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VIDEO :CBC - The Origin of AIDS,Polio

THE ORIGIN OF AIDS  43:49 - 1 year ago 




This documentary profiles the theory that HIV is a Simian Virus which mutated to infect humans when we unknowingly vaccinated millions of Africans with contaminated polio vaccine. The short version - HIV is a human-created pandemic. Serious charges for sure. If you've never heard this theory, watch this video and you'll wanna know more for sure.

State Origin: The Evidence of the Laboratory Birth of AIDS, Issues 0-9587 By Boyd Ed Graves
http://www.huffingtonpost.com/2008/10/01/scientists-trace-the-orig_n_131056.html
http://www.jstor.org/pss/1312149
Read More... VIDEO :CBC - The Origin of AIDS,Polio

Video: An Energy-Independent Future | The Daily Show

Wednesday June 16, 2010
An Energy-Independent Future

Jon Stewart clip 2010.06.16 The history of the dependence on foreign oil, and how and when to stop it. Excellent clip and pretty much says it all on the American political system and the American public's total ignorance on all subjects. It should really be a sad commentary on the system that subjugates its owners. 

The last eight presidents have gone on television and promised to move America towards an energy-independent future.

The Daily Show With Jon StewartMon - Thurs 11p / 10c
An Energy-Independent Future
www.thedailyshow.com
Daily Show Full EpisodesPolitical HumorTea Party

Video: An Energy-Independent Future | The Daily Show | Comedy Central

Read More... Video: An Energy-Independent Future | The Daily Show

Shoe Bomber Sentenced - Judge's Words

Remember the guy who got on a plane with a bomb built into his shoe and tried to light it?
Did you know his trial is over?
Did you know he was sentenced?
Did you see/hear any of the judge's comments on TV or Radio?
Didn't think so.!!!
Everyone should hear what the judge had to say.



Ruling by Judge William Young, US District Court.

Prior to sentencing, the Judge asked the defendant if he had anything to say
His response: After admitting his guilt to the court for the record, Reid
also admitted his 'allegiance to Osama bin Laden, to Islam, and to the
religion of Allah,' defiantly stating, 'I think I will not apologize for my
actions,' and told the court 'I am at war with your country.'

Judge Young then delivered the statement quoted below:

Judge Young: 'Mr. Richard C. Reid, hearken now to the sentence the Court
imposes upon you.

On counts 1, 5 and 6 the Court sentences you to life in prison in the
custody of the United States Attorney General. On counts 2, 3, 4and 7, the
Court sentences you to 20 years in prison on each count, the sentence on
each count to run consecutively. (That's 80 years.)

On count 8 the Court sentences you to the mandatory 30 years again, to be
served consecutively to the 80 years just imposed. The Court imposes upon
you for each of the eight counts a fine of $250,000 that's an aggregate fine
of $2 million. The Court accepts the government's recommendation with
respect to restitution and orders restitution in the amount of $298.17 to
Andre Bousquet and $5,784 to American Airlines.

The Court imposes upon you an $800 special assessment. The Court imposes
upon you five years supervised release simply because the law requires it.
But the life sentences are real life sentences so I need go no further.

This is the sentence that is provided for by our statutes. It is a fair and
just sentence. It is a righteous sentence.

Now, let me explain this to you. We are not afraid of you or any of your
terrorist co-conspirators, Mr. Reid. We are Americans. We have been
through the fire before. There is too much war talk here and I say that to
everyone with the utmost respect. Here in this court, we deal with
individuals as individuals and care for individuals as individuals. As
human beings, we reach out for justice.

You are not an enemy combatant. You are a terrorist. You are not a soldier
in any war. You are a terrorist. To give you that reference, to call you a
soldier, gives you far too much stature. Whether the officers of government
do it or your attorney does it, or if you think you are a soldier, you are
not----- you are a terrorist. And we do not negotiate with terrorists. We
do not meet with terrorists. We do not sign documents with terrorists. We
hunt them down one by one and bring them to justice.

So war talk is way out of line in this court You are a big fellow. But you
are not that big. You're no warrior. I've known warriors. You are a
terrorist. A species of criminal that is guilty of multiple attempted
murders. In a very real sense, State Trooper Santiago had it right when you
first were taken off that plane and into custody and you wondered where the
press and the TV crews were, and he said: 'You're no big deal.'

You are no big deal.

What your able counsel and what the equally able United States attorneys
have grappled with and what I have as honestly as I know how tried to
grapple with, is why you did something so horrific. What was it that led
you here to this courtroom today?

I have listened respectfully to what you have to say. And I ask you to
search your heart and ask yourself what sort of unfathomable hate led you to
do what you are guilty and admit you are guilty of doing? And, I have an
answer for you. It may not satisfy you, but as I search this entire record,
it comes as close to understanding as I know.

It seems to me you hate the one thing that to us is most precious. You hate
our freedom. Our individual freedom. Our individual freedom to live as we
choose, to come and go as we choose, to believe or not believe as we
individually choose. Here, in this society, the very wind carries freedom.
It carries it everywhere from sea to shining sea. It is because we prize
individual freedom so much that you are here in this beautiful courtroom, so
that everyone can see, truly see, that justice is administered fairly,
individually, and discretely. It is for freedom's sake that your lawyers
are striving so vigorously on your behalf, have filed appeals, will go on in
their representation of you before other judges.

We Americans are all about freedom. Because we all know that the way we
treat you, Mr. Reid, is the measure of our own liberties. Make no mistake
though. It is yet true that we will bear any burden; pay any price, to
preserve our freedoms. Look around this courtroom. Mark it well. The
world is not going to long remember what you or I say here. The day after
tomorrow, it will be forgotten, but this, however, will long endure.

Here in this courtroom and courtrooms all across America , the American
people will gather to see that justice, individual justice, justice, not
war, individual justice is in fact being done. The very President of the
United States through his officers will have to come into courtrooms and lay
out evidence on which specific matters can be judged and juries of citizens
will gather to sit and judge that evidence democratically, to mold and shape
and refine our sense of justice.

See that flag, Mr. Reid? That's the flag of the United States of America .
That flag will fly there long after this is all forgotten. That flag stands
for freedom. And it always will.

Mr. Custody Officer. Stand him down.
So, how much of this Judge's comments did we hear on our TV sets? We need
more judges like Judge Young. Pass this around. Everyone should and needs
to hear what this fine judge had to say. Powerful words that strike home.

http://www.snopes.com/politics/soapbox/shoebomb.asp

Read More... Shoe Bomber Sentenced - Judge's Words

I have been tortured by your corrupt system far to long

When will some one care about helping me and not taking my non existent money.
I have nothing left I am hungry and don’t know how to pay the bills any more. But those that are supposed to help me have what I need and they go about their way as if i don’t even exist if I cant pay.

I have been tortured by your corrupt anti man system far to long. It has cost me my family, my children, their and my future, no one cares. It is cruel and inhuman to the point of sickness years of lies and theft goes unanswered, yet all stand by and watch me drown and relish the fact that if I could pay it would be different.

Will some one finally do something?
I doubt it.
Read More... I have been tortured by your corrupt system far to long

Did we really land Men on the Moon?

Did we really land Men on the Moon?
51:16 - 4 years ago

Greatest hoax yet, see astronauts refuse to swear on the bible they flew to the moon. moon landings,

 WIKI "Different Moon landing conspiracy theories claim that some or all elements of the Apollo Project and the associated Moon landings were falsifications staged by NASA and members of other organizations. Since the conclusion of the Apollo program, a number of related accounts espousing a belief that the landings were faked in some fashion have been advanced by various groups and individuals. Some of the more notable of these various claims include allegations that the Apollo astronauts did not set foot on the Moon; instead NASA and others intentionally deceived the public into believing the landings did occur by manufacturing, destroying, or tampering with evidence, including photos, telemetry tapes, transmissions, and rock samples."

http://www.imdb.com/title/tt0277642/
http://en.wikipedia.org/wiki/Moon_landing_conspiracy_theories
http://science.nasa.gov/science-news/science-at-nasa/2001/ast23feb_2/
http://www.unmuseum.org/moonhoax.htm
http://www.jimloy.com/pseudo/apollo.htm

Read More... Did we really land Men on the Moon?

UFO - The Secret NASA Transmissions

The Smoking Gun 2004 1:29:09



EBE Award Winner! Best Film International UFO Congress Film Festival. On March 11, 2000, in front of an assembled audience of UFO enthusiasts and the media, evidence was presented that would appear to indicate the existence of, not one, but two types of unknown extraterrestrial lifeforms. Labeled Phenomena One and Phenomena Two by a man who spent several years recording and logging thousands of hours of NASA space shuttle transmissions, this historic footage and the story that lay behind its discovery can now be revealed. 90 min
 http://www.imdb.com/title/tt0345911/  
Read More... UFO - The Secret NASA Transmissions

CBC - The CIAs Secret War

CBC Passionate Eye:The CIA's Secret War
51:37 - 3 years ago
Sunday October 15, 2006 at 10pm ET/PT on CBC Newsworld
repeating Monday May 28 at 10pm PT on CBC Newsworld
Did the CIA abduct, torture and hold men prisoner on European soil? President Bush recently acknowledged that the CIA has operated secret prisons. What happened in these secret prisons in Europe? Filmmakers Arnaud Muller and Steve Baumann conduct their own investigation around a European Parliament inquiry to help answer these troubling questions.

When several CIA airplanes suspiciously land in northern Poland, it raises questions about CIA activities in Europe. In Macedonia, a German citizen claims he was abducted and held prisoner in Kabul for five months by U.S. agents. Is there evidence these strange activities took place? The CIA's Secret War provides proof, for the first time, that these abductions and confinements are no coincidence, but the result of political decisions to use information obtained through torture in countries where torture is standard practice.

Taking viewers into the heart of a troubling European parliamentary inquiry-an inquiry that in many ways parallels Canada's own Maher Arar inquiry-The CIA's Secret War sparks a debate on the role of democratic nations in the "war on terror". The CIA's Secret War is directed by Arnaud Muller and Steve Baumann.


Read More... CBC - The CIAs Secret War

Medical researchers patented AIDS cure in 1990




Kaali outlined two methods for treating an AIDS patient with this new therapy: One method involved removing a small amount of blood, electrifying it and then returning it to the patient's body. The second method involved sewing a miniature electrifying power supply along with two tiny electrodes directly into the lumen of an artery. For long term treatment, the mini electrifying unit needed to be removed and relocated to a new artery site after 30-45 days since scar tissue and calcification forming around the implant unit would lead to artery blockage. Kaali (along with co-inventor Peter Schwolsky) filed for a patent on this implantable electrifying device on Nov 16, 1990 and nine months later was granted patent #5,139,684 on August 18, 1992.--Juris Doctor Boyd Graves

United States Patent 5,139,684
Kaali, etal. August 18, 1992
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Electrically conductive methods and systems for treatment of blood and other body fluids and/or synthetic fluids with electric forces

Abstract
A new process and system for treatment of blood and/or other body fluids and/or synthetic fluids from a donor to a recipient or storage receptacle or in a recycling system using novel electrically conductive treatment vessels for treating blood and/or other body fluids and/or synthetic fluids with electric field forces of appropriate electric field strength to provide electric current flow through the blood or other body fluids at a magnitude that is biologically compatible but is sufficient to render the bacteria, viruses, and/or fungus ineffective to infect normally healthy cells while maintaining the biological usefulness of the blood or other body fluids. For this purpose the low voltage electric potentials applied to the treatment vessel should be of the order of from about 0.2 to 12 volts and should produce current flow densities of from one microampere per square millimeter of electrode area exposed to the fluid being treated to about one milliampere per square millimeter. Treatment time within this range of parameters may range for a period of time from about one minute to about 12 minutes.
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Inventors: Kaali; Steven (88 Ashford Ave., Dobbs Ferry, NY 10522); Schwolsky; Peter M. (4101 Cathedral Ave., NW., Washington, DC 20016)
Appl. No.: 615800
Filed: November 16, 1990

Current U.S. Class: 205/701; 204/164; 204/275.1; 204/278.5; 210/243; 210/748; 422/22; 422/44; 604/6.08; 607/116
Intern'l Class: B01D 035/06; A61K 041/00
Field of Search: 210/748,243,764 128/419 R,421,783,784 604/4 422/22,44 204/131,186,164,242,275,302,305
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References Cited [Referenced By]

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U.S. Patent Documents
592735 Oct., 1897 Jones 204/242.
672231 Apr., 1901 Lacomme 204/275.
2490730 Dec., 1949 Dubilier 204/305.
2955076 Oct., 1960 Gossling 195/78.
3692648 Sep., 1972 Matloff et al. 204/129.
3753886 Aug., 1973 Myers 204/186.
3878564 Apr., 1975 Yao et al. 210/648.
3965008 Jun., 1976 Dawson 422/22.
3994799 Nov., 1976 Yao et al. 210/321.
4188375 Feb., 1980 Straub 424/88.
4473449 Sep., 1984 Michaels et al. 204/101.
4520113 May., 1985 Gallo et al. 436/504.
4616640 Oct., 1986 Kaali et al. 128/130.
4770167 Sep., 1988 Kaali et al. 128/788.
4932421 Jun., 1990 Kaali et al. 128/831.
5049252 Sep., 1991 Murrell 210/243.
5058065 Oct., 1991 Slovak 128/783.
Foreign Patent Documents
995848 Feb., 1983 SU 210/243.

Other References
Proceedings of the Society for Experimental Biology & Medicine, vol. 161, (1979), pp. 204-209--"Inactivation of Herpes Simples Virus with Methylene Blue, Light and Electricity"--Mitchell R. Swartz et al.
Journal of the Clinical Investigation published by the American Society for Clinical Investigations, Inc., vol. 65, Feb. 1980, pp. 432-438--"Mechanisms of Photodynamic Inactivation of Herpes Simplex Viruses"--Lowell E. Schnipper et al.
Journal of Clinical Microbiology, vol. 17, No. 2, Feb. 1983, pp. 374-376--"Photodynamic Inactivation of Pseudorabier Virus with Methylene Blue Dye, Light and Electricity"--Janine A. Badyisk et al.

Primary Examiner: Dawson; Robert A.
Assistant Examiner: Kim; Sun Uk
Attorney, Agent or Firm: Helzer; Charles W.
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Parent Case Text

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FIELD OF INVENTION

This is a continuation-in-part application of prior U.S. patent application Ser. No. 07/562,721 filed Aug. 6, 1990, now abandoned.
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Claims

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What is claimed is:

1. An electrically conductive vessel for direct electric treatment of bacteria, and/or virus, parasites and/or fungus entrained in blood and/or other body fluids and/or synthetic fluids contained within or flowing through the vessel in the presence of electric field forces, said electrically conductive vessel being fabricated with only biologically compatible material containing the fluid being treated and with an array of at least two or more spaced-apart, opposed electrically conductive electrode segments formed of biologically compatible conductive material on or in the interior surface of the vessel and exposed to blood or other fluids contained in or flowing through the vessel, said electrically conductive electrode segments being electrically isolated from each other and extending over or through a portion of the length of the vessel, and means for applying different polarity low voltage non biologically damaging electric potentials to the electrically conductive electrode segments whereby electrical field forces are produced between the electrically conductive electrode segments that induce biologically compatible current flow through the blood and/or other fluids contained in or flowing through the vessel so as to attenuate bacteria, virus, parasites and/or fungus contained in the blood and/or other fluids by the action of the electric current flow therethrough to thereby render the bacteria, virus, parasites and/or fungus ineffective while not impairing the biological usefulness of the fluids.

2. An electrically conductive vessel according to claim 1 wherein the low voltage electric potentials are in the range from about 0.2 volts to 12 volts and induce electric current flow densities in the blood or other fluids of from one microampere per square millimeter (1 .mu.A/mm.sup.2) to about one milliampere per square millimeter (1 mA/mm.sup.2).

3. An electrically conductive vessel according to claim 2 wherein the walls of the vessel itself are formed from electrically conductive polymer material that is compatible with human tissue and blood and/or other body fluids with the electrically conductive portions being formed into desired patterns of spaced apart electrically conductive electrode segments physically interconnected by integrally formed electrically insulating tubing wall portions which electrically isolate a first array of positive electrode portions from a second opposite polarity array of negative electrode portions.

4. An electrically conductive vessel according to claim 3 wherein the vessel is in the form of tubing and electrically conductive electrode segments are in the form of zebra stripes which extend longitudinally parallel with the longitudinal axis of the tubing with the alternate electrically conductive electrode stripes being separated by alternate electrically insulating stripes for electrically isolating the alternate electrically conductive electrode stripes one from the other, a first set of alternate ones of the electrically conductive electrode stripes being electrically connected in common to a first annular terminal buss formed on and circumferentially surrounding the tubing and electrically isolated from the remaining second set of alternate electrically conductive electrode stripes, said first annular terminal buss being designed for connection to a first polarity source of electric excitation potential, and a second annular terminal buss circumferentially surrounding the tubing and electrically connected to the remaining second set of alternate electrically conductive electrode stripes, said second annular terminal buss being electrically isolated from the first annular terminal buss and the first set of alternate electrically conductive electrode stripes and being designed for connection to a second polarity source of electric excitation potential having a polarity opposite to that of the first polarity source of potential.

5. Electrically conductive tubing according to claim 4 wherein the tubing is inserted in a flow-thru blood treatment system between a hypodermic needle employed to withdraw and/or supply blood from a donor and/or to a recipient and/or a blood storage receptacle or to a patient in a blood recycling system.

6. Electrically conductive tubing according to claim 5 wherein a blood pump is inserted in the tubing between a donor and a recipient and/or a receptacle, and the tubing is part of a system which further includes means for electrically isolating the blood pump from the electrically conductive tubing, means for regulating blood flow from the output of the blood pump, and means for electrically interconnecting the input and output sides of the tubing around the blood pump and blood flow regulating means whereby electrical continuity is maintained throughout a desired length of the tubing.

7. An electrically conductive vessel according to claim 3 wherein the vessel is in the form of tubing and the electrically conductive electrode segments are in the form or zebra stripes which extend radially around the inside diameter of the tubing in alternating conductive and insulating annular bands whereby alternate conductive bands are electrically isolated one from the other by respective insulating bands, a first set of alternate ones of the electrically conductive annular electrode stripes being electrically connected in common to a first longitudinally extending terminal buss that is formed on the tubing in parallel with the longitudinal axis thereof and electrically isolated from the remaining second set of alternate electrically conductive annular electrode stripes, said first longitudinally extending terminal buss being designed for connection to a first polarity source of electric excitation potential, and a second longitudinally extending terminal buss electrically connected to the remaining second set of alternate electrically conductive annular electrode stripes, said second longitudinally extending terminal buss being electrically isolated from the first longitudinally extending terminal buss and the first set of alternate electrically conductive annular electrode stripes and being designed for connection to a second polarity source of electric excitation potential of opposite polarity from that of the first polarity source of excitation potential.

8. Electrically conductive tubing according to claim 7 wherein the tubing is inserted in a flow-thru blood treatment system between a hypodermic needle employed to withdraw and/or supply blood from a donor and/or to a recipient and/or a blood storage receptacle or a patient in a blood recycling system.

9. Electrically conductive tubing according to claim 8 wherein a blood pump is inserted in the tubing between a donor and a recipient and/or a receptacle and the tubing is part of a system that further includes means for electrically isolating the blood pump from the electrically conductive tubing, means for regulating blood flow from the output of the blood pump, and means for electrically interconnecting the input and output sides of the tubing around the blood pump and the blood flow regulating means whereby electrical continuity is maintained throughout a desired length of the tubing.

10. An electrically conductive vessel according to claim 2 wherein the vessel is in the form of tubing and is inserted in a flow-thru blood treatment system between a hypodermic needle employed to withdraw and/or supply from a donor and/or to a recipient and/or a blood storage receptacle or to a patient in a blood recycling system.

11. An electrically conductive vessel according to claim 2 wherein the vessel is part of a system and is in the form of tubing and a blood pump is inserted in the tubing between a donor and a recipient or a receptacle, and the system further includes means for electrically isolating the blood pump from the electrically conductive vessel, means for regulating blood flow rate from the blood pump output and means for maintaining electrical continuity throughout a desired length of the conducting vessel.

12. An electrically conductive vessel according to claim 2 wherein the vessel is in the form of tubing and the electrically conductive electrode segments are in the form of zebra stripes which extend longitudinally parallel with the longitudinal axis of the tubing with the alternate electrically conductive electrode stripes being separated by alternate electrically insulating stripes for electrically isolating the alternate electrically conductive electrode stripes one from the other, a first set of alternate ones of the electrically conductive electrode stripes being electrically connected in common to a first annular terminal buss formed on and circumferentially surrounding the tubing and electrically isolated from the remaining second set of alternate electrically conductive electrode stripes, said first annular terminal buss being designed for connection to a first polarity source of electric excitation potential, and a second annular terminal buss circumferentially surrounding the tubing and electrically connected to the remaining second set of alternate electrically conductive electrode stripes, said second annular terminal buss being electrically isolated from the first annular terminal buss and the first set of alternate electrically conductive electrode stripes and being designed for connection to a second polarity source of electric excitation potential having a polarity opposite to that of the first polarity source of potential.

13. Electrically conductive tubing according to claim 12 wherein the tubing is inserted in a flow-thru blood treatment system between a hypodermic needle employed to withdraw and/or supply blood from a donor and/or a recipient and/or a blood storage receptacle or to a patient in a blood recycling system.

14. Electrically conductive tubing according to claim 12 wherein a blood pump is inserted in the tubing between a donor and a recipient and/or a receptacle, and the tubing is part of a system which further includes means for electrically isolating the blood pump from the electrically conductive tubing, means for regulating blood flow rate from the blood pump output, and means for electrically interconnecting the input and output sides of the tubing around the blood pump and the blood flow regulating means whereby electrical continuity is maintained throughout a desired length of the tubing.

15. An electrically conductive tubing according to claim 2 wherein the vessel is in the form of tubing and the electrically conductive electrode segments are in the form of zebra stripes which extend radially around the inside diameter of the tubing in alternating conductive and insulating annular bands whereby alternate conductive bands are electrically isolated one from the other by respective insulating bands, a first set of alternate ones of the electrically conductive annular electrode stripes being electrically connected in common to a first longitudinally extending terminal buss that is formed on the tubing in parallel with the longitudinal axis thereof and electrically isolated from the remaining second set of alternate electrically conductive annular electrode stripes, said first longitudinally extending terminal buss being designed for connection to a first polarity source of electric excitation potential, and a second longitudinally extending terminal buss electrically connected to the remaining second set of alternate electrically conductive annular electrode stripes, said second longitudinally extending terminal buss being electrically isolated from the first longitudinally extending terminal buss and the first set of alternate electrically conductive annular electrode stripes and being designed for connection to a second polarity source of electric excitation potential of opposite polarity from that of the first polarity source of excitation potential.

16. Electrically conductive tubing according to claim 15 wherein the tubing is inserted in a flow-thru blood treatment system between a hypodermic needle employed to withdraw and/or supply blood from a donor and/or to a recipient and/or a blood storage receptacle or to a patient in a blood recycling system.

17. Electrically conductive tubing according to claim 16 wherein a blood pump is inserted in the tubing between a donor and a recipient and/or a receptacle, and the tubing is part of a system that further includes means for electrically isolating the blood pump from the electrically conductive tubing, means for regulating blood flow from the output of the blood pump, and means for electrically interconnecting the input and output side of the tubing around the blood pump and blood flow regulating means whereby electrical continuity is maintained throughout a desired length of the tubing.

18. A fluid treatment process for attenuating bacteria, and/or virus, parasites, and/or fungus, existing in blood and/or other body fluids and/or synthetic fluids within a treatment vessel having only biologically compatible internal and electrode surfaces therein contacting fluid being treated thereby maintaining the biological usefulness of the blood or other fluids being treated comprising subjecting the fluid within the treatment vessel to low voltage, low current non biologically damaging electric field forces within an electric field for producing a biologically compatible current flow through the blood or other fluids for a predetermined period of time sufficient to attenuate bacteria and/or virus, parasites and/or fungus contained in the blood or other fluids to thereby render them ineffective while maintaining and not impairing the biological usefulness of the fluids being treated.

19. The product of the process according to claim 18.

20. A fluid treatment process according to claim 18 wherein the low voltage electric potentials are in the range from about 0.2 to 12 volts and induce electric current flow densities in the blood or other fluids of from one microampere per square millimeter (1 .mu.A/mm.sup.2) to about one milliampere per square millimeter (1 mA/mm.sup.2).

21. The product of the process according to claim 20.

22. A fluid treatment system for attenuating bacteria, and/or virus, and/or parasites and/or fungus existing in blood and/or other body fluids and/or synthetic fluids being treated without biological damage to the blood or other fluids comprising an electrically conductive vessel formed at least in part of biologically compatible conductive material for contacting blood or other fluids to be treated, means for subjecting the contained blood or other fluids within the conductive vessel to low voltage, low current electric field forces for producing biologically compatible current flow through the blood or other fluids for a predetermined period of time sufficient to attenuate bacteria and/or virus, and/or parasites and/or fungus contained in the blood or other fluids to thereby render such contaminants ineffective while maintaining the biological usefulness of the blood or other fluids.

23. A fluid treatment system according to claim 22 wherein the low voltage electric potentials are in the range from about 0.2 to 12 volts and produce electric current flow densities in the blood or other fluids of from one microampere per square millimeter (1 .mu.A/mm.sup.2) to about one milliampere per square millimeter (1 mA/mm.sup.2).

24. A body fluid treatment system according to claim 22 wherein the system comprises a plurality of components including an electric power source all of which are miniaturized and implanted in the body of a patient being treated to form a closed loop, continuous recirculating body fluid treatment system.

25. A body fluid treatment system according to claim 22 wherein the conductive vessel is in the form of an open ended tube to allow flow-thru treatment of blood and other body fluids and is miniaturized along with an electric power source for supply of electric potentials thereto whereby the system may be implanted in human beings and other mammals to operate as a continuous recirculating body fluid treatment process.

26. A fluid treatment system according to claim 22 wherein the conductive vessel in the vicinity of the low voltage, low current electric field forces is provided with an enlarged cross sectional area wherein increased quantities of blood or other fluids are allowed to flow through the vessel thereby increasing the through-put and/or effectiveness of the treatment accomplished within the vessel for a given dwell time.

27. A fluid treatment system according to claim 26 wherein the electrically conductive vessel comprises an enlarged rectangular-shaped body of electrical insulating material having a plurality of parallel, longitudinally extending tubular openings formed all the way through the insulating material from one end to the other and having spaced-apart electrically conductive metal strips secured to respective opposite sides of all of the tubes in opposed, parallel relationship, the conductive strips of one polarity electric potential extending out of the ends of the tubes on one side or end of the body of electrical insulating material to a conductive surface forming a terminal buss for all conductive strips of a given polarity potential, and the remaining set of conductive strips projecting out of the opposite ends of the respective tubes on the opposite end of the insulating block to engage a conductive terminal surface for the opposite polarity potential, and header reservoirs formed on each of the ends of the body of electrical insulating material into which the ends of the tubular passageways are connected each header having a respective inlet or outlet opening for the supply of blood and/or other body fluids for treatment thereto.

28. A fluid treatment system according to claim 27 wherein the enlarged insulating block member is cylindrically shaped and the header reservoirs at each end of the block member are correspondingly cylindrically shaped.

29. A fluid treatment system according to claim 27 wherein selectively operated gas vents are provided in the top of the respective reservoirs of the electrically conductive vessel.

30. A body fluid treatment system according to claim 26 wherein the electrically conductive vessel is in the form of an enlarged cross sectional area treatment vessel of substantially greater cross sectional area than the inlet and outlet conducts supplying body fluids to be treated to the vessel and wherein the enlarged cross sectional area vessel is included in a blood transfer system between a hypodermic needle employed to withdraw and/or supply blood from a donor and/or to a recipient and/or a blood storage receptacle or to a patient in a continuous flow-thru blood recycling system.

31. A body fluid treatment system according to claim 30 wherein a blood pump is inserted in the flow path of the blood or other body fluid either to or from the enlarged cross sectional area vessel, or both, and are located in a tubing system between the donor and recipient or receptacle, and the system further includes means for regulating blood flow rate from or to the enlarged cross sectional area treatment vessel via the inlet or outlet pumps or both.
--------------------------------------------------------------------------------

Description

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This invention relates to novel electrically conductive methods and systems employing electrically conductive vessels provided with electrically conductive surfaces for use in subjecting blood and/or other body fluids and/or synthetic fluids such as tissue culture medium to direct treatment by electric forces.

BACKGROUND PROBLEM

It is now well known in the medical profession and the general public that blood collected in a blood bank from a large number of donors may be contaminated by contaminants such as bacteria, virus, parasites or fungus obtained from even a single donor. While screening of donors has done much to alleviate this problem, the screening of donors can and does miss occasional donors whose blood is unfit for use. When this occurs and the unfit blood is mixed with otherwise usable blood, the entire batch must be discarded for transfusion purposes. Because of this problem, the present invention has been devised to attenuate any bacteria, virus (including the AIDS HIV virus), parasites and/or fungus contained in blood contributed by a donor to the point that any such contaminant is rendered ineffective for infecting a normally healthy human cell, but does not make the blood biologically unfit for use in humans. Similar problems exist with respect to the treatment of other body fluids, such as amniotic fluids. The treatment method and system is also applicable to mammals other than humans.

In addition to the above, there is a need for methods and systems for the treatment of blood and other body fluids both in in-situ processing wherein the treated blood and/or other body fluids are withdrawn from the body, treated and then returned to the body in a closed loop, recirculating treatment process that is located near but outside the patient's body, or the treatment can be effected through implanted treatment system components.

SUMMARY OF INVENTION

The present invention provides new electrically conductive methods and systems for transferring blood or other body fluids, such as amniotic fluids, and/or synthetic fluids such as tissue culture medium from a donor to a transfusion recipient or to a storage receptacle, or for recirculating a single donor's blood or other body fluids through components of a treatment system external of the body or by implant devices for purging contaminants using a novel electrically conductive vessel for direct electric treatment of blood or other body fluids, such as amniotic fluids, with electric field forces of appropriate electric field strength to attenuate such contaminants to the extent that bacteria, virus, or fungus, or parasites contained in the blood or other body fluids are rendered ineffective to infect or affect normally healthy human cells. The treatment, however, does not render the blood or other body fluids biologically unfit for use in humans or other mammals after the treatment. The new methods and systems according to the invention achieve these ends without requiring time consuming and expensive processing procedures and equipment in addition to those normally required in the handling of blood or other body fluids or synthetic fluids. The invention achieves the electric field force treatment during the normally occurring transfer processing from a donor to a recipient or to a collection receptacle, or recirculation of a single donor's blood or other body fluids, such as amniotic fluids.

BRIEF DESCRIPTION OF DRAWINGS

The above and many other objects, features and attendant advantages of this invention will be appreciated more readily as the invention becomes better understood from a reading of the following detailed description, when considered in connection with the accompanying drawings, wherein like parts in each of the several figures are identified by the same reference characters, and wherein:

FIG. 1 is a diagrammatic, fragmentary, elevational view of a new blood transfer system using a novel electrically conductive treatment vessel in the form of conductive tubing to directly treat blood being transferred to a storage receptacle with electric field forces according to the invention;

FIG. 2 is an enlarged, horizontal cross sectional view of the novel electrically conductive tubing treatment vessel taken across lines 2--2 of FIG. 1;

FIG. 3 is a longitudinal, vertical sectional view of the novel electrically conductive tubing treatment vessel taken along the staggered section lines 3--3 of FIG. 2;

FIG. 4 is a view similar to FIG. 2 showing a different construction of the novel electrically conductive tubing treatment vessel;

FIG. 5 is a view similar to FIG. 3, taken along the staggered section lines 5--5 of FIG. 4;

FIG. 6 is a diagrammatic, fragmentary, elevational view showing a different modification of a novel blood transfer system using the novel electrically conductive tubing treatment vessel, and which employs a blood pump and a blood flow regulator;

FIG. 7 is an enlarged cross sectional view, similar to FIG. 2 that shows an electrically conductive tubing treatment vessel fabricated from longitudinally extending, integrally molded strips of alternate polarity, conductive polymer interconnected by integrally molded, insulating, longitudinally extending strips made of polymer or other insulating material;

FIG. 8 is a diagrammatic, fragmentary elevational view showing a different form of a blood transfer system according to the invention wherein a small electrically conductive vessel in the form of a short piece of tubing and a miniaturized battery power source are implanted in the arm of a human being to provide a novel electrically conductive blood and other body fluid treatment system which operates in a closed loop, recirculating manner;

FIG. 9 is a partial, diagrammatic sectional view of the upper arm portion of a human being and shows in greater detail the construction of a specially designed miniaturized, electrically conductive treatment vessel with associated miniaturized battery electric power source for use in the implant treatment system shown in FIG. 8;

FIG. 10 illustrates the details of construction of a somewhat different form of miniaturized electrified treatment tubing for use in an implanted treatment system of the type shown in FIG. 8 and built according to the invention;

FIGS. 11 and 11A illustrate still a different construction for the electrified treatment tubing for use in practicing the invention wherein the tubing has a square or rectangular cross section with upper and lower conductive sides and intervening right and left sides separating the two conductive sides made from plastic or other suitable electrical insulating material;

FIG. 12 is a perspective top and side view of a novel electrified, closed, octagonally-shaped, flat, box-like treatment vessel having an enlarged cross sectional area relative to the cross sectional diameter of the inlet and outlet tubes supplying the interior of the treatment vessel;

FIG. 12A is a partial, cross sectional view of the enlarged treatment vessel shown in FIG. 12;

FIG. 13 is a perspective view of a second form of enlarged cross sectional area treatment vessel having an exterior shape similar to that of FIG. 12, but wherein the electrically conductive electrodes of the treatment vessel comprise interleaved conductive plates with one set of alternate ones of the plates being electrically insulated from the remaining set, and wherein different polarity electric potentials are applied to the respective sets. If desired, the electrode plates may be formed from an electrically conductive porous material;

FIG. 13A is a partial, cross sectional view taken through the electrically conductive treatment vessel shown in FIG. 13;

FIG. 13B is a sectional view taken through staggered line 13B--13B of FIG. 13A;

FIG. 14 is a longitudinal sectional view of still a different form of enlarged diameter electrified treatment vessel wherein the vessel is in the form of an elongated cylinder, and the sets of conductive electrodes mounted therein are concentrically arrayed within the interior of the treatment vessel and maintained at different electric potentials;

FIG. 14A is a cross sectional view of FIG. 14 taken through plane A--A;

FIG. 15 is an enlarged longitudinal sectional view of still another form of an enlarged cross sectional area treatment vessel according to the invention wherein the electrically conductive electrodes of the treatment vessel are comprised by longitudinally extending needle-like electrodes with alternate ones of the needle-like electrodes being provided with opposite polarity electric potentials;

FIG. 15A is a cross sectional view of the treatment vessel shown in FIG. 15 taken through plane A--A of FIG. 15;

FIG. 16 is a perspective view of still another form of enlarged cross sectional area treatment vessel according to the invention wherein the treatment vessel comprises a relatively large block of insulating material having parallel, longitudinally extending, open ended tubes formed through its length. The tubes are provided with electrically separated, opposed, parallel extending conductive plate electrodes which have opposite polarity electric potentials applied thereto. The ends of the tubes open into and are supplied from, or supply, respective reservoirs formed on the respective ends of the central block of insulating material containing the tubes, with inlet and outlet conduits for body fluids to be treated connected to the free ends of the respective reservoirs;

FIG. 16A is a partial cross-sectional view taken through 16A--16A of FIG. 16;

FIG. 17 is a perspective view of an enlarged cross sectional area treatment vessel similar to FIG. 16 wherein the body of the treatment vessel is cylindrical in nature;

FIG. 18 is a diagrammatic, fragmentary elevational view of a human blood or other body fluid treatment system according to the invention employing one of the larger cross sectional dimension fluid treatment vessels shown in any one of FIGS. 12-16 of the drawings, and which is suitable for use in a continuous flow through recirculating body fluid treatment system;

FIG. 19 is a diagrammatic, fragmentary elevational view of still another human blood or other body fluid, closed loop, recirculating treatment system according to the invention designed for use with the enlarged diameter fluid treatment vessels illustrated in FIGS. 12-16, and which employs both inlet and outlet fluid pumps on each side of the treatment vessel. With this arrangement the system can be operated in an intermittent manner to allow batch treatment of the body fluids to fully take plate before passage of the body fluids being treated back to the patient;

FIG. 20 is a partially disassembled, perspective view of a non-flow through, single batch, body fluid treatment vessel according to the invention which is open to atmosphere on the upper side thereof to allow a clear view of the body fluids being treated during operation of the process; and

FIG. 20A is a diagrammatic, fragmentary side view of an assembled, open sided, treatment vessel of the type shown in FIG. 20 connected to a source of electric power.

BEST MODE OF PRACTICING INVENTION

FIG. 1 is a schematic illustration of one form of novel blood transfer system according to the invention. FIG. 1 shows an electrically conductive blood treatment vessel constructed according to the invention which is in the form of intravenous-type tubing 11 interconnected between a hypodermic needle 12 and a blood storage receptacle 14. The needle 12 is inserted in an artery or vein of the arm 13 of a blood donor and the tubing 11 leads from the arm 13 to the receptacle 14. Alternatively, the system could be set up to transfer blood from the storage receptacle 14 to the arm of a recipient or could be designed to recirculate the blood through electrified tubing 11 back to the donor. The electrically conductive tubing 11 may be of any desired length as indicated by the break at 15 so that it can be appropriately set up to lead from a comfortable position for the donor from whose arm 13 the blood is being taken to a proper storage location for the receptacle 14. The greater the length of the electrified portion of tubing 11, then the more extended is the exposure of the blood (or other body fluid) to the electric field force effects and low level, biologically compatible current flow through the body fluid being treated thereby assuring adequate electrification treatment of the fluid without impairing the biological usefulness of the blood or other body fluid being treated.

FIG. 2 is a cross sectional view of the electrically conductive tubing 11 taken through plane 2--2 of FIG. 1. The tubing 11 may be from 1 to about 20 millimeters in inside diameter, although it may be larger or smaller in diameter depending upon the intended application. For example, if the blood transfer system is for the purpose shown in FIG. 6, then the tubing may have a cross sectional dimension of about 5 millimeters. However, if the intended use is in an implanted blood transfer system as shown in FIG. 8, then the tubing diameter must be designed to result in a flow-through rate corresponding to the natural circulatory blood flow rate of the patient in which the system is implanted, and must be long enough to assure effective electrification treatment at the flow rate selected. The tubing 11 is formed from plastic, rubber, medical grade polymer, or other suitable material which is compatible with human fluids and/or tissue. A plurality of physically separated, electrically conductive surface segments form opposed, parallel electrodes shown at 16 and 16A on the inside of tubing 11 from electrically conductive materials such as platinum, platinum alloys, silver, silver or platinum covered alloys, or other similar conductive materials such as conductive polymers, or silver or platinum covered polymers which are compatible with human fluids and tissue. The spacing between opposed electrodes 16 and 16A is of the order of 1 to 19 millimeters and perhaps may be more or less dependent upon the application and the conductivity of the body fluids being treated.

FIG. 3 is a longitudinally extending sectional view along the axis of tubing 11 taken through staggered section lines 3--3 of FIG. 2. From FIG. 3 of the drawings it will be seen that the electrically conductive surface segments 16 and 16A all comprise longitudinally extending, zebra-like stripe or strip electrodes which extend longitudinally in parallel with the longitudinal axis of the tubing 11. In between each longitudinally extending conductive stripe electrode 16 or 16A is a longitudinally extending electric insulating area 17 which electrically isolates the alternate electrically conductive, zebra-like stripe electrodes 16 and 16A one from the other.

As best shown in FIG. 3, a first set of alternate electrically conductive surface stripes 16 are electrically connected in common to a first annular terminal buss 18 which circumferentially surrounds the tubing 11 and is embedded within the sidewalls of the tubing 11 at a suitable point along it length. The design is such that the first annular terminal buss 18 is electrically isolated from the remaining second set of alternate, electrically conductive surface stripe electrodes 16A and is electrically connected through a conductor terminal 19 to a first polarity (positive) source of electric excitation potential shown in FIG. 1 as a battery 20. As best depicted in FIG. 2, all of the first set of positive electrically conductive stripes 16 are physically and electrically connected in common to the first annular terminal buss 18 so that all of the conductive stripes 16 are maintained at a constant, positive polarity electric excitation potential.

A second annular terminal buss 21, which circumferentially surrounds the tubing 11, is embedded within the tubing 11 at a point along its length displaced from the position of the first annular terminal buss 18 and is spaced inwardly towards the inside diameter of the tubing relative to the first annular buss 18. By this arrangement it is possible to electrically connect the remaining second set of alternate electrically conductive surface stripes 16A in common to the second annular terminal buss 21 in a manner such that the second annular terminal buss is electrically isolated from the first annular terminal buss 18 as well as the first set of alternate electrically conductive surface stripes 16. As shown in FIG. 3, the second annular terminal buss 21 is provided with an outside terminal conductor connection 22 for connecting the annular buss 21 to a negative polarity source of electric potential on the battery 20 as shown in the system drawing of FIG. 1. The second set of alternate electrically conductive surface stripes 16A are all provided with internal connector studs which physically and electrically connect all of the 16A stripes in common to the second annular terminal buss 21 so that all of these conductive stripes will be maintained at a negative polarity potential opposite to that from the positive polarity potential applied to the first set of electrically conductive stripes 16 by annular buss 18.

As best shown in FIG. 1, the source of electric potential may constitute a direct current voltage battery 20 connected to the conductor terminals 19 and 22 through electric supply conductors 23 and 24 preferably by a double pole, double throw, on-off control switch 25. In preferred embodiments of the invention, voltage controlling variable resistors 26 and 27 also are included in the electric supply conductors 23 and 24 in order to control the value of the excitation voltage developed between the alternate sets of conductive surface stripes 16, 16A. While a battery has been illustrated as a source of direct current excitation potential in the system of FIG. 1, it is believed obvious to those skilled in the art that any known direct current source of excitation potential could be used in place of the battery 20.

In operation, the donor whose blood is to be taken, or the recipient who is to be given blood, or is to have his or her blood recycled, is placed on a cot with his or her arm 13 extended and the interconnecting electrically conductive tubing 11 having the hypodermic needle 12 for withdrawal, or supplying, or recycling of blood set up as shown in FIG. 1. When both the donor/recipient and the system is in readiness, the control switch 25 is closed so that an electric field is built up across the oppositely disposed electrically conductive zebra-like stripes 16, 16A, etc. Voltages of the order of from 0.2 to 12 volts are applied to the conductive surfaces 16, 16A. It is important to note that the hypodermic needle should be electrically isolated via conventional electrically insulating IV tubing from any of the zebra stripe electrodes 16, 16A so that the donor/recipient does not receive a shock. By this precaution, he or she will not even be aware of the existence of the electric field within the electrically conductive tubing 11. With the transfer system thus conditioned, the hypodermic needle is inserted into a vein in the donor's/recipient's arm and blood is withdrawn, given, or recycled through tubing 11.

As the blood passes through the electric fields produced within the electric conductive tubing 11 it will be subjected to and treated by biologically compatible electric current flow through the blood or other body fluid with a current density that ranges from from one microampere per square millimeter (1 .mu.A/mm.sup.2) of electrode cross sectional area exposed to the fluid to about one milliampere per square millimeter (1 mA/mm.sup.2) dependent upon field strength of the electric field gradient existing between electrodes 16 and 16A, the distance between the electric electrodes 16, 16A and the conductivity (resistivity) of the body fluid being treated. Recent experiments have proven that exposure to electric fields induced by supply voltages of 2-4 volts produces electric current flow through blood of the order of 1 to 100 microamperes. Effectiveness is dependent primarily upon length of time of treatment (which may range from about one to twelve minutes) and the magnitude of the biologically compatible current flow at current densities within the range noted above. For example, treatment of AIDS virus in media at 100 microamperes for 3 minutes has been observed to substantially attenuate (render ineffective) the AIDS virus. Treatment at other current densities and lengths of time will have a similar attenuating effect. By controlling the length of time and field strength values that blood and/or other body fluids is subjected to the electric field forces, undesirable contaminants such as virus, bacteria, fungus and/or parasites will be adequately attenuated. The contaminants are rendered ineffective by the sustained action of the electric current as the blood travels from the needle 12 to the storage bag 14, or vice versa, or in a recycling mode. The length of travel of the blood through the sustained electric field induced current flow also can be adjusted so that the blood is subjected to the electric field force for time periods of the order of from about 1 to 12 minutes at least. At the current noted above this is believed adequate to attenuate (render ineffective) bacteria, virus (including the AIDS virus), parasites and/or fungus entrained in blood or other body fluids, but does not render the fluids unfit for human use or impair their biological usefulness.

The species of the invention shown in FIGS. 2 and 3 is advantageous since it is possible to fabricate the treatment tubing by preforming the conductive segments 16 and 16A on the tubing walls while it is in a flat planar condition, and then rolling the walls into tubular form using a suitable mandrel. The adjoining longitudinal edges of the planar member after rolling are thereafter heat sealed along a longitudinally extending seam located within one of the electrically insulating sections 17. Particular attention must be paid to the juncture of the ends of the annular terminal busses 18 and 21 during the rolling and heat sealing steps to assure that good electrical interconnection and continuity at these junctures of the annular terminal busses is provided in the completed treatment tubing. The conductive electrode segments 16, 16A may be electro-deposited, chemically formed, separately formed conductive polymer surfaces, or conductive foil or wires adhesively secured to the side walls of the tubing 11 in advance of the rolling and sealing using techniques well known in the printed circuit and integrated circuit manufacturing technologies.

FIG. 6 is a diagrammatic, fragmentary, elevational view of a modified blood transfer system using the novel electrically conductive treatment tubing in accordance with the invention. In the FIG. 6 embodiment of the invention, a blood pump 28 of conventional, commercially available construction is inserted in the tubing 11 at some point along its length. The blood pump 28 is electrically isolated from the zebra striped conductive surfaces 16, 16A by suitable insulators 29 formed on the blood input-output connections of pump 28. Provision for electrically bypassing the blood pump 28 (if need be) is made through the shunt conductors 30, 30A which maintain electrical continuity of the direct current excitation potential applied to the conductive stripes 16, 16A on each side of pump 28. For convenience, the direct current excitation source 20 and its connection to the electrically conductive tubing 11 has not been shown in FIG. 6 but would have to be provided. A separate source of excitation current for running the blood pump 28 is provided from a conventional 110 volt alternating current source through the input terminals 31, 31A.

In systems employing a blood pump, it may be desirable in some applications to provide a blood flow regulating valve 37 inserted in the system at the output of blood pump 28 and within the by-pass loop 30, 30A for the conductive stripes 16, 16A. By thus controlling blood flow, the electrified transfer system safely can be employed in a closed loop recycling system for withdrawing blood from a patient, electrically treating the blood as described above and then returning the electrically treated blood to the patient. This procedure is referred to herein as recycling. The system of FIG. 6 also can be used in those situations where the blood flow of a donor's blood is not sufficient to assure supply of an adequate amount of blood to or from the collection receptacle 14 or other recipient. It may also be desirable to have a blood flow regulating valve such as 37 in non-pump systems.

FIGS. 4 and 5 of the drawings show another embodiment of the invention wherein the electrically conductive treatment tubing 11 includes electrically conductive electrode segments 32 and 32A which are in the form of zebra stripes that extend radially around the inside diameter of tubing 11 in spaced-apart, alternating polarity, conductive annular bands 32 and 32A separated by insulating surface bands 11I which serve to electrically isolate the respective first set of conductive zebra stripes 32 from the second set of conductive zebra stripes 32A. The first set of alternate ones of the electrically conductive annular stripes 32 are electrically connected in common to a first longitudinally extending terminal buss bar 33 that is embedded within tubing 11 in parallel with the longitudinal axis of the tubing and electrically isolated from the remaining second set of alternate electrically conductive annular stripes 32A. The first longitudinally extending terminal buss bar 33 is designed for connection to a first polarity (positive) source of electric excitation potential through a supply conductor connection 35 on the exterior surface of the tubing 11.

A second longitudinally extending terminal buss bar 34 is embedded within the body of tubing 11 and is electrically connected to the remaining second set of alternate electrically conductive annular stripes 32A. The second longitudinally extending terminal buss bar 34 is electrically isolated from the first longitudinally extending terminal buss 33 and the first set of alternate electrically annular stripes 32. Terminal buss bar 33 is designed for connection to a second polarity (negative) source of electric excitation potential of opposite polarity from that of the first polarity source of excitation potential. For this purpose an input supply conductor connection 36 is directly connected through the exterior surface of tubing 11 and to the second longitudinally treatment extending terminal buss bar 34.

In operation, the embodiment of the invention shown in FIGS. 4 and 5 is physically arranged in a blood transfer system in the manner illustrated in FIG. 1 of the drawings with the positive polarity and negative polarity zebra annular stripes being connected to the respective positive polarity and negative polarity terminals of an excitation battery 20 via control switch 25. If required, a blood pump such as 28 and blood flow regulating valve 37 shown in FIG. 6 can be included in the blood transfer system employing electrified tubing shown in FIGS. 4 and 5.

Similar to the system shown in FIG. 1, a blood transfer system employing the embodiment of the invention shown in FIGS. 4 and 5 would be electrically excited in advance of injection of the hypodermic needle 12 into the arm of a blood donor so that all blood passing through the tubing 11 will be subjected to electric forces produced between the alternate polarity annularly formed conductive bands 32 and 32A. Experience with the invention will establish what length is required for the electrification field. However, for initial installations the length of the electrified field as related to the flow of blood through electrified tubing 11 should correspond to at least the 1-6 minute treatment time mentioned earlier. This is achieved by using an extended array of the alternate annular zebra bands 32 and 32A of adequate length to assure thorough subjection of blood to electric current flow produced by the alternate polarity zebra stripes 32 and 32A. The electric field force intensity applied to the blood by means of the electrified tubing is anticipated to be of the order of 2 to 4 volts similar to the embodiment of the invention shown in FIGS. 1-3.

In place of supplying continuous direct current excitation to the conductive stripes 16, 16A of FIGS. 2 and 3 or 32, 32A of FIGS. 4 and 5, it also is possible to excite these electrically conductive segments of tubing 11 with pulsed waveform direction current excitation potentials. For use in this manner, the pulse rate of the pulsed waveform excitation potentials must be sufficiently high to maintain continuous current flow through blood being treated. In addition, it may be desirable to couple a bank of storage capacitors in parallel across respective pairs of opposite polarity electrically conductive segments 16, 16A and 32, 32A where operation in a pulsed DC mode is desired.

FIG. 7 of the drawings is a cross sectional view of another embodiment of the invention which is substantially different from those previously described. In FIG. 7, the material used for fabrication of the tubing 11 is one of the new space-age polymer materials which can be either highly electrically conductive, insulating, or semiconducting and may have values of conductivity ranging from essentially fully conductive to insulating. In the embodiment of the invention of FIG. 7, the conductive surface areas on the inside diameter of the tubing 11 are actually formed into segments, such as 11C, of the cross sectional area of the tubing 11 fabricated from the highly conductive polymer material. The intervening segments of the tubing 11I which separate the conductive segments 11C are integrally formed from the highly insulating polymer material. Suitable positive polarity and negative polarity potentials are applied to the exterior surface areas of alternate ones of the sets of conductive polymer segments 11C from a source of electric potential via the conductors 23 and 24 as illustrated schematically in FIG. 7.

It will be appreciated that the embodiment of the invention shown in FIG. 7 is much simpler and hence less expensive to make in that it requires fewer processing steps than the embodiments of the invention shown in FIGS. 1-6. In other respects, the embodiment of the invention shown in FIG. 7 would be used in a blood transfer system similar to that shown in FIG. 1 or 6 with or without a blood pump 28 and blood flow regulating valve 37 to effect transfer of blood from a donor to a receptacle or recipient in the event of a transfusion or recycling. During the blood transfer process, again it would be necessary to provide alternate polarity, DC electric excitation potentials to the spaced-apart, alternate sets of positive polarity and negative electrically conductive polymer segments 11C prior to passing blood through the tubing 11. This will assure that all of the blood being transferred is subjected to the electric field forces produced between the alternate conductive surfaces 11C. As a variation of the FIG. 7 embodiment, which visualizes that the segments 11C and 11I all extend longitudinally and parallel to the longitudinal axis of tubing 11, it would be possible, but more elaborate to design, to employ alternate radially surrounding annular conductive segments 11C and interlacing insulating segments 11I similar to FIG. 5, but such fabrication would require somewhat more complex terminal buss bar DC electric supply connections 23 and 24 than those shown in FIG. 7.

FIG. 8 is a fragmentary, diagrammatic, elevational view showing a form of blood treatment system according to the invention wherein a small electrically conductive vessel 41 in the form of a short piece of electrified tubing and a miniaturized battery power source 42 are implanted in the arm of a human being. The electrified tubing 41 may be in the form of any of the prior disclosed electrified tubing structures described with relation to FIGS. 1-7, but which are fabricated in miniaturized form so that the tubing 41 can be inserted in a section of or surrounding a vein 44 of the arm 13 of a patient whose blood is being treated. The implantation is such that the blood of the patient 44 naturally is pumped through the short piece of electrified tubing 41 while circulating blood to the hand of the patient and thereby form a closed loop, recirculating, implanted treatment system that comprises an integral part of the circulatory system of the patient being treated. Because the parameters of such an implanted system are necessarily small, a single passage through the implanted electrified tube 14 may accomplish a relatively small attenuation of contaminants in the blood. Therefore, it is the repeated passage of small portions of the patient's blood continuously twenty-four hours a day and for as many days as are needed which will gradually attenuate the contaminants to the point where they are rendered ineffective as described earlier.

FIG. 9 is a partial, fragmentary, sectional view of the upper arm portion 13 of a vein or artery of a patient in which a treatment system according to the invention has been implanted, and shows in greater detail the construction of a specified, miniaturized, electrically conductive treatment vessel with associated miniaturized battery electric power source for use in an implanted treatment system as shown in FIG. 8. In FIG. 9, the electrified vessel 41 is in the form of an outer housing 45 that is in the shape of a football which is implanted within the interior walls 44 of an artery or a vein 44. The outer housing 45 is comprising by a central, cylindrically-shaped portion 45M of solid conductor such as platinum which is biocompatible with human blood and tissue and has integrally formed, conically-shaped porous ends 45C which are attached to and form an electrically conductive screen grid (at the same potential) as the mod portion 45M. The conical end portions 45C both are perforated and may be in the nature of a screen or mesh wire and of the same material composition as the mid portion 45M. Disposed within the outer housing 45 is a inner housing 46 which is tear-drop shaped and secured within the central portion 45M of the outer housing by suitable insulating support spider legs 47. The inner housing 46 likewise is formed from platinum or other suitable biocompatible conductive material and has supported within its interior a miniaturized battery 42 secured to the conductive walls of inner housing 46 by conductive support legs 48. The support legs serve as terminal connectors from one terminal of battery 42 to the inner housing 46 so that it is maintained at one polarity excitation potential. The remaining opposite polarity terminal of miniaturized battery 42 is connected through an insulated conductor 49 to the central portion 45M of outer housing 45 whereby the entire outer housing including the meshed conical end portions 45C are maintained at the opposite polarity potential.

Prior to implantation in a patient, the electrified vessel shown in FIG. 9 is activated by connection to battery 42 so that a difference of potential exists between the inner and outer housings 45 and 46. Following implantation of the activated, electrified treatment vessel 41, its presence in a vein or artery will cause all blood flowing through the vein or artery to pass between the side walls of the inner and outer housings 45 and 46 so as to be subjected to the electric field forces existing in these spaces. The presence of the electric field forces will induce a current flow through the blood passing between the interior and outer housings as explained above which will result in attenuating bacteria, virus, parasites and/or fungus which are present in the blood as contaminants. Here again, because of the relatively small portion of the total blood flowing in a patient that will be treated by the device within a given time period, it is the repeated, recycling process of treatment of the blood over a prolonged period of time that will result in attenuation of the contaminants in the blood to the point where such contaminants are rendered ineffective as described earlier.

In order to further assure adequate treatment of the blood of a patient receiving the implant device, it is recommended that the blood be treated in an external treatment processing facility such as described earlier in FIGS. 1 and 6 or to be described hereinafter with relation to FIGS. 18 and 19 in which the total capacity of the treatment system is greater whereby substantial attenuation effect can be achieved in a comparatively shorter time period yet to be determined, and then the in vitro implant treatment system such as shown in FIGS. 8, 9 and 10 can be used to maintain the attenuated condition and to prevent any subsequent build up of contaminants after the initial treatment.

FIG. 10 is a fragmentary, diagrammatic view of a partial vein or artery 44 showing in greater detail the cylindrical or tubular electrified treatment vessel 41 originally described with relation to FIG. 8. This implant treatment vessel 41 is miniaturized so that it is in effect an open-ended cylinder in shape and has a diameter comparable to that of a large vein or artery and so that is can be grafted or implanted into the vein or artery as illustrated in FIG. 10. The tubular treatment vessel 41 may be designed pursuant to FIGS. 2 and 3 of the drawings, for example. For this application, the battery source of power 42 is annular in shape and is slipped over the tubular treatment vessel 41 in the manner shown. In FIG. 10 only a longitudinal sectional view of the annular collar-shaped battery 42 is illustrated. At the point where the battery 42 fits over the tubular treatment vessel 41, the respective positive and negative terminals of the battery are exposed to engage the corresponding positive and negative supply terminals 19 and 22 of the tube 41 so that the resulting battery powered structure has a minimum exterior profile to facilitate implantation. From a comparison of FIG. 10 to FIG. 9 of the drawings, it will be appreciated that the FIG. 9 treatment vessel introduces some flow restriction in the vein or artery in which it is implanted and for this reason the construction shown in FIG. 10 is preferred.

FIG. 11 and 11A of the drawings illustrate a construction for the electrified treatment vessel 51 wherein the treatment vessel is in the form of square or rectangular cross sectionally-shaped open-ended tubing. The treatment tubing 51 provided with a square or rectangular shape so that provision of opposed, parallel conductive electrode surfaces 51U and 51L is greatly simplified as best seen in FIG. 11A of the drawings which is a cross sectional view taken through plane 11A--11A of FIG. 11. By fabricating the upper and lower surfaces of the tubing 11 from electrically conductive material such as platinum, etc., and separating the upper and lower surfaces 51U and 51L by electrically insulating side walls 52R and 52L, provision of the electrically isolated, opposed, parallel electrode surfaces is simplified and the resulting treatment vessel introduce minimum restriction to flow of blood. By connecting the upper surface 51U to one polarity of electric potential (for example the positive terminal) and connecting the lower surface 51L to the negative polarity terminal of a battery (not shown), electrification of the interior area of the tubing wherein the fluid to be treated flow is readily achieved with a greatly simplified electrode structure. Variations of this structural feature wherein the side insulating surfaces 52R and 52L are curved with their concave surfaces facing each other and the cross sectional area of the upper and lower conductive surfaces 51U and 51L tailored to provide a desired current density, tubular treatment vessels such as shown in FIGS. 11 and 11A could be readily provided for use in implantation devices such as those illustrated in FIGS. 8 and 9 above.

FIG. 12 is a perspective view of a novel, electrified, closed, octagonally-shaped, flat, box-like treatment vessel 60 according to the invention which provides an enlarged cross-sectional area relative to the cross sectional diameter of the inlet and outlet tubing supplying the interior of the treatment vessel whereby increased through-put of a fluid being treated can be achieved in a given time period. The treatment vessel 60 shown in FIG. 12 is comprised essentially of upper and lower, octagonally-shaped, flat insulating plates 61 and 62, respectively, of an insulating material which is compatible with human blood and/or other body fluids. Disposed immediately below and above the upper and lower plates 61 and 62 are octagonally-shaped, conductive electrode members 63 and 64, respectively, which are separated and electrically isolated one from the other by a surrounding electric insulating gasket member 65. The entire structure is sandwiched together and held in assembled relation by threaded thru-pins 66 as best seen in FIG. 12A of the drawings. The insulating gasket 65 which may be of teflon defines an open space 67 between the two conductive electrode members 63 and 64 into which the blood or other body fluid to be treated is introduced via inlet and outlet conduits 68 and 69. Opposite polarity electric potentials are applied to respective conductive plates 63 and 64 to produce an electric field force across the intermediate space 67 through which the fluids being treated flow between electrode plates 63 and 64. By thus structuring the treatment vessel, increased treatment surface area is provided to the blood or other body fluid flowing through the space 67 whereby in a given time period an increased quantity of fluids can be treated.

FIG. 13 is a perspective view of another form of enlarged cross sectional area treatment vessel 70 having an exterior shape similar to the of the treatment vessel shown in FIG. 12. The electrified treatment vessel shown in FIG. 13 differs from that in FIG. 12, however, in the construction of its electrically conductive electrodes which comprise a plurality of inteleaved, conductive, flat, electrode plates 71 and 71A. The electrode plates 71 are secured in and project inwardly from a right hand (RH) conductive end plate 73R as shown in FIG. 13A. The alternate set of flat electrode plates 71A are secured to and project inwardly from a corresponding conductive end plate 73L on the left hand end of the treatment vessel 70. The conductive end plates 73R and 73L and coacting insulating side plates 72 which insulate the conducting end plates from one another, form an octagonally-shaped box frame which is closed by upper and lower insulating top and bottom insulating plates 74 and 75. The conductive end plates 73R and 73L have a central opening formed therein into which inlet and outlet tubes 76 and 77 are secured as best seen in FIG. 13 for providing inlet and outlet flow through connection to the treatment vessel 70.

The alternate sets of flat electrode plates 71 and 71A extend parallel to one another and are provided with different polarity electric potentials supplied to the respective sets of interleaved electrode plates via the respective conductive end members 73R and 73L. If desired, the respective flat conductive electrode plates 71 and 71A may be fabricated from a perforated material as shown in FIG. 13B of the drawings. Also, it may be desirable that some form of thermal insulation, or a thermally controlled chamber be provided around the exterior of the treatment vessel 70 as indicated by the thermal insulation 78 shown in FIG. 13A.

In operation, electrified treatment vessel 70 shown in FIGS. 12, 13A and 13B functions in essentially the same manner as was described earlier with respect to FIGS. 1-7 to effect attenuation of contaminants such as bacteria, virus and fungus contained in blood and/or other body fluids being treated in the flow through treatment vessel of FIG. 13.

FIG. 14 is a longitudinal sectional view of still another form of enlarged cross sectional area, electrified treatment vessel 80. The treatment vessel 80 shown in FIG. 14 is in the form of an open-ended, elongated cylinder 81 whose cylindrical walls are fabricated from an insulating material which is biocompatible with human blood and/or other body fluids and whose open ends are closed by circular-shaped conductive end pieces 82 and 83. Inlet and outlet tubular openings 84 and 85 are provided to the interior of cylindrical housing 81 through centrally formed apertures in the circular end plates 82 and 83. Within the interior of the cylindrical, insulating housing 81 at least two, separate, concentric, perforated, cylindrically-shaped electrode members 86 and 87 are provided which extend longitudinally through the interior of the outer cylindrical housing 81. The first set of concentric, perforated, electrically conductive electrodes 86 is embedded in and supported by the conductive end plate 82 which serves as an electrical terminal for applying electric potentials to all of the concentric electrode member 86. Similarly, the concentric, perforated, conductive electrode member 87 is physically supported by and electrically connected to the conductive end plate 83 for the supply of an opposite polarity potential thereto. Additionally, if desired, one or more additional perforated concentric electrode members similar to 86 may be spaced apart from the inner concentric electrode member 86 outwardly along the diameter of the circular end member 82 with additional perforated concentric electrode members 87 being sandwiched between the two electrode members 86 and spaced apart therefrom so as to provide an electrode field force between all the spaced apart, separated electrically conductive electrode members 86 and 87. Additionally, if desired, a conductive surface 89 may be formed around the interior walls of the outer, insulating cylindrical housing member 81 and electrically connected to the conductive end plate 82 or 83 which is opposite in polarity to the outermost concentric electrode members 86 or 87. This will assure that the entire interior of the treatment 80 vessel cross sectional area is crossed by the electric field force and all blood or other body fluid passing the cylindrical housing member 81 is subjected to biologically compatible low electric current flow as a consequence of the electric fields produced between the different concentric electrode members including the coated surface 89 within the interior insulating housing member 81.

In operation, the embodiment of the invention shown in FIG. 14 and 14A operates in substantially the same manner as described with relation to earlier embodiments of the invention to assure production of biologically compatible electric current flow through the blood or other body fluid being treated in the treatment vessel 80.

FIG. 15 is a longitudinal sectional view of still another embodiment of an enlarged cross-sectional area treatment vessel 90. The treatment vessel 90 again comprises an outer, hollow, open-ended cylindrically-shaped, insulating body member 91 whose open ends are closed by electrically conductive, circular end plates 92 and 93, respectively. Inlet and outlet tubular openings 94 and 95 are provided through the central axial opening in the conductive end plates 92 and 93 for passage of blood and/or other body fluids being treated onto the interior of the treatment vessel 90. The conductive end plates 92 and 93 have respective sets of opposite polarity potential needle-like electrodes 96 and 97, respectively, projecting therefrom inwardly into the interior of the treatment vessel 90. Different polarity electric potentials are applied to the respective conductive end plates 92 and 93 through respective negative and positive polarity terminals indicated at 98 and 99. If desired, and in order to assure complete saturation of the entire volumetric area within treatment vessel 90 with electric fields, a conductive coating similar to that shown at 89 in FIG. 14 can be provided to the inner surface of the hollow, cylindrically-shaped outer body member 91 of treatment vessel 90.

FIG. 15A is a cross sectional view taken through plane A--A of FIG. 15 and shows how the array of needle-like electrodes appear within the interior of the treatment vessel 90. In operation, the treatment vessel 90 will function in substantially the same manner as has been described previously with relation to earlier described embodiments of the invention.

FIG. 16 is a perspective view of still another form of enlarged cross sectional area treatment vessel 100 according to the invention and FIG. 16A is a partial cross sectional view taken through plane 16A--16A of FIG. 16. The treatment vessel 100 comprises a relatively large rectangular-shaped block 101 of electrical insulating material which is biocompatible with blood and/or other human body fluids. The insulating block 101 has a plurality of parallel, longitudinally extending, open-ended, tubular-shaped openings 102 formed therein through the entire length of the block. The tubes 102 are provided with electrically isolated, opposed, parallel extending conductive plate electrodes 109, best seen in FIG. 16A, which have opposite polarity electric potentials applied thereto. One set of these electrodes, formed for example by the lower electrode 109 in each tube, extend out to and engage a conductive surface coating formed on one end of the insulating block, for example 101R, and the remaining upper electrodes 109 form a second set which extend out of the left hand end of the tubes and contact a conductive coating formed on the remaining end 101L of block 101. Respective, opposite polarity electric potentials are supplied to the respective conductive surfaces 101R and 101L so that a potential difference exists between the sets of positive and negative polarity electrodes within each longitudinally extending tube in block 101. The ends of the tubes 102 open into and are supplied from, or supply, respective header reservoirs 103 and 104 formed on the respective opposite ends of the block of insulating material 101. Each of the reservoirs 103 and 104 has a centrally formed opening for receiving either an inlet tube 105 applied to header 103 or an outlet tube 106 secured to header 104 for supply of blood or other body fluids to be treated to and from the treatment vessel 100. If desired, a blood pump or other fluid pump can be inserted between the supply tube 105 and header 103, or between outlet tube 106 and the or outlet from the header reservoir 104, or both. Alternatively, both inlet and outlet pumps can be used. In operation, the electrified treatment vessel 100 shown in FIG. 16 functions in the same manner as those species of treatment vessels described previously.

For some treatment applications, it may be desirable to provide exhaust vents such as shown at 107 and 108 in FIG. 16 to the inlet reservoir 103 and/or the outlet reservoir 104 with the vents that can be selectively operated by valves that can be automatically or manually controlled for venting off gases that might be trapped in the tops of reservoirs and which otherwise might interfere with the proper operation of the electrified treatment vessel. In a similar manner, suitable venting apparatus may be provided to other of the large cross sectional area electrified treatment vessels described previously.

FIG. 17 is a perspective view of still another enlarged cross-sectional area treatment vessel 110 which is similar in all respects to the treatment vessel shown in FIG. 16 with the exception that the body or block of insulating material 101 through which the elongate tubular openings are made, is cylindrically shaped as illustrated in FIG. 17. In other respects, the embodiment of the invention shown in FIG. 17 would be identical to FIG. 16 in the fabrication and operation of its component parts including the reservoir headers 103 and 104 and would operate in a similar manner.

FIG. 18 is a diagrammatic, sketch of a human blood or other body fluid treatment system employing one of the larger cross-sectional dimension fluid treatment vessels 60, such as any one of those shown in FIGS. 12-17 of the drawings. The particular fluid treatment system shown in FIG. 18 is for a continuous flow-through recirculating body fluid treatment wherein blood is withdrawn from the arm 13 of a patient and supplied through IV tubing 111 to a commercially available blood pump 28 and thence to an electrified treatment vessel 60. The treatment vessel 60 may be like any of the treatment vessels described with relation to FIGS. 12-17 of the drawings wherein the blood or other body fluids being treated is exposed to a low voltage, low current electric current flow for attenuating to the point of rendering them ineffective, any contaminants entrained in the blood, such as bacteria, virus and fungus. The treated blood appearing at the output of the treatment vessel 60 then is recirculated back through IV tubing 112 to the arm 13 of the patient whose blood or other body fluid is being treated. If desired, IV tubing 111 and 112 could also be treatment tubing such as described in FIGS. 1-7 and 11. This could provide double treatment for the fluid if that were desirable. In the event that the entire treatment does not take place in an air conditioned, temperature controlled room, then it may be desirable to provide a temperature controlled enclosure indicated by dotted lines 78 around at least the pump 28, electrified treatment vessel 60 and the interconnecting IV tubing sections 111 and 112 in order to assure maintaining a substantially constant viscosity of the blood or body fluid being treated.

Normally, the system of FIG. 18 would be used in a continuous flow-through recirculating treatment system wherein blood from the patient's arm 13 is supplied through pump 28 to the treatment vessel 60 where it is treated and then discharged back through tubing section 112 to the arm of the patient. The flow rate of the blood thus processed would be adjusted to correspond substantially to the natural flow rate of blood circulated through the patient's body to the extend possible.

In addition to operation in the above manner, it would also be possible to operate the system of FIG. 18 in a stopped-flow manner wherein the blood pump is intermittently stopped to allow for more extended electrical treatment of the blood or other body fluid contained in the treatment vessel 60 during the period of time that the blood pump is stopped thereby assuring fuller electrification treatment and the greater attenuation of the bacteria, virus or fungus entrained in the blood.

FIG. 19 is a diagrammatic sketch of a form of closed loop, flow-through recirculating treatment system according to the invention that is somewhat similar to the system shown in FIG. 18. FIG. 19 differs from FIG. 18 in that an inlet pump 28 and an outlet pump 28' are connected to, respectively, the intake to and outlet from the electrified treatment vessel 60. If desired, an inlet control valve 113 and an outlet control valve 114 also can be interconnected between the inlet pump 28 and the intake to the treatment vessel 60 and between the output from the treatment vessel 60 and the intake to the outlet blood pump 28'. These inlet and outlet control valves indicated at 113 and 114 preferably are automatically operated in a time sequence which allows the system of FIG. 19 to be operated as a two pump, start-stop flow through system. When operated in this manner, the first pump 28 is allowed to operate and discharge blood from the arm 13 of the patient to be pumped into the treatment vessel 60 and thereafter is closed off with both the inlet and outlet valves 113 and 114 in their closed condition. At this point electrification treatment of the blood or other body fluid takes place for a predetermined, scheduled time period to assure adequate attenuation to the point of rendering ineffective the contaminant bacteria, virus or fungus. Upon completion of the pre-scheduled treatment period, the outlet valve 114 is opened and outlet pump 28' actuated to return the treated blood to the arm of the patient 13. Operation in the semi-continuous, start-stop, batch fashion will assure that adequate electrified treatment of the blood has been accomplished while achieving this end in a somewhat continuous manner suitable for use in a closed loop, recycling blood treatment process.

FIG. 20 is a partially disassembled, perspective view of a non-flow-thru, single batch, body fluid treatment vessel 120 according to the invention, which is open to atmosphere on its upper side, and which was used in conducting the experiments described hereinafter. FIG. 20A is a diagrammatic sketch of the assembled treatment vessel 120 shown in FIG. 20 connected to a source of direct current electric power 128. Power source 128 was capable of providing substantially constant voltage across the conductive electrodes of the treatment vessel 120 at a given voltage setting, ranging between 0.2 volts and 12 volts DC, and for a given electrical resistivity of a sample being treated, and provided essentially constant current through the batch sample in the treatment vessel. Upon being assembled together with through bolts and nuts 124N that extend through the openings 124 in each of the teflon partitions comprising end walls 121 and 122 and a central partition 123, the parts form a fluid-tight chamber as shown in FIG. 20A. A set of spaced-apart, parallel electrodes 125 and 126 are supported in suitable formed channels in the respective end partitions 121 and 122 by threaded studs (not shown) securing the electrodes 125 and 126 in opposed parallel relationship by means of bolts (not shown) threaded into threaded openings 127 in the tops of the end partitions 121 and 122. The electrodes 125 and 126 were connected to the negative and positive terminals, respectively, of the battery source of direct current electric power shown at 128 in FIG. 20A. When thus assembled, the resulting structure results in a non-flow treatment vessel or cell defined by the vertically extending slot formed in a 1 millimeter wide central portion of the central segment 123 of the vessel. This vertically extending slot defines an open-sided treatment well 129 which is 1 millimeter across between electrodes 125 and 126, 1.56 millimeters in length and 8.32 millimeters in depth. With the experimental test treatment vessel constructed and energized as thus described, the following experiments were conducted.

EXPERIMENTAL RESULTS

Overview

A non-flow vessel or cell included a pair of platinum electrodes 1 mm apart inserted into a well 1.56 mm in length and 8.32 mm in depth. The non-flow vessel was connected to a direct current source capable of creating an electric field at a constant voltage and constant amperage. Into this well was laced a suspension of the human immunodeficiency virus type 1 (HIV-1) at a concentration of 10.sup.6 infections particles per ml. An aliquot of approximately 10 .mu.l of the virus suspension was placed into the well. Thereafter, the viral suspension was exposed to direct currents ranging from 0 microamps for up to 12 minutes to 100 microamp for up to 6 minutes. Intermediate currents of 25, 50 and 75 microamps were used to expose similar viral aliquots. A matrix of current and time was employed as shown in Table 1. After the exposure of the viral suspension to electric currents, the contents of the non-flow vessel were removed and placed into sterile microtubes. Five .mu.l of each sample were removed and diluted with 95 .mu.l tissue culture medium supplemented with 10% fetal calf serum (FCS).

In Experiment 1, the resuspended and treated viral stocks were incubated with a human T lymphoblastoid cell line named CEM-SS. This cell line, upon exposure to HIV-1, forms syncytia. It is well documented that the viral titer used is directly correlated with the number of syncytia formed. Therefore, evaluation of infectivity of HIV-1 can be used with this assay. In contrast, Experiment No. 2 used a different human T lymphoblastoid cell line named H9. This cell line, in contrast to CEM-SS cells, produces, upon exposure to HIV-1, many viral particles. The amount of virus produced is proportional to the amount of virus to which the cells are exposed. Therefore, quantitation of viral particles or, more commonly viral associated protein (in this case reverse transcriptase), can be used as an index of viral infection. In both assays, the CEM syncytia forming assay and the H9 viral protein assay, similar type results were obtained. That is, with the CEM cells, although syncytium formation and quantitation is preferable, one can quantitate the HIV-1 associated protein (reverse transcriptase) activity and conversely with the H9 cells, although reverse transcriptase quantitation is preferred, one can quantitate giant cell (syncytia) formation. Both of these assays are widely used as reproducible measures of viral infection and can be used to determine if alternations in viral infectivity as a product of this electrical treatment can be detected.

Experiment #1

Approximately 10.sup.5 CEM-SS cells per sample were incubated with a treated or untreated (control) viral aliquot for up to 4 days. The cells were placed into microtiter plate wells and monitored for formation of syncytia every 24 hours by microscopic observation. In a standardized fashion, as it has been reported in the literature and is currently being conducted in many laboratories, the number of syncytia at 3 and 4 days was determined. Table 2 summarizes the results from a representative experiment using this assay. As can be noted, the number of syncytia formed was inversely proportional to the amount of electric current. That is, additionally, with increased current (50 vs. 100 microamps) there was a reduction in the number of syncytia formed. These results and those of additional experiments using the CEM-SS cell line indicate a consistent finding that electrical treatment of the RF strain of HIV-1 attenuates the virus potential for inducing syncytium formation in this cell line.

Experiment #2

A separate and independent assay to determine the ability of electric current to alter HIV-1 infectivity using H9 cells was employed. The basic strategy was similar to that used for the CEM cells with the exception that the initial suspension of treated and controlled viral stock was incubated with 10.sup.5 H9 cells for 2 hours at 37.degree. C. Thereafter, the cell virus suspensions were further diluted to 5 ml in standard tissue culture medium. The cell-viral suspensions were then incubated for up to 14 days at 37.degree. C. 5% CO.sub.2. At 3 day intervals (beginning at day 2), aliquots of cell suspension were removed from each sample. The aliquots were centrifuged at 1,000 rpm for 5 minutes in order to pellet the cells. After centrifugation, the supernatant and cell pellets were separated. The supernatant was cryopreserved for subsequent reverse transcriptase assay and the cell pellets were resuspended in fixatives and maintained in a tissue bank for additional studies employing in situ hybridization and innumocytochemistry to detect qualitatively and semi-qualitatively viral infection by HIV-1. At the end of each experiment, the supernatant samples from each of the tests and time points were examined using standard reverse transcriptase assay. The results of the representative experiment are shown in Table 3. The results of this experiment indicate that the ability of HIV-1 to infect H9 cells is attenuated by the magnitude of the electrical currents to which the virus is exposed. Additionally, at lower current magnitude, but with prolonged exposure time, attenuation of viral infectivity is achieved. That is, analogous to the results observed using syncytium formation and the CEM-SS cell line, either increased current or increased duration of exposure time was inversely proportional to the amount of reverse transcriptase produced by the cell line.

In conclusion, these experiments which have been repeated several times and those using the CEM-SS cell line indicate at a statistically significant level that direct electrical current at biocompatible amperages for discrete exposure time intervals can attenuate the ability of HIV-1 to infect normally healthy cells which are susceptible to the HIV-1 AIDS virus.

Although it is uncertain what is specifically causing the attenuation of the contaminants (virus, bacteria, parasites and/or fungus), some possible explanations have been put forward. One is the attenuation is caused simply by the direct affect of the electric current and voltage. Another entails the following. When a voltage is applied to the electrodes, a small current will flow through the electrically conductive medium. The applied voltage and ensuing current will induce changes in the complex biologically active fluid. Current can flow through the media if positive and/or negative charges are transported through said media. The transport might induce changes in the charge distribution of the biologically active molecules thus changing their biological activity.

Furthermore, the voltage and current can induce the production or elimination of different ions, radicals, gases and/or PH levels which may affect, alone or in combination, the biologically active molecules and/or cells. The above products of the electrical processes may either be very short lived and stay in the close proximity of the electrodes or can diffuse or mix in the bulk of the media and react with the biologically active molecules or cells to result in their attenuation.


TABLE 1
______________________________________
Experimental Paradigm
current (.mu.A)
Time (Minutes)
______________________________________
0 1 4 8 12
25 2 4 8 12
50 2 4 8 12
75 2 4 8 12
100 1 3 4 6
______________________________________
TABLE 2
______________________________________
Syncytium Formation
(Number of Syncytia)
Dilution
of virus
______________________________________
1:20 TNTC* TNTC 28 66 15
1:40 TNTC 175 22 42 7
1:80 TNTC 90 20 25 4
1:160 180 44 9 9 2
1:320 115 28 4 6 0
1:640 70 10 0 2 0
1:1280 40 7 0 0 0
1:2560 28 4 0 0 0
1:5120 15 2 0 0 0
1:10,240
10 1 0 0 0
1:20,480
4 0 0 0 0
0 .mu.A8'
25 .mu.A8'
50 .mu.A6'
75 .mu.A4'
100 .mu.A3'
______________________________________
*TNTC = Too numerous to count
TABLE 3
______________________________________
Reverse Transcriptase Activity
(CPM .times. 10.sup.-3)
Days of incubation
.mu. Amps/Time (Min.)
2 4
______________________________________
0/6 0 13.8
0/12 0 11.7
50/3 0 9.1
50/6 0 9.1
50/12 0 4.8
100/3 0 5.7
100/6 0 3.6
______________________________________



PRACTICAL USES OF INVENTION

While the disclosure herein presented has been directed to principally the electrical treatment of blood, it is believed obvious to those skilled in the art that the invention can be applied with corresponding effect to other body fluids which are electrically conductive for the treatment of contaminants such as bacteria, virus and fungus contained therein. Further, while voltages of the order of from about 0.2 volts to 12 volts have been indicated as preferable, it is possible that certain virus may be attenuated (or attenuated at a faster rate) if they are subjected to a greater electric current magnitude of the order of 500 microamperes for shorter time periods. Acceptable current magnitudes normally would require an excitation voltage of from 0.2 to 12 volts. However, in certain cases where faster or more complete attenuation of the contaminants in body fluids may be desired under certain circumstances and conditions, the excitation voltage supplied to the conductive tubing may in fact exceed the 0.2 to 12 volt range indicated for most treatments.

Having described several embodiments of new and improved electrically conductive treatment methods and vessels for use in practicing the novel method for the treatment of blood and/or other body fluids with electric field forces and treatment systems employing the same, it is believed obvious that other modifications and variations of the invention will be suggested to those skilled in the art in the light of the above teachings. It is therefore to be understood that changes may be made in the particular embodiments of the invention described which are within the full intended scope of the invention as defined by the appended claims.




By Juris Doctor Boyd Graves
Forward by Jerry Mazza
Online Journal Associate Editor
Jan 21, 2008, 00:18
I
In the Fall of 1990, two medical researchers, Drs. William Lyman and Steven Kaali, working at Albert Einstein College of Medicine in New York City made an important discovery. They found that they could inactivate the HIV virus by applying a low voltage direct current electrical potential with an extremely small current flow to AIDS infected blood in a test tube. Initially, they discovered this in the lab by inserting two platinum electrodes into a glass tube filled with HIV-1 (type 1) infected blood.
They applied a direct current to the electrodes and found that a current flow in the range of 50-100 microamperes (uA) produced the most effective results. Practically all of the HIV viral particles were adversely affected while normal blood cells remained unharmed. The viral particles were not directly destroyed by the electric current, but rather the outer protein coating of the virus was affected in such a way as to prevent the virus from producing reverse transcriptase, a necessary enzyme needed by the virus to invade human cells.
Reverse transcriptase allows the virus to enter a human T cell line (called CEM-SS) and commandeer the DNA reproduction machinery. After using the host cell to reproduce itself into thousands of new virii, the swollen host cell (now called syncytia or giant cell) will burst and spew the contents into the bloodstream or lymph system. This is how the virus spreads, but lacking reverse transcriptase, the HIV virus can't invade the host cell and it becomes vulnerable to destruction by the body's immune system. (The details of this experiment can be read from Kaali's patent application.)
A brief announcement of this discovery appeared in The Houston Post (Mar 20, 1991), then in Science News (Mar. 30, 1991 pg. 207) and later in Longevity magazine: (Dec.1992 pg. 14). Following their work in the Fall of 1990, Kaali and Lyman presented their findings at the First International Symposium on Combination Therapies (an AIDS conference) in Washington DC on March 14th, 1991. Kaali outlined two methods for treating an AIDS patient with this new therapy: One method involved removing a small amount of blood, electrifying it and then returning it to the patient's body. The second method involved sewing a miniature electrifying power supply along with two tiny electrodes directly into the lumen of an artery. For long term treatment, the mini electrifying unit needed to be removed and relocated to a new artery site after 30-45 days since scar tissue and calcification forming around the implant unit would lead to artery blockage. Kaali (along with co-inventor Peter Schwolsky) filed for a patent on this implantable electrifying device on Nov 16, 1990 and nine months later was granted patent #5,139,684 on August 18, 1992.
It's interesting to note two things here:
1. In order to obtain a patent from the United States Patent Office, Kaali and Schwolsky had to prove that the device works as claimed. Lacking solid proof, US patents are simply not granted.
2. Very often it takes years to obtain a patent, yet this patent was granted in only nine months; a further indication to me of the strength of their demonstrated claims
It's also interesting to note that other than the 3 publications mentioned above and the March '91 AIDS conference, nothing again appeared in print, radio, or TV about this important discovery as a potential treatment and cure for AIDS from Kaali and company. Most knowledgeable observers feel that Kaali and Lyman's discovery was intentionally suppressed following the March '91 AIDS conference presentation.
If AIDS research was on the level and not the sham that it actually is, this should have made front page news around the world. (Around 1999, I was contacted by a woman with AIDS who had managed to reach Dr. William Lyman over the phone. She asked him about his experiments with Kaali regarding blood electrification and if she could obtain the treatment through them. Lyman denied any knowledge of any AIDS treatment or cure. He said he never heard of Dr. Kaali and he had no idea what she was talking about concerning blood electrification and then hung up on her. What does that tell about the power of the people behind the suppression of this discovery?)
Accompanying document and addresses
Boyd Graves wrote:
They have no record of the U.S. Special Virus program (1962 - 1978). They have never mentioned the 1997 CURE for AIDS, "TETRASIL". WHY? Boyd EdGraves, J.D. 619-849-9364
Boyd Graves > wrote:
Date: Mon, 14 Jan 2008 14:14:52 -0800 (PST)
From: Boyd Graves boyded2003@yahoo.com
Subject: Africa and the U.S. AIDS CURE (patent#5676977)
To: Chairman Payne noel.lusane@mail.house.gov
CC: Speaker Nancy Pelosi wendell.primus@mail.house.gov
Senator Harry Reid carolyn_gluck@reid.senate.gov
Congressman BobFilner willie.blair@mail.house.gov. . . .
January 14, 2008
Donald Payne, Chairman
United States House Foreign Affairs Subcommittee on Africa and Global Health
United States Congress
United States of America
Re: Africa and the U.S. AIDS CURE
A Report to the United States House Foreign Affairs Subcommittee on Africa and Global Health
Dear Chairman Payne:
After contacting the Committee staff I hereby submit this request to provide testimony before Congress regarding my “Global Plan to End HIV/AIDS,� and the progress made to date.
During the year 2007, our efforts have led to the brink of clinical trials of the AIDS CURE in both Zambia and Angola. We seek the jurisdiction of the subcommittee for further oversight and direction.
In 1997, the United States patented the CURE for AIDS, U.S. patent#5676977. Go to www.uspto.gov. Part of the “Global Plan to end HIV/AIDS� is the initiation of “clinical trials� of the patented CURE for efficacy, protocol and modality. We believe this Congressional subcommittee is the appropriate Congressional authority to oversee the clinical trial testing of the ten year old patented CURE for AIDS.
Part two of the “PLAN� is a review and investigation of the U.S. Special Virus program (1962 – 1978). According to the experts, this federal program lies at the heart of the origin of HIV/AIDS. Specifically, the U.S. Special Virus program made the esp-1 virus in 1971. Under electron microscope, the esp-1 virus is identical to HIV. This point is further underscored when you compare the 1971 electron microscope of the esp-1 virus to the 2008 government HIV/AIDS poster, “Understanding HIV and AIDS.�
Mr. Chairman, how can the 2008 government poster of HIV/AIDS be identical to a photo from 1971? Further still, Congress funded the development of HIV/AIDS on June 9, 1969. See, U.S. House Resolution 15090, page 129.
The record reveals Congress funded the development of HIV/AIDS as early as May 1946. See, “Better� Than the Bomb, Time Magazine, June 3, 1946.
The record reveals that HIV/AIDS is a product of recombinant genetics, best highlighted by the “sheep� cells in its genome. The “visna� sheep cells alone PROVE HIV/AIDS is a synthetic biological agent EXACTLY as requested by the U.S. Pentagon on June 9, 1969. See, Science, Vol. 227, pp. 173 – 7, January 1985, see also, PROC NAS, Vol. 83, pp. 4007 – 11, June 1986, PROC NAS, Vol. 92, 3283 – 87, April 11, 1995.
According to the Proceedings of the United States of America, HIV/AIDS evolved from an “Icelandic� sheep disease! In fact the very strain is from 1932 (strain ks-1514). When we began giving syphilis to African Americans, we also began testing the infectious agent of HIV/AIDS on the sheep in Iceland. Tuskegee was not an isolated event!
In any testimony before your Committee we can conclude the evidence confirms HIV/AIDS is the result of a century long hunt for a contagious cancer that selectively kills. We also conclude the clinical trials of the patented CURE for AIDS should begin immediately as the health of Africa and the world begins the process of recovery from the greatest man made calamity in the history of the known world.
Respectfully submitted,
Boyd Ed Graves, J.D.
574 Garret Avenue
Chula Vista, CA 91910
619-849-9364
www.boydgraves.com
www.boydgraves.com/graves (bio)
www.boydgraves.com/comments/ (expert reviews)
cc: Nancy Pelosi, House Speaker
Joe Leonard, Congressional Black Caucus
Jerry Mazza is a freelance writer living in New York City. Reach him at gvmaz@verizon.net.
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