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On The Mechanisms Of Toxicity Of Chlorine Oxides
Against Malarial Parasites - An Overview
By Thomas Lee Hesselink, MD
Copyright September 6, 2007
- The purpose of this article is to propose research.
- Nothing in this article is intended as medical advice.
- No claims, promises nor guarantees are made.
ABSTRACT
Sodium chlorite (NaClO2)
can be acidified as a convenient method to produce
chlorine dioxide (ClO2)
which is a strong
oxidant
and a potent disinfectant. A protocol has been
developed whereby a solution of these compounds can be taken
orally. This procedure rapidly eliminates malaria and other
infectious agents in only one dose. Chlorine dioxide (ClO2)
is highly reactive with
thiols (RSH),
polyamines,
purines, certain amino acids and iron, all of which are
necessary for the growth and survival of pathogenic microbes.
Properly dosed this new treatment is tolerable orally
with only transient side effects. More research to better
document efficacy in malaria and in other infections is
urgently called for.
DISCOVERY
Jim Humble, a modern gold prospecting geologist, needed
to travel to malaria infested areas numerous times.
He or his coworkers would on occassion contract malaria.
At times access to modern medical treatment was absolutely
unavailable. Under such dire circumstances it was found
that a solution useful to sanitize drinking water was also
effective to treat malaria if diluted and taken orally.
[1a]
Despite no formal medical training Mr. Humble had the innate
wisdom to experiment with various dosage and administration
techniques. Out of such necessity was invented an easy to
use treatment for malaria which was found rapidly effective
in almost all cases.
[1b,1c]
MATERIALS AND METHODS
The procedure as used by Mr. Humble follows: A 28% stock
solution of 80% (technical grade)
sodium chlorite (NaClO2)
is prepared. The remaining 20% is a mixture of the usual
excipients necessary in the manufacture and stabilization
of sodium chlorite (NaClO2) powder or flake. Such are mostly sodium
chloride (NaCl) ~19%, sodium hydroxide (NaOH) <1%, and
sodium chlorate (NaClO3)
<1%. The actual sodium chlorite (NaClO2) present is
therefore 22.4%. Using a medium caliber dropper (25 drops
per cc), the usual administered dose per treatment is 6 to
15 drops. In terms of milligrams of
sodium chlorite (NaClO2)
, this calculates out to 9mg per drop or 54mg to 135mg per treatment.
Effectiveness is enhanced, if prior to administration the
selected drops are premixed with 2.5 to 5 cc of table vinegar
or lime juice or 5-10%
citric acid
and allowed to react for 3 minutes.
The resultant solution is always mixed into a glass
of water or apple juice and taken orally. The
carboxylic acids
neutralize the sodium hydroxide (NaOH) and at the same time convert
a small portion of the chlorite (ClO2-) to its conjugate acid known as
chlorous acid (HClO2)
. Under such conditions the chlorous acid (HClO2) will oxidize other
chlorite anions (ClO2-) and gradually produce
chlorine dioxide (ClO2)
. Chlorine dioxide (ClO2) appears in
solution as a yellow tint which smells exactly like elemental
chlorine (Cl2). The above described procedure can be repeated
a few hours later if necessary. Considerably lower dosing
should be applied in children or in emaciated individuals
scaled down according to size or weight. The diluted solution
can be taken without food to enhance effectiveness but this
often causes nausea. Drinking extra water usually relieves
this. Nausea is less likely to occur if food is present in
the stomach. Starchy food is preferable to protein as protein
quenches chlorine dioxide. Significant amounts of vitamin C
(ascorbic acid)
must not be present at any point in the
mixtures or else this will quench the chlorine dioxide (ClO2)
and render it ineffective. For the same reason
antioxidant
supplements should not be taken on the day of treatment.
Other side effects reported are transient vomiting, diarrhea,
headache, dizziness, lethargy or malaise.
[2a,2b]
EXPLORING BENEFITS
I first learned of Jim Humble's remarkable discovery in the fall of 2006. That
sodium chlorite (NaClO2)
or
chlorine dioxide (ClO2)
could kill parasites in vivo seemed immediately reasonable to me
at the onset. It is well known that many disease causing
organisms are sensitive to
oxidants
. Various compounds
classifiable as oxides of chlorine such as
sodium hypochlorite (NaClO)
and
chlorine dioxide (ClO2)
are already widely used as disinfectants.
What is novel and exciting here is that Mr. Humble's technique
seems:
- easy to use,
- rapidly acting,
- successful,
- apparently lacking in toxicity, and
- affordable.
If this treatment continues to prove effective, it could be
used to help rid the world of one of the most devasting of all
known plagues.
[3a-3e]
Especially moving in me is the
empathy I feel for anyone with a debilitating febrile illness.
I cannot forget how horrible I feel whenever I have caught
influenza. How much more miserable it must be to suffer like
that again and again every 2 to 3 days as happens in malaria.
Millions of people suffer this way year round. 1 to 3 million
die from malaria every year mostly children. Thus motivated I
sought to learn all I could about the chemistry of the oxides
of chlorine.
[4a-4hh]
I wanted to understand their probable mechanisms of toxicity
towards the causative agents of malaria (Plasmodium species).
I wanted to check available literature pertaining to issues
of safety or risk in human use.
OXIDANTS AS PHYSIOLOGIC AGENTS
Oxidants
are atoms or molecules which take up electrons.
Reductants
are atoms or molecules which donate electrons
to oxidants. I was already very familiar with most of the
medicinally useful oxidants. I had taught at numerous
seminars on their use and explained their mechanisms of
action on the biochemical level. Examples are:
hydrogen peroxide (H2O2),
zinc peroxide (ZnO2), various
quinones, various
glyoxals,
ozone,
ultraviolet light, hyperbaric
oxygenation,
benzoyl peroxide,
anodes,
artemisinin,
methylene blue,
allicin,
iodine and permanganate.
Some work has been done using dilute solutions of
sodium chlorite (NaClO2)
internally to treat fungal infections,
chronic fatigue, and cancer; however, little has been
published in that regard.
[5a-5h]
Low dose
oxidant
exposure to living red blood cells induces a
change in
oxyhemoglobin (Hb-O2)
activity so that more
oxygen (O2)
is released to tissues throughout the body.
[6a-6d]
Hyperbaric
oxygenation
(oxygen under pressure) is:
- a powerful detoxifier against
carbon monoxide (CO);
- a powerful support for natural healing in burns,
crush injuries, and ischemic strokes; and
- an effective aid to treat most bacterial infections.
[7a-7d]
Taken internally, intermittently and in low doses many
oxidants
have been found to be powerful immune stimulants.
Sodium chlorite (NaClO2)
with
lactic acid
as in the product
"WF10" has similarly been shown to modulate immune activation.
Exposure of live blood to
ultraviolet light
also has immune enhancing effects.
These treatments work through a natural physiologic
trigger
mechanism, which induces peripheral white blood cells
to express and to release
cytokines
. These cytokines serve as a control system to down-regulate
allergic reactions and as an alarm system to increase
cellular attack
against pathogens.
[8a-8v]
Activated cells
of the immune system naturally produce strong
oxidants
as part of the inflammatory process at sites
of infection or cancer to rid the body of these diseases.
Examples are:
superoxide (*OO-),
hydrogen peroxide (H2O2),
hydroxyl radical (HO*),
singlet oxygen (O=O) and
ozone (O3).
[9a-9v]
Another is
peroxynitrate (-OONO)
the
coupled
product of
superoxide (*OO-) and
nitric oxide (*NO)
radicals.
[10a-10h]
Yet another
killer cell
product is hypochlorous acid (HOCl) the conjugate acid of
hypochlorite (ClO-) anion
. [11a,11b,11c]
The immune system uses these same oxidants to attack various parasites.
[12a,12b,12c]
OXIDES OF CHLORINE AS DISINFECTANTS
All bacteria have been shown to be incabable of growing in
any medium in which the
oxidants
(electron grabbers) out-number the
reducants
(electron donors).
[13a]
Therefore, oxidants are at least bacteriostatic and at most bacteriocidal.
[13b]
Many oxidants have been proven useful as antibacterial disinfectants.
[13c,13d]
Hypochlorites (ClO-)
are commonly used as bleaching agents,
as swimming pool sanitizers, and as disinfectants. At low concentrations
chlorine dioxide (ClO2)
has been shown to kill many types of bacteria
[14a-14j], viruses
[15a-15L] and protozoa
[16a-16f].
Ozone (O3)
or chlorine dioxide (ClO2) are often used to disinfect public water
supplies or to sanitize and deodorize waste water.
[17a-17L]
Sodium chlorite (NaClO2)
or chlorine dioxide (ClO2) solutions are used
in certain mouth washes to clear mouth odors and oral bacteria.
[18a-18i]
Chlorine dioxide sanitizes food preparation facilities.
[19a]
Acidified sodium chlorite is FDA approved as a spray in the
meat packing industry to sanitized meat.
[20a-20g]
This can also be used to sanitize vegetables and other foods.
[21a,21b]
Farmers use this to cleanse the udders of cows to prevent mastitis,
[22a,22b,22c]
or to rid eggs of pathogenic bacteria. Chlorine dioxide
can be used to disinfect endoscopes.
[23a]
Oxidants such as iodine, various peroxides, permanganate and
chlorine dioxide can be applied topically to the skin to
treat infections caused by bacteria or fungi.
[24a-24d]
MALARIA IS OXIDANT SENSITIVE
From November 2006 through May of 2007 I spent hundreds
of hours searching biochemical literature and medical
literature pertaining to the biochemistry of Plasmodia.
Four species are commonly pathogenic in humans namely:
Plasmodium vivax, Plasmodium falciparum, Plasmodium ovale
and Plasmodium malariae. What I found was an abundance
of confirmation that, just like bacteria, Plasmodia are
indeed quite sensitive to
oxidants.
[25a-25p]
. Examples of oxidants toxic to Plasmodia include:
artemisinin, artemether
[26a-26n],
t-butyl hydroperoxide
[27a]
, xanthone
[28a]
, various
quinones
(e.g. atovaquone,
lapachol,
beta-lapachone,
menadione)
[29a-29m] and
methylene blue
[30a-30i] .
TARGETING THIOLS
Like bacteria, fungi and tumor cells, the ability of
Plasmodia to live and grow depends heavily on an internal
abundance of
reductants
. This is especially true regarding
thiol (RSH)
compounds also known as
sulfhydryl compounds (RSH).
[31a,31b]
Thiols (RSH) as a class behave as reductants (electron
donors). As such they are especially sensitive to
oxidants
(electron grabbers). Thiols (RSH) such as
glutathione (GSH)
[32a-32L]
and other sulfur compounds
[33a,33b,33c]
are reactive with
sodium chlorite (NaClO2)
and with
chlorine dioxide (ClO2).
These are the very agents present in Mr. Humble's solution.
The products of
oxidation
of thiols (RSH) using various oxides of chlorine are:
disulfides (RSSR),
disulfide monoxides (RSSOR), sulfenic acids (RSOH),
sulfinic acids (RSO2H), and sulfonic acids (RSO3H).
None of these can support the life
processes of the parasite. Upon sufficient removal of the
parasite's life sustaining thiols (RSH) by oxidation,
the parasite rapidly dies.
[34a-34e]
A list of thiols (RSH) upon which survival of Plasmodium
species heavily depend includes:
lipoic acid and dihydrolipoic acid
[35a-35h],
coenzyme A and acyl carrier protein
[36a-36f],
glutathione
[37a-37m],
glutathione reductase
[38a-38e],
glutathione-S-transferase
[39a-39g],
peroxiredoxin
[40a-40L],
thioredoxin
[41a-41g],
glutaredoxin
[42a,42b,42c],
plasmoredoxin
[43a],
thioredoxin reductase
[44a-44g],
falcipain
[45a-45i], and
ornithine decarboxylase
[46a-46e].
HEME IS AN OXIDANT SENSITIZER
Of particular relevance to treating malaria is the fact that
Plasmodial trophozoites living inside red blood cells must
digest hemoglobin (Hb) as their preferred protein source.
[47a,47b]
They accomplish this by ingesting hemoglobin (Hb) into an
organelle known as the "acid food vacuole".
[47c-47h]
Incidently, the high concentration of
acid (H+)
in this organelle
could serve as an additional site of conversion of
chlorite (ClO2-)
to the more active
chlorous acid (HClO2)
and
chlorine dioxide (ClO2)
right inside the parasite.
Furthermore, Plasmodia consume 50 to 100 times more glucose
than noninfected red blood cells most of which is metabolized to
lactic acid
a known activator of chlorite (ClO2-).
[48a-48b]
Next falcipain (a hemoglobin digesting enzyme)
hydrolyzes
hemoglobin (Hb) protein to release its nutritional amino acids.
[49a-49e]
A necessary byproduct of this digestion is the
release of 4 heme molecules from each hemoglobin molecule (Hb)
digested. Free heme (also known as ferriprotoporphyrin IX) is
redox active
and can react with ambient
diatomic oxygen (O2)
, an abundance of which is always present in red blood cells.
This produces
superoxide radical (*OO-),
hydrogen peroxide (H2O2)
and other reactive oxidant toxic species (ROTS).
[50a-50bb]
. These can rapidly poison the parasite internally.
To protect themselves against this dangerous side-effect
of eating blood protein, Plasmodia must maintain a high
reductant
capacity (an abundance of reduced
NADPH
and
thiols)
to quench these ROTS. This is their main mechanism of
antioxidant
defense.
[51a-51n]
Plasmodia must also rapidly and continuously eliminate heme ,
which is accomplished by two methods.
1) heme is polymerized producing hemozoin.
[52a-52k]
2) heme is metabolized in a detoxification process
that requires reduced
glutathione (GSH).
[53a,53b]
Therefore any method (especially exposure to oxidants) which
limits the availability of reduced glutathione (GSH) will
cause a toxic build up of heme and of ROTS inside the
parasite cells. Sodium chlorite (NaClO2) and chlorine dioxide (ClO2)
(the exact agents present in Mr. Humble's treatment) readily
oxidize glutathione (GSH).
[54a,54b]
Therefore, a rapid killing of Plasmodia upon taking acidified
sodium chlorite orally should be expected.
OVERCOMING ANTIBIOTIC RESISTANCE WITH OXIDATION
Now the issue of resistance of Plasmodium species to commonly
used antiprotozoal antibiotics must be addressed. Quinine,
chloroquine, mefloquine, quinacrine, amodiaquine, primaquine
and other quinoline-like antibiotics all work by blocking the
heme detoxifying system inside the trophozoites.
[55a-55gg]
Many Plasmodial strains against which quinolines have
repeatedly been used have found ways to adapt to these drugs
and to acquire resistance. Research into the mechanisms of
resistance has found that often resistance is accomplished
by a meere upregulation of
glutathione
production and utilization.
[56a-56j]
Consequently oxidizing or otherwise depleting glutathione (GSH)
inside the parasite usually restores sensitivity to the quinoline antibiotics.
[57a-57f]
Therefore, protocols combining the use of oxidants with quinolines
are under developement and already showing signs of success.
[57g]
In this context let us consider that no
amount of intraplasmodial glutathione (GSH) could ever resist
exposure to a suffient dose of
chlorine dioxide (ClO2).
Note that each molecule of ClO2 can disable 1 to 5 molecules
of glutathione (GSH) depending on the reaction mechanism.
2(GSH) + 2(ClO2) -> 1(GSSG) + 2(H+) + 2(ClO2-)
or 10(GSH) + 2(ClO2) -> 5(GSSG) + 2(H+) + 2(Cl-) + 4(H2O)
SOME INCOMPATIBILITIES
Acidified sodium chlorite could provide a powerful new
opportunity to improve or to restore sensitivity to
quinolines by virtue of its oxidative power.
However, quinolines contain secondary (RNHR') or tertiary
(RNR'R") amino groups which react with chlorine dioxide
(ClO2) in such a way that both could destroy each other.
Some possible strategies to resolve this incompatibility
are suggested below.
- Acidified sodium chlorite could be used as
explained above only as a solo therapy.
- Quinoline administration could be withheld
until after the acidified sodium chorite has
completed its action.
- Patients already preloaded with a quinoline
could stop this, wait a suitable period of time
for this to wash out, then administer the
acidified sodium chlorite.
- The quinoline could remain in use and while
the less active sodium chlorite is administered
without acid. This should retain plenty of oxidant
effectiveness without destroying any quinoline or
wasting too much oxidant.
- Switch from a quinoline to an endoperoxide
(such as artemisinin) or to a quinone (such as
atovaquone) before using acidified sodium chlorite,
as these may be less sensitive toward destruction
by chlorine dioxide.
Similar problems apply to
methylene blue
and many other drugs if they have an unoxidized sulfur atom,
a phenol group, a secondary amine (RNHR') or a tertiary amine (RNR'R").
Such are also very reactive with the chlorine dioxide (ClO2) component.
[58a]
REDUCTANT RECOVERY SYSTEMS
Living things possess a recovery system to rescue oxidized
sulfur compounds. It operates through the
donation of hydrogen atoms
to these compounds and thereby restores their original condition as
thiols (RSH).
[59a,59b]
2 [H] + (RSSR) -> 2(RSH)
This system is known as the
hexose monophophate shunt.
[59c,59d]
A key player in this system is the
enzyme
glucose-6-phosphate-dehydrogenase (G6PDH)
. Patients with a genetic defect of G6PDH, known as
glucose-6-phosphate-dehydrogenase deficiency disease,
are especially sensitive to
oxidants
and to
prooxidant
drugs. However, this genetic disease has a benefit
in that such individuals are naturally resistant to
malaria. They can still catch malaria, but it is much less
severe in them, since they permanently lack the enzyme
necessary to assist the parasite in
reactivating
glutathione disulfide (GSSG)
and other oxidized thiols.
[60a-60i]
Chlorine dioxide (ClO2)
has been shown to
oxidize
L-tyrosine and L-tryptophan residues inside G6PDH irreversibly
inhibiting
this enzyme.
[61a]
Furthermore, G6PDH is sensitive to inhibition by
sodium chlorate (NaClO3)
, another member of the chlorine oxide family of compounds.
[61b,61c,61d]
Sodium chlorate (NaClO3) is a trace ingredient present in Jim Humble's
antimalarial solution. Some sodium chlorate (NaClO3) should also
be produced in vivo by a slow reaction of chlorine dioxide (ClO2)
with water under alkaline conditions.
[61e]
2(ClO2) + 2(OH-) -> (ClO2-) + (ClO3-) + H2O
The Plasmodia may attempt to restore any thiols (RSH) lost to oxidation.
However, this becomes more difficult as G6PDH is inhibited by chlorine
dioxide (ClO2) or by chlorate (ClO3-).
TARGETING IRON
While most available literature refers to redox imbalances
causing depletion of necessary
thiols (RSH)
. Other mechanisms of toxicity of the oxides of chlorine against
Plasmodia should also be considered. Oxides of chlorine are generally
rapidly reactive with
ferrous iron (Fe++)
converting it to
ferric (Fe+++).
[62a-62d]
This explains why in cases of overdosed exposures to oxides
of chlorine such as
sodium chlorite (NaClO2)
there was a notable rise in
methemoglobin levels.
[63a,63b]
Methemoglobin is a metabolically inactive
form of hemoglobin in which its ferrous iron (Fe++) cofactor
has been oxidized to ferric (Fe+++). In living things
including parasites iron is a necessary
cofactor
for many other important
enzymes.
[64a-64f]
Thus it is reasonable to expect that any damage to Plasmodia
caused by various oxides of chlorine may be compounded
by conversion of ferrous (Fe++) cofactors to ferric (Fe+++) or other alterations of iron compounds.
[65a-65g]
The enzyme
superoxide dismutase (SOD)
inside Plasmodial cells also utilizes iron in its active center.
[66a-66m]
Chlorine dioxide (ClO2) also readily oxidizes
manganese (Mn++).
[67a]
TARGETING POLYAMINES
Other metabolites necessary for survival and growth in
tumors, bacteria and parasites are the
polyamines.
[68a-68d]
Plasmodia quit growing and die, when polyamines are lacking
[69a-69k]
, or when their functions are blocked
[70a-70L]
. Polyamines are also sensitive to
oxidation
and can be eliminated by strong
oxidants
. When oxidized, polyamines are converted to
aldehydes
, which are deadly to parasites and to tumors.
[71a-71e]
Chlorine dioxide (ClO2)
is known to be
especially reactive against secondary amines.
[72a]
This includes
spermine
and
spermidine
the two main biologically important polyamines.
Thus any procedure which is successful to oxidize both
thiols (RSH)
and
polyamines
does quadruple damage to the pathogen:
- oxidation of the thiol containing enzyme
ornithine decarboxylase
inhibits
polyamine synthesis;
- oxidation of the thiol containing enzyme
S-adenosyl-L-methionine
decarboxylase
also inhibits polyamine synthesis;
(see references with "TARGETING THIOLS" above)
- oxidation of the secondary amines
spermidine
and
spermine
directly eliminates these essential polyamines;
- the products of polyamine oxidation are toxic
aldehydes.
TARGETING PURINES
Purines are essential to many life processes. These molecules
have a double ring structure. The rings are heterocyclic
being composed of both carbon and nitrogen. Their nitrogen
atoms are vulnerable to reaction with
chlorine dioxide (ClO2).
[73a]
Examples of important biologic purines are
xanthine
, hypoxanthine, inosine, guanine and adenine. Guanine and
adenine are essential components of DNA and RNA necessary
for all genetic functions and for all protein syntheses.
Adenine is an essential component of the
cofactors
NADH,
NADPH,
FAD and
ATP
, all of which are necessary for many metabolic functions including
oxidation-reduction
and energy metabolism.
Any purines lost by chlorine dioxide (ClO2)
exposure can readily be replaced by host cells.
[74a]
Plasmodia and other apicomplexae are uniquely vulnerable
to purine deficiency as they lack the
enzymes
necessary to produce purines for themselves.
[75a,75b,75c]
Instead these must be scavenged from host cells and imported
across the plasma membranes of the parasite cells.
[76a-76i]
Drugs are under development to inhibit purine
utilization by Plasmodia and are already
showing signs of success.
[77a-77g]
Temporarily destroying some of the purines
in the blood as should occur upon brief exposure
to chlorine dioxide (ClO2) in vivo is very likely
an additional stress that Plasmodia cannot tolerate.
TARGETING PROTEINS
Chlorine dioxide (ClO2)
is highly reactive with
thiols (RSH),
phenols
, secondary amines and tertiary amines. Therefore,
proteins composed of amino acids which present these
reactive groups are vulnerable to
oxidation
by this agent.
Proteins which present residue(s) of the amino acid
L-cysteine
are discussed above under TARGETING THIOLS. L-tyrosine
presents a phenol group and is therefore similarly vulnerable.
L-tryptophan and L-histidine present secondary amino groups (RNR')
which are also especially reactive with chlorine dioxide (ClO2).
[78a-78d]
SAFETY ISSUES
A remaining concern is safety. So far, at least anecdotally,
the dosages of the oxides of chlorine as administered orally
per Jim Humble's protocol have produced no definite toxicity.
Some have taken this as often as 1 to 3 times weekly and
on the surface seem to suffer no ill effects. To be certain
if this is safe more research is warranted for such long term
or repeated use. The concern is that too much or too frequent
administration of oxidants could excessively deplete the body's
reductants
and promote
oxidative stress
. One useful
way to monitor this may be to periodically check
methemoglobin
levels in frequent users.
Sodium chlorite (NaClO2)
, as found in municipal water supplies after disinfection by
chlorine dioxide (ClO2)
, has been studied and proven safe.
[79a-79j]
Animal studies using much higher oral or topical
doses have proven relatively safe.
[80a-80t]
In a suicide attempt 10g of sodium chlorite (NaClO2)
taken orally caused nearly fatal kidney failure and
methemoglobinemia
refractory to treatment with
methylene blue.
[81a]
Inhalation or aerosol exposure to chlorine dioxide (ClO2) gas
is highly irritating and generally not recommended.
[82a-82g]
Special precautions must be employed in cases of
glucose-6-phosphate-dehydrogenase
deficiency disease, as these patients
are especially sensitive to oxidants of all kinds.
[83a-83g]
Nevertheless, oral acidified sodium chlorite solutions
might even be found safe
[84a,84b]
and effective in them, but probably will
need to be administered at lower doses.
MORE RESEARCH
It is hoped that this overview will spark a flurry of
interest, and stimulate more research into the use of
acidified sodium chlorite in the treatment of malaria.
The above appreciated observations need to be proven
more rigorously and published
[85a]
. The biochemistry most likely
involved suggests that other members of the phylum
Apicomplexa should also be sensitive to this treatment.
[86a]
This phylum includes: Plasmodium, Babesia, Toxoplasma
[87a]
, Cryptosporidium
[88a]
, Eimeria, Theileria, Sarcocystis,
Cyclospora, Isospora and Neospora. These pathogens are
responsible for widespread diseases in humans, pets and
cattle. Other thiol (RSH) dependent parasites should also
be susceptible to acidified sodium chlorite. For example
Trypanosoma and Leishmania extensively utilize and cannot
survive without the cofactor known as trypanothione. Each
molecule of trypanothione presents 2 sulfur atoms and 5
secondary amino groups all of which are vulnerable to
oxidative destruction from chlorine dioxide (ClO2).
[89a-89p]
Chlorine dioxide (ClO2) has been proven to be cidal
to almost all known infectious agents in vitro using
remarkably low concentrations. This includes parasites,
fungi, bacteria and viruses. The experiences noted above
imply that this compound is tolerable orally at effective
concentrations.
[90a,90b]
Therefore extensive research is warranted
to determine if acidified sodium chlorite is effective
in treating other infections. We may be on the verge of
discovering the most potent and broad spectrum antimicrobial agent
yet known. Special thanks go to Jim Humble for his
willingness to share his discovery with the world.
by Thomas Lee Hesselink, MD
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