Zinc Pyrithione although the exact mechanism of action of the "activated"
zinc
pyrithione preparation is unknown it may be speculated that the
possible anti-proliferative mechanism of action of zinc pyrithione
may involve the regulation of DNA transcription factors containing
"zinc finger" binding domains.(9,10) It is also well recognized that
many enzymes require the binding of metal ions for activation.
Perhaps one of these (zinc requiring) enzymes or transcription
factors plays a key role in the regulation of cellular
proliferation. It is also well known that a deficiency of zinc
produces a disease state (acrodermatitis enteropathica) that
includes psoriasiform lesions (11,12). Perhaps the vehicle or the
activated form of zinc pyrithione permits a physiologic level of
zinc to be reached in the target cells, either epidermal and/or
lymphocytic. The combination of zinc pyrithione with the other
vehicle including isopropyl myristate may also have significant
additional influence on clinical effectiveness..
Zinc pyrithione is also used extensively in adhesive coatings for
floorings and for fungal protection of carpet backing. It is
registered with the U.S. Environmental Protection Agency as zinc
OMADINE® fungicide by Arch for applications such as dry-film
preservation of architectural and industrial paints and coatings, as
well as adhesives, sealants and grouts. Zinc OMADINE® fungicide is
available in standard and fine-particle, 48% aqueous-dispersion form
with a negligible VOC content.
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Zinc pyrithione is also known as zinc 2-pyridinethiol-n-oxide. It
has a water solubility of 8 ppm at neutral pH. This low solubility
makes the zinc pyrithione suitable for use in outdoor products that
require protection against microorganisms, because it will not
easily leach out of a paint film.
Zinc Pyrithione though still relatively new to the industry, has
been well-received by the industry as both a fungicide and
algaecide. During the last 10 years, the industry has not had many
choices of new dry-film preservatives. However, zinc pyrithione
actually is not a new fungicide -- it has been used for more than 30
years as the fungicide in anti dandruff shampoos and similar
personal care products.
UV degradation of zinc pyrithione in a paint film is gradual, and
therefore, efficacy in direct sunlight can be expected for years.
Its stability at high temperatures is also very good -- zinc
pyrithione can withstand temperatures of 100°C for at least 120
hours, with a decomposition temperature of 240°C. Another concern
for fungicides in latex paints is alkaline stability.
The stability of zinc pyrithione is presently being studied at up
to pH 11.0. After nine months at pH 11.0, a 0.5 % zinc pyrithione
dispersion is still stable, and the study will continue.
Because pyrithione is an excellent chelating agent, zinc
pyrithione cannot be used in paints that relies on metal
carboxalates for film cure. The metal, particularly cobalt will
transchelate with the zinc and lose the ability to catalyze the film
curing. Also, in latex paints, if the water supply contains high
concentrations of soluble iron, a sequestering agent should be used
to preferentially chelate with the iron.
Since zinc pyrithione shows little tendency to yellow in paint
films and does not cause acceleration of chalking or fading, the
same fungicide can be used for both whites and colors. This reduces
inventory and helps formulators avoid the inadvertent addition of
the wrong fungicide to a batch of paint. Photo below
illustrates the negligible effect zinc pyrithione has on the fading
of a blue tint, acrylic latex paint when compared to a commonly used
fungicide.
We present here a report of a case using a novel topical
preparation of zinc pyrithione for the treatment of psoriasis.
Topical zinc pyrithione appears to be a safe and effective treatment
for psoriasis.
This report describes the use of a preparation containing zinc
pyrithione (0.25%) in a vehicle containing isopropyl myristate to
treat a case of psoriasis.
We have recently become aware of a new anti-psoriatic treatment
containing zinc pyrithione (which is also recognized as the active
ingredient in a major anti-dandruff shampoo). The effectiveness of
zinc pyrithione to treat seborrheic dermatitis and psoriasis has
been well documented (4,5,6,7,8,13). Since some believe that
seborrheic dermatitis and psoriasis may lie on different ends of the
same spectrum, it seemed reasonable to try a topical preparation of
zinc pyrithione to treat psoriasis. The mechanism of action of
zinc
pyrithione on psoriasis and seborrheic dermatitis has been reported
to be anti-proliferative via "DNA interactions", anti-yeast,
antiseptic, and keratinolytic mechanisms.(4,5,6,8)
We report here the clinical results of a psoriatic patient treated
with a topical spray containing zinc pyrithione.
A 39 year old man with a 14 year history of moderate plaque
psoriasis was instructed to spray the topical zinc pyrithione
preparation, twice per day, to the left elbow. The right elbow was
to be used as a control and received no treatment of any kind during
the trial. The treatment preparation contains zinc pyrithione
(0.25%) in a vehicle containing isopropyl myristate.
zinc pyrithione preparation to the left elbow only. At the end of
the 3 week treatment period the left (treated) elbow was essentially
clear. The right (control) elbow remained virtually unchanged, if
not slightly worse. The patient also reported a complete
disappearance of pruritus approximately 3 days into treatment, on
the zinc pyrithione preparation treated plaque only, that was
sustained throughout the treatment period.
In this preliminary report, an aerosol preparation of zinc
pyrithione (0.25%) in a vehicle containing isopropyl myristate
appears to be a safe and effective treatment for psoriasis. Each ml
of the liquid preparation will cover an area the size of a palm,
approximately 6-8 times.
Because of the promising results in this case report and a plethora
of anecdotal reports, we are initiating a 60 patient, double-blind,
vehicle- controlled clinical study evaluating the use of topical
zinc pyrithione for the treatment of psoriasis. If additional
controlled research confirms these encouraging results, topical zinc
pyrithione may represent one of the major advances n the treatment
of psoriasis.
At the four-week follow up, the combination of zinc pyrithione demonstrated great efficacy in all parameters. For
erythema, zinc pyrithione propionate demonstrated a 50 percent
improvement.
For hyperkeratosis, zinc pyrithione success rate as compared with
generic. There was a slight improvement of 23 percent with negative
control cream. For thickness, zinc pyrithione once again had the
greatest improvement, 58 percent
We found zinc pyrithione more effective than generic.
There appears to be a synergistic effect associated with the
combination of zinc pyrithione proliferation with the zinc and anti-inflammatory
of anti-immune effect. Zinc has already been demonstrated to work in
conditions such as seborrheic dermatitis in which epidermal cells
proliferate.