Povidone is completely soluble in cold and
mild-warm water, ethyl alcohol, isopropyl alcohol, polyethylene glycol, and
glycerol. Its stability in solution is much greater than that of tincture of
iodine or Lugol's solution. Its CAS NO is 9003-39-8.
It was discovered at the Industrial
Toxicology Laboratories in Philadelphia
by H. A. Shelanski and M. V. Shelanski. They carried out tests in vitro to
demonstrate anti-bacterial activity, and found that the complex was less toxic
than tincture of iodine in mice. Human clinical trials showed the product to be
superior to other iodine formulations. It was first sold in 1955, and has since
become the universally preferred iodine antiseptic.
Free iodine, slowly liberated from the povidone
complex in solution, it kills eukaryotic or prokaryotic cells through
iodination of lipids and oxidation of cytoplasmic and membrane compounds. This
agent exhibits a broad range of microbicidal activity against bacteria, fungi,
protozoa, and viruses. Slow release of iodine from the PVPI complex in solution
minimizes iodine toxicity towards mammalian cells.
Povidone is a broad spectrum antiseptic for
topical application in the treatment and prevention of infection in wounds. It
may be used in first aid for minor cuts, grazes, burns, abrasions and blisters.
Following the discovery of iodine by
Bernard Courtois in 1811, it has been broadly used for the prevention and
treatment of skin infections, and the treatment of wounds. Iodine has been
recognized as an effective broad-spectrum bactericide, and it is also effective
against yeasts, molds, fungi, viruses, and protozoans. Drawbacks to its use in
the form of aqueous solutions include irritation at the site of application,
toxicity and the staining of surrounding tissues. These deficiencies were
overcome by the discovery and use of POVIDONE, in which the iodine is carried
in a complexed form and the concentration of free iodine is very low.
The product thus serves as an iodophor. In
addition, it has been demonstrated that bacteria do not develop resistance to Povidone,
and the sensitization rate to the product is only 0.7% Consequently, Povidone
has found broad application in medicine as a surgical scrub; for pre- and
post-operative skin cleansing; for the treatment and prevention of infections
in wounds, ulcers, cuts and burns; for the treatment of infections in decubitus
ulcers and stasis ulcers; in gynecology for vaginitis associated with candidal,
trichomonal or mixed infections.
For these purposes Povidone has been
formulated at concentrations of 7.5–10.0% in solution, spray, surgical scrub,
ointment, and swab dosage forms. It is available without a prescription under
the generic name povidone-iodine or the brand name Polydine and Betadine.
It is used in pleurodesis (fusion of the
pleura because of incessant pleural effusions). For this purpose,
povidone-iodine is equally effective and safe as talc, and may be preferred
because of easy availability and low cost.
2.5 percent of buffered Povidone solution
can be used for prophylaxis of neonatal conjunctivitis (Ophthalmia neonatorum)
which can lead to blindness, especially if it is caused by Neisseria
gonorrhoeae, or Chlamydia trachomatis. Povidone appears to be very suitable for
this purpose because unlike other substances it is efficient also against fungi
and viruses (including HIV and Herpes simplex).
Povidone can be loaded into hydrogels
(based on carboxymethyl cellulose, poly(vinyl alcohol) and gelatin, or on
crosslinked polyacrylamide). These hydrogels can be used for wound dressing.
The rate of release of the iodine in the POVIDONE is heavily dependent on the
hydrogel composition. The release rate increases with more CMC/PVA and decreases
with more gelatin.
Povidone can also be used to reduce skin
damage from mustard gas, although it must be applied immediately post-exposure
to have any effect, and mustard gas exposure is usually not noticed until the
onset of skin irritation, by which point POVIDONE administration is useless.
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