Zinc pyrithione is a coordination complex of zinc. This colourless solid is used as an antifungal and antibacterial agent. This coordination complex, which has many names, was first reported in the 1930s.
Structure of the compound
The pyrithione ligands, which are formally mono
anions, are
chelated to Zn
2+ via
oxygen and
sulfur centers. In the crystalline state, zinc pyrithione exists a centrosymmetric dimer (see figure). Each zinc is bonded to two sulfur and three oxygen centers. In solution, however, the dimers dissociate via scission of one Zn-O bond.
Pyrithione is the conjugate base derived from 2-mercaptopyridine-N-oxide (CAS# 1121-31-9), a derivative of pyridine-N-oxide.
Uses
Medical
Zinc pyrithione is best known for its use in treating
dandruff and seborrheic dermatitis. It also has antibacterial properties and is effective against many
pathogens from the
streptococcus and
staphylococcus class. Its other medical applications include treatments of
psoriasis,
eczema,
ringworm,
fungus,
athletes foot,
dry skin,
atypical dermatitis,
tinea, and
vitiligo.
Zinc pyrithione is approved for over-the-counter topical use in the United States as a treatment for dandruff. It is the active ingredient in several anti-dandruff shampoos such as Head & Shoulders. However, in its industrial forms and strengths, it may be harmful by contact or ingestion.
In paint
Due to its low
solubility in
water (8 ppm at neutral pH), zinc pyrithione is suitable for use in outdoor
paints and other products that provide protection against
mildew and
algae. It is an effective
algaecide. It is chemically incompatible with paints relying on metal carboxylate curing agents. When used in latex paints and the water contains high amount of
iron, a sequestering agent that will preferentially bind the iron ions is needed. Its decomposition by
ultraviolet light is slow, providing years of protection even against direct sunlight.
In sponges
Zinc pyrithione is also used as an
antibacterial treatment for household
sponges, most notably by the
3M Corporation.
Mechanism of action
Its antifungal effect is proposed to derive from its ability to disrupt
membrane transport by blocking the proton pump that energizes the transport mechanism. Fungi are capable of inactivating pyrithione in low concentrations.
References
External links