povidone

(redirected from Polyvinylpyrrolidone)
Also found in: Medical, Acronyms, Wikipedia.

po·vi·done

 (pō′vĭ-dōn′)
n.
A polymer used as a vehicle for a drug, especially iodine.

[po(ly)vi(nylpyrroli)done.]
Mentioned in ?
References in periodicals archive ?
06LiNbO3 Piezoelectric Ceramics Prepared from the Solid State Reaction Modified with Polyvinylpyrrolidone (PVP) of Different Molecular Weights, Ceramics International, 38, 2513 (2012).
4] polymorphs subjected to high-energy mechanochemical ball milling in polyvinylpyrrolidone (PVP) solution as nonionic stabilizer.
Effect of polyvinylpyrrolidone on bovine oocyte maturation in vitro and subsequent fertilization and embryonic development.
Soleimani said that next, cobalt alumina nano pigments were produced through co-precipitation method in the presence of surfactants, cetyltrimethylammonium bromide (CTAB), polyvinylpyrrolidone (PVP), and a combination of PVP and CTAB.
The prepared sperm was diluted 1:1 with 12% polyvinylpyrrolidone in PBS immediately, just before microinjection.
The cyst cavities were irrigated with hypertonic saline solution and polyvinylpyrrolidone, and then filled with bone allograft.
Schwartz, PVP--A Critical Reviewof the Kinetics and Toxicology of Polyvinylpyrrolidone (Povidone), Lewis, Chelsea, Mich, USA, 1990.
Briefly, the AgNPs were made by adding 100 mM silver nitrate to a 1% (w/v) tannic acid solution (pH adjusted to 8 by adding 150 mM potassium carbonate) of polyvinylpyrrolidone (PVP) with stirring.
When polyvinylpyrrolidone was used to inhibit polyphenol oxidase activity, the yield and integrity of RNA had improved significantly.
An aqueous solution (B) of sodium lauryl sulphate (2 g) in distilled water (20 ml) was added drop-wise with magnetic stirring to the organic phase (A) obtained by mixing the solution of polyvinylpyrrolidone (PVP) (2 g) in dichloromethane (20 ml) with the solution of technical grade larvicide (0.
Heifers were given 100 mg of FSH (Folltropin[R]-V) dissolved in 10 ml of 30% (wt/vol) polyvinylpyrrolidone (PVP) to form FSHp (Chasombat and Vongpralub, 2011) by a single dose administration 24 h after follicular ablation.