Please use this identifier to cite or link to this item: https://doi.org/10.1081/PDT-200033004
Title: Complexation between PVP and Gantrez polymer and its effect on release and bioadhesive properties of the composite PVP/Gantrez films
Authors: Jin, S.H. 
Lai, W.C. 
Ze, X.S.
Heng, P.W.S. 
Keywords: Bioadhesion
Diclofenac sodium
Interpolymer complexation
Poly(methyl vinyl ether-maleic anhydride) copolymer
Polyvinylpyrrolidone
Release
Issue Date: 2004
Citation: Jin, S.H., Lai, W.C., Ze, X.S., Heng, P.W.S. (2004). Complexation between PVP and Gantrez polymer and its effect on release and bioadhesive properties of the composite PVP/Gantrez films. Pharmaceutical Development and Technology 9 (4) : 379-386. ScholarBank@NUS Repository. https://doi.org/10.1081/PDT-200033004
Abstract: Complexation between poly(methyl vinyl ether-maleic anhydride) copolymer (Gantrez AN 169) and polyvinylpyrrolidone (PVP K-90D) in aqueous solutions were investigated using a viscometric method and Raman spectroscopy. The composite films with different weight ratios of PVP to Gantrez were prepared in the presence of N-methyl-2-pyrrolidone. The release profiles of diclofenac sodium (DS) from these films were determined and the bioadhesive properties measured. An interpolymer complex was formed through hydrogen bonding between the carbonyl groups of PVP and the hydroxyl groups of Gantrez. The formation of interpolymer hydrogen bonds reduced the interaction of the polymers with water molecules, thus resulting in a lower solubility of the complex in water and a further retarded release of DS from the composite films. The interpolymer complexation was also found to increase the bioadhesive properties of the composite films to a silicone elastomer substrate. The complexation of PVP and the Gantrez copolymer in the composite films was a critical factor affecting the release of DS from the films and the bioadhesive properties of the films.
Source Title: Pharmaceutical Development and Technology
URI: http://scholarbank.nus.edu.sg/handle/10635/105765
ISSN: 10837450
DOI: 10.1081/PDT-200033004
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