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In vitro drug release of natamycin from...
Journal article

In vitro drug release of natamycin from β-cyclodextrin and 2-hydroxypropyl-β-cyclodextrin-functionalized contact lens materials

Abstract

PURPOSE: The antifungal agent natamycin can effectively form inclusion complexes with beta-cyclodextrin (β-CD) and 2-hydroxypropyl-β-cyclodextrin (HP-βCD) to improve the water solubility of natamycin by 16-fold and 152-fold, respectively (Koontz, J. Agric. Food. Chem. 2003). The purpose of this study was to develop contact lens materials functionalized with methacrylated β-CD (MβCD) and methacrylated HP-βCD (MHP-βCD), and to evaluate their …

Authors

Phan C-M; Subbaraman LN; Jones L

Journal

Journal of Biomaterials Science Polymer Edition, Vol. 25, No. 17, pp. 1907–1919

Publisher

Taylor & Francis

Publication Date

November 22, 2014

DOI

10.1080/09205063.2014.958016

ISSN

0920-5063