Penciclovir solubility in Eudragit films: a comparison of X-ray, thermal, microscopic and release rate techniques

被引:25
作者
Ahmed, A
Barry, BW
Williams, AC [1 ]
Davis, AF
机构
[1] Univ Bradford, Sch Pharm, Drug Delivery Grp, Bradford BD7 1DP, W Yorkshire, England
[2] GlaxoSmithKline Consumer Healthcare Brands, Weybridge, Surrey, England
基金
英国工程与自然科学研究理事会;
关键词
Eudragit films; drug solubility; X-ray powder diffraction; differential scanning calorimetry; light microscopy; release kinetics; penciclovir;
D O I
10.1016/j.jpba.2003.11.018
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The solubility of penciclovir(C10N5O3H17) in a novel film formulation designed for the treatment of cold sores was determined using X-ray, thermal, microscopic and release rate techniques. Solubilities of 0.15-0.23, 0.44, 0.53 and 0.42% (w/w) resulted for each procedure. Linear calibration lines were achieved for experimentally and theoretically determined differential scanning calorimetry (DSC) and X-ray powder diffractometry (XRPD) data. Intra- and inter-batch data precision values were determined; intra values were more precise. Microscopy was additionally useful for examining crystal shape, size distribution and homogeneity of drug distribution within the film. Whereas DSC also determined melting point, XRPD identified polymorphs and release data provided relevant kinetics. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:945 / 956
页数:12
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