Quantitative determination of polymorphic composition in intact compacts by parallel-beam X-ray powder diffractometry

被引:29
作者
Cao, WJ
Bates, S
Peck, GE
Wildfong, PLD
Qiu, ZH
Morris, KR
机构
[1] Purdue Univ, Sch Pharm, Dept Ind & Phys Pharm, W Lafayette, IN 47907 USA
[2] Kratos Analyt Inc, Chestnut Ridge, NY 10977 USA
基金
美国国家科学基金会;
关键词
parallel-beam X-ray powder diffraction; chlorpropamide; glycine; polymorph; quantitation; compact; process-induced transformation;
D O I
10.1016/S0731-7085(02)00419-3
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This paper details the development of a method using parallel-beam X-ray powder diffractometry as a novel means of determining polymorphic composition in intact compacts. Two polyrnorphic systems, chlorpropamide and glycine, were selected. The polymorphic components were weighed, mixed, and compressed using a Carver press with 3/8-in. concave tooling. The compacts were then analyzed using parallel-beam X-ray powder diffractometry in transmission geometry. The data were processed using the profile-fitting module in the Shimadzu XRD-6000 software V 4.1 (for NT 4.0/98). The integrated intensity ratio of a selected peak for each crystal form was used for quantitation of each polymorph. Excellent linear correlation was observed for both polymorphic systems. The convex shape of the compact surface had no effect on the XRD patterns. Since parallel-beam X-ray diffractometry is not sensitive to the shape of the sample surface, it provides a simple method for quantifying polymorphs in intact compacts. Further work to extend this to formulated tablets is ongoing. The relatively larger variation in one of the peaks in the chlorpropamide study was found to be consistent with the computational analysis of the slip behavior of the stable polymorph. This method provides the first reported non-invasive X-ray diffraction pattern quantitation of crystal forms in intact compacts. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:1111 / 1119
页数:9
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