DSC screening of potential prochlorperazine-excipient interactions in preformulation studies

被引:14
作者
Brown, ME [1 ]
Antunes, EM [1 ]
Glass, BD [1 ]
Lebete, M [1 ]
Walker, RB [1 ]
机构
[1] Rhodes Univ, Dept Chem, ZA-6140 Grahamstown, South Africa
来源
JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY | 1999年 / 56卷 / 03期
关键词
cyclodextrins; drugs; DSC; excipients; prochlorperazine;
D O I
10.1023/A:1010150305542
中图分类号
O414.1 [热力学];
学科分类号
摘要
Differential scanning calorimetry was used to examine the thermal behaviour of mixtures of the drug prochlorperazine with standard excipients, to assess potential interactions, and of mixtures with cyclodextrins, to investigate inclusion complexation which could increase the photostability of the drug. For most of the excipients (magnesium stearate, stearic acid, Explotab(R), Ac-Di-Sol(R), Encompress(R) and Ludipress(R), lactose and Starch 1500) disappearance or broadening of the melting endotherm of the drug indicated interactions. Lubritab(R) was the only 'inert' excipient tested. Mixtures of prochlorperazine and the cyclodextrins gave incomplete inclusion complexation as;shown by only partial disappearance of the melting endotherm of the drug.
引用
收藏
页码:1317 / 1322
页数:6
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