Excipient Stability in Oral Solid Dosage Forms: A Review

被引:66
作者
Darji, Mittal A. [1 ]
Lalge, Rahul M. [1 ]
Marathe, Sushrut P. [1 ]
Mulay, Tarul D. [1 ]
Fatima, Tasnim [1 ]
Alshammari, Alia [1 ]
Lee, Hyung Kyung [1 ]
Repka, Michael A. [1 ]
Murthy, S. Narasimha [1 ,2 ]
机构
[1] Univ Mississippi, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
[2] Inst Drug Delivery & Biomed Res, Bangalore, Karnataka, India
关键词
drug-excipient interactions; solid dosage form; excipient stability; chemical incompatibility; oxidative degradation; AQUEOUS POLYMERIC DISPERSIONS; DRUG-EXCIPIENT; LYMPHATIC TRANSPORT; TITANIUM-DIOXIDE; DELIVERY-SYSTEMS; WATER; DISSOLUTION; PROTEIN; BIOAVAILABILITY; HYDROCHLORIDE;
D O I
10.1208/s12249-017-0864-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The choice of excipients constitutes a major part of preformulation and formulation studies during the preparation of pharmaceutical dosage forms. The physical, mechanical, and chemical properties of excipients affect various formulation parameters, such as disintegration, dissolution, and shelf life, and significantly influence the final product. Therefore, several studies have been performed to evaluate the effect of drug-excipient interactions on the overall formulation. This article reviews the information available on the physical and chemical instabilities of excipients and their incompatibilities with the active pharmaceutical ingredient in solid oral dosage forms, during various drug-manufacturing processes. The impact of these interactions on the drug formulation process has been discussed in detail. Examples of various excipients used in solid oral dosage forms have been included to elaborate on different drug-excipient interactions.
引用
收藏
页码:12 / 26
页数:15
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