Advances in coamorphous drug delivery systems

被引:139
|
作者
Shi, Qin [1 ]
Moinuddin, Sakib M. [1 ]
Cai, Ting [1 ]
机构
[1] China Pharmaceut Univ, Sch Pharm, Dept Pharmaceut, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Coamorphous; Preparation; Characterization; Physical stability; Dissolution; Bioavailability; AMORPHOUS SOLID DISPERSIONS; ENHANCED PHYSICAL STABILITY; HUGGINS INTERACTION PARAMETER; WATER-SOLUBLE DRUGS; PHYSICOCHEMICAL PROPERTIES; CRYSTAL-GROWTH; MOLECULAR MOBILITY; AMINO-ACIDS; DISSOLUTION BEHAVIOR; PHASE-SEPARATION;
D O I
10.1016/j.apsb.2018.08.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In recent years, the coamorphous drug delivery system has been established as a promising formulation approach for delivering poorly water-soluble drugs. The coamorphous solid is a single-phase system containing an active pharmaceutical ingredient (API) and other low molecular weight molecules that might be pharmacologically relevant APIs or excipients. These formulations exhibit considerable advantages over neat crystalline or amorphous material, including improved physical stability, dissolution profiles, and potentially enhanced therapeutic efficacy. This review provides a comprehensive overview of coamorphous drug delivery systems from the perspectives of preparation, physicochemical characteristics, physical stability, in vitro and in vivo performance. Furthermore, the challenges and strategies in developing robust coamorphous drug products of high quality and performance are briefly discussed. (C) 2019 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.
引用
收藏
页码:19 / 35
页数:17
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