Proniosomes: A novel drug carrier preparation (vol 185, pg 23, 1999)

被引:45
作者
Hu, CJ
Rhodes, DG [1 ]
机构
[1] Univ Connecticut, Dept Pharmaceut Sci, Storrs, CT 06269 USA
[2] Univ Texas, Coll Pharm, Div Pharmaceut, Austin, TX 78712 USA
关键词
D O I
10.1016/S0378-5173(00)00513-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A procedure is described for producing a dry product which may be hydrated immediately before use to yield aqueous niosome dispersions similar to those produced by more cumbersome conventional methods. These 'proniosomes' minimize problems of niosome physical stability such as aggregation, fusion and leaking, and provide additional convenience in transportation, distribution, storage, and dosing. This report describes the preparation of dispersions of proniosome-derived niosomes, comparison of these niosomes to conventional niosomes, and optimization of proniosome formulations. In addition, conventional and proniosome-derived niosomes are compared in terms of their morphology, particle size, particle size distribution, and drug release performance in synthetic gastric or intestinal fluid. In all comparisons, proniosome-derived niosomes are as good or better than conventional niosomes. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:109 / 122
页数:14
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