Submicron emulsions as drug carriers - Studies on destabilization potential of various drugs

被引:42
作者
Sznitowska, M [1 ]
Janicki, S [1 ]
Dabrowska, E [1 ]
Zurowska-Pryczkowska, K [1 ]
机构
[1] Med Acad Gdansk, Dept Pharmaceut Technol, PL-80416 Gdansk, Poland
关键词
submicron emulsions; parenteral emulsions; stability; drug concentration;
D O I
10.1016/S0928-0987(00)00115-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Few drugs have been successfully formulated as submicron emulsions. The physicochemical stability of submicron emulsions on admixture of drugs is the main factor limiting a wider use of this type of vehicle for parenteral or other routes of administration. In a short-term stability studies we have investigated 35 drugs with regard to their compatibility with 20 or 5% parenteral fat emulsions. The study has shown that interaction of drugs with submicron emulsions is complex in nature. Taking into consideration the physicochemical properties: of a drug e.g. lipophilicity or ionization, it is difficult to predict changes in the physical stability of the system. If destabilization occurs it is maximal at saturated concentrations and the presence of even significant amounts of the solid phase formed by undissolved drug does not influence the short-term stability of the system. Due to the increased ratio of emulgator to oil, emulsions containing 5% of oily phase are less susceptible to destabilization than 20% emulsions. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:175 / 179
页数:5
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