Development of nobiliside A loaded liposomal formulation using response surface methodology

被引:43
作者
Xiong, Yang [1 ,2 ]
Guo, Dan [1 ]
Wang, Lili [2 ]
Zheng, Xiaoli [1 ]
Zhang, Yue [1 ]
Chen, Jianming [1 ]
机构
[1] Second Mil Med Univ, Sch Pharm, Dept Pharmaceut Sci, Shanghai 200433, Peoples R China
[2] Zhejiang Chinese Med Univ, Hangzhou 310053, Zhejiang, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
Nobiliside; Liposome; Response surface methodology; Hemolysis; Encapsulation efficiency; Acute toxicity; HEMOLYTIC-ACTIVITY; PHOSPHOLIPID-MEMBRANES; OPTIMIZING CONDITIONS; FACTORIAL DESIGN; WATER EXTRACTION; CHOLESTEROL; PEPTIDES; OPTIMIZATION; MECHANISM; SYSTEMS;
D O I
10.1016/j.ijpharm.2008.12.031
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
To reduce the hemolysis and toxicity of nobiliside A (Nob), liposomes were used as a carrier in this study. Response surface methodology (RSM) based on central composite rotatable design (CCRD) was applied for formulation optimization. Phosphatidyl choline (PC) proportion, cholesterol (CH) proportion, and lipids/drug ratio were selected as the independent variables while the encapsulation efficiency (EE) and hemolytic rate (HR) of the liposomes as the dependent variables. The results indicated CH proportion and lipids/drug ratio were the major contributing variables for EE and PC/CH ratio was the major contributing variables for HR. The optimum formulation of Nob liposomes, in which PC proportion of 2% (w/v), CH proportion of 0.9% (w/v), and lipids/drug ratio (w/w) of 40, had higher EE (>95%) and lower HR (<1% at the concentration of 80 mu gmL(-1))with spherical shape and uniform sizes. The intravenous LD50 increased to 9.5 mgkg(-1) compared to 4.1 mgkg(-1) of Nob solution. In conclusion, the liposome was a safety and effective carrier for intravenous Nob. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:197 / 203
页数:7
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