Formulation optimization of chelerythrine loaded O-carboxymethylchitosan microspheres using response surface methodology

被引:37
|
作者
Li, Gui-yin [1 ]
Zhong, Ming [2 ]
Zhou, Zhi-de [1 ]
Zhong, Yue-dan [3 ]
Ding, Ping [3 ]
Huang, Yong [1 ]
机构
[1] Guilin Univ Elect Technol, Sch Life & Environm Sci, Guilin 541014, Guangxi, Peoples R China
[2] Hunan Inst Sci & Technol, Sch Chem & Chem Engn, Yueyang 414006, Hunan, Peoples R China
[3] Cent S Univ, Sch Publ Hlth, Changsha 410078, Hunan, Peoples R China
关键词
O-carboxymethylchitosan; Chelerythrine; Response surface methodology; Controlled release; DRUG-DELIVERY; CHITOSAN; NANOPARTICLES; ALKALOIDS; ALGINATE; RELEASE; CELLS;
D O I
10.1016/j.ijbiomac.2011.08.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aims of this investigation were to develop a procedure to prepare chelerythrine (CHE) loaded O-carboxymethylchitosan (O-CMCS) microspheres by emulsion cross-linking method and optimize the process and formulation variables using response surface methodology (RSM) with a three-level, three-factor Box-Behnken design (BBD). The independent variables studied were O-CMCS/CHE ratio, O/W phase ratio, and O-CMCS concentration, dependent variables (responses) were drug loading content and encapsulation efficiency. Mathematical equations and response surface plots were used to relate the dependent and independent variables. The process and formulation variables were optimized to achieve maximum drug loading content and entrapment efficiency by the desirability function. The optimized microsphere formulation was characterized for particle size, shape, morphology and in vitro drug release. Results for mean particle size, drug loading content, entrapment efficiency, and in vitro drug release of CHE-loaded O-CMCS microspheres were found to be of 12.18 mu m, 4.16 +/- 3.36%, 57.40 +/- 2.30%, and 54.5% at pH 7.4 after 70 h, respectively. The combination use of RSM, BBD and desirability function could provide a promising application for O-CMCS as controlled drug delivery carrier and help to develop procedures for a lab-scale microemulsion process. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:970 / 978
页数:9
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