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引用本文:朱波.Box-Behnken响应面法优化益母草碱脂质纳米粒处方[J].中国现代应用药学,2021,38(10):1205-1210.
ZHU Bo.Formulation Optimization of Leonurine Lipid Nanoparticles by Box-Behnken Response Surface Methodology[J].Chin J Mod Appl Pharm(中国现代应用药学),2021,38(10):1205-1210.
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Box-Behnken响应面法优化益母草碱脂质纳米粒处方
朱波
中国科学院大学宁波华美医院, 浙江 宁波 315010
摘要:
目的 制备益母草碱脂质纳米粒并优化处方。方法 采用pH梯度结合逆向蒸发法制备益母草碱脂质纳米粒,以粒径、包封率和载药量为评价指标,药物和脂质比例、胆固醇和脂质比例、药物终浓度为考察因素,采用Box-Behnken效应面法优化纳米粒处方,并考察纳米粒体外释放情况。结果 益母草碱脂质纳米粒最优处方为药物和脂质比例为9.8%,胆固醇和脂质为1.0%,药物终浓度为10 mg·mL-1。制得的纳米粒粒径为(83.9±5.6)nm、包封率(73.3±2.2)%、载药量(4.0±0.0)%,实测值与预测值RSD均<5%。体外释放结果显示,与原料相比,益母草碱脂质纳米粒具有一定的缓释作用。结论 Box-Behnken响应面优化法应用简便、预测性好,所得益母草碱脂质纳米粒包封率和载药量高,符合设计要求。
关键词:  益母草碱  pH梯度结合逆向蒸发法  Box-Behnken效应面法  体外释放
DOI:10.13748/j.cnki.issn1007-7693.2021.10.009
分类号:R284.2
基金项目:
Formulation Optimization of Leonurine Lipid Nanoparticles by Box-Behnken Response Surface Methodology
ZHU Bo
Hwa Mei Hospital, University of Chinese Academy of Sciences, Ningbo 315010, China
Abstract:
OBJECTIVE To optimize the formulation of leonurine lipid nanoparticles.METHODS The leonurine lipid nanoparticles were prepared by pH-gradients method coupled with reverse evaporation method.Final drug concentration, drug-lipid ratio, cholesterol and lipid ratio were selected as influences factors, the formulation was optimized by Box-Behnken response surface method with particle, the particle size, encapsulation efficiency and loading content as the evaluation parameters.The in vitro release was determined.RESULTS The optimal formulation parameters were as follows: the drug-lipid ratio was 9.8%, cholesterol and lipid ratio was 1.0% and the final drug concentration was 10 mg·mL-1.The mean particle size, entrapment efficiency, and the drug loading were (83.9±5.6)nm, (73.3±2.2)% and (4.0±0.0)%, respectively.RSD of measured and predicted values were all less than 5%.In vitro release test results showed that leonurine lipid nanoparticles had a sustained release effect compared with the raw materials.CONCLUSION The Box-Behnken response surface method is simple and predictable, and have high encapsulation efficiency and drug loading of the obtained leonurine lipid nanoparticles, which meets the design requirements.
Key words:  leonurine  pH-gradients method coupled with reverse evaporation method  Box-Behnken response surface method  in vitro release
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