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Spray drying of fenofibrate loaded nanostructured lipid carriers
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作者 Dengning Xia Neha Shrestha +2 位作者 Jacco van de Streek Huiling Mu Mingshi Yang 《Asian Journal of Pharmaceutical Sciences》 SCIE CAS 2016年第4期507-515,共9页
The conversion of aqueous dispersion of nanostructured lipid carriers(NLCs) into dry powder by spray drying could be a useful approach to render NLCs with better physical chemical stability than the aqueous dispersion... The conversion of aqueous dispersion of nanostructured lipid carriers(NLCs) into dry powder by spray drying could be a useful approach to render NLCs with better physical chemical stability than the aqueous dispersion. In this study, aqueous NLC dispersion containing fenofibrate was converted into dry, easily reconstitutable powder using spray drying. A central composite face centered design(CCFD) was used to investigate the influence of the ratio of lipid to protectant(mannitol and trehalose) and crystallinity of spray-dried powder on the particle size, yield and residual moisture content of the dried powder. A linear relationship(R2= 0.9915) was established between the crystalline content of the spray-dried powders against the ratio of mannitol to trehalose from 3:7 to 10:0(w/w). Spray drying of NLC aqueous dispersion using a mannitol and trehalose mixture resulted in an increase in particle size of the NLCs after reconstitution in water as compared to that in the initial aqueous dispersion. The decrease in crystallinity of the dry powder by reducing the ratio of mannitol to trehalose could improve the reconstitution of the NLCs in water. However the yield and residual moisture content of dry powder decreased with an increase in the ratio of mannitol to trehalose. Lipid nanoparticles were able to retain the drug incorporation and the prolonged drug release profile after spray drying. The experimental model was robust, and suggested that spray drying is a viable technique for the conversion of NLCs into dry powder. 展开更多
关键词 FENOFIBRATE NANOSTRUCTURED LIPID carriers SPRAY DRYING design of experiments central composite face-centered design
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利用实验设计筛选并优化SARS-CoV-2单抗F61亲和层析阶段工艺参数
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作者 孙文泽 陈莹 +7 位作者 詹珊珊 邓小杰 黄嘉欣 王炯 宋刚 刘建邦 桂芳 潘勇兵 《中国生物制品学杂志》 CAS CSCD 2024年第6期731-738,共8页
目的利用实验设计(Design of Experiment,DoE)筛选及优化实验对SARS-CoV-2单抗F61亲和层析工艺参数进行筛选及优化,获得最佳工艺条件。方法选择8个可能在亲和层析中影响实验响应结果的工艺参数并制定其水平范围,利用DoE筛选实验对选择... 目的利用实验设计(Design of Experiment,DoE)筛选及优化实验对SARS-CoV-2单抗F61亲和层析工艺参数进行筛选及优化,获得最佳工艺条件。方法选择8个可能在亲和层析中影响实验响应结果的工艺参数并制定其水平范围,利用DoE筛选实验对选择的工艺参数进行8因子2水平筛选实验,通过检测响应值,用统计学软件拟合数学模型,经帕累托图分析获得3个显著影响关键质量属性的关键工艺参数(P<0.05),再选择DoE响应曲面法对关键工艺参数进行优化实验。首先完成全析因实验设计部分,检测响应结果拟合数学模型,分析弯曲项P值判断显著因子的工艺参数范围处于最佳范围内(弯曲P<0.05)后,再根据实验的序贯性补齐中心复合表面设计(central composite face-centered design,CCF)实验,通过检测响应结果拟合响应曲面模型,获得工艺最佳条件范围,最终通过重复试验验证最佳参数值的稳定性。结果在筛选实验中获得在亲和层析阶段影响F61的显著因子为洗脱缓冲液pH、洗脱缓冲液盐浓度、中间淋洗缓冲液盐浓度、平衡缓冲液盐浓度。通过CCF实验最终获得亲和层析中关键工艺参数的最佳条件,当洗脱缓冲液pH为3.2、洗脱缓冲液盐浓度为0.07 mol/L NaCl、中间淋洗缓冲液盐浓度为0.31 mol/L NaCl,F61在亲和层析阶段收率达95.25%,宿主细胞蛋白(host cell protein,HCP)残留量为97.33 ppm,样品单体纯度达98.51%。结论用不同类型DoE方法进行了F61亲和层析阶段工艺参数的筛选和优化,获得了最佳工艺条件,为F61纯化工艺的建立奠定了基础。 展开更多
关键词 实验设计 亲和层析 SARS-CoV-2单抗 筛选实验 优化实验 中心复合表面设计
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