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Development and Optimization of Osmotically Controlled Asymmetric Membrane Capsules for Delivery of Solid Dispersion of Lycopene

机译:渗透控制的番茄红素固体分散膜的不对称膜胶囊的研制与优化

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摘要

The aim of the present investigation is to develop and statistically optimize the osmotically controlled asymmetric membrane capsules of solid dispersion of lycopene. Solid dispersions of lycopene with β-cyclodextrin in different ratios were prepared using solvent evaporation method. Solubility studies showed that the solid dispersion with 1 : 5 (lycopene : β-cyclodextrin) exhibited optimum solubility (56.25 mg/mL) for osmotic controlled delivery. Asymmetric membrane capsules (AMCs) were prepared on glass mold pins via dip coating method. Membrane characterization by scanning electron microscopy showed inner porous region and outer dense region. Central composite design response surface methodology was applied for the optimization of AMCs. The independent variables were ethyl cellulose (X 1), glycerol (X 2), and NaCl (X 3) which were varied at different levels to analyze the effect on dependent variables (percentage of cumulative drug release (Y 1) and correlation coefficient of drug release (Y 2)). The effect of independent variables on the response was significantly influential. The F18 was selected as optimized formulation based on percentage of CDR (cumulative drug release) of 85.63% and correlation coefficient of 0.9994. The optimized formulation was subjected to analyze the effect of osmotic pressure and agitational intensity on percentage of CDR. The drug release was independent of agitational intensity but was dependent on osmotic pressure of dissolution medium.
机译:本研究的目的是开发和统计优化番茄红素固体分散体的渗透控制不对称膜胶囊。采用溶剂蒸发法制备番茄红素与β-环糊精的不同比例的固体分散体。溶解度研究表明,具有1:5(番茄红素:β-环糊精)的固体分散体具有最佳的溶解度(56.25 mg / mL),可用于渗透控制的递送。通过浸涂法在玻璃模具销上制备不对称膜胶囊(AMC)。通过扫描电子显微镜对膜的表征显示出内部的多孔区域和外部的致密区域。中央复合设计响应面方法被应用于AMC的优化。自变量是乙基纤维素(X 1),甘油(X 2)和NaCl(X 3),它们在不同的水平上变化以分析对因变量的影响(累积药物释放百分比(Y 1)和相关系数)。药物释放(Y 2))。自变量对反应的影响具有显着影响。基于CDR(累积药物释放)百分比为85.63%,相关系数为0.9994,选择F18作为优化配方。对优化的制剂进行分析渗透压和搅动强度对CDR百分比的影响。药物释放与搅拌强度无关,但与溶出介质的渗透压有关。

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