槲皮素固体自纳米乳化给药体系的研制

Roma Mathew, Joyamma Varkey
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引用次数: 1

摘要

本研究旨在开发槲皮素固体自乳化给药系统,以提高槲皮素的生物利用度。从剂型来看,固体自乳化给药系统是指具有自乳化性质的固体剂型。制备了含有15mg /ml槲皮素的液体自乳化给药体系,并通过吸附在各种固体载体上转化为固体自乳化给药体系。通过对槲皮素的微观性质和药物含量分析,选择Aerosil®200作为吸附剂,开发槲皮素固体自乳化给药系统。通过不同用量的组分制备不同配方,优化后的配方粒径为264.2 nm,药物含量为93.95%。优化后的槲皮素固体自乳化给药体系表现出良好的自乳化性、无相互作用(FTIR分析)、药物在混合物中的可溶性(DSC和XRD分析)和表面光滑(SEM分析)。槲皮素固体自乳化给药系统的体外释药率为99.70±0.227%。研究结果表明,固体自乳化技术是开发口服吸收不良的稳定剂型的一种很有前途的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of Solid Self Nanoemulsifying Drug Delivery System of Quercetin
This work aims to develop Solid Self Emulsifying Drug Delivery System of Quercetin for enhancing its bioavailability. From the perspective of dosage forms, Solid Self Emulsifying Drug Delivery System mean solid dosage forms with self-emulsification properties. Liquid Self Emulsifying Drug Delivery System containing 15 mg/ml of Quercetin was prepared and converted to Solid Self Emulsifying Drug Delivery System by adsorption onto various solid carriers. Based on micromeritic properties and drug content analysis Aerosil ® 200 was selected as the adsorbent for development of Solid Self Emulsifying Drug Delivery System of Quercetin.Various formulation were prepared by variying amounts of the components and optimized fornulation showed particle size of 264.2 nm and drug content of 93.95 %.Optimized Solid Self Emulsifying Drug Delivery System of Quercetin showed good self emulsification ,absence of interactions(FTIR analyis), solubilization of the drug in the mixture (DSC and XRD analysis)and smooth surface (SEM analysis ) . In-vitro drug release of Solid Self Emulsifying Drug Delivery System of Quercetin revealed percentage drug release of 99.70±0.227% within 30 min . Results of the study indicates the Solid Self emulsification technique is a promising approach for development of stable dosage form of drugs with poor oral absorption.
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