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首页> 外文期刊>Research journal of pharmacy and technology >Formulation and evaluation of mucoadhesive microcsapsules of Aceclofenac for Oral controlled release by Emulsification-gelation Technique
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Formulation and evaluation of mucoadhesive microcsapsules of Aceclofenac for Oral controlled release by Emulsification-gelation Technique

机译:乳化-胶凝技术制备醋氯芬酸粘膜粘附微胶囊口服控释制剂

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摘要

Microencapsulation by emulsification-ionic gelation technique is an approach to achieve controlled release of drug and mucoadhesive microcapsules were designed to improve the absorption and bioavailability of drug. Microcapsules of Aceclofenac were formulated by employing sodium alginate, two natural polymers-gum kondagogu and gum karaya. The prepared microcapsules were free flowing, discrete spherical shape was characterised by scanning electron microscopy (SEM). Microencapsulation efficiency was in the range of 60-80% and they exhibited good mucoadhesive property. Invitro dissolution data revealed that formulations exhibit the zero order kinetics and followed non-fickian diffusion transport mechanism. In-vitro release profile of formulation (F3) was found similar to that of marketed formulation. Pre-clinical pharmacological activity i.e. analgesic activity was conducted and optimized formulation exhibited the significant analgesic activity Mucoadhesive microcapsules prepared with sodium alginate, gum karaya and gum kondagogu found to be suitable for oral controlled release.
机译:通过乳化-离子凝胶技术微囊化是一种实现药物控制释放的方法,并设计了粘膜粘附性微胶囊以改善药物的吸收和生物利用度。醋氯芬酸的微胶囊是通过使用藻酸钠,两种天然聚合物-口香糖和口香糖制成的。制备的微胶囊自由流动,通过扫描电子显微镜(SEM)表征离散的球形。微囊化效率在60-80%的范围内,并且它们表现出良好的粘膜粘附特性​​。体外溶出数据显示,制剂表现出零级动力学,并且遵循非菲克扩散扩散机制。发现制剂(F3)的体外释放曲线类似于市售制剂。进行了临床前药理活性,即镇痛活性,优化的制剂表现出了显着的镇痛活性。发现藻酸胶,角ya胶和角onda胶制备的粘膜粘附微胶囊适合口服控释。

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