首页> 外文期刊>Indian journal of pharmaceutical sciences. >Formulation design, optimization and pharmacodynamic evaluation of sustained release mucoadhesive microcapsules of venlafaxine HCl
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Formulation design, optimization and pharmacodynamic evaluation of sustained release mucoadhesive microcapsules of venlafaxine HCl

机译:盐酸文拉法辛缓释粘膜粘附微胶囊的制剂设计,优化和药效学评价

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摘要

The objective of present research work was to design and characterize the venlafaxine HCl-loaded sodium alginate-based mucoadhesive microcapsules by ionic gelation technique using HPMC K100M as mucoadhesive polymer. The Placket-Burman Design was applied for preliminary screening of the formulations and systematic optimization by using Box-Behnken Design. The prepared microcapsules were characterized for drug content, entrapment efficiency, micromeritic properties, particle size, swelling index, mucoadhesive strength, in vitro drug release and in vivo antidepressant activity. FTIR and differential scanning calorimetry studies showed no incompatibility. Surface morphology studies revealed spherical nature of the prepared microcapsules. In vitro drug release studies revealed sustained release by diffusion mechanism. Further, the microcapsules were effective in reducing the depression induced by forced swimming test in Sprague-Dawley rats compared to the pure drug. The microcapsules were found to be stable under accelerated stability conditions, which suggest them as better alternative delivery systems for enhanced therapeutic efficacy of antidepressant drug, venlafaxine HCl.
机译:本研究的目的是使用HPMC K100M作为黏膜黏附聚合物,通过离子凝胶技术设计和表征盐酸文拉法辛负载海藻酸钠的黏膜黏附微胶囊。 Placket-Burman设计用于通过Box-Behnken Design进行配方的初步筛选和系统优化。制备的微胶囊的特征在于药物含量,包封率,微链性能,粒径,溶胀指数,粘膜粘附强度,体外药物释放和体内抗抑郁活性。 FTIR和差示扫描量热法研究显示不相容。表面形态学研究显示了制备的微胶囊的球形性质。体外药物释放研究显示通过扩散机制持续释放。此外,与纯药物相比,微胶囊在减轻Sprague-Dawley大鼠的强迫游泳试验引起的抑郁方面有效。发现微胶囊在加速的稳定性条件下是稳定的,这表明它们是用于增强抗抑郁药文拉法辛盐酸盐治疗功效的更好的替代递送系统。

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