乙酰唑胺缓释胶囊处方的体外研究。

Bollettino chimico farmaceutico Pub Date : 2003-10-01
V P Pandey, K Kannan, R Manavalan, N Desai
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引用次数: 0

摘要

本研究采用非平行种子制备乙酰唑胺250 mg缓释胶囊。用药物、聚乙烯吡咯烷酮、单硬脂酸甘油、微晶蜡和二硬脂酸甘油单独或联合包被非pareil种子,以获得250 mg的缓释胶囊。在成功的配方中,采用20%的药物包衣微丸和80%的蜡包衣微丸。成功配方的蜡包被微丸在相同浓度1.6% w/w的药物包被微丸上包被微晶蜡和二硬脂酸甘油。将成功配制的乙酰唑胺250 mg缓释胶囊与wagner建议的理论缓释配方和一种市售的250 mg缓释胶囊进行体外研究比较。配方胶囊的效果优于市售胶囊或与市售胶囊相当。对于成功的配方,将颗粒填充在'1'大小的硬明胶胶囊中,并在室温和45℃的热空气中进行稳定性研究,为期5周。该制剂在药物含量和释放率方面稳定。
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In vitro study on sustained release capsule formulation of acetazolamide.

In the present study formulation of sustained release capsule of acetazolamide 250 mg was tried using nonpareil seeds. Nonpareil seeds were coated with drug, polyvinylpyrrolidone, glyceryl monostearate, microcrystalline wax, and glyceryl distearate either individually or in combination to achieve sustained release capsule 250 mg. In successful formulation 20% drug coated pellets and 80% wax coated pellets were taken. Wax coated pellets for successful formulation contained coating of microcrystalline wax and glyceryl distearate on drug coated pellets of the same concentration of 1.6% w/w. Successful formulated sustained release capsule 250 mg of acetazolamide was compared in in vitro study with theoretical sustained release formulation suggested by wagner and one marketed sustained release capsule 250 mg. Formulated capsule showed result superior to or on par with marketed capsule. For successful formulation pellets were filled in '1' size hard gelatin capsule and stability study was carried out in hot air over at room temperature and 45 degrees C for 5 weeks. The formulation was found stable in respect of drug content and release rate.

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