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首页> 外文期刊>Acta Poloniae Pharmaceutica: Durg Research >Evaluation of microcrystalline chitosan properties as a drug carrier. Part II. The influence of microcrystalline chitosan on release rate of ketoprofen.
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Evaluation of microcrystalline chitosan properties as a drug carrier. Part II. The influence of microcrystalline chitosan on release rate of ketoprofen.

机译:评价微晶壳聚糖作为药物载体的性能。第二部分微晶壳聚糖对酮洛芬释放速率的影响。

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摘要

The effect of microcrystalline chitosan (MCCh) as hydrogel and dried gel (film) on the release of ketoprofen (KTA) was studied in vitro. Commercial ketoprofen gel (Profenid gel) was applied as a reference preparation for MCCh hydrogel, pure as well as in combination with methylcellulose (MC) and hydrophilising agents (1,2-propylene glycol and glycerol). The quantity of the released drug was determined by ultraviolet spectroscopy. IR spectroscopic analysis, proton magnetic resonance (1H NMR), powder X-ray diffraction, and differential scanning calorimetry (DSC) studies verified physical and chemical interactions between chitosan and ketoprofen. The influence of these interactions on the ketoprofen release from the hydrogel and film was analysed. It was found that microcrystalline chitosan may be used as a polymer drug carrier.
机译:体外研究了微晶壳聚糖(MCCh)作为水凝胶和干燥凝胶(薄膜)对酮洛芬(KTA)释放的影响。商用酮洛芬凝胶(Profenid凝胶)用作纯净的MCCh水凝胶的参考制剂,并与甲基纤维素(MC)和亲水剂(1,2-丙二醇和甘油)结合使用。释放的药物量通过紫外光谱法确定。红外光谱分析,质子磁共振(1H NMR),粉末X射线衍射和差示扫描量热法(DSC)研究证实了壳聚糖和酮洛芬之间的物理和化学相互作用。分析了这些相互作用对酮洛芬从水凝胶和薄膜中释放的影响。发现微晶壳聚糖可以用作聚合物药物载体。

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