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首页> 外文期刊>Research journal of pharmacy and technology >Rectal Suppository of Mucoadhesive Microspheres of Alverine Citrate for irritable Bowel Disease: In vitro Evaluation
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Rectal Suppository of Mucoadhesive Microspheres of Alverine Citrate for irritable Bowel Disease: In vitro Evaluation

机译:亚汞粘附性微球的直肠栓塞烟酸藻类毒液:体外评价

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The aim of present investigation was to develop chitosan based mucoadhesive microspheres of alverine citrate (ALV) for rectal delivery. Mucoadhesive microspheres of alverine citrate were prepared by simple emulsification crosslinking technique and evaluated for surface morphology, particle size, equilibrium swelling degree, drug content, in vitro bioadhesion and in vitro drug release. The suppositories of optimized batch of microspheres (AM5) were prepared by fusion method using cocoa butter, polyethylene glycol (PEG) 2000, PEG 4000 alone or in combinations with different ratios and evaluated for weight variation, hardness, drug content uniformity, liquefaction tune, micro-melting range, in v/frodissolution and compatibility study by Attenuated total reflectance- Fourier transform infrared spectroscopy (ATR-FTIR). Chitosan based mucoadhesive microspheres of all batches of ALV except AM3 and AM4 showed spherical shape and particle s ize in the range of 76.56 to 294.32|im. All the formulations showed drug encapsulation efficiency in the range of 43.91 to 98.36% and bioadhesion in the range of 58.25 to 82.65%. AM5 batch showed 94.65% drug release at the end of lOh. Formulations of solid suppositories showed all the physical parameters within prescribed pharmacopoeial standard limits. Drug content of all the batches of suppositories was found to be in the range of 70.94 to 91.65%. All the batches of suppositories retarded the release of drug at the end of lOh. Suppository batch E showed 86.33% drug release at the end of lOh. Developed rectal formulation of ALV could be able to relieve the symptoms of irritable bowel disease and may overcome the disadvantages of oral delivery.
机译:目前调查的目的是开发壳聚糖的亚亚硝酸盐(ALV)的粘膜粘附微球,用于直肠递送。通过简单的乳化交联技术制备亚汞酸丝粘膜微球,并评估表面形态,粒度,平衡溶胀度,药物含量,体外生物粘附和体外药物释放。通过使用可可脂,聚乙二醇(PEG)2000,PEG 4000单独或用不同比例的组合的融合方法制备优化的微球(AM5)的栓剂制备,并评估重量变异,硬度,药物含量均匀性,液化曲调,微熔化范围,在V / Frodissolution和兼容性研究中通过减弱的总反射率 - 傅里叶变换红外光谱(ATR-FTIR)。除am3和am4外,壳聚糖的粘膜粘附微球,除am3和am4外,均显示球形和粒子的形状和粒子s含量在76.56至294.32 | Im。所有配方在43.91至98.36%的范围内显示出药物包封效率,生物粘附在58.25至82.65%的范围内。 AM5批次在LOH结束时显示出94.65%的药物释放。固体栓剂的配方在规定的药典标准限制内显示出所有物理参数。发现所有批次栓剂的药物含量在70.94至91.65%的范围内。所有批次的栓剂在LOH末端延迟了药物的释放。栓剂批量E显示LOH末端的86.33%的药物释放。 Alv的直肠制剂可以能够缓解肠疾病疾病的症状,并可能克服口腔递送的缺点。

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