首页> 外文期刊>Indian drugs >FORMULATION DEVELOPMENT AND PHARMACODYNAMIC EVALUATION OF COLON TARGETED CONTROLLED RELEASE LORNOXICAM PELLETS FOR PAIN MANAGEMENT OF RHEUMATOID ARTHRITIS
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FORMULATION DEVELOPMENT AND PHARMACODYNAMIC EVALUATION OF COLON TARGETED CONTROLLED RELEASE LORNOXICAM PELLETS FOR PAIN MANAGEMENT OF RHEUMATOID ARTHRITIS

机译:结肠靶向控释洛诺克西兰粒子的配方开发和药效学评价用于类风湿性关节炎的疼痛管理

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The aim of the present research work was to formulate and evaluate colon targeted pellets of lornoxicam for the pain management of rheumatoid arthritis. The product and process parameters were optimized by screening methods. Pellets were prepared by extrusion spheronization method using microcrystalline cellulose (MCC) as spheronizing aid and ethyl cellulose (EC) as controlled release polymer, in different ratios. Based on the physical appearance, sphericity and % in wfradrug release, batch B17 containing EC: MCC (6:4) was optimized for core pellets. The site specificity was obtained by screening Eudragit FS30D and Eudragit S100 as coating polymers and the core pellets were coated with Eudragit S100. The batch C4 (6%) showed appropriate physical appearance and % in vitro drug release upto 24 h, indicating controlled release property. The pharmacodynamic studies performed on rat model indicated the anti-inflammatory activity of pellet formulation. Thus, it is concluded that the coated pellets can be a good candidate for site specific delivery of lornoxicam to colon by decreasing the gastric irritation, reducing dose frequency and improving patient compliance.
机译:目前研究工作的目的是制定和评估林洛昔康的结肠靶向颗粒,用于类风湿性关节炎的疼痛管理。通过筛选方法优化产品和工艺参数。通过使用微晶纤维素(MCC)作为球形辅助辅助和乙基纤维素(EC)作为控释聚合物,以不同比例,通过挤出球纤维素(MCC)制备粒料。基于WFradrug释放的外观,球形度和%,含有EC的批量B17:MCC(6:4)针对核心颗粒进行了优化。通过筛选Eudragit FS30D和Eudragit S100作为涂料聚合物,核心粒料涂有Eudragit S100,获得了位点特异性。批量C4(6%)显示出适当的物理外观和体外药物释放的%,高达24小时,表明控释性。对大鼠模型进行的药效学研究表明了颗粒制剂的抗炎活性。因此,得出结论是通过降低胃刺激,减少剂量频率并改善患者依从性,涂覆的颗粒可以是现场特异性培养物到结肠的良好候选者。

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