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Composite Microspheres of Rosin Gum and Ethyl cellulose for Controlled Release of an Anti-diabetic Drug: in-vitro and in-vivo Assessment

机译:松香胶和乙基纤维素复合微球用于抗糖尿病药物的控释:体外和体内评估

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In the present work, an attempt was made to develop and evaluate composite microspheres for controlled release of an anti-diabetic drug, nateglinide (NTG). The composite microspheres were prepared using rosin gum and ethyl cellulose as retardant polymers for drug release by solvent evaporation method. DSC and XRD analysis indicated the uniform dispersion of drug in the microspheres. The microspheres were capable of releasing drug for 24 h and the drug release mechanism followed non-Fickian transport. In vivo anti-diabetic activity conducted on wistar rats indicated that the plain (unformulated) NTG showed maximum percent reduction in blood glucose up to 2 h and then the blood glucose was increased. While in case of rats treated with test microspheres (RN6), the percent reduction in glucose level was slow up to 2 h as compared to plain drug, then it was gradually increased to 72.83 % at the end of 24 h. Histopathology of rat pancreas suggested that the regeneration of beta cells was seen in the rats treated with RN6 microspheres. It can be concluded from the study that, the prepared microspheres are versatile delivery systems for nateglinide, which could release drug for longer period of time.
机译:在目前的工作中,已尝试开发和评估复合微球以控制释放抗糖尿病药物那格列奈(NTG)。以松香胶和乙基纤维素为阻聚剂,通过溶剂蒸发法制备了复合微球。 DSC和XRD分析表明药物在微球中均匀分散。微球能够释放药物24小时,并且药物释放机制遵循非菲克转运。对wistar大鼠进行的体内抗糖尿病活性表明,普通(未配制)的NTG在2小时内显示出最大的血糖降低百分比,然后血糖升高。在用受试微球(RN6)治疗的大鼠中,与普通药物相比,葡萄糖水平的降低百分比在2小时之内缓慢,然​​后在24小时结束时逐渐增加至72.83%。大鼠胰腺的组织病理学表明,在用RN6微球治疗的大鼠中可见β细胞的再生。从研究中可以得出结论,所制备的微球是那格列奈的通用递送系统,可以长时间释放药物。

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