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首页> 外文期刊>International Journal of Pharmaceutics >Preparation, in vitro and in vivo evaluation of PLGA/Chitosan based nano-complex as a novel insulin delivery formulation
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Preparation, in vitro and in vivo evaluation of PLGA/Chitosan based nano-complex as a novel insulin delivery formulation

机译:基于PLGA /壳聚糖的纳米复合物的制备,体外和体内评价为新的胰岛素递送制剂

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摘要

The smart self-regulated drug delivery systems for insulin administration are desirable to achieve glycemic control, and decrease the long-term micro- and macro vascular complications. In this study, we developed an injectable nano-complex formulation for closed-loop insulin delivery after subcutaneous administration and release of insulin in response to increased blood glucose levels. The nano-complex was prepared by mixing oppositely charged chitosan and PLGA nanoparticles. PLGA nanoparticles were prepared using double-emulsion solvent diffusion method, and were loaded with glucose oxidase (GOx) and catalase (CAT) enzymes. These negatively charged particles decrease micro-environmental pH, by gluconic acid production in the glucose molecules presence. Positively charged chitosan nanoparticles were prepared using ionic gelation method, and were loaded with insulin. These nanoparticles (NPs) released insulin by dissociation in acidic pH caused by the GOx activity. Following in vitro studies, in vivo evaluation of nano-complex formulations in streptozocin induced diabetic rats showed significant glycemic regulation up to 98 h after subcutaneous administration.
机译:用于胰岛素给药的智能自调节药物递送系统是理想的,以实现血糖控制,并降低长期微观和宏观血管并发症。在这项研究中,我们开发了一种可注射的纳米复合物配方,用于在皮下给药后闭环胰岛素递送,响应血糖水平增加而释放胰岛素。通过混合相反带电的壳聚糖和PLGA纳米颗粒制备纳米配合物。使用双乳液溶剂扩散方法制备PLGA纳米粒子,并用葡萄糖氧化酶(GOX)和过氧化氢酶(猫)酶负载。这些带负电荷的颗粒通过葡萄糖分子存在的葡萄糖酸产生减少微环境pH。使用离子凝胶化方法制备正电壳聚糖纳米粒子,并用胰岛素装载。这些纳米颗粒(NPS)通过对GOX活性引起的酸性pH解离释放胰岛素。在体外研究之后,体内评价链脲素诱导的糖尿病大鼠的纳米复合物制剂在皮下施用后显着血糖调节至98小时。

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