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Enhancing Lysozyme Loading in Powderized Liposomes by Controlling Encapsulation Processes

机译:通过控制包封过程增强粉状脂质体中溶菌酶的负载

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Liposomes have demonstrated great potentials as protein carriers in various pharmaceutical applications. However, low loading amount of proteins in liposomes have been a major challenge for maximizing the therapeutics potential of the proteins. We thus aimed to enhance the loading amount of a model protein, lysozyme, in liposomes by controlling key experimental variables of a reverse phase evaporation method. The loading amount of lysozyme in liposomes was evaluated with changing type of organic solvents used, weight ratio of lysozyme/phosphatidylcholine, and volume ratio of aqueous to organic phase along with particle characterization before and after freezea??drying procedure. As a result, the loading amount of lysozyme in liposomes was considerably enhanced and the physical stability of the liposomes was maintained without any significant changes in the particle characteristics for 7 days. The findings of this study would be useful for highly efficient loading of protein therapeutics in liposomes, leading to improved therapeutic effects of the drugs.
机译:脂质体已显示出在各种药物应用中作为蛋白质载体的巨大潜力。然而,脂质体中蛋白质的低负载量一直是使蛋白质的治疗潜力最大化的主要挑战。因此,我们旨在通过控制反相蒸发方法的关键实验变量来提高脂质体中模型蛋白溶菌酶的负载量。通过改变所用有机溶剂的类型,溶菌酶/磷脂酰胆碱的重量比,水相与有机相的体积比以及冷冻干燥前后的颗粒特性,评价脂质体中溶菌酶的负载量。结果,脂质体中溶菌酶的负载量大大增加,并且脂质体的物理稳定性得以维持,而颗粒特性在7天内没有任何显着变化。这项研究的发现将对脂质体中蛋白质治疗剂的高效负载有用,从而改善药物的治疗效果。

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