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Preparation of chitosan-coated liposomes as a novel carrier system for the antiviral drug Triazavirin

机译:壳聚糖涂层脂质体作为抗病毒药物三氮素的新型载体系统的制备

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摘要

Novel method for the coating of positively charged liposomes with modified chitosan was elaborated. Liposomes were prepared by stepwise extrusion through inorganic membranes (Anotop) of 0.2 and 0.1 糾 pore sizes. Chitosan derivatives were synthesized via the Ugi multicomponent reaction. Several series of liposomal compositions were produced and their properties were compared in terms of particle size, polydispersity index (PDI), zeta potential and stability. The effect of various additives was investigated and the optimal composition of the lipid film was determined. The addition of the uncharged fatty esters allowed the diameter of the liposomes obtained by extrusion to be reduced to 145150 nm with a PDI of 0.130.15. The prepared liposomes were loaded with the novel antiviral drug Triazavirin and used to determine the release profile. Triazavirin was included into liposome layer as a salt with biocompatible choline derivatives of limiting fatty acids. The appropriate lipid composition was used for the preparation of a larger quantity of liposomes coated by modified chitosan. It was shown that an appropriate combination of liposomes and polysaccharide layer potentially extended colloidal stability by up to 3 months and exhibited broad functional capabilities for surface modification. ?2016 Informa UK Limited, trading as Taylor & Francis Group.
机译:阐述了用改性壳聚糖涂覆带正电荷脂质体的新方法。通过逐步挤出通过0.2和0.1孔径的无机膜(Anotop)逐步挤出制备脂质体。通过UGI多组分反应合成壳聚糖衍生物。产生了几种脂质体组合物,并在粒度,多分散指数(PDI),Zeta电位和稳定性方面进行了它们的性质。研究了各种添加剂的效果,测定了脂膜的最佳组成。加入不带电的脂肪酯允许通过挤出获得的脂质体的直径减少至145150nm,PDI为0.130.15。将制备的脂质体加载着新的抗病毒药物三唑林,并用于确定释放曲线。将三氮素林包含在脂质体层中作为具有限制脂肪酸的生物相容性胆碱衍生物的盐。合适的脂质组合物用于制备由改性壳聚糖涂覆的较大量的脂质体。结果表明,脂质体和多糖层的适当组合可能会延长胶体稳定性长达3个月,并表现出用于表面改性的广泛功能能力。 ?2016年Informa UK Limited,贸易为泰勒和弗朗西斯集团。

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