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Liposomes encapsulating polymeric chitosan based vesicles - a vesicle in vesicle system for drug delivery

机译:脂质体,封装基于聚合物壳聚糖的囊泡-囊泡系统中的囊泡,用于药物输送

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摘要

Drug delivery systems comprising vesicles prepared from one amphiphile encapsulating vesicles prepared from a second amphiphile have not been prepared previously due to a tendency of the bilayer components of the different vesicles to mix during preparation. Recently we have developed polymeric vesicles using the new polymer-palmitoyl glycol chitosan and cholesterol in a 2:1 weight ratio. These polymeric vesicles have now been encapsulated within egg phosphatidylcholine (egg PC), cholesterol (2:1 weight ratio) liposomes yielding a vesicle in vesicle system. The vesicle in vesicle system was visualised by freeze fracture electron microscopy. The mixing of the different bilayer components was studied by monitoring the excimer fluorescence of pyrene-labelled polymeric vesicles after their encapsulation within egg PC liposomes or hexadecyl diglycerol ether niosomes. A minimum degree of lipid mixing was observed with the polymeric vesicle-egg PC liposome system when compared to the polymeric vesicle-hexadecyl diglycerol ether niosome system. The polymeric vesicle-egg PC vesicle in vesicle system was shown to retard the release of encapsulated solutes. 28% of 5(6)-carboxyfluorescein (CF) encapsulated in the polymeric vesicle compartment of the vesicle in vesicle system was released after 4 h compared to the release of 62% of encapsulated CF from plain polymeric vesicles within the same time period.
机译:由于不同囊泡的双层成分在制备过程中有混合的趋势,因此尚未预先制备包含由一种两亲菌制备的囊泡和由另一种两亲菌制备的囊泡的药物递送系统。最近,我们使用重量比为2:1的新型聚合物-棕榈酰乙二醇壳聚糖和胆固醇开发了聚合物囊泡。这些聚合物囊泡现已被封装在卵磷脂酰胆碱(卵磷脂PC),胆固醇(重量比为2:1)脂质体中,从而在囊泡系统中形成囊泡。通过冷冻断裂电子显微镜观察囊泡系统中的囊泡。通过将pyr标记的聚合物囊泡包封在卵PC脂质体或十六烷基二甘油醚脂质体中后,通过监测label标记的聚合物囊泡的准分子荧光来研究不同双层成分的混合。当与聚合囊泡-十六烷基二甘油醚脂质体系统相比时,使用聚合囊泡-PC PC脂质体系统观察到最小程度的脂质混合。囊泡系统中的聚合物囊泡-卵泡PC囊泡显示出延迟了包封的溶质的释放。囊泡系统中囊泡的聚合物囊泡腔室中封装的5(6)-羧基荧光素(CF)中有28%在4小时后释放,而在同一时间段内从普通聚合物囊泡中释放了62%的封装CF。

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