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Polymeric vesicle prepared from poly-l-lysine modified amphiphilic graft copolymer

机译:由聚-1-赖氨酸改性的两亲性接枝共聚物制备的聚合物囊泡

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Phospholipid vesicels (liposomes) and non-ionic surfactant based vesicles (niosomes) have been extensively studied as carriers of bioactive materials~1,2. In an effort to improve the stability of these vesicles, several polymerised vesicles have been developed~3,4, in which amphiphilic monomers containing polymerizable groups have been assembled into vesicles and later polymerised. In addition specially synthesised amphiphilic polymers in which the bilayer forming phospholipid amphiphiles are separated from the polymer backbone by an obligatory hydrophilic spacer unit have been used to make vesicles~5. In this laboratory, a novel poly-L-lysine based amphiphilic copolymer (PLP) has been developed by grafting hydrophobic palmitoyl groups and hydrophilic polyethylene glycol chains onto a poly-L-lysine backbone (Figure 1). It has been found that certain PLP variants can assemble into unilamellar vesicles on sonication in the presence of cholesterol and such vesicles are being investigated as gene delivery agents~6.
机译:磷脂囊泡(脂质体)和基于非离子表面活性剂的囊泡(脂质体)已被广泛研究为生物活性物质的载体〜1,2。为了提高这些囊泡的稳定性,已经开发了几种聚合的囊泡[3,4],其中将含有可聚合基团的两亲单体组装成囊泡,然后进行聚合。另外,使用特殊合成的两亲聚合物,其中形成双层的磷脂两亲物通过必不可少的亲水性间隔单元与聚合物主链分开,从而制成囊泡〜5。在这个实验室中,通过将疏水性棕榈酰基和亲水性聚乙二醇链接枝到聚-L-赖氨酸主链上,开发了一种新型的基于聚-L-赖氨酸的两亲共聚物(PLP)(图1)。已经发现某些PLP变体可以在胆固醇存在下经超声处理组装成单层囊泡,并且正在研究这种囊泡作为基因递送剂[6]。

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