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A pH/reduction dual-sensitive copolymer inserted in liposomal bilayer acts as a protective 'umbrella'

机译:插入脂质体双层的pH /还原双敏化共聚物充当保护性“伞”

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摘要

Developing a targeted intelligent drug delivery system with excellent controllability of drug release remains an ongoing challenge in chemotherapy. A multistage responsive liposome was constructed by inserting a folate (FA) modified lipid and a pH/reduction dual-sensitive copolymer into the liposome bilayer. The properties of liposome were studied by fluorescence polarization, dynamic light scattering and in vitro drug release. Since the PDPA segment of the copolymer could embed in or escape from the liposomal bilayer depending on pH value, the membrane stability of the liposome was improved at pH 7.4 and decreased at pH 5.0. As a result, the drug leakage of the liposome was significantly suppressed at pH 7.4 but promoted at an acidic pH. Moreover, the liposome Lipo5-FA, which contained negatively charged FA groups protected by the longer PEG, was found to undergo membrane fusion with the positively charged Lipo( + ) to verify the longer PEG was cut by GSH. All results indicated that the smart copolymer acted as a switch on liposomal bilayer for drug release and also a protective "umbrella" for FA.
机译:开发具有优异的药物释放可控性的目标智能药物递送系统仍然是化疗的持续挑战。通过将叶酸(Fa)改性的脂质和pH /还原双敏化共聚物插入脂质体双层来构建多级敏感脂质体。通过荧光极化,动态光散射和体外药物释放研究了脂质体的性质。由于共聚物的PDPA区段可以根据pH值嵌入或逸出或逸出,因此在pH7.4的pH7.4下改善脂质体的膜稳定性并在pH 5.0下降低。结果,在pH7.4下显着抑制了脂质体的药物泄漏,但在酸性pH下促进。此外,含有受较长栓较长佩格保护的带负电荷的FA组的脂质体Lipo5-Fa被发现与带正电荷的Lipo(+)进行膜融合以验证通过GSH切割较长的佩格。所有结果表明,智能共聚物用作脂质体双层的开关,用于药物释放,也是FA的保护性“伞”。

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