Design and evaluation of pH-sensitive liposomes constructed by poly(2-ethyl-2-oxazoline)-cholesterol hemisuccinate for doxorubicin delivery

被引:55
作者
Xu, Huan [1 ]
Hu, Meina [1 ]
Yu, Xiu [1 ]
Li, Yan [1 ]
Fu, Yuanshan [2 ]
Zhou, Xiaoxia [1 ]
Zhang, Di [1 ]
Li, Jianying [1 ]
机构
[1] Liaoning Normal Univ, Dept Pharm, Sch Chem & Chem Engn, Dalian 116029, Peoples R China
[2] Dlian Med Univ, Coll Basic Med Sci, Dept Anat, Dalian, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Poly(2-ethyl-2-oxazoline); Cholesterol hemisuccinate; Liposomes; pH-sensitive; PEGylation; PEG dilemma; PEGYLATED LIPOSOMES; CIRCULATION TIME; GENE DELIVERY; SYSTEMS; EFFICIENT; PROTEINS; POLYMERS; VESICLES; RECEPTOR; PEPTIDE;
D O I
10.1016/j.ejpb.2015.01.030
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this study, a novel material, poly(2-ethyl-2-oxazoline)-cholesterol hemisuccinate (PEtOz-CHEMS), was synthesized to construct pH-sensitive liposomes. The structure of PEtOz-CHEMS was confirmed by thin-layer chromatography, Fourier transform infrared spectroscopy, and H-1 NMR. Anticancer fluorescent drug doxorubicin (DOX) was encapsulated into the liposomes. Compared with conventional liposomes (CL), CHEMS modified liposomes (CH-L) and PEGylated liposomes (PEG-L), the PEtOzylated liposomes (PEtOz-L) showed an acidic pH-induced increase in particle size. At pH 6.4, the heme release of PEtOz-L group was close to that of the positive control group, whereas that of CL, CH-L and PEG-L was close to that of the negative control group. In vitro drug release studies demonstrated that DOX was released from PEtOz-L in a pH-dependent manner, and the release of DOX from conventional DOX liposomes (CL-DOX), DOX loaded CH-L (CH-DOX-L) and PEGylated DOX liposomes (PEG-DOX-L) had no pronounced differences under each pH medium. In vitro cellular uptake assays showed that PEtOz-DOX-L indicated a significant fluorescence intensity at pH 6.4 compared with at pH 7.4. CL-DOX, CH-DOX-L and PEG-DOX-L did not achieve any obvious diversity at different pH conditions. Confocal laser scanning microscopy images showed that PEtOz-DOX-L can fuse with the endosomal membrane under acidic conditions of endosome, release DOX into the cytoplasm, then gather into the nucleus. Therefore, PEtOz can help liposomes achieve "endosomal escape". The in vitro cytotoxicity experiment results on A375 cells showed that PEtOz-DOX-L resulted in lower cell viability than CL-DOX, CH-DOX-L and PEG-DOX-L under low pH conditions. These results confirm that the pH-responsive PEtOz was a promising material for intracellular targeted delivery system and might be used for overcoming the "PEG dilemma". (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:66 / 74
页数:9
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