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RGD修饰的脂质盘作为肿瘤靶向给药的药物载体。

RGD-modified lipid disks as drug carriers for tumor targeted drug delivery.

作者信息

Gao Jie, Xie Cao, Zhang Mingfei, Wei Xiaoli, Yan Zhiqiang, Ren Yachao, Ying Man, Lu Weiyue

机构信息

Department of Pharmaceutics, School of Pharmacy, Fudan University & Key Laboratory of Smart Drug Delivery (Fudan University), Ministry of Education, Shanghai, 201203, P. R. China.

出版信息

Nanoscale. 2016 Apr 7;8(13):7209-16. doi: 10.1039/c5nr05577f. Epub 2016 Mar 14.

Abstract

Melittin, the major component of the European bee venom, is a potential anticancer candidate due to its lytic properties. However, in vivo applications of melittin are limited due to its main side effect, hemolysis, especially when applied through intravenous administration. The polyethylene glycol-stabilized lipid disk is a novel type of nanocarrier, and the rim of lipid disks has a high affinity to amphiphilic peptides. In our study, a c(RGDyK) modified lipid disk was developed as a tumor targeted drug delivery system for melittin. Cryo-TEM was used to confirm the shape and size of lipid disks with or without c(RGDyK) modification. In vitro and in vivo hemolysis analyses revealed that the hemolysis effect significantly decreased after melittin associated with lipid disks. Importantly, the results of our in vivo biodistribution and tumor growth inhibitory experiments showed that c(RGDyK) modification increased the distribution of lipid disks in the tumor and the anticancer efficacy of melittin loaded lipid disks. Thus, we successfully achieved a targeted drug delivery system for melittin and other amphiphilic peptides with a good therapeutic effect and low side effects.

摘要

蜂毒明肽是欧洲蜜蜂毒液的主要成分,因其具有溶解特性而成为一种潜在的抗癌候选物。然而,由于其主要副作用溶血,尤其是通过静脉给药时,蜂毒明肽的体内应用受到限制。聚乙二醇稳定的脂质盘是一种新型纳米载体,脂质盘的边缘对两亲性肽具有高亲和力。在我们的研究中,开发了一种c(RGDyK)修饰的脂质盘作为蜂毒明肽的肿瘤靶向给药系统。冷冻透射电子显微镜用于确认有无c(RGDyK)修饰的脂质盘的形状和大小。体外和体内溶血分析表明,蜂毒明肽与脂质盘结合后溶血效应显著降低。重要的是,我们的体内生物分布和肿瘤生长抑制实验结果表明,c(RGDyK)修饰增加了脂质盘在肿瘤中的分布以及负载蜂毒明肽的脂质盘的抗癌效果。因此,我们成功实现了一种针对蜂毒明肽和其他两亲性肽的靶向给药系统,具有良好的治疗效果和低副作用。

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