Preparation and characterization of amphiphilic nanoparticles based on chondroitin sulfate A conjugated with hydrophobic drug for enhanced doxorubicin delivery

被引:8
|
作者
Xie, Xin [1 ]
Yuan, Zhen [2 ]
Yuan, Qinglan [3 ]
Huang, Yuyou [2 ]
Yu, Qunying [2 ]
Ren, Jin [2 ]
Liang, Liang [4 ]
Jin, Hongguang [2 ]
Yu, Jingmou [1 ,2 ]
机构
[1] Jiujiang Univ, Key Lab Jiangxi Prov Syst Biomed, Jiujiang 332000, Peoples R China
[2] Jiujiang Univ, Sch Pharm & Life Sci, Jiujiang 332000, Peoples R China
[3] Jiujiang Univ, Univ Hosp, Jiujiang 332005, Peoples R China
[4] Jiujiang Univ, Analyt & Testing Ctr, Jiujiang 332005, Peoples R China
关键词
Chondroitin sulfate A; Doxorubicin; Polymer-drug conjugate; Self-assembled nanoparticles; POLYMERIC MICELLES; TARGETED DELIVERY; IN-VITRO;
D O I
10.1007/s00396-020-04778-2
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Novel chondroitin sulfate A conjugated doxorubicin (CSA-DOX) was synthesized and characterized. The mean diameter of CSA-DOX was 152 nm analyzed by dynamic light scattering (DLS). Further, DOX was physically encapsulated into the CSA-DOX nanoparticles. Total amounts of DOX in three kinds of DOX-loaded CSA-DOX (CSA-DOX/DOX) nanoparticles were from 21.8 to 24.2%. The mean diameters of three CSA-DOX/DOX nanoparticles were in the range of 167-177 nm. The shape of CSA-DOX/DOX nanoparticles was almost spherical. DOX released from DOX-loaded nanoparticles exhibited a biphasic way in phosphate buffered saline (PBS, pH 7.4). Cellular uptake studies exhibited that CSA-DOX and CSA-DOX/DOX nanoparticles could enhance the uptake of DOX into CD44 receptor-positive A549 cells. Moreover, the cytotoxicity of CSA-DOX/DOX nanoparticles against A549 cells significantly improved in contrast with free DOX and CSA-DOX nanoparticles. These results suggested that CSA-DOX copolymer could be a potential carrier for antitumor drug delivery.
引用
收藏
页码:129 / 136
页数:8
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