Amphiphilic nanoparticles based on poly(vinyl pyrrolidone) and stearoyl modified chitosan as drug vehicles for paclitaxel delivery

被引:6
|
作者
Liu, Zhao [1 ]
Zhang, Teng [2 ,3 ]
Tang, Cui [1 ]
Yin, Chunhua [1 ]
机构
[1] Fudan Univ, Sch Life Sci, Shanghai 200438, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Yueyang Hosp, Shanghai 200437, Peoples R China
[3] Shanghai Univ Tradit Chinese Med, Clin Res Inst Integrat Med, Shanghai 200437, Peoples R China
关键词
Polymers; Nanoparticles; Hydrophilic modification; Hydrophobic modification; Antitumor efficacy;
D O I
10.1016/j.matlet.2016.08.145
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Poly(vinyl pyrrolidone) (PVP) and stearoyl chloride (SC) double-grafted chitosan (PCS) nanoparticles (NPs) were prepared for paclitaxel (PTX) delivery. PTX could be effectively loaded into PCS NPs with encapsulation efficiency of 92.8%. PTX-loaded PCS NPs (PTX/PCS NPs), which possessed particle sizes of 144 nm and Zeta potentials of -7.5 mV, exhibited a sustained release behavior. In H-22 tumor bearing mice, significantly enhanced antitumor efficacies were achieved by PTX/PCS NPs with the tumor inhibition ratio (TIR) of 76.1% as compared with PTX injection. Furthermore, no signs of sub-acute toxicity were detected in healthy mice, indicating the safety of PCS NPs. Therefore, PCS NPs could be served as an effective and safe carrier for PTX delivery. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:226 / 229
页数:4
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