结合
紫杉醇
纳米载体
细胞毒性
化学
药理学
维甲酸
药物输送
药代动力学
毒品携带者
药品
阿霉素
化疗
生物化学
维甲酸
医学
体外
有机化学
外科
数学分析
基因
数学
作者
Lin Hou,Ying Fan,Jing Yao,Jianping Zhou,Caocao Li,Zhengjie Fang,Qiang Zhang
标识
DOI:10.1016/j.carbpol.2011.06.008
摘要
As a novel nanocarrier for simultaneous delivery of multiple anticancer drugs, low molecular weight heparin-all-trans-retinoid acid (ATRA) (LHR) conjugate was developed. Amphiphilic LHR conjugate had markedly lower anticoagulant activity, and could self-assemble to form nanoparticles for loading hydrophobic drugs. The critical aggregation concentrations of LHR conjugates were varied from 407 to 40 mg/L. Paclitaxel (PTX)-loaded LHR nanoparticles were prepared by the dialysis method, with particle sizes in the range of 228.0–108.9 nm. The maximum drug-loading was as much as 33.1% with an entrapment efficiency of 93.1%. They displayed enhanced PTX-induced cytotoxicity to HepG2 cells compared to PTX solution. Hemolysis and cytotoxicity studies showed that LHR conjugate was a safe material for intravenous administration. Moreover, the pharmacokinetic profiles indicated that PTX-loaded LHR nanoparticles contributed to an extended circulation of PTX and ATRA. These results suggest that PTX-loaded LHR nanoparticles can be considered as promising anticancer drug delivery system for combination chemotherapy.
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