Erythrocyte membrane encapsulated gambogic acid nanoparticles as a therapeutic for hepatocellular carcinoma

被引:9
作者
Liu, Ruijie [1 ]
He, Li [2 ]
Liu, Maoyu [3 ]
Chen, Lu [3 ]
Hou, Jun [1 ]
Shi, Jianyou [3 ]
Bai, Lan [3 ]
机构
[1] Southwest Jiaotong Univ, Affiliated Hosp, Chengdu Peoples Hosp 3, Dept Cardiol, Chengdu 610031, Peoples R China
[2] Jianyang Chinese Med Hosp, Dept Pharm, Chengdu 641499, Peoples R China
[3] Univ Elect Sci & Technol China, Sichuan Acad Med Sci & Sichuan Prov Peoples Hosp, Sch Med, Dept Pharm,Personalized Drug Therapy Key Lab Sichu, Chengdu 610072, Peoples R China
基金
中国国家自然科学基金;
关键词
Gambogic acid; Erythrocyte membrane; Drug delivery systems; Biomimetic nanoparticles; Hepatocellular carcinoma; DRUG-DELIVERY; BIOMIMETIC NANOPARTICLES; SYSTEMS;
D O I
10.1016/j.cclet.2022.05.089
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Gambogic acid (GA) is a potential clinical anticancer drug that can exert antitumor effects via various molecular mechanisms. Notwithstanding, GA's low water solubility, poor stability, short half-life, and un-avoidable toxic side effects have significantly hampered its clinical application. Erythrocyte membrane-coated nanoparticles (RBCM-NPs) improve drug's physicochemical properties, biocompatibility, and phar-macokinetic behaviors, allowing for long-term drug circulation and passive targeting. In this study, a novel biomimetic drug delivery system (DDS) against hepatocellular carcinoma was prepared by covering RBCM on GPP-NPs (GA-loaded mPEG-PLA NPs) to develop the RBC@GPP-NPs. In comparison to RBCM-free nanoparticles and free GA, RBC@GPP-NPs improved the drug's water solubility, stability, safety, and anti-tumor activity in vivo. We expect that this bionic nanoparticle composite can expand the clinical applica-bility of GA and provide a feasible solution for the research and development of GA's nano-formulation.& COPY; 2022 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
引用
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页数:4
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