The development and evaluation of hyaluronic acid coated mitochondrial targeting liposomes for celastrol delivery

被引:14
|
作者
Xiao, Simeng [1 ]
Huang, Siying [1 ]
Yang, Xiaojing [1 ]
Lei, Yujie [3 ]
Chang, Mingxiang [4 ]
Hu, Junjie [1 ]
Meng, Yan [1 ]
Zheng, Guohua [2 ,6 ]
Chen, Xinyan [1 ,5 ]
机构
[1] Hubei Univ Chinese Med, Pharm Fac, Wuhan, Peoples R China
[2] Hubei Univ Chinese Med, Key Lab Chinese Med Resource & Cpd Prescript, Minist Educ, Wuhan, Peoples R China
[3] Wuxue No 1 Peoples Hosp, Pharm Dept, Wuxue, Peoples R China
[4] Hubei Hosp Tradit Chinese Med, Lab Cell & Mol Biol, Wuhan, Peoples R China
[5] Hubei Univ Chinese Med, Pharm Fac, Wuhan 430065, Peoples R China
[6] Hubei Univ Chinese Med, Key Lab Chinese Med resource & Cpd Prescript, Minist Educ, Wuhan 430065, Peoples R China
关键词
Celastrol; mitochondrial targeting; tumor targeting; delivery system; anticancer effect; BREAST-CANCER; CO-DELIVERY; NANOPARTICLES; MICELLES; SIRNA;
D O I
10.1080/10717544.2022.2162156
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In order to precisely deliver celastrol into mitochondria of tumor cells, improve antitumor efficacy of celastrol and overcome its troublesome problems in clinical application, a novel multistage-targeted celastrol delivery system (C-TL/HA) was developed via electrostatic binding of hyaluronic acid (HA) to celastrol-loaded cationic liposomes composed of natural soybean phosphatidylcholine and cholesterol modified with mitochondrial targeting molecular TPP. Study results in this article showed that C-TL/HA successfully transported celastrol into mitochondria, effectively activated apoptosis of mitochondrial pathway, exerted higher tumor inhibition efficiency and lower toxic side effects compared with free celastrol. More importantly, HA coating not only enabled this delivery system to have good stability and safety in vivo, but also increased drug uptake and facilitated tumor targeting through recognizing CD44 receptors rich on the surface of tumor cells. Conclusively, this HA-coated mitochondrial targeting liposomes may provide a prospect for the clinical application of celastrol in tumor therapy.
引用
收藏
页数:12
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