10-hydroxycamptothecin-loaded starch-based microcapsules with the stepwise responsive release strategy for targeted controlled release

被引:2
|
作者
Meng, Qingye [1 ]
Zhong, Shuangling [2 ]
Wang, Jia [1 ]
Gao, Yan [1 ,3 ,4 ]
Cui, Xuejun [1 ,4 ]
机构
[1] Jilin Univ, Coll Chem, Changchun 130012, Peoples R China
[2] Jilin Agr Univ, Coll Resources & Environm, Changchun 130118, Peoples R China
[3] Jilin Univ, State Key Lab Supramol Struct & Mat, Changchun 130012, Peoples R China
[4] Jilin Univ, Weihai Inst Bion, Weihai 264400, Peoples R China
关键词
Starch; Microcapsules; Controlled release; DRUG-DELIVERY; FOLIC-ACID; FABRICATION; CHITOSAN; NANOPARTICLES; BREAST; SMART;
D O I
10.1016/j.ijbiomac.2023.126424
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Controlled and accurate drug release at the target site have been the focus of research. Especially in cancer therapy, economical, convenient and accurate delivery strategies could help to reduce the toxic effects of drugs on normal tissues and improve drug availability. In the study, glutathione (GSH)-responsive microcapsules (FARSMCs) were prepared by sonochemical method based on thiolated modified starch. 10-Hydroxycamptothecin (HCPT) was designed as a reactive oxygen species (ROS)-responsive polyprodrug (polyHCPT), which was loaded into the core of the microcapsules to obtain stepwise released drug delivery carriers. In the tumor microenvironment, FA-RSMCs first triggered GSH-responsive cleavage to release polyHCPT, followed by ROSresponsive cleavage of polyHCPT to release intact HCPT drug molecules. The results of experiments in simulated tumor microenvironment showed that FA-RSMCs exhibited good cascade-response release properties in vitro. It exhibited good anti-tumor ability and protection of normal cells in cytotoxicity in vitro. This strategy enhanced the accuracy and safety of targeted delivery of HCPT via microcapsules, which has potential for clinical application.
引用
收藏
页数:10
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