纳米载体
阿霉素
细胞毒性
体内
药物输送
透明质酸
离体
化学
谷胱甘肽
靶向给药
毒品携带者
MTT法
药理学
生物物理学
体外
生物化学
医学
生物
化疗
有机化学
外科
生物技术
解剖
酶
作者
Athar Mahdieh,Hamidreza Motasadizadeh,Hamid Yeganeh,Bo Nyström,Rassoul Dinarvand
标识
DOI:10.1016/j.ijpharm.2022.122275
摘要
Nanocarriers of different origins that respond to stimuli have been synthesized and used in various biomedical applications, such as intracellular drug delivery. To develop highly efficient nanocarriers, novel clickable and cleavable soybean oil-based polyurethane nanomicelles (CPUM), and polyurethane-hyaluronic acid nanomicelles (CPUM-HA) were prepared. The prepared nanocarriers exhibited controlling self-assembly properties, stimuli-responsiveness, good cytocompatibility, and high loading capacity for doxorubicin (DOX). The addition of the reducing agent glutathione (GSH) to the drug release medium resulted in GSH-triggered species size change (aggregation of nanomicelles) and enhanced release of DOX, leading to higher cytotoxicity in tumors. MTT, confocal laser scanning microscopy (CLSM), and flow cytometry results showed that the CPUM-HA-DOX nanocarriers exhibited increased cytotoxicity and cellular uptake compared to the CPUM-DOX nanocarriers. The in vivo and ex vivo results suggested that the CPUM-HA nanomicelles could provide a potential platform for effective targeted delivery of cytotoxic drug molecules to the tumor tissue and breast cancer therapy in the clinic.
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