Esterase-responsive and size-optimized prodrug nanoparticles for effective intracranial drug delivery and glioblastoma treatment

被引:7
作者
Ye, Zhang
Gao, Lun
Cai, Jiayang
Wang, Yixuan
Li, Yong
Tong, Shiao
Yan, Tengfeng
Sun, Qian
Qi, Yangzhi
Xu, Yang
Jiang, Hongxiang
Zhang, Si
Zhao, Linyao
Zhang, Shenqi
Chen, Qianxue
机构
[1] Wuhan Univ, Renmin Hosp, Dept Neurosurg, Wuhan 430060, Hubei, Peoples R China
[2] Wuhan Univ, Renmin Hosp, Cent Lab, Wuhan 430060, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
GBM; CXCR4; PLGA nanoparticle; Tandutinib; Prodrug; MULTIDRUG-RESISTANCE; MOLECULAR-MECHANISMS; TANDUTINIB MLN518; ISCHEMIC-STROKE; STRATEGIES; RELEASE; SYSTEM;
D O I
10.1016/j.nano.2022.102581
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Glioblastoma multiforme (GBM) is the intracranial malignancy with the highest rates of morbidity and mortality. Chemotherapy is often ineffective against GBM due to the presence of the blood-brain barrier (BBB); however, the application of nanotechnology is expected to overcome this limitation. Poly(lactic-co-glycolic acid) (PLGA) is a degradable and nontoxic functional polymer with good biocompatibility that is widely used in the pharmaceutical industry. Previous studies have shown that the ability of PLGA nanoparticles (NPs) to penetrate the BBB is largely determined by their size; however, determination of the optimal PLGA NP size requires further research. Here, we report a tandutinib-based prodrug (proTan), which responds to the GBM microenvironment, that was combined with NPs to overcome the BBB. AMD3100-PLGA NPs loaded with proTan inhibited tumor growth and effectively prolonged the survival of tumor-bearing mice. (c) 2022 Published by Elsevier Inc.
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页数:12
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