Stimuli-Responsive Polymeric Nanocarriers Accelerate On-Demand Drug Release to Combat Glioblastoma

被引:6
|
作者
Ismail, Muhammad [1 ,2 ,3 ]
Wang, Yibin [3 ]
Li, Yundong [3 ]
Liu, Jiayi [3 ]
Zheng, Meng [1 ,2 ,3 ]
Zou, Yan [1 ,2 ,3 ,4 ]
机构
[1] Henan Univ, Huaihe Hosp, Dept Radiotherapy, Kaifeng 475000, Henan, Peoples R China
[2] Henan Univ, Huaihe Hosp, Translat Med Ctr, Kaifeng 475000, Henan, Peoples R China
[3] Henan Univ, Sch Life Sci, Henan Macquarie Univ Joint Ctr Biomed Innovat, Henan Key Lab Brain Targeted Bionanomedicine, Kaifeng 475004, Henan, Peoples R China
[4] Macquarie Univ, Fac Med Hlth & Human Sci, Macquarie Med Sch, Sydney, NSW 2109, Australia
基金
中国国家自然科学基金;
关键词
BLOOD-BRAIN-BARRIER; MESOPOROUS SILICA NANOPARTICLES; PHOTODYNAMIC THERAPY; TARGETED DELIVERY; X-RAY; TEMOZOLOMIDE INTERMEDIATE; LIPOSOMAL DOXORUBICIN; 5-AMINOLEVULINIC ACID; COMBINATION THERAPY; BLOCK-COPOLYMER;
D O I
10.1021/acs.biomac.4c00722
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
Glioblastoma multiforme (GBM) is a highly malignant brain tumor with a poor prognosis and limited treatment options. Drug delivery by stimuli-responsive nanocarriers holds great promise for improving the treatment modalities of GBM. At the beginning of the review, we highlighted the stimuli-active polymeric nanocarriers carrying therapies that potentially boost anti-GBM responses by employing endogenous (pH, redox, hypoxia, enzyme) or exogenous stimuli (light, ultrasonic, magnetic, temperature, radiation) as triggers for controlled drug release mainly via hydrophobic/hydrophilic transition, degradability, ionizability, etc. Modifying these nanocarriers with target ligands further enhanced their capacity to traverse the blood-brain barrier (BBB) and preferentially accumulate in glioma cells. These unique features potentially lead to more effective brain cancer treatment with minimal adverse reactions and superior therapeutic outcomes. Finally, the review summarizes the existing difficulties and future prospects in stimuli-responsive nanocarriers for treating GBM. Overall, this review offers theoretical guidelines for developing intelligent and versatile stimuli-responsive nanocarriers to facilitate precise drug delivery and treatment of GBM in clinical settings.
引用
收藏
页码:6250 / 6282
页数:33
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