替莫唑胺
胶质瘤
医学
体内
癌症研究
药物输送
血脑屏障
基因传递
遗传增强
生物相容性
药理学
化学
材料科学
中枢神经系统
纳米技术
内科学
生物
基因
生物技术
有机化学
生物化学
作者
Tingting Yang,Nan Zhang,Yuanyuan Liu,Ruyue Yang,Zhaoyi Wei,Futai Liu,Dan Song,Longwei Wang,Jiangyan Wei,Yuanpei Li,Deliang Shen,Gaofeng Liang
标识
DOI:10.1186/s12951-024-02895-6
摘要
Abstract Gliomas are one of the most frequent primary brain tumors and pose a serious threat to people’s lives and health. Platelets, a crucial component of blood, have been applied as drug delivery carriers for disease diagnosis and treatment. In this study, we designed engineered nanoplatelets for targeted delivery of therapeutic miR-375 and temozolomide (TMZ, a first-line glioma treatment agent) to enhance glioma therapy. Nanoplatelets were prepared through mild ultrasound, TMZ and miR-375 were co-loaded through ultrasound and electrostatic interactions, respectively, to combine chemotherapy with gene therapy against glioma. To improve the blood brain barrier (BBB) crossing efficiency and glioma targeting ability, the nanoplatelets were modified with central nervous system-specific rabies viral glycoprotein peptide (RVG) through thiol-maleimide click reaction. The RVG modified nanoplatelets co-loaded TMZ and miR-375 (NR/TMZ/miR-375) not only inherited the good stability and remarkable biocompatibility of platelets, but also promoted the cellular uptake and penetration of glioma tissues, and effectively induced cell apoptosis to enhance the therapeutic effect of drugs. In vivo studies showed that NR/TMZ/miR-375 significantly increased the circulation time of TMZ, and exhibited superior combined antitumor effects. In summary, this multifunctional ‘natural’ nanodrug delivery system provides a potent, scalable, and safety approach for platelet-based combined cancer chemotherapy and gene therapy.
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