Exosome-mediated delivery platform of biomacromolecules into the brain: Cetuximab in combination with doxorubicin for glioblastoma therapy

阿霉素 胶质母细胞瘤 微泡 外体 西妥昔单抗 医学 癌症研究 脑瘤 药物输送 化学 药理学 化疗 内科学 免疫学 病理 单克隆抗体 抗体 生物化学 小RNA 有机化学 基因
作者
Liuxiang Chu,Yuchen Sun,Yanyan Zhao,Aiping Wang,Yiying Sun,Xinliu Duan,Nuannuan Li,Hangyu Xia,Yijie Liu,Kaoxiang Sun
出处
期刊:International Journal of Pharmaceutics [Elsevier BV]
卷期号:660: 124262-124262 被引量:5
标识
DOI:10.1016/j.ijpharm.2024.124262
摘要

Monoclonal antibodies (mAbs) have become the predominant treatment modality for various diseases due to their high affinity and specificity. Although antibodies also have great potential for neurological diseases, they couldn't fully meet the therapeutic requirements due to their high molecular weight and limitations in crossing the blood–brain barrier (BBB). Herein, an innovative strategy based on exosomes (Exos) platform was developed to enhance the delivery of cetuximab (CTX) into the brain, and in combination with doxorubicin (DOX) for the synergistic targeted therapy of glioblastoma (GBM). The in vitro/vivo experiments have shown that exosomes could effectively promote BBB penetration and increase the content of CTX in glioma cells and brain lesions. Cytotoxicity and wound healing experiments have shown that CTX-Exo-DOX could significantly inhibit the proliferation of tumor cells. Finally, in vivo results showed that CTX-Exo-DOX significantly prolonged the survival time of tumor-bearing rats to 28 days, which was 1.47 times that of the DOX group. In summary, exosomes could deliver more antibodies into the brain, and CTX-Exo-DOX is a promising co-delivery system for the treatment of GBM. The results of this study will also provide a prospective strategy for antibody drugs in the treatment of neurological diseases.
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