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通过嵌入同型癌细胞膜增强柠檬来源的细胞外囊泡的肿瘤自靶向性以实现高效药物递送。

Enhanced tumor self-targeting of lemon-derived extracellular vesicles by embedding homotypic cancer cell membranes for efficient drug delivery.

作者信息

Yang Lu-Yao, Liang Guo-Wu, Cai Bing-Jie, Xu Ke-Min, Zhao Yu-Jie, Xie Xiao-Ting, Zhang Yu-Lin, Li Chao-Qing, Zhang Guo-Jun

机构信息

School of Laboratory Medicine, Hubei University of Chinese Medicine, 16 Huangjia Lake West Road, Wuhan, 430065, P. R. China.

Department of Clinical Laboratory, Institute of Translational Medicine, Renmin Hospital of Wuhan University, Wuhan, Hubei, 430060, PR China.

出版信息

J Nanobiotechnology. 2025 Feb 1;23(1):74. doi: 10.1186/s12951-025-03161-z.

Abstract

Plant-derived nanovesicles (PDVs) as nanodrug delivery carriers have gained recognition due to their satisfactory biosafety. However, there remains a challenge to target tumor sites accurately due to the uncertain membrane protein components on the surface of vesicles. Herein, a composite nanodrug delivery system by encapsulating the chemotherapy drug DOX is establish to efficiently target breast cancer. The novel nanoplatform (LEVBD) is formed by embedding the membrane fragments from breast cancer cell with the lemon-derived nanovesicles (LEVs) as the foundational skeleton. LEVBD reveal wonderful homologous tumor targeting due to fusion of cancer cell membrane components with LEVs, and the encapsulation of hybrid vesicles facilitates the transcellular transport of drugs. After intravenous injection, LEVBD could efficiently and selectively home to homologous tumor sites even under competition from heterologous tumors and significantly inhibit tumor growth without any observable toxic side effects. The doping of homologous cancer cell membranes provides a paradigm for the precise delivery of drug delivery vehicles using plant-derived vesicles as the backbone.

摘要

植物源纳米囊泡(PDVs)作为纳米药物递送载体,因其令人满意的生物安全性而受到认可。然而,由于囊泡表面膜蛋白成分不确定,准确靶向肿瘤部位仍然是一个挑战。在此,通过封装化疗药物阿霉素建立了一种复合纳米药物递送系统,以有效靶向乳腺癌。新型纳米平台(LEVBD)由以柠檬源纳米囊泡(LEVs)为基础骨架,嵌入乳腺癌细胞膜片段形成。由于癌细胞膜成分与LEVs融合,LEVBD显示出良好的同源肿瘤靶向性,并且杂合囊泡的封装促进了药物的跨细胞转运。静脉注射后,即使在异源肿瘤竞争的情况下,LEVBD也能有效且选择性地归巢到同源肿瘤部位,并显著抑制肿瘤生长,且无任何明显的毒副作用。同源癌细胞膜的掺杂为以植物源囊泡为骨架的药物递送载体的精确递送提供了一种范例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faf9/11786351/c1f7bdbb8057/12951_2025_3161_Sch1_HTML.jpg

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