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仿生自适应微药物增强恶性脑胶质瘤的化疗:超越纳米药物。

Bioinspired Adaptive Microdrugs Enhance the Chemotherapy of Malignant Glioma: Beyond Their Nanodrugs.

机构信息

Cancer Research Institute, Experimental Education/Administration Center, School of Basic Medical Sciences, Southern Medical University, Guangzhou, 510515, P. R. China.

South China Advanced Institute for Soft Matter Science and Technology, School of Emergent Soft Matter, South China University of Technology, Guangzhou, 510515, P. R. China.

出版信息

Adv Mater. 2024 Aug;36(32):e2405165. doi: 10.1002/adma.202405165. Epub 2024 Jun 16.

Abstract

Solid nanoparticle-mediated drug delivery systems are usually confined to nanoscale due to the enhanced permeability and retention effect. However, they remain a great challenge for malignant glioma chemotherapy because of poor drug delivery efficiency and insufficient tumor penetration resulting from the blood-brain barrier/blood-brain tumor barrier (BBB/BBTB). Inspired by biological microparticles (e.g., cells) with excellent adaptive deformation, it is demonstrated that the adaptive microdrugs (even up to 3.0 µm in size) are more efficient than their nanodrugs (less than 200 nm in size) to cross BBB/BBTB and penetrate into tumor tissues, achieving highly efficient chemotherapy of malignant glioma. The distinct delivery of the adaptive microdrugs is mainly attributed to the enhanced interfacial binding and endocytosis via adaptive deformation. As expected, the obtained adaptive microdrugs exhibit enhanced accumulation, deep penetration, and cellular internalization into tumor tissues in comparison with nanodrugs, significantly improving the survival rate of glioblastoma mice. It is believed that the bioinspired adaptive microdrugs enable them to efficiently cross physiological barriers and deeply penetrate tumor tissues for drug delivery, providing an avenue for the treatment of solid tumors.

摘要

固体纳米颗粒介导的药物传递系统通常由于增强的通透性和保留效应而局限于纳米级。然而,由于血脑屏障/血脑肿瘤屏障(BBB/BBTB)导致的药物传递效率差和肿瘤穿透不足,它们仍然是恶性脑胶质瘤化疗的巨大挑战。受具有优异适应性变形的生物微粒(例如细胞)的启发,已经证明适应性微药物(甚至达到 3.0 µm 大小)比其纳米药物(小于 200nm 大小)更有效地穿过 BBB/BBTB 并渗透到肿瘤组织中,从而实现恶性脑胶质瘤的高效化疗。适应性微药物的独特传递主要归因于通过适应性变形增强的界面结合和内吞作用。不出所料,与纳米药物相比,所获得的适应性微药物在肿瘤组织中的积累、深层渗透和细胞内化得到增强,显著提高了脑胶质母细胞瘤小鼠的存活率。人们相信,受生物启发的适应性微药物能够有效地穿过生理屏障并深入渗透肿瘤组织进行药物传递,为治疗实体瘤提供了一种途径。

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