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用于深度缺血穿透和抑制铁死亡以进行缺血性中风神经保护治疗的仿生纳米马达

Biomimetic Nanomotors for Deep Ischemia Penetration and Ferroptosis Inhibition in Neuroprotective Therapy of Ischemic Stroke.

作者信息

Wang Rui, Nie Weimin, Yan Xin, Luo Kuankuan, Zhang Qi, Wang Tao, Lu Enhao, Chen Yiting, Luo Yu, Zhang Zhiwen, Wang He, Zhao Jing, Sha Xianyi

机构信息

Department of Pharmaceutics, School of Pharmacy, Fudan University, Key Laboratory of Smart Drug Delivery (Ministry of Education), Shanghai, 201203, China.

Key Laboratory of Computational Neuroscience and Brain-Inspired Intelligence (Ministry of Education), Institute of Science and Technology for Brain-Inspired Intelligence, Fudan University, Shanghai, 200 433, China.

出版信息

Adv Mater. 2025 Jan;37(3):e2409176. doi: 10.1002/adma.202409176. Epub 2024 Nov 26.

Abstract

Nerve injury represents the primary reason of mortality and disability in ischemic stroke, but effective drug delivery to the region of cerebral ischemia and hypoxia poses a significant challenge in neuroprotective treatment. To address these clinical challenges, a biomimetic nanomotor, Pt@LF is designed, to facilitate deep delivery of neuroprotective agents and inhibit ferroptosis in ischemic stroke. Pt@LF traverses the blood-brain barrier (BBB) and penetrates into deep cerebral ischemic-hypoxic areas due to the active targeting capacity of apo-lactoferrin (Apo-LF) and the self-propelling motion properties of nanomotors. Subsequently, Pt@LF loosens thrombus and alleviates the "no reflow" phenomenon via mechanical thrombolysis. Thanks to the various enzyme-like abilities and multi-target ferroptosis inhibition capability, Pt@LF ameliorates the inflammatory microenvironment and rescues dying neurons. In conclusion, Pt@LF demonstrates efficiently deep penetration and neuroprotective effects in vitro and vivo. And this study provides a promising therapeutic platform for the treatment of ischemic stroke.

摘要

神经损伤是缺血性卒中致死和致残的主要原因,但在神经保护治疗中,向脑缺血缺氧区域有效递送药物面临重大挑战。为应对这些临床挑战,设计了一种仿生纳米马达Pt@LF,以促进神经保护剂的深度递送并抑制缺血性卒中中的铁死亡。由于脱铁乳铁蛋白(Apo-LF)的主动靶向能力和纳米马达的自推进运动特性,Pt@LF能够穿越血脑屏障(BBB)并渗透到脑深部缺血缺氧区域。随后,Pt@LF通过机械溶栓作用松解血栓并减轻“无复流”现象。得益于多种类酶能力和多靶点铁死亡抑制能力,Pt@LF改善了炎症微环境并挽救濒死神经元。总之,Pt@LF在体外和体内均表现出高效的深度渗透和神经保护作用。本研究为缺血性卒中的治疗提供了一个有前景的治疗平台。

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