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用于活性氧激活的动脉粥样硬化诊疗的仿生铈辅助超碳点组装

Biomimetic Cerium-Assisted Supra-Carbon Dots Assembly for Reactive Oxygen Species-Activated Atherosclerosis Theranostic.

作者信息

Chen Qiao, Yang Xu, Yu Yao, Duan Xinmei, Ni Rongrong, Song Guojing, Zhu Li, Zhong Yuan, Qu Kai, Qin Xian, Zhang Kun, Luo Yang, Wu Wei

机构信息

Key Laboratory for Biorheological Science and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, Bioengineering College of Chongqing University, Chongqing University Three Gorges Hospital, Chongqing, 400044, China.

Thyroid Breast Surgery Department, Dazhou Central Hospital, Dazhou, 635000, China.

出版信息

Small. 2025 Feb;21(8):e2408980. doi: 10.1002/smll.202408980. Epub 2025 Jan 7.

Abstract

Theranostic applications in atherosclerosis plaque microenvironment-triggered nanoplatforms are significantly compromised by the complex synthesis procedure, non-specific distribution, and limited therapeutic function. Therefore, development of a facile and feasible method to construct a pathology-based stimuli-responsive nanoplatform with satisfactory theranostic performance remains a demanding and highly anticipated goal. Herein, a novel class of multifunctional supra-carbon dots (CDs), denoted as MM@Ce-CDs NPs, by a simple nanoassembly and a subsequent coating with macrophage membrane (MM), is developed for the targeted reactive oxygen species-trigged theranostic and positive regulation of the pathological plaque microenvironment in AS. The harvested MM@Ce-CDs NPs exhibit activatable fluorescence properties, photoacoustic characteristics, and cascade enzyme performances, which can be effectively activated under ROS stimulation in the plaque pathological microenvironment, enabling precise control over theranostic functions, while markedly enhancing diagnostic accuracy and therapeutic efficacy for AS management. Besides, MM@Ce-CDs NPs can effectively manipulate the plaque microenvironment by reducing ROS levels and inflammation, alleviating M1 macrophage infiltration, and inhibiting foam cell formation, all together suppressing the pathological plaque development through the synergistic mechanisms. In addition, MM@Ce-CDs NPs inherit the biomimetic biological functions from MM, facilitating a highly specific target delivery to AS.

摘要

在动脉粥样硬化斑块微环境触发的纳米平台中的诊疗应用,因合成过程复杂、非特异性分布和治疗功能有限而受到显著影响。因此,开发一种简便可行的方法来构建具有令人满意的诊疗性能的基于病理学的刺激响应纳米平台,仍然是一个迫切且备受期待的目标。在此,通过简单的纳米组装以及随后用巨噬细胞膜(MM)包覆,开发了一类新型的多功能超碳点(CDs),记为MM@Ce-CDs NPs,用于靶向活性氧触发的诊疗以及对动脉粥样硬化中病理斑块微环境的正向调节。所制备的MM@Ce-CDs NPs具有可激活的荧光特性、光声特性和级联酶性能,在斑块病理微环境中的活性氧刺激下可被有效激活,从而实现对诊疗功能的精确控制,同时显著提高动脉粥样硬化管理的诊断准确性和治疗效果。此外,MM@Ce-CDs NPs可通过降低活性氧水平和炎症、减轻M1巨噬细胞浸润以及抑制泡沫细胞形成来有效调控斑块微环境,共同通过协同机制抑制病理斑块发展。此外,MM@Ce-CDs NPs继承了MM的仿生生物学功能,有助于高度特异性地靶向递送至动脉粥样硬化部位。

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