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工程化 P2Y 过表达细胞膜包裹纳米粒子逆转替格瑞洛和氯吡格雷的功能。

Engineered P2Y-Overexpressing Cell-Membrane-Wrapped Nanoparticles for the Functional Reversal of Ticagrelor and Clopidogrel.

机构信息

College of Pharmacy, Beihua University, Jilin 132013, PR China.

School of Nanoscience and Engineering, School of Chemical Sciences, University of Chinese Academy of Sciences, Beijing 101408, PR China.

出版信息

Nano Lett. 2024 Aug 28;24(34):10482-10489. doi: 10.1021/acs.nanolett.4c02207. Epub 2024 Aug 14.

Abstract

Antiplatelet agents, particularly P2Y receptor inhibitors, are critical medicines in the prevention and treatment of thrombotic diseases in the clinic. However, their long-term use introduces a significant risk of bleeding in patients with cardiovascular diseases. Whether the bleeding is caused by the drug itself or due to surgical procedures or trauma, the need to rapidly reverse the effects of antiplatelet agents in the circulation is essential; however, no such agents are currently available. To address this need, here we describe a strategy that uses cell-membrane-wrapped nanoparticles (CM-NPs) for the rapid reversal of P2Y inhibitors. CM-NPs are fabricated with membranes derived from 293T cells genetically engineered to overexpress the P2Y receptor. Our findings support the potential of CM-NPs as a strategy for managing bleeding complications associated with P2Y receptor inhibitors, offering an approach to improve the safety in the use of these drugs in clinical settings.

摘要

抗血小板药物,特别是 P2Y 受体抑制剂,是临床预防和治疗血栓性疾病的关键药物。然而,它们的长期使用会使心血管疾病患者出血的风险显著增加。无论出血是由药物本身引起,还是由于手术或外伤引起,都需要迅速逆转抗血小板药物在循环中的作用;然而,目前尚无此类药物。为了解决这一需求,我们在这里描述了一种使用细胞膜包裹的纳米颗粒(CM-NPs)快速逆转 P2Y 抑制剂的策略。CM-NPs 是用来源于 293T 细胞的膜制成的,该细胞经过基因工程改造以过表达 P2Y 受体。我们的研究结果支持 CM-NPs 作为管理与 P2Y 受体抑制剂相关的出血并发症的策略的潜力,为改善这些药物在临床环境中的使用安全性提供了一种方法。

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