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生物材料介导的心肌缺血再灌注损伤靶向治疗。

Biomaterials-mediated targeted therapeutics of myocardial ischemia-reperfusion injury.

机构信息

Department of Cardiology, The Second Hospital of Jilin University, 4026 Yatai Street, Changchun 130041, PR China; Key Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022, PR China.

Respiratory and Critical Care Medicine, The Second Hospital of Jilin University, 4026 Yatai Street, Changchun 130041, PR China.

出版信息

Biomaterials. 2023 Dec;303:122368. doi: 10.1016/j.biomaterials.2023.122368. Epub 2023 Oct 30.

Abstract

Reperfusion therapy is widely used to treat acute myocardial infarction. However, its efficacy is limited by myocardial ischemia-reperfusion injury (MIRI), which occurs paradoxically due to the reperfusion therapy and contributes to the high mortality rate of acute myocardial infarction. Systemic administration of drugs, such as antioxidant and anti-inflammatory agents, to reduce MIRI is often ineffective due to the inadequate release at the pathological sites. Functional biomaterials are being developed to optimize the use of drugs by improving their targetability and bioavailability and reducing side effects, such as gastrointestinal irritation, thrombocytopenia, and liver damage. This review provides an overview of controlled drug delivery biomaterials for treating MIRI by triggering antioxidation, calcium ion overload inhibition, and/or inflammation regulation mechanisms and discusses the challenges and potential applications of these treatments clinically.

摘要

再灌注疗法被广泛用于治疗急性心肌梗死。然而,其疗效受到心肌缺血再灌注损伤(MIRI)的限制,这种损伤是由于再灌注治疗而产生的,导致急性心肌梗死的死亡率居高不下。为了减少 MIRI,全身给予药物(如抗氧化剂和抗炎剂)的方法往往效果不佳,因为这些药物在病理部位的释放不足。功能性生物材料的开发旨在通过提高药物的靶向性和生物利用度,以及减少胃肠道刺激、血小板减少和肝损伤等副作用,来优化药物的使用。本文综述了通过触发抗氧化、钙离子超载抑制和/或炎症调节机制来治疗 MIRI 的控释药物生物材料,并讨论了这些治疗方法在临床上的挑战和潜在应用。

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