缺血
再灌注损伤
医学
氢
心肌缺血
药理学
心脏病学
化学
有机化学
作者
Chaoqun Nie,A Rong,Jing Wang,Shuang Pan,Rentong Zou,Bin Wang,Shuiqing Xi,Xiaojian Hong,Meifang Zhou,Haoyu Wang,Mengshu Yu,Lina Wu,Xilin Sun,Wei Yang
标识
DOI:10.1002/advs.202304178
摘要
Abstract Hydrogen gas is recently proven to have anti‐oxidative and anti‐inflammation effects on ischemia‐reperfusion injury. However, the efficacy of hydrogen therapy is limited by the efficiency of hydrogen storage, targeted delivery, and controlled release. In this study, H 2 ‐PFOB nanoemulsions (NEs) is developed with high hydrogen loading capacity for targeted ischemic myocardium precision therapy. The hydrogen‐carrying capacity of H 2 ‐PFOB NEs is determined by gas chromatography and microelectrode methods. Positive uptake of H 2 ‐PFOB NEs in ischemia‐reperfusion myocardium and the influence of hydrogen on 19 F‐MR signal are quantitatively visualized using a 9.4T MR imaging system. The biological therapeutic effects of H 2 ‐PFOB NEs are examined on a myocardial ischemia‐reperfusion injury mouse model. The results illustrated that the developed H 2 ‐PFOB NEs can efficaciously achieve specific infiltration into ischemic myocardium and exhibit excellent antioxidant and anti‐inflammatory properties on myocardial ischemia‐reperfusion injury, which can be dynamically visualized by 19 F‐MR imaging system. Moreover, hydrogen burst release induced by low‐intensity focused ultrasound (LIFU) irradiation further promotes the therapeutic effect of H 2 ‐PFOB NEs with a favorable biosafety profile. In this study, the potential therapeutic effects of H 2 ‐PFOB NEs is fully unfolded, which may hold great potential for future hydrogen‐based precision therapeutic applications tailored to ischemia‐reperfusion injury.
科研通智能强力驱动
Strongly Powered by AbleSci AI