Key result
An injectable thermosensitive hydrogel encapsulating tanshinone IIA-loaded ROS-sensitive microspheres effectively released the drug into infarcted myocardium, mitigating left ventricular remodeling.
Why the study?
Tanshinone IIA is a promising therapeutic agent for myocardial infarction, but efficient delivery remains a major issue limiting its clinical translation.
Does an injectable thermosensitive hydrogel delivering tanshinone IIA improve cardiac function and reduce remodeling in a preclinical model of myocardial infarction?
Does an injectable thermosensitive hydrogel delivering tanshinone IIA improve cardiac function and reduce remodeling in a preclinical model of myocardial infarction?
A novel ROS-sensitive, thermosensitive hydrogel delivery system for tanshinone IIA shows promise in preclinical models for preventing adverse remodeling and restoring cardiac function after myocardial infarction.
Myocardial damage resulting from acute myocardial infarction often leads to progressive heart failure and sudden death, highlighting the urgent clinical need for effective therapies. Recently, tanshinone IIA has been identified as a promising therapeutic agent for myocardial infarction. However, efficient delivery remains a major issue that limits clinical translation. To address this problem, an injectable thermosensitive poly (lactic acid‐co‐glycolic acid)‐block‐poly (ethylene glycol)‐block‐poly (lactic acid‐co‐glycolic acid) gel (PLGA‐PEG‐PLGA) system encapsulating tanshinone IIA‐loaded reactive oxygen species‐sensitive microspheres (Gel−MS/tanshinone IIA) has been designed and synthesized in this study. The thermosensitive hydrogel exhibits good mechanical properties after reaching body temperature. Microspheres initially immobilized by the gel exhibit excellent reactive oxygen species‐triggered release properties in a high‐reactive oxygen species environment after myocardial infarction onset. As a result, encapsulated tanshinone IIA is effectively released into the infarcted myocardium, where it exerts local anti‐pyroptotic and anti‐inflammatory effects. Importantly, the combined advantages of this technique contribute to the mitigation of left ventricular remodeling and the restoration of cardiac function following tanshinone IIA. Therefore, this novel, precision‐guided intra‐tissue therapeutic system allows for customized local release of tanshinone IIA, presenting a promising alternative treatment strategy aimed at inducing beneficial ventricular remodeling in the post‐infarct heart.
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Yu et al. (2022) studied Myocardial infarction. Gel−MS/tanshinone IIA (injectable thermosensitive PLGA-PEG-PLGA gel encapsulating tanshinone IIA-loaded ROS-sensitive microspheres) was evaluated on Mitigation of left ventricular remodeling and restoration of cardiac function. An injectable thermosensitive hydrogel encapsulating tanshinone IIA-loaded ROS-sensitive microspheres effectively released the drug into infarcted myocardium, mitigating left ventricular remodeling.
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