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Nanoparticle-based therapeutic strategies for mitochondrial dysfunction in cardiovascular disease.

Isabella Suzuki, Huihua Xing, Joshua Giblin, Anisa Ashraf, E. J. ChungJanuary 12, 20246 citations
DOI10.1002/jbm.a.37668
Sourcehttps://dx.doi.org/10.1002/jbm.a.37668
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Abstract

Although cardiovascular diseases (CVD) are the leading cause of global mortality, there is a lack of therapies that target and revert underlying pathological processes. Mitochondrial dysfunction is involved in the pathophysiology of CVD, and thus is a potential target for therapeutic development. To target the mitochondria and improve therapeutic efficacy, nanoparticle-based delivery systems have been proposed as promising strategies for the delivery of therapeutic agents to the mitochondria. This review will first discuss how mitochondrial dysfunction is related to the progression of several CVD and then delineate recent progress in mitochondrial targeting using nanoparticle-based delivery systems including peptide-based nanosystems, polymeric nanoparticles, liposomes, and lipid nanoparticles. In addition, we summarize the advantages of these nanocarriers and remaining challenges in targeting the mitochondria as a therapeutic strategy for CVD treatment.