Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2015 Aug:34:225-31.
doi: 10.1016/j.copbio.2015.03.016. Epub 2015 Apr 11.

Developing injectable nanomaterials to repair the heart

Affiliations
Review

Developing injectable nanomaterials to repair the heart

Mary M Nguyen et al. Curr Opin Biotechnol. 2015 Aug.

Abstract

Injectable nanomaterials have been designed for the treatment of myocardial infarction, particularly during the acute stages of inflammation and injury. Among these strategies, injectable nanofibrous hydrogel networks or nanoparticle complexes may be delivered alone or with a therapeutic to improve heart function. Intramyocardial delivery of these materials localizes treatments to the site of injury. As an alternative, nanoparticles may be delivered intravenously, which provides the ultimate minimally invasive approach. These systems take advantage of the leaky vasculature after myocardial infarction, and may be designed to specifically target the injured region. The translational applicability of both intramyocardial and intravenous applications may provide safe and effective solutions upon optimizing the timing of the treatments and biodistribution.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Therapeutic delivery routes to the infarcted heart. Nanomaterials can be delivered to the heart through catheter-based intracoronary infusion, intramyocardial injection either via a transendocardial catheter or surgical-based direct injection, or through IV delivery and subsequent targeting to the site of infarction. Nanofibrous hydrogels or nanocomplexes have been delivered via intramyocardial injection, while nanoparticles have been delivered IV and have the potential for intracoronary infusion.

References

    1. Go AS, Mozaffarian D, Roger VL, Benjamin EJ, Berry JD, Borden WB, Bravata DM, Dai S, Ford ES, Fox CS, Franco S, et al. Heart disease and stroke statistics--2013 update: A report from the american heart association. Circulation. 2013;127:e6–e245. - PMC - PubMed
    1. Dobaczewski M, Gonzalez-Quesada C, Frangogiannis NG. The extracellular matrix as a modulator of the inflammatory and reparative response following myocardial infarction. Journal of Molecular and Cellular Cardiology. 2010;48(3):504–511. - PMC - PubMed
    1. Sutton MGS, Sharpe N. Left ventricular remodeling after myocardial infarction - pathophysiology and therapy. Circulation. 2000;101(25):2981–2988. - PubMed
    1. Vanhoutte D, Schellings M, Pinto Y, Heymans S. Relevance of matrix metalloproteinases and their inhibitors after myocardial infarction: A temporal and spatial window. Cardiovascular Research. 2006;69(3):604–613. - PubMed
    1. Nelson DM, Ma Z, Fujimoto KL, Hashizume R, Wagner WR. Intra-myocardial biomaterial injection therapy in the treatment of heart failure: Materials, outcomes and challenges. Acta Biomaterialia. 2011;7(1):1–15. - PMC - PubMed

Publication types

MeSH terms

Substances