posted on 2022-08-29, 23:44authored byHaiting Chen, Lu Fan, Ningxin Peng, Yong Yin, Dan Mu, Jun Wang, Ran Meng, Jun Xie
Uncontrolled and excessive fibrosis after myocardial
infarction
(MI) in the peri-infarct zone leads to left ventricular remodeling
and deterioration of cardiac function. Inhibiting fibroblast activation
during the mature phase of cardiac repair improves cardiac remodeling
and function after MI. Here, we engineered a biocompatible microneedle
(MN) patch using gelatin methacryloyl and loaded it with galunisertib,
a transforming growth factor-beta (TGF-β)-specific inhibitor,
to treat excessive cardiac fibrosis after MI. The MN patch could sustainably
release galunisertib for more than 2 weeks and provide mechanical
support for the fragile ventricular wall. After being applied to a
rat model of MI, the galunisertib-loaded MN patch improved long-term
cardiac function and reduced cardiac fibrosis by effectively inhibiting
TGF-β depending on fibroblast activation. This strategy shows
the potential of the MN patch as an advanced platform to locally deliver
direct antifibrotic drugs to prevent myocardial fibrosis for the treatment
of MI and the promotion of cardiac repair.