In recent years, cardiac patches have been developed for the treatment of myocardial infarction. However, the fixation approaches onto the tissue through suture or phototriggered reaction inevitably cause new tissue damage. Herein, a paintable hydrogel is constructed based on Fe -triggered simultaneous polymerization of covalently linked pyrrole and dopamine in the hyperbranched chains where the in situ formed conductive polypyrrole also uniquely serves to crosslink network. This conductive and adhesive hydrogel can be conveniently painted as a patch onto the heart surface without adverse liquid leakage. The functional patch whose conductivity is equivalent to that of normal myocardium is strongly bonded to the beating heart within 4 weeks, accordingly efficiently boosting the transmission of electrophysiological signals. Eventually, the reconstruction of cardiac function and revascularization of the infarct myocardium are remarkably improved. The translatable suture-free strategy reported in this work is promising to address the human clinical challenges in cardiac tissue engineering.
Over
the past decade, tissue-engineering strategies, mainly involving injectable
hydrogels and epicardial biomaterial patches, have been pursued to
treat myocardial infarction. However, only limited therapeutic efficacy
is achieved with a single means. Here, a combined therapy approach
is proposed, that is, the coadministration of a conductive hydrogel
patch and injectable hydrogel to the infarcted myocardium. The self-adhesive
conductive hydrogel patch is fabricated based on Fe3+-induced
ionic coordination between dopamine–gelatin (GelDA) conjugates
and dopamine-functionalized polypyrrole (DA–PPy), which form
a homogeneous network. The injectable and cleavable hydrogel is formed
in situ via a Schiff base reaction between oxidized sodium hyaluronic
acid (HA-CHO) and hydrazided hyaluronic acid (HHA). Compared with
a single-mode system, injecting the HA-CHO/HHA hydrogel intramyocardially
followed by painting a conductive GelDA/DA–PPy hydrogel patch
on the heart surface results in a more pronounced improvement of the
cardiac function in terms of echocardiographical, histological, and
angiogenic outcomes.
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