Combined local delivery of tacrolimus and stem cells in hydrogel for enhancing peripheral nerve regeneration.
Tiam Mana SaffariKatelyn ChanSara SaffariKevin J ZuoRenee M McGovernJoel M ReidGregory H BorschelAlexander Y ShinPublished in: Biotechnology and bioengineering (2021)
The application of scaffold-based stem cell transplantation to enhance peripheral nerve regeneration has great potential. Recently, the neuroregenerative potential of tacrolimus (a U.S. Food and Drug Administration-approved immunosuppressant) has been explored. In this study, a fibrin gel-based drug delivery system for sustained and localized tacrolimus release was combined with rat adipose-derived mesenchymal stem cells (MSC) to investigate cell viability in vitro. Tacrolimus was encapsulated in poly(lactic-co-glycolic) acid (PLGA) microspheres and suspended in fibrin hydrogel, using concentrations of 0.01 and 100 ng/ml. Drug release over time was measured. MSCs were cultured in drug-released media collected at various days to mimic systemic exposure. MSCs were combined with (i) hydrogel only, (ii) empty PLGA microspheres in the hydrogel, (iii) 0.01, and (iv) 100 ng/ml of tacrolimus PLGA microspheres in the hydrogel. Stem cell presence and viability were evaluated. A sustained release of 100 ng/ml tacrolimus microspheres was observed for up to 35 days. Stem cell presence was confirmed and cell viability was observed up to 7 days, with no significant differences between groups. This study suggests that combined delivery of 100 ng/ml tacrolimus and MSCs in fibrin hydrogel does not result in cytotoxic effects and could be used to enhance peripheral nerve regeneration.
Keyphrases
- stem cells
- peripheral nerve
- drug delivery
- drug release
- wound healing
- stem cell transplantation
- hyaluronic acid
- tissue engineering
- mesenchymal stem cells
- molecularly imprinted
- cell therapy
- high dose
- low dose
- drug administration
- emergency department
- mass spectrometry
- insulin resistance
- metabolic syndrome
- umbilical cord
- oxidative stress
- drug induced
- human health