Human mesenchymal stem cells (hMSCs),
which have the ability to
differentiate into osteoblasts, show promise for bone tissue engineering
and bone defect treatment. While there are a number of approaches
currently available to accomplish this, e.g., utilizing biodegradable
materials loaded with the synthetic glucocorticoid osteogenic inducer
dexamethasone (DEX), there are still many disadvantages with the current
technologies. Here, we generated light-responsive microgels that we
showed are capable of loading and releasing DEX in a light-triggered
fashion, with the released DEX being able to induce hMSC differentiation
into osteoblasts. Specifically, light-responsive poly(N-isopropylacrylamide-co-nitrobenzyl methacrylate)
(pNIPAm-co-NBMA) microgels were synthesized via free
radical precipitation polymerization and their size, morphology, and
chemical composition were characterized. We then went on to show that
the microgels could be loaded with DEX (via what we think are hydrophobic
interactions) and released upon exposure to UV light. We went on to
show that the DEX released from the microgels was still capable of
inducing osteogenic differentiation of hMSCs using an alamarBlue assay
and normalized alkaline phosphatase (ALP) activity assay. We also
investigated how hMSC differentiation was impacted by intermittent
DEX released from UV-exposed microgels. Finally, we confirmed that
the microgels themselves were not cytotoxic to hMSCs. Taken together,
the DEX-loaded light-responsive microgels reported here may find a
use for niche clinical applications, e.g., bone tissue repair.