4.7 Article

Synthesis and Evaluation of AlgNa-g-Poly(QCL-co-HEMA) Hydrogels as Platform for Chondrocyte Proliferation and Controlled Release of Betamethasone

Journal

Publisher

MDPI
DOI: 10.3390/ijms22115730

Keywords

hydrogels; sodium alginate; betamethasone; drug delivery; cartilage tissue engineering

Funding

  1. EuropeanUnion through Erasmus PLUS doctoral fellowship [2015-1-NL01-KA 107-008639]
  2. European Commission H2020MSCA-RISE [644373-PRISAR]
  3. European Commission H2020-MSCA-RISE [777682-CANCER]
  4. European Commission H2020-WIDESPREAD-05-2017Twinning [807281-ACORN]
  5. European Commission H2020-WIDESPREAD-2018-03 [852985-SIMICA]
  6. European Commission H2020-SCARISE-2016 [734684-CHARMED]
  7. European Commission MSCA-ITN-2015-ETN [675743-ISPIC]
  8. PAVE [861190]
  9. CAST [857894]
  10. NOVA-MRI [859908]
  11. PRISAR2 [872860]
  12. VIDI personal grant [723.012.110]
  13. Agencia Nacional de Investigacion y Desarrollo (ANID, Chile) through projects FONDECYT REGULAR [1210107]

Ask authors/readers for more resources

Hydrogels obtained from combining different polymers are evaluated for their applicability in controlled release system platforms and tissue engineering scaffolds in this study. Characterization of the hydrogels was done through Fourier transform-infrared spectroscopy, scanning electron microscopy, and analysis of swelling degree. The results show that these hydrogels are promising materials for pharmaceutical and biomedical applications due to their biocompatibility and controlled release behavior.
Hydrogels obtained from combining different polymers are an interesting strategy for developing controlled release system platforms and tissue engineering scaffolds. In this study, the applicability of sodium alginate-g-(QCL-co-HEMA) hydrogels for these biomedical applications was evaluated. Hydrogels were synthesized by free-radical polymerization using a different concentration of the components. The hydrogels were characterized by Fourier transform-infrared spectroscopy, scanning electron microscopy, and a swelling degree. Betamethasone release as well as the in vitro cytocompatibility with chondrocytes and fibroblast cells were also evaluated. Scanning electron microscopy confirmed the porous surface morphology of the hydrogels in all cases. The swelling percent was determined at a different pH and was observed to be pH-sensitive. The controlled release behavior of betamethasone from the matrices was investigated in PBS media (pH = 7.4) and the drug was released in a controlled manner for up to 8 h. Human chondrocytes and fibroblasts were cultured on the hydrogels. The MTS assay showed that almost all hydrogels are cytocompatibles and an increase of proliferation in both cell types after one week of incubation was observed by the Live/Dead(R) assay. These results demonstrate that these hydrogels are attractive materials for pharmaceutical and biomedical applications due to their characteristics, their release kinetics, and biocompatibility.

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