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Thermoresponsive Alginate-Graft-pNIPAM/Methyl Cellulose 3D-Printed Scaffolds Promote Osteogenesis In Vitro.

Aikaterini GialouriSofia Falia SaravanouKonstantinos LoukelisMaria ChatzinikolaidouGeorge PasparakisNicolaos Bouropoulos
Published in: Gels (Basel, Switzerland) (2023)
In this work, a sodium alginate-based copolymer grafted by thermoresponsive poly( N -isopropylacrylamide) (PNIPAM) chains was used as gelator (Alg-g-PNIPAM) in combination with methylcellulose (MC). It was found that the mechanical properties of the resulting gel could be enhanced by the addition of MC and calcium ions (Ca 2+ ). The proposed network is formed via a dual crosslinking mechanism including ionic interactions among Ca 2+ and carboxyl groups and secondary hydrophobic associations of PNIPAM chains. MC was found to further reinforce the dynamic moduli of the resulting gels (i.e., a storage modulus of ca. 1500 Pa at physiological body and post-printing temperature), rendering them suitable for 3D printing in biomedical applications. The polymer networks were stable and retained their printed fidelity with minimum erosion as low as 6% for up to seven days. Furthermore, adhered pre-osteoblastic cells on Alg-g-PNIPAM/MC printed scaffolds presented 80% viability compared to tissue culture polystyrene control, and more importantly, they promoted the osteogenic potential, as indicated by the increased alkaline phosphatase activity, calcium, and collagen production relative to the Alg-g-PNIPAM control scaffolds. Specifically, ALP activity and collagen secreted by cells were significantly enhanced in Alg-g-PNIPAM/MC scaffolds compared to the Alg-g-PNIPAM counterparts, demonstrating their potential in bone tissue engineering.
Keyphrases
  • tissue engineering
  • induced apoptosis
  • cell cycle arrest
  • ionic liquid
  • mesenchymal stem cells
  • oxidative stress
  • human health
  • signaling pathway
  • drug delivery
  • quantum dots
  • vascular smooth muscle cells
  • network analysis