6533b854fe1ef96bd12aea10

RESEARCH PRODUCT

κ-Carrageenan and PVA blends as bioinks to 3D print scaffolds for cartilage reconstruction.

Emanuela MuscolinoAnna Barbara Di StefanoMarco TrapaniMaria Antonietta SabatinoDaniela GiacomazzaSabina AlessiEmanuele CammarataFrancesco MoschellaAdriana CordovaFrancesca ToiaClelia Dispenza

subject

CartilageTissue ScaffoldsTissue EngineeringStructural BiologyPrinting Three-DimensionalHydrogelsGeneral MedicineCarrageenanMolecular BiologyBiochemistryspheroids from human adipose stem cells 3D printing hydrogel bioinks

description

3D printing of polymeric scaffolds and autologous stem cells is a promising tool for damaged facial cartilage reconstruction surgeries. To this end, suitable bioinks are needed to generate scaffolds with the required morphological and functional features. We formulated hydrogel bioinks using k-Carrageen (kC) and poly(vinyl alcohol) (PVA) in three different weight ratios. The kC gives the systems the ability to undergo rapid sol-to-gel transitions upon cooling from 60 °C and above to body temperature, while the PVA is used as rheology modifier and porogen. The latter is crosslinked after molding or printing by freeze-thaw cycling for 1 day (FT1) or 5 days (FT5). To select the most suitable formulation for 3D printing, the sol-to-gel transition and the physico-chemical, mechanical and morphological properties of obtained hydrogels were studied. Moreover, the absence of cytotoxic effects of the material on SASCs was assessed in both stemness-preserving or chondro-inductive media. Printing trials were performed to identify optimal process parameters and co-printing and post-printing seeding approaches of SASCs were evaluated. Cells were found to be viable after co-printing and also after the FT1 treatment. Viable adherent cells were also found in the FT5 system, where cells were plated after freezing and thawing treatment.

10.1016/j.ijbiomac.2022.09.275https://pubmed.ncbi.nlm.nih.gov/36208815