6533b834fe1ef96bd129ce07

RESEARCH PRODUCT

Development of injectable and durable kefiran hydro-alcoholic gels.

SabatinoMaria AntoniettaPaviaFrancesco CarfiRigogliusoSalvatriceGiacomazzaDanielaGhersiGiulioLa CarrubbaVincenzoDispenzaClelia

subject

GelationXYLOGLUCANCell Survival02 engineering and technologyBiochemistryPolyvinyl alcoholSCAFFOLDSCULTURE03 medical and health scienceschemistry.chemical_compoundViscosityDrug Delivery SystemsRheologyStructural BiologyPolysaccharidesmedicineHumansKefiran gelsMolecular BiologyKINETICS030304 developmental biologyCell Proliferationchemistry.chemical_classification0303 health sciencesIn-situ forming gelsIn-situ forming gelKefiranHydrogelsGeneral MedicineBuffer solutionPolymer021001 nanoscience & nanotechnologyPropylene GlycolChemical engineeringchemistryAlcoholsDrug deliverySettore CHIM/07 - Fondamenti Chimici Delle TecnologieSwellingmedicine.symptom0210 nano-technologyRheology

description

Injectable, in-situ forming kefiran gels have been developed for potential applications as implantable drug delivery devices or scaffolds for tissue regeneration. Concentrated solutions (4, 5 and 6%w) of kefiran, extracted from kefir grains, have been assessed in term of viscosity and injectability through G26 syringe needles, and for their ability to undergo gelation upon mixing with different alcohols. Propylene glycol (PG) has been selected as gelling agent because it ensures homogenous gelation in relatively short times (from few minutes up to 6 h). The investigation of the rheological behavior of kefiran/PG gels varying polymer concentration and temperature (25 degrees C and 37 degrees C) has provided interesting hints to support a possible gelation mechanism that accounts also for the observed influence of the alcohol type. Finally, the study of kefiran/PG gels has been complemented with the investigation on selected formulations of the swelling/degradation behavior upon immersion in isotonic buffer solution for up to 40 days at 37 et; of the ability of the gels to retain and/or release two model molecules; and within vitro cell viability and cytotoxicity tests, to support the absence of toxic effects on cells induced by direct contact with the gels or by leached components from these gels. (C) 2020 Elsevier B.V. All rights reserved.

10.1016/j.ijbiomac.2020.01.244https://pubmed.ncbi.nlm.nih.gov/31987942