6533b831fe1ef96bd129846a

RESEARCH PRODUCT

New biodegradable hydrogels based on a photocrosslinkable modified polyaspartamide: synthesis and characterization

Gaetano GiammonaSilvestre BuscemiGennara CavallaroFilippo SaianoGiovanna Pitarresi

subject

Glycidyl methacrylateMagnetic Resonance SpectroscopyDouble bondPolymersUltraviolet RaysBiophysicsBiochemistryEsterasechemistry.chemical_compoundDrug Delivery SystemsEnzymatic hydrolysisSpectrophotometrySpectroscopy Fourier Transform InfraredPolymer chemistrymedicineCopolymerMolecular Biologychemistry.chemical_classificationAcrylamidesAqueous solutionmedicine.diagnostic_testChemistryWaterHydrogelsHydrogen-Ion ConcentrationBiodegradation EnvironmentalSelf-healing hydrogelsEpoxy CompoundsMethacrylatesPeptides

description

Abstract α,β-Poly( N -2-hydroxyethyl)- dl -aspartamide (PHEA), a synthetic water-soluble biocompatible polymer, was derivatized with glycidyl methacrylate (GMA), in order to introduce in its structure chemical residues having double bonds and ester groups. The obtained copolymer (PHG) contained 29 mol% of GMA residues. PHG aqueous solutions at various concentrations ranging from 30 to 70 mg/ml were exposed to a source of UV rays at λ 254 nm in the presence or in the absence of N , N ′-methylenebisacrylamide (BIS); the formation of compact gel phases was observed beginning from 50 mg/ml. The obtained networks were characterized by FT-IR spectrophotometry and swelling measurements which evidenced the high affinity of PHG hydrogels towards aqueous media at different pH values. In vitro chemical or enzymatic hydrolysis studies suggested that the prepared samples undergo a partial degradation both at pH 1 and pH 10 and after incubation with enzymes such as esterase, pepsin and α-chymotrypsin. Finally, the effect of irradiation time on the yield and the properties of these hydrogels was investigated and the sol fractions coming from irradiated samples, properly purified, were characterized by FT-IR and 1 H-NMR analyses.

https://doi.org/10.1016/s0304-4165(99)00051-3