Dynamic shear oscillation measurements at small strain were used to charact
erize the viscoelastic properties and related differences in the molecular
structure of hydrogels based on gelatin methacrylamide. Gelatin was derivat
ized with methacrylamide side groups and was subsequently cross-linked by r
adical polymerization via photoinitiation. The light treatment of methacryl
amide gelatin solutions resulted in the production of hydrogel films with h
igh storage modulus (G'). Mechanical spectra and thermal scanning rheology
of the obtained hydrogels are described. The temperature scan of the networ
k below and above melting point of gelatin allowed us to identify the respe
ctive contributions of chemical and physical cross-linkage to the hydrogel
elastic modulus. The results indicate that the rheological properties of th
e gelatin-based hydrogels can be controlled by the degree of substitution,
polymer concentration, initiator concentration, and UV irradiation conditio
ns.