Light induced fluidization of azopolysiloxane: exposure to 488 nm light generates instantaneous mass transfer as a result of trans – cis isomerization in azophenol polymers. Viscoelastic mapping confirms the changes of rheological properties upon exposure to the light.

The formation of double cross-linked (ionic and covalent) gelatin (G) and chitosan (CS) hydrogels was studied. The covalent cross-linking consists in the reaction between the carbonyl groups of glutaraldehyde with the free amine groups from the two polymers; the ionic cross-linking is based on sulfate anions interaction with protonated amine groups of the polymers solubilized in acetic acid. The structural and morphological characterization of the obtained hydrogels was performed using FT-IR and scanning electron microscopy (SEM). The influence of different parameters on the cross-linking density (indirectly assessed by water swelling capacity) and the ability to include hydrosoluble active principles such as the ratio between polymers (G/CS), the amount of ionic cross-linker, and the cross-linking time were investigated. The morphological and structural characteristics, mechanical stability, elasticity of the network, the interaction with aqueous weak alkaline solutions, and the capacity to load and release a model drug were analyzed for the obtained hydrogels. Rheological tests were performed to study the mechanical stability of the hydrogels and the results show, generally, elastic and stable networks.