Development and characterization of photo-responsive cinnamoly modified alginate

A photo-crosslinkable hydrogel derived from cinnamoyl modified alginate (Alg-CN) was prepared via hydrazide intermediate and employed as an efficient drug carrier using the painkiller drug paracetamol. Methyl ester of the alginic acid was first prepared and converted into the corresponding hydrazide intermediate (Alg-Hyd) and then the cinnamoyl units were incorporated using cinnamoyl chloride. The synthesized derivatives were characterized by spectral and instrumental methods to confirm their suggested chemical structures. The obtained Alg-CN derivatives displayed initiator-free crosslinking capabilities upon the UV exposure for adequate periods of time, which was demonstrated due to the formation of cyclobutane bridges connecting the alginate polysaccharide chains through the [2 pi+2 pi] cycloaddition reaction carried out by the -CH=CH- units of the inserted cinnamoyl moieties. The cross-linking of the Alg-CN was monitored by observing the lowering of the UV spectral band related to the cinnamoyl units and then the gelation efficiency along with the swelling degree was investigated over the UV light exposure time. Moreover, the developed hydrogel derivatives present considerable potentials as drug carriers that enable the control of the drug release by varying the degree of hydrogel crosslinking either by cinnamoyl functionalization or UV light exposure time.

Automated summary

The photo-crosslinkable hydrogel derived from cinnamoyl modified alginate shows potential as an efficient drug carrier with the ability to control drug release. The gel can be crosslinked without the need for initiators through UV exposure, and the extent of crosslinking can be adjusted through cinnamoyl functionalization or UV light exposure time.