Stimuli-responsive drug delivery systems are gaining
importance
in personalized medicine to deliver therapeutic doses in response
to disease-specific stimulation. Pancreas-mimicking glucose-responsive
insulin delivery systems offer improved therapeutic outcomes in the
treatment of type 1 and advanced stage of type 2 diabetic conditions.
Herein, we present a glucose-responsive smart hydrogel platform based
on phenylboronic acid-functionalized natural silk fibroin protein
for regulated insulin delivery. The modified protein was synergistically
self-assembled and cross-linked through β-sheet and phenylboronate
ester formation. The dynamic nature of the bonding confers smooth
injectability through the needle. The cross-linked hydrogel structures
firmly hold the glucose-sensing element and insulin in its pores and
contribute to long-term sensing and drug storage. Under hyperglycemic
conditions, the hydrogen peroxide generated from the sensing element
induces hydrogel matrix degradation by oxidative cleavage, enabling
insulin release. In vivo studies in a type 1 diabetic
Wistar rat model revealed that the controlled insulin release from
the hydrogel restored diabetic glucose level to physiological conditions
for 36 h. This work establishes the functional modification of silk
fibroin into a glucose-responsive hydrogel platform for regulated
and functional insulin delivery application