A light responsive single amino acid-based supramolecular hydrogel for photo-controlled vitamin release

Abstract

Light responsive low-molecular-weight hydrogelators (LMWHs) offer a promising platform for controlled delivery applications via light triggered structural changes in the hydrogel network. In this study, we report the facile synthesis of a tyrosine-derived LMWH, FmocY-Azo, incorporating a photoresponsive azobenzene moiety. Self-assembly of FmocY-Azo under ambient conditions provides the supramolecular hydrogel material that displays thixotropic behavior, as well as thermal and light responsiveness. The hydrogel material effectively encapsulates vitamin B12 within its fibrous network and enables its controlled release upon light irradiation, driven by structural changes in the FmocY-Azo framework. The release kinetics follows the Korsmeyer–Peppas model in the presence of light irradiation, whereas it follows zero-order kinetics in the dark, indicating a combined effect of diffusion and light-induced network disassembly. This work presents a single amino acid-based light responsive fibrous hydrogel with potential for developing light-triggered drug delivery systems.

Graphical abstract: A light responsive single amino acid-based supramolecular hydrogel for photo-controlled vitamin release

Supplementary files

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Article information

Article type
Communication
Submitted
09 Jul 2025
Accepted
06 Nov 2025
First published
07 Nov 2025
This article is Open Access
Creative Commons BY-NC license

Mater. Adv., 2026, Advance Article

A light responsive single amino acid-based supramolecular hydrogel for photo-controlled vitamin release

D. Chauhan and C. Maity, Mater. Adv., 2026, Advance Article , DOI: 10.1039/D5MA00736D

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