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Updated: May 3, 2026

An Injectable and Drug-loaded Supramolecular Hydrogel for Local Catheter Injection into the Pig Heart
Published on: June 7, 2015
Bioactive peptide based supramolecular hydrogel as an efficient drug/cell delivery platform for ophthalmic
Lulu Du1, Yiping Wu1, Qipeng Liu1
1National Engineering Research Center of Ophthalmology and Optometry, Eye Hospital, Wenzhou Medical University, Wenzhou 325027, China.
None:
In this work, we reported the generation of a bioactive peptide based supramolecular hydrogel as platform for efficient cell and drug delivery for ophthalmic application. The supramolecular hydrogelator was composed of a self-assembly motif (i.e., NapFF) and a biofunctional moiety (i.e., RGD) using glycine (G) as a linker. Self-assembly behavior of amphiphiles could be finely tuned by the number of glycine, and the optimized NapFFGGRGD amphiphile could self-assemble into supramolecular hydrogel in aqueous solution after a heating-cooling procedure. The formed hydrogel was thoroughly characterized by transmissionelectronmicroscopy (TEM), scanning electron microscopy (SEM) and a rheometer. The proposed NapFFGGRGD hydrogel exhibits great in vitro stability upon incubation in cell culture medium for 7 days and supports human corneal epithelial cells (HCECs) proliferation in both 2D and 3D culture models. Both hydrophobic and hydrophilic drugs (i.e., curcumin, vancomycin hydrochloride) could be readily encapsulated into the NapFFGGRGD hydrogel without compromising their pharmacological activities. Using a rat model of bacterial keratitis (BK), we evidently demonstrated that vancomycin loaded NapFFGGRGD hydrogel (Van/NapFFGGRGD) effectively cured BK by the elimination of invaded bacteria and the promotion of corneal re-epithelization. As a result, the developed NapFFGGRGD supramolecular hydrogel might be a promising platform for efficient ophthalmic cell/drug delivery.
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