DOI: 10.3390/pharmaceutics18070812 ISSN: 1999-4923

Design and Characterization of GelMA Nanogels (nanoGelMA) via Desolvation and Photopolymerization for Drug Delivery Applications

Roberta Pappalardo, Rossella Laurano, Claudio Cassino, Stefano Bianchi, Valeria Chiono, Gianluca Ciardelli, Monica Boffito

Background/Objectives: Micro- and nano-scale hydrogels (microgels and nanogels) have attracted increasing attention as carriers for drug delivery due to their high-water content, responsiveness to external stimuli, tunable properties, and versatility. In this work, gelatin methacryloyl (GelMA) with a medium degree of methacryloylation (DoM ca. 60%) was ad hoc synthesized as a constituent material for nanogel production. For the first time in the literature, GelMA-based nanogels (nanoGelMA) were developed through an optimized two-step desolvation method combined with photo-crosslinking. Methods: The influence of key process parameters, including the pH, volume of desolvating agent, photo-initiator concentration, and UV exposure time, was systematically investigated to identify optimal conditions for nanoGelMA preparation. To assess its potential as a drug delivery nanocarrier, the nanoGelMA was loaded with ibuprofen (IBU) as a model anti-inflammatory drug via in situ encapsulation during nanogel preparation. Results: The formulated nanoGelMA exhibited an average hydrodynamic diameter (d) of ca. 250 nm, a polydispersity index of 0.2, and a production yield of approximately 30%. The nanogels demonstrated stability in water and in phosphate buffer at pH 5 over 96 h, while exhibiting significant swelling in physiological-like conditions and enzymatic degradation (d of ca. 421 ± 91 nm and 609 ± 182 nm at 96 h, respectively). The cytocompatibility evaluation demonstrated high cell viability (86–96%) of the nanoGelMA at different concentrations (1–5 mg/mL). IBU-loaded nanoGelMA particles were successfully developed via direct drug encapsulation during nanogel formation, achieving a maximum encapsulation efficiency of ca. 30%, and exhibited environment-responsive release, with kinetics modulated by the ionic strength, pH, and enzymatic activity. Conclusions: Overall, the nanoGelMA developed herein represents a promising nanogel platform with great potential for the development of advanced and controlled drug delivery therapies.

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