top of page

Presentation: 2025 ND EPSCoR Annual conference 

October 21, 2025, NDSU Memorial Union, Fargo, North Dakota

Synthesis and Characterization of Gelatin Methacrylate Hydrogel Microparticles for Biomedical Applications

Kiana

Mahmoudian

Master's Student

North Dakota State University

Co-author: Selvakumar Prakash Parthiban, Assistant Professor, Mechanical Engineering Department

Session

Poster number: 108

Ballroom

Hydrogels are attractive biomaterials for tissue engineering, but size limits nutrient, oxygen, and drug transport, reducing their effectiveness. Hydrogel microparticles (HMPs) overcome these challenges by enhancing diffusion, injectability, and modular assembly, making them strong candidate for injectable scaffolds, drug carriers, and bioinks. Here, photocrosslinkable gelatin methacrylate (GelMA) hydrogels were synthesized and fabricated into microparticles of various sizes and shapes using 3D printing. Nuclear magnetic resonance confirmed successful methacrylation to gelatin backbone; rheometry measured the Young’s modulus to be ~60 ± 8 kPa; scanning electron microscopy revealed a porous architecture which allows cellular penetration. Swelling studies showed a ~380-fold increase in water retention compared to dry GelMA. The GelMA HMPs could be delivered through standard syringe needles without clogging, thereby supporting minimally invasive applications. Dissolution studies showed that HMPs degraded completely within 108 hours, while bulk hydrogel discs retained ~30% of their mass after 120 hours. Drug release studies established controlled release during the first week, in contrast to the delayed burst observed in bulk hydrogel discs. Live/Dead fluorescence further verified high viability, with predominantly live cells observed at both day 1 and day 3, indicating sustained growth within the HMP environment. These findings show that GelMA HMPs integrate tunable mechanics, high print fidelity, injectability, and favorable degradation and release profiles with strong cytocompatibility. Their ability to support cell viability and controlled drug delivery underscores their potential as injectable biomaterials for localized drug release for bone tissue engineering.

ND EPSCoR logo

Physical/shipping address
ND EPSCoR
1805 NDSU Research Park Dr N
Fargo, ND 58102

Phone: (701) 231-8400

NSF EPSCoR logo

Mailing/billing address
ND EPSCoR
NDSU Dept. 4450
PO Box 6050
Fargo, ND 58108-6050

  • Facebook
  • LinkedIn
  • Bluesky icon2
  • YouTube
Sign up for our newsletter
bottom of page