Interpenetrating alginate network as drug delivery matrix: Effects on protein stability and release

J Biomed Mater Res B Appl Biomater. 2024 Jan;112(1):e35354. doi: 10.1002/jbm.b.35354. Epub 2023 Nov 20.

Abstract

The study investigates the rheological properties and protein release capacity of a uniform hydrogel composed of sodium alginate (SA) and poloxamer (P407). The hydrogel is prepared through the sustained release of calcium ions, resulting in a reinforced and homogeneous interpenetrating networks (IPNs) of SA and P407 polymeric chains. By adjusting the amount of crosslink agent, the hydrogel exhibites an adjustable dissolution ratio and adaptable gelling time. Moreover, the composite showed a well-structured network and superior mechanical strength, enabling the sustained release of both calcium ions and Soybean Trypsin Inhibitor (STI) protein, a model of Bone Morphogenic Protein (BMP). Importantly, the protein release kinetic can be tuned based on the SA content in the polymeric blend, highlighting the versatile nature of this hydrogel for drug delivery purposes.

Keywords: drug delivery; hydrogel; poloxamer; soybean trypsin inhibitor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alginates* / pharmacology
  • Calcium*
  • Delayed-Action Preparations / pharmacology
  • Hydrogels / pharmacology
  • Ions
  • Polymers
  • Protein Stability

Substances

  • Delayed-Action Preparations
  • Alginates
  • Calcium
  • Hydrogels
  • Polymers
  • Ions