open access publication

Article, 2024

Mechanically reinforced hydrogel vehicle delivering angiogenic factor for beta cell therapy

Journal of Colloid and Interface Science, ISSN 0021-9797, 1095-7103, Volume 667, Pages 54-63, 10.1016/j.jcis.2024.04.050

Contributors

Toftdal, Mette Steen [1] [2] Christensen, Natasja Porskjær [1] Kadumudi, Firoz Babu 0000-0002-1329-4015 [3] Dolatshahi-Pirouz, Alireza 0000-0001-6326-0836 [3] Grunnet, Lars Groth 0000-0003-2298-2597 [2] Chen, Menglin 0000-0002-2721-651X (Corresponding author) [1]

Affiliations

  1. [1] Aarhus University
  2. [NORA names: AU Aarhus University; University; Denmark; Europe, EU; Nordic; OECD];
  3. [2] Novo Nordisk (Denmark)
  4. [NORA names: Novo Nordisk; Private Research; Denmark; Europe, EU; Nordic; OECD];
  5. [3] Technical University of Denmark
  6. [NORA names: DTU Technical University of Denmark; University; Denmark; Europe, EU; Nordic; OECD]

Abstract

Type 1 diabetes mellitus (T1DM) is a chronic disease affecting millions worldwide. Insulin therapy is currently the golden standard for treating T1DM; however, it does not restore the normal glycaemic balance entirely, which increases the risk of secondary complications. Beta-cell therapy may be a possible way of curing T1DM and has already shown promising results in the clinic. However, low retention rates, poor cell survival, and limited therapeutic potential are ongoing challenges, thus increasing the need for better cell encapsulation devices. This study aimed to develop a mechanically reinforced vascular endothelial growth factor (VEGF)-delivering encapsulation device suitable for beta cell encapsulation and transplantation. Poly(l-lactide-co-ε-caprolactone) (PLCL)/gelatin methacryloyl (GelMA)/alginate coaxial nanofibres were produced using electrospinning and embedded in an alginate hydrogel. The encapsulation device was physically and biologically characterised and was found to be suitable for INS-1E beta cell encapsulation, vascularization, and transplantation in terms of its biocompatibility, porosity, swelling ratio and mechanical properties. Lastly, VEGF was incorporated into the hydrogel and the release kinetics and functional studies revealed a sustained release of bioactive VEGF for at least 14 days, making the modified alginate system a promising candidate for improving the beta cell survival after transplantation.

Keywords

INS-1, T1DM, VEGF, alginate, alginate hydrogel, alginate system, angiogenic factors, balance, beta, beta cell survival, beta cell therapy, beta-cells, bioactive VEGF, biocompatibility, cell encapsulation, cell encapsulation device, cell survival, cell therapy, cells, chronic disease affecting millions, clinic, complications, cure T1DM, days, devices, disease affecting millions, encapsulated devices, encapsulation, factors, functional studies, glycaemic balance, golden standard, hydrogel vehicle, hydrogels, insulin, insulin therapy, kinetics, low retention rates, mechanical properties, mechanism, mellitus, methacryloyl, millions, nanofibres, poor cell survival, porosity, potential, properties, rate, ratio, release, release kinetics, results, retention rate, risk, risk of secondary complications, secondary complications, standards, study, survival, swelling, swelling ratio, system, therapeutic potential, therapy, transplantation, treat T1DM, type, type 1 diabetes mellitus, vascularization, vehicle

Funders

  • Innovation Fund Denmark
  • Novo Nordisk (Denmark)

Data Provider: Digital Science