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Sustained delivery of growth factors with high loading efficiency in a layer by layer assemblyElectronic supplementary information (ESI) available. See DOI: 10.1039/c9bm00979e

Authors :
Damanik, Febriyani F. R.
Brunelli, Marzia
Pastorino, Laura
Ruggiero, Carmelina
van Blitterswijk, Clemens
Rotmans, Joris
Moroni, Lorenzo
Source :
Biomaterials Science; 2019, Vol. 8 Issue: 1 p174-188, 15p
Publication Year :
2019

Abstract

Layer by layer (LBL) assembly has garnered considerable interest due to its ability to generate multifunctional films with high tunability and versatility in terms of substrates and polyelectrolytes, allowing the option to use complex devices and drugs. Polyelectrolytes, such as growth factors (GFs), are essential, but costly, delicate, biological molecules that have been used in various tissue regeneration applications. For this reason, the controlled drug delivery of efficiently loaded GFs viaLBL assembly (GF-LBL) can contribute to the establishment of cost-effective biologically triggered biomedical applications. We have developed an LBL method to load GFs (specifically, transforming growth factor beta 1, platelet-derived growth factor ββ, and insulin growth factor 1), with up to 90% efficiency approximately, by gas plasma surface activation and tuning the pH to increase the ionic strength of polyelectrolytes. Poly(styrenesulfonate) (PSS) and poly(ethyleneimine) (PEI) have been used to provide the initial necessary charge for multilayer build-up. Heparin and dextran sulphate have been investigated as counter polyelectrolytes to enhance the activity of GFs by protecting their ligands, where heparin resulted in the highest achievable loading efficiency for all GFs. Oxygen gas plasma and acidic pH levels also resulted in a significant increase in GF loading efficiency. The three GFs were released by diffusion and erosion in a controlled manner over lengthy time scales and the bioactivity was maintained for up to 14 days. When tested as implants in vitro, GF-LBL constructs increased fibroblast proliferation, influenced cell morphology and migration, and enhanced myofibroblast differentiation, indicating that the biological functionalities of the GFs were preserved. In conclusion, this developed LBL assembly method can provide a simple drug delivery system, which may yield more effective applications for tissue regeneration as well as biomedical sciences at large.

Details

Language :
English
ISSN :
20474830 and 20474849
Volume :
8
Issue :
1
Database :
Supplemental Index
Journal :
Biomaterials Science
Publication Type :
Periodical
Accession number :
ejs51747703
Full Text :
https://doi.org/10.1039/c9bm00979e