Title
Gelatin microgel incorporated poly(ethylene glycol)-based bioadhesive with enhanced adhesive property and bioactivity
Document Type
Article
Publication Date
4-25-2016
Abstract
Up to 7.5 wt % of chemically cross-linked gelatin microgel was incorporated into dopamine-modified poly(ethylene glycol) (PEGDM) adhesive to simultaneously improve the material property and bioactivity of the PEG-based bioadhesive. Incorporation of gelatin microgel reduced cure time while it increased the elastic modulus and cross-linking density of the adhesive network. Most notably, the loss modulus values for microgel-containing adhesive were an order of magnitude higher when compared to microgel-free control. This drastic increase in the viscous dissipation ability of the adhesive is attributed to the introduction of reversible physical bonds into the adhesive network with the incorporation of the gelatin microgel. Additionally, incorporation of the microgel increased the adhesive properties of PEGDM by 1.5- to 2-fold. From in vitro cell culture studies, the composite adhesive is noncytotoxic and the incorporation of microgels provided binding site for promoting fibroblast attachment and viability. The subcutaneous implantation study indicated that the microgel-containing PEGDM adhesive is biocompatible and the incorporated microgels provided pockets for rapid cellular infiltration. Gelatin microgel incorporation was demonstrated to be a facile method to simultaneously enhance the adhesive property and the bioactivity of PEG-based adhesive
Publication Title
Applied Materials and Interfaces
Recommended Citation
Li, Y.,
Meng, H.,
Liu, Y.,
Narkar, A.,
&
Lee, B. P.
(2016).
Gelatin microgel incorporated poly(ethylene glycol)-based bioadhesive with enhanced adhesive property and bioactivity.
Applied Materials and Interfaces,
8(19), 11980-11989.
http://doi.org/10.1021/acsami.6b01364
Retrieved from: https://digitalcommons.mtu.edu/biomedical-fp/5
Publisher's Statement
© 2016 American Chemical Society. Publisher's version of record: http://dx.doi.org/10.1021/acsami.6b01364