Browsing by Author "Bragg, John C."

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    Designing Visible Light-Cured Thiol-Acrylate Hydrogels for Studying the HIPPO Pathway Activation in Hepatocellular Carcinoma Cells
    (Wiley Blackwell (John Wiley & Sons), 2016-04) Lin, Tsai-Yu; Bragg, John C.; Lin, Chien-Chi; Department of Biomedical Engineering, School of Engineering and Technology
    Various polymerization mechanisms have been developed to prepare peptide-immobilized poly(ethylene glycol) (PEG) hydrogels, a class of biomaterials suitable for studying cell biology in vitro. Here, a visible light mediated thiol-acrylate photopolymerization scheme is reported to synthesize dually degradable PEG-peptide hydrogels with controllable crosslinking and degradability. The influence of immobilized monothiol pendant peptide is systematically evaluated on the crosslinking of these hydrogels. Further, methods are proposed to modulate hydrogel crosslinking, including adjusting concentration of comonomer or altering the design of multifunctional peptide crosslinker. Due to the formation of thioether ester bonds, these hydrogels are hydrolytically degradable. If the dithiol peptide linkers used are susceptible to protease cleavage, these thiol-acrylate hydrogels can be designed to undergo partial proteolysis. The differences between linear and multiarm PEG-acrylate (i.e., PEGDA vs PEG4A) are also evaluated. Finally, the use of the mixed-mode thiol-acrylate PEG4A-peptide hydrogels is explored for in situ encapsulation of hepatocellular carcinoma cells (Huh7). The effects of matrix stiffness and integrin binding motif (e.g., RGDS) on Huh7 cell growth and HIPPO pathway activation are studied using PEG4A-peptide hydrogels. This visible light poly-merized thiol-acrylate hydrogel system represents an alternative to existing light-cured hydrogel platforms and shall be useful in many biomedical applications.
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    Improving Cross-linking of Degradable Thiol-acrylate Hydrogels via Peptide Design
    (Office of the Vice Chancellor for Research, 2015-04-17) Bragg, John C.; Lin, Chien-Chi
    Hydrogels fabricated from poly (ethylene glycol) (PEG) based macromers are ideal for drug delivery and tissue engineering applications. Recently, a new visible light-mediated photopolymerization scheme was developed to fabricate cytocompatible and degradable poly (ethylene glycol)-diacrylate (PEGDA) hydrogels. Co-polymerization of mono-cysteine peptides (e.g. CRGDS) with PEGDA offers the gels with cell adhesion property. However, this approach causes significant reduction in network crosslinking density, in part due to chain transfer of thiols to acrylates. The goal of the project is to improve the network cross-linking efficiency of this peptide-immobilized PEGDA hydrogel for cell culture. We hypothesized that the incorporation of bi-functional bis-cysteine peptides or silk fibroin will produce hydrogels with enhanced stiffness. The shear moduli of the gels were characterized via oscillatory rheometry in strain-sweep (0.1-5%) mode. Hydrolytic degradation of the gels as a function of time was also evaluated by rheometry. Cytocompatibility of the hydrogel system will be assessed by in situ encapsulation of 3T3 fibroblasts. Cell metabolic activity was determined by Alamar-Blue assay. We found that the bis-cysteine peptide enhanced gel crosslinking, as compared with mono-cysteine peptide. Incorporation of silk fibroin protein also exhibited enhancement in gel stiffness. However, the optimum concentration of incorporated silk fibroin presented an increased shear modulus compared to gels containing only the mono-cysteine peptide. Ongoing work is focused on fine-tuning gel formulations and degradation, as well as on evaluating the cytocompatibility of these visible-light cured thiol-acrylate hydrogels.
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    In situ formation of silk-gelatin hybrid hydrogels for affinity-based growth factor sequestration and release
    (RSC, 2016) Bragg, John C.; Kweon, HaeYong; Jo, You-Young; Lee, Kwang Gill; Lin, Chien-Chi; Department of Biomedical Engineering, School of Engineering and Technology
    Silk fibroin (SF) and gelatin are natural polymers suitable for biomedical applications, including controlled protein release. SF offers high mechanical strength and slow enzymatic degradability, whereas gelatin contains bioactive motifs that can provide biomimicry to the resulting scaffolds. Owing to their complementary material properties, SF and gelatin are increasingly being used together to afford hybrid scaffolds with adjustable properties. Here, we report the use of in situ crosslinked SF/gelatin hydrogels as a platform for tunable growth factor sequestration and delivery. We demonstrate that the physical assembly of SF into insoluble networks could be accelerated by sonication even in the presence of gelatin. However, the processing conditions from which to prepare SF aqueous solution (e.g., heating duration and number of processing steps) drastically altered the resulting hydrogel physical properties. Furthermore, the stiffness of SF/gelatin hybrid gels displayed temperature dependency. Specifically, incorporation of gelatin increased gel stiffness at 25 °C but decreases hydrogel mechanical stability at 37 °C. The thermostability of SF/gelatin gels can be restored by using a low concentration of genipin, a naturally derived chemical crosslinker. We also incorporate heparin-conjugated gelatin (GH) into the hydrogels to create a hybrid matrix capable of sequestering growth factors, such as basic fibroblast growth factor (bFGF). Both sonicated SF (SSF) and hybrid SSF-GH gels exhibit moderate bFGF sequestration, but only SSF-GH gels afford slow release of bFGF. On the other hand, genipin-stabilized network exhibited the highest retention and sustained release of bFGF, suggesting the suitability of this particular formulation as a scaffold for tissue engineering applications.