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      One-pot synthesis of superabsorbent hybrid hydrogels based on methacrylamide gelatin and polyacrylamide. Effortless control of hydrogel properties through composition design

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          Abstract

          Network-forming polymerization of methacrylamide gelatin and acrylamide generates scaffolds with controlled biocompatibility and water affinity.

          Abstract

          Biocompatible methacrylamide-modified gelatin (GELMA) hydrogels with tuned characteristics, obtained through network-forming photopolymerization, have recently attracted increasing attention due to their wide range of possible applications such as drug release, tissue regeneration and generation of bioartificial implants. Due to the controlled number of CC bonds, GELMA may simultaneously act as macromonomer and crosslinker leading through polymerization to hydrogels with rationally designed performances. This study provides effortless one-pot synthesis of hybrid hydrogels based on covalently linked GELMA and polyacrylamide (PAA), using photo-induced network-forming polymerization. Conventional synthesis of similar hydrogels leads to interpenetrating gelatin and PAA networks, usually involving multistep crosslinking of the components and the use of toxic crosslinkers. Through the described one-pot chemistry, the synthetic water superabsorbent PAA with its well-recognized advantages can rationally benefit from the high biocompatibility and cell-adherence of GELMA in a simple covalent way. This work provides a correlation between the composition and the corresponding hydrogel properties (including swelling, pH influence, mechanical behaviour, ability to generate porous scaffolds, enzymatic degradation). The addition of PAA modulated the network density and the water affinity allowing the control of elasticity and degradability. Supplementary crosslinking of the synthetic component provided additional control over hydrophilicity. The capacity of such hydrogels to generate porous scaffolds was proved; interesting morphologies were developed only by varying the composition. In vitro cellular studies indicated that the presence of GELMA conferred controlled cell-affinity properties to the bicomponent hydrogels. Nevertheless, the drug release potential of such hydrogels was preliminarily investigated using sodium nafcillin. GELMA–PAA hydrogels may be useful for tissue regeneration due to effortless synthesis, compositional flexibility and variable properties.

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          Most cited references25

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          Laser fabrication of three-dimensional CAD scaffolds from photosensitive gelatin for applications in tissue engineering.

          In the present work, 3D CAD scaffolds for tissue engineering applications were developed starting from methacrylamide-modified gelatin (GelMOD) using two-photon polymerization (2PP). The scaffolds were cross-linked employing the biocompatible photoinitiator Irgacure 2959. Because gelatin is derived from collagen (i.e., the main constituent of the ECM), the developed materials mimic the cellular microenvironment from a chemical point of view. In addition, by applying the 2PP technique, structural properties of the cellular microenvironment can also be mimicked. Furthermore, in vitro degradation assays indicated that the enzymatic degradation capability of gelatin is preserved for the methacrylamide-modified derivative. An in depth morphological analysis of the 2PP-fabricated scaffolds demonstrated that the parameters of the CAD model are reproduced with great precision, including the ridge-like surface topography on the order of 1.5 μm. The developed scaffolds showed an excellent stability in culture medium. In a final part of the present work, the suitability of the developed scaffolds for tissue engineering applications was verified. The results indicated that the applied materials are suitable to support porcine mesenchymal stem cell adhesion and subsequent proliferation. Upon applying osteogenic stimulation, the seeded cells differentiated into the anticipated lineage. Energy dispersive X-ray (EDX) analysis showed the induced calcification of the scaffolds. The results clearly indicate that 2PP is capable of manufacturing precisely constructed 3D tissue engineering scaffolds using photosensitive polymers as starting material.
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            Synthesis and characterization of photocrosslinkable gelatin and silk fibroin interpenetrating polymer network hydrogels.

            To effectively repair or replace damaged tissues, it is necessary to design scaffolds with tunable structural and biomechanical properties that closely mimic the host tissue. In this paper, we describe a newly synthesized photocrosslinkable interpenetrating polymer network (IPN) hydrogel based on gelatin methacrylate (GelMA) and silk fibroin (SF) formed by sequential polymerization, which possesses tunable structural and biological properties. Experimental results revealed that IPNs, where both the GelMA and SF were independently crosslinked in interpenetrating networks, demonstrated a lower swelling ratio, higher compressive modulus and lower degradation rate as compared to the GelMA and semi-IPN hydrogels, where only GelMA was crosslinked. These differences were likely caused by a higher degree of overall crosslinking due to the presence of crystallized SF in the IPN hydrogels. NIH-3T3 fibroblasts readily attached to, spread and proliferated on the surface of IPN hydrogels, as demonstrated by F-actin staining and analysis of mitochondrial activity (MTT). In addition, photolithography combined with lyophilization techniques was used to fabricate three-dimensional micropatterned and porous microscaffolds from GelMA-SF IPN hydrogels, furthering their versatility for use in various microscale tissue engineering applications. Overall, this study introduces a class of photocrosslinkable, mechanically robust and tunable IPN hydrogels that could be useful for various tissue engineering and regenerative medicine applications.
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              A biomimetic hydrogel based on methacrylated dextran-graft-lysine and gelatin for 3D smooth muscle cell culture.

              Many synthetic hydrogels for cell encapsulation have hitherto been based on polyethylene glycol which is non-natural, non-biodegradable and only terminal-functionalizable, all of which are drawbacks for tissue engineering or cell delivery. The polysaccharide dextran is also highly hydrophilic but biodegradable and pendant-functionalizable and more closely resembles glycosaminoglycans to mimic the natural extracellular matrix. This study reports synthesis of a methacrylate and lysine functionalized dextran and development of hydrogel composite systems based on this material and methacrylamide modified gelatin. The mechanical stiffness and degree of swelling of the hydrogels were varied by manipulation of the degree of functionalization of dextran and gelatin and concentration/composition of precursor solution. Human umbilical artery smooth muscle cells (SMCs) were encapsulated inside hydrogels during gel hardening with photopolymerization. Rapid cell spreading, extensive cellular network formation and high SMC proliferation occurred within softer hydrogels (with shear storage moduli ranging from 898 to 3124Pa). The encapsulated SMCs appear to be relatively contractile in the initial culture than on tissue culture polystyrene dish due to physical constraint imposed by the hydrogels but they become more synthetic with time possibly due to the inability of cells to reach confluence inside these cell-mediated degradable hydrogels. From the impressive cell proliferation and network formation, these new hydrogels combining polysaccharide and protein derivatives appear to be excellent candidates for further development as bioactive scaffolds for use in vascular tissue engineering and regeneration.
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                Author and article information

                Journal
                NJCHE5
                New J. Chem.
                New J. Chem.
                Royal Society of Chemistry (RSC)
                1144-0546
                1369-9261
                2014
                2014
                : 38
                : 7
                : 3112-3126
                Affiliations
                [1 ]Advanced Polymer Materials Group
                [2 ]University Politehnica of Bucharest
                [3 ]Bucharest, Romania
                [4 ]“Cantacuzino” National Institute for Research and Development in Microbiology and Immunology
                [5 ]050096 Bucharest, Romania
                [6 ]Polymer Chemistry and Biomaterials Group
                [7 ]Ghent University
                [8 ]Ghent, Belgium
                Article
                10.1039/C4NJ00161C
                a04518dc-c6eb-44d6-82cb-7394d891f93f
                © 2014
                History

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