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In situ assembly of fibrinogen/hyaluronic acid hydrogel via knob-hole interaction for 3D cellular engineering

机译:纤维蛋白原/透明质酸水凝胶通过旋钮孔相互作用原位组装用于3D细胞工程

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摘要

Hyaluronic acid (HA)-based hydrogels have applied widely for biomedical applications due to its biocompatibility and biodegradability. However, the use of initiators or crosslinkers during the hydrogel formation may cause cytotoxicity and thereby impair the biocompatibility. Inspired by the crosslinking mechanism of fibrin gel, a novel HA-based hydrogel was developed via the in situ supramolecular assembly based on knob-hole interactions between fibrinogen and knob-grafted HA (knob-g-HA) in this study. The knob-grafted HA was synthesized by coupling knob peptides (GPRPAAC, a mimic peptide of fibrin knob A) to HA via Michael addition. Then the translucent fibrinogen/knob-g-HA hydrogels were prepared by simply mixing the solutions of knob-g-HA and fibrinogen at the knob/hole ratio of 1.2. The rheological behaviors of the fibrinogen/knob-g-HA hydrogels with the fibrinogen concentrations of 50, 100 and 200 mg/mL were evaluated, and it was found that the dynamic storage moduli (G′) were higher than the loss moduli (G″) over the whole frequency range for all the groups. The SEM results showed that fibrinogen/knob-g-HA hydrogels presented the heterogeneous mesh-like structures which were different from the honeycomb-like structures of fibrinogen/MA-HA hydrogels. Correspondingly, a higher swelling ratio was obtained in the groups of fibrinogen/knob-g-HA hydrogel. Finally, the cytocompatibility of fibrinogen/knob-g-HA hydrogels was proved by live/dead stainings and MTT assays in the 293T cells encapsulation test. All these results highlight the biological potential of the fibrinogen/knob-g-HA hydrogels for 3D cellular engineering.
机译:基于透明质酸(HA)的水凝胶具有生物相容性和生物降解性,因此已广泛应用于生物医学应用。但是,在水凝胶形成过程中使用引发剂或交联剂可能会引起细胞毒性,从而损害生物相容性。受纤维蛋白凝胶交联机理的启发,在这项研究中,基于纤维蛋白原和结瘤嫁接的HA(结节-g-HA)之间的结孔相互作用,通过原位超分子组装技术开发了一种新型的基于HA的水凝胶。通过Michael加成将结节肽(GPRPAAC,血纤蛋白结节A的模拟肽)偶联至HA来合成结节嫁接的HA。然后,通过简单地以旋钮/孔比为1.2混合旋钮-g-HA和纤维蛋白原的溶液来制备半透明的纤维蛋白原/旋钮-g-HA水凝胶。评价了纤维蛋白原浓度为50、100和200 mg / mL的纤维蛋白原/旋钮g-HA水凝胶的流变行为,发现动态储能模量(G')高于损耗模量(G ”)在所有组的整个频率范围内。 SEM结果表明,纤维蛋白原/旋钮-g-HA水凝胶呈现出异质的网状结构,不同于纤维蛋白原/ MA-HA水凝胶的蜂窝状结构。相应地,在纤维蛋白原/旋钮-g-HA水凝胶组中获得了更高的溶胀率。最后,在293T细胞包封试验中,通过活/死染色和MTT测定法证明了纤维蛋白原/旋钮-g-HA水凝胶的细胞相容性。所有这些结果突出了纤维蛋白原/旋钮-g-HA水凝胶在3D细胞工程中的生物学潜力。

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