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首页> 外文期刊>Journal of biomaterials science >Effects of Precursor and Cross-linking Parameters on the Properties of Dextran-Allyl Isocyanate-Ethylamine/Poly(ethylene glycol diacrylate) Biodegradable Hydrogels and Their Release of Ovalbumin
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Effects of Precursor and Cross-linking Parameters on the Properties of Dextran-Allyl Isocyanate-Ethylamine/Poly(ethylene glycol diacrylate) Biodegradable Hydrogels and Their Release of Ovalbumin

机译:前驱物和交联参数对葡聚糖-异氰酸烯丙酯-乙胺/聚(乙二醇二丙烯酸乙二醇酯)可生物降解水凝胶性能及卵清蛋白释放的影响

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摘要

In this paper, we studied the effects of molecular weight of poly(ethylene glycol diacrylate) (PEGDA) precursor, the degree of substitution (DS) of both allyl isocyanate (AI) and amine groups in dextran-based precursor (Dex-AE), and photoinitiator concentration on Dex-AE/PEGDA hydrogel formation and its ovalbumin (OVA) release. FT-IR spectra showed chemical bond interaction between amine and urethane groups of the hydrogel carriers with OVA. The increase in PEGDA molecular weight led to a faster OVA release because of a more open gel network structure. The study on the DS of AI in Dex-AE precursor showed that an increase in AI did not result in a prominent gel network structure difference. However, the urethane groups in Dex-AE precursor showed some interactions with OVA and, thus, resulted in a slower release rate. The incorporation of amine group into Dex-AE precursor did not affect the gel network structure, but reduced the OVA release rate, and the level of reduction increased with an increasing amine group substitution into the Dex-AE precursor. This reduction could be attributed to the interaction between the amine groups in the gel carrier and OVA. An increase in the photoinitiator concentration showed no effect on the gel network structure or OVA release.
机译:在本文中,我们研究了聚乙二醇二丙烯酸酯(PEGDA)前体的分子量,异氰酸烯丙酯(AI)和胺基在右旋糖酐基前体(Dex-AE)中的取代度(DS)的影响。 ,以及光引发剂浓度对Dex-AE / PEGDA水凝胶形成及其卵白蛋白(OVA)释放的影响。 FT-IR光谱表明OVA在水凝胶载体的氨基和氨基甲酸酯基团之间具有化学键相互作用。 PEGDA分子量的增加由于更开放的凝胶网络结构而导致OVA释放更快。对Dex-AE前体中AI的DS的研究表明,AI的增加并未导致明显的凝胶网络结构差异。但是,Dex-AE前体中的氨基甲酸酯基团显示出与OVA的某些相互作用,因此导致释放速率较慢。将胺基并入Dex-AE前体中并不影响凝胶网络结构,但降低了OVA释放速率,并且随着胺基向Dex-AE前体中取代基的增加,还原水平增加。该减少可以归因于凝胶载体中的胺基和OVA之间的相互作用。光引发剂浓度的增加对凝胶网络结构或OVA释放没有影响。

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