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Swelling Dynamics of a DNA-Polymer Hybrid Hydrogel Prepared Using Polyethylene Glycol as a Porogen

机译:聚乙二醇为致孔剂制备的DNA-聚合物杂化水凝胶的溶胀动力学

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摘要

DNA-polyacrylamide hybrid hydrogels designed with covalent and double-stranded (dsDNA) crosslinks respond to specific single-stranded DNA (ssDNA) probes by adapting new equilibrium swelling volume. The ssDNA probes need to be designed with a base pair sequence that is complementary to one of the strands in a dsDNA supported network junction. This work focuses on tuning the hydrogel swelling kinetics by introducing polyethylene glycol (PEG) as a pore-forming agent. Adding PEG during the preparation of hydrogels, followed by removal after polymerization, has been shown to improve the swelling dynamics of DNA hybrid hydrogels upon specific ssDNA probe recognition. The presence of porogen did not influence the kinetics of osmotic pressure-driven (2-acrylamido-2-methylpropane sulfonic acid)-co-acrylamide (AMPSA-co-AAm) hydrogels’ swelling, which is in contrast to the DNA-sensitive hydrogels. The difference in the effect of using PEG as a porogen in these two cases is discussed in view of processes leading to the swelling of the gels.
机译:具有共价和双链(dsDNA)交联设计的DNA-聚丙烯酰胺杂化水凝胶可通过适应新的平衡溶胀量来响应特定的单链DNA(ssDNA)探针。 ssDNA探针需要设计有与dsDNA支持的网络连接中的一条链互补的碱基对序列。这项工作的重点是通过引入聚乙二醇(PEG)作为成孔剂来调节水凝胶的溶胀动力学。研究表明,在水凝胶的制备过程中加入PEG,然后在聚合反应后将其除去,可改善DNA杂化水凝胶在特异性ssDNA探针识别后的溶胀动力学。致孔剂的存在并不影响渗透压驱动的(2-丙烯酰胺基-2-甲基丙烷磺酸)-共丙烯酰胺(AMPSA-co-AAm)水凝胶的动力学,这与对DNA敏感的水凝胶相反。鉴于导致凝胶膨胀的过程,讨论了在这两种情况下使用PEG作为致孔剂的效果差异。

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