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用于富集钙离子的聚合物网络

Polymer Networks for Enrichment of Calcium Ions.

作者信息

Heinze Marcus, Horn Christoph, Pospiech Doris, Boldt Regine, Kobsch Oliver, Eckstein Kathrin, Jehnichen Dieter, Voit Brigitte, Baudis Stefan, Liska Robert, Naumova Anna, Saalwächter Kay, Lendenmann Urs, Moszner Norbert

机构信息

Leibniz-Institut für Polymerforschung Dresden e.V., Hohe Str. 6, 01069 Dresden, Germany.

Organic Chemistry of Polymers, Technische Universität Dresden, 01069 Dresden, Germany.

出版信息

Polymers (Basel). 2021 Oct 12;13(20):3506. doi: 10.3390/polym13203506.

Abstract

In this study, solvogels containing (2-((2-(ethoxycarbonyl)prop-2-en-1-yl)oxy)-ethyl) phosphonic acid (ECPA) and ,'-diethyl-1,3-bis-(acrylamido)propane (BNEAA) as the crosslinker are synthesized by UV induced crosslinking photopolymerization in various solvents. The polymerization of the ECPA monomer is monitored by the conversion of double bonds with attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy. The morphology of the networks is characterized by photorheology, solid state NMR spectroscopy, and scanning electron microscopy (SEM) of the dried gels. It is demonstrated that the storage modulus is not only determined by the crosslinker content in the gel, but also by the solvent used for preparation. The networks turn out to be porous structures with being governed by a rigid, phase-separated polymer phase rather than by entropic elasticity. The external and internal values of the poly(ECPA--BNEAA) gels were determined by titration with a specially designed method and compared to the calculated values. The polymer-immobilized phosphonic acid groups in the hydrogels induce buffering behavior into the system without using a dissolved buffer. The calcium accumulation in the gels is studied by means of a double diffusion cell filled with calcium ion-containing solutions. The successful accumulation of hydroxyapatite within the gels is shown by a combination of SEM, energy-dispersive X-ray spectroscopy (EDX) and wide-angle X-ray scattering (WAXS).

摘要

在本研究中,通过紫外线诱导交联光聚合反应,在各种溶剂中合成了含有(2-((2-(乙氧基羰基)丙-2-烯-1-基)氧基)乙基)膦酸(ECPA)和作为交联剂的N,N'-二乙基-1,3-双(丙烯酰胺基)丙烷(BNEAA)的溶胶凝胶。通过衰减全反射傅里叶变换红外光谱(ATR-FTIR)监测ECPA单体的双键转化率来跟踪聚合反应。通过光流变学、固态核磁共振光谱以及干燥凝胶的扫描电子显微镜(SEM)对网络结构的形态进行表征。结果表明,储能模量不仅取决于凝胶中的交联剂含量,还取决于用于制备的溶剂。这些网络结构最终呈现出多孔结构,其结构由刚性的、相分离的聚合物相决定,而非由熵弹性决定。采用一种专门设计的方法通过滴定测定了聚(ECPA-BNEAA)凝胶的外部和内部pH值,并与计算值进行了比较。水凝胶中聚合物固定化的膦酸基团在不使用溶解缓冲剂的情况下赋予系统缓冲性能。通过填充含钙离子溶液的双扩散池研究了凝胶中的钙积累情况。通过扫描电子显微镜(SEM)、能量色散X射线光谱(EDX)和广角X射线散射(WAXS)相结合的方法,证明了凝胶中成功积累了羟基磷灰石。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4758/8538138/33cf391513e6/polymers-13-03506-g002.jpg

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