School of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland 4072, Australia.
Biomacromolecules. 2011 Apr 11;12(4):889-97. doi: 10.1021/bm1011773. Epub 2011 Mar 7.
Phosphorylation of alginate was achieved using a heterogeneous urea/phosphate reaction. The degree and stereoselectivity of phosphorylation as well as the effects on the physical properties of the polysaccharide were investigated by Fourier transform infrared (FTIR) and nuclear magnetic resonance (NMR) spectroscopies, inductively coupled plasma optical-emission spectroscopy (ICP-OES), and size exclusion chromatography (SEC). Multidimensional NMR studies of the phosporylated alginate revealed that phosphorylation of the M residues occurred predominantly at the C3 (equatorial) carbon of the polysaccharide ring. In addition, a more comprehensive assignment of the (1)H NMR spectrum of alginate, compared with those previously reported in the literature, is provided here. Hydrogel materials were formed from ionically cross-linked blends of phosphorylated alginate and alginate. These blended hydrogels showed an enhanced resistance to degradation by chelating agents compared with cross-linked alginate hydrogels and a reduction in their mineralization potential.
利用非均相脲/磷酸盐反应实现了褐藻胶的磷酸化。通过傅里叶变换红外(FTIR)和核磁共振(NMR)光谱、电感耦合等离子体光学发射光谱(ICP-OES)和尺寸排阻色谱(SEC)研究了磷酸化的程度和立体选择性以及对多糖物理性质的影响。磷酸化褐藻胶的多维 NMR 研究表明,M 残基的磷酸化主要发生在多糖环的 C3(赤道)碳原子上。此外,与文献中先前报道的相比,本文还提供了褐藻酸盐(1)H NMR 光谱的更全面的归属。离子交联的磷酸化褐藻酸盐和褐藻酸盐共混物形成了水凝胶材料。与交联褐藻酸盐水凝胶相比,这些共混水凝胶对螯合剂的降解具有更高的抵抗力,并且其矿化潜力降低。