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Development of NMR Methods for the Characterization of Heparin and its Impurities.

机译:开发用于表征肝素及其杂质的NMR方法。

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摘要

The goal of this dissertation is to develop and apply NMR methods for the analysis of heparin and its impurities. As a result of the intentional contamination of heparin with oversulfated chondroitin sulfate (OSCS), significant efforts have been placed on the development of analytical methods to evaluate heparin purity. To advance the suite of analytical methods available for heparin analysis, HPLC-NMR and diffusion NMR methods were developed for its characterization. Our HPLC-NMR method focuses on the WAX separation of intact glycosaminoglycans (GAGs) coupled to on-line UV and NMR spectroscopy for detection and identification of heparin contaminants. The weak anion exchange (WAX) method developed allows for the timely separation of heparin and its impurities, OSCS, dermatan sulfate, and chondroitin sulfate A. In addition to the study of heparin impurities using WAX-HPLC, the characterization of intact and digested heparin samples was investigated using diffusion NMR. Because the diffusion behavior of the intact biopolymers can be dominated by viscosity and molecular crowding effects even in dilute GAG solutions, NMR diffusion results must only be interpreted qualitatively. These limitations can be largely overcome by digesting heparin to low molecular weight oligosaccharides, significantly improving the resolution of heparin and its biopolymer impurities.;The second part of this dissertation is on the characterization of heparin-derived oligosaccharides. Because of the structural complexity and heterogeneity of heparin and heparan sulfate, extensive or partial digestion of the full length polysaccharides is a common practice. Size-exclusion chromatography was used to separate digested heparin oligosaccharides into size-based fractions while SAX-HPLC was used to further purify individual oligosaccharides for NMR characterization. Although, NMR spectroscopy is a powerful tool for structure determination, it trails other analytical techniques in sensitivity. Microcoil NMR is an inexpensive method for enhancing the mass sensitivity of NMR allowing structure elucidation with 5--10 mug of isolated material. Results are presented showing the utility of microcoil NMR for the structure characterization of microgram amounts of heparin-derived tetrasaccharides, reducing the NMR sample requirements by 2-fold when compared to analysis in a Shigemi tube.;In Chapter 6, an IMPACT-HNMBC experiment was used in the detection of 15N in amino sugars through long-range couplings to carbon-bound protons of the sugar ring. Comparison of the ge-HMBC, IMPACT-HMBC and a modified IMPACT-HNMBC pulse sequence revealed improved sensitivity, resolution and reduced F 1 noise with the IMPACT-HNMBC experiment.
机译:本文的目的是开发和应用NMR方法分析肝素及其杂质。由于肝素被过度硫酸化的软骨素硫酸盐(OSCS)故意污染,因此已经在开发评估肝素纯度的分析方法上付出了巨大的努力。为了改进可用于肝素分析的分析方法套件,开发了HPLC-NMR和扩散NMR方法进行表征。我们的HPLC-NMR方法专注于完整糖胺聚糖(GAG)的WAX分离,并结合在线UV和NMR光谱用于检测和鉴定肝素污染物。开发的弱阴离子交换(WAX)方法可以及时分离肝素及其杂质,OSCS,硫酸皮肤素和硫酸软骨素A。除了使用WAX-HPLC研究肝素杂质外,还可以鉴定完整和消化的肝素使用扩散NMR研究样品。因为即使在稀释的GAG溶液中,完整生物聚合物的扩散行为也受粘度和分子拥挤效应的支配,所以NMR扩散结果只能定性地解释。通过将肝素消化成低分子量的寡糖可以大大克服这些局限性,从而显着提高肝素及其生物聚合物杂质的分离度。本论文的第二部分是对肝素衍生的寡糖的表征。由于肝素和硫酸乙酰肝素的结构复杂性和异质性,全长多糖的广泛或部分消化是一种常见的做法。使用尺寸排阻色谱法将消化的肝素寡糖分离为基于大小的馏分,而使用SAX-HPLC进一步纯化单个寡糖以进行NMR表征。尽管NMR光谱法是确定结构的强大工具,但其灵敏度却落后于其他分析技术。 Microcoil NMR是一种廉价的方法,可以提高NMR的质量灵敏度,允许使用5--10杯分离的材料来阐明结构。结果显示微线圈NMR可用于微克量肝素衍生的四糖的结构表征,与Shigemi管中的分析相比,将NMR样品需求减少了2倍。;在第6章中,IMPACT-HNMBC实验通过与糖环的碳键质子进行长距离偶联,Norman可以用于检测氨基糖中的15N。 ge-HMBC,IMPACT-HMBC和改良的IMPACT-HNMBC脉冲序列的比较显示,IMPACT-HNMBC实验提高了灵敏度,分辨率并降低了F 1噪声。

著录项

  • 作者

    Limtiaco, John Kuper.;

  • 作者单位

    University of California, Riverside.;

  • 授予单位 University of California, Riverside.;
  • 学科 Chemistry Analytical.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 272 p.
  • 总页数 272
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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