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New development of theory and application in capillary electrophoresis: Extended dissociation model for predicting electroosmotic mobility, correction of electrokinetic sampling bias, and enantiomeric separations.

机译:毛细管电泳理论和应用的新进展:扩展的解离模型,用于预测电渗迁移率,校正电动采样偏差和对映体分离。

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摘要

Although the theoretical research of capillary electrophoresis (CE) is quite active in past twenty years and the technology of capillary electrophoresis has been accepted and widely used in chemical and pharmaceutical industries, quantitative control of electroosmotic mobility, the driving separation force in capillary electrophoresis, is still very limited. So far, there was no thorough study conducted on the quantitative control of electroosmotic mobility from theoretical approach. In this thesis, a new equilibrium ion adsorption model was developed based upon the chemical kinetic theory and Langmuir isotherm theory. This theory was successfully confirmed by the experimental results.; In Chapter 1, a historical review of the development of capillary electrophoresis technology, the development of theories involved in CE, and the landmarks of the application of CE are presented.; In Chapter 2, the detailed derivation of the equilibrium ion adsorption model is provided. In addition, the theoretical model was verified by using three types of buffer systems: buffers containing monovalent cations only; buffers containing multiple cations; and buffers containing cations and neutral additives.; Chapter 3 presents the study of suppressing the electroosmotic mobility by using multiply charged cations along with the microemulsion system for the purpose of dual opposite injection, which further qualitatively confirmed the theoretical model described in Chapter 2. An improvement of bias correction factor for an electrokinetic injection of sample was also presented.; Chapter 4 presents a development of a new analytical method for the quantitation of chiral impurities in sertraline hydrochloride, a therapeutic drug. The highly sulfated γ-cyclodextrin was used as the chiral selector. The method is capable to separate and accurately quantitate the stereoisomeric impurities at 0.1% of the active. In addition, the van't Hoff plot demonstrates a non-linear relationship between ln α and 1/T. The effect of temperature on separation also supported by the theoretical model described in Chapter 2.
机译:尽管毛细管电泳(CE)的理论研究在过去的二十年中非常活跃,并且毛细管电泳技术已被接受并广泛应用于化学和制药行业,但电渗迁移率的定量控制,毛细管电泳的驱动分离力却是公认的。仍然非常有限。迄今为止,还没有从理论角度对电渗迁移率进行定量控制的深入研究。本文基于化学动力学理论和朗缪尔等温理论,建立了新的平衡离子吸附模型。实验结果成功证实了这一理论。在第一章中,对毛细管电泳技术的发展,毛细管电泳涉及的理论的发展以及毛细管电泳的应用的历史性进行了回顾。在第二章中,提供了平衡离子吸附模型的详细推导。此外,通过使用三种类型的缓冲液系统验证了理论模型:仅含一价阳离子的缓冲液;含有多种阳离子的缓冲液;以及含有阳离子和中性添加剂的缓冲液。第3章介绍了通过使用带双电荷的阳离子和微乳液系统来抑制双重渗透的电渗迁移率的研究,进一步定性地证实了第2章中描述的理论模型。电动注入的偏置校正因子的改进还提供了样品。第4章介绍了一种新的分析方法的开发方法,该方法用于定量治疗药物舍曲林盐酸盐中的手性杂质。将高度硫酸化的γ-环糊精用作手性选择剂。该方法能够以活性成分的0.1%分离并准确定量立体异构体杂质。此外,范霍夫图显示了lnα与1 / T 之间的非线性关系。第2章中描述的理论模型也支持了温度对分离的影响。

著录项

  • 作者

    Zhou, Marilyn Xiaohong.;

  • 作者单位

    Drexel University.;

  • 授予单位 Drexel University.;
  • 学科 Chemistry Analytical.
  • 学位 Ph.D.
  • 年度 2004
  • 页码 228 p.
  • 总页数 228
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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