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Capillary electrophoresis separation of neutral organic compounds, pharmaceutical drugs, proteins and peptides, enantiomers and anions

机译:中性有机化合物,药物,蛋白质和肽,对映异构体和阴离子的毛细管电泳分离

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摘要

Addition of a novel anionic surfactant, namely lauryl polyoxyethylene sulfate, to an aqueous-acetonitrile electrolyte makes it possible to separate nonionic organic compounds by capillary electrophoresis. Separation is based on differences in the association between analytes and the surfactant. Highly hydrophobic compounds such as polyaromatic hydrocarbons are well separated by this new surfactant. Migration times of analytes can be readily changed over an unusually large range by varying the additive concentration and the proportion of acetonitrile in the electrolyte. Several examples are given, including the separation of four methylbenz (a) anthracene isomers and the separation of normal and deuterated acetophenone;The effect of adding this new surfactant to the acidic electrolyte was also investigated. Working at acidic condition at pH 2.4 has the advantage that electroosmotic flow is virtually eliminated. Neutral compounds are dragged by their association with the surfactant, moving as the same direction as the surfactant, resulting in fast separations. Basic compounds are also investigated under the same conditions. Excellent resolution of a mixture of 19 polyaromatic hydrocarbons was obtained in only 20 min;Incorporation of cetyltrimethylammonium bromide in the electrolyte is shown to dynamically coat the capillary and reverse electroosmotic flow. The coating prevents basic proteins and peptides adsorption into the capillary wall, resulting in high separation efficiencies. A systematic study of experimental parameters demonstrated the importance of selecting a suitable buffer and an appropriate pH;Chiral recognition mechanism is studied using several novel synthetic surfactants as chiral selectors, which are made from amino acids reacting with alkyl chloroformates. It was found that enantiomeric resolution can be readily manipulated by varying the alkyl groups (different chain lengths), amino acids and surfactant concentrations. Sulfonated [beta]-cyclodextrin is also employed as a chiral selector to compare chiral selectivity with these synthetic surfactants. A duo-chiral selectors system is further investigated for the possibility of eliminating some tedious steps in chiral compounds method development;A satisfactory separation of both inorganic and organic anions is obtained using electrolyte solutions as high as 5 M sodium chloride using direct photometric detection. The temperature inside the capillary that resulted from Joule heating is calculated, and used to explain the unexpected fast and efficient separations. Since electroosmotic flow is suppressed, a quaternary ammonium additive (Q+), which is normally used to reverse the electroosmotic flow in anion separations, is not utilized in our study. The effect of various salts on electrophoretic and electroosmotic mobility is further discussed. Several examples are given under high-salt conditions.
机译:在水性乙腈电解质中添加新型阴离子表面活性剂,即月桂基聚氧乙烯硫酸盐,可以通过毛细管电泳分离非离子有机化合物。分离基于分析物和表面活性剂之间缔合的差异。这种新型表面活性剂可以很好地分离出高度疏水的化合物,例如聚芳烃。通过改变电解液中添加剂的浓度和乙腈的比例,可以轻松地在很大的范围内改变分析物的迁移时间。给出了几个实例,包括四种甲基苯并(a)蒽异构体的分离以及正和氘代苯乙酮的分离;还研究了将这种新型表面活性剂添加到酸性电解质中的效果。在pH为2.4的酸性条件下工作具有消除电渗流的优势。中性化合物由于与表面活性剂的缔合而受到拖累,其移动方向与表面活性剂相同,从而导致快速分离。在相同条件下还研究了碱性化合物。仅20分钟就获得了19种聚芳烃混合物的出色分离度;在电解液中掺入鲸蜡基三甲基溴化铵可动态包覆毛细管并逆渗透电。该涂层可防止碱性蛋白质和肽吸附到毛细管壁中,从而提高分离效率。对实验参数的系统研究表明,选择合适的缓冲液和合适的pH值的重要性;使用几种新型合成表面活性剂作为手性选择剂,研究了手性识别机理,这些表面活性剂是由氨基酸与烷基氯甲酸酯反应制得的。发现通过改变烷基(不同链长),氨基酸和表面活性剂浓度可以容易地控制对映体拆分。磺化的β-环糊精也用作手性选择剂,以与这些合成表面活性剂比较手性选择性。进一步研究了双手性选择器系统,以消除手性化合物方法开发过程中的一些繁琐步骤;使用直接光度法检测的高达5 M氯化钠的电解质溶液,可以令人满意地分离无机和有机阴离子。计算了因焦耳热而产生的毛细管内部温度,并用于解释意想不到的快速有效分离。由于电渗流受到抑制,因此在我们的研究中未使用通常用于在阴离子分离中逆转电渗流的季铵添加剂(Q +)。进一步讨论了各种盐对电泳和电渗迁移率的影响。在高盐条件下给出了几个例子。

著录项

  • 作者

    Ding, Wei-Liang;

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  • 年度 1998
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  • 原文格式 PDF
  • 正文语种 en
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