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受限进样介质捕集柱对小分子进行在线捕集的效率及捕集容量评估。

Evaluation of efficiency and trapping capacity of restricted access media trap columns for the online trapping of small molecules.

作者信息

Baghdady Yehia Z, Schug Kevin A

机构信息

Department of Chemistry & Biochemistry, The University of Texas at Arlington, Arlington, TX, USA.

出版信息

J Sep Sci. 2016 Nov;39(21):4183-4191. doi: 10.1002/jssc.201600777. Epub 2016 Sep 22.

Abstract

Restricted access media are generally composed from multi-modal particles that combine a size excluding outer surface and an inner-pore retention mechanism for small molecules. Such materials can be used for either online isolation and pre-concentration of target small molecules or removal of small molecule interferences from large macromolecules, such as proteins in complex biological matrices. Thus, they are considered as enhanced online solid-phase extraction materials. We evaluated the efficiency and trapping capacity of different semi-permeable surface restricted access media columns (C , C , and C inner pores) for four model small molecule compounds (dopamine hydrochloride, acetaminophen, 4-hydroxybenzoic acid, and diethyl phthalate) having variable physicochemical properties. We further studied the effect of mobile phase flow rate (0.25, 0.5, 1, and 2 mL/min) and pH, using 98:2 0.5% acetic acid in water/ methanol (pH 2.88) and 5 mM ammonium acetate in 98:2 water/methanol (pH 6.61) as mobile phases. Breakthrough curves generated using frontal analysis were analyzed to determine important chromatographic parameters specific for each of the studied compounds. Experimental determination of these parameters allowed selection of the most efficient trap column and the best loading mobile phase conditions for maximal solute enrichment and pre-concentration on restricted access media trap columns.

摘要

受限-access介质通常由多模态颗粒组成,这些颗粒结合了一种排除小分子的外表面尺寸和一种用于小分子的内孔保留机制。这类材料可用于在线分离和预浓缩目标小分子,或从复杂生物基质中的大分子(如蛋白质)中去除小分子干扰物。因此,它们被视为增强型在线固相萃取材料。我们评估了不同半透性表面受限-access介质柱(C、C和C内孔)对四种具有不同物理化学性质的模型小分子化合物(盐酸多巴胺、对乙酰氨基酚、4-羟基苯甲酸和邻苯二甲酸二乙酯)的效率和捕获能力。我们进一步研究了流动相流速(0.25、0.5、1和2 mL/min)和pH值的影响,使用98:2的0.5%乙酸水溶液/甲醇(pH 2.88)和5 mM乙酸铵的98:2水/甲醇溶液(pH 6.61)作为流动相。通过前沿分析生成的突破曲线进行分析,以确定每种研究化合物特有的重要色谱参数。通过实验测定这些参数,可以选择最有效的捕获柱和最佳的加载流动相条件,以在受限-access介质捕获柱上实现最大溶质富集和预浓缩。

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