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Micellar liquid chromatographic separation of amino acids using pre- and post-column o-phthalaldehyde/N-acetylcysteine derivatization

机译:柱前和柱后邻苯二甲醛/ N-乙酰基半胱氨酸衍生化的氨基酸的胶束液相色谱分离

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The isocratic analysis of primary proteic amino acids using a C-18 column, micellar mobile phases of sodium dodecyl sulphate (SDS) and 1-propanol at varying pH, and pre- and po st-column formation of the o-phthalaldehyde (OPA)/N-acetyl-L-cysteine (NAC) isoindoles, is examined. An interpretive optimization strategy was applied to find the best separation conditions. For this purpose, empirical polynomial models were used to describe the elution behavior of the isoindoles and free amino acids, using as separation factors the concentrations of surfactant and modifier (two-factor problem), or these two factors and the pH of the mobile phase (three-factor problem). The separation of the OPA/NAC amino acid isoindoles was very poor: only eight compounds could be separated satisfactorily. In contrast, 14 free amino acids (ordered according to their elution times: aspartic acid, glutamine, threonine, cysteine, alanine, tyrosine, valine, methionine, phenylalanine, leucine, lysine, histidine, tryptophan and arginine) could be well resolved with 0.05 M SDS-1.2% propanol at pH 3 in 42 min, partially due to the higher efficiencies frequently five- to 10-fold those achieved for the isoindoles at this pH. A mobile phase of 0.05 M SDS without alcohol allowed the resolution of a mixture of aspartic acid, glutamine, asparagine, glutamic acid, threonine, cysteine and alanine, which eluted at the lower retention times. In these conditions, only serine and glycine overlapped with glutamine and threonine, respectively. (C) 2000 Elsevier Science B.V. All rights reserved. [References: 28]
机译:使用C-18色谱柱,十二烷基硫酸钠(SDS)和1-丙醇在不同pH下的胶束流动相以及邻苯二甲醛(OPA)的柱前和柱后形成,对一级蛋白质氨基酸进行等度分析检查了/ N-乙酰基-L-半胱氨酸(NAC)异吲哚。采用解释性优化策略来找到最佳分离条件。为此,使用经验多项式模型来描述异吲哚和游离氨基酸的洗脱行为,使用表面活性剂和改性剂的浓度(两因素问题)或这两个因素以及流动相的pH作为分离因子。 (三因素问题)。 OPA / NAC氨基酸异吲哚的分离非常差:只能令人满意地分离出8种化合物。相反,用0.05可以很好地解析14种游离氨基酸(根据其洗脱时间排序:天冬氨酸,谷氨酰胺,苏氨酸,半胱氨酸,丙氨酸,酪氨酸,缬氨酸,蛋氨酸,苯丙氨酸,亮氨酸,赖氨酸,组氨酸,色氨酸和精​​氨酸)在42分钟内于pH值为3的情况下使用M SDS-1.2%丙醇,部分原因是在此pH值条件下,通常效率达到异吲哚的5至10倍。不含酒精的0.05 M SDS流动相可分离出天冬氨酸,谷氨酰胺,天冬酰胺,谷氨酸,苏氨酸,半胱氨酸和丙氨酸的混合物,并在较低的保留时间洗脱。在这些条件下,只有丝氨酸和甘氨酸分别与谷氨酰胺和苏氨酸重叠。 (C)2000 Elsevier Science B.V.保留所有权利。 [参考:28]

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