Kubán Pavel, Hauser Peter C
Department of Chemistry, University of Basel, Spitalstrasse 51, 4004 Basel, Switzerland.
J Chromatogr A. 2006 Sep 22;1128(1-2):97-104. doi: 10.1016/j.chroma.2006.06.046. Epub 2006 Jun 30.
The application of gradient methods in HPLC determinations with capacitively coupled contactless conductivity detection was successfully demonstrated for non-UV-absorbing amino acids as well as for small peptides as analytes. The drift in baseline which is caused by the change in the conductivity of the mobile phase during the elution could be minimized by careful optimization of the composition of the mobile phase. For such conditions the remaining baseline drift could be corrected for either by subtraction of a blank chromatogram or by baseline normalization using a software package for chromatographic data processing. Reverse phase separations were carried out using aqueous eluents containing either methanol or acetonitrile and acetic acid or trifluoroacetic acid. Detection limits between 1 and 40 microM were achieved for the amino acids and the di- and tri-peptides investigated. The reproducibilities for the peak areas were typically found to be about 2% and good linearity was obtained for the concentration range tested (up to 1000 microM).
梯度方法在采用电容耦合非接触式电导检测的高效液相色谱测定中的应用,已成功证明适用于非紫外吸收氨基酸以及作为分析物的小肽。洗脱过程中流动相电导率变化所导致的基线漂移,可通过仔细优化流动相组成将其降至最低。在这种条件下,剩余的基线漂移可通过减去空白色谱图或使用色谱数据处理软件包进行基线归一化来校正。反相分离使用含有甲醇或乙腈以及乙酸或三氟乙酸的水性洗脱剂进行。所研究的氨基酸以及二肽和三肽的检测限在1至40微摩尔之间。峰面积的重现性通常约为2%,并且在所测试的浓度范围(高达1000微摩尔)内获得了良好的线性关系。