Begley D J, Reichel A, Ermisch A
Biomedical Sciences Division, King's College London, UK.
J Chromatogr B Biomed Appl. 1994 Jul 1;657(1):185-91. doi: 10.1016/0378-4347(94)80085-5.
The quantitation of 16 acidic, basic, small and large neutral amino acids was performed using 10-microliters sample aliquots of cisternal cerebrospinal fluid (CSF) and blood plasma of rats. The analytical technique is based upon a two-buffer HPLC system with fluorimetric detection of pre-column derivatized primary amino acids with o-phthaldialdehyde (OPA). A modification of a well established method, the power of the present technique comes from an improved resolution and sensitivity by installing a column heater adjusted to 43 degrees C and strictly reducing any contamination by background amino acids. The analysis is simplified by separating the amino acid derivatives with a linear buffer gradient and less time consuming by the use of a short analytical column with a higher flow-rate. Analytical precision, linearity of response and reproducibility were highly acceptable at both CSF and plasma concentrations of amino acids without changing any of the separation or detection parameters.
使用大鼠脑池脑脊液(CSF)和血浆的10微升等分试样对16种酸性、碱性、小分子和大分子中性氨基酸进行定量分析。该分析技术基于双缓冲高效液相色谱系统,采用邻苯二甲醛(OPA)对柱前衍生的伯氨基酸进行荧光检测。作为一种成熟方法的改进,本技术的优势在于通过安装调节至43摄氏度的柱加热器提高了分辨率和灵敏度,并严格减少了背景氨基酸的污染。通过线性缓冲液梯度分离氨基酸衍生物简化了分析过程,使用短分析柱和更高流速减少了分析时间。在脑脊液和血浆氨基酸浓度下,分析精度、响应线性和重现性均高度可接受,且无需改变任何分离或检测参数。