Pronce T, Tilquin B
Université Catholique de Louvain, Ecole de Pharmacie, Unité d'Analyse Chimique et Physico-Chimique des Médicaments (CHAM 72.30), Bruxelles, Belgium.
J Pharm Biomed Anal. 1996 Jun;14(8-10):1175-84. doi: 10.1016/s0731-7085(96)01746-3.
A Crownpack CR(+) column was used for the highly sensitive quantitation of amino acid enantiomers. The use of a mobile phase of exclusively aqueous perchloric acid enabled the use of low-wavelength UV detection (200 nm) before on-line derivatization with o-phthaldialdehyde for fluorimetric detection. The use of simultaneous UV and fluorimetric detection permitted the simultaneous quantification of the impurity and its parent compound. The method was used for the evaluation of some commercially available amino acid standards. Enantiomeric impurities as low as 0.001% (10 ppm) can be determined in some cases. High precision for the determination of trace levels of D-amino acids in the presence of large amounts of corresponding L-enantiomer is demonstrated.
使用Crownpack CR(+) 柱对氨基酸对映体进行高灵敏度定量分析。仅使用高氯酸水溶液作为流动相,能够在与邻苯二甲醛进行在线衍生化以进行荧光检测之前,采用低波长紫外检测(200 nm)。同时使用紫外和荧光检测可同时对杂质及其母体化合物进行定量。该方法用于评估一些市售氨基酸标准品。在某些情况下,可测定低至0.001%(10 ppm)的对映体杂质。结果表明,在存在大量相应L-对映体的情况下,该方法对痕量D-氨基酸的测定具有很高的精密度。