Clark Shona, Francis Paul S, Conlan Xavier A, Barnett Neil W
School of Life and Environmental Sciences, Deakin University, Geelong, Victoria 3217, Australia.
J Chromatogr A. 2007 Aug 17;1161(1-2):207-13. doi: 10.1016/j.chroma.2007.05.085. Epub 2007 Jun 2.
A high-performance liquid chromatography (HPLC) method for the determination of urea that incorporates automated derivatisation with xanthydrol (9H-xanthen-9-ol) is described. Unlike the classic xanthydrol approach for the determination of urea, which involves the precipitation of dixanthylurea (N,N'-di-9H-xanthen-9-ylurea), the derivatisation procedure employed in this method produces N-9H-xanthen-9-ylurea, which remains in solution and can be quantified using fluorescence detection (lambda(ex)=213 nm; lambda(em)=308 nm) after chromatographic separation from interferences. The limit of detection for urea was 5 x 10(-8) M (0.003 mg L(-1)). This method was applied to the determination of urea in human and animal urine and in wine.
描述了一种采用与呫吨醇(9H-呫吨-9-醇)自动衍生化的高效液相色谱(HPLC)法测定尿素。与经典的呫吨醇法测定尿素不同,经典方法涉及二呫吨基脲(N,N'-二-9H-呫吨-9-基脲)沉淀,而该方法采用的衍生化程序生成N-9H-呫吨-9-基脲,其保留在溶液中,在与干扰物进行色谱分离后,可使用荧光检测(激发波长λ(ex)=213 nm;发射波长λ(em)=308 nm)进行定量。尿素的检测限为5×10(-8) M(0.003 mg L(-1))。该方法应用于人和动物尿液及葡萄酒中尿素的测定。