Selander S, Cramér K
Br J Ind Med. 1968 Apr;25(2):139-43. doi: 10.1136/oem.25.2.139.
A method for the determination of lead in urine by means of atomic absorption spectrophotometry (AAS) is described. A combination of wet ashing and extraction with ammonium pyrrolidine dithiocarbamate into butylmethylketone was used. The sensitivity was about 0·02 μg./ml. for 1% absorption, and the detection limit was about 0·02 μg./ml. with an instrumental setting convenient for routine analyses of urines. Using the scale expansion technique, the detection limit was below 0·01 μg./ml., but it was found easier to determine urinary lead concentrations below 0·05 μg./ml. by concentrating the lead in the organic solvent by increasing the volume of urine or decreasing that of the solvent. The method was applied to fresh urines, stored urines, and to urines, obtained during treatment with chelating agents, of patients with lead poisoning. Urines with added inorganic lead were not used. The results agreed well with those obtained with a colorimetric dithizone extraction method (r = 0·989). The AAS method is somewhat more simple and allows the determination of smaller lead concentrations.
本文描述了一种用原子吸收分光光度法(AAS)测定尿中铅的方法。采用湿灰化法,并以吡咯烷二硫代氨基甲酸铵萃取至丁基甲基酮中。对于1%的吸光度,灵敏度约为0·02μg./ml,在便于尿液常规分析的仪器设置下,检测限约为0·02μg./ml。使用量程扩展技术时,检测限低于0·01μg./ml,但发现通过增加尿液体积或减少溶剂体积来浓缩有机溶剂中的铅,更容易测定低于0·05μg./ml的尿铅浓度。该方法应用于新鲜尿液、储存尿液以及铅中毒患者在螯合剂治疗期间获得的尿液。未使用添加无机铅的尿液。结果与用比色双硫腙萃取法得到的结果吻合良好(r = 0·989)。AAS法更为简便一些,并且能够测定更低的铅浓度。