Schmidt M, Eisenburg J, Huger F
Fortschr Med. 1977 Mar 17;95(11):727-33.
A rapid method for quantitative determination of concentration of urobilinoids of fresh urine was developed. The method is based upon extraction of urinary urobilinoids using a mixture of acetic acid and ether and followed by the extraction of the ethereal phase with Ehrlich reagent and a solution of sodium acetate. Readings of absorbance from the absorption band of reaction products from urobilinoids and Ehrlich reagent are done. Performance of the rapid method: 2 ml urine + 10 ml ether + 2 ml acetic acid were thoroughly mixed for about 15 seconds. The ethereal extract was shaken after addition of 12 ml Ehrlich-reagent for 1 minute and 15 ml half-saturated sodium acetate solution were added. 0-3 minutes afterwards reading of absorption at 560 nm respectively filter Hg 578 nm. Photometer:mg/dl=29 X A578 nm, 1 cm -0,4. Spectrophotometer:mg/dl urobilinoids=13,7 X A560 nm X 1/d -0,22 (d=optical pathway). Photometrical determination of concentration of urobilinoid can also be done using table 1. Accuracy, reproducibility and specificity are fully satisfying for clinical use of the method.
建立了一种快速定量测定新鲜尿液中尿胆素原浓度的方法。该方法基于用乙酸和乙醚的混合物提取尿中尿胆素原,然后用埃利希试剂和乙酸钠溶液萃取醚相。读取尿胆素原与埃利希试剂反应产物吸收带的吸光度。快速方法的操作:将2ml尿液 + 10ml乙醚 + 2ml乙酸充分混合约15秒。加入12ml埃利希试剂后,将醚提取物振荡1分钟,然后加入15ml半饱和乙酸钠溶液。0 - 3分钟后分别在560nm处读取吸光度,滤光片汞灯578nm。光度计:mg/dl = 29×A578nm,1cm - 0.4。分光光度计:尿胆素原mg/dl = 13.7×A560nm×1/d - 0.22(d = 光路)。也可使用表1进行尿胆素原浓度的光度测定。该方法的准确性、重现性和特异性完全满足临床使用要求。