Furuya E
Am J Clin Pathol. 1975 Sep;64(3):315-26. doi: 10.1093/ajcp/64.3.315.
In the determination of urinary 17-hydroxycorticosteroids, the urine is saturated with NaHSO3 after hydrolysis with beta-glucuronidase and then extracted with methylene chloride. Sodium bisfulfite removes almost all non-steroidal impurities in the urines from patients medicated with acetylspiramycin, leucomycin, erythromycin, triacetylolenadomycin, rifampicin and tranquilizers such as chlorpromazine, which interfere with the absorption at 410 nm. in the subsquent Porter-Silber reaction. In order to increase the specificity of a routine method, a procedure conducted by Allen has been often employed: The sum of 370- and 450-nm. absorbances is subtracted from twice absorbance at 410 nm. However, the procedure could not be used in the medicated urines mentioned above, because the spectral absorption curve of these drugs and their metabolites in the Porter-Silber reaction was not a straight but a strongly convex or concave line in the 370-450-nm. range. Using the present method, interference with the Porter-Silber reaction was not found in the urines from patients medicated with chloramphenicol, minocycline, chlordiazepoxide, meprobamate, methyprylon, nitrazepam, synthetic penicillins such as hetacillin, oxacillin and cloxacillin, or cephalosporins such as cephalexin and cephalothin. However, to obtain correct values in urines from patients medicated with spironolactone, it was necessary to subject the urines to treatment with methylene chloride before enzyme hydrolysis.
在测定尿17-羟皮质类固醇时,尿液先用β-葡萄糖醛酸酶水解,然后用亚硫酸氢钠饱和,再用二氯甲烷萃取。亚硫酸氢钠可去除服用乙酰螺旋霉素、柱晶白霉素、红霉素、三乙酰竹桃霉素、利福平以及氯丙嗪等镇静剂的患者尿液中几乎所有的非甾体杂质,这些杂质会干扰后续波特-西尔伯反应中410nm处的吸光度。为提高常规方法的特异性,常采用艾伦的方法:从410nm处吸光度的两倍中减去370nm和450nm处吸光度之和。然而,上述用药后的尿液不能采用该方法,因为这些药物及其代谢产物在波特-西尔伯反应中的光谱吸收曲线在370 - 450nm范围内不是直线,而是强烈的凸线或凹线。采用本方法时,服用氯霉素、米诺环素、氯氮卓、甲丙氨酯、甲乙哌酮、硝西泮、海他西林、苯唑西林和氯唑西林等合成青霉素或头孢氨苄和头孢噻吩等头孢菌素的患者尿液中未发现对波特-西尔伯反应有干扰。然而,为了获得服用螺内酯患者尿液的正确值,在酶水解前必须先用二氯甲烷对尿液进行处理。