Morris M E, Levy G
J Pharm Sci. 1983 Jun;72(6):612-7. doi: 10.1002/jps.2600720609.
Two high-performance liquid chromatographic (HPLC) assay procedures were developed for the determination of salicylamide and its metabolites in serum, urine, and saliva. One method involves reverse-phase ion-pair chromatography and UV detection, and is used to determine salicylamide, salicylamide glucuronide, and salicylamide sulfate. The other method, with a different mobile phase and without the ion-pairing reagent, is used to determine gentisamide (the hydroxylated metabolite of salicylamide), gentisamide glucuronide, and gentisamide sulfate. The assays are performed by direct injection of the sample after protein precipitation with ethanol containing the internal standard. Increased sensitivity for the determination of low concentrations of salicylamide is obtained by organic extraction of this drug from serum or saliva. Calibration curves for the conjugates of salicylamide and gentisamide were obtained, in the absence of authentic standards, by partial enzymatic hydrolysis, using the decrease of the conjugate peaks and the concomitant increase of free salicylamide or gentisamide concentrations to determine peak area ratio-concentration relationships. Application of the HPLC assay procedures to the determination of salicylamide excretion products in the urine of three normal human subjects resulted in 98.6% (range:97.1-100.1%) recovery of a 1-g oral dose of the drug. All five metabolites of salicylamide were found in urine, but only salicylamide glucuronide, salicylamide sulfate, and gentisamide glucuronide were found consistently and in appreciable quantities. Salicylamide and all of its metabolites except gentisamide sulfate were found in human and rat serum, and unconjugated salicylamide as well as gentisamide were found in human saliva.
开发了两种高效液相色谱(HPLC)分析方法,用于测定血清、尿液和唾液中的水杨酰胺及其代谢物。一种方法涉及反相离子对色谱法和紫外检测,用于测定水杨酰胺、水杨酰胺葡萄糖醛酸苷和水杨酰胺硫酸盐。另一种方法使用不同的流动相且不使用离子对试剂,用于测定龙胆酰胺(水杨酰胺的羟基化代谢物)、龙胆酰胺葡萄糖醛酸苷和龙胆酰胺硫酸盐。分析通过用含内标的乙醇进行蛋白质沉淀后直接进样来进行。通过从血清或唾液中有机萃取该药物,可提高低浓度水杨酰胺测定的灵敏度。在没有真实标准品的情况下,通过部分酶促水解获得水杨酰胺和龙胆酰胺结合物的校准曲线,利用结合物峰的降低和游离水杨酰胺或龙胆酰胺浓度的相应增加来确定峰面积比-浓度关系。将HPLC分析方法应用于三名正常人类受试者尿液中水杨酰胺排泄产物的测定,1 g口服剂量药物的回收率为98.6%(范围:97.1 - 100.1%)。在尿液中发现了水杨酰胺的所有五种代谢物,但仅始终一致且大量发现了水杨酰胺葡萄糖醛酸苷、水杨酰胺硫酸盐和龙胆酰胺葡萄糖醛酸苷。在人和大鼠血清中发现了水杨酰胺及其除龙胆酰胺硫酸盐外的所有代谢物,在人唾液中发现了未结合的水杨酰胺以及龙胆酰胺。