Belsey Sarah L, Couchman Lewis, Flanagan Robert J
Toxicology Unit, Department of Clinical Biochemistry, King's College Hospital, Bessemer Wing, Denmark Hill, London SE5 9RS, UK
Toxicology Unit, Department of Clinical Biochemistry, King's College Hospital, Bessemer Wing, Denmark Hill, London SE5 9RS, UK.
J Anal Toxicol. 2014 Sep;38(7):438-43. doi: 10.1093/jat/bku060. Epub 2014 Jun 12.
A sensitive liquid chromatographic-high-resolution mass spectrometric (LC-HR-MS) assay for buprenorphine and its urinary metabolites has been developed that requires minimal sample preparation. The results obtained have been compared with those given by (i) cloned enzyme donor immunoassay (CEDIA) and (ii) homogeneous enzyme immunoassay (HEIA) in the analysis of patient urines submitted for buprenorphine analysis. Centrifuged urine (100 µL) was diluted with internal standard solution (25 µL) + LC eluent (875 µL), and 50 µL of the prepared sample were analyzed (Accucore Phenyl-Hexyl column). MS detection was in alternating positive and negative mode using heated electrospray ionization (ThermoFisher Q Exactive). Intra- and inter-assay accuracy and precision were 104-128 and <11%, respectively, at 5 µg/L. Limits of detection were 1.3 µg/L (buprenorphine, norbuprenorphine and buprenorphine glucuronide) and 2.5 µg/L (norbuprenorphine glucuronide). Immunoassay sensitivity and selectivity were 97 and 100% (HEIA) and 99 and 84% (CEDIA), respectively, compared with LC-HR-MS. In 120 patient urines, norbuprenorphine glucuronide was easily the most abundant analyte except when adulteration with buprenorphine had occurred. The median immunoreactive buprenorphine species present (unhydrolysed urine) were 7.5 and 13% for HEIA and CEDIA, respectively. However, codeine, dihydrocodeine, morphine and morphine-3-glucuronide did not interfere in the HEIA assay.
已开发出一种用于丁丙诺啡及其尿液代谢物的灵敏液相色谱 - 高分辨率质谱(LC - HR - MS)分析方法,该方法所需的样品前处理极少。在对提交进行丁丙诺啡分析的患者尿液进行分析时,将所获得的结果与以下两种方法给出的结果进行了比较:(i)克隆酶供体免疫分析(CEDIA)和(ii)均相酶免疫分析(HEIA)。将离心后的尿液(100μL)用内标溶液(25μL)+ LC洗脱液(875μL)稀释,然后对50μL制备好的样品进行分析(Accucore苯基 - 己基柱)。使用加热电喷雾电离(ThermoFisher Q Exactive)以交替正离子和负离子模式进行质谱检测。在5μg/L时,批内和批间准确度分别为104 - 128,精密度分别<11%。检测限为1.3μg/L(丁丙诺啡、去甲丁丙诺啡和丁丙诺啡葡萄糖醛酸苷)和2.5μg/L(去甲丁丙诺啡葡萄糖醛酸苷)。与LC - HR - MS相比,免疫分析的灵敏度和选择性分别为HEIA的97%和100%以及CEDIA的99%和84%。在120份患者尿液中,除非发生丁丙诺啡掺假,去甲丁丙诺啡葡萄糖醛酸苷很容易成为含量最丰富的分析物。对于HEIA和CEDIA,未水解尿液中存在的免疫反应性丁丙诺啡种类的中位数分别为7.5%和13%。然而,可待因、二氢可待因、吗啡和吗啡 - 3 - 葡萄糖醛酸苷在HEIA分析中不产生干扰。