Kacinko Sherri L, Jones Hendree E, Johnson Rolley E, Choo Robin E, Concheiro-Guisan Marta, Huestis Marilyn A
Chemistry and Drug Metabolism, Intramural Research Program, National Institute on Drug Abuse, NIH, Baltimore, MD, USA.
Clin Chem. 2009 Jun;55(6):1177-87. doi: 10.1373/clinchem.2008.113712. Epub 2009 Mar 26.
Buprenorphine (BUP) is under investigation as a medication therapy for opioid-dependent pregnant women. We investigated BUP and metabolite disposition in urine from women maintained on BUP during the second and third trimesters of pregnancy and postpartum.
We measured BUP, norbuprenorphine (NBUP), buprenorphine glucuronide (BUP-Gluc), and NBUP-Gluc concentrations in 515 urine specimens collected thrice weekly from 9 women during pregnancy and postpartum. Specimens were analyzed using a fully validated liquid chromatography-mass spectrometry method with limits of quantification of 5 microg/L for BUP and BUP-Gluc and 25 microg/L for NBUP and its conjugated metabolite. We examined ratios of metabolites across trimesters and postpartum to identify possible changes in metabolism during pregnancy.
NBUP-Gluc was the primary metabolite identified in urine and exceeded BUP-Gluc concentrations in 99% of specimens. Whereas BUP-Gluc was identified in more specimens than NBUP, NBUP exceeded BUP-Gluc concentrations in 77.9% of specimens that contained both analytes. Among all participants, the mean BUP-Gluc:NBUP-Gluc ratio was significantly higher in the second trimester compared to the third trimester, and there were significant intrasubject differences between trimesters in 71% of participants. In 3 women, the percent daily dose excreted was higher during pregnancy than postpregnancy, consistent with other data indicating increased renal elimination of drugs during pregnancy.
These data are the first to evaluate urinary disposition of BUP and metabolites in a cohort of pregnant women. Variable BUP excretion during pregnancy may indicate metabolic changes requiring dose adjustment during later stages of gestation.
丁丙诺啡(BUP)作为一种用于阿片类药物依赖孕妇的药物疗法正在接受研究。我们调查了妊娠中期和晚期以及产后维持使用BUP的女性尿液中丁丙诺啡及其代谢物的情况。
我们测量了9名女性在孕期和产后每周三次采集的515份尿液样本中丁丙诺啡(BUP)、去甲丁丙诺啡(NBUP)、丁丙诺啡葡萄糖醛酸苷(BUP-Gluc)和去甲丁丙诺啡葡萄糖醛酸苷(NBUP-Gluc)的浓度。使用经过充分验证的液相色谱-质谱法对样本进行分析,丁丙诺啡和丁丙诺啡葡萄糖醛酸苷的定量限为5微克/升,去甲丁丙诺啡及其结合代谢物的定量限为25微克/升。我们检查了各孕期和产后代谢物的比例,以确定孕期代谢可能发生的变化。
NBUP-Gluc是尿液中鉴定出的主要代谢物,在99%的样本中超过BUP-Gluc的浓度。虽然鉴定出BUP-Gluc的样本比NBUP多,但在同时含有两种分析物的样本中,77.9%的样本中NBUP超过BUP-Gluc的浓度。在所有参与者中,与妊娠晚期相比,妊娠中期BUP-Gluc:NBUP-Gluc的平均比值显著更高,71%的参与者在不同孕期之间存在显著的个体内差异。在3名女性中,孕期排泄的每日剂量百分比高于产后,这与其他表明孕期肾脏药物清除增加的数据一致。
这些数据首次评估了一组孕妇尿液中丁丙诺啡及其代谢物的情况。孕期丁丙诺啡排泄的变化可能表明代谢发生了改变,需要在妊娠后期调整剂量。