Department of Anesthesiology, Division of Clinical and Translational Research, Washington University in St. Louis, St. Louis, MO, United States.
J Chromatogr B Analyt Technol Biomed Life Sci. 2013 Nov 15;939:23-31. doi: 10.1016/j.jchromb.2013.09.004. Epub 2013 Sep 8.
A new method using ultra-fast liquid chromatography and tandem mass spectrometry (UFLC-MS/MS) was developed for the simultaneous determination of buprenorphine and the metabolites norbuprenorphine, buprenorphine-3β-glucuronide, and norbuprenorphine-3β-glucuronide in plasma and urine. Sample handling, sample preparation and solid-phase extraction procedures were optimized for maximum analyte recovery. All four analytes of interest were quantified by positive ion electrospray ionization tandem mass spectrometry after solid-phase microextraction. The lower limits of quantification in plasma were 1pg/mL for buprenorphine and buprenorphine glucuronide, and 10pg/mL for norbuprenorphine and norbuprenorphine glucuronide. The lower limits of quantitation in urine were 10pg/mL for buprenorphine, norbuprenorphine and their glucuronides. Overall extraction recoveries ranged from 68-100% in both matrices. Interassay precision and accuracy was within 10% for all four analytes in plasma and within 15% in urine. The method was applicable to pharmacokinetic studies of low-dose buprenorphine.
建立了一种新的超快速液相色谱-串联质谱(UFLC-MS/MS)方法,用于同时测定血浆和尿液中的丁丙诺啡及其代谢物去甲丁丙诺啡、丁丙诺啡-3β-葡糖苷酸和去甲丁丙诺啡-3β-葡糖苷酸。优化了样品处理、样品制备和固相萃取程序,以实现最大分析物回收率。所有四种感兴趣的分析物均采用正离子电喷雾串联质谱法,经固相微萃取后定量。血浆中丁丙诺啡和丁丙诺啡葡糖苷酸的定量下限为 1pg/mL,去甲丁丙诺啡和去甲丁丙诺啡葡糖苷酸的定量下限为 10pg/mL。尿液中丁丙诺啡、去甲丁丙诺啡及其葡糖苷酸的定量下限均为 10pg/mL。在两种基质中,总提取回收率均在 68-100%之间。在血浆中,所有四种分析物的批内精密度和准确度均在 10%以内,在尿液中,均在 15%以内。该方法适用于低剂量丁丙诺啡的药代动力学研究。