Ackermans M T, Ruiter A F, Endert E
Laboratory of Endocrinology and Radiochemistry, Academic Medical Centre, Amsterdam, 1105 AZ, The Netherlands.
Anal Biochem. 1998 Apr 10;258(1):80-6. doi: 10.1006/abio.1997.2535.
An analytical method is presented to determine glycerol concentrations and stable isotope tracer enrichments in human plasma after intravenous tracer infusion in a single analytical run, using gas chromatography coupled to mass spectrometry. The method uses an internal standard, which is also a stable isotope labeled form of glycerol. Three substances were tested as model compounds viz. [2-13C]glycerol, and [1,2,3-13C3]glycerol, and [1,1,2,3, 3-2H5]glycerol. Any combination of two can be used (one as internal standard, one as tracer), even if overlapping of the mass spectra occurs. The method is precise (recovery of spiked glycerol and tracer are, respectively, 99.7 and 99.8%) and reproducible (intraassay variation <1.5%, interassay variation <6%) and needs only a small amount of plasma (100 microl).
本文介绍了一种分析方法,可在单次分析运行中,通过气相色谱-质谱联用技术测定静脉注射示踪剂后人体血浆中的甘油浓度和稳定同位素示踪剂富集情况。该方法使用内标物,其也是甘油的稳定同位素标记形式。测试了三种物质作为模型化合物,即[2-¹³C]甘油、[1,2,3-¹³C₃]甘油和[1,1,2,3,3-²H₅]甘油。即使质谱发生重叠,也可使用任意两种物质的组合(一种作为内标物,一种作为示踪剂)。该方法精确(加标甘油和示踪剂的回收率分别为99.7%和99.8%)且可重复(批内变异<1.5%,批间变异<6%),且仅需少量血浆(100微升)。