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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Determination of 1-(3-fluoro-4-hydroxy-5-mercaptomethyltetrahydrofuran-2-yl)-5-methyl-1H-pyrimidine-2,4-dione in rat plasma and urine by high-performance liquid chromatography
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Determination of 1-(3-fluoro-4-hydroxy-5-mercaptomethyltetrahydrofuran-2-yl)-5-methyl-1H-pyrimidine-2,4-dione in rat plasma and urine by high-performance liquid chromatography

机译:通过高效液相色谱法测定大鼠等离子体和尿液中1-(3-氟-4-羟基-5-巯基甲基四氢呋喃-2-甲基-1H-嘧啶-2,4-二酮

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A high-performance liquid chromatographic method using liquid–liquid extraction was developed for the determination of 1-(3-fluoro-4-hydroxy-5-mercaptomethyl-tetrahydrofuran-2-yl)-5-methyl-1H-pyrimidine-2,4-dione (L-FMAUS; I) in rat plasma and urine. A 100 μl aliquot of distilled water containing -cysteine (100 mg/ml) was added to a 100 μl aliquot of biological sample. L-Cysteine was employed to protect binding between the 5'-thiol of I and protein in the biological sample. After vortex-mixing for 30 s and adding a 50 μl aliquot of the mobile phase containing the internal standard (10 μg/ml of 3-aminophenyl sulfone), 1 ml of ethyl acetate was used for extraction. After vortex-mixing, centrifugation, and evaporating the ethyl acetate, the residue was reconstituted with a 100 μl aliquot of the mobile phase. A 50 μl aliquot was injected onto a C18 reversed-phase column. The mobile phases, 50 mM KH_2PO_4 (pH=2.5):acetonitrile (85:15, v/v) for rat plasma and 50 mM KH_2PO_4 (pH 2.5):acetonitrile:methanol (85:10:5, v/v/v) for urine samples, were run at a flow-rate of 1.2 ml/min. The column effluent was monitored by an ultraviolet detector set at 265 nm. The retention times for I and the internal standard were approximately 9.7 and 12.5 min, respectively, in plasma samples and the corresponding values in urine samples were 16.8 and 14.9 min. The quantitation limits of I in rat plasma and urine were 0.1 and 0.5 μg/ml, respectively.
机译:使用液 - 液萃取的高性能液相色谱法用于测定1-(3-氟-4-羟基-5-巯基甲基 - 四氢呋喃-2-基)-5-甲基-1H-嘧啶-2,大鼠血浆和尿液中的4-二酮(L-FMAUS; i)。将100μl含有 - 琥珀酸盐(100mg / ml)的蒸馏水(100mg / ml)加入到100μl等分试样的生物样品中。使用L-半胱氨酸以保护生物样品中5'-硫醇和蛋白质之间的结合。在涡旋混合后30秒并加入含有内标(10μg/ mL的3-氨基苯基砜)的50μl等分试样,使用1ml乙酸乙酯进行萃取。在涡旋混合,离心和蒸发乙酸乙酯后,将残余物用100μL等分试样的流动相重构。将50μL等分试样注入C18反相柱。移动相,50mm KH_2PO_4(pH = 2.5):大鼠等离子体和50mM KH_2PO_4(pH 2.5):乙腈:甲醇(85:10:5,v / v / v)的乙腈(85:15 )对于尿液样品,以1.2mL / min的流速进行。通过在265nm处设定的紫外探测器监测柱流出物。 I的保留时间和内标在等离子体样品中分别为9.7和12.5分钟,尿液样品中的相应值为16.8和14.9分钟。在大鼠等离子体和尿液中I的定量限制分别为0.1和0.5μg/ ml。

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