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首页> 外文期刊>Journal of mass spectrometry: JMS >Ultrasensitive method to quantify intracellular zidovudine mono-, di- and triphosphate concentrations in peripheral blood mononuclear cells by liquid chromatography-tandem mass spectrometry
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Ultrasensitive method to quantify intracellular zidovudine mono-, di- and triphosphate concentrations in peripheral blood mononuclear cells by liquid chromatography-tandem mass spectrometry

机译:液相色谱-串联质谱法定量测定外周血单核细胞中细胞内齐多夫定单磷酸,二磷酸和三磷酸的浓度的超灵敏方法

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Although zidovudine (AZT) is not the preferred antiretroviral drug for adult HIV-infected patients, it is still widely used in infants for both prevention of mother-to-infant HIV-1 transmission and treatment of HIV-infected children. However, it is difficult to measure intracellular concentrations of AZT metabolites in small blood samples due to their extremely low concentrations in peripheral blood mononuclear cells and interference by endogenous nucleotide triphosphates, residual plasma phosphates and electrolytes. We developed an ultrasensitive assay using liquid chromatography-tandem mass spectrometry (LC-MS/MS) for measurement of intracellular concentrations of zidovudine (AZT)-monophosphate (AZT-MP), -diphosphate (AZT-DP) and - triphosphate (AZT-TP). The high sensitivity was due to the improvement of peripheral blood mononuclear cells extraction for complete removal of plasma and electrolytes, alkalization of LC buffer and use of alkaline-stable high performance liquid chromatography column and tetrabutylammoniumhydroxide as the ion pair. Using this method, the lower limits of quantification of AZT, AZT-MP, -DP and -TP were 6, 6, 10 and 10 fmol per sample, respectively. Accuracy ranged 89-115% and precision was lower than 15% in the quantification range of 6-6000 fmol/sample for plasma AZT and intracellular AZT-MP and 10-10 000 fmol/sample for AZT-DP and -TP. The validation parameters met the international requirements. Among nine AZT-treated HIV-infected adult patients, five had low AZT-TP levels (< 10fmol/10(6) cells). Our assay has high sensitivity and is advantageous for evaluation of AZT phosphates in children and infants based on minimum blood sampling requirement. Copyright (C) 2015 John Wiley & Sons, Ltd.
机译:尽管齐多夫定(AZT)不是成人HIV感染患者首选的抗逆转录病毒药物,但它仍广泛用于婴儿中,以预防母婴HIV-1传播和治疗HIV感染的儿童。但是,由于小血样中AZT代谢产物在外周血单核细胞中的浓度极低,并且受到内源核苷酸三磷酸,残留血浆磷酸盐和电解质的干扰,因此很难测量其在血浆中的浓度。我们开发了一种使用液相色谱-串联质谱(LC-MS / MS)的超灵敏测定法,用于测量齐多夫定(AZT)-单磷酸盐(AZT-MP),-二磷酸盐(AZT-DP)和-三磷酸盐(AZT- TP)。高灵敏性归因于改善了外周血单核细胞提取以完全去除血浆和电解质,LC缓冲液碱化以及使用碱稳定的高效液相色谱柱和四丁基氢氧化铵作为离子对的改进。使用此方法,每个样品的AZT,AZT-MP,-DP和-TP定量下限分别为6、6、10和10 fmol。血浆AZT和细胞内AZT-MP的定量范围为6-6000 fmol /样品,而​​AZT-DP和-TP的定量范围为10-10 000 fmol /样品,准确度范围为89-115%,精密度低于15%。验证参数符合国际要求。在9例接受AZT治疗的HIV感染的成年患者中,有5例的AZT-TP水平较低(<10fmol / 10(6)细胞)。我们的测定具有很高的灵敏度,并且根据最低的血液采样要求,对于评估儿童和婴儿的AZT磷酸盐具有优势。版权所有(C)2015 John Wiley&Sons,Ltd.

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