首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Determination of para-aminohippuric acid (PAH) in human plasma and urine by liquid chromatography-tandem mass spectrometry
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Determination of para-aminohippuric acid (PAH) in human plasma and urine by liquid chromatography-tandem mass spectrometry

机译:液相色谱-串联质谱法测定人血浆和尿液中的对氨基马尿酸(PAH)

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摘要

In this manuscript, we present a simple and reliable method for the quantitation of para-aminohippuric acid (PAH; 2-(4-aminobenzamido)acetic acid) in human plasma and urine using liquid chromatography coupled to electrospray ionisation low-energy collision-induced dissociation tandem mass spectrometry (HPLC-ESI-CID-MS/MS) analysis (negative ion mode) via multiple reaction monitoring (MRM). Sample preparation involved protein precipitation of plasma samples with acetonitrile and subsequent dilution of urine samples with the mobile phase. The internal standard (IS) adopted was para-aminosalicylic acid (PAS; 4-amino-2-hydroxybenzoic acid). Chromatographic separation was achieved on a Cosmosil HILIC column using an isocratic mobile phase consisting of ammonium acetate buffer (20 mM) and acetonitrile (45:55, v/v) at a flow rate of 200 mu l/min. The transactions monitored were m/z 192.9 -> 149.1 for PAH and m/z 152.1 -> 108.1 for IS. Linear calibration curves were generated over the PAH concentration range of 0.2-100 mg/L in human plasma and urine. The method was validated for selectivity, accuracy, precision, recovery and stability according to USFDA criteria, and has been successfully applied to a pharmacokinetic study in healthy volunteers administered an intravenous dose of 440 mg PAH.
机译:在本手稿中,我们提出了一种简单可靠的方法,采用液相色谱与电喷雾电离低能碰撞诱导的定量方法,可定量测定人血浆和尿液中的对氨基马尿酸(PAH; 2-(4-氨基苯甲酰胺基)乙酸)通过多反应监测(MRM)进行解离串联质谱(HPLC-ESI-CID-MS / MS)分析(负离子模式)。样品制备涉及用乙腈沉淀血浆样品的蛋白质,然后用​​流动相稀释尿液样品。所采用的内标(IS)为对氨基水杨酸(PAS; 4-氨基-2-羟基苯甲酸)。在Cosmosil HILIC色谱柱上,使用由乙酸铵缓冲液(20 mM)和乙腈(45:55,v / v)组成的等度流动相,以200μl/ min的流速进行色谱分离。对于PAH,监视的事务为m / z 192.9-> 149.1,对于IS,m / z 152.1-> 108.1。在人血浆和尿液中PAH浓度在0.2-100 mg / L范围内产生线性校准曲线。该方法已根据USFDA标准进行了选择性,准确性,精密度,回收率和稳定性验证,已成功应用于健康志愿者静脉注射440 mg PAH的药代动力学研究。

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