首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Simultaneous determination of triptolide, tripdiolide and tripterine in human urine by high-performance liquid chromatography coupled with ion trap atmospheric-pressure chemical ionization mass spectrometry.
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Simultaneous determination of triptolide, tripdiolide and tripterine in human urine by high-performance liquid chromatography coupled with ion trap atmospheric-pressure chemical ionization mass spectrometry.

机译:高效液相色谱-离子阱大气压化学电离质谱联用同时测定人尿中雷公藤内酯醇,雷公藤内酯和雷公藤碱的含量。

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摘要

An accurate and selective method for the simultaneous determination of triptolide, tripdiolide and tripterine in human urine using hydrocortisone as an internal standard (IS) by high-performance liquid chromatography coupled with atmospheric-pressure chemical ionization mass spectrometry in negative ion mode has been developed. After triptolide, tripdiolide and tripterine in human urine were extracted with ethyl acetate and cleaned by solid-phase extraction with C(18) cartridges, a satisfactory separation was achieved on an XDB C(18) short column (30 x 2.1 mm i.d., 3 microm) using the mobile phase of acetic acid-ammonium acetate (5 mmol/L, pH = 4.5)-acetonitrile-methanol in gradient elution. Detection was operated by APCI in selected ion monitoring mode. The target ions m/z 359, m/z 375, m/z 449 and m/z 419 were selected for the quantification of triptolide, tripdiolide, tripterine and IS, respectively. The linear range was 1.0-100.0 ng mL(-1), and the limits of quantification in human urine were foundto be 0.1-0.5 ng mL(-1) for the three compounds. The precisions (CV%) and accuracies were 6.6-12.9 and 85.1-97.0%, respectively. The developed method could be applied to the determination of triptolide, tripdiolide and tripterine in human urine for diagnosis of the intoxication and for forensic purposes.
机译:建立了一种以氢化可的松为内标(IS)的高效液相色谱-负离子模式大气压化学电离质谱联用同时测定人尿中雷公藤内酯醇,雷公藤内酯和雷公藤碱的准确,选择性的方法。用乙酸乙酯萃取雷公藤内酯,雷公藤内酯和雷公藤碱后,用乙酸乙酯萃取,并用C(18)柱通过固相萃取进行清洗,在XDB C(18)短柱(30 x 2.1 mm内径,3乙酸-乙酸铵(5 mmol / L,pH = 4.5)-乙腈-甲醇的流动相进行梯度洗脱。通过APCI在选定的离子监测模式下进行检测。选择目标离子m / z 359,m / z 375,m / z 449和m / z 419分别对雷公藤内酯醇,雷公藤内酯,雷公藤碱和IS进行定量。线性范围为1.0-100.0 ng mL(-1),发现这三种化合物在人尿中的定量限为0.1-0.5 ng mL(-1)。精度(CV%)和准确度分别为6.6-12.9和85.1-97.0%。所开发的方法可用于测定人尿中雷公藤内酯醇,雷公藤内酯和雷公藤碱的含量,以用于中毒诊断和法医鉴定。

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