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高效液相色谱-电喷雾串联质谱法同时测定大鼠肝组织中腺嘌呤核苷酸、磷酸肌酸和肌酸

Simultaneous determination of adenine nucleotides, creatine phosphate and creatine in rat liver by high performance liquid chromatography-electrospray ionization-tandem mass spectrometry.

机构信息

West China School of Public Health, Sichuan University, No. 17, Section 3, South Renmin Road, Chengdu, Sichuan 610041, People's Republic of China.

出版信息

J Pharm Biomed Anal. 2012 Jul;66:258-63. doi: 10.1016/j.jpba.2012.03.027. Epub 2012 Mar 24.

DOI:10.1016/j.jpba.2012.03.027
PMID:22494519
Abstract

A high performance liquid chromatography-electrospray ionization-tandem mass spectrometric method (HPLC-ESI-MS/MS) was developed for simultaneous determination of adenosine 5'-triphosphate (ATP), adenosine 5'-diphosphate (ADP), adenosine 5'-monophosphate (AMP), creatine phosphate (CP), and creatine in rat liver. After extraction with pre-cooled (4 °C) methanol/water (1:1, v/v), the analytes were separated on a porous graphitic carbon (Hypercarb) column (2.1 mm × 150 mm, 5 μm) using a programmed gradient elution with a mobile phase consisting of 2 mmol/L ammonium acetate in water and 2 mmol/L ammonium acetate in acetonitrile (pH=10.0). The analytes were detected in a way of multiple reaction monitoring (MRM) under negative scan mode by a triple quadrupole mass spectrometer with electrospray ionization (ESI). An external calibration method with linear ranges from 10 to 5000 ng/mL for the five target compounds was used for quantification with a correlation coefficients≥0.9973. The limits of detection and limits of quantification for all analytes were in ranges from 0.50 to 1.5 ng/mL and 1.6 to 0.5 ng/mL, respectively. The average recoveries spiked in three levels were from 77.2% to 102% and precisions expressed in RSDs were from 0.2% to 4.8%. The established method was successfully applied to determination of ATP, ADP, AMP, CP and creatine in liver tissue.

摘要

建立了一种高效液相色谱-电喷雾串联质谱(HPLC-ESI-MS/MS)法,用于同时测定大鼠肝组织中的腺苷 5'-三磷酸(ATP)、腺苷 5'-二磷酸(ADP)、腺苷 5'-一磷酸(AMP)、磷酸肌酸(CP)和肌酸。经预冷(4°C)甲醇/水(1:1,v/v)提取后,采用梯度洗脱程序,以含 2 mmol/L 乙酸铵的水和含 2 mmol/L 乙酸铵的乙腈(pH=10.0)为流动相,在多孔石墨碳(Hypercarb)柱(2.1 mm×150 mm,5 μm)上进行分离。采用电喷雾(ESI)负扫描模式的多重反应监测(MRM)方式对分析物进行检测。采用外标法进行定量,五个目标化合物的线性范围为 10-5000 ng/mL,相关系数≥0.9973。所有分析物的检测限和定量限范围分别为 0.50-1.5 ng/mL 和 1.6-0.5 ng/mL。三种浓度水平的平均回收率为 77.2%-102%,相对标准偏差(RSD)表示的精密度为 0.2%-4.8%。该方法成功应用于肝组织中 ATP、ADP、AMP、CP 和肌酸的测定。

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