首页 | 本学科首页   官方微博 | 高级检索  
     检索      

反相离子对高效液相色谱法测定心肌组织中的三磷酸腺苷
引用本文:张燕婉,龙村,史世勇.反相离子对高效液相色谱法测定心肌组织中的三磷酸腺苷[J].色谱,2000,18(4):322-324.
作者姓名:张燕婉  龙村  史世勇
作者单位:中国医学科学院,中国协和医科大学,阜外心血管病医院,北京,100037
摘    要: 采用反相离子对高效液相色谱法测定心肌组织中三磷酸腺苷 (ATP)的含量。样品经高氯酸溶液沉淀蛋白 ,上清液用KOH溶液中和后用反相离子对高效液相色谱法分离测定。色谱柱为SpherisorbODS2柱 ,流动相为甲醇 KH2 PO4缓冲液 (内含 5mmol/LIPR A离子对试剂 ) ,在 2 59nm波长处检测。方法最低检测限为 2mg/L,在 5mg/L~ 1 0 0 mg/L范围内有良好的线性关系 (r=0 9998) ,方法的回收率为 97 8%~ 1 0 4 % ,日内精密度 <4 85% ,日间精密度 <8 81 %。方法准确、灵敏、快速 ,适用于动物和人心肌组织中ATP含量的测定。

关 键 词:反相离子对高效液相色谱法  三磷酸腺苷  心肌组织

Determination of the Adenosine Triphosphate in Myocardial Tissue by Ion-Pair Reversed-Phase High Performance Liquid Chromatography
ZHANG Yan-wan,LONG Cun,SHI Shi-yong.Determination of the Adenosine Triphosphate in Myocardial Tissue by Ion-Pair Reversed-Phase High Performance Liquid Chromatography[J].Chinese Journal of Chromatography,2000,18(4):322-324.
Authors:ZHANG Yan-wan  LONG Cun  SHI Shi-yong
Institution:Fu Wai Hospital for Cardiology, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100037, China.
Abstract:ATP depletion is an important factor contributing to the incomplete recovery of ventricular function following ischemia and reperfusion. A simple and rapid method for determination of adenosine triphosphate(ATP) in myocardial tissue by RP-HPLC was developed. The chromatographic conditions were as follows: Spherisorb ODS2 column, V(40 mmol/L KH2PO4 and 5 mmol/L TBAP):V(methanol) = 74:26 (pH 6.2) mobile phase and UV detector at 259 nm. The ATP in myocardium was extracted with 0.4 mol/L HClO4. The calibration curve showed a good linearity in 5 mg/L-100 mg/L(r = 0.9998). The recovery ranged from 97.8% to 104.1%. The limit of detection was 2 mg/L. The verified results demonstrated that this method is precise, accurate and can be used for determination of ATP in myocardial tissue.
Keywords:ion  pair reversed  phase high performance liquid chromatography  adenosine triphosphate  myocardial tissue
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《色谱》浏览原始摘要信息
点击此处可从《色谱》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号