• 首页期刊简介编委会刊物订阅专栏专刊电子刊学术动态联系我们English
引用本文:陈晓红.HPLC-FLD同时测定全血中加替沙星和莫西沙星含量[J].中国现代应用药学,2009,(5):412-414.
CHEN Xiaohong.Determination of Gatifloxacin and Moxifloxacin in Whole Blood by HPLC Coupled with Fluorescence Detection[J].Chin J Mod Appl Pharm(中国现代应用药学),2009,(5):412-414.
【打印本页】   【HTML】   【下载PDF全文】   查看/发表评论  【EndNote】   【RefMan】   【BibTex】
←前一篇|后一篇→ 过刊浏览    高级检索
本文已被:浏览 2079次   下载 1377 本文二维码信息
码上扫一扫!
分享到: 微信 更多
HPLC-FLD同时测定全血中加替沙星和莫西沙星含量
陈晓红
作者单位
陈晓红  
摘要:
目的建立一种灵敏、可靠的全血中加替沙星和莫西沙星的高效液相色谱荧光检测方法。方法样品经磷酸盐缓冲液提取后,用Waters Oasis MAX 小柱进行净化,甲醇-乙腈-0.2%甲酸(15∶15∶70)为流动相,采用Cloversil - C18柱(3.0 mm ×150 mm, 5 μm)分离,荧光检测波长:λex 288 nm和λem 493 nm,内标法定量。结果加替沙星和莫西沙星在15.0~240.0 μg·L-1内呈良好线性,方法回收率在97.7%~101.3% 之间,日内RSD<6.0%,其定量限为15.0 μg·L-1。结论本方法简便、灵敏、干扰少,特异性好,能满足血液中加替沙星和莫西沙星的检测要求。
关键词:  高效液相色谱-荧光法  全血  加替沙星  莫西沙星
DOI:
分类号:
基金项目:
Determination of Gatifloxacin and Moxifloxacin in Whole Blood by HPLC Coupled with Fluorescence Detection
CHEN Xiaohong
Abstract:
OBJECTIVE To develop a sensitive and accurate method for the determination of gatifloxacin and moxifloxacin in whole blood by high-performance liquid chromatography coupled with fluorescence detection(HPLC-FLD). METHODS After gatifloxacin and moxifloxacin in whole blood were extracted by phosphate buffer, the sample was cleaned with solid-phase extraction (SPE) using Oasis MAX cartridges.The separation was performed on Cloversil - C18 column(3.0 mm ×150 mm, 5 μm)using the mobile phase consisting of methanol-acetonitrile-0.2% formic acid(15∶15∶70).Detection was carried out on a fluorescence detection at λex 288 nm and λem 493 nm. RESULTS Calibration curves were linear within the range of 15.0-240.0 μg·L-1, and the extraction recoveries were from 97.7% to 101.3%, the RSDs were less than 6.0%.The limits of quantification were found to be 15.0 μg·L-1.CONCLUSION This method is found to be simple,sensitive,little interferential and good specificity for the determination of gatifloxacin and moxifloxacin in whole blood.
Key words:  HPLC-FLD  whole blood  gatifloxacin  moxifloxacin
扫一扫关注本刊微信