首页> 外文OA文献 >Automated method for the determination of a new matrix metalloproteinase inhibitor in ovine plasma and serum by coupling of restricted access material for on-line sample clean-up to liquid chromatography
【2h】

Automated method for the determination of a new matrix metalloproteinase inhibitor in ovine plasma and serum by coupling of restricted access material for on-line sample clean-up to liquid chromatography

机译:限制进样的在线进样与液相色谱耦合的自动测定羊血浆和血清中新型基质金属蛋白酶抑制剂的方法

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

A fully automated liquid chromatographic method was developed for the determination of Ro 28-2653, a new synthetic inhibitor of matrix metalloproteinases (MMPs), in ovine serum and plasma. The method was based on the coupling of a pre-column packed with restricted access material, namely LiChrospher RP-8 ADS (alkyl diol silica), for sample clean-up to an analytical column containing octyl silica stationary phase. One hundred mul of biological sample, to which 2-propanol was automatically added, were injected onto the ADS pre-column, which was then washed with a washing liquid consisting of a mixture of 25 mM phosphate buffer (pH 7.0) and acetonitrile (90: 10; v/v) for 10 min. By rotation of the switching valve, the analyte was then eluted in the back-flush mode with the LC mobile phase composed of a mixture of acetonitrile and 25 mM phosphate buffer (pH 7.0) (57:43; v/v). The UV detection was performed at 395 nm. The main parameters likely to influence the sample preparation technique were investigated. The method was then validated over a concentration range from 17.5 to 1950 ng/mI, the first concentration level corresponding to the lower limit of quantitation. At this concentration level, the mean bias and the R.S.D. value for intermediate precision were -2.4% and 4.2%, respectively. (C) 2004 Elsevier B.V. All rights reserved.
机译:开发了一种全自动液相色谱方法,用于测定绵羊血清和血浆中新型的基质金属蛋白酶(MMPs)合成抑制剂Ro 28-2653。该方法基于填充有限制进入材料的预柱(即LiChrospher RP-8 ADS(烷基二醇二氧化硅))的耦合,以将样品净化至包含辛基二氧化硅固定相的分析柱。将100摩尔自动添加了2-丙醇的生物样品注入ADS预色谱柱,然后将其用由25 mM磷酸盐缓冲液(pH 7.0)和乙腈(90的混合物)组成的洗涤液洗涤:10; v / v)10分钟。通过旋转切换阀,然后将分析物以由乙腈和25 mM磷酸盐缓冲液(pH 7.0)(57:43; v / v)组成的LC流动相以反吹模式洗脱。 UV检测在395nm下进行。研究了可能影响样品制备技术的主要参数。然后在17.5至1950 ng / ml的浓度范围内验证了该方法,第一浓度水平对应于定量下限。在此浓度水平下,平均偏差和R.S.D.中等精度值分别为-2.4%和4.2%。 (C)2004 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号