首页> 外文会议>American Society for Mass Spectrometry Conference on Mass Spectrometry and Allied Topics >Analysis of Non-steroidal Anti-inflammatory Drugs in Food Matrices by means of HPLC-MS/MS
【24h】

Analysis of Non-steroidal Anti-inflammatory Drugs in Food Matrices by means of HPLC-MS/MS

机译:通过HPLC-MS / MS分析食物基质中的非甾体类抗炎药

获取原文

摘要

Non-steroidal anti-inflammatory drugs (NSAIDs) are a class of medications that provide analgesic and antipyretic (fever-reducing) effects, and, in higher doses, anti-inflammatory effects. The widespread use of NSAIDs has meant that the adverse effects of these drugs have become increasingly prevalent. The two main adverse drug reactions associated with NSAIDs relate to the gastrointestinal (GI) and renal effects of NSAIDs. These effects are dosedependent, and in many cases severe enough to pose the risk of ulcer perforation, upper gastrointestinal bleeding, and death, limiting the use of NSAID therapy. NSAIDs, like all drugs, may interact with other medications. For example, concurrent use of NSAIDs and quinolenes may increase the risk of quinolones' adverse central nervous system effects, including seizure. Most NSAIDs act as nonselective inhibitors of the enzyme cyclooxygenase (COX), inhibiting both the cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) isoenzymes. This inhibition is competitively reversible (albeit at varying degrees of reversibility), as opposed to the mechanism of aspirin, which is irreversible inhibition. COX catalyzes the formation of prostaglandins and thromboxane from arachidonic acid (itself derived from the cellular phospholipid bilayer by phospholipase A2). Prostaglandins act (among other things) as messenger molecules in the process of inflammation. Due to such a danger the necessity for the development of highly sensitive and selective analytical methods for detection of NSAIDs has been appeared. MRLs for NSAIDs are set in EC directives. Here we present the LC-MS method for quantification of NSAID residues in food matrices at the level of 1 ppb.
机译:非甾体抗炎药(NSAIDs)是一类提供镇痛,解热(退烧)作用的药物,并在更高的剂量,抗炎作用。广泛使用NSAID意味着这些药物的不利影响已变得越来越普遍。用的NSAID相关联的两个主要的药物不良反应涉及胃肠(GI)和NSAID的肾功能的影响。这些作用是剂量依赖性的,而且在许多情况下,严重的足以造成溃疡穿孔,上消化道出血和死亡的风险,限制使用NSAID治疗。 NSAIDs的,像所有的药物,可与其他药物相互作用。例如,NSAIDs和quinolenes的同时使用可能会增加的喹诺酮类不良中枢神经系统影响的风险,包括扣押。大多数的NSAID充当酶环加氧酶(COX)的非选择性抑制剂,抑制环氧合酶-1(COX-1)和环氧合酶-2(COX-2)同工酶两者。这种抑制是竞争性可逆的(虽然是在不同程度的可逆性的),相对于阿司匹林的机制,这是不可逆抑制。 Cox催化前列腺素和来自花生素酸的前列腺蛋白的形成(通过磷脂酶A 2从细胞磷脂双层衍生自源自磷脂双层)。前列腺素(尤其是其他事情)作为炎症过程中的信使分子。由于这种危险的必要性的检测NSAIDs的高灵敏度和选择性分析方法的发展已经出现了。对于NSAIDs的最大残留限量是在欧盟指令集。在这里,我们在1ppb以下的电平呈现为在食物基质NSAID残基的定量LC-MS方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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