用DPPH自由基清除法研究吡啶甜菜碱的抗氧化活性

Malki Fatiha, Touati Abdelkader
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引用次数: 15

摘要

自由基引起各种人类疾病抗氧化剂是一种消除自由基的物质,并作为防御自由基在体内的作用的因素。抗氧化剂在预防自由基引起的疾病中起着重要作用,并通过降低自由基的浓度来系统地降低其风险它们的作用是抑制起始和增殖步骤,导致反应结束并延缓氧化过程在生物系统中,抗氧化剂具有多种功能,例如,它通过参与主要的细胞信号传导途径和防止活性氧(ROS)引起的细胞损伤来防御氧化损伤。因此,食用抗氧化剂和在食品材料中添加抗氧化剂可以保护身体和食物免受氧化变质许多评估特定化合物抗氧化活性的方法已经被描述,但最广泛记录的是2,2 -二苯基-1-吡啶肼基自由基(DPPH)。6-9 DPPH是一种稳定的自由基,接受电子或氢成为稳定的抗磁性分子。在DPPH自由基清除试验中,抗氧化剂与DPPH反应,并将其转化为黄色的二苯基吡啶肼。褪色程度间接证明了抗氧化剂清除自由基的能力通过517 nm处吸光度的下降来评价抗氧化剂对DPPH自由基的还原作用。抗氧化剂对DPPH自由基吸光度的降低是由于抗氧化剂分子与自由基进程发生反应,自由基被供氢清除所致文献中提供的DPPH测试基于BrandWilliams等人所描述的相同原理8,但分析方案在几个参数上有所不同。对DPPH法测定自由基清除活性的方法和改进的评价表明,影响重现性的主要因素是溶剂、反应时间、样品与试剂的比以及测定反应混合物脱色吸光度的波长因此,这些因素显然对所测化合物的自由基清除活性具有重要意义。吡啶甜菜碱是一类介离子化合物,作为具有生物活性的化合物引起了人们极大的兴趣由于在其结构中存在嘧啶环,吡啶甜菜碱仍然是一类重要的生物活性杂环化合物。文献表明,具有嘧啶核的化合物具有广泛的生物活性。由于其显著的药理活性,对嘧啶衍生物的深入研究一直集中在其活性上,从而构成了制药工业的一个组成部分
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Study of antioxidant activity of pyrimidinium betaines by DPPH radical scavenging method
Free radicals cause various human diseases.1 Antioxidants are substances that eliminate free radicals and serve as a defensive factor against their effects in the body. Antioxidants play an important role in the prevention of diseases induced by free radicals2 and systematically reduce their risk by reducing their concentrations.3 They act by inhibiting the initiation and propagation steps, resulting in the end of the reaction and delaying the oxidation process.4 In biological systems, antioxidants have multiple functions, eg it defends against oxidative damage by participating in the main cell signaling pathways and by preventing cell damage caused by the action of reactive oxygen species (ROS). Therefore, antioxidant consumption and the addition of antioxidant in food materials protect the body as well as food from deterioration of oxidation.5 Numerous methods to evaluate the antioxidant activity of specific compounds have been described, but the most widely documented relates to the 2, 2-diphenyl-1-picrylhydrazyl radical (DPPH).6–9 DPPH is stable free radical that accepts an electron or hydrogen to become a stable diamagnetic molecule. In the DPPH radical-scavenging assay, antioxidants react with DPPH, and convert it to yellowcolored diphenylpicrylhydrazine. The color fading extent proves indirectly the radical-scavenging capacity of the antioxidant.6 The reduction of DPPH radical by antioxidants is evaluated by the decrease in absorbance at 517 nm. The decrease in absorbance of DPPH radical caused by antioxidants is due to the reaction between antioxidant molecules and radical progress which results in the scavenging of the radical by hydrogen donation.10 The DPPH tests provided in the literature are based on the same principle as described by BrandWilliams et al.,8 but the analytical protocols differ in several parameters. Evaluation of the methods and modifications for determination of the radical scavenging activity by DPPH shows that the main factors influenced the reproducibility are the solvent, duration of the reaction, sample to reagent ratio and the wave length for absorbance measurement of the decolouration of the reaction mixture.11 Therefore, it is obvious that these factors are of significance for the radical scavenging activity of the tested compounds. Pyrimidinium betaines constitute a class of mesoionic compounds12 which have raised much interest as biologically active compounds.13 Pyrimidinium betaines remain an important class of bioactive heterocyclics due to the presence of the pyrimidine ring in their structure. The literatures indicated that compounds having pyrimidine nucleus have a broad range of biological activities. As a result of their remarkable pharmacological activity, intensive research on pyrimidine derivatives has been focused on their activity, thus constituting an integral part of pharmaceutical industry.14
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