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Lipid Peroxidation Induced by Expandable Clay Minerals

机译:膨胀黏土矿物引起的脂质过氧化

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摘要

Small-sized environmental particles such as 2:1 phyllosilicates induce oxidative stress, a primary indicator of cell damage and toxicity. Herein, potential hazards of clay particle uptake are addressed. This paper reports thatthe content and distribution of structural Fe influence the ability of expandable clay minerals to induce lipid peroxidation (LP), a major indicator of oxidative stress, in biological matrices. Three smectite clays, hectorite (SHCa-1) and two nontronites (NAu-1) and (NAu-2) containing varying total content and coordination environment of structural Fe, were selected. Screening and monitoring of LP was conducted using a thiobarbituric acid reactive substances (TBARS) assay. The higher content of TBARS in nontronites than that in SHCa-1 suspensions was explained because structural Fe contributes to LP. The observed lack of correlation between TBARS content and the extent of Fe dissolution indicated that the formation of TBARS is surface controlled. Results showing a high TBARS content in SHCa-1 but not in nontronite supernatant solutions was explained because the former contains distinct soluble chemical componen(s) that could (i) induce LP by its (their) own right and (ii) whose chemical affinity for organic ligands used as inhibitors is weak. Clays serve as stronger inductors than 2,2'-azobis(2-amidinopropane) dihydrochloride (AAPH) but are much weaker than FeSO_4. The outcome of this work shows that LP is clay surface-controlled and dependent on clay structural composition.
机译:诸如2:1的层状硅酸盐之类的小型环境颗粒会诱导氧化应激,这是细胞损伤和毒性的主要指标。在此,解决了粘土颗粒吸收的潜在危险。本文报道结构铁的含量和分布影响生物基质中可膨胀粘土矿物诱导脂质过氧化(LP)的能力,脂质过氧化是氧化应激的主要指标。选择了三种蒙脱石粘土,锂蒙脱石(SHCa-1)和两种斑脱石(NAu-1)和(NAu-2),它们的总铁含量和结构铁的配位环境各不相同。使用硫代巴比妥酸反应性物质(TBARS)分析进行LP的筛选和监测。解释说,囊铁中TBARS的含量高于SHCa-1悬浮液中的TBARS,因为结构铁有助于形成LP。观察到的TBARS含量和Fe溶解程度之间没有相关性,表明TBARS的形成受表面控制。解释了在SHCa-1中显示高TBARS含量但在囊脱石上清液中没有的结果,因为前者包含不同的可溶性化学成分,这些成分可以(i)通过其自身的权利诱导LP,并且(ii)其化学亲和力对于用作抑制剂的有机配体来说是弱的。黏土比2,2'-偶氮二(2-ami基丙烷)二盐酸盐(AAPH)更强,但比FeSO_4弱得多。这项工作的结果表明,LP是粘土表面控制的,并且取决于粘土的结构组成。

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  • 来源
    《Environmental Science & Technology》 |2009年第19期|7550-7555|共6页
  • 作者单位

    Facultad de Quimica, Universidad National Autonoma de Mexico,Circuito Exterior sin, Ciudad Universitaria, Coyoacan, Mexico, DF 04510, Mexico;

    Institute de Quimica, Vniversidad National Autonoma de Mexico,Circuito Exterior sin, Ciudad Universitaria, Coyoacan, Mexico, DF 04510, Mexico;

    Departnmento de Procesos y Tecnologia, Divisidn de Ciencias Naturales e Ingenieria, Universidad Autonoma Metropolitana, Unidad Cuajimalpa (UAM-C), Artificios No. 40,6° Piso, CP. 01120 Mexico NASA Astrobiology Institute,1 Cyclotron Rd., Berkeley, CA 94720 Earth Sciences Division, Lawrence Berkeley National Laboratory,1 Cyclotron Rd., Berkeley, CA 94720;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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