首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Determination of Malondialdehyde as Dithiobarbituric Acid Adduct in Biological Samples by HPLC with Fluorescence Detection: Comparison with Ultraviolet-Visible Spectrophotometry
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Determination of Malondialdehyde as Dithiobarbituric Acid Adduct in Biological Samples by HPLC with Fluorescence Detection: Comparison with Ultraviolet-Visible Spectrophotometry

机译:高效液相色谱-荧光检测法测定生物样品中作为二硫代巴比妥酸加合物的丙二醛:与紫外可见分光光度法比较

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Living cells are constantly exposed to reactive oxygen species, some of which are capable of initiating lipid peroxidation by abstraction of an allylic proton from a polyunsaturated fatty acid. This process, by multiple stages leading to the formation of lipid hydroperoxides, is a known contributor to the development of atherosclerosis (1).The thiobarbituric acid (TBA) test is an easy and quick assay for the assessment of lipid peroxidation in which malondialdehyde (MDA) is derivatized. The rationale and methodology have been discussed in detail elsewhere (2)(3) and have rightfully been criticized for low specificity and artifact formation because only a fraction of the MDA measured was generated in vivo (1)(3). Furthermore, the TBA derivatization procedure itself leads to the formation of several MDA-unrelated ultraviolet (UV)-absorbing and fluorescent species, the latter as shown in Fig. 1? , A–C. Despite this fact, the method remains one of the most useful and commonly used measurements of oxidative damage because of its simplicity. In recent years, several HPLC-based TBA assays have evolved with increased specificity (4)(5)(6)(7), but nevertheless the spectrophotometric methods remain commonly used. In the present report, MDA was quantified in plasma, erythrocytes, and liver homogenates from 3-month-old guinea pigs by either our “modern” TBA test based on HPLC with fluorescence detection, which quantifies only the genuine MDA(TBA)2 adduct, or by the original less specific and less sensitive spectrophotometric method, which measures the total absorbance of several species. The purpose was to evaluate the use of the original TBA test by today’s standards by assessing the overestimation and sensitivity in the various applications that are routinely performed in several laboratories.All compounds were of the highest quality available. Specifically, butylated hydroxytoluene (BHT), tetramethoxypropane, TBA, and phosphotungstic acid were from Fluka.Sample …
机译:活细胞不断暴露于活性氧中,其中一些能够通过从多不饱和脂肪酸中提取烯丙基质子来引发脂质过氧化。这个过程由多个阶段导致脂质过氧化氢的形成,是导致动脉粥样硬化发展的已知因素(1)。硫代巴比妥酸(TBA)测试是一种简便,快速的测定脂质过氧化的测定方法,其中丙二醛( MDA)已衍生化。其原理和方法已在其他地方(2)(3)进行了详细讨论,并因其低特异性和伪影形成而受到批评,因为在体内仅产生了一部分MDA(1)(3)。此外,TBA的衍生过程本身会导致形成几种与MDA无关的紫外线(UV)吸收和荧光物质,后者如图1所示。 ,AC。尽管有这个事实,但由于其简便性,该方法仍是最有用和最常用的氧化损伤测量方法之一。近年来,一些基于HPLC的TBA测定法已经发展为具有更高的特异性(4)(5)(6)(7),但是分光光度法仍然是常用的方法。在本报告中,通过我们基于HPLC的“现代” TBA测试和荧光检测,对3个月大豚鼠的血浆,红细胞和肝匀浆中的MDA进行了定量,仅对真正的MDA(TBA)2加合物进行了定量,或采用原始的特异性较低,灵敏度较低的分光光度法,该方法可测量几种物种的总吸光度。目的是通过评估在几个实验室中常规执行的各种应用中的高估和敏感性,来评估按当今标准进行的原始TBA测试的使用。所有化合物均具有最高质量。具体来说,丁基化羟基甲苯(BHT),四甲氧基丙烷,TBA和磷钨酸来自Fluka.Sample…

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