首页> 外文期刊>Toxicon: An International Journal Devoted to the Exchange of Knowledge on the Poisons Derived from Animals, Plants and Microorganisms >Use of egg yolk antibody (IgY) as an immunoanalytical tool in the detection of Indian cobra (Naja naja naja) venom in biological samples of forensic origin
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Use of egg yolk antibody (IgY) as an immunoanalytical tool in the detection of Indian cobra (Naja naja naja) venom in biological samples of forensic origin

机译:卵黄抗体(IgY)作为免疫分析工具在法医来源生物样品中检测印度眼镜蛇(Naja naja naja)毒液中的用途

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摘要

An immunoglobulin Y (IgY) based indirect double antibody sandwich enzyme linked immunosorbent assay (ELISA) was developed for the detection of Indian cobra (Naja naja naja) venom in the biological samples of forensic origin. Polyclonal antibodies were raised and purified from chick egg yolk and rabbit serum. The cobra venom was sandwiched between immobilized affinity purified IgY and the rabbit IgG. The detection concentration of cobra venom was in the range of 0.1 to 300ng. The calibration plot was based on linear regression analysis (y=0.2581x+0.4375, r(2)=0.9886). The limit of detection of the assay was found to be 0.1ng. The coefficient of variation (CV) of different concentrations of working range in inter (n=6) and intra-assay (n=6) was observed to be less than 10%. The recovery of venom was found to be in the range of 80-99%, when different concentrations (0.002, 0.1, 0.2, 1, and 2microg) of cobra venom were spiked to pooled normal human serum (ml(-1)). No cross reactivity was observed with krait and viper venom in the immunoassay system in the concentration range of 0.1-1000ng. The method was initially, validated by analyzing specimens (autopsy) of experimental rats injected with cobra venom (1.2mgkg(-1) body mass). Further, human specimens (autopsy and biopsy) of snake bite victims of forensic origin were also analyzed. The methodology developed may find diagnostic application in forensic laboratories.
机译:建立了一种基于免疫球蛋白Y(IgY)的间接双抗体夹心酶联免疫吸附测定(ELISA)方法,用于检测法医来源的生物样品中的印度眼镜蛇(Naja naja naja)毒液。产生多克隆抗体,并从鸡卵黄和兔血清中纯化。眼镜蛇毒被夹在固定的亲和纯化的IgY和兔IgG之间。眼镜蛇毒的检出浓度为0.1〜300ng。校准图基于线性回归分析(y = 0.2581x + 0.4375,r(2)= 0.9886)。测定的检测极限为0.1ng。在内部(n = 6)和分析内(n = 6),不同浓度工作范围的变异系数(CV)小于10%。当将不同浓度(0.002、0.1、0.2、1和2微克)的眼镜蛇毒加标到合并的正常人血清(ml(-1))中时,发现毒液的回收率在80-99%的范围内。在免疫测定系统中,浓度范围为0.1-1000ng时,没有发现与krait和毒蛇毒有关的交叉反应。该方法最初是通过分析注射眼镜蛇毒(1.2mgkg(-1)体重)的实验大鼠的标本(尸检)进行验证的。此外,还对法医来源的蛇咬受害者的人体标本(尸检和活检)进行了分析。所开发的方法可以在法医实验室中找到诊断应用。

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