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An immunological determination of somatostatin in pharmaceutical by sandwich ELISA based on IgY and polyclonal antibody

机译:基于IgY和多克隆抗体的夹心ELISA制药生长抑素的免疫测定

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A sensitive and specific enzyme-linked immunosorbent assay (ELISA) for the detection of Somatostatin based on double antibody sandwich method was studied in this paper. The Somatostatin specific Yolk antibody (IgY) and polyclonal antibody were available to Somatostatin-conjugated KLH immunized rabbits and chickens used to construct the sandwich ELISA for the measurement of Somatostatin. The limit of detection was 0.1 mu g/mL and the half maximal inhibitory concentration (IC50) was 0.859 pg/mL. The method developed in the study showed no evident cross-reactivity with other similar analogs. The recoveries of Somatostatin spiked mannitols were in the range of 98.45% to 103.90% with infra- and inter-day coefficient of variants (CVs) 8.71% and 4.60% respectively. The detection standard curve of Somatostatin exhibited a good linearity (R-2 = 0.9931, n = 3). Therefore, the methods could be selectively used for rapid screening of Somatostatin in pharmaceutical.
机译:本文研究了基于双抗体夹层法检测生长抑制素的敏感和特异性酶联免疫吸附测定(ELISA)。 生长抑素特异性蛋黄抗体(IgY)和多克隆抗体可用于生长抑制素 - 缀合的KLH免疫兔和鸡,用于构建夹心ELISA以测量生长抑素。 检测限为0.1μg/ ml,半最大抑制浓度(IC 50)为0.859pg / ml。 该研究中开发的方法显示出与其他类似类似物的明显交叉反应性。 生长抑素掺入甘露醇的回收率在98.45%至103.90%的范围内,具有内部变体和日间变体系数(CVS)& 分别为8.71%和4.60%。 生长抑素的检测标准曲线表现出良好的线性度(R-2 = 0.9931,n = 3)。 因此,可以选择性地用于在药物中快速筛选生长抑素的方法。

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