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Sensitive quantitative analysis of the bitter glycoside amarogentin by specific monoclonal antibody-based indirect competitive enzyme-linked immunosorbent assay

机译:基于特异性单克隆抗体的间接竞争酶联免疫吸附法灵敏定量分析苦味苷a菜素

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Amarogentin (AG) is a naturally occurring secoiridoid glycoside produced mainly in the plant genera Swertia and Gentiana . Extracts of these plants have a long history of use in Japan as bitter stomachics because of their strong bitterness. Because the AG content directly reflects the potential activity of the extract, the quality control of these plant extracts through the quantitative analysis of AG is important. In the present study, we aimed to develop a quantitative analysis of AG using a monoclonal antibody (MAb) against AG (MAb 1E9) in the plant family Gentianaceae. Surprisingly, production of MAb 1E9 was successfully achieved by immunizing AG–bovine serum albumin (BSA) conjugates into mice although the number of AG bound to BSA was only one. The characterization of MAb 1E9 revealed that it shows high specificity to AG, enabling the development of an icELISA for the specific determination of AG. In addition, the detectable concentration of AG in the developed icELISA ranged from 1.95 to 62.5 ng mL ~(?1) with a limit of detection of 1.28 ng mL ~(?1) , which is approximately 30–625 times higher in sensitivity compared with the conventional HPLC method. Validation analysis revealed that the icELISA using MAb 1E9 is precise (intra-assay variation <3.9%, inter-assay variation <8.8%) and accurate (recovery rates of spiked samples were between 91.0% and 106.4%). This method can be used for the quality control of plant extracts using AG as an index.
机译:Amarogentin(AG)是一种天然存在的类蛇药苷,主要在Swertia和Gentiana属植物中产生。这些植物的提取物因其强烈的苦味而在日本用作苦味胃药已有很长的历史。由于AG含量直接反映了提取物的潜在活性,因此通过AG的定量分析对这些植物提取物进行质量控制非常重要。在本研究中,我们旨在使用植物龙胆科中针对AG(MAb 1E9)的单克隆抗体(MAb)开发AG的定量分析。出人意料的是,尽管将与牛血清白蛋白结合的AG数量只有一个,但通过将AG-牛血清白蛋白(BSA)结合物免疫小鼠成功地实现了MAb 1E9的生产。 MAb 1E9的表征表明,它对AG具有高特异性,从而可以开发用于特异性测定AG的icELISA。此外,在已开发的icELISA中,可检测到的AG浓度范围为1.95至62.5 ng mL〜(?1),检测极限为1.28 ng mL〜(?1),其灵敏度约为30-625倍。使用常规HPLC方法。验证分析显示,使用MAb 1E9的icELISA准确(批内变异度<3.9%,批间变异度<8.8%)且准确(加标样品的回收率在91.0%至106.4%之间)。该方法可用于以AG为指标的植物提取物的质量控制。

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