...
首页> 外文期刊>Journal of Medical Biochemistry >Development of a Quantitative Detection Card for Heart-type Fatty Acid-binding Protein based on Background Fluorescence Quenching Immune Chromatography
【24h】

Development of a Quantitative Detection Card for Heart-type Fatty Acid-binding Protein based on Background Fluorescence Quenching Immune Chromatography

机译:基于背景荧光猝灭免疫色谱的心脏型脂肪酸结合蛋白定量检测卡的研制

获取原文
           

摘要

Summary Background To establish a fast and simple quantitative method for detection of heart-type fatty acid-binding protein (H-FABP) in serum based on a background fluorescence quenching immunochromatographic assay. Methods A detection card based on the double-antibody sandwich double-antibody method with background fluorescence quenching was developed for quantitative measurement of H-FABP in serum. The optimal concentrations of control for coating the test and control lines were determined as well as the concentrations of gold-labeled antibodies used in preparing the detection system. The detection method for H-FABP in serum was established and validated using real-world clinical samples. Results The optimal concentrations of labeling antibody and coating antibody were 5.0 μg/mL and 1.0 mg/mL, respectively. The test card had a sensitivity of 1.15 ng/mL over a linear concentration range of 0–100 ng/mL. Based on three batches prepared for testing the card, the relative standard deviation (RSD) within batches was less than 15% without a significant difference (P=0.942). The detection method was tested against common interfering substances in serum, such as bilirubin, triglyceride and serum anticoagulants ethylenediamine tetraacetic acid (EDTA), heparin, and sodium citrate, and no significant cross-reaction was detected. The test method was further validated with 50 clinical serum samples, and the test results were comparable with standard reference detection methods with good correlation (R=0.95). Conclusion Our study presents a new method with strong specificity and sensitivity for the detection of H-FABP in serum, which could promote H-FABP detection in a broad range of applications.
机译:发明背景基于背景荧光猝灭免疫色谱测定法,建立一种快速简单的定量血清中心脏型脂肪酸结合蛋白(H-FABP)的定量方法。方法建立了基于双抗体夹心双抗体法和背景荧光猝灭的检测卡,用于定量检测血清中的H-FABP。确定用于涂覆测试线和对照线的最佳对照浓度,以及用于制备检测系统的金标记抗体的浓度。建立了血清中H-FABP的检测方法,并使用了真实的临床样本进行了验证。结果标记抗体和包被抗体的最佳浓度分别为5.0μg/ mL和1.0 mg / mL。在0–100 ng / mL的线性浓度范围内,测试卡的灵敏度为1.15 ng / mL。基于准备测试卡的三个批次,批次内的相对标准偏差(RSD)小于15%,无显着差异(P = 0.942)。测试了针对血清中常见干扰物质(例如胆红素,甘油三酸酯和血清抗凝剂乙二胺四乙酸(EDTA),肝素和柠檬酸钠)的检测方法,未检测到明显的交叉反应。用50个临床血清样品进一步验证了该测试方法,该测试结果与具有良好相关性的标准参考检测方法相当(R = 0.95)。结论我们的研究提出了一种检测血清中H-FABP的强特异性和灵敏性的新方法,可以促进H-FABP在广泛应用中的检测。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号