首页> 外文学位 >Development platform for immunoassays with up-converting phosphors.
【24h】

Development platform for immunoassays with up-converting phosphors.

机译:具有上转换荧光粉的免疫分析开发平台。

获取原文
获取原文并翻译 | 示例

摘要

For medical diagnostic applications, immunoassays provide a relatively simple, quick, and reliable method to measure analytes. Immunoassays identify and quantify substances by harnessing the sensitivity and specificity of nature's antibody-antigen detection system. Since clinically relevant analytes tend to have lower concentrations in physiological fluids other than blood, sensitive immunoassays with low detection limits would facilitate safer and painless noninvasive measurements of these analytes. Practical limitations to immunoassays, such as autofluorescence and nonspecific binding, often confine detection limits to higher levels, and functional immunoassays with extremely low detection limits are rare, particularly ones with rapid turnaround times.; To address these issues, an engineering approach to immunoassay development, as opposed to the typical empirical one, was used to characterize and optimize an immunoassay that utilized up-converting phosphor (UCP) technology. With this immunoassay development platform, which featured 2-D imaging and quantification of UCP labels in immunoassays, as well as temperature control, a microfluidic immunoassay for interferon-gamma (IFN-gamma) was developed to demonstrate a UCP-based immunoassay for cytokines (regulatory proteins involved in the body's immune response) for potential use as an early indicator of infection and stress. Image processing techniques were employed to extract the signals from the 2-D images, which were proportional to the IFN-gamma concentrations present in the samples. Concentrations as low as 3 pM (50 pg/mL) and as high as 600 pM (10 ng/mL) were detected from 100-muL samples with a total assay time of under an hour, including the 8-minute readout time.; To enhance immunoassay sensitivity, a novel mathematical model for immunoassays that incorporates the effects of both temperature and nonspecific binding was used to predict the kinetic behavior of the immunoassay based on reagent and substrate properties. Temperature-controlled immunoassays experimentally verified that temperature modulation could be employed to significantly reduce nonspecific binding levels by over 50%. This model used in conjunction with the immunoassay development platform provides a valuable tool to speed development, reduce errors, and potentially improve the accuracy and sensitivity of immunoassays, whether they are applied to biological research or medical diagnostics.
机译:对于医学诊断应用,免疫分析提供了一种相对简单,快速和可靠的方法来测量分析物。免疫分析利用自然界的抗体-抗原检测系统的敏感性和特异性来鉴定和定量物质。由于临床上相关的分析物在血液以外的生理液中的浓度往往较低,因此检测限低的灵敏免疫分析将有助于对这些分析物进行更安全,无痛的无创测量。免疫测定的实际限制,例如自发荧光和非特异性结合,通常将检测极限限制在较高水平,而极低检测极限的功能免疫测定却很少,尤其是周转时间短的免疫测定。为了解决这些问题,与典型的经验方法相反,采用了一种工程化的免疫分析方法来表征和优化利用上转换荧光粉(UCP)技术的免疫分析方法。借助此免疫测定开发平台,该平台具有2-D成像和免疫测定中UCP标记的定量以及温度控制的功能,因此开发了用于干扰素-γ(IFN-γ)的微流体免疫测定,以证明基于UCP的细胞因子免疫测定(参与人体免疫反应的调节蛋白)可潜在地用作感染和压力的早期指标。使用图像处理技术从二维图像中提取信号,这些信号与样品中存在的IFN-γ浓度成比例。从100-μL样品中检出的浓度低至3 pM(50 pg / mL),高至600 pM(10 ng / mL),总测定时间不到一小时,包括8分钟的读出时间。为了增强免疫测定的敏感性,结合了温度和非特异性结合作用的新型免疫测定数学模型被用于基于试剂和底物性质来预测免疫测定的动力学行为。温度控制的免疫测定实验证明,可以采用温度调节将非特异性结合水平显着降低50%以上。将该模型与免疫分析开发平台结合使用,无论将其应用于生物学研究还是医学诊断,都可提供宝贵的工具来加快开发速度,减少错误并潜在地提高免疫分析的准确性和灵敏度。

著录项

  • 作者

    Li, Janice Joyce.;

  • 作者单位

    Stanford University.;

  • 授予单位 Stanford University.;
  • 学科 Engineering Biomedical.; Engineering Electronics and Electrical.
  • 学位 Ph.D.
  • 年度 2007
  • 页码 132 p.
  • 总页数 132
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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