Peng Weiyu, Athukorale Sumudu, Hu Juan, Cui Xin, Zhang Dongmao
Department of Chemistry, Mississippi State University, Mississippi State, MS, 39762, United States.
Department of Mathematical Sciences, DePaul University, Chicago, IL, 60604, United States.
Anal Chim Acta. 2021 Apr 8;1153:338293. doi: 10.1016/j.aca.2021.338293. Epub 2021 Feb 5.
Kinetic chromogenic (CG) and fluorogenic (FG) quantification deduces analyte concentration based on the reaction rate between the CG/FG probe and its targeted molecule. Little progress has been made in the past half century in either the theory or the applications of the kinetic spectroscopic quantification methods. Current kinetic CG/FG quantification is limited only to a subset of CG/FG reactions that can be approximated as the single-step process, and more problematically, to research samples with no matrix interferences. Reported herein is a kinetic quantification model established for multistep CG/FG reactions and a proof-of-concept demonstration of direct kinetic FG quantification of biomarkers in practical samples. The kinetic spectral intensity of the CG/FG reactions with two rate-limiting steps comprises three temporal regions: an accelerating period where rate of signal change is increasingly rapid, a linear region where the rate of signal change is approximately constant, and a deceleration region where the rate of signal increase becomes progressively small. Kinetic quantification is performed through simple linear-curve-fitting of the kinetic signal in its linear time-course region. The theoretical model is validated with the dual CG/FG 2-thiobarbituric acid (TBA) and malondialdehyde (MDA) reaction. Proof-of-concept kinetic spectroscopic quantification of analytes in practical samples is demonstrated with the FG quantification of MDA in canned chicken. The only sample preparation is bench-top centrifugation followed by two sequential syringe filtrations. The total kinetic FG assay time is less than 10 min, more than 10 times more efficient than the current equilibrium-based MDA assay. The theoretical model and the measurement design strategies offered by this work should help transform the current kinetic spectroscopic quantification from a niche research tool to an indispensable technique for time-sensitive applications.
动力学显色(CG)和荧光(FG)定量分析是基于CG/FG探针与其靶向分子之间的反应速率来推断分析物浓度的。在过去的半个世纪里,动力学光谱定量分析方法在理论和应用方面都进展甚微。目前的动力学CG/FG定量分析仅限于一小部分可近似为单步过程的CG/FG反应,更成问题的是,仅限于无基质干扰的研究样本。本文报道了一种针对多步CG/FG反应建立的动力学定量模型,以及在实际样本中对生物标志物进行直接动力学FG定量分析的概念验证。具有两个限速步骤之CG/FG反应的动力学光谱强度包括三个时间区域:信号变化速率越来越快的加速期、信号变化速率近似恒定的线性区域以及信号增加速率逐渐变小的减速区域。动力学定量分析是通过对动力学信号在线性时间进程区域进行简单的线性曲线拟合来实现的。该理论模型通过双CG/FG 2-硫代巴比妥酸(TBA)和丙二醛(MDA)反应得到验证。通过对罐装鸡肉中MDA的FG定量分析,展示了在实际样本中对分析物进行概念验证的动力学光谱定量分析。唯一的样本制备是台式离心,然后进行两次连续的注射器过滤。总的动力学FG分析时间不到10分钟,比目前基于平衡的MDA分析效率高10倍以上。这项工作提供的理论模型和测量设计策略应有助于将当前的动力学光谱定量分析从一种小众的研究工具转变为对时间敏感应用不可或缺的技术。