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Quantification of C-Reactive protein in human blood plasma using near-infrared Raman spectroscopy

机译:使用近红外拉曼光谱对人血浆中C反应蛋白的定量

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摘要

In this paper a new biological application of quantitative Raman spectroscopy is proposed. Native human plasma C-Reactive Protein (CRP) is used as a clinical biomarker of bacterial infection and tissue damage. The protein circulates in the blood and the concentration rises as inflammation occurs. For the first time the Raman spectrum of CRP in a buffered aqueous solution has been acquired using 785 nm excitation. The concentration of CRP has been measured in blood plasma, using near-infrared (NIR) Raman spectroscopy . Spectra were acquired with an in situ Inspector Raman spectrometer using 785 nm excitation. Raman spectra were collected from blood plasma drawn from 40 individuals. Quantitative predictions of CRP were made by means of Partial Least Squares (PLS) analysis and a variable selection method Interval PLS (IPLS). The similarity of the features in the PLS regression vector to that of CRP's Raman spectrum illustrates that the prediction is sensitive to the molecular information carried by the Raman scattered light. The IPLS algorithm is applied to optimize the calibration model to near clinical accuracy. This demonstrates the feasibility of using Raman spectroscopy for quantitative measurements of CRP in blood plasma.
机译:本文提出了定量拉曼光谱的一种新的生物学应用。天然人血浆C反应蛋白(CRP)被用作细菌感染和组织损伤的临床生物标志物。蛋白质在血液中循环,并且随着发炎而浓度升高。首次使用785 nm激发获得了缓冲水溶液中CRP的拉曼光谱。已使用近红外(NIR)拉曼光谱法测量了血浆中CRP的浓度。光谱是通过使用785 nm激发的原位Inspector拉曼光谱仪获得的。从从40个人抽取的血浆中收集拉曼光谱。 CRP的定量预测是通过偏最小二乘(PLS)分析和变量选择方法间隔PLS(IPLS)进行的。 PLS回归向量中的特征与CRP拉曼光谱的特征相似,表明该预测对拉曼散射光所携带的分子信息敏感。 IPLS算法用于优化校准模型,使其接近临床准确性。这证明了使用拉曼光谱法定量测定血浆中CRP的可行性。

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  • 来源
    《The Analyst》 |2009年第10期|p.2123-2127|共5页
  • 作者单位

    Institute of Sensors, Signals and Electrotechnics (SENSE), The Technical Faculty, University of Southern Denmark, Campusvej 55, DK 5230, Odense M, Denmark;

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