Near infrared spectroscopy for hemoglobin quantification in a single drop of blood with improved pretreatment and wavelength selection

IF 3.3 Q2 MULTIDISCIPLINARY SCIENCES
Fatima Ezzahra El Kamouny , Hassan Oukhouya , Younes Wadiai , Abdellah Madani , Khadija El Kamouny , Aziz Lmakri
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Abstract

Clinical diagnostics and patient monitoring depend heavily on hemoglobin (HGB) quantification; however, traditional techniques are frequently intrusive, time-consuming, and require comparatively large blood volumes. By investigating the possibility of using Near Infrared (NIR) spectroscopy to predict hemoglobin concentration from a single drop of blood, this study addresses the demand for a quick and minimally invasive alternative. The primary goal is to increase prediction accuracy by using optimized wavelength selection and spectral preprocessing. A total of 400 blood samples, including those from healthy individuals and patients receiving medical treatment with hemoglobin values ranging from 2.5 to 20 g/dL, were collected from AL QODS Medical Analysis Laboratory. To improve spectral clarity, spectral preprocessing methods such as the Savitzky–Golay Method (SGM), Standard Normal Variate (SNV), and Multiplicative Scatter Correction (MSC) were applied. An optimal subset of wavelengths was then selected using the Interval Partial Least Squares (IPLS) regression technique. Compared to conventional Partial Least Squares (PLS) using the entire spectrum, the results demonstrate that IPLS significantly improves model performance. A strong correlation between laboratory data and a selection of 39 spectral bands (2238.758–2307.405 nm) was also observed. This study demonstrates how advanced preprocessing and wavelength selection can be combined to quantify hemoglobin from a single blood drop accurately. The results highlight the potential of NIR spectroscopy as a fast, reliable, and easily accessible clinical monitoring tool, particularly for the diagnosis and monitoring of anemia and other blood disorders.
改进前处理和波长选择的近红外光谱法测定单滴血中的血红蛋白
临床诊断和患者监测严重依赖血红蛋白(HGB)定量;然而,传统技术通常是侵入性的,耗时的,并且需要相对较大的血容量。通过研究使用近红外(NIR)光谱预测单滴血中血红蛋白浓度的可能性,本研究解决了对快速微创替代方案的需求。主要目的是通过优化波长选择和光谱预处理来提高预测精度。从AL QODS医学分析实验室采集了400份血液样本,包括健康个体和接受治疗的患者,血红蛋白值在2.5 ~ 20 g/dL之间。为了提高光谱清晰度,采用了Savitzky-Golay方法(SGM)、标准正态变量(SNV)和乘法散射校正(MSC)等光谱预处理方法。然后使用区间偏最小二乘(IPLS)回归技术选择波长的最佳子集。与使用全谱的传统偏最小二乘(PLS)相比,结果表明,IPLS显著提高了模型的性能。实验数据与39个光谱波段(2238.758-2307.405 nm)之间有很强的相关性。这项研究展示了如何将先进的预处理和波长选择结合起来,准确地定量单滴血中的血红蛋白。这些结果突出了近红外光谱作为一种快速、可靠和易于获取的临床监测工具的潜力,特别是在贫血和其他血液疾病的诊断和监测方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Scientific African
Scientific African Multidisciplinary-Multidisciplinary
CiteScore
5.60
自引率
3.40%
发文量
332
审稿时长
10 weeks
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