Near-infrared spectrometric determination of blood pH.

N. Rosen, W. Charash, E. Hirsch
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引用次数: 22

Abstract

BACKGROUND Reflectance near-infrared spectroscopy (600-2200 nm) can noninvasively probe deep into tissues. Blood is the predominant absorber of near-infrared light in biological tissues. We investigated the feasibility of using reflectance near-infrared spectroscopy to measure blood pH in vitro. METHODS Reflectance near-infrared spectra (600-2200 nm) were obtained with a fiberoptic probe immersed in diluted human packed red blood cells maintained at 37 degrees C. Changes in pH (6.800-7.600) were induced by: (1) varying the partial pressure of carbon dioxide by the bubbling of mixtures of humidified carbon dioxide and nitrogen gas through the blood; and (2) adding 1 N HCl/NaOH. Humidified oxygen gas was bubbled through the blood to generate variations in oxygen saturation. After each titration of pH, the spectrum was recorded and blood was sampled for the measurement of: pH, pCO(2), and pO(2) using blood gas analysis; and hemoglobin concentration and oxygen saturation using co-oximetry. Samples from three separate pH titrations were combined (120 total samples) and analyzed using partial least-squares analysis to generate a mathematical model relating spectral changes to pH (calibration set). This model was then used to predict the pH of a set of 36 pH titrations (prediction set). RESULTS Quantitative and qualitiative analyses of the spectra in the calibration set found that spectral changes in the wavelength range, 650-1050 nm, were directly related to changes in pH. First-derivative-treated spectra from the calibration set, analyzed using partial least-squares analysis, generated a mathematical model with a cross-validated r(2) of 0.939 and a standard error of calibration of 0.046 pH unit. When this model was applied to the prediction set, with an offset correction, the r(2) was 0.936 with a standard error of prediction of 0.050 pH unit. CONCLUSION Blood pH can be predicted in vitro with clinical significance using reflectance near-infrared spectroscopy (650-1050 nm) within a standard error of 0.050 pH unit.
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近红外光谱法测定血液pH值。
反射近红外光谱(600- 2200nm)可以无创地探测到组织深处。血液是生物组织中主要的近红外光吸收剂。我们探讨了用反射近红外光谱法测定体外血液pH值的可行性。方法将光纤探针浸入稀释后的人红细胞中,在37℃下获得近红外光谱(600 ~ 2200 nm),通过以下方法改变pH值(6.800 ~ 7.600):(1)使加湿后的二氧化碳和氮气的混合物在血液中起泡,改变二氧化碳的分压;(2)加入1 N HCl/NaOH。加湿的氧气在血液中冒泡,产生氧饱和度的变化。每次pH滴定后,记录光谱并采血,通过血气分析测定pH、pCO(2)和pO(2);血红蛋白浓度和血氧饱和度。将三种不同pH滴定的样品(总共120个样品)组合在一起,并使用偏最小二乘分析生成光谱变化与pH(校准集)相关的数学模型。然后使用该模型预测一组36个pH滴定(预测集)的pH值。结果对校准集中的光谱进行定量和定性分析发现,光谱在650 ~ 1050 nm波长范围内的变化与pH的变化直接相关。对校准集中的光谱进行一阶导数处理后的数学模型进行偏最小二乘分析,交叉验证的r(2)为0.939,校准标准误差为0.046 pH单位。将该模型应用于预测集,经偏移量校正后,r(2)为0.936,预测标准误差为0.050 pH单位。结论反射近红外光谱法(650 ~ 1050 nm)可在0.050 pH单位的标准误差范围内预测血液pH值,具有临床意义。
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