Filik Jacob, Stone Nicholas
Biophotonics Research, Gloucester Royal Hospital, Great Western Road, Gloucester, UK.
Analyst. 2007 Jun;132(6):544-50. doi: 10.1039/b701541k. Epub 2007 Apr 23.
The technique of drop coating deposition Raman (DCDR) spectroscopy has been shown to be a highly reproducible and sensitive method of obtaining Raman spectra from low concentration protein solutions. This study assesses the ability of DCDR to analyse changes in the relative protein concentrations of aqueous tertiary protein mixtures, with protein levels similar to that found in human tear fluid. The three proteins used to make the mixtures were lysozyme, lactoferrin and albumin. The combination of DCDR spectroscopy and principal components analysis is found to be sensitive enough to detect small changes in the relative protein concentrations, from very small sample volumes (1.5 microl). With certain mixtures it was found that the deposition of proteins was not homogeneous across the width of the ring, but averaging spectra taken at different positions could compensate for this. Principal components regression was able to predict the protein concentrations of test solutions with a good degree of accuracy (root-mean-square errors of prediction of 0.083, 0.112, and 0.082 mg ml(-1) or 8.3, 11.2 and 8.2% of the mean concentration value, for lysozyme, lactoferrin and albumin concentrations respectively). The results of this study suggest that DCDR spectroscopy could be a simple, fast, near-patient technique capable of assisting the diagnosis of ocular infection.
滴涂沉积拉曼(DCDR)光谱技术已被证明是一种从低浓度蛋白质溶液中获取拉曼光谱的高度可重复且灵敏的方法。本研究评估了DCDR分析与人类泪液中蛋白质水平相似的水性三级蛋白质混合物相对蛋白质浓度变化的能力。用于制备混合物的三种蛋白质是溶菌酶、乳铁蛋白和白蛋白。发现DCDR光谱与主成分分析相结合足够灵敏,能够从非常小的样品体积(1.5微升)中检测相对蛋白质浓度的微小变化。对于某些混合物,发现蛋白质在环的宽度上沉积不均匀,但对不同位置采集的光谱进行平均可以弥补这一点。主成分回归能够以较高的准确度预测测试溶液的蛋白质浓度(溶菌酶、乳铁蛋白和白蛋白浓度的预测均方根误差分别为0.083、0.112和0.082毫克/毫升,或平均浓度值的8.3%、11.2%和8.2%)。本研究结果表明,DCDR光谱可能是一种简单、快速、接近床边的技术,能够辅助眼部感染的诊断。