Group for Applied Instrumental Analysis, Department of Chemistry, Federal University of São Carlos, Rod. Washington Luís, km 235, 13565-905 São Carlos, São Paulo State, Brazil.
Department of Analytical Chemistry, Institute of Chemistry, São Paulo State University (Unesp), Rua Professor Francisco Degni, 55, 14800-060 Araraquara, São Paulo State, Brazil.
Food Res Int. 2017 Apr;94:72-78. doi: 10.1016/j.foodres.2017.01.027. Epub 2017 Jan 31.
This study describes the application of laser-induced breakdown spectroscopy (LIBS) for the direct determination of Ca, K and Mg in powdered milk and solid dietary supplements. The following two calibration strategies were applied: (i) use of the samples to calculate calibration models (milk) and (ii) use of sample mixtures (supplements) to obtain a calibration curve. In both cases, reference values obtained from inductively coupled plasma optical emission spectroscopy (ICP OES) after acid digestion were used. The emission line selection from LIBS spectra was accomplished by analysing the regression coefficients of partial least squares (PLS) regression models, and wavelengths of 534.947, 766.490 and 285.213nm were chosen for Ca, K and Mg, respectively. In the case of the determination of Ca in supplements, it was necessary to perform a dilution (10-fold) of the standards and samples to minimize matrix interference. The average accuracy for powdered milk ranged from 60% to 168% for Ca, 77% to 152% for K and 76% to 131% for Mg. In the case of dietary supplements, standard error of prediction (SEP) varied from 295 (Mg) to 3782mgkg (Ca). The proposed method presented an analytical frequency of around 60 samples per hour and the step of sample manipulation was drastically reduced, with no generation of toxic chemical residues.
本研究描述了激光诱导击穿光谱(LIBS)在粉末状牛奶和固体膳食补充剂中直接测定 Ca、K 和 Mg 的应用。应用了以下两种校准策略:(i)使用样品计算校准模型(牛奶)和(ii)使用样品混合物(补充剂)获得校准曲线。在这两种情况下,均使用酸消解后电感耦合等离子体发射光谱(ICP OES)获得的参考值。通过分析偏最小二乘(PLS)回归模型的回归系数来选择 LIBS 光谱中的发射线,分别选择 534.947nm、766.490nm 和 285.213nm 作为 Ca、K 和 Mg 的波长。在测定补充剂中的 Ca 时,需要对标准品和样品进行 10 倍稀释,以最小化基质干扰。对于粉末状牛奶,Ca 的平均准确度在 60%至 168%之间,K 在 77%至 152%之间,Mg 在 76%至 131%之间。对于膳食补充剂,预测标准误差(SEP)在 295(Mg)至 3782mgkg(Ca)之间变化。该方法的分析频率约为每小时 60 个样品,样品处理步骤大大减少,且不会产生有毒化学残留物。