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衰减全反射-傅里叶变换红外(ATR-FTIR)光谱结合化学计量学分析检测和定量薰衣草和香茅精油中的掺假。

Attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy coupled with chemometric analysis for detection and quantification of adulteration in lavender and citronella essential oils.

机构信息

Department of Life Sciences, University of Modena and Reggio Emilia, via G. Campi 103, Modena, 41125, Italy.

Doctorate School in Clinical and Experimental Medicine (CEM), University of Modena and Reggio Emilia, Modena, 41125, Italy.

出版信息

Phytochem Anal. 2021 Nov;32(6):907-920. doi: 10.1002/pca.3034. Epub 2021 Feb 10.

Abstract

INTRODUCTION

The growing consumer interest in "naturals" led to an increased application of essential oils (EOs). The market outbreak induced the intensification of EO adulterations, which could affect their quality.

OBJECTIVES

Nowadays, little is known about the illegal practice of adulteration of EOs with vegetable oils. Therefore, the application of mid-infrared spectroscopy coupled with chemometrics was proposed for the detection of EO counterfeits.

MATERIALS AND METHODS

Two EOs, three seed oils, and their mixtures were selected to build the adulteration model. EO-adulterant mixtures for model calibration and validation were analyzed by attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy. The spectral data were analyzed with principal component analysis (PCA) and partial least-squares (PLS) regression.

RESULTS

PCA allowed the discrimination of the EO and adulterant percentages by explaining 97.47% of the total spectral variance with two principal components. A PLS regression model was generated with three factors explaining 97.73% and 99.69% of the total variance in X and Y, respectively. The root mean square error of calibration and the root mean square error of cross-validation were 0.918 and 1.049, respectively. The root mean square error of prediction value obtained from the external validation set was 1.588 and the coefficients of determination R and R were 0.997 and 0.996, respectively.

CONCLUSIONS

The results highlighted the robustness of the developed method in quantifying counterfeits in the range from 0 to 50% of adulterants, disregarding the type of EO and adulterant employed. The present work offers a research advance and makes an important impact in phytochemistry, revealing an easily applicable method for EO quality assessment.

摘要

简介

消费者对“天然产品”的兴趣日益浓厚,导致对精油(EOs)的应用不断增加。市场的爆发促使 EO 掺假现象加剧,这可能会影响其质量。

目的

目前,人们对 EO 与植物油掺假的非法行为知之甚少。因此,提出了中红外光谱结合化学计量学的应用,以检测 EO 假冒品。

材料和方法

选择两种精油、三种籽油及其混合物来建立掺假模型。通过衰减全反射傅里叶变换红外(ATR-FTIR)光谱分析对模型校准和验证的 EO-掺杂物混合物进行分析。对光谱数据进行主成分分析(PCA)和偏最小二乘(PLS)回归分析。

结果

PCA 通过用两个主成分解释总光谱方差的 97.47%,允许区分 EO 和掺杂物的百分比。生成了一个具有三个因子的 PLS 回归模型,分别解释了 X 和 Y 方向总方差的 97.73%和 99.69%。校准和交叉验证的均方根误差分别为 0.918 和 1.049。从外部验证集获得的预测值的均方根误差为 1.588,决定系数 R 和 R 分别为 0.997 和 0.996。

结论

结果突出了所开发方法在量化从 0 到 50%掺杂物范围内假冒品的稳健性,而不考虑使用的 EO 和掺杂物的类型。本工作在植物化学领域提供了研究进展,对 EO 质量评估具有重要影响,展示了一种易于应用的方法。

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