4.7 Article

A comprehensive quality evaluation method by FT-NIR spectroscopy and chemometric: Fine classification and untargeted authentication against multiple frauds for Chinese Ganoderma lucidum

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.saa.2017.03.074

Keywords

Near-infrared spectroscopy (NIR); Chemometrics; Ganoderma lucidum (GL); Fine classification; Untargeted analysis

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Funding

  1. National Natural Science Foundation of China [21576297, 21205145, 21665022]
  2. Key Projects of Technological Innovation of Hubei Province [2016ACA138]
  3. State Key Laboratory Breeding Base of Green Chemistry Synthesis Technology (Zhejiang University of Technology) [GCTKF2014007]
  4. Research Fund for the Doctoral Program of Tongren University [trxyDH1501]
  5. Education Department of Guizhou Province [GZKY[2015]498]
  6. Students Innovation and Entrepreneurship Training Center of Food Science and Technology in Tongren University [2016SJDCZX001]
  7. Modernization Engineering Technology Research Center of Ethnic Minority Medicine of Hubei province (South-Central University for Nationalities) [2015ZY006, 2015ZD001, 2015ZD002]

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The origins and authenticity against frauds are two essential aspects of food quality. In this work, a comprehensive quality evaluation method by FT-NIR spectroscopy and chemometrics were suggested to address the geographical origins and authentication of Chinese Ganoderma lucidum (GL). Classification for 25 groups of GL samples (7 common species from 15 producing areas) was performed using near-infrared spectroscopy and interval -combination One-Versus-One least squares support vector machine (IC-OVO-LS-SVM). Untargeted analysis of 4 adulterants of cheaper mushrooms was performed by one-class partial least squares (OCPLS) modeling for each of the 7 GL species. After outlier diagnosis and comparing the influences of different preprocessing methods and spectral intervals on classification, IC-OVO-LS-SVM with standard normal variate (SNV) spectra obtained a total classification accuracy of 0.9317, an average sensitivity and specificity of 0.9306 and 0.9971, respectively. With SNV or second-order derivative (D2) spectra, OCPLS could detect at least 2% or more doping levels of adulterants for 5 of the 7 GL species and 5% or more doping levels for the other 2 GL species. This study demonstrates the feasibility of using new chemometrics and NIR spectroscopy for fine classification of GL geographical origins and species as well as for untargeted analysis of multiple adulterants. (C) 2017 Elsevier B.V. All rights reserved.

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