Abstract

Edible gelatin has been widely used as a food additive in the food industry, and illegal adulteration with industrial gelatin will cause serious harm to human health. The present work used laser-induced breakdown spectroscopy (LIBS) coupled with the partial least square–support vector machine (PLS-SVM) method for the fast and accurate estimation of edible gelatin adulteration. Gelatin samples with 11 different adulteration ratios were prepared by mixing pure edible gelatin with industrial gelatin, and the LIBS spectra were recorded to analyze their elemental composition differences. The PLS, SVM, and PLS-SVM models were separately built for the prediction of gelatin adulteration ratios, and the hybrid PLS-SVM model yielded a better performance than only the PLS and SVM models. Besides, four different variable selection methods, including competitive adaptive reweighted sampling (CARS), Monte Carlo uninformative variable elimination (MC-UVE), random frog (RF), and principal component analysis (PCA), were adopted to combine with the SVM model for comparative study; the results further demonstrated that the PLS-SVM model was superior to the other SVM models. This study reveals that the hybrid PLS-SVM model, with the advantages of low computational time and high prediction accuracy, can be employed as a preferred method for the accurate estimation of edible gelatin adulteration.

Highlights

  • Edible gelatin has been frequently used in the food industry and pharmaceutical industry—for example, yogurt, gumdrops, jelly, and gelatin capsules—due to its high protein and abundant amino acids

  • The results further demonstrated that the partial least square–support vector machine (PLS-support vector machine (SVM)) model can be used as an optimal method for quantifying gelatin adulteration by using the laser-induced breakdown spectroscopy (LIBS)

  • LIBS coupled with a hybrid partial least squares (PLS)-SVM model was applied for the fast and accurate determination of gelatin adulteration ratios, with a computation time of 3 s and a limit of detection (LOD) of

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Summary

Introduction

Edible gelatin has been frequently used in the food industry and pharmaceutical industry—for example, yogurt, gumdrops, jelly, and gelatin capsules—due to its high protein and abundant amino acids. It is extremely important to distinguish edible gelatin from industrial gelatin in food and pharmaceutical products. Some analytical techniques such as electrophoretic methods [1,2], enzyme linked immune sorbent assay (ELISA) [3,4,5], high performance liquid chromatography (HPLC) [6,7], and polymerase chain. We have utilized NIRS coupled with supervised pattern recognition methods for the identification of adulterated edible gelatin [14]. Few studies have attempted to explore the potential of the quantitative evaluation of adulteration ratios

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