Attenuated Total Reflectance-FTIR Spectra Combined with Multivariate Calibration and Discrimination Analysis for Analysis of Patchouli Oil Adulteration
Author(s) -
Zaki Fahmi,
Mudasir Mudasir,
Abdul Rohman
Publication year - 2019
Publication title -
indonesian journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.273
H-Index - 14
eISSN - 2460-1578
pISSN - 1411-9420
DOI - 10.22146/ijc.36955
Subject(s) - chemistry , chemometrics , principal component analysis , partial least squares regression , principal component regression , analytical chemistry (journal) , calibration , fourier transform infrared spectroscopy , chromatography , attenuated total reflection , mean squared error , coefficient of determination , infrared spectroscopy , mathematics , statistics , organic chemistry , physics , quantum mechanics
The adulteration of high priced oils such as patchouli oil with lower price ones is motivated to gain the economical profits. The aim of this study was to use FTIR spectroscopy combined with chemometrics for the authentication of patchouli oil (PaO) in the mixtures with Castor Oil (CO) and Palm Oil (PO). The FTIR spectra of PaO and various vegetable oils were scanned at mid infrared region (4000–650 cm –1 ), and were subjected to principal component analysis (PCA). Quantitative analysis of PaO adulterated with CO and PO were carried out with multivariate calibration of Partial Least Square (PLS) regression. Based on PCA, PaO has the close similarity to CO and PO. From the optimization results, FTIR normal spectra in the combined wavenumbers of 1200–1000 and 3100–2900 cm –1 were chosen to quantify PaO in PO with coefficient of determination (R 2 ) value of 0.9856 and root mean square error of calibration (RMSEC) of 4.57% in calibration model. In addition, R 2 and root mean square error of prediction (RMSEP) values of 0.9984 and 1.79% were obtained during validation, respectively. The normal spectra in the wavenumbers region of 1200–1000 cm –1 were preferred to quantify PaO in CO with R 2 value of 0.9816 and RMSEC of 6.89% in calibration, while in validation model, the R 2 value of 0.9974 and RMSEP of 2.57% were obtained. Discriminant analysis was also successfully used for classification of PaO and PaO adulterated with PO and CO without misclassification observed. The combination of FTIR spectroscopy and chemometrics provided an appropriate model for authentication study of PaO adulterated with PO and CO.
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