Cargando…
Rapid Iodine Value Estimation Using a Handheld Raman Spectrometer for On-Site, Reagent-Free Authentication of Edible Oils
[Image: see text] Edible oil adulteration is a common and serious issue faced by human societies across the world. Iodine value (IV), the total unsaturation measure, is an authentication tool used by food safety officers and industries for edible oils. Current wet titrimetric methods (e.g., Wijs met...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8945061/ https://www.ncbi.nlm.nih.gov/pubmed/35350360 http://dx.doi.org/10.1021/acsomega.1c05123 |
_version_ | 1784673862548455424 |
---|---|
author | Pulassery, Sanoop Abraham, Bini Ajikumar, Nandu Munnilath, Arun Yoosaf, Karuvath |
author_facet | Pulassery, Sanoop Abraham, Bini Ajikumar, Nandu Munnilath, Arun Yoosaf, Karuvath |
author_sort | Pulassery, Sanoop |
collection | PubMed |
description | [Image: see text] Edible oil adulteration is a common and serious issue faced by human societies across the world. Iodine value (IV), the total unsaturation measure, is an authentication tool used by food safety officers and industries for edible oils. Current wet titrimetric methods (e.g., Wijs method) employed for IV estimation use dangerous chemicals and elaborate procedures for analysis. Alternate approaches for oil analysis require sophisticated and costly equipment such as gas chromatography (GC), liquid chromatography, high-performance liquid chromatography, mass spectrometry (MS), UV-Visible, and nuclear magnetic resonance spectroscopies. Mass screening of the samples from the market and industrial environment requires a greener, fast, and more robust technique and is an unmet need. Herein, we present a handheld Raman spectrometer-based methodology for fast IV estimation. We conducted a detailed Raman spectroscopic investigation of coconut oil, sunflower oil, and intentionally adulterated mixtures with a handheld device having a 785 nm excitation source. The obtained data were analyzed in conjunction with the GC–MS results and the conventional wet Wijs titrimetric estimated IVs. Based on these studies, a specific equation for IV estimation is derived from the intensity of identified Raman spectral bands. Further, an algorithm is designed to automate the signal processing and IV estimation, and a stand-alone graphical user interface is created in user-friendly LabVIEW software. The data acquisition and analysis require < 2 minutes, and the estimated statistical parameters such as the R(2) value (0.9), root-mean-square error of calibration (1.3), and root-mean-square error of prediction (0.9) indicate that the demonstrated method has a high precision level. Also, the limit of detection and the limit of quantification for IV estimation through the current approach is ∼1 and ∼3 gI(2)/100 g oil, respectively. The IVs of different oils, including hydrogenated vegetable oils, were evaluated, and the results show an excellent correlation between the estimated and reported ones. |
format | Online Article Text |
id | pubmed-8945061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-89450612022-03-28 Rapid Iodine Value Estimation Using a Handheld Raman Spectrometer for On-Site, Reagent-Free Authentication of Edible Oils Pulassery, Sanoop Abraham, Bini Ajikumar, Nandu Munnilath, Arun Yoosaf, Karuvath ACS Omega [Image: see text] Edible oil adulteration is a common and serious issue faced by human societies across the world. Iodine value (IV), the total unsaturation measure, is an authentication tool used by food safety officers and industries for edible oils. Current wet titrimetric methods (e.g., Wijs method) employed for IV estimation use dangerous chemicals and elaborate procedures for analysis. Alternate approaches for oil analysis require sophisticated and costly equipment such as gas chromatography (GC), liquid chromatography, high-performance liquid chromatography, mass spectrometry (MS), UV-Visible, and nuclear magnetic resonance spectroscopies. Mass screening of the samples from the market and industrial environment requires a greener, fast, and more robust technique and is an unmet need. Herein, we present a handheld Raman spectrometer-based methodology for fast IV estimation. We conducted a detailed Raman spectroscopic investigation of coconut oil, sunflower oil, and intentionally adulterated mixtures with a handheld device having a 785 nm excitation source. The obtained data were analyzed in conjunction with the GC–MS results and the conventional wet Wijs titrimetric estimated IVs. Based on these studies, a specific equation for IV estimation is derived from the intensity of identified Raman spectral bands. Further, an algorithm is designed to automate the signal processing and IV estimation, and a stand-alone graphical user interface is created in user-friendly LabVIEW software. The data acquisition and analysis require < 2 minutes, and the estimated statistical parameters such as the R(2) value (0.9), root-mean-square error of calibration (1.3), and root-mean-square error of prediction (0.9) indicate that the demonstrated method has a high precision level. Also, the limit of detection and the limit of quantification for IV estimation through the current approach is ∼1 and ∼3 gI(2)/100 g oil, respectively. The IVs of different oils, including hydrogenated vegetable oils, were evaluated, and the results show an excellent correlation between the estimated and reported ones. American Chemical Society 2022-03-08 /pmc/articles/PMC8945061/ /pubmed/35350360 http://dx.doi.org/10.1021/acsomega.1c05123 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Pulassery, Sanoop Abraham, Bini Ajikumar, Nandu Munnilath, Arun Yoosaf, Karuvath Rapid Iodine Value Estimation Using a Handheld Raman Spectrometer for On-Site, Reagent-Free Authentication of Edible Oils |
title | Rapid Iodine Value Estimation Using a Handheld Raman
Spectrometer for On-Site, Reagent-Free Authentication of Edible Oils |
title_full | Rapid Iodine Value Estimation Using a Handheld Raman
Spectrometer for On-Site, Reagent-Free Authentication of Edible Oils |
title_fullStr | Rapid Iodine Value Estimation Using a Handheld Raman
Spectrometer for On-Site, Reagent-Free Authentication of Edible Oils |
title_full_unstemmed | Rapid Iodine Value Estimation Using a Handheld Raman
Spectrometer for On-Site, Reagent-Free Authentication of Edible Oils |
title_short | Rapid Iodine Value Estimation Using a Handheld Raman
Spectrometer for On-Site, Reagent-Free Authentication of Edible Oils |
title_sort | rapid iodine value estimation using a handheld raman
spectrometer for on-site, reagent-free authentication of edible oils |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8945061/ https://www.ncbi.nlm.nih.gov/pubmed/35350360 http://dx.doi.org/10.1021/acsomega.1c05123 |
work_keys_str_mv | AT pulasserysanoop rapidiodinevalueestimationusingahandheldramanspectrometerforonsitereagentfreeauthenticationofedibleoils AT abrahambini rapidiodinevalueestimationusingahandheldramanspectrometerforonsitereagentfreeauthenticationofedibleoils AT ajikumarnandu rapidiodinevalueestimationusingahandheldramanspectrometerforonsitereagentfreeauthenticationofedibleoils AT munnilatharun rapidiodinevalueestimationusingahandheldramanspectrometerforonsitereagentfreeauthenticationofedibleoils AT yoosafkaruvath rapidiodinevalueestimationusingahandheldramanspectrometerforonsitereagentfreeauthenticationofedibleoils |