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Development of a Sequential Injection Analysis System for the Determination of Saccharin
Saccharin is a powerfully sweet nonnutritive sweetener that has been approved for food-processing applications within the range of 100–1200 mg/kg. A simple, rapid, and cost-effective sequential injection analysis (SIA) technique was developed to determine the saccharin level. This method is based on...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5751712/ https://www.ncbi.nlm.nih.gov/pubmed/29231885 http://dx.doi.org/10.3390/s17122891 |
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author | Wibowotomo, Budi Eun, Jong-Bang Rhee, Jong Il |
author_facet | Wibowotomo, Budi Eun, Jong-Bang Rhee, Jong Il |
author_sort | Wibowotomo, Budi |
collection | PubMed |
description | Saccharin is a powerfully sweet nonnutritive sweetener that has been approved for food-processing applications within the range of 100–1200 mg/kg. A simple, rapid, and cost-effective sequential injection analysis (SIA) technique was developed to determine the saccharin level. This method is based on the reaction of saccharin with p-chloranil in an ethanol medium with a hydrogen peroxide (H(2)O(2)) acceleration, and the resultant violet-red compound was detected using a UV-Vis spectrophotometer at λ(max) = 420 nm. To ascertain the optimal conditions for the SIA system, several parameters were investigated, including buffer flow rate and volume, p-chloranil concentration, and reactant volumes (saccharin, p-chloranil, and H(2)O(2)). The optimum setup of the SIA system was achieved with a buffer flow rate, buffer volume, and draw-up time of 1.2 mL/min, 2900 µL, and ~145 s, respectively. The optimal p-chloranil concentration is 30 mM, and the best reactant volumes, presented in an ordered sequence, are as follows: 30 µL of H(2)O(2), 450 µL of saccharin, and 150 µL of p-chloranil. The optimized SIA configuration produced a good linear calibration curve with a correlation coefficient (R(2) = 0.9812) in the concentration range of 20–140 mg/L and with a detection limit of 19.69 mg/L. Analytical applications in different food categories also showed acceptable recovery values in the range of 93.1–111.5%. This simple and rapid SIA system offers great feasibility for the saccharin quality control in food-product processing. |
format | Online Article Text |
id | pubmed-5751712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-57517122018-01-10 Development of a Sequential Injection Analysis System for the Determination of Saccharin Wibowotomo, Budi Eun, Jong-Bang Rhee, Jong Il Sensors (Basel) Article Saccharin is a powerfully sweet nonnutritive sweetener that has been approved for food-processing applications within the range of 100–1200 mg/kg. A simple, rapid, and cost-effective sequential injection analysis (SIA) technique was developed to determine the saccharin level. This method is based on the reaction of saccharin with p-chloranil in an ethanol medium with a hydrogen peroxide (H(2)O(2)) acceleration, and the resultant violet-red compound was detected using a UV-Vis spectrophotometer at λ(max) = 420 nm. To ascertain the optimal conditions for the SIA system, several parameters were investigated, including buffer flow rate and volume, p-chloranil concentration, and reactant volumes (saccharin, p-chloranil, and H(2)O(2)). The optimum setup of the SIA system was achieved with a buffer flow rate, buffer volume, and draw-up time of 1.2 mL/min, 2900 µL, and ~145 s, respectively. The optimal p-chloranil concentration is 30 mM, and the best reactant volumes, presented in an ordered sequence, are as follows: 30 µL of H(2)O(2), 450 µL of saccharin, and 150 µL of p-chloranil. The optimized SIA configuration produced a good linear calibration curve with a correlation coefficient (R(2) = 0.9812) in the concentration range of 20–140 mg/L and with a detection limit of 19.69 mg/L. Analytical applications in different food categories also showed acceptable recovery values in the range of 93.1–111.5%. This simple and rapid SIA system offers great feasibility for the saccharin quality control in food-product processing. MDPI 2017-12-12 /pmc/articles/PMC5751712/ /pubmed/29231885 http://dx.doi.org/10.3390/s17122891 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wibowotomo, Budi Eun, Jong-Bang Rhee, Jong Il Development of a Sequential Injection Analysis System for the Determination of Saccharin |
title | Development of a Sequential Injection Analysis System for the Determination of Saccharin |
title_full | Development of a Sequential Injection Analysis System for the Determination of Saccharin |
title_fullStr | Development of a Sequential Injection Analysis System for the Determination of Saccharin |
title_full_unstemmed | Development of a Sequential Injection Analysis System for the Determination of Saccharin |
title_short | Development of a Sequential Injection Analysis System for the Determination of Saccharin |
title_sort | development of a sequential injection analysis system for the determination of saccharin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5751712/ https://www.ncbi.nlm.nih.gov/pubmed/29231885 http://dx.doi.org/10.3390/s17122891 |
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