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Fully-automated magnetic stirring-assisted lab-in-syringe dispersive liquid–liquid microextraction for the determination of arsenic species in rice samples

Fully-automated magnetic stirring-assisted lab-in-syringe dispersive liquid–liquid microextraction (MAS-LIS-DLLME), combined with graphite furnace atomic absorption spectrometry (GFAAS) was developed for the fast and efficient separation and preconcentration of trace levels of inorganic arsenic spec...

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Detalles Bibliográficos
Autores principales: Wang, Xiaojun, Xu, Guoliang, Chen, Peng, Sun, Yueshu, Yao, Xiaoting, Lv, Yan, Guo, Weiwei, Wang, Guozhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080300/
https://www.ncbi.nlm.nih.gov/pubmed/35540556
http://dx.doi.org/10.1039/c8ra00875b
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author Wang, Xiaojun
Xu, Guoliang
Chen, Peng
Sun, Yueshu
Yao, Xiaoting
Lv, Yan
Guo, Weiwei
Wang, Guozhen
author_facet Wang, Xiaojun
Xu, Guoliang
Chen, Peng
Sun, Yueshu
Yao, Xiaoting
Lv, Yan
Guo, Weiwei
Wang, Guozhen
author_sort Wang, Xiaojun
collection PubMed
description Fully-automated magnetic stirring-assisted lab-in-syringe dispersive liquid–liquid microextraction (MAS-LIS-DLLME), combined with graphite furnace atomic absorption spectrometry (GFAAS) was developed for the fast and efficient separation and preconcentration of trace levels of inorganic arsenic species in rice samples. This totally automated analytical procedure combines the advantages of lab-in-syringe flow system and dispersive liquid–liquid microextraction (DLLME) aiming at separation of trace arsenite and arsenate species from natural matrix for the first time. With a single syringe pump that is coupled with a multiposition valve, the whole lab-in-syringe microextraction process including cleaning, mixing, microextraction, phase separation, and target analyte collection was implemented in a fully-automated way. Significant factors of the MAS-LIS-DLLME method were sample acidity, concentration of the chelating agent, amounts of ionic liquids (ILs), aspiration speed and matrix interference. Using the present method, the limits of detection (LODs) for As(v) was 0.005 μg L(−1). The relative standard deviation (RSDs) for seven replicate measurements of 2.0 μg L(−1) of As(v) was 3.7%. The linear dynamic range (LDR) was 0.04–5.0 μg L(−1) and the determination coefficients was 0.9990. Under the optimum conditions, the developed totally automated analytical procedure was successfully applied for the trace arsenite and arsenate species studies in natural rice samples and standard reference materials with satisfactory results.
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spelling pubmed-90803002022-05-09 Fully-automated magnetic stirring-assisted lab-in-syringe dispersive liquid–liquid microextraction for the determination of arsenic species in rice samples Wang, Xiaojun Xu, Guoliang Chen, Peng Sun, Yueshu Yao, Xiaoting Lv, Yan Guo, Weiwei Wang, Guozhen RSC Adv Chemistry Fully-automated magnetic stirring-assisted lab-in-syringe dispersive liquid–liquid microextraction (MAS-LIS-DLLME), combined with graphite furnace atomic absorption spectrometry (GFAAS) was developed for the fast and efficient separation and preconcentration of trace levels of inorganic arsenic species in rice samples. This totally automated analytical procedure combines the advantages of lab-in-syringe flow system and dispersive liquid–liquid microextraction (DLLME) aiming at separation of trace arsenite and arsenate species from natural matrix for the first time. With a single syringe pump that is coupled with a multiposition valve, the whole lab-in-syringe microextraction process including cleaning, mixing, microextraction, phase separation, and target analyte collection was implemented in a fully-automated way. Significant factors of the MAS-LIS-DLLME method were sample acidity, concentration of the chelating agent, amounts of ionic liquids (ILs), aspiration speed and matrix interference. Using the present method, the limits of detection (LODs) for As(v) was 0.005 μg L(−1). The relative standard deviation (RSDs) for seven replicate measurements of 2.0 μg L(−1) of As(v) was 3.7%. The linear dynamic range (LDR) was 0.04–5.0 μg L(−1) and the determination coefficients was 0.9990. Under the optimum conditions, the developed totally automated analytical procedure was successfully applied for the trace arsenite and arsenate species studies in natural rice samples and standard reference materials with satisfactory results. The Royal Society of Chemistry 2018-05-08 /pmc/articles/PMC9080300/ /pubmed/35540556 http://dx.doi.org/10.1039/c8ra00875b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Wang, Xiaojun
Xu, Guoliang
Chen, Peng
Sun, Yueshu
Yao, Xiaoting
Lv, Yan
Guo, Weiwei
Wang, Guozhen
Fully-automated magnetic stirring-assisted lab-in-syringe dispersive liquid–liquid microextraction for the determination of arsenic species in rice samples
title Fully-automated magnetic stirring-assisted lab-in-syringe dispersive liquid–liquid microextraction for the determination of arsenic species in rice samples
title_full Fully-automated magnetic stirring-assisted lab-in-syringe dispersive liquid–liquid microextraction for the determination of arsenic species in rice samples
title_fullStr Fully-automated magnetic stirring-assisted lab-in-syringe dispersive liquid–liquid microextraction for the determination of arsenic species in rice samples
title_full_unstemmed Fully-automated magnetic stirring-assisted lab-in-syringe dispersive liquid–liquid microextraction for the determination of arsenic species in rice samples
title_short Fully-automated magnetic stirring-assisted lab-in-syringe dispersive liquid–liquid microextraction for the determination of arsenic species in rice samples
title_sort fully-automated magnetic stirring-assisted lab-in-syringe dispersive liquid–liquid microextraction for the determination of arsenic species in rice samples
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080300/
https://www.ncbi.nlm.nih.gov/pubmed/35540556
http://dx.doi.org/10.1039/c8ra00875b
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