In-tip solid-phase microextraction: a method for determination of sulphonamide residues in environmental water samples
This study involved the development of an in-pipette tip solid-phase microextraction (SPME) method using activated charcoal as an adsorbent. Simultaneous determination of three sulphonamide antibiotic residues in environmental water was performed using this method, coupled with high-performance liqu...
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my.um.eprints.443402024-07-09T04:18:30Z http://eprints.um.edu.my/44340/ In-tip solid-phase microextraction: a method for determination of sulphonamide residues in environmental water samples Lu, Tan Lei Shahriman, Mohamad Shariff Sambasevam, Kavirajaa Pandian Zain, Nur Nadhirah Mohamad Yahaya, Noorfatimah Lim, Vuanghao Raoov, Muggundha QD Chemistry S Agriculture (General) This study involved the development of an in-pipette tip solid-phase microextraction (SPME) method using activated charcoal as an adsorbent. Simultaneous determination of three sulphonamide antibiotic residues in environmental water was performed using this method, coupled with high-performance liquid chromatography-photodiode array (HPLC-PDA) detection. Seven extraction parameters were optimised by one-variable-at-a-time (OVAT) and response surface (RSM) methods. Optimum extraction efficiency was achieved when 10 mL of sample solution at a natural pH (pH 5-6) was loaded through a 1 mL pipette tip packed with 10 mg of adsorbent, washed with 1 mL of hexane and eluted with 500 mu L of 1% ammonium in methanol solution. Under the optimised experimental condition, this method manifested good linearity (5-500 mu g L-1) at the coefficient of determination, R-2 of 0.9992 to 0.9993, high sensitivity (limit of detection, LOD: 0.38-1.14 mu g L-1; limit of quantification, LOQ: 1.14-3.35 mu g L-1), and satisfactory recoveries (82.8-108.7%) with acceptable reproducibility (RSD < 4.6%). Real sample analysis of five environmental water samples sourced from Universiti Malaya, Kuala Lumpur and Malacca showed that the samples contained either none or traces of the target sulphonamides (SAs) with their concentration lower than the LOQs. In contrast to other methods, the comparison outcomes depicted that this in-tip SPME method was beneficial in terms of its simple, reusable, cost-saving setup together with a significant reduction in chemical consumption. Taylor & Francis 2024-01-26 Article PeerReviewed Lu, Tan Lei and Shahriman, Mohamad Shariff and Sambasevam, Kavirajaa Pandian and Zain, Nur Nadhirah Mohamad and Yahaya, Noorfatimah and Lim, Vuanghao and Raoov, Muggundha (2024) In-tip solid-phase microextraction: a method for determination of sulphonamide residues in environmental water samples. International Journal of Environmental Analytical Chemistry, 104 (2). pp. 261-276. ISSN 0306-7319, DOI https://doi.org/10.1080/03067319.2021.2019721 <https://doi.org/10.1080/03067319.2021.2019721>. https://doi.org/10.1080/03067319.2021.2019721 10.1080/03067319.2021.2019721 |
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QD Chemistry S Agriculture (General) Lu, Tan Lei Shahriman, Mohamad Shariff Sambasevam, Kavirajaa Pandian Zain, Nur Nadhirah Mohamad Yahaya, Noorfatimah Lim, Vuanghao Raoov, Muggundha In-tip solid-phase microextraction: a method for determination of sulphonamide residues in environmental water samples |
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This study involved the development of an in-pipette tip solid-phase microextraction (SPME) method using activated charcoal as an adsorbent. Simultaneous determination of three sulphonamide antibiotic residues in environmental water was performed using this method, coupled with high-performance liquid chromatography-photodiode array (HPLC-PDA) detection. Seven extraction parameters were optimised by one-variable-at-a-time (OVAT) and response surface (RSM) methods. Optimum extraction efficiency was achieved when 10 mL of sample solution at a natural pH (pH 5-6) was loaded through a 1 mL pipette tip packed with 10 mg of adsorbent, washed with 1 mL of hexane and eluted with 500 mu L of 1% ammonium in methanol solution. Under the optimised experimental condition, this method manifested good linearity (5-500 mu g L-1) at the coefficient of determination, R-2 of 0.9992 to 0.9993, high sensitivity (limit of detection, LOD: 0.38-1.14 mu g L-1; limit of quantification, LOQ: 1.14-3.35 mu g L-1), and satisfactory recoveries (82.8-108.7%) with acceptable reproducibility (RSD < 4.6%). Real sample analysis of five environmental water samples sourced from Universiti Malaya, Kuala Lumpur and Malacca showed that the samples contained either none or traces of the target sulphonamides (SAs) with their concentration lower than the LOQs. In contrast to other methods, the comparison outcomes depicted that this in-tip SPME method was beneficial in terms of its simple, reusable, cost-saving setup together with a significant reduction in chemical consumption. |
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Article |
author |
Lu, Tan Lei Shahriman, Mohamad Shariff Sambasevam, Kavirajaa Pandian Zain, Nur Nadhirah Mohamad Yahaya, Noorfatimah Lim, Vuanghao Raoov, Muggundha |
author_facet |
Lu, Tan Lei Shahriman, Mohamad Shariff Sambasevam, Kavirajaa Pandian Zain, Nur Nadhirah Mohamad Yahaya, Noorfatimah Lim, Vuanghao Raoov, Muggundha |
author_sort |
Lu, Tan Lei |
title |
In-tip solid-phase microextraction: a method for determination of sulphonamide residues in environmental water samples |
title_short |
In-tip solid-phase microextraction: a method for determination of sulphonamide residues in environmental water samples |
title_full |
In-tip solid-phase microextraction: a method for determination of sulphonamide residues in environmental water samples |
title_fullStr |
In-tip solid-phase microextraction: a method for determination of sulphonamide residues in environmental water samples |
title_full_unstemmed |
In-tip solid-phase microextraction: a method for determination of sulphonamide residues in environmental water samples |
title_sort |
in-tip solid-phase microextraction: a method for determination of sulphonamide residues in environmental water samples |
publisher |
Taylor & Francis |
publishDate |
2024 |
url |
http://eprints.um.edu.my/44340/ https://doi.org/10.1080/03067319.2021.2019721 |
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1805881162081501184 |
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13.211869 |