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Salting-out induced liquid–liquid microextraction for alogliptin benzoate determination in human plasma by HPLC/UV
Salting-out induced liquid–liquid microextraction method has been developed for plasma sample treatment before determination of alogliptin by high performance liquid chromatography with UV detection. Several parameters were optimized to achieve maximum enrichment, including type of extractant, volum...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809805/ https://www.ncbi.nlm.nih.gov/pubmed/33451337 http://dx.doi.org/10.1186/s13065-020-00729-8 |
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author | Hammad, Sherin F. Abdallah, Inas A. Bedair, Alaa Mansour, Fotouh R. |
author_facet | Hammad, Sherin F. Abdallah, Inas A. Bedair, Alaa Mansour, Fotouh R. |
author_sort | Hammad, Sherin F. |
collection | PubMed |
description | Salting-out induced liquid–liquid microextraction method has been developed for plasma sample treatment before determination of alogliptin by high performance liquid chromatography with UV detection. Several parameters were optimized to achieve maximum enrichment, including type of extractant, volume of extractant, type of anion, type of cation, salt amount and pH. The optimum conditions were attained using 500 µL of acetonitrile, added to 1 mL of aqueous sample containing 250 mg of sodium chloride at pH 12. An RP-HPLC method was developed and validated according to the International Conference on Harmonization guidelines M10. The method was linear in the concentration range of 0.1 to 50 µg/mL (correlation coefficient = 0.997). The limit of detection was 0.019 µg/mL and limit of quantitation was 0.06 µg/mL. The method was accurate and precise with an average % recovery of 99.7% and a % relative standard deviation ranging between 1.5 and 2.5. These results showed that the salting-out induced liquid–liquid microextraction methods could be better than other sample preparation protocols in terms of sensitivity, easiness, solvent consumption and waste reduction. |
format | Online Article Text |
id | pubmed-7809805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-78098052021-01-18 Salting-out induced liquid–liquid microextraction for alogliptin benzoate determination in human plasma by HPLC/UV Hammad, Sherin F. Abdallah, Inas A. Bedair, Alaa Mansour, Fotouh R. BMC Chem Research Article Salting-out induced liquid–liquid microextraction method has been developed for plasma sample treatment before determination of alogliptin by high performance liquid chromatography with UV detection. Several parameters were optimized to achieve maximum enrichment, including type of extractant, volume of extractant, type of anion, type of cation, salt amount and pH. The optimum conditions were attained using 500 µL of acetonitrile, added to 1 mL of aqueous sample containing 250 mg of sodium chloride at pH 12. An RP-HPLC method was developed and validated according to the International Conference on Harmonization guidelines M10. The method was linear in the concentration range of 0.1 to 50 µg/mL (correlation coefficient = 0.997). The limit of detection was 0.019 µg/mL and limit of quantitation was 0.06 µg/mL. The method was accurate and precise with an average % recovery of 99.7% and a % relative standard deviation ranging between 1.5 and 2.5. These results showed that the salting-out induced liquid–liquid microextraction methods could be better than other sample preparation protocols in terms of sensitivity, easiness, solvent consumption and waste reduction. Springer International Publishing 2021-01-15 /pmc/articles/PMC7809805/ /pubmed/33451337 http://dx.doi.org/10.1186/s13065-020-00729-8 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Hammad, Sherin F. Abdallah, Inas A. Bedair, Alaa Mansour, Fotouh R. Salting-out induced liquid–liquid microextraction for alogliptin benzoate determination in human plasma by HPLC/UV |
title | Salting-out induced liquid–liquid microextraction for alogliptin benzoate determination in human plasma by HPLC/UV |
title_full | Salting-out induced liquid–liquid microextraction for alogliptin benzoate determination in human plasma by HPLC/UV |
title_fullStr | Salting-out induced liquid–liquid microextraction for alogliptin benzoate determination in human plasma by HPLC/UV |
title_full_unstemmed | Salting-out induced liquid–liquid microextraction for alogliptin benzoate determination in human plasma by HPLC/UV |
title_short | Salting-out induced liquid–liquid microextraction for alogliptin benzoate determination in human plasma by HPLC/UV |
title_sort | salting-out induced liquid–liquid microextraction for alogliptin benzoate determination in human plasma by hplc/uv |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809805/ https://www.ncbi.nlm.nih.gov/pubmed/33451337 http://dx.doi.org/10.1186/s13065-020-00729-8 |
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