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High-throughput quantitation method for amodiaquine and desethylamodiaquine in plasma using supported liquid extraction technology
Amodiaquine is a drug used for treatment of malaria and is often used in combination with artesunate in areas where malaria parasites are still susceptible to amodiaquine. Liquid chromatography tandem-mass spectrometry was used to quantify amodiaquine and its active metabolite, desethylamodiaquine,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8417464/ https://www.ncbi.nlm.nih.gov/pubmed/34364298 http://dx.doi.org/10.1016/j.jchromb.2021.122887 |
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author | Kaewkhao, Karnrawee Tarning, Joel Blessborn, Daniel |
author_facet | Kaewkhao, Karnrawee Tarning, Joel Blessborn, Daniel |
author_sort | Kaewkhao, Karnrawee |
collection | PubMed |
description | Amodiaquine is a drug used for treatment of malaria and is often used in combination with artesunate in areas where malaria parasites are still susceptible to amodiaquine. Liquid chromatography tandem-mass spectrometry was used to quantify amodiaquine and its active metabolite, desethylamodiaquine, in plasma samples. A low sample volume of 100 µl, and high-throughput extraction technique using a supported liquid extraction (SLE(+)) technique on an automated liquid handler platform for faster sample processing are some of the advantages of this method. Separation of amodiaquine from desethylamodiaquine was achieved using a reversed phase Zorbax SB-CN 50 mm × 4.6 mm, I.D. 3.5 µm column with acetonitrile and 20 mM ammonium formate with 1% formic acid pH ~ 2.6 (15–85, v/v) as mobile phase. The absolute recoveries of amodiaquine and desethylamodiaquine were 66% to 76%, and their isotope label internal standard were in the range of 73% to 85%. Validation results of the developed method demonstrated intra-batch and inter-batch precisions within the acceptance criteria range of ± 15.0%. There were no matrix or carry-over effects observed. The lower limit of quantification was 1.08 ng/ml for amodiaquine and 1.41 ng/ml for desethylamodiaquine. The method showed robust and accurate performance with high sensitivity. Thus, the validated method was successfully implemented and applied in the evaluation of a clinical trial where participants received artemether–lumefantrine plus amodiaquine twice daily for three days (amodiaquine dose of 10 mg base/kg/day). |
format | Online Article Text |
id | pubmed-8417464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-84174642021-09-08 High-throughput quantitation method for amodiaquine and desethylamodiaquine in plasma using supported liquid extraction technology Kaewkhao, Karnrawee Tarning, Joel Blessborn, Daniel J Chromatogr B Analyt Technol Biomed Life Sci Article Amodiaquine is a drug used for treatment of malaria and is often used in combination with artesunate in areas where malaria parasites are still susceptible to amodiaquine. Liquid chromatography tandem-mass spectrometry was used to quantify amodiaquine and its active metabolite, desethylamodiaquine, in plasma samples. A low sample volume of 100 µl, and high-throughput extraction technique using a supported liquid extraction (SLE(+)) technique on an automated liquid handler platform for faster sample processing are some of the advantages of this method. Separation of amodiaquine from desethylamodiaquine was achieved using a reversed phase Zorbax SB-CN 50 mm × 4.6 mm, I.D. 3.5 µm column with acetonitrile and 20 mM ammonium formate with 1% formic acid pH ~ 2.6 (15–85, v/v) as mobile phase. The absolute recoveries of amodiaquine and desethylamodiaquine were 66% to 76%, and their isotope label internal standard were in the range of 73% to 85%. Validation results of the developed method demonstrated intra-batch and inter-batch precisions within the acceptance criteria range of ± 15.0%. There were no matrix or carry-over effects observed. The lower limit of quantification was 1.08 ng/ml for amodiaquine and 1.41 ng/ml for desethylamodiaquine. The method showed robust and accurate performance with high sensitivity. Thus, the validated method was successfully implemented and applied in the evaluation of a clinical trial where participants received artemether–lumefantrine plus amodiaquine twice daily for three days (amodiaquine dose of 10 mg base/kg/day). Elsevier 2021-08-01 /pmc/articles/PMC8417464/ /pubmed/34364298 http://dx.doi.org/10.1016/j.jchromb.2021.122887 Text en © 2021 The Authors. Published by Elsevier B.V. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kaewkhao, Karnrawee Tarning, Joel Blessborn, Daniel High-throughput quantitation method for amodiaquine and desethylamodiaquine in plasma using supported liquid extraction technology |
title | High-throughput quantitation method for amodiaquine and desethylamodiaquine in plasma using supported liquid extraction technology |
title_full | High-throughput quantitation method for amodiaquine and desethylamodiaquine in plasma using supported liquid extraction technology |
title_fullStr | High-throughput quantitation method for amodiaquine and desethylamodiaquine in plasma using supported liquid extraction technology |
title_full_unstemmed | High-throughput quantitation method for amodiaquine and desethylamodiaquine in plasma using supported liquid extraction technology |
title_short | High-throughput quantitation method for amodiaquine and desethylamodiaquine in plasma using supported liquid extraction technology |
title_sort | high-throughput quantitation method for amodiaquine and desethylamodiaquine in plasma using supported liquid extraction technology |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8417464/ https://www.ncbi.nlm.nih.gov/pubmed/34364298 http://dx.doi.org/10.1016/j.jchromb.2021.122887 |
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