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Development and validation of a new analytical method for determination of linagliptin in bulk by visible spectrophotometer
A simple, economical, and specific analytical method has been developed for determining and validating linagliptin (LNG) in bulk. This method is based on a condensation reaction between a primary amine in LNG and an aldehyde group in P-dimethylaminobenzaldehyde (PDAB) to form the yellow Schiff base...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008578/ https://www.ncbi.nlm.nih.gov/pubmed/36906687 http://dx.doi.org/10.1038/s41598-023-31202-w |
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author | Sahloul, Lujain Salami, Maisam |
author_facet | Sahloul, Lujain Salami, Maisam |
author_sort | Sahloul, Lujain |
collection | PubMed |
description | A simple, economical, and specific analytical method has been developed for determining and validating linagliptin (LNG) in bulk. This method is based on a condensation reaction between a primary amine in LNG and an aldehyde group in P-dimethylaminobenzaldehyde (PDAB) to form the yellow Schiff base with a wavelength of 407 nm. The optimum experimental conditions for the formulation of the colored complex have been studied. The optimum conditions were 1 mL of 5% w/v reagent solution with methanol and distilled water as a solvent for both PDAB, LNG respectively, also adding 2 mL of HCl as an acidic medium, heating to 70–75 °C on a water bath for 35 min. Furthermore, the stoichiometry of the reaction has been studied according to Job’s and Molar ratio method which was expressing 1:1 for LNG and PDAB. The researcher modified the method. The results show that the linearity in the concentration range (5–45 µg/mL) with correlation coefficient R(2) = 0.9989 with percent recovery (99.46–100.8%) and RSD was less than 2%, LOD and LOQ 1.5815 − 4.7924 μg/mL respectively. This method can show high quality and there is no significant interference with excipients and in pharmaceutical forms. None of the studies showed the development of this method before. |
format | Online Article Text |
id | pubmed-10008578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100085782023-03-13 Development and validation of a new analytical method for determination of linagliptin in bulk by visible spectrophotometer Sahloul, Lujain Salami, Maisam Sci Rep Article A simple, economical, and specific analytical method has been developed for determining and validating linagliptin (LNG) in bulk. This method is based on a condensation reaction between a primary amine in LNG and an aldehyde group in P-dimethylaminobenzaldehyde (PDAB) to form the yellow Schiff base with a wavelength of 407 nm. The optimum experimental conditions for the formulation of the colored complex have been studied. The optimum conditions were 1 mL of 5% w/v reagent solution with methanol and distilled water as a solvent for both PDAB, LNG respectively, also adding 2 mL of HCl as an acidic medium, heating to 70–75 °C on a water bath for 35 min. Furthermore, the stoichiometry of the reaction has been studied according to Job’s and Molar ratio method which was expressing 1:1 for LNG and PDAB. The researcher modified the method. The results show that the linearity in the concentration range (5–45 µg/mL) with correlation coefficient R(2) = 0.9989 with percent recovery (99.46–100.8%) and RSD was less than 2%, LOD and LOQ 1.5815 − 4.7924 μg/mL respectively. This method can show high quality and there is no significant interference with excipients and in pharmaceutical forms. None of the studies showed the development of this method before. Nature Publishing Group UK 2023-03-11 /pmc/articles/PMC10008578/ /pubmed/36906687 http://dx.doi.org/10.1038/s41598-023-31202-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Sahloul, Lujain Salami, Maisam Development and validation of a new analytical method for determination of linagliptin in bulk by visible spectrophotometer |
title | Development and validation of a new analytical method for determination of linagliptin in bulk by visible spectrophotometer |
title_full | Development and validation of a new analytical method for determination of linagliptin in bulk by visible spectrophotometer |
title_fullStr | Development and validation of a new analytical method for determination of linagliptin in bulk by visible spectrophotometer |
title_full_unstemmed | Development and validation of a new analytical method for determination of linagliptin in bulk by visible spectrophotometer |
title_short | Development and validation of a new analytical method for determination of linagliptin in bulk by visible spectrophotometer |
title_sort | development and validation of a new analytical method for determination of linagliptin in bulk by visible spectrophotometer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008578/ https://www.ncbi.nlm.nih.gov/pubmed/36906687 http://dx.doi.org/10.1038/s41598-023-31202-w |
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