DEVELOPMENT AND VALIDATION OF AN ECOLOGICAL, NEW AND RAPID STABILITY-INDICATING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY FOR QUANTITATIVE DETERMINATION OF AZTREONAM IN LYOPHILIZED POWDER FOR INJECTION
Aztreonam is a monocyclic synthetic antimicrobial with bactericidal activity against Gram-negative bacteria, the first agent from the monobactam family to be therapeutically approved. It was developed and validated analytical method using high performance liquid chromatography with UV detection at...
Main Authors: | , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Universidade Federal do Rio Grande do Sul
2017-08-01
|
Series: | Drug Analytical Research |
Online Access: | https://seer.ufrgs.br/index.php/dar/article/view/73755 |
_version_ | 1797271658145251328 |
---|---|
author | Andressa Leme Figueiredo Ana Carolina Kogawa Hérida Regina Nunes Salgado |
author_facet | Andressa Leme Figueiredo Ana Carolina Kogawa Hérida Regina Nunes Salgado |
author_sort | Andressa Leme Figueiredo |
collection | DOAJ |
description |
Aztreonam is a monocyclic synthetic antimicrobial with bactericidal activity against Gram-negative bacteria, the first agent from the monobactam family to be therapeutically approved. It was developed and validated analytical method using high performance liquid chromatography with UV detection at 292 nm to quantify the aztreonam. Furthermore, assessing stability through stress tests was carried out. The chromatographic separation was carried out by reverse phase on an Agilent C18 column (250 x 4.6 mm, 5 µm) with a mobile phase composed of water:ethanol (70:30, v/v) adjusted to pH 2.5 with acetic acid, pumped isocratically at a flow rate of 0.5 mL/min. The validation parameters linearity, selectivity, precision, accuracy, robustness, limits of detection and quantification were determined. The method proposed provides linear response within the concentration range of 45-95 µg/mL for aztreonam. Results obtained were found to be satisfactory. The proposed method is linear, accurate, precise, selective, and robust being able to quantify the aztreonam in raw material and in pharmaceutical preparations. The validated method was suitable for applications in quality control laboratories.
|
first_indexed | 2024-03-07T14:08:38Z |
format | Article |
id | doaj.art-413baf3d6d044b99aea06ffd8eeeec0e |
institution | Directory Open Access Journal |
issn | 2527-2616 |
language | English |
last_indexed | 2024-03-07T14:08:38Z |
publishDate | 2017-08-01 |
publisher | Universidade Federal do Rio Grande do Sul |
record_format | Article |
series | Drug Analytical Research |
spelling | doaj.art-413baf3d6d044b99aea06ffd8eeeec0e2024-03-06T18:15:35ZengUniversidade Federal do Rio Grande do SulDrug Analytical Research2527-26162017-08-0111DEVELOPMENT AND VALIDATION OF AN ECOLOGICAL, NEW AND RAPID STABILITY-INDICATING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY FOR QUANTITATIVE DETERMINATION OF AZTREONAM IN LYOPHILIZED POWDER FOR INJECTIONAndressa Leme Figueiredo0Ana Carolina Kogawa1Hérida Regina Nunes Salgado2Universidade Estadual PaulistaUniversidade Estadual PaulistaUniversidade Estadual Paulista Aztreonam is a monocyclic synthetic antimicrobial with bactericidal activity against Gram-negative bacteria, the first agent from the monobactam family to be therapeutically approved. It was developed and validated analytical method using high performance liquid chromatography with UV detection at 292 nm to quantify the aztreonam. Furthermore, assessing stability through stress tests was carried out. The chromatographic separation was carried out by reverse phase on an Agilent C18 column (250 x 4.6 mm, 5 µm) with a mobile phase composed of water:ethanol (70:30, v/v) adjusted to pH 2.5 with acetic acid, pumped isocratically at a flow rate of 0.5 mL/min. The validation parameters linearity, selectivity, precision, accuracy, robustness, limits of detection and quantification were determined. The method proposed provides linear response within the concentration range of 45-95 µg/mL for aztreonam. Results obtained were found to be satisfactory. The proposed method is linear, accurate, precise, selective, and robust being able to quantify the aztreonam in raw material and in pharmaceutical preparations. The validated method was suitable for applications in quality control laboratories. https://seer.ufrgs.br/index.php/dar/article/view/73755 |
spellingShingle | Andressa Leme Figueiredo Ana Carolina Kogawa Hérida Regina Nunes Salgado DEVELOPMENT AND VALIDATION OF AN ECOLOGICAL, NEW AND RAPID STABILITY-INDICATING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY FOR QUANTITATIVE DETERMINATION OF AZTREONAM IN LYOPHILIZED POWDER FOR INJECTION Drug Analytical Research |
title | DEVELOPMENT AND VALIDATION OF AN ECOLOGICAL, NEW AND RAPID STABILITY-INDICATING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY FOR QUANTITATIVE DETERMINATION OF AZTREONAM IN LYOPHILIZED POWDER FOR INJECTION |
title_full | DEVELOPMENT AND VALIDATION OF AN ECOLOGICAL, NEW AND RAPID STABILITY-INDICATING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY FOR QUANTITATIVE DETERMINATION OF AZTREONAM IN LYOPHILIZED POWDER FOR INJECTION |
title_fullStr | DEVELOPMENT AND VALIDATION OF AN ECOLOGICAL, NEW AND RAPID STABILITY-INDICATING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY FOR QUANTITATIVE DETERMINATION OF AZTREONAM IN LYOPHILIZED POWDER FOR INJECTION |
title_full_unstemmed | DEVELOPMENT AND VALIDATION OF AN ECOLOGICAL, NEW AND RAPID STABILITY-INDICATING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY FOR QUANTITATIVE DETERMINATION OF AZTREONAM IN LYOPHILIZED POWDER FOR INJECTION |
title_short | DEVELOPMENT AND VALIDATION OF AN ECOLOGICAL, NEW AND RAPID STABILITY-INDICATING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY FOR QUANTITATIVE DETERMINATION OF AZTREONAM IN LYOPHILIZED POWDER FOR INJECTION |
title_sort | development and validation of an ecological new and rapid stability indicating high performance liquid chromatography for quantitative determination of aztreonam in lyophilized powder for injection |
url | https://seer.ufrgs.br/index.php/dar/article/view/73755 |
work_keys_str_mv | AT andressalemefigueiredo developmentandvalidationofanecologicalnewandrapidstabilityindicatinghighperformanceliquidchromatographyforquantitativedeterminationofaztreonaminlyophilizedpowderforinjection AT anacarolinakogawa developmentandvalidationofanecologicalnewandrapidstabilityindicatinghighperformanceliquidchromatographyforquantitativedeterminationofaztreonaminlyophilizedpowderforinjection AT heridareginanunessalgado developmentandvalidationofanecologicalnewandrapidstabilityindicatinghighperformanceliquidchromatographyforquantitativedeterminationofaztreonaminlyophilizedpowderforinjection |