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Stability of Ampicillin plus Ceftriaxone Combined in Elastomeric Infusion Devices for Outpatient Parenteral Antimicrobial Therapy

Currently, ampicillin plus ceftriaxone (AC) is one of the preferred treatments for Enterococcus faecalis infective endocarditis. However, there is a lack of stability data for the combination of both drugs in elastomeric devices, so the inclusion of AC in Outpatient Parenteral Antimicrobial Therapy...

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Autores principales: Fernández-Rubio, Beatriz, Herrera-Hidalgo, Laura, Luque-Márquez, Rafael, de Alarcón, Arístides, López-Cortés, Luis E., Luque-Pardos, Sonia, Gutiérrez-Urbón, José María, Fernández-Polo, Aurora, Gil-Navarro, María V., Gutiérrez-Valencia, Alicia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044682/
https://www.ncbi.nlm.nih.gov/pubmed/36978299
http://dx.doi.org/10.3390/antibiotics12030432
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author Fernández-Rubio, Beatriz
Herrera-Hidalgo, Laura
Luque-Márquez, Rafael
de Alarcón, Arístides
López-Cortés, Luis E.
Luque-Pardos, Sonia
Gutiérrez-Urbón, José María
Fernández-Polo, Aurora
Gil-Navarro, María V.
Gutiérrez-Valencia, Alicia
author_facet Fernández-Rubio, Beatriz
Herrera-Hidalgo, Laura
Luque-Márquez, Rafael
de Alarcón, Arístides
López-Cortés, Luis E.
Luque-Pardos, Sonia
Gutiérrez-Urbón, José María
Fernández-Polo, Aurora
Gil-Navarro, María V.
Gutiérrez-Valencia, Alicia
author_sort Fernández-Rubio, Beatriz
collection PubMed
description Currently, ampicillin plus ceftriaxone (AC) is one of the preferred treatments for Enterococcus faecalis infective endocarditis. However, there is a lack of stability data for the combination of both drugs in elastomeric devices, so the inclusion of AC in Outpatient Parenteral Antimicrobial Therapy (OPAT) programs is challenging. The objective of the study was to determine the stability of AC in elastomeric pumps when stored at 8 ± 2 °C, 25 ± 2 °C, 30 ± 2 °C and 37 ± 2 °C using LC-MS/MS. The combination was diluted in 0.9% sodium chloride and the final concentrations were ampicillin 24 g/L plus ceftriaxone 8 g/L. Physical and chemical stability were evaluated at 12, 20, 24, 36 and 48 h after preparation. Stability was met at each time point if the percentage of intact drug was ≥90% of its respective baseline concentration and color and clearness remained unchanged. The drug combination was stable for 48 h when it was kept at 8 ± 2 °C. At 25 ± 2 °C and 30 ± 2 °C, they were stable for 24 h of storage. At 37 ± 2 °C, the stability criterion was not met at any time point. These results prove that AC could be included in OPAT programs using elastomeric infusion devices for the treatment of E. faecalis infections.
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spelling pubmed-100446822023-03-29 Stability of Ampicillin plus Ceftriaxone Combined in Elastomeric Infusion Devices for Outpatient Parenteral Antimicrobial Therapy Fernández-Rubio, Beatriz Herrera-Hidalgo, Laura Luque-Márquez, Rafael de Alarcón, Arístides López-Cortés, Luis E. Luque-Pardos, Sonia Gutiérrez-Urbón, José María Fernández-Polo, Aurora Gil-Navarro, María V. Gutiérrez-Valencia, Alicia Antibiotics (Basel) Article Currently, ampicillin plus ceftriaxone (AC) is one of the preferred treatments for Enterococcus faecalis infective endocarditis. However, there is a lack of stability data for the combination of both drugs in elastomeric devices, so the inclusion of AC in Outpatient Parenteral Antimicrobial Therapy (OPAT) programs is challenging. The objective of the study was to determine the stability of AC in elastomeric pumps when stored at 8 ± 2 °C, 25 ± 2 °C, 30 ± 2 °C and 37 ± 2 °C using LC-MS/MS. The combination was diluted in 0.9% sodium chloride and the final concentrations were ampicillin 24 g/L plus ceftriaxone 8 g/L. Physical and chemical stability were evaluated at 12, 20, 24, 36 and 48 h after preparation. Stability was met at each time point if the percentage of intact drug was ≥90% of its respective baseline concentration and color and clearness remained unchanged. The drug combination was stable for 48 h when it was kept at 8 ± 2 °C. At 25 ± 2 °C and 30 ± 2 °C, they were stable for 24 h of storage. At 37 ± 2 °C, the stability criterion was not met at any time point. These results prove that AC could be included in OPAT programs using elastomeric infusion devices for the treatment of E. faecalis infections. MDPI 2023-02-22 /pmc/articles/PMC10044682/ /pubmed/36978299 http://dx.doi.org/10.3390/antibiotics12030432 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fernández-Rubio, Beatriz
Herrera-Hidalgo, Laura
Luque-Márquez, Rafael
de Alarcón, Arístides
López-Cortés, Luis E.
Luque-Pardos, Sonia
Gutiérrez-Urbón, José María
Fernández-Polo, Aurora
Gil-Navarro, María V.
Gutiérrez-Valencia, Alicia
Stability of Ampicillin plus Ceftriaxone Combined in Elastomeric Infusion Devices for Outpatient Parenteral Antimicrobial Therapy
title Stability of Ampicillin plus Ceftriaxone Combined in Elastomeric Infusion Devices for Outpatient Parenteral Antimicrobial Therapy
title_full Stability of Ampicillin plus Ceftriaxone Combined in Elastomeric Infusion Devices for Outpatient Parenteral Antimicrobial Therapy
title_fullStr Stability of Ampicillin plus Ceftriaxone Combined in Elastomeric Infusion Devices for Outpatient Parenteral Antimicrobial Therapy
title_full_unstemmed Stability of Ampicillin plus Ceftriaxone Combined in Elastomeric Infusion Devices for Outpatient Parenteral Antimicrobial Therapy
title_short Stability of Ampicillin plus Ceftriaxone Combined in Elastomeric Infusion Devices for Outpatient Parenteral Antimicrobial Therapy
title_sort stability of ampicillin plus ceftriaxone combined in elastomeric infusion devices for outpatient parenteral antimicrobial therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044682/
https://www.ncbi.nlm.nih.gov/pubmed/36978299
http://dx.doi.org/10.3390/antibiotics12030432
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