Stability Studies of Antipseudomonal Beta Lactam Agents for Outpatient Therapy

Outpatient parenteral antimicrobial therapy (OPAT) is a useful treatment strategy against <i>Pseudomonas aeruginosa</i> and other multidrug-resistant bacteria. However, it is hindered by the lack of stability data for the administration of antibiotics under OPAT conditions. Our objective...

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Main Authors: Beatriz Fernández-Rubio, Laura Herrera-Hidalgo, Arístides de Alarcón, Rafael Luque-Márquez, Luis E. López-Cortés, Sònia Luque, José María Gutiérrez-Urbón, Aurora Fernández-Polo, Alicia Gutiérrez-Valencia, María V. Gil-Navarro
Format: Article
Language:English
Published: MDPI AG 2023-11-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/15/12/2705
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author Beatriz Fernández-Rubio
Laura Herrera-Hidalgo
Arístides de Alarcón
Rafael Luque-Márquez
Luis E. López-Cortés
Sònia Luque
José María Gutiérrez-Urbón
Aurora Fernández-Polo
Alicia Gutiérrez-Valencia
María V. Gil-Navarro
author_facet Beatriz Fernández-Rubio
Laura Herrera-Hidalgo
Arístides de Alarcón
Rafael Luque-Márquez
Luis E. López-Cortés
Sònia Luque
José María Gutiérrez-Urbón
Aurora Fernández-Polo
Alicia Gutiérrez-Valencia
María V. Gil-Navarro
author_sort Beatriz Fernández-Rubio
collection DOAJ
description Outpatient parenteral antimicrobial therapy (OPAT) is a useful treatment strategy against <i>Pseudomonas aeruginosa</i> and other multidrug-resistant bacteria. However, it is hindered by the lack of stability data for the administration of antibiotics under OPAT conditions. Our objective was to investigate the stability of nine antipseudomonal and broad-spectrum beta lactam antibiotics (aztreonam, cefepime, cefiderocol, ceftazidime, ceftazidime/avibactam, ceftolozane/tazobactam, meropenem, meropenem/vaborbactam, and piperacillin/tazobactam) to allow the spread of OPAT programs. All the antibiotics were diluted in 500 mL 0.9% sodium chloride and stored at 4, 25, 32, and 37 °C for 72 h in two different devices (infusion bags and elastomeric pumps). The solutions were considered stable if the color, clearness, and pH remained unchanged and if the percentage of intact drug was ≥90%. All the antimicrobials remained stable 72 h under refrigerated conditions and at least 30 h at 25 °C. At 32 °C, all the antibiotics except for meropenem and meropenem/vaborbactam remained stable for 24 h or more. At 37 °C, only aztreonam, piperacillin/tazobactam, cefepime, cefiderocol, and ceftolozane/tazobactam were stable for at least 24 h. The stability results were the same in the two devices tested. All the antibiotics studied are actual alternatives for the treatment of antipseudomonal or multidrug-resistant infections in OPAT programs, although the temperature of the devices is crucial to ensure antibiotic stability.
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spelling doaj.art-680f851222f848f4a1d41c8aea0d97792023-12-22T14:32:04ZengMDPI AGPharmaceutics1999-49232023-11-011512270510.3390/pharmaceutics15122705Stability Studies of Antipseudomonal Beta Lactam Agents for Outpatient TherapyBeatriz Fernández-Rubio0Laura Herrera-Hidalgo1Arístides de Alarcón2Rafael Luque-Márquez3Luis E. López-Cortés4Sònia Luque5José María Gutiérrez-Urbón6Aurora Fernández-Polo7Alicia Gutiérrez-Valencia8María V. Gil-Navarro9Unidad de Gestión Clínica de Farmacia, Hospital Universitario Virgen del Rocío/Instituto de Biomedicina de Sevilla (IBiS), 41013 Seville, SpainUnidad de Gestión Clínica de Farmacia, Hospital Universitario Virgen del Rocío/Instituto de Biomedicina de Sevilla (IBiS), 41013 Seville, SpainUnidad de Gestión Clínica de Enfermedades Infecciosas, Microbiología y Parasitologia, Hospital Universitario Virgen del Rocío/Instituto de Biomedicina de Sevilla (IBiS), 41013 Seville, SpainUnidad de Gestión Clínica de Enfermedades Infecciosas, Microbiología y Parasitologia, Hospital Universitario Virgen del Rocío/Instituto de Biomedicina de Sevilla (IBiS), 41013 Seville, SpainCentro de Investigación en Red de Enfermedades Infecciosas (CIBERINFEC), Instituto de Salud Carlos III, 28029 Madrid, SpainCentro de Investigación en Red de Enfermedades Infecciosas (CIBERINFEC), Instituto de Salud Carlos III, 28029 Madrid, SpainUnidad de Gestión Clínica de Farmacia, Complexo Hospitalario Universitario de A Coruña, 15006 A Coruña, SpainUnidad de Gestión Clínica de Farmacia, Hospital Universitari Vall d’Hebron, Institut de Recerca Vall d’Hebron, 08035 Barcelona, SpainUnidad de Gestión Clínica de Enfermedades Infecciosas, Microbiología y Parasitologia, Hospital Universitario Virgen del Rocío/Instituto de Biomedicina de Sevilla (IBiS), 41013 Seville, SpainUnidad de Gestión Clínica de Farmacia, Hospital Universitario Virgen del Rocío/Instituto de Biomedicina de Sevilla (IBiS), 41013 Seville, SpainOutpatient parenteral antimicrobial therapy (OPAT) is a useful treatment strategy against <i>Pseudomonas aeruginosa</i> and other multidrug-resistant bacteria. However, it is hindered by the lack of stability data for the administration of antibiotics under OPAT conditions. Our objective was to investigate the stability of nine antipseudomonal and broad-spectrum beta lactam antibiotics (aztreonam, cefepime, cefiderocol, ceftazidime, ceftazidime/avibactam, ceftolozane/tazobactam, meropenem, meropenem/vaborbactam, and piperacillin/tazobactam) to allow the spread of OPAT programs. All the antibiotics were diluted in 500 mL 0.9% sodium chloride and stored at 4, 25, 32, and 37 °C for 72 h in two different devices (infusion bags and elastomeric pumps). The solutions were considered stable if the color, clearness, and pH remained unchanged and if the percentage of intact drug was ≥90%. All the antimicrobials remained stable 72 h under refrigerated conditions and at least 30 h at 25 °C. At 32 °C, all the antibiotics except for meropenem and meropenem/vaborbactam remained stable for 24 h or more. At 37 °C, only aztreonam, piperacillin/tazobactam, cefepime, cefiderocol, and ceftolozane/tazobactam were stable for at least 24 h. The stability results were the same in the two devices tested. All the antibiotics studied are actual alternatives for the treatment of antipseudomonal or multidrug-resistant infections in OPAT programs, although the temperature of the devices is crucial to ensure antibiotic stability.https://www.mdpi.com/1999-4923/15/12/2705<i>Pseudomonas aeruginosa</i>multidrug-resistant bacteriabeta lactamsstabilityoutpatient parenteral antimicrobial therapy
spellingShingle Beatriz Fernández-Rubio
Laura Herrera-Hidalgo
Arístides de Alarcón
Rafael Luque-Márquez
Luis E. López-Cortés
Sònia Luque
José María Gutiérrez-Urbón
Aurora Fernández-Polo
Alicia Gutiérrez-Valencia
María V. Gil-Navarro
Stability Studies of Antipseudomonal Beta Lactam Agents for Outpatient Therapy
Pharmaceutics
<i>Pseudomonas aeruginosa</i>
multidrug-resistant bacteria
beta lactams
stability
outpatient parenteral antimicrobial therapy
title Stability Studies of Antipseudomonal Beta Lactam Agents for Outpatient Therapy
title_full Stability Studies of Antipseudomonal Beta Lactam Agents for Outpatient Therapy
title_fullStr Stability Studies of Antipseudomonal Beta Lactam Agents for Outpatient Therapy
title_full_unstemmed Stability Studies of Antipseudomonal Beta Lactam Agents for Outpatient Therapy
title_short Stability Studies of Antipseudomonal Beta Lactam Agents for Outpatient Therapy
title_sort stability studies of antipseudomonal beta lactam agents for outpatient therapy
topic <i>Pseudomonas aeruginosa</i>
multidrug-resistant bacteria
beta lactams
stability
outpatient parenteral antimicrobial therapy
url https://www.mdpi.com/1999-4923/15/12/2705
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