Stability of ceftolozane and tazobactam in different peritoneal dialysis solutions

Author:

Harmanjeet Harmanjeet1,Jani Het1,Zaidi Syed Tabish R12,Wanandy Troy13,Castelino Ronald L145,Sud Kamal56,Peterson Gregory M1,Patel Rahul P1ORCID

Affiliation:

1. Division of Pharmacy, School of Medicine, University of Tasmania, Australia

2. School of Healthcare, University of Leeds, UK

3. Department of Pharmacy, Royal Hobart Hospital, Australia

4. School of Nursing, University of Sydney, Australia

5. Peritoneal Dialysis Unit, Regional Dialysis Centre, Blacktown Hospital, Australia

6. Department of Renal Medicine, Nepean Hospital and Nepean Clinical School, The University of Sydney, Australia

Abstract

Background: Peritonitis is a common and serious complication of peritoneal dialysis (PD). PD-associated peritonitis (PDAP) caused by Pseudomonas is usually resistant to most antibiotics, resulting in high failure rates. Ceftolozane/tazobactam (C/T) has been shown to be effective in treating urinary tract and intra-abdominal infections caused by beta-lactam resistant Pseudomonas and other gram-negative bacteria. Given its favourable adverse effects profile, it has a potential role in the treatment of PDAP caused by Pseudomonas species resistant to other antibiotics. Intraperitoneal administration of antibiotics admixed with PD solutions for the treatment of PDAP is associated with superior outcomes. However, there is a lack of published data on the stability of C/T in PD solutions. Therefore, this study investigated the physical and chemical stability of C/T in commonly used PD solutions at different temperatures. Methods: A total of 27 PD bags (3 PD bags for each type of PD solution including Dianeal®, Extraneal®, Balance® and Physioneal® PD bags) containing C/T were prepared and stored at 25°C for 6 h, followed by 4°C for 168 h and then 37°C for 12 h. An aliquot from each PD bag was withdrawn, and the concentration of C/T before (0 h) and after predefined time points was determined using a stability-indicating high-performance liquid chromatography assay. Samples were also assessed for pH, colour change and particulate matter immediately after preparation and on each day of analysis. Results: C/T retained more than 97% of their initial concentration when stored at 25°C for 6 h followed by storage at 4°C for 168 h and then at 37°C for 12 h. Particle formation was not detected at any time under the tested storage conditions. The pH and colour remained essentially unchanged throughout the study. Conclusions: These results provide a platform for clinical studies to determine the safety and therapeutic efficacy of intraperitoneal C/T for the treatment of PDAP caused by resistant Pseudomonas species.

Funder

merck sharp and dohme

Publisher

SAGE Publications

Subject

Nephrology,General Medicine

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