1. Academic Validation
  2. Stability of 90 mg/mL cefuroxime sodium solution for administration by continuous infusion

Stability of 90 mg/mL cefuroxime sodium solution for administration by continuous infusion

  • J Chemother. 2018 Oct-Dec;30(6-8):371-374. doi: 10.1080/1120009X.2018.1535950.
Christelle Vercheval 1 Sophie Streel 2 Anne-Catherine Servais 3 Marianne Fillet 3 Thierry Van Hees 1
Affiliations

Affiliations

  • 1 a Department of Clinical Pharmacy , University Hospital of Liège , Liège , Belgium.
  • 2 b Department of Hospital Pharmacy , University Hospital of Liège , Liège , Belgium.
  • 3 c Laboratory for the Analysis of Medicines (LAM) , CIRM (Center for Interdisciplinary Research on Medicines), University of Liège , Liège , Belgium.
Abstract

Continuous infusions of β-lactam Antibiotics increase pharmacokinetic/pharmacodynamic target attainment. However, this way of administration brings about some practical issues such as stability. This study aims to determine the stability of a 90 mg/mL cefuroxime sodium solution. Cefuroxime sodium was reconstituted and mixed with 50-mL 0.9% saline to produce 90 mg/mL solution in polypropylene syringes which were stored at 4 °C, 25 °C and 40 °C. Cefuroxime sodium concentration was determined periodically over 14 days using a stability-indicating high-performance liquid chromatographic method with ultra-violet detection. The loss in concentration was less than 10% after 2 days of storage at 25 °C and less than 5% after 14 days of storage at 4 °C. The concentration fell below 60% after 1 day at 40 °C. Solutions darken in appearance with time and heat. A 90 mg/mL cefuroxime sodium solution stored in polypropylene syringes is stable for 2 days at 25 °C and for at least 14 days at 4 °C.

Keywords

Cefuroxime; Continuous infusion; Drug stability; High-performance liquid chromatography; Polypropylene syringes.

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