Compatibility studies of selected multichamber bag parenteral nutrition with fluconazole

Katarzyna Dettlaff1, Gabriela Anglart1, Agnieszka Gruszczyńska1

  • 1Department of Pharmaceutical Chemistry, Poznan University of Medical Sciences, Poznań, Poland.

Abstract

Insights

Fluconazole (FLZ) is compatible with six parenteral nutrition (PN) formulations, confirming safety for co-administration in critically ill patients. This ensures safe Y-site administration of FLZ and PN in one infusion line.

Area of Science:

  • Pharmaceutical Sciences
  • Clinical Pharmacy
  • Critical Care Medicine

Background:

  • Fluconazole (FLZ) is essential for treating fungal infections, especially in immunocompromised, HIV-infected, and cancer patients.
  • Critically ill patients often require co-administration of medications with parenteral nutrition (PN).
  • Ensuring the safety of combining FLZ with PN in a single infusion line is crucial for patient care.

Purpose of the Study:

  • To evaluate the physicochemical compatibility of Fluconazole (FLZ) with six different multichamber bag parenteral nutrition (PN) formulations.
  • To determine if FLZ can be safely administered simultaneously with PN via a Y-site connection.

Main Methods:

  • FLZ solutions were combined with six PN formulations in clinically relevant proportions.
  • Visual assessment, pH, osmolality, turbidity, particle size (DLS and light obscuration), and zeta potential were measured.
  • Analyses were conducted immediately after mixing and after 4 hours of storage at room temperature.

Main Results:

  • No visual changes were observed upon combining FLZ with PN.
  • Turbidity remained below 0.4 NTU, and lipid emulsion particle size was under 300 nm (PFAT5 ≤0.02%).
  • pH and osmolality changes were within acceptable limits, and zeta potential indicated stable mixtures.

Conclusions:

  • Fluconazole (FLZ) is compatible with the tested six multichamber bag parenteral nutrition (PN) formulations.
  • This compatibility supports the co-administration of FLZ and PN through a single infusion line (Y-site).
  • The findings provide evidence for the safe use of this drug-PN combination in clinical settings.

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