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Physicochemical stability of a polysorbate-80-containing solvent compounded in the hospital pharmacy and used to reconstitute a biologic for nebulisation
  1. Laura Négrier1,2,
  2. Marine Roche1,2,
  3. Damien Lannoy1,2,
  4. Christophe Berneron2,
  5. Léa Pacqueu2,
  6. Christophe Carnoy3,
  7. Antoine Guillon4,
  8. Benjamin Hamzé5,
  9. Jean-Claude Sirard3,
  10. Bertrand Décaudin1,2,
  11. Pascal Odou1,2,
  12. Cécile Danel2,6
  1. 1University of Lille, CHU Lille, ULR 7365-GRITA - Groupe de Recherche sur les formes Injectables et les Technologies Associées, Lille, France
  2. 2CHU Lille, Institut de Pharmacie, Lille, France
  3. 3University of Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019 - UMR 9017 - CIIL - Center for Infection and Immunity of Lille, Lille, France
  4. 4INSERM, Centre d’Etude des Pathologies Respiratoires (CEPR), UMR 1100, Université de Tours, CHRU de Tours, Service de Médecine Intensive Réanimation, Tours, France
  5. 5Pôle Recherche Clinique, Inserm, Paris, France
  6. 6University of Lille, Lille, Hauts-de-France, France
  1. Correspondence to Dr Cécile Danel; cecile.danel{at}univ-lille.fr

Abstract

Objectives To assess the long-term physicochemical stability of a solvent (10 mM phosphate buffer pH 6.5 containing sodium chloride (145 mM) and polysorbate 80 (PS80) 0.02%) used to reconstitute a biologic for nebulisation. The solvent was compounded in the hospital pharmacy and stored in amber glass vials at −20°C for 1 year.

Methods Samples were analysed immediately on compounding and then 1, 3, 6, 9 and 12 months after storage at −20°C (immediately after thawing, and also 1 month later keeping the vials at 2–8°C). The assays included a visual examination, measurement of the pH, osmolality, sub-visible particulate contamination, the concentration of PS80, and the concentration of oleic acid and peroxides (both major markers of PS80 degradation). Quantification of PS80 was challenging due to the substance’s molecular heterogeneity and the lack of a good chromophore. The strategy adopted consisted of hydrolysis in a strong base and then liquid-liquid extraction of the oleic acid (PS80’s hydrolysis product). The oleic acid content was determined using reversed phase high performance liquid chromatography with ultraviolet detection. The peroxide content was determined spectrophotometrically using a ferrous oxidation with xylenol orange assay.

Results Over 12 months, there was no significant change in the samples’ visual appearance, pH and osmolality. The PS80 concentration remained above 90% of the initial value. The subvisible particle counts remained far below the European Pharmacopoeia thresholds. The oleic acid content of the non-hydrolysed samples remained constant, and no peroxide was detected.

Conclusions A PS80-containing solvent is stable for 1 year when stored at −20°C (±5°C) in amber glass vials. Moreover, the solvent is stable for up to 1 month after thawing if stored at 2–8°C.

  • Chemistry, Pharmaceutical
  • Pharmacopoeia
  • Quality Control
  • Drug Stability
  • Excipients

Data availability statement

All data relevant to the study are included in the article or uploaded as supplementary information.

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Data availability statement

All data relevant to the study are included in the article or uploaded as supplementary information.

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