Evidence map›Paper›PMID 35853692›Full record

ArticleEuropean journal of hospital pharmacy : science and practice2022

Short-term study on in-use stability of opened bevacizumab biosimilar PF-06439535 vials.

Mona Abdel-Tawab, Markus Waßmuth, Florian Gegenfurtner, Andrea Hawe, Jan H Schefe, Anke M Strunz, Joachim Wübert

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Article in European journal of hospital pharmacy : science and practice, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Mona Abdel-TawabCentral Laboratory of German Pharmacists, Eschborn, Germany m.tawab@zentrallabor.com.
Markus WaßmuthCentral Laboratory of German Pharmacists, Eschborn, Germany.
Florian GegenfurtnerCoriolis Pharma Research GmbH, Martinsried, Bayern, Germany.
Andrea HaweCoriolis Pharma Research GmbH, Martinsried, Bayern, Germany.
Jan H SchefePfizer Deutschland GmbH, Berlin, Germany.
Anke M StrunzPfizer Deutschland GmbH, Berlin, Germany.
Joachim WübertCentral Laboratory of German Pharmacists, Eschborn, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesAggregation is one of the key critical points limiting the stability of monoclonal antibodies in solution. The present study aimed to investigate the in-use stability of a residual monoclonal antibody solution after withdrawal of most of the filling volume of PF-06439535 (bevacizumab biosimilar), addressing the physical and chemical stability with respect to aggregation and fragmentation.

methodsThe stability of residual PF-06439535 solution (25 mg/mL) after withdrawal of 80% (12.8 mL) filling volume with a 20G needle was monitored over a light-protected storage period of 8 days at 2-8°C and 25°C with measurement time points at D0 (start of storage), D2, D4, and D8 (2, 4, and 8 days of storage after start, respectively). Unopened vials stored under the same conditions served as control. For this purpose, the analytical results from size exclusion chromatography, dynamic light scattering, and micro-flow imaging obtained after the individual measurement time points up to 8 days were compared with those obtained at D0 and with those obtained for unopened vials stored under the same conditions.

resultsNo aggregation or ongoing fragmentation due to partial withdrawal of filling volume could be observed in the residual PF-06439535 solution. Moreover, no changes in the particle size distribution at D8 compared with the D0 values were identified upon storage at either 2-8°C or 25°C (both opened and unopened vials). The total concentration of particles ≥10 µm of all samples was <100 particles/mL. In addition, no variations in the pH values or in the visual appearance were detected over the whole study period in all samples at all storage conditions.

conclusionsConsequently, residual PF-06439535 solution (25 mg/mL) in opened vials may be regarded as stable when stored light-protected over a period of 8 days in the refrigerator (2-8°C) or at 25°C.

Indexed as

CLINICAL MEDICINEDrug MonitoringMEDICAL ONCOLOGYOPHTHALMOLOGYPHARMACEUTICAL PREPARATIONS

Identifiers

PMID35853692
PMCPMC10895173

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