TY - JOUR
T1 - Stability of ipilimumab in its original vial after opening allows its use for at least 4 weeks and facilitates pooling of residues
AU - Bardo-Brouard, Pascale
AU - Vieillard, Victoire
AU - Shekarian, Tala
AU - Marabelle, Aurélien
AU - Astier, Alain
AU - Paul, Muriel
N1 - Publisher Copyright:
© 2016 Elsevier Ltd
PY - 2016/5/1
Y1 - 2016/5/1
N2 - Purpose Well-documented stability data of monoclonal antibodies are generally missing. That is why we studied the physicochemical and biological stability of undiluted ipilimumab (IPI) in glass vial (5 mg/ml) over 28 d after opening, stored at 4°C and 25°C. Method A stressed study (60°C) was performed to validate our analytical methods as ‘stability indicating’. The different methods used were turbidimetry, dynamic light scattering (DLS), second-derivative ultraviolet and chromatographic methods as size-exclusion chromatography (SEC) and cation-exchange (CEX). Biological characterisation was performed by an in vitro functional binding inhibition bioassay. Results We demonstrated that ipilimumab in opened vials stored at 4°C and 25°C remained stable for at least 28 d. No physical, chemical or structural instability was found. No aggregation was observed by turbidimetry, SEC and DLS. Hydrodynamic diameters remained unchanged, as chromatographic profiles in CEX and thermal aggregation curves. Functionally, the ability of IPI to antagonise CTLA-4/B7.2 binding remained stable over 1 month at 4°C. Conclusion These results indicate that unused residues of IPI in their original vials can be safely kept up to 28 d, following good manufacturing procedures, allowing re-use for another patient or in case of cold-chain rupture.
AB - Purpose Well-documented stability data of monoclonal antibodies are generally missing. That is why we studied the physicochemical and biological stability of undiluted ipilimumab (IPI) in glass vial (5 mg/ml) over 28 d after opening, stored at 4°C and 25°C. Method A stressed study (60°C) was performed to validate our analytical methods as ‘stability indicating’. The different methods used were turbidimetry, dynamic light scattering (DLS), second-derivative ultraviolet and chromatographic methods as size-exclusion chromatography (SEC) and cation-exchange (CEX). Biological characterisation was performed by an in vitro functional binding inhibition bioassay. Results We demonstrated that ipilimumab in opened vials stored at 4°C and 25°C remained stable for at least 28 d. No physical, chemical or structural instability was found. No aggregation was observed by turbidimetry, SEC and DLS. Hydrodynamic diameters remained unchanged, as chromatographic profiles in CEX and thermal aggregation curves. Functionally, the ability of IPI to antagonise CTLA-4/B7.2 binding remained stable over 1 month at 4°C. Conclusion These results indicate that unused residues of IPI in their original vials can be safely kept up to 28 d, following good manufacturing procedures, allowing re-use for another patient or in case of cold-chain rupture.
KW - Immunotherapy
KW - Ipilimumab
KW - Monoclonal antibody
KW - Stability
UR - http://www.scopus.com/inward/record.url?scp=84977507216&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2016.01.008
DO - 10.1016/j.ejca.2016.01.008
M3 - Article
C2 - 26922168
AN - SCOPUS:84977507216
SN - 0959-8049
VL - 58
SP - 8
EP - 16
JO - European Journal of Cancer
JF - European Journal of Cancer
ER -