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Edetate Disodium as a Polysorbate Degradation and Monoclonal Antibody Oxidation Stabilizer.
Yarbrough, Melissa; Hodge, Tamara; Menard, Daniele; Jerome, Richard; Ryczek, Jeff; Moore, David; Baldus, Phoebe; Warne, Nick; Ohtake, Satoshi.
Afiliación
  • Yarbrough M; Pharmaceutical Research and Development, Pfizer Biotherapeutics Pharmaceutical Sciences, Chesterfield, Missouri 63017. Electronic address: Melissa.Yarbrough@pfizer.com.
  • Hodge T; Pharmaceutical Research and Development, Pfizer Biotherapeutics Pharmaceutical Sciences, Chesterfield, Missouri 63017.
  • Menard D; Pharmaceutical Research and Development, Pfizer Biotherapeutics Pharmaceutical Sciences, Chesterfield, Missouri 63017.
  • Jerome R; Pharmaceutical Research and Development, Pfizer Biotherapeutics Pharmaceutical Sciences, Chesterfield, Missouri 63017.
  • Ryczek J; Pharmaceutical Research and Development, Pfizer Biotherapeutics Pharmaceutical Sciences, Chesterfield, Missouri 63017.
  • Moore D; Pharmaceutical Research and Development, Pfizer Biotherapeutics Pharmaceutical Sciences, Chesterfield, Missouri 63017.
  • Baldus P; Pharmaceutical Research and Development, Pfizer Biotherapeutics Pharmaceutical Sciences, Chesterfield, Missouri 63017.
  • Warne N; Pharmaceutical Research and Development, Pfizer Biotherapeutics Pharmaceutical Sciences, Chesterfield, Missouri 63017.
  • Ohtake S; Pharmaceutical Research and Development, Pfizer Biotherapeutics Pharmaceutical Sciences, Chesterfield, Missouri 63017.
J Pharm Sci ; 108(4): 1631-1635, 2019 04.
Article en En | MEDLINE | ID: mdl-30502482
ABSTRACT
Polysorbates are frequently used in biotherapeutic formulations. Interest in assessing their stability, in particular the impact of their degradation products on the stability of therapeutic proteins, has been steadily growing in the past decade. The work presented summarizes a case study of a monoclonal antibody formulation that demonstrated a simultaneous loss of polysorbate and an increase in methionine oxidation. Spiking studies were conducted to determine both the cause and a potential mitigation for the monoclonal antibody (mAb) oxidation and polysorbate 80 (PS80) loss. The results indicated that a different source material exhibited different rates of mAb oxidation and PS80 loss and that in all evaluated materials, the addition of edetate disodium to the formulation mitigated both observed issues. The mAb was assessed for the presence of lipases and lipoprotein lipase was detected at low levels. It is proposed that edetate disodium was effective in mitigating the mAb oxidation and PS80 loss by chelating calcium in the formulation and therefore decreasing the activity of the lipases.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polisorbatos / Tensoactivos / Ácido Edético / Excipientes / Anticuerpos Monoclonales Idioma: En Revista: J Pharm Sci Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polisorbatos / Tensoactivos / Ácido Edético / Excipientes / Anticuerpos Monoclonales Idioma: En Revista: J Pharm Sci Año: 2019 Tipo del documento: Article
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