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Global intercompany assessment of ICIEF platform comparability for the characterization of therapeutic proteins
Authors:Seth Madren  Will McElroy  Kristin Schultz-Kuszak  Boris Boumajny  Yao Shu  Sabine Sautter  Helen C Zhao  Abby Schadock-Hewitt  Chris Chumsae  Nancy Ball  Xiaoying Zhang  Kimberly Rish  Shukui Zhang  Christine Wurm  Sumin Cai  Scott P Bauer  Cinzia Stella  Laura Zheng  Brian Roper  David A Michels  Gang Wu  Bostjan Kocjan  Matej Birk  Simon Erik Erdmann  Xiaoping He  Brad Whittaker  Yvonne Song  Hannah Barrett  Kevin Strozyk  Ye Jing  Long Huang  Vishal Mhatre  Paul McLean  Tiantian Yu  Huijuan Yang  Minna Mattila
Institution:1. Technical Development, Biogen Research Triangle Park, Durham, NC, USA;2. ProteinSimple, San Jose, CA, USA;3. Analytical Sciences, Biopharmaceutical Development, R&D, AstraZeneca, Gaithersburg, MD, USA;4. Analytical Development, Biogen, Cambridge, MA, USA;5. Bio Process + Analytical Development, Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach an der Riss, Germany;6. Quality Control/Clinical Supply Transfer, Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach an der Riss, Germany;7. Global Process Development Analytics, Biologics Development, Bristol Myers Squibb, Devens, MA, USA;8. Biologics, Catalent Pharma Solutions, Kansas City, MO, USA;9. Institute of Biologics, Chia Tai Tianqing Pharmaceutical Group Co., Ltd., Jiangsu, P. 10. R. 11. China;12. Coriolis Pharma Research GmbH, Martinsried, Germany;13. BioTechnology Discovery Research Lead Optimization, Eli Lilly and Company, Indianapolis, IN, USA;14. Department of Protein Analytical Chemistry, Genentech, South San Francisco, CA, USA;15. Key Laboratory of the Ministry of Health for Research on Quality and Standardization of Biotech Products, National Institutes for Food and Drug Control, Beijing, P. R. China;16. Process Analytical Sciences, Novartis, Mengeš, Slovenia;17. Novo Nordisk A/S, Hillerød, Denmark;18. Analytical R&D, Biotherapeutics Pharmaceutical Sciences, Pfizer, Chesterfield, MO, USA;19. BioProcess Analytics, Sanofi Genzyme, Framingham, MA, USA;20. Analytical Development, Sanofi Genzyme, Framingham, MA, USA;21. Analytical Sciences, Seagen Inc., Bothell, WA, USA;22. Analytical Science and Development, Shanghai Henlius Biotech Inc., Shanghai, P. 23. Quality Research Department and Quality Control Department, Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd., Sichuan, P. 24. Analytical Development, Takeda, Lexington, MA, USA;25. Shanghai Analytical Sciences, WuXi Biologics, Shanghai, P. 26. Immunodiagnostic Reagents Business Unit, Medix Biochemica, Espoo, Finland
Abstract:An international team spanning 19 sites across 18 biopharmaceutical and in vitro diagnostics companies in the United States, Europe, and China, along with one regulatory agency, was formed to compare the precision and robustness of imaged CIEF (ICIEF) for the charge heterogeneity analysis of the National Institute of Standards and Technology (NIST) mAb and a rhPD-L1-Fc fusion protein on the iCE3 and the Maurice instruments. This information has been requested to help companies better understand how these instruments compare and how to transition ICIEF methods from iCE3 to the Maurice instrument. The different laboratories performed ICIEF on the NIST mAb and rhPD-L1-Fc with both the iCE3 and Maurice using analytical methods specifically developed for each of the molecules. After processing the electropherograms, statistical evaluation of the data was performed to determine consistencies within and between laboratory and outlying information. The apparent isoelectric point (pI) data generated, based on two-point calibration, for the main isoform of the NIST mAb showed high precision between laboratories, with RSD values of less than 0.3% on both instruments. The SDs for the NIST mAb and the rhPD-L1-Fc charged variants percent peak area values for both instruments are less than 1.02% across different laboratories. These results validate the appropriate use of both the iCE3 and Maurice for ICIEF in the biopharmaceutical industry in support of process development and regulatory submissions of biotherapeutic molecules. Further, the data comparability between the iCE3 and Maurice illustrates that the Maurice platform is a next-generation replacement for the iCE3 that provides comparable data.
Keywords:Antibody  Biopharmaceutical analysis  Fusion protein  ICIEF  Imaged capillary Isoelectric focusing
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