Increasing robustness, reliability and storage stability of critical reagents by freeze-drying

Author:

Emrich Thomas1ORCID,Stracke Jan Olaf2,Guo Xiaoying1,Damhjell Kari1,Moelleken Joerg3,Vogel Rudolf4,Stubenrauch Kay-Gunnar1,Staack Roland F1

Affiliation:

1. Roche Pharma Research & Early Development, Pharmaceutical Sciences, Large Molecule Bioanalytical Sciences, Roche Innovation Center Munich, Nonnenwald 2, Penzberg, 82377, Germany

2. Analytical Development & Quality Control, Roche Pharma Technical Development Europe, F Hoffmann-La Roche AG, Basel, 4070, Switzerland

3. Roche Pharma Research & Early Development, Therapeutic Modalities, Large Molecule Research, Roche Innovation Center Munich, Nonnenwald 2, Penzberg, 82377, Germany

4. Roche Diagnostics, CPS R&D Early Development & Reagent Design, Biological Rare Reagents, Protein Chemistry, Nonnenwald 2, Penzberg, 82377, Germany

Abstract

Aim: Stabilization of critical reagents by freeze-drying would facilitate storage and transportation at ambient temperatures, and simultaneously enable constant reagent performance for long-term bioanalytical support throughout drug development. Freeze-drying as a generic process for stable performance and storage of critical reagents was investigated by establishing an universal formulation buffer and lyophilization process. Results: Using a storage-labile model protein, formulation buffers were evaluated to preserve reagent integrity during the freeze-drying process, and to retain functional performance after temperature stress. Application to critical reagents used in pharmacokinetics and anti-drug antibodies assays demonstrated stable functional performance of the reagents after 11 month at +40°C. Conclusion: Stabilization and storage of critical assay reagents by freeze-drying is an attractive alternative to traditional deep freezing.

Publisher

Future Science Ltd

Subject

Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry

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