Biotechnology and Bioengineering · 2021 · 17 citations · 19 references
PharmacyPharmaceutical AnalysisPharmaceuticsAnalytical ChemistryChromatographic AnalysisImpurity ProfilingAnalytical ChromatographyAntibody PurificationChromatographyLiquid ChromatographyExcipient Quality AttributesOn-line ChromatographyPat Method DevelopmentProcess Analytical MonitoringProcess Analytical TechnologyPurificationSize-exclusion Liquid ChromatographyTangential Flow Filtration
Process analytical technology (PAT) is a fast-growing field within bioprocessing that enables innovation in biological drug manufacturing. This study demonstrates novel PAT methods for monitoring multiple quality attributes simultaneously during the ultrafiltration and diafiltration (UF/DF) process operation, the final step of monoclonal antibody (mAb) purification. Size exclusion chromatography (SEC) methods were developed to measure excipients arginine, histidine, and high molecular weight (HMW) species using a liquid chromatography (LC) system with autosampler for both on-line and at-line PAT modes. The methods were applied in UF/DF studies for the comparison of single-use tangential flow filtration (TFF) cassettes to standard reusable cassettes to achieve very high concentration mAb drug substance (DS) in the order of 100-200 g/L. These case studies demonstrated that single-use TFF cassettes are a functionally equivalent, low-cost alternative to standard reusable cassettes, and that the on-line PAT measurement of purity and excipient concentration was comparable to orthogonal offline methods. These PAT applications using an on-line LC system equipped with onboard sample dilution can become a platform system for monitoring of multiple attributes over a wide dynamic range, a potentially valuable tool for biological drug development and manufacturing.
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Inhibition of Protein Aggregation: Supramolecular Assemblies of Arginine Hold the Key
Utpal Das, Gururao Hariprasad, A.S. Ethayathulla et al. · PLoS ONE · 2007 · 234 citations · Full text