Literature DB >> 28710854

Opportunities and challenges of real-time release testing in biopharmaceutical manufacturing.

Mo Jiang1, Kristen A Severson1, John Christopher Love1, Helena Madden2, Patrick Swann2, Li Zang2, Richard D Braatz1.   

Abstract

Real-time release testing (RTRT) is defined as "the ability to evaluate and ensure the quality of in-process and/or final drug product based on process data, which typically includes a valid combination of measured material attributes and process controls" (ICH Q8[R2]). This article discusses sensors (process analytical technology, PAT) and control strategies that enable RTRT for the spectrum of critical quality attributes (CQAs) in biopharmaceutical manufacturing. Case studies from the small-molecule and biologic pharmaceutical industry are described to demonstrate how RTRT can be facilitated by integrated manufacturing and multivariable control strategies to ensure the quality of products. RTRT can enable increased assurance of product safety, efficacy, and quality-with improved productivity including faster release and potentially decreased costs-all of which improve the value to patients. To implement a complete RTRT solution, biologic drug manufacturers need to consider the special attributes of their industry, particularly sterility and the measurement of viral and microbial contamination. Continued advances in on-line and in-line sensor technologies are key for the biopharmaceutical manufacturing industry to achieve the potential of RTRT. Related article: http://onlinelibrary.wiley.com/doi/10.1002/bit.26378/full.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  biopharmaceutical manufacturing; biopharmaceuticals; critical quality attributes; process control; real-time release; real-time release testing

Mesh:

Substances:

Year:  2017        PMID: 28710854     DOI: 10.1002/bit.26383

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  10 in total

1.  Microfluidic capillary zone electrophoresis mass spectrometry analysis of alkaloids in Lobelia cardinalis transgenic and mutant plant cell cultures.

Authors:  Zachary D Kelley; D Trent Rogers; John M Littleton; Bert C Lynn
Journal:  Electrophoresis       Date:  2019-10-04       Impact factor: 3.535

2.  Continuous integrated antibody precipitation with two-stage tangential flow microfiltration enables constant mass flow.

Authors:  Daniel Burgstaller; Alois Jungbauer; Peter Satzer
Journal:  Biotechnol Bioeng       Date:  2019-01-23       Impact factor: 4.530

3.  Real-time monitoring and model-based prediction of purity and quantity during a chromatographic capture of fibroblast growth factor 2.

Authors:  Dominik Georg Sauer; Michael Melcher; Magdalena Mosor; Nicole Walch; Matthias Berkemeyer; Theresa Scharl-Hirsch; Friedrich Leisch; Alois Jungbauer; Astrid Dürauer
Journal:  Biotechnol Bioeng       Date:  2019-04-17       Impact factor: 4.530

4.  In-Solution IgG Titer Determination in Fermentation Broth Using Affibodies and Flow-Induced Dispersion Analysis.

Authors:  Morten E Pedersen; Jesper Østergaard; Henrik Jensen
Journal:  ACS Omega       Date:  2020-04-28

5.  Raman spectra-based deep learning: A tool to identify microbial contamination.

Authors:  Murali K Maruthamuthu; Amir Hossein Raffiee; Denilson Mendes De Oliveira; Arezoo M Ardekani; Mohit S Verma
Journal:  Microbiologyopen       Date:  2020-10-16       Impact factor: 3.139

6.  Proton-transfer-reaction mass spectrometry (PTR-MS) for online monitoring of glucose depletion and cell concentrations in HEK 293 gene therapy processes.

Authors:  Benjamin Bayer; Andreas Maccani; Johanna Jahn; Mark Duerkop; Ewald Kapeller; Robert Pletzenauer; Barbara Kraus; Gerald Striedner; Juan A Hernandez Bort
Journal:  Biotechnol Lett       Date:  2021-11-12       Impact factor: 2.461

Review 7.  Recent Advances and Future Directions in Downstream Processing of Therapeutic Antibodies.

Authors:  Allan Matte
Journal:  Int J Mol Sci       Date:  2022-08-04       Impact factor: 6.208

Review 8.  Process Analytical Technology Tools for Monitoring Pharmaceutical Unit Operations: A Control Strategy for Continuous Process Verification.

Authors:  Eun Ji Kim; Ji Hyeon Kim; Min-Soo Kim; Seong Hoon Jeong; Du Hyung Choi
Journal:  Pharmaceutics       Date:  2021-06-21       Impact factor: 6.321

Review 9.  A critical review of recent trends, and a future perspective of optical spectroscopy as PAT in biopharmaceutical downstream processing.

Authors:  Laura Rolinger; Matthias Rüdt; Jürgen Hubbuch
Journal:  Anal Bioanal Chem       Date:  2020-03-07       Impact factor: 4.142

10.  Technology transfer of a monitoring system to predict product concentration and purity of biopharmaceuticals in real-time during chromatographic separation.

Authors:  Anna Christler; Theresa Scharl; Dominik G Sauer; Johannes Köppl; Anne Tscheließnig; Cabir Toy; Michael Melcher; Alois Jungbauer; Astrid Dürauer
Journal:  Biotechnol Bioeng       Date:  2021-07-03       Impact factor: 4.530

  10 in total

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