Recent developments in bioprocessing of recombinant proteins: expression hosts and process development

NK Tripathi, A Shrivastava - Frontiers in Bioengineering and …, 2019 - frontiersin.org
Infectious diseases, along with cancers, are among the main causes of death among
humans worldwide. The production of therapeutic proteins for treating diseases at large …

Protein–excipient interactions: Mechanisms and biophysical characterization applied to protein formulation development

TJ Kamerzell, R Esfandiary, SB Joshi… - Advanced drug delivery …, 2011 - Elsevier
The purpose of this review is to demonstrate the critical importance of understanding protein–
excipient interactions as a key step in the rational design of formulations to stabilize and …

Developing therapeutic monoclonal antibodies at pandemic pace

B Kelley - Nature biotechnology, 2020 - nature.com
Developing therapeutic monoclonal antibodies at pandemic pace | Nature Biotechnology Skip
to main content Thank you for visiting nature.com. You are using a browser version with limited …

Recovery and purification process development for monoclonal antibody production

HF Liu, J Ma, C Winter, R Bayer - MAbs, 2010 - Taylor & Francis
Hundreds of therapeutic monoclonal antibodies (mAbs) are currently in development, and
many companies have multiple antibodies in their pipelines. Current methodology used in …

Biopharmaceutical manufacturing: Historical perspectives and future directions

AC Szkodny, KH Lee - Annual Review of Chemical and …, 2022 - annualreviews.org
This review describes key milestones related to the production of biopharmaceuticals—
therapies manufactured using recombinant DNA technology. The market for …

Purifying biopharmaceuticals: knowledge-based chromatographic process development

AT Hanke, M Ottens - Trends in biotechnology, 2014 - cell.com
The purification of biopharmaceuticals is commonly considered the bottleneck of the
manufacturing process. Increasing product diversity, along with growing regulatory and …

High-throughput process development for biopharmaceutical drug substances

R Bhambure, K Kumar, AS Rathore - Trends in biotechnology, 2011 - cell.com
Quality by Design (QbD) is gaining industry acceptance as an approach towards
development and commercialization of biotechnology therapeutic products that are …

Downstream processing of cell culture-derived virus particles

MW Wolf, U Reichl - Expert Review of Vaccines, 2011 - Taylor & Francis
Manufacturing of cell culture-derived virus particles for vaccination and gene therapy is a
rapidly growing field in the biopharmaceutical industry. The process involves a number of …

High-throughput isotherm determination and thermodynamic modeling of protein adsorption on mixed mode adsorbents

BK Nfor, M Noverraz, S Chilamkurthi… - … of Chromatography A, 2010 - Elsevier
The thermodynamic modeling of protein adsorption on mixed-mode adsorbents
functionalized with ligands carrying both hydrophobic and electrostatic groups was …

Challenges in scaling up AAV-based gene therapy manufacturing

Z Jiang, PA Dalby - Trends in Biotechnology, 2023 - cell.com
Accelerating the scale up of adeno-associated virus (AAV) manufacture is highly desirable
to meet the increased demand for gene therapies. However, the development of …