Harnessing Amino Acid Derivatives for Enhanced Viscosity Reduction and Stability of Monoclonal Antibodies

Most monoclonal antibodies (mAbs) are developed with low protein concentrations, and typically delivered to the patient in liquid form via injection or intravenous infusion (IV). However, there are a growing number of indications that prefer intramuscular or subcutaneous injections - mainly so that a patient can self-administer the drug at home and reduce hospital stays and/or treatment costs, increasing patient compliance.

While drugs delivered subcutaneously have significant patient benefits, they add additional manufacturing challenges - mainly due to pain and pressure at the injection site when volumes exceed 1 - 2 ml. This limited volume means that mAbs must be formulated in higher concentrations to administer an efficacious dose to the patient. Higher concentrations create high viscosity, and can also create undesirable protein-protein attractive interactions that leads to protein aggregation.

This article summarizes our research to identify novel excipients that not only reduce viscosity of high-concentration formulation but also improve stability across a wide concentration range.

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Authors

ARVIND SRIVASTAVA, PH.D.

Technical Fellow, Research - Bioprocessing

Dr. Arvind Srivastava is a Vice President at Avantor, leading contract development and manufacturing organization (CDMO). Before joining Avantor, Dr. Srivastava was Research Advisor at Eli Lilly and Company, where he managed drug product development from early development stage through commercial registration. Dr. Srivastava did his postdoctoral training from the University of North Carolina at Chapel Hill, NC, USA. He got his Ph.D. degree in biochemistry from the prestigious Tata Institute of Fundamental Research (TIFR) and M.S. in chemistry from the Banaras Hindu University (BHU). Dr. Srivastava has published numerous papers in international journals and has been frequently invited to present his research at the national and international conferences.

SUMAN McLINDEN

Senior Scientist at Avantor

Suman McLinden is a Sr. Research Scientist in Avantor’s Technology and Innovation group in Bridgewater, NJ for the past 3 years. She is currently working on analytical method and product development, also providing bio-analytical support to ongoing projects focused to improve bioprocess workflow. Prior to working at Avantor, Suman spent 15+ years on biophysical characterization and various aspects of analytical techniques of monoclonal antibody.

COURTNEY O’DELL, MS

Senior Scientist

Courtney is currently a senior scientist with Avantor’s Technology and Innovation group in Bridgewater, NJ for the past 5 years. She is currently working on projects related to cell lysis for viral vector release, optimizing viral vector titer production in suspension cells, spent media analysis, and additionally, novel protein additives to enhance stability of monoclonal antibody formulations. Prior to her position with Avantor, Courtney spent 11 years working in solution formulation development of monoclonal antibodies at ImClone Systems and then Eli Lilly & Co., focusing on stability, structural characterization, and use-time compatibility studies for parenteral drug delivery.

LORI A. FORTIN, PHD

Senior Manager, Research, Upstream Processes

Lori Fortin is currently the Senior Research Manager, Upstream Processes for Avantor’s Technology and Innovation group in Bridgewater, NJ. She has worked for Avantor for over 7 years focusing on product development and application studies for new product innovations used in monoclonal antibody and AAV production workflows. She also plays a role in the development of processes used to produce recombinant proteins from bacteria and mammalian cells used in NPI development of chromatography resins or in the testing of the efficacy of those resins. Prior to coming to Avantor, she worked at Sanofi Pasteur in Swiftwater, PA for 12 years as a Senior Process Development Scientist, where she was responsible for developing and optimizing ACF upstream processes for bacterial seedbanks and fermentations to produce antigens used in vaccine production. Lori holds a PhD and MS from Lehigh University in Chemical Engineering with a Biochemical focus

EVON BOLESSA

Manager, R&D

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DR. NANDU DEORKAR

Ph.D., MBA, Senior Vice President, Research & Development – Biopharma Production, Avantor

Nandu Deorkar is Senior Vice President, Biopharma Production Research & Development for Avantor. He is responsible for innovation strategy and planning, and execution of new products and technology development. During his more than 25-year career in research & development, Dr. Deorkar has been leading teams working on various aspects of upstream and downstream bioprocessing, single use systems, chemical/polymer R&D, drug development, formulation, drug delivery technologies, process development, and technology transfer. He has published more than 30 articles and holds more than 20 patents. Dr. Deorkar received Ph.D. from Indian Institute of Technology, Mumbai, India and MBA in Marketing from Fairleigh Dickinson University, Madison, NJ, USA.

Avantor®, a Fortune 500 company, is a leading global provider of mission-critical products and services to customers in the biopharma, healthcare, education & government, and advanced technologies & applied materials industries. Our portfolio is used in virtually every stage of the most important research, development and production activities in the industries we serve. Our global footprint enables us to serve more than 300,000 customer locations and gives us extensive access to research laboratories and scientists in more than 180 countries. We set science in motion to create a better world.