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Genetic Encoding of a Non-Canonical Amino Acid for the Generation of Antibody-Drug Conjugates Through a Fast Bioorthogonal Reaction
Published on: September 14, 2018
Continuous Processing for Manufacturing of Antibody-Drug Conjugates (ADCs)
Subhankar Metya1, Pragya Prakash2, Anurag S Rathore1,2
1School of Interdisciplinary Research, Indian Institute of Technology Delhi, New Delhi 110016, India.
Continuous manufacturing using a coiled flow inverter reactor (CFIR) significantly improves antibody-drug conjugate (ADC) production. This novel bioprocessing method enhances efficiency and lowers costs compared to traditional batch methods.
Area of Science:
- Biopharmaceutical Manufacturing
- Chemical Engineering
- Drug Delivery Systems
Background:
- Antibody-drug conjugates (ADCs) merge monoclonal antibodies (mAbs) with cytotoxic drugs for targeted therapy.
- Current ADC manufacturing faces challenges including inefficiency, waste, and control over drug-to-antibody ratio (DAR).
Purpose of the Study:
- To develop and evaluate a novel continuous conjugation process for ADCs.
- To improve manufacturing efficiency, reduce costs, and enhance safety in ADC production.
Main Methods:
- Utilized a coiled flow inverter reactor (CFIR) for continuous thiol-maleimide conjugation at mAb interchain cysteines.
- Screened process parameters for thiol reduction and conjugation.
- Optimized key parameters (mAb/drug concentration, duration, temperature) using Design of Experiments (DoE).
Main Results:
- The CFIR demonstrated 64.40% higher productivity than traditional batch conjugation.
- Achieved a 70% reduction in production costs.
- Produced ADCs with clinically relevant DAR and offered a safer manufacturing alternative.
Conclusions:
- Continuous processing with CFIR offers a more efficient, scalable, and sustainable platform for ADC manufacturing.
- This approach addresses key challenges in current ADC production, paving the way for improved biotherapeutic development.
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