Accelerating high-concentration monoclonal antibody development with large-scale viscosity data and ensemble deep learning

Highly concentrated antibody solutions are necessary for developing subcutaneous injections but often exhibit high viscosities, posing challenges in antibody-drug development, manufacturing, and administration. Previous computational models were only limited to a few dozen data points for training, a bottleneck for generalizability. In this study, we measured the viscosity of a panel of 229 monoclonal antibodies (mAbs) to develop predictive models for high concentration mAb screening. We developed DeepViscosity, consisting of 102 ensemble artificial neural network models to classify low-viscosity (≤20 cP) and high-viscosity (>20 cP) mAbs at 150 mg/mL, using 30 features from a sequence-based DeepSP model. Two independent test sets, comprising 16 and 38 mAbs with known experimental viscosity, were used to assess DeepViscosity's generalizability. The model exhibited an accuracy of 87.5% and 89.5% on both test sets, respectively, surpassing other predictive methods. DeepViscosity will facilitate early-stage antibody development to select low-viscosity antibodies for improved manufacturability and formulation properties, critical for subcutaneous drug delivery. The webserver-based application can be freely accessed via https://devpred.onrender.com/DeepViscosity.

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Publication Details

Journal
mAbs
Published
2025-04-01
DOI
https://doi.org/10.1080/19420862.2025.2483944
Citations
14
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
19.04

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article

Accelerating high-concentration monoclonal antibody development with large-scale viscosity data and ensemble deep learning

Pin‐Kuang Lai, Valentin Stanev, Andrew Hinton, J. Timothy Caldwell et al.
14 citations
mAbs
Monoclonal and Polyclonal Antibodies Research
19.04
article

Accelerating high-concentration monoclonal antibody development with large-scale viscosity data and ensemble deep learning

Pin‐Kuang Lai, Valentin Stanev, Andrew Hinton, J. Timothy Caldwell, Gilad Kaplan, I-En Wu, Mark R. Hutchinson, Neil Mody, Andrew Dippel, Jia‐Min Chu, Mitali Shah, Austin Gallegos, Chacko Chakiath, Melissa Damschroder, Lateefat Kalejaye, Mohammad Ali Boroumand, A. Lee, Maryam Pouryahya, Bismark Amofah, Madison Kreitz
article en
14 citations

Abstract

Highly concentrated antibody solutions are necessary for developing subcutaneous injections but often exhibit high viscosities, posing challenges in antibody-drug development, manufacturing, and administration. Previous computational models were only limited to a few dozen data points for training, a bottleneck for generalizability. In this study, we measured the viscosity of a panel of 229 monoclonal antibodies (mAbs) to develop predictive models for high concentration mAb screening. We developed DeepViscosity, consisting of 102 ensemble artificial neural network models to classify low-viscosity (≤20 cP) and high-viscosity (>20 cP) mAbs at 150 mg/mL, using 30 features from a sequence-based DeepSP model. Two independent test sets, comprising 16 and 38 mAbs with known experimental viscosity, were used to assess DeepViscosity's generalizability. The model exhibited an accuracy of 87.5% and 89.5% on both test sets, respectively, surpassing other predictive methods. DeepViscosity will facilitate early-stage antibody development to select low-viscosity antibodies for improved manufacturability and formulation properties, critical for subcutaneous drug delivery. The webserver-based application can be freely accessed via https://devpred.onrender.com/DeepViscosity.

mAbsVol. 17(1)
Stevens Institute of Technology (US), AstraZeneca (Australia) (AU), AstraZeneca (Brazil) (BR), AstraZeneca (United States) (US)
Stevens Institute of Technology
Openalex Percentile: Top 0%
Monoclonal and Polyclonal Antibodies Research
19.04
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