Process Analytical Approach towards Quality Controlled Process Automation for the Downstream of Protein Mixtures by Inline Concentration Measurements Based on Ultraviolet/Visible Light (UV/VIS) Spectral Analysis

Downstream of pharmaceutical proteins, such as monoclonal antibodies, is mainly done by chromatography, where concentration determination of coeluting components presents a major problem. Inline concentration measurements (ICM) by Ultraviolet/Visible light (UV/VIS)-spectral data analysis provide a l...

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Main Authors: Steffen Zobel-Roos, Mourad Mouellef, Christian Siemers, Jochen Strube
Format: Article
Language:English
Published: MDPI AG 2017-12-01
Series:Antibodies
Subjects:
Online Access:https://www.mdpi.com/2073-4468/6/4/24
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spelling doaj-427b7fb7776e49a797e7584c9277cea82020-11-24T21:53:28ZengMDPI AGAntibodies2073-44682017-12-01642410.3390/antib6040024antib6040024Process Analytical Approach towards Quality Controlled Process Automation for the Downstream of Protein Mixtures by Inline Concentration Measurements Based on Ultraviolet/Visible Light (UV/VIS) Spectral AnalysisSteffen Zobel-Roos0Mourad Mouellef1Christian Siemers2Jochen Strube3Institute for Separation and Process Technology, Clausthal University of Technology, Leibnizstraße 15, 38678 Clausthal-Zellerfeld, GermanyInstitute for Separation and Process Technology, Clausthal University of Technology, Leibnizstraße 15, 38678 Clausthal-Zellerfeld, GermanyInstitute for Process Control, Clausthal University of Technology, Arnold-Sommerfeld-Straße 1, 38678 Clausthal-Zellerfeld, GermanyInstitute for Separation and Process Technology, Clausthal University of Technology, Leibnizstraße 15, 38678 Clausthal-Zellerfeld, GermanyDownstream of pharmaceutical proteins, such as monoclonal antibodies, is mainly done by chromatography, where concentration determination of coeluting components presents a major problem. Inline concentration measurements (ICM) by Ultraviolet/Visible light (UV/VIS)-spectral data analysis provide a label-free and noninvasive approach to significantly speed up the analysis and process time. Here, two different approaches are presented. For a test mixture of three proteins, a fast and easily calibrated method based on the non-negative least-squares algorithm is shown, which reduces the calibration effort compared to a partial least-squares approach. The accuracy of ICM for analytical separations of three proteins on an ion exchange column is over 99%, compared to less than 85% for classical peak area evaluation. The power of the partial least squares algorithm (PLS) is shown by measuring the concentrations of Immunoglobulin G (IgG) monomer and dimer under a worst-case scenario of completely overlapping peaks. Here, the faster SIMPLS algorithm is used in comparison to the nonlinear iterative partial least squares (NIPALS) algorithm. Both approaches provide concentrations as well as purities in real-time, enabling live-pooling decisions based on product quality. This is one important step towards advanced process automation of chromatographic processes. Analysis time is less than 100 ms and only one program is used for all the necessary communications and calculations.https://www.mdpi.com/2073-4468/6/4/24inline concentration measurementsUV/VIS spectral analysisPAT for monoclonal antibodieslive poolingpeak deconvolution
collection DOAJ
language English
format Article
sources DOAJ
author Steffen Zobel-Roos
Mourad Mouellef
Christian Siemers
Jochen Strube
spellingShingle Steffen Zobel-Roos
Mourad Mouellef
Christian Siemers
Jochen Strube
Process Analytical Approach towards Quality Controlled Process Automation for the Downstream of Protein Mixtures by Inline Concentration Measurements Based on Ultraviolet/Visible Light (UV/VIS) Spectral Analysis
Antibodies
inline concentration measurements
UV/VIS spectral analysis
PAT for monoclonal antibodies
live pooling
peak deconvolution
author_facet Steffen Zobel-Roos
Mourad Mouellef
Christian Siemers
Jochen Strube
author_sort Steffen Zobel-Roos
title Process Analytical Approach towards Quality Controlled Process Automation for the Downstream of Protein Mixtures by Inline Concentration Measurements Based on Ultraviolet/Visible Light (UV/VIS) Spectral Analysis
title_short Process Analytical Approach towards Quality Controlled Process Automation for the Downstream of Protein Mixtures by Inline Concentration Measurements Based on Ultraviolet/Visible Light (UV/VIS) Spectral Analysis
title_full Process Analytical Approach towards Quality Controlled Process Automation for the Downstream of Protein Mixtures by Inline Concentration Measurements Based on Ultraviolet/Visible Light (UV/VIS) Spectral Analysis
title_fullStr Process Analytical Approach towards Quality Controlled Process Automation for the Downstream of Protein Mixtures by Inline Concentration Measurements Based on Ultraviolet/Visible Light (UV/VIS) Spectral Analysis
title_full_unstemmed Process Analytical Approach towards Quality Controlled Process Automation for the Downstream of Protein Mixtures by Inline Concentration Measurements Based on Ultraviolet/Visible Light (UV/VIS) Spectral Analysis
title_sort process analytical approach towards quality controlled process automation for the downstream of protein mixtures by inline concentration measurements based on ultraviolet/visible light (uv/vis) spectral analysis
publisher MDPI AG
series Antibodies
issn 2073-4468
publishDate 2017-12-01
description Downstream of pharmaceutical proteins, such as monoclonal antibodies, is mainly done by chromatography, where concentration determination of coeluting components presents a major problem. Inline concentration measurements (ICM) by Ultraviolet/Visible light (UV/VIS)-spectral data analysis provide a label-free and noninvasive approach to significantly speed up the analysis and process time. Here, two different approaches are presented. For a test mixture of three proteins, a fast and easily calibrated method based on the non-negative least-squares algorithm is shown, which reduces the calibration effort compared to a partial least-squares approach. The accuracy of ICM for analytical separations of three proteins on an ion exchange column is over 99%, compared to less than 85% for classical peak area evaluation. The power of the partial least squares algorithm (PLS) is shown by measuring the concentrations of Immunoglobulin G (IgG) monomer and dimer under a worst-case scenario of completely overlapping peaks. Here, the faster SIMPLS algorithm is used in comparison to the nonlinear iterative partial least squares (NIPALS) algorithm. Both approaches provide concentrations as well as purities in real-time, enabling live-pooling decisions based on product quality. This is one important step towards advanced process automation of chromatographic processes. Analysis time is less than 100 ms and only one program is used for all the necessary communications and calculations.
topic inline concentration measurements
UV/VIS spectral analysis
PAT for monoclonal antibodies
live pooling
peak deconvolution
url https://www.mdpi.com/2073-4468/6/4/24
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