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In-line fiber optical sensor for detection of IgG aggregates in affinity chromatography

Tran, Thuy (author)
Linköpings universitet,Biofysik och bioteknik,Tekniska fakulteten,ArgusEye AB, Fridtunagatan 24, S-58213 Linkoping, Sweden,Laboratory of Molecular Materials
Gustavsson Lindberg, Robert (author)
Linköpings universitet,Biofysik och bioteknik,Tekniska fakulteten,Laboratory of Molecular Materials
Martinsson, Erik (author)
ArgusEye AB, Fridtunagatan 24, S-58213 Linkoping, Sweden
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Bergqvist, Filip (author)
Cytiva Sweden AB, Sweden
Axen, Andreas (author)
Cytiva Sweden AB, Sweden
Lundström, Ingemar (author)
Linköpings universitet,Sensor- och aktuatorsystem,Tekniska fakulteten
Mandenius, Carl-Fredrik (author)
Linköpings universitet,Biofysik och bioteknik,Tekniska fakulteten,Laboratory of Molecular Materials
Aili, Daniel (author)
Linköpings universitet,Biofysik och bioteknik,Tekniska fakulteten,Laboratory of Molecular Materials
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 (creator_code:org_t)
ELSEVIER, 2024
2024
English.
In: Journal of Chromatography A. - : ELSEVIER. - 0021-9673 .- 1873-3778. ; 1730
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Therapeutic monoclonal antibodies (mAbs) are critical for treatment of a wide range of diseases. Immunoglobulin G (IgG) is the most predominant form of mAb but is prone to aggregation during production. Detection and removal of IgG aggregates are time-consuming and laborious. Chromatography is central for purification of biopharmaceuticals in general and essential in the production of mAbs. Protein purification systems are usually equipped with detectors for monitoring pH, UV absorbance, and conductivity, to facilitate optimization and control of the purification process. However, specific in-line detection of the target products and contaminating species, such as aggregates, is currently not possible using convectional techniques. Here we show a novel fiber optical in-line sensor, based on localized surface plasmon resonance (LSPR), for specific detection of IgG and IgG aggregates during affinity chromatography. A flow cell with a Protein A sensor chip was connected to the outlet of the affinity column connected to three different chromatography systems operating at lab scale to pilot scale. Samples containing various IgG concentrations and aggregate contents were analyzed in-line during purification on a Protein A column using both pH gradient and isocratic elution. Because of avidity effects, IgG aggregates showed slower dissociation kinetics than monomers after binding to the sensor chips. Possibilities to detect aggregate concentrations below 1 % and difference in aggregate content smaller than 0.3 % between samples were demonstrated. In-line detection of aggregates can circumvent time-consuming off-line analysis and facilitate automation and process intensification.

Subject headings

NATURVETENSKAP  -- Kemi -- Analytisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Analytical Chemistry (hsv//eng)

Keyword

In -line sensor; Monoclonal antibodies; LSPR; Chromatography; IgG aggregate; Process analytical technology

Publication and Content Type

ref (subject category)
art (subject category)

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