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Microfluidic Cartridge for Bead-Based Affinity Assays

Pinto, Ines Fernandes (author)
KTH,Nanobioteknologi,Science for Life Laboratory, SciLifeLab
Chotteau, Véronique, Docent, 1963- (author)
KTH,Industriell bioteknologi
Russom, Aman, Prof. 1976- (author)
KTH,Nanobioteknologi,Science for Life Laboratory, SciLifeLab,Center for the Advancement of Integrated Medical and Engineering Sciences, AIMES
 (creator_code:org_t)
Springer Nature, 2024
2024
English.
In: Methods in Molecular Biology. - : Springer Nature. - 1064-3745 .- 1940-6029. ; 2804, s. 127-138
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Within the vast field of medical biotechnology, the biopharmaceutical industry is particularly fast-growing and highly competitive, so reducing time and costs associated to process optimization becomes instrumental to ensure speed to market and, consequently, profitability. The manufacturing of biopharmaceutical products, namely, monoclonal antibodies (mAbs), relies mostly on mammalian cell culture processes, which are highly dynamic and, consequently, difficult to optimize. In this context, there is currently an unmet need of analytical methods that can be integrated at-line in a bioreactor, for systematic monitoring and quantification of key metabolites and proteins. Microfluidic-based assays have been extensively and successfully applied in the field of molecular diagnostics; however, this technology remains largely unexplored for Process Analytical Technology (PAT), despite holding great potential for the at-line measurement of different analytes in bioreactor processes, combining low reagent/molecule consumption with assay sensitivity and rapid turnaround times.Here, the fabrication and handling of a microfluidic cartridge for protein quantification using bead-based affinity assays is described. The device allows geometrical multiplexed immunodetection of specific protein analytes directly from bioreactor samples within 2.5 h and minimal hands-on time. As a proof-of-concept, quantification of Chinese hamster ovary (CHO) host cell proteins (HCP) as key impurities, IgG as product of interest, and lactate dehydrogenase (LDH) as cell viability marker was demonstrated with limits of detection (LoD) in the low ng/mL range. Negligible matrix interference and no cross-reactivity between the different immunoassays on chip were found. The results highlight the potential of the miniaturized analytical method for PAT at reduced cost and complexity in comparison with sophisticated instruments that are currently the state-of-the-art in this context.

Subject headings

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

Keyword

Biopharmaceuticals
Colorimetry
Immunoassays
Microfluidics
Monoclonal antibodies
Multiplexing
Process analytical technology

Publication and Content Type

ref (subject category)
art (subject category)

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