Samenvatting
In therapies involving therapeutic antibodies, therapeutic drug monitoring (TDM) has the potential to substantially increase clinical efficacy and to enable more economical drug use, because the clearance from the bloodstream after administration is patient dependent. Since TDM must be performed continuously and over extended time periods, it should ideally be achieved through an economical and easy to perform point-of-care (POC) assay. Here, we introduce a new analytical method for POC TDM of the clinically important therapeutic antibody cetuximab, using microfluidic thread-based analytical devices (µTADs) as a platform for a bioluminescence resonance energy-transfer (BRET) switching sensor protein for simple quantitative antibody detection. The µTAD is pre-treated with NaCl for blood plasma separation and a BRET switching sensor protein and its substrate for cetuximab detection, integrating all elements required for a reagent-free, single-step assay. A change in bioluminescence emission color depending on cetuximab concentrations occurs after whole blood application. The device design enables the quantification of cetuximab within the therapeutically relevant blood concentration range in 2.5 min using only 2 µL of whole blood. The results obtained are independent of the blood volume. This µTAD can be stored for about one month at − 20 °C, a temperature compatible with commonly available freezers. The application of mathematical morphology recognition (MMR)-integrated image processing techniques for the automatic selection of regions of interest (ROIs) yields results with minimal error. The simplicity of use, rapidity, and cost-effectiveness of this µTAD are expected to offer the possibility of achieving TDM of therapeutic antibodies at POC for individual patients.
Originele taal-2 | Engels |
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Artikelnummer | 131002 |
Aantal pagina's | 9 |
Tijdschrift | Sensors and Actuators, B: Chemical |
Volume | 352 |
DOI's | |
Status | Gepubliceerd - 1 feb. 2022 |
Bibliografische nota
Publisher Copyright:© 2021 Elsevier B.V.
Financiering
The authors acknowledge financial support by a Grant-in-Aid for Scientific Research (B) (grant no. 18H02008 ) from the Japan Society for the Promotion of Science (JSPS, Japan) to D.C. and Y.H., Terumo Life Science Foundation grant (Japan) to D.C., as well as by an European Research Council (ERC) proof-of-concept grant ( ERC- 2016-PoC 755471 ), an NWO-Take-off-1 grant ( NWO , 17820 ) from the Dutch Research Council (NWO, The Netherlands), and a Regieorgaan SIA (The Netherlands) grant RAAK.PRO Printing makes sense ( RAAK.PRO02.066 ) to M.M.
Financiers | Financiernummer |
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European Union’s Horizon Europe research and innovation programme | 755471 |
European Research Council | |
Japan Society for the Promotion of Science | |
Nederlandse Organisatie voor Wetenschappelijk Onderzoek | 17820 |
Terumo Foundation for Life Sciences and Arts | |
Regieorgaan SIA | RAAK.PRO02.066 |