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Improved sensitivity and automation of a multi-step upconversion lateral flow immunoassay using a 3D-printed actuation mechanism.
Raiko, Kirsti; Nääjärvi, Oskari; Ekman, Miikka; Koskela, Sonja; Soukka, Tero; Martiskainen, Iida; Salminen, Teppo.
  • Raiko K; Biotechnology Unit, Department of Life Technologies, Faculty of Technology, University of Turku, Kiinamyllynkatu 10, 20520, Turku, Finland. kisrai@utu.fi.
  • Nääjärvi O; Biotechnology Unit, Department of Life Technologies, Faculty of Technology, University of Turku, Kiinamyllynkatu 10, 20520, Turku, Finland.
  • Ekman M; Biotechnology Unit, Department of Life Technologies, Faculty of Technology, University of Turku, Kiinamyllynkatu 10, 20520, Turku, Finland.
  • Koskela S; Biotechnology Unit, Department of Life Technologies, Faculty of Technology, University of Turku, Kiinamyllynkatu 10, 20520, Turku, Finland.
  • Soukka T; Biotechnology Unit, Department of Life Technologies, Faculty of Technology, University of Turku, Kiinamyllynkatu 10, 20520, Turku, Finland.
  • Martiskainen I; Biotechnology Unit, Department of Life Technologies, Faculty of Technology, University of Turku, Kiinamyllynkatu 10, 20520, Turku, Finland.
  • Salminen T; Biotechnology Unit, Department of Life Technologies, Faculty of Technology, University of Turku, Kiinamyllynkatu 10, 20520, Turku, Finland.
Anal Bioanal Chem ; 416(6): 1517-1525, 2024 Mar.
Article en En | MEDLINE | ID: mdl-38280018
ABSTRACT
The development of sensitive point-of-care (POC) assay platforms is of interest for reducing the cost and time of diagnostics. Lateral flow assays (LFAs) are the gold standard for POC systems, but their sensitivity as such is inadequate, for example, in the case of cardiac diagnostics. The performance can be improved by incorporating different steps, such as pre-incubation to prolong the interaction time between sample and reporter for immunocomplex formation, and washing steps for background reduction. However, for POC assays, manual steps by the assay conductor are not desired. In this research, upconverting nanoparticles (UCNPs) were coated with poly(acrylic acid) (PAA) and conjugated to anti-cTnI antibodies, yielding non-clustering particles with low non-specific binding. The performance of cTnI-LFA in the PAA-anti-cTnI-UCNPs was compared to the same UCNPs with a commercial carboxyl surface. A kitchen-timer mechanism was embedded in a 3D-printed housing to produce a low-cost actuator facilitating a timed pre-incubation step for reporter and sample, and a washing step, to enable a multi-step cTnI-LFA with minimized manual labour. PAA-UCNPs showed improved mobility on nitrocellulose compared to those with a commercial surface. The mechanical actuator system was shown to improve sensitivity compared to a labour-intensive multi-step dipstick method, despite pre-incubation occurring during shaking and heating in the dipstick method. The limit of detection decreased from 7.6 to 1.5 ng/L cTnI in human plasma. The presented actuator can be easily modified for sensitivity improvement in the LFA for different analytes via pre-incubation and washing steps.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Nanopartículas Tipo de estudio: Diagnostic_studies / Guideline Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Nanopartículas Tipo de estudio: Diagnostic_studies / Guideline Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article