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Development of a Point-of-Care System Based on White Light Reflectance Spectroscopy: Application in CRP Determination

The development of methods and miniaturized systems for fast and reliable quantitative determinations at the Point-of-Care is a top challenge and priority in diagnostics. In this work, a compact bench-top system, based on White Light Reflectance Spectroscopy, is introduced and evaluated in an applic...

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Detalles Bibliográficos
Autores principales: Tsounidi, Dimitra, Koukouvinos, Georgios, Christianidis, Vasilios, Legaki, Evangelia, Giogli, Vasiliki, Panagiotopoulou, Konstantina, Taka, Styliani, Ekaterinidi, Zoi, Kakabakos, Sotirios, Raptis, Ioannis, Petrou, Panagiota
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8394791/
https://www.ncbi.nlm.nih.gov/pubmed/34436070
http://dx.doi.org/10.3390/bios11080268
Descripción
Sumario:The development of methods and miniaturized systems for fast and reliable quantitative determinations at the Point-of-Care is a top challenge and priority in diagnostics. In this work, a compact bench-top system, based on White Light Reflectance Spectroscopy, is introduced and evaluated in an application with high clinical interest, namely the determination of C-Reactive protein (CRP) in human blood samples. The system encompassed all the necessary electronic and optical components for the performance of the assay, while the dedicated software provided the sequence and duration of assay steps, the reagents flow rate, the real-time monitoring of sensor response, and data processing to deliver in short time and accurately the CPR concentration in the sample. The CRP assay included two steps, the first comprising the binding of sample CRP onto the chip immobilized capture antibody and the second the reaction of the surface immunosorbed CRP molecules with the detection antibody. The assay duration was 12 min and the dynamic range was from 0.05 to 200 μg/mL, covering both normal values and acute inflammation incidents. There was an excellent agreement between CRP values determined in human plasma samples using the developed device with those received for the same samples by a standard diagnostic laboratory method.