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Fluorescence-polarization immunoassays within glass fiber micro-chambers enable tobramycin quantification in whole blood for therapeutic drug monitoring at the point of care.
Bojescu, E-Diana; Prim, Denis; Pfeifer, Marc E; Segura, Jean-Manuel.
Afiliación
  • Bojescu ED; Institute of Life Technologies - School of Engineering, HES-SO // University of Applied Sciences Western Switzerland, Sion, Switzerland. Electronic address: diana.bojescu@gmail.com.
  • Prim D; Institute of Life Technologies - School of Engineering, HES-SO // University of Applied Sciences Western Switzerland, Sion, Switzerland. Electronic address: denis.prim@hevs.ch.
  • Pfeifer ME; Institute of Life Technologies - School of Engineering, HES-SO // University of Applied Sciences Western Switzerland, Sion, Switzerland. Electronic address: marc.pfeifer@hevs.ch.
  • Segura JM; Institute of Life Technologies - School of Engineering, HES-SO // University of Applied Sciences Western Switzerland, Sion, Switzerland. Electronic address: jmanuel.segura@hevs.ch.
Anal Chim Acta ; 1225: 340240, 2022 Sep 08.
Article en En | MEDLINE | ID: mdl-36038239
Many therapeutic drugs require monitoring of their concentration in blood followed by dose adjustments in order to ensure efficacy while minimizing adverse effects. It would be highly desirable to perform such measurements rapidly and with reduced sample volumes to support point-of-care testing. Here, we demonstrate that the concentration of small therapeutics can be determined in whole blood within paper-like membranes using Fluorescence Polarization Immunoassay (FPIA). Different types of paper-like materials such as glass microfibers, cellulose and filter paper were investigated for artefacts such as scattering or autofluorescence. Accurate determination of the fluorescence polarization of red-emitting fluorophores at sub-nanomolar concentrations was feasible within glass fiber membranes. This enabled the development of a competitive immunoassay for the quantification of the antibiotic tobramycin using only 1 µL of plasma in glass fiber micro-chambers. Furthermore, the same membrane was used for transversal separation of blood cells followed by accurate FPIA read-out at the bottom part of the micro-chamber. For quantification of tobramycin, 1 µL of whole blood was incubated with the immunoassay reagents during only 3 min before deposition in the micro-chamber and analysis. Within the therapeutic window, coefficients of variation were around 20% and recoveries between 80 and 105%. Owing to the simplified procedure requiring no centrifugation, the reduced blood sample volume and the rapid analysis time, we envision that this novel method supports the performance of therapeutic drug monitoring directly at the point of care.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tobramicina / Monitoreo de Drogas Idioma: En Revista: Anal Chim Acta Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tobramicina / Monitoreo de Drogas Idioma: En Revista: Anal Chim Acta Año: 2022 Tipo del documento: Article
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