Microfluidic fluorescence immunosensor using ZnONFs for invasive aspergillosis determination

•A sensitive microfluidic fluorescence immunosensor was developed.•This sensor was applied to GM determination in human serum samples.•The ZnONFs were used as a bioaffinity nanoplatform.•The proposed method can be applied to the IA early diagnosis. Galactomannan (GM) is a polysaccharide cell-wall co...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Microchemical journal 2020-12, Vol.159, p.105371, Article 105371
Hauptverfasser: Piguillem, Sofía V., Regiart, Matias, Bertotti, Mauro, Raba, Julio, Messina, Germán A., Fernández-Baldo, Martín A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:•A sensitive microfluidic fluorescence immunosensor was developed.•This sensor was applied to GM determination in human serum samples.•The ZnONFs were used as a bioaffinity nanoplatform.•The proposed method can be applied to the IA early diagnosis. Galactomannan (GM) is a polysaccharide cell-wall component released by Aspergillus species, used as a biological marker for invasive aspergillosis (IA) screening. A fluorescence microfluidic immunosensor for GM detection was developed by using ZnO nanoflowers (ZnONFs) synthesized by a wet chemical method and characterized by scanning electron microscopy and energy dispersive spectrometry. The ZnONFs were covalently linked to the microfluidic channel through a silanization process with 3-aminopropyl triethoxysilane and then used as a bioaffinity nanoplatform for the immobilization of monoclonal anti-GM antibodies, which react specifically with the GM present in human serum samples. Subsequently, the GM amount that reacted was quantified by an HRP-anti-GM antibody (type sandwich immunoassay), which in the presence of H2O2 catalyzes the oxidation of 10-acetyl-3,7-dihydroxyphenoxacine to a highly fluorescent resorufin, which was measured by a laser-induced fluorescence (LIF) detector (excitation at 561 nm and emission at 585 nm). The measured fluorescence is directly proportional to the concentration of GM present in the patient serum sample. The fluorescence method was compared with a previously published electrochemical method, and a commercial ELISA test, showing outstanding properties. This immunosensor can be applied to the IA early diagnosis since it offers several attractive advantages such as high selectivity and sensitivity.
ISSN:0026-265X
DOI:10.1016/j.microc.2020.105371