Publication Type Journal Article
Title In situ synthesis of fluorescent polydopamine nanoparticles coupled with enzyme-controlled dissolution of MnO2 nanoflakes for a sensitive immunoassay of cancer biomarkers
Authors Zhenzhen Lin Meijin Li Shuzhen Lv Kangyao Zhang Minghua Lu Dianping Tang Joshua Oconnor Taylor Jackson
Groups G3 G1
Journal JOURNAL OF MATERIALS CHEMISTRY B
Year 2017
Month November
Volume 5
Number 43
Pages 8506-8513
Abstract Herein, a novel immunosensing strategy was designed for the sensitive fluorescence/visual detection of alpha-fetoprotein (AFP), by combining the enzyme-controlled formation of polydopamine (PDA) nanoparticles with the dissolution of manganese dioxide (MnO2) nanoflakes. Initially, a sandwich-type immunoreaction was fabricated on a capture antibody-coated microplate by using detection antibody/ascorbate oxidase-conjugating gold nanoparticles (AOX-AuNP-Ab(2)) as the detection probe. The ascorbate oxidase, carried within the immunocomplex, oxidized ascorbic acid (AA) to dehydroascorbic acid (DAA) to inhibit the dissolution of the MnO2 nanoflakes. This resulted in an increment in fluorescent PDA nanoparticles from the oxidation of dopamine (DA) into its quinone derivative with the aid of the MnO2 nanoflakes. Under optimal conditions, the fluorescence intensity of the PDA nanoparticles increased with increasing AFP concentration within the dynamic working range of 0.05-20 ng mL(-1), with a detection limit (LOD) of 17.3 pg mL(-1). The sensor also showed high specificity and acceptable accuracy for the detection of target AFP against other potential cancer biomarkers. Importantly, this study demonstrated for the first time that fluorescent PDA nanoparticles could be used as signal-generation tags and applied to an enzyme immunoassay. Although this methodology focused on AFP detection, it would be suitable for the detection of other cancer biomarkers if the corresponding antibodies were employed.
DOI http://dx.doi.org/10.1039/c7tb02291c
ISBN
Publisher
Book Title
ISSN 2050-750X
EISSN 2050-7518
Conference Name
Bibtex ID ISI:000414782200009
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