4.8 Article

Magneto-Fluorescent Microbeads for Bacteria Detection Constructed from Superparamagnetic Fe3O4 Nanoparticles and AIS/ZnS Quantum Dots

Journal

ANALYTICAL CHEMISTRY
Volume 91, Issue 20, Pages 12661-12669

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.9b01812

Keywords

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Funding

  1. Federal Target Program for Research and Development of the Ministry of Science and Higher Education of the Russian Federation [14.587.21.0047, RFMEFI58718X0047]
  2. Irish Research Council (IRC) [GOIPD/2018/504]
  3. BEACON, Bioeconomy Research Centre [SFI 16/RC/3889]
  4. M-Eranet Project ICENAP [RE1203/17-1]
  5. German Research Council (DFG) [RE1203/12-3]
  6. EraNetRus Project TARQUIS (Federal Ministry of Education and Research (BMBF)) [01DJ18001]
  7. Adolf-Martens fellowship - BAM
  8. BAM-internal research program Menschen, Ideen and Innovation (MI-Typ III)

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The efficient and sensitive detection of pathogenic microorganisms in aqueous environments, such as water used in medical applications, drinking water, and cooling water of industrial plants, requires simple and fast methods suitable for multiplexed detection such as flow cytometry (FCM) with optically encoded carrier beads. For this purpose, we combine fluorescent Cd-free Ag-In-S ternary quantum dots (t-QDs) with fluorescence lifetimes (LTs) of several hundred nanoseconds and superparamagnetic Fe3O4 nanoparticles (SPIONs) with mesoporous CaCO3 microbeads to a magneto-fluorescent bead platform that can be surface-functionalized with bioligands, such as antibodies. This inorganic bead platform enables immuno-magnetic separation, target enrichment, and target quantification with optical readout. The beads can be detected with steady-state and time-resolved fluorescence microscopy and flow cytometry (FCM). Moreover, they are suited for readout by time gated emission. In the following, the preparation of these magneto-fluorescent CaCO3 beads, their spectroscopic and analytic characterization, and their conjugation with bacteria-specific antibodies are presented as well as proof-of-concept measurements with Legionella pneumophila including cell cultivation and plating experiments for bacteria quantification. Additionally, the possibility to discriminate between the long-lived emission of the LT-encoded capture and carrier CaCO3 beads and the short-lived emission of the dye-stained bacteria with time-resolved fluorescence techniques and single wavelength excitation is demonstrated.

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