Design, Synthesis and Characterization of Fluorescent MIP Particles for Labelling of Malignant Cells

  • Cancer is a leading cause of death worldwide, and its early detection and resultant treatment contributes significantly to patient recovery and survival. Detection is currently based on magnetic resonance imaging and computed tomography, methods that are expensive, while processing of the results is time-consuming1. There is a need for low-cost cancer detection techniques that give conclusive results in the shortest time possible. When equipped with a reporter function, molecularly imprinted polymers (MIPs) targeting tumor markers on cancerous cells may provide a cheaper solution for imaging-based cancer detection. Thin MIP layers immobilized on particle platforms are ideal in this regard, because a fluorescence reporter can be integrated into the particle core and/or MIP shell and such core/shell nanoparticles show faster response times and increased selectivity in comparison to bulk MIPs. Changes in sialylation patterns of cell surface glycans indicate malignancy2. Here, weCancer is a leading cause of death worldwide, and its early detection and resultant treatment contributes significantly to patient recovery and survival. Detection is currently based on magnetic resonance imaging and computed tomography, methods that are expensive, while processing of the results is time-consuming1. There is a need for low-cost cancer detection techniques that give conclusive results in the shortest time possible. When equipped with a reporter function, molecularly imprinted polymers (MIPs) targeting tumor markers on cancerous cells may provide a cheaper solution for imaging-based cancer detection. Thin MIP layers immobilized on particle platforms are ideal in this regard, because a fluorescence reporter can be integrated into the particle core and/or MIP shell and such core/shell nanoparticles show faster response times and increased selectivity in comparison to bulk MIPs. Changes in sialylation patterns of cell surface glycans indicate malignancy2. Here, we present the design, synthesis and characterization of MIPs that target sialic acid-terminated glycans (SA MIPs), prepared as a thin layer on a polystyrene core/silica shell nanoparticle platform. The MIP particles contain fluorescent emitters and can be applied in fluorescence imaging of malignant tumors. Dynamic light scattering (DLS) and transmission electron microscopy (TEM) are used for structural characterization. Binding capacity of the MIPs to target glycans and competing sugars is also evaluated and compared to that of the corresponding non-imprinted polymer particles (NIP).zeige mehrzeige weniger

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Metadaten
Autor*innen:Martha Wamaitha KimaniORCiD
Koautor*innen:Evgeniia Kislenko, Kornelia Gawlitza, Knut Rurack
Dokumenttyp:Vortrag
Veröffentlichungsform:Präsentation
Sprache:Englisch
Jahr der Erstveröffentlichung:2020
Organisationseinheit der BAM:1 Analytische Chemie; Referenzmaterialien
1 Analytische Chemie; Referenzmaterialien / 1.9 Chemische und optische Sensorik
DDC-Klassifikation:Naturwissenschaften und Mathematik / Chemie / Analytische Chemie
Freie Schlagwörter:Cancer; MIPs; Sialic acid
Themenfelder/Aktivitätsfelder der BAM:Umwelt
Umwelt / Sensorik
Veranstaltung:Mini MIP Conference
Veranstaltungsort:Online meeting
Beginndatum der Veranstaltung:16.06.2020
Enddatum der Veranstaltung:16.06.2020
Verfügbarkeit des Dokuments:Datei im Netzwerk der BAM verfügbar ("Closed Access")
Datum der Freischaltung:18.06.2020
Referierte Publikation:Nein
Eingeladener Vortrag:Nein
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