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Carbon Nanodots (CNDs) Doped Molecularly Imprinted Polymers (MIPs) for Tumor- Associated Glycan Imaging

  • Glycosylation is heavily altered in tumor cells compared with healthy cells, because of the different levels of expression of glycosyltransferases, glycosidases and monosaccharide transporters within a cancerous microenvironment. 1 Tumor-associated glycans, especially sialic acid (SA) conjugates, which are good candidates of tumor markers, can be used for Cancer early diagnosis. 2 However, studies on SA-binding lectins demonstrate that the type of SAlinkage and the glycosylation position of carbohydrate can greatly influence the affinity. 3 Therefore, there is a need for diagnostic tools owning high specificity and strong affinity to analyze and determine SA glycosylation motifs. 4 Herein, we report the development of fluorescent core/shell/shell nanoparticles where the outermost layer is a thin molecularly imprinted polymer (MIP) film binding to tumor cells in vitro by targeting cell surface SA. The core is made of N-doped red carbon nanodots (R-CNDs) which were prepared byGlycosylation is heavily altered in tumor cells compared with healthy cells, because of the different levels of expression of glycosyltransferases, glycosidases and monosaccharide transporters within a cancerous microenvironment. 1 Tumor-associated glycans, especially sialic acid (SA) conjugates, which are good candidates of tumor markers, can be used for Cancer early diagnosis. 2 However, studies on SA-binding lectins demonstrate that the type of SAlinkage and the glycosylation position of carbohydrate can greatly influence the affinity. 3 Therefore, there is a need for diagnostic tools owning high specificity and strong affinity to analyze and determine SA glycosylation motifs. 4 Herein, we report the development of fluorescent core/shell/shell nanoparticles where the outermost layer is a thin molecularly imprinted polymer (MIP) film binding to tumor cells in vitro by targeting cell surface SA. The core is made of N-doped red carbon nanodots (R-CNDs) which were prepared by hydrothermal synthesis, emitting intense red fluorescence under fluorescence microscopy imaging conditions. Silica coating of R-CNDs was achieved by a microemulsion method, resulting in ca. 40 nm large silica-coated CNDs (named R-CSNs). Finally, a thin MIP-shell was accomplished by using a combination of non-fluorescent monomer (3), functional monomers (1, 2) and cross-linker (EGDMA) for polymerization (Figure 1). Transmission electron microscopy (TEM) is used for structural characterization of the formation of MIP layer, and the results of cell-based binding tests show a promising binding affinity of MIPs to tumor cells, allowing a relatively robust, specific and rapid analytical method for cancer biopsies.zeige mehrzeige weniger

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Metadaten
Autor*innen:Shan Jiang
Koautor*innen:T. Wang, Kornelia GawlitzaORCiD, J. Persson, Knut RurackORCiD
Dokumenttyp:Vortrag
Veröffentlichungsform:Präsentation
Sprache:Englisch
Jahr der Erstveröffentlichung:2019
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:Carbon Nanodots; Glycan; MIP
Themenfelder/Aktivitätsfelder der BAM:Umwelt
Umwelt / Sensorik
Veranstaltung:GSSMIP2019
Veranstaltungsort:Berlin, Germany
Beginndatum der Veranstaltung:28.08.2019
Enddatum der Veranstaltung:30.08.2019
URL:https://sites.google.com/view/gssmip2019/gss-mip-2019
Verfügbarkeit des Dokuments:Datei im Netzwerk der BAM verfügbar ("Closed Access")
Datum der Freischaltung:14.10.2019
Referierte Publikation:Nein
Eingeladener Vortrag:Nein
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