HER2 aptamer-conjugated iron oxide nanoparticles with PDMAEMA-b-PMPC coating for breast cancer cell identification - supplementary data

Aim: To synthesize HER2 aptamer-conjugated iron oxide nanoparticles with a coating of poly(2- (dimethylamino) ethyl methacrylate)–poly(2-methacryloyloxyethylphosphorylcholine) block copolymer (IONPPPs). Methods: Characterization covered molecular structure, chemical composition, thermal stability, m...

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Hauptverfasser: von Zuben de Valega Negrao, Cyro, NP Cerize, Natalia, da Silva Justo-Junior, Amauri, Bester Liszbinski, Raquel, Pastore Meneguetti, Giovanna, Araujo, Larissa, A Rocco, Silvana, de Almeida Goncalves, Kaliandra, R Cornejo, Daniel, Leo, Patrıcia, Perecin, Caio, Adamoski, Douglas, M Gomes Dias, Sandra
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Sprache:eng
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Zusammenfassung:Aim: To synthesize HER2 aptamer-conjugated iron oxide nanoparticles with a coating of poly(2- (dimethylamino) ethyl methacrylate)–poly(2-methacryloyloxyethylphosphorylcholine) block copolymer (IONPPPs). Methods: Characterization covered molecular structure, chemical composition, thermal stability, magnetic characteristics, aptamer interaction, crystalline nature and microscopic features. Subsequent investigations focused on IONPPPs for in vitro cancer cell identification. Results: Results demonstrated high biocompatibility of the diblock copolymer with no significant toxicity up to 150 μg/ml. The facile coating process yielded the IONPP complex, featuring a 13.27 nm metal core and a 3.10 nm polymer coating. Functionalized with a HER2-targeting DNA aptamer, IONPPP enhanced recognition in HER2-amplified SKBR3 cells viamagnetization separation. Conclusion: These findings underscore IONPPP’s potential in cancer research and clinical applications, showcasing diagnostic efficacy and HER2 protein targeting in a proof-of-concept approach.
DOI:10.25402/nnm.25102169