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

被引:3
作者
Negrao, Cyro von Zuben de Valega [1 ,2 ,3 ]
Cerize, Natalia N. P. [3 ]
Justo Jr, Amauri da Silva [2 ]
Liszbinski, Raquel Bester [1 ,2 ]
Meneguetti, Giovanna Pastore [3 ]
Araujo, Larissa [3 ]
Rocco, Silvana A. [2 ]
Goncalves, Kaliandra de Almeida [2 ]
Cornejo, Daniel R. [4 ]
Leo, Patricia [3 ]
Perecin, Caio [3 ]
Adamoski, Douglas [2 ]
Dias, Sandra M. Gomes [2 ]
机构
[1] Univ Campinas UNICAMP, Inst Biol, Grad Program Genet & Mol Biol, BR-13083864 Campinas, SP, Brazil
[2] Brazilian Ctr Res Energy & Mat CNPEM, Brazilian Biosci Natl Lab LNBio, BR-13083970 Campinas, SP, Brazil
[3] Inst Technol Res IPT, Bionanomanufacturing Ctr, BR-05508901 Sao Paulo, SP, Brazil
[4] Univ Sao Paulo, Inst Phys, Dept Mat & Mech, BR-05508090 Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
aptamers; block copolymers; breast cancer; diagnostics; hybrid nanoparticles; RAFT-POLYMERIZATION; REVERSIBLE-ADDITION; MOLECULAR-WEIGHT; IN-VITRO; METHACRYLATE; COPOLYMERS; DELIVERY; FUNCTIONALIZATION; CYTOTOXICITY; CHALLENGES;
D O I
10.2217/nnm-2023-0225
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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 mu g/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 via magnetization 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.
引用
收藏
页码:231 / 254
页数:24
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