The physicochemical and biological characterization of a 24-month-stored nanocomplex based on gold nanoparticles conjugated with cetuximab demonstrated long-term stability, EGFR affinity and cancer cell death due to apoptosis

被引:20
作者
Andrade, Lidia M. [1 ]
Martins, Estefania M. N. [1 ,2 ]
Versiani, Alice F. [1 ,3 ]
Reis, Daniela S. [4 ]
da Fonseca, Flavio G. [5 ]
de Souza, Ivina P. [6 ,7 ]
Paniago, Roberto M. [1 ]
Pereira-Maia, Elene [6 ]
Ladeira, Luiz O. [1 ]
机构
[1] Univ Fed Minas Gerais, Dept Fis, Nanobiomed Res Grp, Belo Horizonte, MG, Brazil
[2] Ctr Desenvolvimento Tecnol Nucl, Belo Horizonte, MG, Brazil
[3] Fac Med Sao Jose do Rio Preto, Dept Doencas Dermatol Infecciosas & Parasitarias, Sao Jose Do Rio Preto, SP, Brazil
[4] Univ Fed Minas Gerais, Dept Bioquim & Imunol, Belo Horizonte, MG, Brazil
[5] Univ Fed Minas Gerais, Dept Microbiol, Belo Horizonte, MG, Brazil
[6] Univ Fed Minas Gerais, Dept Quim, Belo Horizonte, MG, Brazil
[7] Ctr Fed Educ Tecnol Minas Gerais, Dept Quim, Belo Horizonte, MG, Brazil
来源
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2020年 / 107卷
关键词
Long-term stability; Gold nanoparticles; Cetuximab; Apoptosis; Cancer; DRUG-DELIVERY SYSTEM; ANTIBODY; IMMOBILIZATION; OPPORTUNITIES; TRAFFICKING; MECHANISMS; RESISTANCE; THERAPY; MODEL; SIZE;
D O I
10.1016/j.msec.2019.110203
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Nanotechnology is one of the most promising tools for future diagnosis and therapy. Thus, we have produced gold nanoparticles coated with cetuximab at a dose-range from 5 mu g up to 200 mu g, and prolonged stable nanocomplexes were obtained. The nanocomplexes were characterized by UV-Vis, zeta potential, TEM, fluorometry, infrared regions, XPS and atomic absorption spectrometry. For biological characterization the A431 cell line was used. Cellular uptake, target affinity and cell death were assessed using ICP-OES, immunocytochemistry and flow cytometry, respectively. The immobilization of cetuximab on the AuNPs surfaces was confirmed. The nanocomplex with 24 months of manufacturing promoted efficient EGFR binding and induced tumour cell death due to apoptosis. Significant (p < 0.05) cell death was achieved using relatively low cetuximab concentration for AuNPs coating compared to the antibody alone. Therefore, our results provided robust physicochemical and biological characterization data corroborating the cetuximab-bioconjugate AuNPs as a feasible nanocomplex for biomedical applications.
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页数:12
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