Peptide functionalized magneto-plasmonic nanoparticles obtained by microfluidics for inhibition of β-amyloid aggregation

被引:13
|
作者
Hassan, N. [1 ]
Cordero, M. L. [2 ]
Sierpe, R. [3 ,4 ]
Almada, M. [5 ]
Juarez, J. [6 ]
Valdez, M. [6 ]
Riveros, A. [3 ,4 ]
Vargas, E. [7 ]
Abou-Hassan, A. [8 ]
Ruso, J. M. [9 ]
Kogan, M. J. [3 ,4 ]
机构
[1] Univ Tecnol Metropolitana, Programa Inst Fomento I D I, Ignacio Valdivieso 2409, Santiago, Chile
[2] Univ Chile, Fac Ciencias Fis & Matemat, Dept Fis, Av Blanco Encalada 2008, Santiago, Chile
[3] Univ Chile, Fac Ciencias Quim & Farmaceut, Dept Quim Farmacol & Toxicol, Santos Dumont 964, Santiago, Chile
[4] Adv Ctr Chron Dis ACCDis, Santos Dumont 964, Santiago, Chile
[5] Catedras CONACYT Inst Tecnol Nuevo Leon, Av Alianza 507,Parque Invest & Innovac Tecnol, Monterrey 66629, NL, Mexico
[6] Univ Sonora, Dept Fis, Hermosillo 83000, Sonora, Mexico
[7] Ctr Dev Nanosci & Nanotechnol, Santiago 9170124, Chile
[8] Sorbonne Univ, CNRS, PHysicochim Electrolytes & Nanosyst InterfaciauX, PHENIX, F-75005 Paris, France
[9] Univ Santiago de Compostela, Dept Appl Phys, Soft Matter & Mol Biophys Grp, Santiago De Compostela 15782, Spain
关键词
CONTROLLED DRUG-RELEASE; GOLD NANORODS; BIOMEDICAL APPLICATIONS; INORGANIC NANOPARTICLES; ALZHEIMERS-DISEASE; THERAPY; DELIVERY; CANCER; CHITOSAN; MICROPARTICLES;
D O I
10.1039/c8tb00206a
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
In the present work, we report on the synthesis of peptide functionalized magneto-plasmonic nanoparticles in a simple microfluidic platform. Superparamagnetic nanoparticles and gold nanorods were selected for this study. Magnetic nanoparticles were functionalized with peptide D1, which can bind selectively to toxic aggregates of the beta-amyloid peptide associated with Alzheimer's disease. Gold nanorods were functionalized with chitosan replacing the surfactant cetyltrimethylammonium bromide to reduce the cytotoxic effect. The selected microfluidic strategy yields structures with plasmonic and magnetic properties in a nanostructure. Cytotoxic assays with SH-SY5Y cells demonstrate that nanoparticles obtained by microfluidics do not affect cell viability at the studied concentrations. Additionally, these magneto-plasmonic nanoparticles inhibit fibril formation demonstrating that the magneto-plasmonic nanoparticles obtained by microfluidics could be applied for a potential treatment and diagnosis of Alzheimer's disease.
引用
收藏
页码:5091 / 5099
页数:9
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