Development of label-free plasmonic Au-TiO2 thin film immunosensor devices

被引:22
作者
Barbosa, Ana I. [1 ,2 ]
Borges, Joel [3 ]
Meira, Diana I. [3 ]
Costa, Diogo [3 ]
Rodrigues, Marco S. [3 ]
Rebelo, Rita [2 ]
Correlo, Vitor M. [1 ,2 ,4 ]
Vaz, Filipe [3 ]
Reis, Rui L. [1 ,2 ,4 ]
机构
[1] Univ Minho, Headquarters European Inst Excellence Tissue Engn, Res Inst Biomat Biodegradables & Biomimet I3Bs, Res Grp 3Bs, AvePk,Parque Ciencia & Tecnol, P-4805017 Barco, Guimaraes, Portugal
[2] ICVS 3Bs PT Govt Associate Lab, Braga, Guimaraes, Portugal
[3] Univ Minho, Ctr Fis, Campus Gualtar, P-4710057 Braga, Portugal
[4] Headquarters Univ Minho, Discoveries Ctr Regenerat & Precis Med, AvePk, P-4805017 Barco, Guimaraes, Portugal
来源
MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2019年 / 100卷
关键词
Nanoplasmonic Au-TiO2 thin films; Plasma treatment; Immunosensor; Antibody immobilization; Localized surface plasmon resonance; RESONANCE SENSORS; REFRACTIVE-INDEX; SURFACE; SENSITIVITY; BIOSENSORS; ANTIBODY; DENSITY; QUANTITATION; IMMUNOASSAY; OCHRATOXIN;
D O I
10.1016/j.msec.2019.03.029
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
This work reports on the development of a label-free immunosensor technology, based on nanoplasmonic AuTiO2 thin films. The Au-TiO2 thin films were prepared by cost-effective reactive DC magnetron sputtering, followed by a thermal annealing procedure. The latter promoted the growth of the Au nanoparticles throughout the TiO2 matrix and induced some morphological changes, which are the base for the immunosensor device functionality. A posterior plasma etching treatment was required to partially expose the nanoparticles to the biological environment. It gave rise to a 6-fold increase of the total area of gold exposed, allowing further possibilities for the sensor sensitivity enhancement. Experimental results demonstrated the successful functionalization of the films' surface with antibodies, with the immobilization occurring preferentially in the exposed nanoparticles and negligibly on the TiO2 matrix. Antibody adsorption surface coverage studies revealed antibody low affinity to the film's surface. Nevertheless, immunoassay development experiments showed a strong and active immobilized antibody monolayer at an optimized antibody concentration. This allowed a 236 signal-tonoise-ratio in a confocal microscope, using mouse IgG and 100 ng/ml of Fab-specific anti-mouse IgG-FITC conjugated. Label-free detection of the optimized antibody monolayer on Au-TiO2 thin films was also tested, revealing an expected redshift in the LSPR band, which demonstrates the suitability for the development of cost-effective, label-free LSPR based immunosensor devices.
引用
收藏
页码:424 / 432
页数:9
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