Laser-assembled conductive 3D nanozyme film-based nitrocellulose sensor for real-time detection of H2O2 released from cancer cells

被引:8
|
作者
Bukhari, Qurat U. A. [1 ,2 ,3 ]
Della Pelle, Flavio [3 ]
Alvarez-Diduk, Ruslan [1 ,2 ]
Scroccarello, Annalisa [3 ]
Nogues, Carme [4 ]
Careta, Oriol [4 ]
Compagnone, Dario [3 ]
Merkoci, Arben [1 ,2 ,5 ]
机构
[1] CSIC, Catalan Inst Nanosci & Nanotechnol ICN2, Nanobioelect & Biosensors Grp, Campus UAB, Bellaterra, Barcelona, Spain
[2] BIST, Campus UAB, Bellaterra, Barcelona, Spain
[3] Univ Teramo, Dept Biosci & Technol Food Agr & Environm, Campus Aurelio Saliceti Via R Balzarini 1, I-64100 Teramo, Italy
[4] Univ Autonoma Barcelona UAB, Dept Biol Cellular Fisiol & Immunol, Fac Biociencies, Campus UAB, Barcelona 08193, Spain
[5] ICREA Inst Catalana Recerca & Estudis Avancats i, Passeig Lluis Companys 23, Barcelona 08010, Spain
来源
关键词
Biosensors; Paper -based sensors; Nanozymes; IR laser; Cells; Nanomaterial film; REDUCED GRAPHENE OXIDE; SCRIBED GRAPHENE; IN-SITU; NANOPARTICLES; CARBON; ELECTRODES; XPS;
D O I
10.1016/j.bios.2024.116544
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this work, a nanostructured conductive film possessing nanozyme features was straightforwardly produced via laser-assembling and integrated into complete nitrocellulose sensors; the cellulosic substrate allows to host live cells, while the nanostructured film nanozyme activity ensures the enzyme-free real-time detection of hydrogen peroxide (H2O2) released by the sames. In detail, a highly exfoliated reduced graphene oxide 3D film decorated with naked platinum nanocubes was produced using a CO2-laser plotter via the simultaneous reduction and patterning of graphene oxide and platinum cations; the nanostructured film was integrated into a nitrocellulose substrate and the complete sensor was manufactured using an affordable semi-automatic printing approach. The linear range for the direct H2O2 determination was 0.5-80 mu M (R2 = 0.9943), with a limit of detection of 0.2 mu M. Live cell measurements were achieved by placing the sensor in the culture medium, ensuring their adhesion on the sensors' surface; two cell lines were used as non-tumorigenic (Vero cells) and tumorigenic (SKBR3 cells) models, respectively. Real-time detection of H2O2 released by cells upon stimulation with phorbol ester was carried out; the nitrocellulose sensor returned on-site and real-time quantitative information on the H2O2 released proving useful sensitivity and selectivity, allowing to distinguish tumorigenic cells. The proposed strategy allows low-cost in-series semi-automatic production of paper-based point-of-care devices using simple benchtop instrumentation, paving the way for the easy and affordable monitoring of the cytopathology state of cancer cells.
引用
收藏
页数:10
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