Synthesis and characterization of a stable, label-free optical biosensor from TiO2-coated porous silicon

2014 ◽  
Vol 55 ◽  
pp. 372-378 ◽  
Author(s):  
Jianlin Li ◽  
Michael J. Sailor
2018 ◽  
Vol 1003 ◽  
pp. 012087 ◽  
Author(s):  
Roaa A abbas ◽  
Alwan M Alwan ◽  
Zainab T Abdulhamied

Chemosensors ◽  
2021 ◽  
Vol 9 (8) ◽  
pp. 228
Author(s):  
Dashananda Nanda Kumar ◽  
Zina Baider ◽  
Daniel Elad ◽  
Shlomo E. Blum ◽  
Giorgi Shtenberg

Botulinum neurotoxins (BoNT) are the most potent toxins, which are produced by Clostridium bacteria and cause the life-threatening disease of botulism in all vertebrates. Specifically, animal botulism represents a serious environmental and economic concern in animal production due to the high mortality rates observed during outbreaks. Despite the availability of vaccines against BoNT, there are still many outbreaks of botulism worldwide. Alternative assays capable of replacing the conventional in vivo assay in terms of rapid and sensitive quantification, and the applicability for on-site analysis, have long been perused. Herein, we present a simple, highly sensitive and label-free optical biosensor for real-time detection of BoNT serotype C using a porous silicon Fabry–Pérot interferometer. A competitive immunoassay coupled to a biochemical cascade reaction was adapted for optical signal amplification. The resulting insoluble precipitates accumulated within the nanostructure changed the reflectivity spectra by alternating the averaged refractive index. The augmented optical performance allowed for a linear response within the range of 10 to 10,000 pg mL−1 while presenting a detection limit of 4.8 pg mL−1. The practical aspect of the developed assay was verified using field BoNT holotoxins to exemplify the potential use of the developed optical approach for rapid bio-diagnosis of BoNT. The specificity and selectivity of the assay were successfully validated using an adjacent holotoxin relevant for farm animals (BoNT serotype D). Overall, this work sets the foundation for implementing a miniaturized interferometer for routine on-site botulism diagnosis, thus significantly reducing the need for animal experimentation and shortening analysis turnaround for early evidence-based therapy.


2010 ◽  
Vol 107 (1) ◽  
pp. 014513 ◽  
Author(s):  
Ilaria Rea ◽  
Annalisa Lamberti ◽  
Ivo Rendina ◽  
Giuseppe Coppola ◽  
Mariano Gioffrè ◽  
...  

Proceedings ◽  
2020 ◽  
Vol 60 (1) ◽  
pp. 32
Author(s):  
Giuliano Zanchetta ◽  
Thomas Carzaniga ◽  
Luka Vanjur ◽  
Luca Casiraghi ◽  
Giovanni Tagliabue ◽  
...  

MicroRNAs are widely studied as circulating biomarkers for early stage diagnosis of several diseases, but the procedures for their detection and quantification are currently complex and time consuming. We demonstrate a rapid, multiplex, one-pot detection method based on two-step amplification of the signal measured by a recent label-free optical biosensor, Reflective Phantom Interface (RPI). The specific capture with surface DNA probes is combined with mass amplification by an antibody targeting DNA–RNA hybrids and polyclonal secondary antibody, all performed without washing steps. Through this method, we achieved linear, sub-pM quantification of different miRNAs in 1.5 h. The RPI enabled the characterization of equilibrium and kinetics of each individual interaction involved in this multi-step process, which allowed us to model and optimize the relative concentrations and the time intervals of the assay.


Silicon ◽  
2017 ◽  
Vol 10 (3) ◽  
pp. 967-974 ◽  
Author(s):  
Falah A-H Mutlak ◽  
Ahmed B. Taha ◽  
Uday Muhsin Nayef

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