Highly sensitive evanescent wave combination tapered fiber optic fluorosensor for protein detection

2008 ◽  
Author(s):  
Vincent Nardone ◽  
Rakesh Kapoor

The study of refractive index of liquids over a range of 10oC to 60oC shows very interesting results to design and develop a highly sensitive passive fiber optic sensor based on a U-shaped glass probe. The depth of penetration of light that escaping from the core of the fiber into the cladding plays a crucial role in the development of a highly sensitive fiber optic evanescent wave sensor. The depth of penetration of an optical fiber striped off its cladding is directly related to the wavelength of the light, the index of refraction of the surrounding medium, the angle of incidence of light, the bending radius and thickness of the U-shaped probe. In the design of the sensor a U-shaped glass probe is used to replace the core of the fiber in the region of sensing, the diameter of which is same as that of the cores of a pair of insensitive fibers which in-turn connected to a tunable light source and an optical detector. The sensor is highly reliable, robust and easy to configure using multimode PCS fibers and the source operating at the wavelengths of 630nm, 660nm, 820nm and 850nm.


2006 ◽  
Vol 321-323 ◽  
pp. 1168-1171 ◽  
Author(s):  
Gi Young Kim ◽  
Mark T. Morgan ◽  
Daniel Ess ◽  
Byoung Kwon Hahm ◽  
Aparna Kothapalli ◽  
...  

Fiber-optic biosensor uses light transmittable tapered fiber to send excitation laser light and receive emitted fluorescent light. The fluorescent light excited by an evanescent wave generated by the laser is quantitatively related to biomolecules immobilized on the fiber surface [1]. An automated fiber-optic biosensor based detection method for Listeria monocytogenes was developed in this research. Detections of Listeria monocytogenes in hotdog sample were performed to evaluate the method. By using the detection method with automated fiber-optic biosensor, 5.4×107 cfu/ml of Listeria monocytogenes was able to detect.


Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3732
Author(s):  
Agnieszka Dabrowska ◽  
Aleksandra Milewska ◽  
Joanna Ner-Kluza ◽  
Piotr Suder ◽  
Krzysztof Pyrc

Mass spectrometry (MS) used in proteomic approaches is able to detect hundreds of proteins in a single assay. Although undeniable high analytical power of MS, data acquired sometimes lead to confusing results, especially during a search of very selective, unique interactions in complex biological matrices. Here, we would like to show an example of such confusing data, providing an extensive discussion on the observed phenomenon. Our investigations focus on the interaction between the Zika virus NS3 protease, which is essential for virus replication. This enzyme is known for helping to remodel the microenvironment of the infected cells. Several reports show that this protease can process cellular substrates and thereby modify cellular pathways that are important for the virus. Herein, we explored some of the targets of NS3, clearly shown by proteomic techniques, as processed during infection. Unfortunately, we could not confirm the biological relevance of protein targets for viral infections detected by MS. Thus, although mass spectrometry is highly sensitive and useful in many instances, also being able to show directions where cell/virus interaction occurs, we believe that deep recognition of their biological role is essential to receive complete insight into the investigated process.


2018 ◽  
Vol 18 (13) ◽  
pp. 5361-5367
Author(s):  
Raffaele Caroselli ◽  
David Martin Sanchez ◽  
Salvador Ponce-Alcantara ◽  
Francisco Prats Quilez ◽  
Luis Torrijos Moran ◽  
...  

2016 ◽  
Vol 168 ◽  
pp. 117-120 ◽  
Author(s):  
S. Chauhan ◽  
N. Punjabi ◽  
D. Sharma ◽  
S. Mukherji

2019 ◽  
Vol 37 (11) ◽  
pp. 2756-2761 ◽  
Author(s):  
Dandan Sun ◽  
Li-Peng Sun ◽  
Tuan Guo ◽  
Bai-Ou Guan
Keyword(s):  

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