Optical signal recording from optogenetic stimulation of human pulp dental cells using twin-core fiber optic biosensor based on Mach-Zender interoferometer

• Type: Article in International Conference Proceedings Book
• Date: 2019

Authors

Akbari, F (Author) Other; Layeghi, A (Author) Other; Nazari, MHS (Author) Other; Ghorbani, A (Author) Other; Nejad, SC (Author) Other; Dragahi, L (Author) Other; Frazao, O (Author) FCUP; Santos, JL (Author) Other; Latifi, H (Author) Other; Zibaii, MI (Author) Other

Conference proceedings International

Title: 2019 Conference on Lasers and Electro-Optics Europe and European Quantum Electronics Conference, CLEO/Europe-EQEC 2019

2019 Conference on Lasers and Electro-Optics Europe and European Quantum Electronics Conference, CLEO/Europe-EQEC 2019

23 June 2019 through 27 June 2019

Indexing

Scopus - 0 Citations

Other information

Authenticus ID: P-00R-907

DOI: 10.1109/cleoe-eqec.2019.8872177

Abstract (EN): In this study, an optical signal recording method for optogenetics stimulation of ChR2 channels expressed in human pulp dental (HPD) cells by using a fiber optic refractive index (RI) sensor based on all fiber Mach-Zehnder interferometer was proposed. All-fiber Mach-Zender interferometric biosensor is composed of a specially fabricated twin-core fiber spliced between two pieces of a single-mode fiber which one of the cores was doped with germanium and the other with phosphorous [1]. The interference pattern in the fiber Mach-Zehnder interferometer is occurred by coupling of the propagation lights of both fiber cores. For coupling the light into both cores, a short length of a coreless fiber optic was used. The length of twin-core fiber was 40 cm. Here, one core of the fiber acts as a reference arm and the other cores as sensing arm. For increasing evanescent wave around the sensing arm of the fiber optic biosensor, a short section of the cladding of the twin-core fiber about 2 cm was etched with HF solution. For this propose, after determining the direction of the cores so that the two cores were in the vertical direction, one side of the twin-core fiber was fixed on Plexiglas substrate by using UV glow and the upper side of the sensor was etched. The thickness of remained clad around the upper core was about 1 micrometer. In the experimental setup as is shown in Fig. 1(a), light from an SLD at 1550 nm after passing an isolator arrived at the sensor and output spectrum was monitored with an optical spectrum analyzer which has 10 pm wavelength resolution. The best RI sensitivity of the sensor in the range of 1.39 to 1.43 was obtained to be 675.74 nm/RIU. For detecting of cell signal by using optogenetic stimulation which ChR2 opsin was expressed on HPD cells, it needs that high concentrations of cells were immobilized to the etched fiber surface by PLL biopolymer. Optogenetic stimulation of ChR2 channel was done using a 470 nm laser diode [2] pulse with a frequency of 15 Hz, a number of pulses 120, duty cycle 50 in 60 seconds, and 300 second rest time. As a result of optogenetic stimulation and activation of light-sensitive ion channels, effective RI around the fiber optic biosensor changes [3]. Obtained results were shown in Fig. 1(b). Changes in the RI lead to a wavelength shift of the sensor spectrum. © 2019 IEEE.

Language: English

Type (Professor's evaluation): Scientific