Optical signal recording of cellular activity in optogenetic stimulation of human pulp dental cells using a twin-core fiber-based Mach-Zehnder interferometer biosensor

TL;DR

This paper presents a novel fiber-optic Mach-Zehnder interferometer sensor capable of detecting refractive index changes in cell media during optogenetic stimulation of human dental pulp stem cells, enabling real-time monitoring of cellular activity.

Contribution

The study introduces a new twin-core fiber-based MZI biosensor for optogenetic cell activity monitoring, with validated high sensitivity and successful detection of RI changes during stimulation.

Findings

Sensor achieved 675.74 nm/RIU sensitivity.

Blue light effectively stimulated light-sensitive cells.

Sensor successfully detected RI changes during optogenetic stimulation.

Abstract

This paper introduces an innovative two-core fiber (TCF) optic sensor employing a Mach-Zehnder interferometer (MZI) to monitor the optogenetic response of light-sensitive human dental pulp stem cells (hDPSCs). The in-fiber MZI, formed using a segment of TCF optic, detects refractive index (RI) changes in the surrounding medium. The sensor utilizes the evanescent wave of one core as the sensing arm, necessitating a thin cladding achieved through one-sided chemical etching. This design allows the sensor to detect subtle alterations in the RI of the environment by observing displacements in the interference spectrum. The optogenetic stimulation of light-sensitive cells induces variations in ion concentrations, leading to a corresponding change in refractive index. The fabricated sensor, with a peak sensitivity of 675.74 nm/RIU within the RI range of 1.39-1.43, can detect these changes. A computer simulation validated the sensitivity and optimized fabrication parameters, exhibiting satisfactory agreement with experimental results. Spectrum displacements were recorded for both light-sensitive hDPSCs and regular hDPSCs (as a control test). Results from the experiment, analyzed and compared using data analysis software, revealed that 473 nm blue light effectively stimulated light-sensitive hDPSCs. Notably, the proposed sensor, a novel structure, demonstrated its capability to detect RI changes in the cell medium during optogenetic applications.