Ultrasensitive biosensor based on magnetic microspheres enhanced microfiber interferometer.

Biosens Bioelectron

National Engineering Laboratory for Destructive Testing and Optoelectronic Sensing Technology and Application, Nanchang HangKong University, Nanchang, 330063, China; Faculty of Engineering and Environment, Northumbria University, Newcastle Upon Tyne, NE1 8ST, United Kingdom. Electronic address:

Published: December 2019

A critical barrier for the successful development of fiber sensors for bio-chemical processes is their limitedly improved sensitivity, restricted by the sensor structural design. To solve this, in this paper, a novel concept was proposed using functionalised modified magnetic microspheres (MMSs) to "amplify" the effect of target bio-chemical analytes to significantly improve the fiber sensor's sensitivity, which has been demonstrated using human chorionic gonadotropin (hCG) as an example. Two types of antibody hCG, (β and α, both can specifically bind with hCG), were adhered on the surface of fibre sensor and MMSs respectively. Both hCG and MMSs will be specifically captured by the fibre sensor, where MMSs act as an "amplifier" to improve the sensor sensitivity. Experimentally immunomagnetic detection limit of 0.0001 mIU/mL has been achieved, which is the highest reported so far. This newly developed methodology opens a new direction for sensitivity improvement and could be further explored to applications require ultrahigh sensitivity detections such as earlier medical diagnostics.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.bios.2019.111563DOI Listing

Publication Analysis

Top Keywords

magnetic microspheres
8
fibre sensor
8
sensor mmss
8
sensitivity
5
ultrasensitive biosensor
4
biosensor based
4
based magnetic
4
microspheres enhanced
4
enhanced microfiber
4
microfiber interferometer
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!