Issue 6, 2005

Magnetic force-based multiplexed immunoassay using superparamagnetic nanoparticles in microfluidic channel

Abstract

This paper describes a novel microfluidic immunoassay utilizing binding of superparamagnetic nanoparticles to beads and deflection of these beads in a magnetic field as the signal for measuring the presence of analyte. The superparamagnetic 50 nm nanoparticles and fluorescent 1 µm polystyrene beads are immobilized with specific antibodies. When target analytes react with the polystyrene beads and superparamagnetic nanoparticles simultaneously, the superparamagnetic nanoparticles can be attached onto the microbeads by the antigen–antibody complex. In the poly(dimethylsiloxane) (PDMS) microfluidic channel, only the microbeads conjugated with superparamagnetic nanoparticles by analytes consequently move to the high gradient magnetic fields under the specific applied magnetic field. In this study, the magnetic force-based microfluidic immunoassay is successfully applied to detect the rabbit IgG and mouse IgG as model analytes. The lowest concentration of rabbit IgG and mouse IgG measured over the background is 244 pg mL−1 and 15.6 ng mL−1, respectively. The velocities of microbeads conjugated with superparamagnetic nanoparticles are demonstrated by magnetic field gradients in microfluidic channels and compared with the calculated magnetic field gradients. Moreover, dual analyte detection in a single reaction is also performed by the fluorescent encoded microbeads in the microfluidic device. Detection range and lower detection limit can be controlled by the microbeads concentration and the higher magnetic field gradient.

Graphical abstract: Magnetic force-based multiplexed immunoassay using superparamagnetic nanoparticles in microfluidic channel

Supplementary files

Article information

Article type
Paper
Submitted
15 Feb 2005
Accepted
11 Apr 2005
First published
29 Apr 2005

Lab Chip, 2005,5, 657-664

Magnetic force-based multiplexed immunoassay using superparamagnetic nanoparticles in microfluidic channel

K. Sung Kim and J. Park, Lab Chip, 2005, 5, 657 DOI: 10.1039/B502225H

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements