Issue 3, 2007

Label-free detection of neuron–drug interactions using acoustic and Kelvin vibrational fields

Abstract

Kelvin and acoustic fields of high-frequency have been employed in the non-invasive investigation of immortalized hypothalamic neurons, in order to assess their response to different concentrations of specific drugs, toxins, a stress-reducing hormone and neurotrophic factors. In an analytical systems biology approach, this work constitutes a first study of living neuron cultures by scanning Kelvin nanoprobe (SKN) and thickness shear mode (TSM) acoustic wave techniques. N-38 hypothalamic mouse neurons were immobilized on the gold electrode of 9 MHz TSM acoustic wave devices and gold-coated slides for study by SKN. The neurons were exposed to the neurochemicals betaseron, forskolin, TCAP, and cerebrolysin. Signals were collected with the TSM in real-time mode, and with the SKN in scanning and real-time modes, as the drugs were applied at biologically significant concentrations. With the TSM, for all drugs, some frequency and resistance shifts were in the same direction, contrary to normal functioning for this type of instrument. Possible mechanisms are presented to explain this behaviour. An oscillatory signal with periodicity of approximately 2 min was observed for some neuron-coated surfaces, where the amplitude of these oscillations was altered upon application of certain neurotrophic factors. These two new techniques present novel and non-invasive electrodeless methods for detecting changes at the cellular level caused by a variety of neuroactive compounds, without killing or destroying the neurons.

Graphical abstract: Label-free detection of neuron–drug interactions using acoustic and Kelvin vibrational fields

Article information

Article type
Paper
Submitted
24 Oct 2006
Accepted
02 Jan 2007
First published
18 Jan 2007

Analyst, 2007,132, 242-255

Label-free detection of neuron–drug interactions using acoustic and Kelvin vibrational fields

L. Cheran, S. Cheung, A. Al Chawaf, J. S. Ellis, D. D. Belsham, W. A. MacKay, D. Lovejoy and M. Thompson, Analyst, 2007, 132, 242 DOI: 10.1039/B615476J

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