Principles for Measurement of Chemical Exposure Based on Recognition-Driven Anchoring Transitions in Liquid Crystals

Author:

Shah Rahul R.1,Abbott Nicholas L.1

Affiliation:

1. Department of Chemical Engineering, University of Wisconsin, Madison, WI 53706, USA.

Abstract

The competitive binding of a molecule forming a liquid crystal and a targeted analyte to a common molecular receptor presented at a solid surface possessing nanometer-scale topography is used to trigger an easily visualized surface-driven change in the orientation of a micrometer-thick film of liquid crystal. Diffusion of the targeted analyte from atmosphere to surface-immobilized receptor across the micrometer-thick film of liquid crystal is fast (on the order of seconds), and the competitive interaction of the targeted analyte and liquid crystal with the receptor provides a high level of tolerance to nontargeted species (water, ethanol, acetone, and hexanes). Systems that provide parts-per-billion (by volume) sensitivity to either organoamine or organophosphorus compounds are demonstrated, and their use for imaging of spatial gradients in concentration is reported. This approach does not require complex instrumentation and could provide the basis of wearable personalized sensors for measurement of real-time and cumulative exposure to environmental agents.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference45 articles.

1. B. E. Rittmann P. McCarty Environmental Biotechnology: Principles and Applications (McGraw Hill New York 2000).

2. Cisper M. E., Hemberger P. H., Rapid Commun. Mass Spectrosc. 11, 1449 (1997).

3. Methods for detection of toxic compounds or their metabolites such as those based on mass-sensitive oscillators (33) microfabricated cantilevers (34 35) fluorescence quenching (36) and enzymatic detection (37) are not suitable as the basis of personal dosimeters.

4. Past studies have reported detection of vapors (to ∼1 ppmv) by their absorption into the bulk of a LC (5 6). The bulk absorption of the analyte results in a color change caused by a change in the pitch of a cholesteric phase. The sensitivity and selectivity reported in these past studies are low.

5. Poziomek E. J., Novak T. J., Mackay R. A., Mol. Cryst. Liq. Cryst. 27, 175 (1974).

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