In-Plane Parallel Scanning: A Microarray Technology for Point-of-Care Testing

Reuven Duer*, Russell Lund, Richard Tanaka, Douglas A. Christensen, and James N. Herron*§
PLC Diagnostics, Inc., 192 Odebolt Drive, Thousand Oaks, California 91360, United States, Departments of Bioengineering and Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, Utah 84112, United States
Anal. Chem., 2010, 82 (21), pp 8856–8865
DOI: 10.1021/ac101571b
Publication Date (Web): October 14, 2010
Copyright © 2010 American Chemical Society
* To whom correspondence should be addressed. Phone: 805-405-4620 (R.D.), (801) 581-7303 (J.N.H.). Fax: 805-265-6025 (R.D.), (801) 585-5151 (J.N.H.). E-mail: rduer@plcds.com (R.D.), james.herron@utah.edu (J.N.H.)., †

PLC Diagnostics, Inc.

, ‡

Department of Bioengineering, University of Utah.

, §

Department of Pharmaceutics and Pharmaceutical Chemistry, University of Utah.

Abstract

Abstract Image

A new microarray technology is described for rapid, inexpensive, multiplex diagnostics assays. Referred to as “in-plane parallel scanning” (IPPS), this technology replaces expensive laser scanning with a grid of 100-μm-wide waveguides embedded in the chip’s substrate, enabling real-time quantification of molecular complex formation on the chip’s surface. Compared to conventional microarray technology, IPPS has advantages of shorter assay time and lower instrument cost and complexity so that the platform can potentially be used in point-of-care (POC) settings. Two different chip formats are described: a low-density microarray with 10 sensing wells (IPPS-10) and a medium-density one with 100 sensing wells (IPPS-100). Performance was evaluated in two different proof-of-principle immunoassays: interleukin-1β (IL-1β) and Clostridium difficile toxin A. The two assays gave similar limits of detection of 0.67 and 0.94 pM, respectively. A saturation kinetics model described the sensor response with apparent dissociation constants of 511 pM for IL-1β and 6.47 nM for C. difficile toxin A toxoid. The multiplexing capabilities of the IPPS technology were also demonstrated in a multiplex assay for both analytes on the same IPPS-10 chip. Based on these results, the IPPS technology holds promise for translating diagnostic microarrays into near-patient environments.

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History

  • Published In Issue November 01, 2010
  • Article ASAPOctober 14, 2010
  • Received: June 12, 2010
    Accepted: September 28, 2010

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