4.2 Article

Enhanced Colorimetric Differentiation between Staphylococcus aureus and Pseudomonas aeruginosa Using a Shape-Encoded Sensor Hydrogel

Journal

ACS APPLIED BIO MATERIALS
Volume 3, Issue 7, Pages 4398-4407

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsabm.0c00403

Keywords

bacteria detection; bacteria differentiation; biosensors; fluorescent probe; hydrogels

Funding

  1. EPSRC
  2. University of Bath
  3. National Institutes of Health
  4. Robert A. Welch Foundation
  5. Medical Research Council (MRC)/UKRI [MR/N0137941/1]
  6. Royal Society
  7. European Research Council (ERC) [279202]
  8. equality office of the University of Siegen
  9. MaxBuchner-Forschungsstiftung Dechema [MBFSt-Kennziffer: 3671]
  10. University of Siegen
  11. MRC [MR/N006496/1] Funding Source: UKRI

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Herein, we demonstrate a combined fluorescent probe/shapeencoded hydrogel strategy for the fast, sensitive, and selective detection of bacterial species via their characteristic enzymes. A poly(vinyl alcohol) (PVA) hydrogel loaded with the fluorescent probe N,N'-(3-oxo-3H- spiro-[isobenzofuran-1,9'-xanthene]- 3',6'-diyl) bis(2,2,3,3,3-pentafluoropropanamide) (ACS-HNE) was designed for the detection of elastase, an enzyme produced by Pseudomonas aeruginosa. Likewise, a chitosan-derived hydrogel was loaded with the fluorescent probe 4-methylumbelliferyl-a-D-glucopyranoside (MUD) by entrapment for the selective detection of a-glucosidase, an enzyme produced by Staphylococcus aureus. For an observation time of 60 min, limits of detection (LODs) of <= 20 nM for elastase and <= 30 pM for alpha-glucosidase were obtained, which in the latter case is 3 orders of magnitude better than related chitosan systems with covalently coupled substrate. To illustrate the potential utility of these highly sensitive sensor hydrogels as a simple point-of-care test system, shaped hydrogel slabs representing the letters P and S were manufactured to detect P. aeruginosa and S. aureus, respectively. These shapes were shown to provide an additional unique color code under UV illumination corresponding to the characteristic enzyme produced by the corresponding bacteria. This study shows potential for the future development of an effective and simple point-of-care test for the rapid identification of bacterial species that can be operated by nonspecialists.

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