Next‐Generation Wound Care: Aptamer‐Conjugated Polydiacetylene/Polyurethane Nanofibrous Biosensors for Selective In Situ Colorimetric Detection of Pseudomonas

Author:

Currie Sarah1ORCID,Cortes de la Torre Alan Jesus2,Kumar Ayush3,Logsetty Sarvesh4,Liu Song15ORCID

Affiliation:

1. Department of Biosystems Engineering Faculty of Agricultural and Food Sciences University of Manitoba Winnipeg Manitoba Canada

2. Research Laboratory on Optimal Design Devices and Advanced Materials − OPTIMA Department of Mathematics and Physics ITESO Tlaquepaque Jalisco Mexico

3. Department of Microbiology Faculty of Science University of Manitoba Winnipeg Manitoba Canada

4. Departments of Surgery Psychiatry and Children's health Rady Faculty of Health Sciences University of Manitoba Winnipeg Manitoba Canada

5. Biomedical Engineering Faculty of Engineering University of Manitoba Winnipeg Manitoba Canada

Abstract

AbstractBiosensors for wound dressings can enable point‐of‐care monitoring of wound bed health by exhibiting a color change visible to the naked eye, to alert healthcare providers of the presence of pathogenic bacteria. Here, a polydiacetylene‐based electrospun nanofibrous wound dressing for the detection of Pseudomonas aeruginosa is reported. Using conventional blend electrospinning, two diacetylene monomers—10,12‐pentacosadiynoic acid (PCDA) and 10,12‐tricosadiynoic acid (TCDA)—are separately electrospun alongside polyurethane as a supporting matrix polymer. The differences in side‐chain length impact the sensitivity of the nanofibers in detecting P. aeruginosa. Furthermore, two DNA aptamers are conjugated to the polydiacetylenes to achieve targeted detection of P. aeruginosa. The aptamer‐modified dressings show improved sensitivity of detection toward eight strains of P. aeruginosa compared to the unmodified membranes. Furthermore, the aptamer‐modified membranes do not respond to non‐target bacteria methicillin‐resistant Staphylococcus aureus (MRSA), Staphylococcus aureus, and Escherichia coli within 3 h of direct contact. Reducing the chain‐length of the diacetylene monomer by substituting PCDA with TCDA boosts the colorimetric response by a factor of >2x compared to the aptamer‐modified PCDA membranes, at the cost of reduced specificity. The aptamer‐conjugated polydiacetylene membranes show promise for application in point‐of‐care wound dressings for improved specificity of detection of bacterial infections.

Funder

Canada Foundation for Innovation

Natural Sciences and Engineering Research Council of Canada

Cystic Fibrosis Foundation

Publisher

Wiley

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