Nanofibrous theranostic biosensor for visual detection of infections and triggered drug release: Utilizing ROS-responsive nanoparticles to combat bacterial resistance

The need for new technologies to treat infections in wound care is increasingly urgent, especially with the rise of antibiotic-resistant bacteria. In this study, we developed a nanofibrous theranostic biosensor that provides both visual infection detection and on-demand drug release to combat bacterial resistance. The biosensor incorporates a hemicyanine dye, citric acid and ciprofloxacin (Cip)-loaded NPs within a nanofibrous matrix. The cleavage of the hemicyanine dye in the presence of bacteria triggers a colorimetric response, while the responsive release of Cip from the NPs upon exposure to elevated ROS enables targeted antibacterial agent delivery. The results of testing biosensors indicated a detection limit of 1.0 × 10 5 CFU/cm 2 , the biosensor provided vivid visual results within 5 h. In direct antibacterial tests, 100 % bacterial reduction for E. coli, MRSA, and P. aeruginosa was achieved within 4 h in the presence of H 2 O 2 (1.0 mM). Citric acid provided untargeted antibacterial action (99.9 % for E. coli and 99.999 % for MRSA and P. aeruginosa ). While ROS-responsive Cip release, in addition to citric acid, ensured sustained triggered bacterial elimination (100.0 % and 8.0 log reduction), significantly enhancing overall efficacy. Cytocompatibility tests with 3-day elution confirmed that the biosensor was non-cytotoxic, maintaining over 90.0 % fibroblast viability even after complete drug release. This theranostic biosensor effectively prevents untargeted antibiotic release, reducing the risk of bacterial resistance while supporting fibroblast health and proliferation. These results suggest that this biosensor is a promising tool for wound care, offering real-time infection monitoring and targeted antibacterial treatment. • A nanofibrous theranostic biosensor was developed for in situ bacterial detection and treatment. • Detection is triggered by bacterial lipase at concentrations producing a visible yellow-to-green color change detectable by the naked eye. • Treatment is achieved through the release of antibiotics from reactive oxygen species (ROS)-responsive nanoparticles. • The system achieved complete bacterial eradication, with an 8-log reduction within 24 h, while detection occurred within 5 h. • 90 % Human Fibroblast viability was achieved using the developed biosensor.

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Journal
Materials Today Chemistry
Published
2025-09-25
DOI
https://doi.org/10.1016/j.mtchem.2025.103060
Primary Topic
Biosensors and Analytical Detection
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article
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article

Nanofibrous theranostic biosensor for visual detection of infections and triggered drug release: Utilizing ROS-responsive nanoparticles to combat bacterial resistance

Sarvesh Logsetty, Farinaz Jonidi Shariatzadeh, Song Liu
Materials Today Chemistry
Biosensors and Analytical Detection
article

Nanofibrous theranostic biosensor for visual detection of infections and triggered drug release: Utilizing ROS-responsive nanoparticles to combat bacterial resistance

Sarvesh Logsetty, Farinaz Jonidi Shariatzadeh, Song Liu
article en

Abstract

The need for new technologies to treat infections in wound care is increasingly urgent, especially with the rise of antibiotic-resistant bacteria. In this study, we developed a nanofibrous theranostic biosensor that provides both visual infection detection and on-demand drug release to combat bacterial resistance. The biosensor incorporates a hemicyanine dye, citric acid and ciprofloxacin (Cip)-loaded NPs within a nanofibrous matrix. The cleavage of the hemicyanine dye in the presence of bacteria triggers a colorimetric response, while the responsive release of Cip from the NPs upon exposure to elevated ROS enables targeted antibacterial agent delivery. The results of testing biosensors indicated a detection limit of 1.0 × 10 5 CFU/cm 2 , the biosensor provided vivid visual results within 5 h. In direct antibacterial tests, 100 % bacterial reduction for E. coli, MRSA, and P. aeruginosa was achieved within 4 h in the presence of H 2 O 2 (1.0 mM). Citric acid provided untargeted antibacterial action (99.9 % for E. coli and 99.999 % for MRSA and P. aeruginosa ). While ROS-responsive Cip release, in addition to citric acid, ensured sustained triggered bacterial elimination (100.0 % and 8.0 log reduction), significantly enhancing overall efficacy. Cytocompatibility tests with 3-day elution confirmed that the biosensor was non-cytotoxic, maintaining over 90.0 % fibroblast viability even after complete drug release. This theranostic biosensor effectively prevents untargeted antibiotic release, reducing the risk of bacterial resistance while supporting fibroblast health and proliferation. These results suggest that this biosensor is a promising tool for wound care, offering real-time infection monitoring and targeted antibacterial treatment. • A nanofibrous theranostic biosensor was developed for in situ bacterial detection and treatment. • Detection is triggered by bacterial lipase at concentrations producing a visible yellow-to-green color change detectable by the naked eye. • Treatment is achieved through the release of antibiotics from reactive oxygen species (ROS)-responsive nanoparticles. • The system achieved complete bacterial eradication, with an 8-log reduction within 24 h, while detection occurred within 5 h. • 90 % Human Fibroblast viability was achieved using the developed biosensor.

Materials Today ChemistryVol. 49
University of Manitoba (CA)
Openalex Percentile: Top 75%
Biosensors and Analytical Detection
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