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March 14, 2026Biosensors0 citationsOpen Access

A Chemiresistive Nanosensor Array for Rapid and Sensitive VOC-Based Detection and Differentiation of Prosthetic Joint Infection-Relevant Pathogens in Enriched Human Synovial Fluid

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DGDerese GetnetTKTaejun KoDLDeyu Liu

Key Points

  • The study aims to develop a rapid and specific method for identifying pathogens related to prosthetic joint infection.
  • Validated a 19-channel chemiresistive nanosensor array in vitro against ESKAPEE pathogens.
  • Used machine learning with a radial-basis-function support vector machine for data analysis.
  • Optimized the sensor array to a six-sensor format while maintaining high signal-to-noise performance.
  • Evaluated the platform with human synovial fluid spiked with specific pathogens at varying concentrations.
  • Achieved 96% mean classification accuracy for pathogen detection.
  • Detected all infected samples within 9 hours with distinct VOC signatures for each pathogen.
  • Demonstrated strong inverse correlation between time-to-detection and initial bacterial concentration.
  • Negative controls showed no signal changes throughout testing.

Abstract

Rapid and actionable pathogen identification remains a major unmet need in the diagnosis of prosthetic joint infection (PJI). Current diagnostic approaches either provide rapid host response information without pathogen specificity or identify pathogens with delays of days to weeks. Here, we report a chemiresistive nanosensor array combined with machine learning analysis for same-day, pathogen-specific detection based on volatile organic compound (VOC) profiling. A 19-channel nanosensor array was first validated in vitro against a panel of ESKAPEE pathogens, achieving 96% mean classification accuracy using a radial-basis-function support vector machine (SVM) classifier. Data-driven optimization yielded a reduced six-sensor array with high signal-to-noise performance. The optimized platform was evaluated using pooled, uninfected human synovial fluid enriched 1:1 with nutrient media and spiked with Staphylococcus aureus, Staphylococcus epidermidis, or Pseudomonas aeruginosa across a range of 1–106 CFU/mL. All infected samples were detected within 9 h, with distinct VOC signatures enabling accurate pathogen differentiation. Time-to-detection (TTD) demonstrated a strong inverse correlation with initial bacterial concentration, supporting semi-quantitative estimation of bacterial load. Negative controls remained at baseline throughout testing. This chemiresistive VOC-based biosensor platform demonstrates the potential to deliver rapid, integrated detection, identification, and burden estimation of metabolically active PJI pathogens, highlighting its promise for future point-of-care diagnostic applications.

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Cite This Study

Getnet et al. (2026) studied this question.

synapsesocial.com/papers/69b4fc33b39f7826a300cf5ahttps://doi.org/10.3390/bios16030156
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