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Demonstrates enhanced sepsis detection with a novel immunochromatographic assay, implying improved clinical outcomes.
Accurate bedside diagnosis of sepsis is essential for timely treatment and reducing mortality, yet technical limitations persist. Here, we present a multiplex-compatible lateral flow immunoassay (LFIA) that integrates a universal click-chemistry conjugation strategy with highly dispersible, film-like magnetic fluorescent probes (GFDQD@Si) to enable precise diagnosis through concurrent monitoring of pathogens and protein biomarkers. GFDQD@Si combines a two-dimensional high-area reactive interface; a magnetic interlayer for target enrichment and signal amplification; a multilayer of quantum dots for fluorescence enhancement; and an outer silica shell that suppresses background fluorescence and confers superior flowability. This architecture overcomes the size disparity between bacteria and proteins, enabling efficient cocapture of multiple proteins/bacteria and achieving faster, more sensitive detection on an LFIA platform. The platform quantitatively detects two key sepsis biomarkers─procalcitonin (PCT) and interleukin-6 (IL6)─as well as the pathogen Pseudomonas aeruginosa, with limits of detection of 4.44 pg mL–1 for PCT, 0.94 pg mL–1 for IL6, and 7 CFU mL–1 for bacteria. Validation in 75 clinical whole-blood samples demonstrated high sensitivity, ease of operation, and robustness, underscoring its potential for real-time bedside sepsis diagnosis. By simultaneously providing dual readouts of host-response biomarkers and pathogen detection, the GFDQD@Si-LFIA platform is expected to accelerate and improve clinical decision-making for sepsis.
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Zhang et al. (2026) studied this question.
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