ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025
A Promising Point-of-Care Testing Strategy: Ultrasmooth Gold Nanogroove Arrays Biosensor Combined with Initial Rate Analysis.
Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
2 citing papers in PubMed.
- Nanobiosensors for Rheumatoid Arthritis Biomarkers: Advances and Clinical Translational Potential.International journal of nanomedicine · 2026Review
- A Promising Point-of-Care Testing Strategy: Ultrasmooth Gold Nanogroove Arrays Biosensor Combined with Initial Rate Analysis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025Article
Corrections and comments
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Authors and funding
7 authors.
Funding
Abstract
Nowadays, plasmonic biosensors have achieved the limit of detection (LOD) far beyond the clinical or professional standards in the sensing field through material and structural optimizations. However, it remains predominantly a research tool due to the challenge to simultaneously achieve mass production, ultrasensitive and rapid detection, high-reproducibility, and ease of integration, which are extremely desired in point-of-care testing (POCT)-based commercial products. Here, a label-free, ultrasensitive, and rapid assay protocol is described for quantitative protein detections in serum samples, which integrates an ultrasmooth gold nanogroove arrays (UGNA) biosensor with an initial rate analysis (IRA) method. i) Compared with the existing plasmonic biosensors, miscellaneous-protein-mixed scheme substantially accelerates the binding kinetics of analytes by passivation of all channel inner surfaces. Combined with the IRA method, a wide linear range of AFP detection (1-10
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Registered trials
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