Cryo-Assembled AuNP/QD Probe Pairs Enabling Single-Step Ochratoxin A Detection

The extensive utilization of nanomaterials and aptamers in biosensing has positioned the construction of efficient, stable, and user-friendly nanoprobe systems as a pivotal strategy for rapid small-molecule detection. This study developed a dual-probe fluorescence detection system utilizing gold nanoparticles (AuNPs) and quantum dots (QDs) for ochratoxin A (OTA) analysis. The AuNP probes were functionalized via an innovative freeze-driven asymmetric conjugation approach, while a distinct freeze-driven labeling strategy was applied to QDs. Compared to conventional labeling protocols, the freeze-driven methodology reduced conjugation duration from several hours to merely 20 min and was successfully implemented for QD-aptamer conjugation for the first time, facilitating efficient dual-probe assembly. The complete process, spanning from probe preparation to OTA quantification, was accomplished within 1.5 h. Under optimized parameters, the biosensor demonstrated a linear detection range of 0.5-50 ng/mL, achieved a detection limit of 0.183 ng/mL, and exhibited satisfied specificity, reproducibility, and matrix interference resistance. Validation experiments across various herbal specimens confirmed its accuracy and practical applicability. This research not only establishes a rapid and efficient platform for OTA monitoring but also provides a generalized framework for developing nanomaterial-based biosensing systems.

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Publication Details

Journal
Bioconjugate Chemistry
Published
2026-03-23
DOI
https://doi.org/10.1021/acs.bioconjchem.5c00617
Primary Topic
Mycotoxins in Agriculture and Food
Type
article
Field-Weighted Citation Impact
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article

Cryo-Assembled AuNP/QD Probe Pairs Enabling Single-Step Ochratoxin A Detection

Rentang Huang, Yuxin Huang, Xinyu Zhao, Xiuling Cui et al.
Bioconjugate Chemistry
Mycotoxins in Agriculture and Food
article

Cryo-Assembled AuNP/QD Probe Pairs Enabling Single-Step Ochratoxin A Detection

Rentang Huang, Yuxin Huang, Xinyu Zhao, Xiuling Cui, Qing Cao, Lei Zhang
article en

Abstract

The extensive utilization of nanomaterials and aptamers in biosensing has positioned the construction of efficient, stable, and user-friendly nanoprobe systems as a pivotal strategy for rapid small-molecule detection. This study developed a dual-probe fluorescence detection system utilizing gold nanoparticles (AuNPs) and quantum dots (QDs) for ochratoxin A (OTA) analysis. The AuNP probes were functionalized via an innovative freeze-driven asymmetric conjugation approach, while a distinct freeze-driven labeling strategy was applied to QDs. Compared to conventional labeling protocols, the freeze-driven methodology reduced conjugation duration from several hours to merely 20 min and was successfully implemented for QD-aptamer conjugation for the first time, facilitating efficient dual-probe assembly. The complete process, spanning from probe preparation to OTA quantification, was accomplished within 1.5 h. Under optimized parameters, the biosensor demonstrated a linear detection range of 0.5-50 ng/mL, achieved a detection limit of 0.183 ng/mL, and exhibited satisfied specificity, reproducibility, and matrix interference resistance. Validation experiments across various herbal specimens confirmed its accuracy and practical applicability. This research not only establishes a rapid and efficient platform for OTA monitoring but also provides a generalized framework for developing nanomaterial-based biosensing systems.

Bioconjugate Chemistry
Guangdong Pharmaceutical University (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), State Administration of Traditional Chinese Medicine of the People's Republic of China (CN), Peking Union Medical College Hospital (CN), Institute of Medicinal Plant Development (CN)
Openalex Percentile: Top 12%
Mycotoxins in Agriculture and Food
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Cryo-Assembled AuNP/QD Probe Pairs Enabling Single-Step Ochratoxin A Detection — Rentang Huang, Yuxin Huang, et al. · Bioconjugate Chemistry (2026) | TGRS Research Map | TGRS