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Human papillomavirus, a leading cause of cervical cancer, poses a global health threat. Rapid and accurate point-of-care testing (POCT) is crucial for early detection and disease control. Here, we present an electrochemical sensor on a thermally controllable paper-based digital microfluidic (e-pDMF) device for detecting human papillomavirus type 16 DNA (HPV16 DNA) via target-induced hairpin opening and enzyme-assisted signal amplification strategy. The e-pDMF device operates in transport and thermal modes to enable programmable droplet manipulation and precise temperature control via an integrated thermal platform capable of heating to 125 °C. In this study, the platform maintained a 37.5 ± 0.14 °C isothermal state with a 0.09 °C/s ramp rate to support efficient Exonuclease III activity during signal amplification. The integrated system facilitates multiple processes, from sample loading and mixing to signal amplification and electrochemical detection, and completes the whole assay within 75 min. The products from the enzyme-amplified target-induced hairpin opening process can be captured on the probe-immobilized electrode. Differential pulse voltammetry measures the current decrease caused by electron transfer of redox indicator, indicating the presence of target HPV16 DNA. The sensing platform demonstrated a detection range from 1 fM to 10 pM (R = 0.9968), with an experimental detection limit of 1 fM. It showed high specificity for HPV16 DNA, with no cross-reactivity to mismatched sequences or related genital tract pathogens. The platform was validated using clinical cervical swab samples, showing 100 % agreement with PCR results. This portable and automated e-pDMF device shows great potential as an alternative POCT tool for DNA diagnosis.
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http://dx.doi.org/10.1016/j.bios.2025.117898 | DOI Listing |
Anal Chim Acta
November 2025
College of Chemical Engineering, Xiangtan University, Xiangtan, 411105, China. Electronic address:
Background: Aflatoxin B1 (AFB1) is a highly carcinogenic mycotoxin frequently found in contaminated food products, posing a significant threat to public health and food safety. Therefore, the development of rapid, sensitive, and reliable detection methods for AFB1 is critical for early warning and prevention. However, traditional detection techniques often require expensive equipment, skilled personnel, and complex procedures, limiting their suitability for on-site applications.
View Article and Find Full Text PDFBiosens Bioelectron
August 2025
Department of Chemistry and Institute of Biological Interfaces, Sogang University, Seoul, 04107, Republic of Korea. Electronic address:
Human papillomavirus, a leading cause of cervical cancer, poses a global health threat. Rapid and accurate point-of-care testing (POCT) is crucial for early detection and disease control. Here, we present an electrochemical sensor on a thermally controllable paper-based digital microfluidic (e-pDMF) device for detecting human papillomavirus type 16 DNA (HPV16 DNA) via target-induced hairpin opening and enzyme-assisted signal amplification strategy.
View Article and Find Full Text PDFAnalyst
July 2025
Key Laboratory of Luminescence Analysis and Molecular Sensing, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.
Owing to their high affinity and specificity for antigen target molecules, therapeutic monoclonal antibodies (mAbs) have been increasingly used for the treatment of different diseases. The sensitive and accurate detection of mAbs is crucial for the evaluation of their efficacy and safety. With a new design of a thiophosphate-modified and self-folding hairpin primer, herein, we described the establishment of an aptamer-based, highly sensitive and simple fluorescent trastuzumab mAb assay method target-induced recycling and low-temperature LAMP activation of CRISPR/Cas12a signal amplifications.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
July 2025
Food Inspection and Quarantine Technology Center of Shenzhen Customs, Shenzhen Academy of Inspection and Quarantine, Shenzhen 518045, China. Electronic address:
Ochratoxin A (OTA) is a highly hazardous mycotoxin widely found in food ingredients and processed products. In response to the demand for food safety, there is an urgent need to establish a highly sensitive, reliable, and cost-effective method for the detection of OTA. In this study, a simple, enzyme-free, sensitive cascade amplification fluorescent strategy was developed to detect OTA based on a magnetic separation system-assisted, multicomponent nuclease (MNAzyme) and its induced catalytic hairpin assembly (CHA).
View Article and Find Full Text PDFMikrochim Acta
January 2025
Department of Chemistry and Biochemistry, National Chung Cheng University, 621301, Chia-Yi, Taiwan.
A fluorescent aptasensor was developed based on target-induced hairpin conformation switch coupled with nicking enzyme-assisted signal amplification (NESA) to detect the oligomeric form of ß-amyolid peptide (AβO) in cerebrospinal fluid. The hairpin DNA probe (HP) was specifically designed to recognize AβO. When AβO is present in the sensing system, it induces an HP conformational switch and triggers the NESA reaction.
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