Electrochemical Detection of miR-29a and miR-34a Using AuNPs Immobilized by a Silsesquioxane Polyelectrolyte: Potential Early Alzheimer’s Disease Biomarkers Detection

Alzheimer’s Disease (AD) is the leading cause of dementia worldwide, and early diagnosis is crucial to minimize neurological damage and loss of quality of life. Here, we report an electrochemical biosensor for detecting miRNAs 29a and 34a, potential non-invasive biomarkers associated with AD. The biosensor consisted of a glassy carbon electrode (GCE) modified with a novel nanohybrid of gold nanoparticles stabilized by 3-n-propyl(4-dimethylaminopyridinium) silsesquioxane chloride (AuNPs–Si4DMAP+Cl−). Thiolated anti-miRNA probes were immobilized separately on the GCE/AuNPs-Si4DMAP+Cl−, followed by BSA blocking. Target miRNAs were detected via hybridization with complementary probes using electrochemical impedance spectroscopy. The nanohybrid, characterized by spectroscopic and morphological techniques, significantly enhanced the electrochemical response and was effective detecting both miRNAs, showing suspension stability over 600 days. LOD and LOQ were 1.79 pM and 5.87 pM for miRNA-29a, and 2.21 pM and 11.01 pM for miRNA-34a. These results highlight the platform’s potential for electrochemical detection of these miRNAs in blood, supporting earlier detection of AD and other neurodegenerative diseases.

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Journal
Sensors
Published
2026-03-27
DOI
https://doi.org/10.3390/s26072089
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article
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article

Electrochemical Detection of miR-29a and miR-34a Using AuNPs Immobilized by a Silsesquioxane Polyelectrolyte: Potential Early Alzheimer’s Disease Biomarkers Detection

Paulo H. S. Picciani, Felipe Zahrebelnei, João Paulo Winiarski, Karen Wohnrath et al.
Sensors
Advanced biosensing and bioanalysis techniques
article

Electrochemical Detection of miR-29a and miR-34a Using AuNPs Immobilized by a Silsesquioxane Polyelectrolyte: Potential Early Alzheimer’s Disease Biomarkers Detection

Paulo H. S. Picciani, Felipe Zahrebelnei, João Paulo Winiarski, Karen Wohnrath, Christiana Andrade Pessôa, Amanda Loos Vargas Zinser
article en

Abstract

Alzheimer’s Disease (AD) is the leading cause of dementia worldwide, and early diagnosis is crucial to minimize neurological damage and loss of quality of life. Here, we report an electrochemical biosensor for detecting miRNAs 29a and 34a, potential non-invasive biomarkers associated with AD. The biosensor consisted of a glassy carbon electrode (GCE) modified with a novel nanohybrid of gold nanoparticles stabilized by 3-n-propyl(4-dimethylaminopyridinium) silsesquioxane chloride (AuNPs–Si4DMAP+Cl−). Thiolated anti-miRNA probes were immobilized separately on the GCE/AuNPs-Si4DMAP+Cl−, followed by BSA blocking. Target miRNAs were detected via hybridization with complementary probes using electrochemical impedance spectroscopy. The nanohybrid, characterized by spectroscopic and morphological techniques, significantly enhanced the electrochemical response and was effective detecting both miRNAs, showing suspension stability over 600 days. LOD and LOQ were 1.79 pM and 5.87 pM for miRNA-29a, and 2.21 pM and 11.01 pM for miRNA-34a. These results highlight the platform’s potential for electrochemical detection of these miRNAs in blood, supporting earlier detection of AD and other neurodegenerative diseases.

SensorsVol. 26(7)
Universidade Federal do Rio de Janeiro (BR), Universidade Federal de Santa Catarina (BR), Universidade Estadual de Ponta Grossa (BR), BorgWarner (Brazil) (BR)
Openalex Percentile: Top 5%
Advanced biosensing and bioanalysis techniques
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