Evidence map›Paper›PMID 41711970›Full record

ArticleMikrochimica acta2026

Development and human samples validation of a plasma pTau‑217 electrochemical sensor for Alzheimer's detection in Vietnamese patients.

Hoai Bao Pham, Mai Trang Tong, Nguyen Thuy Linh Tran, Tien Tai Tran, Thien Luan Phan, Congo Tak Shing Ching, Chan Khon Huynh, Thi Thanh Huong Ha, Cong Thang Tran

Abstract readValidation Study
PubMed Publisher
In one paragraph

Article in Mikrochimica acta, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Hoai Bao PhamSchool of Biomedical Engineering, International University, Ho Chi Minh City, Vietnam.
Mai Trang Tong *Department of Neurology, University Medical Center, Ho Chi Minh City, Vietnam.
Nguyen Thuy Linh Tran *School of Biomedical Engineering, International University, Ho Chi Minh City, Vietnam.
Tien Tai TranDepartment of Physiology, Pathophysiology and Immunology, Pham Ngoc Thach University of Medicine, Ho Chi Minh City, Vietnam.
Thien Luan PhanVietnam National University, Ho Chi Minh City, Vietnam.
Congo Tak Shing ChingGraduate Institute of Biomedical Engineering, National Chung Hsing University, Taichung, Taiwan.
Chan Khon HuynhSchool of Biomedical Engineering, International University, Ho Chi Minh City, Vietnam.
Thi Thanh Huong HaSchool of Biomedical Engineering, International University, Ho Chi Minh City, Vietnam. htthuong@hcmiu.edu.vn.
Cong Thang TranSchool of Medicine, University of Medicine and Pharmacy at HCMC VN, Ho Chi Minh City, Vietnam. trancongthang@ump.edu.vn.

Funding

Vietnam National University HoChiMinh City (VNU-HCM) B2024-28-06
6 · The paper itself

Abstract

A multi-walled carbon nanotube - poly (allylamine hydrochloride acid)/platinum nanoparticle (MWCNT-PAH/PtNP) biosensor for phosphorylated Tau-217 (pTau-217) detection and validated using Alzheimer’s disease (AD) plasma samples is described. Morphological characterization confirmed successful deposition of MWCNT-PAH/PtNP, which enhanced the sensor’s surface height range (bare sensor |∆| = 2.2 μm vs. modified sensor |∆| = 5.7 μm) and electrochemical properties. The sensor achieved a detection limit of 9.85 pg/mL by cyclic voltammetry (CV) and 3.83 pg/mL by chronoamperometry (CA), and could detect pTau-217 in the presence of interfering molecules and in complex protein-rich matrices such as fetal bovine serum (FBS). When validated on clinical samples, the sensor could distinguish AD from cognitive normal (CN ) samples more effectively than ELISA (AUCCV: 90.75%; AUCCA: 87.13%; AUCELISA: 52.52%). Subgroup analysis revealed that sensor output primarily reflected disease status, with minimal confounding effects from demographic or social factors. However, a key limitation is that current intensity cannot be directly converted into plasma pTau-217 concentration, restricting the sensor to qualitative AD screening rather than precise quantification. Taken together, this biosensor holds great potential as a cost-effective tool for distinguishing AD and CN plasma samples, with promising prospects for on-site application.

Indexed as

Alzheimer DiseaseBiosensing TechniquesElectrochemical Techniquestau ProteinsFemaleHumansLimit of DetectionMetal NanoparticlesNanotubes, CarbonPlatinumPolyaminesNanotubes, CarbonPlatinumpolyallylaminePolyaminestau ProteinsAlzheimer’s diseaseClinical samplesElectrochemical biosensorMWCNTPTau-217PtNPSPCE

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.