Evidence map›Paper›PMID 41836728›Full record

ArticleInternational journal of nanomedicine2026

DNA Aptamer-Functionalized Fluorescent Silica Nanoparticles: A Robust Strategy for Specific Detection and Bioimaging of HER2-Overexpressing Breast Cancer.

Juntao Tan, Zixi Hu, Da Huang, Suqing Cheng, Lu Chen, Liangliang Min, Jianhong Tu, Zhihua Li

Abstract read
In one paragraph

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

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0citing papers in PubMed
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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

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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

8 authors.

Juntao Tan *Jiangxi Province Key Laboratory of Breast Diseases, Nanchang People's Hospital, Nanchang People's Hospital Affiliated of Nanchang Medical College, Nanchang, Jiangxi, People's Republic of China.
Zixi Hu *Clinical Laboratory Center, The First affiliated hospital of Guilin Medical University, Guilin, Guangxi Zhuang Autonomous Region, People's Republic of China.
Da Huang *Jiangxi Province Key Laboratory of Breast Diseases, Nanchang People's Hospital, Nanchang People's Hospital Affiliated of Nanchang Medical College, Nanchang, Jiangxi, People's Republic of China.
Suqing Cheng *Department of Pathology, Nanchang People's Hospital, Nanchang People's Hospital Affiliated of Nanchang Medical College, Nanchang, Jiangxi, People's Republic of China.
Lu ChenJiangxi Province Key Laboratory of Breast Diseases, Nanchang People's Hospital, Nanchang People's Hospital Affiliated of Nanchang Medical College, Nanchang, Jiangxi, People's Republic of China.
Liangliang MinJiangxi Province Key Laboratory of Breast Diseases, Nanchang People's Hospital, Nanchang People's Hospital Affiliated of Nanchang Medical College, Nanchang, Jiangxi, People's Republic of China.
Jianhong TuDepartment of Pathology, Nanchang People's Hospital, Nanchang People's Hospital Affiliated of Nanchang Medical College, Nanchang, Jiangxi, People's Republic of China.
Zhihua LiJiangxi Province Key Laboratory of Breast Diseases, Nanchang People's Hospital, Nanchang People's Hospital Affiliated of Nanchang Medical College, Nanchang, Jiangxi, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Precise detection of HER2-positive breast cancer is vital for targeted therapy. This study integrates HER2-specific DNA aptamers with fluorescent silica nanoparticles (FSNPs) to develop a targeted imaging probe. Methods: HER2 aptamer-conjugated FSNPs (HApt-FSNPs) were synthesized and characterized. Specificity was evaluated in HER2-positive/negative cells and tumor sections via flow cytometry and microscopy. Targeting efficacy and biodistribution were assessed in tumor-bearing mice through systemic injection and real-time fluorescence imaging. Photostability and biosafety were systematically examined. Results: HApt-FSNPs showed uniform size, excellent dispersity, and enhanced photostability. They selectively bound HER2-positive cells and tumor tissues, with binding effectively blocked by free aptamer. In vivo imaging revealed specific accumulation in HER2-positive tumors, peaking at 6 hours post-injection, with minimal off-target signals. The probe demonstrated good biocompatibility in vitro and in vivo. Conclusion: The HApt-FSNP platform enables specific detection and in vivo imaging of HER2-positive breast cancer, highlighting its potential for diagnostic and bioimaging applications.

Indexed as

Aptamers, NucleotideBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesFluorescent DyesNanoparticlesSilicon DioxideAnimalsCell Line, TumorFemaleHumansMiceMice, Inbred BALB CMice, NudeMicroscopy, FluorescenceOptical ImagingTissue DistributionAptamers, NucleotideERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesFluorescent DyesSilicon Dioxideaptamerfluorescent silica nanoparticlesHER2-positive breast cancerin vivo imagingtargeted detection

Identifiers

PMID41836728
PMCPMC12984057

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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.