Evidence map›Paper›PMID 42145784›Full record

ArticleParticle & particle systems characterization : measurement and description of particle properties and behavior in powders and other disperse systems2026

Theranostic Nanoparticles for Fluorosensitive Visualization and Inhibition of Amyloid Beta-Induced Neuroinflammation.

Umme Tamima, Hoda M Gebril, Md Ragib Hasan, Miguel A Quintero, Aravind Aryasomayajula, Diya Chengappa, Imran Attarwala, Bradley L Truong, Prabhas V Moghe, Kathryn E Uhrich

Abstract read
In one paragraph

Article in Particle & particle systems characterization : measurement and description of particle properties and behavior in powders and other disperse systems, 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

10 authors.

Umme TamimaDepartment of Chemistry University of California Riverside California USA.
Hoda M GebrilDepartment of Biomedical Engineering Rutgers University Piscataway New Jersey USA.ORCID https://orcid.org/0000-0001-5797-9406
Md Ragib HasanDepartment of Chemistry University of California Riverside California USA.
Miguel A QuinteroDepartment of Chemistry University of California Riverside California USA.
Aravind AryasomayajulaCooper Medical School Rowan University Camden New Jersey USA.
Diya ChengappaDepartment of Biomedical Engineering Rutgers University Piscataway New Jersey USA.
Imran AttarwalaDepartment of Biomedical Engineering Rutgers University Piscataway New Jersey USA.
Bradley L TruongDepartment of Chemistry University of California Riverside California USA.
Prabhas V MogheDepartment of Biomedical Engineering Rutgers University Piscataway New Jersey USA.
Kathryn E UhrichDepartment of Chemistry University of California Riverside California USA.

Funding

Nanotechnology for Glial Targeting and Inhibition of Neuroinflammation for Alzheimer’s DiseaseR21AG085394 · NIA · RUTGERS, THE STATE UNIV OF N.J. · PI GEBRIL, HODA, MOGHE, PRABHAS V · 2024 to 2024
$446k
NIA NIH HHS R21 AG085394
6 · The paper itself

Abstract

The emerging field of microglial therapies has significant potential to alleviate fibrillar amyloid beta (fAβ)-associated neuroinflammation, which exacerbates neurodegeneration in Alzheimer's disease (AD). New therapeutic strategies integrate with diagnostic capabilities to robustly elucidate the mechanisms and consequences of intervention. Amphiphilic macromolecules (AMs), comprising a hydrophilic sugar backbone, hydrophobic aliphatic side chains, and poly(ethylene glycol) (PEG) segments for enhanced stability, exhibit significant potential for biomedical applications due to their biocompatibility and self-assembled nanoscale structures. This study presents rhodamine B-tagged (Rh) AMs (Rh-AMs) that create stable nanoparticles (Rh-AM-NPs) with potential neurotherapeutic and diagnostic applications. Rh-AMs were successfully synthesized and validated using NMR, FTIR, UV-vis, and fluorescent spectroscopy. The ratio of labeled to unlabeled AMs necessary for Rh-AM-NPs formation was optimized via flash nanoprecipitation to confirm the minimum quantity required for direct visualization within cells. Using an in vitro BV2 microglial model, we demonstrated that Rh-AM-NPs exhibit multifunctional properties, suppressing the microglial inflammatory response and reducing microglial uptake of fAβ within a low-toxicity range, while simultaneously enabling in situ tracking of cellular interactions. This work validates a novel nanoplatform for combined AD therapy and diagnostics.

Indexed as

amphiphilic macromoleculesfibril amyloid betamicrogliananoparticlesneuroinflammationrhodamine‐tagged macromolecules

Identifiers

PMID42145784
PMCPMC13173615

What OpenQuestion holds

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Registered trials

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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.