Evidence map›Paper›PMID 42311212›Full record

ArticleAnalytical chemistry2026

Mapping Morphology-Dependent Stability of Gold Nanostars in Immune Cells Using Hyperspectral Imaging.

Lakhvir Singh, Ngoc Nhu Vu, Elizabeth A Bullard, Erin M Stout, Samuel Mabbott, Alex J Walsh

Abstract read
In one paragraph

Article in Analytical chemistry, 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

6 authors.

Lakhvir SinghDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas 77843, United States.ORCID 0009-0001-9869-6071
Ngoc Nhu VuDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas 77843, United States.ORCID 0009-0006-4494-104X
Elizabeth A BullardDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas 77843, United States.
Erin M StoutDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas 77843, United States.
Samuel MabbottDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas 77843, United States.ORCID 0000-0003-4926-5467
Alex J WalshDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas 77843, United States.ORCID 0000-0003-3832-8207

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gold nanoparticles (AuNPs) are widely applied in nanomedicine, cellular and tissue biology, nanoscopy, photothermal therapy, and a range of diagnostic and clinical technologies. Among them, gold nanostars (AuNSs) have emerged as particularly promising due to their highly tunable optical and chemical properties. However, like other nanostructures, the stability of AuNSs remains a key challenge, especially within complex cellular microenvironments. Here, wide-field hyperspectral microscopy is evaluated for the real-time characterization of the morphology-dependent stability of AuNS formulations in immune-cell microenvironments. A computationally efficient image processing pipeline extracts statistical features from reflectance images, enabling the real-time analysis of hyperspectral data. UMAP-based visualization of spectral data revealed distinct, time- and formulation-dependent spectral shifts, with smaller seed volume formulations (larger overall diameter) for AuNSs exhibiting rapid destabilization and aggregation in THP-1 cells. In contrast, larger seed volume formulations (smaller overall diameter) for AuNS demonstrated enhanced colloidal stability and spectral uniformity. Compared to conventional ensemble measurements, hyperspectral reflectance measurements provided a rapid and resource-efficient approach that enabled macroscale imaging while retaining the spectral detail necessary to resolve AuNS transformations. Overall, the hyperspectral microscopy techniques presented here provide a label-free, high-throughput platform for evaluating AuNS stability and biocompatibility, with strong potential to guide the rational design of AuNSs for immunotherapeutic and diagnostic applications.

Indexed as

GoldHyperspectral ImagingMetal NanoparticlesHumansParticle SizeTHP-1 CellsGold

Identifiers

PMID42311212
PMCPMC13325451

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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.