Evidence map›Paper›PMID 42328797›Full record

ArticleAdvanced healthcare materials2026

Sea Urchin-Like Platinum-Coated Gold Nanozymes-Based Ultra-Sensitive Colorimetric Detection and Mechanism Differentiation Platform for Dual-Marker Guided Genotoxicity Assessment.

Hongtan Zhu, Lu Xu, Xueying Wang, Yutong Xiao, Feng Feng, Feng Zheng, Xiaoli Meng, Dean Naisbitt, Wenyuan Liu, Lingfei Han

Abstract read
In one paragraph

Article in Advanced healthcare materials, 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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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

10 authors.

Hongtan ZhuDepartment of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing, China.
Lu XuDepartment of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing, China.
Xueying WangDepartment of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing, China.
Yutong XiaoDepartment of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing, China.
Feng FengTaizhou University, Taizhou, China.
Feng ZhengDepartment of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing, China.
Xiaoli MengMRC Centre for Drug Safety Science, Department of Pharmacology and Therapeutic, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK.
Dean NaisbittMRC Centre for Drug Safety Science, Department of Pharmacology and Therapeutic, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK.
Wenyuan LiuDepartment of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing, China.ORCID https://orcid.org/0000-0002-0838-8877
Lingfei HanDepartment of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing, China.ORCID https://orcid.org/0000-0002-1345-5763

Funding

Jiangsu Funding Program for Excellent Postdoctoral Talent 2022ZB295National Natural Science Foundation of China 82204340Natural Science Foundation of Jiangsu Province BK20221048
6 · The paper itself

Abstract

The evaluation of compound genotoxicity is of great significance for drug safety assurance, and the existing evaluation methods have the problems of false-positive/negative, low throughput, or complicated operation. Although enzyme-linked immunosorbent assays (ELISA) kits targeting some genotoxic targets have high throughput, there are limitations in sensitivity and stability due to the use of horseradish peroxidase (HRP). In this study, an integrated evaluation platform based on novel sea urchin-like platinum-coated gold nanoparticles (Pt/Au NPs) was developed to address the above problems. Pt/Au NPs nanozymes were synthesized by deposition of a platinum layer on the surface of gold seeds. The nanozymes exhibited excellent peroxidase activity as well as superior stability compared to natural enzymes. Pt/Au NPs nano-enzymes were replaced for the construction of nano-enzyme-linked immunosorbent assay (NLISA), which has better sensitivity and stability, decreasing the acquired amount of test compounds. Through quantification of genotoxicity damage markers, phosphorylated histone H2AX (γH2AX) and phosphorylated histone H3 (p-H3) in metabolic human hepatocytes, this study has proposed a "see-saw" model to differentiate the genotoxic compounds of DNA breakage or aneuploidy: the breakage agent can significantly increase γH2AX levels, whereas the aneuploidy agent can increase p-H3 levels. Therefore, this microplate-based high-throughput colorimetric detection method can provide an efficient assessment tool for drug safety.

Indexed as

ColorimetryGoldMetal NanoparticlesPlatinumAnimalsBiomarkersDNA DamageEnzyme-Linked Immunosorbent AssayHepatocytesHistonesHumansMutagenicity TestsSea UrchinsBiomarkersGoldH2AX protein, humanHistonesPlatinumELISAgenotoxicity evaluationp‐H3POD‐active nanozymeγH2AX

Identifiers

PMID42328797
PMCPMC13410460

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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.