Evidence map›Paper›PMID 41208861›Full record

ArticleFrontiers in pharmacology2025

Integrated chemometric evaluation of morphological traits, chemical composition, and hepatotoxicity of

Yanyi Li, Qi Wang, Yanrong Yang, Xiaobin Huang, Yujie Zhang

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2025. 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

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yanyi LiSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, China.
Qi WangInstitute of Chinese Traditional Medicine and Ethnic Medicine, National Institutes for Food and Drug Control, Beijing, China.
Yanrong YangSchool of Functional Food and Wine, Shenyang Pharmaceutical University, Shenyang, Liaoning, China.
Xiaobin HuangSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, China.
Yujie ZhangSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ethnopharmacological relevance: The toxicity of Aim: This study aims to establish a new evaluation model that integrates multiparameter chemometric analysis with combined statistical approaches to assess and monitor the toxicity of PM. The multi-index framework included crude drug morphological traits, main chemical constituents (anthraquinones, stilbene glycosides, flavonoids and phenols), and hepatotoxicity across different PM batches. Materials and methods: An ultra-performance liquid chromatography-electrospray ionization-triple-quadrupole tandem mass spectrometry (UPLC-ESI-QqQ-MS/MS) method was first developed to quantify 26 compounds in 61 batches of commercial PM samples. Chemometric analyses, including principal component analysis (PCA) and hierarchical cluster analysis (HCA), were then applied to classify the samples into four groups based on chemical composition. Hepatotoxicity comparisons among these groups were conducted using the Cell Counting Kit-8 assay in HepaRG cells. Subsequently, toxicity-related morphological traits were investigated by quantifying chromaticity values of crude drugs from groups with distinct toxicity profiles. Two key between-group toxicity variables were identified through chemometric analyses, including orthogonal partial least squares discriminant analysis (OPLS-DA) and Results: The established chemical profiling library of PM demonstrated a strong correlation with hepatocytotoxicity. White decoction pieces of PM were found to be safer, while THSG and EG were identified as potential hepatotoxic constituents. Moreover, THSG enhanced the hepatotoxicity of EG, indicating a synergistic effect. Conclusion: The proposed model offers a novel framework linking morphological traits, chemical composition, and hepatotoxicity of PM, offering a reference for the safety evaluation of other medicinal herbs.

Indexed as

chemometricscomponent analysishepatotoxic constituentsmorphological traitsmulti-index comprehensive evaluation modelPolygonum multiflorum

Identifiers

PMID41208861
PMCPMC12588903

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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.