Evidence map›Paper›PMID 42181734›Full record

ArticleRSC advances2026

The cocrystals of isorhamnetin and isoliquiritigenin with 4,4'-bipyridine: system characterization, stability, dissolution and anticancer activity.

Yu Liu, Jian Lei, Ting Li, Aiyu Zhong, Zihan Zhu, Junxiao Lu, Zhipeng Wang, Panpan Zhao, Zhigang Wu

Abstract read
In one paragraph

Article in RSC advances, 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

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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

The trial behind it

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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

9 authors.

Yu LiuHebei Key Laboratory of Neuropharmacology, Department of Pharmacy, Hebei North University Zhangjiakou 075000 China wangzp0128@sina.com wuzhigang1982@126.com.
Jian LeiHebei Key Laboratory of Neuropharmacology, Department of Pharmacy, Hebei North University Zhangjiakou 075000 China wangzp0128@sina.com wuzhigang1982@126.com.
Ting LiHebei Key Laboratory of Neuropharmacology, Department of Pharmacy, Hebei North University Zhangjiakou 075000 China wangzp0128@sina.com wuzhigang1982@126.com.
Aiyu ZhongHebei Key Laboratory of Neuropharmacology, Department of Pharmacy, Hebei North University Zhangjiakou 075000 China wangzp0128@sina.com wuzhigang1982@126.com.
Zihan ZhuHebei Key Laboratory of Neuropharmacology, Department of Pharmacy, Hebei North University Zhangjiakou 075000 China wangzp0128@sina.com wuzhigang1982@126.com.
Junxiao LuHebei Key Laboratory of Neuropharmacology, Department of Pharmacy, Hebei North University Zhangjiakou 075000 China wangzp0128@sina.com wuzhigang1982@126.com.
Zhipeng WangHebei Key Laboratory of Neuropharmacology, Department of Pharmacy, Hebei North University Zhangjiakou 075000 China wangzp0128@sina.com wuzhigang1982@126.com.ORCID https://orcid.org/0000-0003-2308-3622
Panpan ZhaoDepartment of Endocrinology and Metabolic Diseases, The First Affiliated Hospital of Hebei North University Zhangjiakou 075000 China zpanpan0903@sina.com.
Zhigang WuHebei Key Laboratory of Neuropharmacology, Department of Pharmacy, Hebei North University Zhangjiakou 075000 China wangzp0128@sina.com wuzhigang1982@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As two natural products, isorhamnetin and isoliquiritigenin have been demonstrated to have significant anticancer activity. However, various pharmaceutical defects, such as low solubility and poor bioavailability, impede their anticancer efficacy. To optimize the anticancer efficacy of isorhamnetin and isoliquiritigenin, a scientific cocrystal design was performed to obtain two newly prepared cocrystals in this study. Leveraging multiple analytical techniques including single-crystal X-ray diffraction, powder X-ray diffraction, Fourier transform infrared spectroscopy, differential scanning calorimetry and thermogravimetric analysis, the isorhamnetin-4,4'-bipyridine (2 : 3) and isoliquiritigenin-4,4'-bipyridine (1 : 1) cocrystals were systematically characterized. The results of a series of evaluations on their stabilities, dissolution and anticancer activities demonstrated that these two cocrystals could remain stable under three different extreme environments, and the isorhamnetin-4,4'-bipyridine (2 : 3) cocrystal achieved significant improvement in solubility, dissolution rate and anticancer efficacy compared to isorhamnetin. For the isoliquiritigenin-4,4'-bipyridine (1 : 1) cocrystal, there was no increase in its solubility and dissolution rate compared to isoliquiritigenin. Nevertheless, a slight increase in the anticancer activity of isoliquiritigenin was achieved by the formation of the cocrystal. This study was a meaningful investigation, which not only laid an innovative material foundation for the development of isorhamnetin and isoliquiritigenin but also provided a new strategy to optimize the pharmaceutical properties of natural products.

Identifiers

PMID42181734
PMCPMC13191744

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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.