Evidence map›Paper›PMID 39697549›Full record

ArticleFrontiers in pharmacology2024

Development of a UPLC-MS/MS method for the determination of sulfatinib and its no interaction with myricetin in rats.

Dongxin Chen, Jie Chen, Hailun Xia, Xiaohai Chen, Jinyu Hu, Guangliang Wu, Xuegu Xu

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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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

7 authors.

Dongxin Chen *The Affiliated Lihuili Hospital, Ningbo University, Ningbo, Zhejiang, China.
Jie Chen *The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Hailun XiaThe First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Xiaohai ChenThe First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Jinyu HuThe First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Guangliang WuThe Affiliated Lihuili Hospital, Ningbo University, Ningbo, Zhejiang, China.
Xuegu XuThe Eye Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Sulfatinib is a novel oral tyrosine kinase inhibitor (TKI) with selective inhibition of fibroblast growth factor (FGFR), colony-stimulating factor 1 receptor (CSF-1R) and vascular endothelial growth factor receptor (VEGFR) 1, 2, and 3. It has been approved for the therapy of neuroendocrine tumors arising in the non-pancreatic (December 2020) and pancreatic (June 2021) glands. Until now, there has no research on the determination of sulfatinib in biological medium by ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method. Methods: The current study validated a sensitive and reliable quantitative detection of sulfatinib in plasma using UPLC-MS/MS for the first time, and investigated the interaction with myricetin in rats. Acetonitrile was used to precipitate the plasma protein, and lenvatinib was employed as the internal standard (IS). Results: The method demonstrated that sulfatinib presented high linearity over the concentration of 11-2,000 ng/mL with the lower limit of quantification (LLOQ) of 1 ng/mL. It was validated methodologically that the precision, matrix effect, stability, accuracy and extraction recovery were all within the allowable values. Moreover, male Sprague-Dawley (SD) rats were assigned randomly to assess the interaction between sulfatinib (30 mg/kg) and myricetin (50 mg/kg). Nevertheless, no significant differences of the main pharmacokinetic parameters were revealed. This may be due to insufficient doses of myricetin, or failure of myricetin to act in a timely manner Discussion: The findings contributed to a better understanding of the metabolism and drug-drug interaction of sulfatinib, but the presence or absence of interactions needs to be confirmed by further studies.

Indexed as

drug-drug interactionmyricetinpharmacokineticssulfatinibUPLC-MS/MS

Identifiers

PMID39697549
PMCPMC11653107

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