Evidence map›Paper›PMID 36424804›Full record

ArticleCurrent drug metabolism2022

Comprehensive Metabolism Study of Tangeretin in Rat Plasma, Urine and Faeces Using Ultra-High Performance Liquid Chromatography-Q Exactive Hybrid Quadrupole- Orbitrap High-Resolution Accurate Mass Spectrometry.

Xiaojun Yu, Zhufeng Cong, Changlin Wang, Shengguang Wang, Zhi Yan, Bin Wang, Xiaonan Liu, Zhen Li, Peng Gao, Huaixing Kang

Abstract read
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Article in Current drug metabolism, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.5field-weighted citation impact, top 16% of its field
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

3 citing papers in PubMed, 7 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Xiaojun YuCollege of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan, Shandong Province, China.
Zhufeng CongShandong Cancer Hospital & Institute, Jinan, Shandong Province, China.
Changlin WangCollege of Traditional Chinese Medicine, Shandong University of Traditional Chinese Medicine, Jinan, Shandong Province, China.
Shengguang WangCollege of Traditional Chinese Medicine, Shandong University of Traditional Chinese Medicine, Jinan, Shandong Province, China.
Zhi YanCollege of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan, Shandong Province, China.
Bin WangCollege of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan, Shandong Province, China.
Xiaonan LiuCollege of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan, Shandong Province, China.
Zhen LiCollege of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan, Shandong Province, China.
Peng GaoCollege of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan, Shandong Province, China.
Huaixing KangCollege of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan, Shandong Province, China.
Shandong University of Traditional Chinese Medicine · CNShandong First Medical University · CN

Funding

Major scientific and technological innovation projects in Shandong Province 2019JZZY020906
6 · The paper itself

Abstract

backgroundTangeretin, present in citrus fruits, is a polymethoxy flavone with extensive pharmacological effects. It has been widely used in the clinic, but there were no detailed studies on the in vivo metabolism of tangeretin.

objectiveThis study aimed to establish a rapid and effective strategy to identify the metabolites of tangeretin and evaluate the biotransformation pathways of tangeretin in rats.

methodsThe ultra-high performance liquid chromatography (UHPLC) equipped with a Q-Exactive Orbitrap mass spectrometer was used to identify the metabolites of tangeretin in plasma, urine and faeces of rats after intragastric administration. Based on high-resolution extracted ion chromatograms (HREICs) and parallel reaction monitoring mode (PRM), metabolites of tangeretin were identified by comparing the accurate mass, chromatographic retention times, diagnostic product ions (DPIs) and neutral loss fragments (NLFs) with those of tangeretin reference standard. Isomers were distinguished by ClogP values.

resultsAn efficient and integrated strategy was established for the comprehensive screening and characterizing of tangeretin metabolites through Rapid Profiling. Based on this strategy, a total of 52 metabolites were detected and identified, among which 25 metabolites were found in rat plasma, while 48 and 16 metabolites were characterized from rat urine and faeces, respectively. These metabolites were produced by demethylation, demethoxylation, hydroxylation, methoxylation, glucuronidation, glycosylation, sulfation, and their composite reactions. Interestingly, tangeretin is easy to lose methyl in vivo and becomes an intermediate product, and then other phase I and phase II reactions occur. Moreover, the characteristic fragmentation pathways of tangeretin were summarized for the subsequent metabolite identification.

conclusionThe analytical method based on UHPLC-Q-Exactive mass spectrometer has the ability to quickly clarify unknown metabolism. And the the comprehensive metabolism study of tangeretin provided an overall metabolic profile, which will be of great scientific basis for further studies on tangeretin in determining its pharmacokinetics, the bioactivity of the metabolites, and clinical applications.

Indexed as

bioactive components.data-mining methodsflavonoidmetabolitesspectrometryTangeretinUHPLC-Q-Exactive Orbitrap mass spectrometer

Identifiers

PMID36424804
OpenAlexW4310049180

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.