Evidence map›Paper›PMID 40652826›Full record

ArticleInternational journal for parasitology. Drugs and drug resistance2025

Pharmacokinetics and metabolism of artemisinin (ART) in Plasmodium yoelii: ART-heme adduct as a potential biomarker for its resistance.

Shanshan Du, Kun Xu, Zhaohua Liu, Jie Xing

Abstract read
In one paragraph

Article in International journal for parasitology. Drugs and drug resistance, 2025. 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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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

1 citing paper in PubMed.

  1. Review
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

4 authors.

Shanshan DuSchool of Pharmaceutical Sciences, Shandong University, Jinan, China.
Kun XuSchool of Pharmaceutical Sciences, Shandong University, Jinan, China.
Zhaohua LiuThe Model Animal Research Center, Cheeloo College of Medicine, Shandong University, Jinan, China.
Jie XingSchool of Pharmaceutical Sciences, Shandong University, Jinan, China. Electronic address: xingjie@sdu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPlasmodium falciparum in Southeast Asia and Africa is developing resistance to the antimalarial drug artemisinin (ART). In this study, the metabolite of ART in P. yoelii parasites was evaluated as a potential biomarker for its antimalarial activity as well as its resistance.

methodsThe induced strain of P. yoelii (iPy) was first established after long-time pressure of ART in P. yoelii (Py)-infected mice. The metabolic and pharmacokinetic profiles of ART were then studied in both P. yoelii parasites and infected mice. The pharmacokinetic-pharmacodynamic behaviors of ART in two strains of P. yoelii (Py and iPy) were compared. The pharmacokinetic parameters (e.g., AUC and C

resultsLower antimalarial activity was found for ART against iPy than Py, in terms of the 90 % growth inhibitory dose (ED

conclusionsPlasma ART concentration merely reflected drug exposure in the host. ART-heme adduct was the major metabolite for ART in P. yoelii parasites, and it could be a potential biomarker for the antimalarial activity of ART as well as its resistance.

Indexed as

AntimalarialsArtemisininsDrug ResistanceHemeMalariaPlasmodium yoeliiAnimalsBiomarkersFemaleMiceAntimalarialsartemisininArtemisininsBiomarkersHemeAntimalarial activityArtemisininBiomarkerHeme adductResistance

Identifiers

PMID40652826
PMCPMC12366529

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