Evidence map›Paper›PMID 41939443›Full record

ArticleInternational journal of pharmaceutics: X2026

Allicin-based biomimetic nanoparticles of the erythrocyte membrane for the delivery of lumefantrine to enhance its antimalarial effect.

Chuyi Yu, Xiaobo Li, Keneng Cai, Weichi Jiang, Wanying Chen, Run Xia, Mengyao Xu, Jianjia Feng, Chengli Ling, Sheng Zhou and 7 more

Abstract read
In one paragraph

Article in International journal of pharmaceutics: X, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Chuyi YuArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Xiaobo LiArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Keneng CaiArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Weichi JiangArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Wanying ChenArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Run XiaArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Mengyao XuArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Jianjia FengArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Chengli LingHunan Academy of Chinese Medicine, Yuehua Road, Yuelu District, Changsha 410013, China.
Sheng ZhouArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Yinhuan ChenThe First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou 510405, China.
Feng ZengArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Qin XuArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Xiao HeArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Mingqiang LiArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Jianping SongArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Jianming LiangArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Owing to the emergence of drug resistance and the lack of effective vaccines, malaria continues to seriously harm the physical and mental health of a multitude of individuals, warranting the need to explore new antimalarial strategies. In this study, we developed allicin-based biomimetic nanoparticles of the erythrocyte membrane (PECm-Allicin@LM) through a sonication method for the delivery of lumefantrine (LM), a hydrophobic antimalarial drug. PECm-Allicin@LM showed regular spherical morphology with a mean diameter of 120 nm and retained most of the major proteins on the erythrocyte membrane. PECm-Allicin@LM was stable and sustained the release of LM. Flow cytometry analysis showed that PECm-Allicin@LM could deliver LM to

Indexed as

AllicinErythrocyte membrane biomimetic nanoparticlesLumefantrineMultiple pathwaysPbANKA-infected malaria

Identifiers

PMID41939443
PMCPMC13049907

What OpenQuestion holds

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Registered trials

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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.