Evidence map›Paper›PMID 37143036›Full record

ArticleBMC complementary medicine and therapies2023

Preclinical evaluation of antimalarial activity of CPF-1 formulation as an alternative choice for the treatment of malaria.

Prapaporn Chaniad, Tachpon Techarang, Arisara Phuwajaroanpong, Walaiporn Plirat, Prasit Na-Ek, Atthaphon Konyanee, Parnpen Viriyavejakul, Abdi Wira Septama, Chuchard Punsawad

Abstract read
In one paragraph

Article in BMC complementary medicine and therapies, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. From "traditional" to modern medicine: A medical and historical analysis ofJournal of traditional and complementary medicine · 2025
    Review
  3. Article
  4. Article
  5. Article
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

9 authors.

Prapaporn ChaniadDepartment of Medical Sciences, School of Medicine, Walailak University, Nakhon Si Thammarat, 80160, Thailand.
Tachpon TecharangDepartment of Tropical Pathology, Faculty of Tropical Medicine, Mahidol University, Bangkok, 10400, Thailand.
Arisara PhuwajaroanpongDepartment of Medical Sciences, School of Medicine, Walailak University, Nakhon Si Thammarat, 80160, Thailand.
Walaiporn PliratDepartment of Medical Sciences, School of Medicine, Walailak University, Nakhon Si Thammarat, 80160, Thailand.
Prasit Na-EkDepartment of Medical Sciences, School of Medicine, Walailak University, Nakhon Si Thammarat, 80160, Thailand.
Atthaphon KonyaneeDepartment of Medical Sciences, School of Medicine, Walailak University, Nakhon Si Thammarat, 80160, Thailand.
Parnpen ViriyavejakulDepartment of Tropical Pathology, Faculty of Tropical Medicine, Mahidol University, Bangkok, 10400, Thailand.
Abdi Wira SeptamaResearch Center for Pharmaceutical Ingredient and Traditional Medicine, Cibinong Science Center, National Research and Innovation Agency (BRIN), West Java, 16915, Indonesia.
Chuchard PunsawadDepartment of Medical Sciences, School of Medicine, Walailak University, Nakhon Si Thammarat, 80160, Thailand. chuchard.pu@wu.ac.th.

Funding

Thailand Science Research and Innovation Fund FRB650082/0227
6 · The paper itself

Abstract

backgroundKheaw Hom remedy is a traditional Thai medicine used to treat fever. Some plants used in the Kheaw Hom remedy show promising in vitro antimalarial activity. This study prepared novel formulations of plants from the Kheaw Hom remedy and evaluated their antimalarial and toxicological activities.

methodsSeven new formulations were prepared by combining at least three herbs of six selected plants from the Kheaw Hom remedy, namely Mammea siamensis Kosterm., Mesua ferrea L., Dracaena loureiroi Gagnep., Pogostemon cablin (Blanco) Benth., Kaempferia galanga L, and Eupatorium stoechadosmum Hance. In vitro antimalarial activities of each formulation's aqueous and ethanolic extracts were evaluated using the parasite lactate dehydrogenase (pLDH) assay. Cytotoxicity in Vero and HepG2 cells was assessed using the MTT assay. An extract with good antimalarial potency and selectivity index (SI) was selected for in vivo antimalarial activity using Peter's 4-day suppressive test and acute oral toxicity test in mice. In addition, bioactive compounds were identified using Gas chromatography-mass spectrometry (GC-MS) analysis.

resultsAmong the seven new formulations, ethanolic extracts of CPF-1 (Formulation 1) showed the highest activity with an IC

conclusionThe ethanolic extract of CPF-1 showed promising in vitro and in vivo antimalarial efficacy, with no toxic effects at a dose of 2000 mg/kg, suggesting that the ethanolic extract of CPF-1 may serves as a new herbal formulation for the treatment of malaria. Additional research is required for safety and clinical pharmacology studies.

Indexed as

AntimalarialsMalariaAnimalsDracaenaMedicine, TraditionalMicePlant ExtractsAntimalarialsPlant ExtractsAcute toxicityAntimalarial activityKheaw Hom remedyNew formulationPlasmodium bergheiPlasmodium falciparum

Identifiers

PMID37143036
PMCPMC10158254

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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.