Evidence map›Paper›PMID 39046555›Full record

ArticleParasitology research2024

Spiramycin-loaded maltodextrin nanoparticles as a promising treatment of toxoplasmosis on murine model.

Ayman A Abdel-Wahab, Dalia A Shafey, Sahar M Selim, Soraya A Sharaf, Khloud K Mohsen, Dina M Allam, Sally W Elkhadry, Marwa A Gouda

Abstract read
In one paragraph

Article in Parasitology research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
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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

8 authors.

Ayman A Abdel-WahabDepartment of Clinical and Molecular Parasitology, National Liver Institute, Menoufia University, Menoufia, Egypt.
Dalia A ShafeyDepartment of Clinical and Molecular Parasitology, National Liver Institute, Menoufia University, Menoufia, Egypt.
Sahar M SelimDepartment of Clinical and Molecular Parasitology, National Liver Institute, Menoufia University, Menoufia, Egypt.
Soraya A SharafDepartment of Clinical and Molecular Parasitology, National Liver Institute, Menoufia University, Menoufia, Egypt.
Khloud K MohsenDepartment of Clinical and Molecular Parasitology, National Liver Institute, Menoufia University, Menoufia, Egypt. drkhloud.kamel@liver.menofia.edu.eg.ORCID http://orcid.org/0009-0009-0572-1855
Dina M AllamDepartment of Pathology, Faculty of Medicine, Menoufia University, Shibin Elkom, Egypt.
Sally W ElkhadryDepartment of Epidemiology and Preventive Medicine, National Liver Institute, Menoufia University, Menoufia, Egypt.
Marwa A GoudaDepartment of Clinical and Molecular Parasitology, National Liver Institute, Menoufia University, Menoufia, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite being the initial choice for treating toxoplasmosis, sulfadiazine and pyrimethamine have limited effectiveness in eliminating the infection and were linked to a variety of adverse effects. Therefore, the search for new effective therapeutic strategies against toxoplasmosis is still required. The current work is the first research to assess the efficacy of spiramycin-loaded maltodextrin nanoparticles (SPM-loaded MNPs) as a novel alternative drug therapy against toxoplasmosis in a murine model. Fifty laboratory-bred Swiss albino mice were divided into five groups: normal control group (GI, n = 10), positive control group (GII, n = 10), orally treated with spiramycin (SPM) alone (GIII, n = 10), intranasal treated with SPM-loaded MNPs (GIV, n = 10), and orally treated with SPM-loaded MNPs (GV, n = 10). Cysts of Toxoplasma gondii ME-49 strain were used to infect the mice. Tested drugs were administered 2 months after the infection. Drug efficacy was assessed by counting brain cysts, histopathological examination, and measures of serum CD19 by flow cytometer. The orally treated group with SPM-loaded MNPs (GV) showed a marked reduction of brain cyst count (88.7%), histopathological improvement changes, and an increasing mean level of CD19 (80.2%) with significant differences. SPM-loaded MNPs showed potent therapeutic effects against chronic toxoplasmosis. Further research should be conducted to assess it in the treatment of human toxoplasmosis, especially during pregnancy.

Indexed as

Disease Models, AnimalNanoparticlesPolysaccharidesSpiramycinToxoplasmosis, AnimalAnimalsAntiprotozoal AgentsBrainDrug CarriersFemaleMiceToxoplasmaToxoplasmosisAntiprotozoal AgentsDrug CarriersmaltodextrinPolysaccharidesSpiramycinMaltodextrin nanoparticlesSpiramycinToxoplasmosisTreatment

Identifiers

PMID39046555
PMCPMC11269460

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.