Evidence map›Paper›PMID 39953569›Full record

ArticleBMC pharmacology & toxicology2025

Development of nanospray loaded with ciclopirox for dermal fungus treatment: determination of pro-inflammatory interleukin IL-2 mRNA expression.

Yasir Mehmood, Hira Shahid, Rabbia Nazir, Mohammad N Uddin, Mohammad Nur-E-Alam, Mohammed Bourhia, Khalid S Almaary, Mohsin Kazi, Ousman B Mahamat

Abstract read
In one paragraph

Article in BMC pharmacology & toxicology, 2025. 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
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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

9 authors.

Yasir MehmoodRiphah Institute of Pharmaceutical Sciences (RIPS), Riphah International University Faisalabad, PO. Box 38000, Faisalabad, Pakistan.
Hira ShahidDepartment of Pharmacology, Faculty of Pharmaceutical Sciences, Government College University Faisalabad, P.O. Box 38000, Faisalabad, Pakistan.
Rabbia NazirUniversity College of Pharmacy, University of the Punjab, Allama Iqbal Campus, Lahore, Pakistan.
Mohammad N UddinCollege of Pharmacy, Mercer University, Atlanta, GA, 30341, USA.
Mohammad Nur-E-AlamDepartment of Pharmacognosy, College of Pharmacy, King Saud University, PO BOX-2457, Riyadh, 11451, Saudi Arabia. mohnalam@ksu.edu.sa.
Mohammed BourhiaLaboratory of Biotechnology and Natural Resources Valorization, Faculty of Sciences, Ibn Zohr University, Agadir, 80060, Morocco. bourhia.mohamed@gmail.com.
Khalid S AlmaaryDepartment of Botany and Microbiology, College of Science, King Saud University, P. O. BOX 2455, Riyadh, 11451, Saudi Arabia.
Mohsin KaziDepartment of Pharmaceutics, College of Pharmacy, King Saud University, P.O. Box 11451, Riyadh, Saudi Arabia.
Ousman B MahamatNational Federation of Associations of Medical Practitioners in Chad (FENAPMT), Ministry of Health, N'Djamena, N'Djamena City, Republic of Chad.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to develop a ciclopirox (CXP) topical nano spray using nanotechnology to enhance drug bioavailability and skin absorption. A precipitation method was employed to incorporate CXP in its nano particulate form, using chitosan as the polymer. Chitosan nanoparticles (CT NPs) possess unique properties that make them highly suitable for biological applications. The study focused on investigating the penetration behavior of chitosan nanoparticles (nano spray) through artificial skin, with the goal of developing them as effective skin delivery systems for medications. The nanoparticles had an average size of 640 nm, with a positive or negative surface potential and a polydispersity index (PDI) of 0.298. A thorough analysis of the nano spray was conducted using several scientific techniques, including X-ray diffractometry, scanning electron microscopy, Fourier transform infrared spectroscopy, differential scanning calorimetry (DSC), as well as in vitro release and diffusion studies. Additionally, cell viability was evaluated using the MTT assay, and blood compatibility was tested through a hemolysis test. The study also assessed the levels of the anti-inflammatory cytokine IL-2 in the lungs of mice using RNA extraction, reverse transcription, and polymerase chain reaction (RT-PCR). The drug dissolution and diffusion rates showed a significant improvement compared to the pure reference sample. Therefore, the CXP nano spray appears to be an efficient and practical method to enhance skin penetration, bioavailability, and permeability. Based on the results, the CXP nano spray holds potential as a promising treatment for fungal infections, particularly for skin diseases.

Indexed as

Antifungal AgentsCiclopiroxInterleukin-2NanoparticlesAnimalsCell SurvivalChitosanHumansLungMaleMiceRNA, MessengerSkinSkin AbsorptionAntifungal AgentsChitosanCiclopiroxInterleukin-2RNA, MessengerCytokinesDiameterDiffusionIn vitroSkin penetration

Identifiers

PMID39953569
PMCPMC11827433

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.