Evidence map›Paper›PMID 39025925›Full record

ArticleScientific reports2024

Posaconazole-hemp seed oil loaded nanomicelles for invasive fungal disease.

Anjali Rathee, Pavitra Solanki, Nasr A Emad, Iqra Zai, Saeem Ahmad, Shadab Alam, Ali S Alqahtani, Omar M Noman, Kanchan Kohli, Yasmin Sultana

Abstract read
In one paragraph

Article in Scientific reports, 2024. 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

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

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

10 authors.

Anjali RatheeDepartment of Pharmaceutics, School of Pharmaceutical Education and Research, Jamia Hamdard, 110062, New Delhi, India.
Pavitra SolankiDepartment of Pharmaceutics, Delhi Pharmaceutical Sciences and Research University (DPSRU), New Delhi, 110017, India.
Nasr A EmadDepartment of Pharmaceutics, School of Pharmaceutical Education and Research, Jamia Hamdard, 110062, New Delhi, India.
Iqra ZaiDepartment of Pharmaceutics, School of Pharmaceutical Education and Research, Jamia Hamdard, 110062, New Delhi, India.
Saeem AhmadDepartment of Pharmaceutics, School of Pharmaceutical Education and Research, Jamia Hamdard, 110062, New Delhi, India.
Shadab AlamDepartment of Pharmaceutics, School of Pharmaceutical Education and Research, Jamia Hamdard, 110062, New Delhi, India.
Ali S AlqahtaniDepartment of Pharmacognosy, College of Pharmacy, King Saud University, PO Box 2457, 11451, Riyadh, Saudi Arabia.
Omar M NomanDepartment of Pharmacognosy, College of Pharmacy, King Saud University, PO Box 2457, 11451, Riyadh, Saudi Arabia.
Kanchan KohliDepartment of Pharmaceutics, School of Pharmaceutical Education and Research, Jamia Hamdard, 110062, New Delhi, India.
Yasmin SultanaDepartment of Pharmaceutics, School of Pharmaceutical Education and Research, Jamia Hamdard, 110062, New Delhi, India. ysultana@jamiahamdard.ac.in.

Funding

King Saud University RSP2024R132
6 · The paper itself

Abstract

Invasive fungal infections (IFI) pose a significant health burden, leading to high morbidity, mortality, and treatment costs. This study aims to develop and characterize nanomicelles for the codelivery of posaconazole and hemp seed oil for IFI via the oral route. The nanomicelles were prepared using a nanoprecipitation method and optimized through the Box Behnken design. The optimized nanomicelles resulted in satisfactory results for zeta potential, size, PDI, entrapment efficiency, TEM, and stability studies. FTIR and DSC results confirm the compatibility and amorphous state of the prepared nanomicelles. Confocal laser scanning microscopy showed that the optimized nanomicelles penetrated the tissue more deeply (44.9µm) than the suspension (25µm). The drug-loaded nanomicelles exhibited sustained cumulative drug release of 95.48 ± 3.27% for 24 h. The nanomicelles showed significant inhibition against Aspergillus niger and Candida albicans (22.4 ± 0.21 and 32.2 ± 0.46 mm, respectively). The pharmacokinetic study on Wistar rats exhibited a 1.8-fold increase in relative bioavailability for the nanomicelles compared to the suspension. These results confirm their therapeutic efficacy and lay the groundwork for future research and clinical applications, providing a promising synergistic antifungal nanomicelles approach for treating IFIs.

Indexed as

Antifungal AgentsPlant OilsAnimalsAspergillus nigerCandida albicansDrug CarriersDrug LiberationInvasive Fungal InfectionsMaleMicellesNanoparticlesRatsRats, WistarSeedsTriazolesAntifungal AgentsDrug CarriersMicellesPlant OilsposaconazoleTriazolesAntifungal activityDockingHemp seed oilIn vitro drug releaseNanomicellesPharmacokinetic studyPosaconazole

Identifiers

PMID39025925
PMCPMC11258229

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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.