Evidence map›Paper›PMID 40844557›Full record

ArticleBrazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]2025

Encapsulation of Flucytosine into nanoliposomes for enhanced antifungal activity against Candida glabrata and Candida albicans.

Haniyeh Dianati, Payam Esmailpour, Azita Dilmaghani, Ali Shayanfar, Nastaran Hashemzadeh, Behzad Baradaran, Somayeh Hallaj-Nezhadi

Abstract read
In one paragraph

Article in Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology], 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Haniyeh DianatiStudent Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
Payam EsmailpourStudent Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
Azita DilmaghaniDepartment of Pharmaceutical Biotechnology, Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran.
Ali ShayanfarPharmaceutical Analysis Research Center, Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran.
Nastaran HashemzadehPharmaceutical Analysis Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Behzad BaradaranImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Somayeh Hallaj-NezhadiDepartment of Pharmaceutical & Food Control, Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, 51664-14766, Iran. nezhadis@yahoo.com.ORCID http://orcid.org/0000-0003-4730-205X

Funding

Tabriz University of Medical Sciences 60341
6 · The paper itself

Abstract

Flucytosine (FC) is currently used as an antifungal drug for the treatment of infectious diseases. However, due to the development of drug resistance, the monotherapy of FC is limited. Recently, nanoliposomes have been studied as promising approaches to overcome microbial resistance. In this study, we encapsulate FC in the nanoliposomes and investigate their physicochemical properties as well as antifungal activities against Candida glabrata and Candida albicans in-vitro. Various liposomal formulations of FC were prepared based on the modified freeze-drying of a monophase solution method. The nanoliposomes were characterized in terms of size, zeta potential, transmission electron microscopy image, encapsulation efficiency, stability, release, crystallography, and cytotoxicity. Also, the minimum inhibitory concentration and minimum fungicidal concentration were determined against C. glabrata and C. albicans. The size and zeta potential of the selected nanoliposomes were 147.33 ± 23.25 nm and - 31.20 ± 9.05 mV, respectively. Encapsulation efficiency was 46.7 ± 7.5% in the selected formulation. TEM results revealed that the nanoliposomes were nano-sized and spherical. Release results indicated that the nanoliposomes had a slow-release rate of FC. The fungal eradication of nanoliposomal FC was at least two times higher than that of the free drug for C. glabrata and C. albicans. Cytotoxicity studies demonstrated no significant toxicity at effective concentrations of nanoliposomal FC. The stability of the nano-formulation was temperature-dependent, and the refrigerator showed the best condition for long-term storage. Nanoliposomal FC prepared using the modified freeze-drying of a monophase solution method seems promising and may be used to overcome the fungal resistance relative to FC.

Indexed as

Antifungal AgentsCandida albicansCandida glabrataFlucytosineLiposomesNanoparticlesCell SurvivalDrug CompoundingHumansMicrobial Sensitivity TestsParticle SizeAntifungal AgentsFlucytosineLiposomesCandida albicansCandida glabrataFlucytosineFreeze-drying of monophase solutionNanoliposomes

Identifiers

PMID40844557
PMCPMC12660535

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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.