Evidence map›Paper›PMID 41622218›Full record

ArticleBMC chemistry2026

Acemetacin-loaded bilosomal gel formulations prepared using different polymers for topical application: Box-Behnken design for bilosomes formulation optimization and in vitro evaluation of the formulations.

Esra Demirturk, Tilbe Çevikelli, Aylin Balcı Özyurt, Liban Barre, Meltem Cetin, Mustafa Sinan Kaynak

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Article in BMC chemistry, 2026. 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

What it found

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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

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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

6 authors.

Esra DemirturkDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Çukurova University, Adana, Turkey. demirturkesra@hotmail.com.
Tilbe ÇevikelliDepartment of Pharmaceutical Technology, School of Pharmacy, Bahçeşehir University, İstanbul, Turkey.
Aylin Balcı ÖzyurtDepartment of Pharmaceutical Toxicology, School of Pharmacy, Bahçeşehir University, İstanbul, Turkey.
Liban BarreDepartment of Pharmaceutical Technology, Graduate School, Anadolu University, Eskisehir, Turkey.
Meltem CetinDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Atatürk University, Erzurum, Turkey.
Mustafa Sinan KaynakDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Anadolu University, Eskisehir, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acemetacin (ACIN) is a poorly water-soluble nonsteroidal anti-inflammatory drug, which limits its effectiveness in topical therapeutic applications. This study aimed to enhance the delivery potential and dermal applicability of ACIN through the development of bilosome-loaded hydrogel formulations. Bilosomes were prepared using the thin-film hydration method and optimized using Box-Behnken Design (BBD). The amount of phosphotidylcholine (lecithin), cholesterol and sodium taurocholate were chosen as the formulation parameters and their effects were evaluated on the resulting vesicle size, zeta potential and entrapemnet efficiency percentage (EE%). The optimized formulation displayed a vesicle size of 137.3 nm, a zeta potential of -30.1 mV, a polydispersity index (PDI) of 0.384 and EE% of 84.5%. Bilosomes were incorporated into hydrogel bases containing hydroxypropyl methylcellulose (HPMC) or Carbopol. HPMC-based gels exhibited a favorable pH (~4) for skin application and were selected for further evaluation. These gels provided sustained drug release for up to eight hours. Cytocompatibility testing on L929 fibroblasts using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay demonstrated cell viability above 90% within the tested concentration range (0.05-2 µg/mL), indicating good biocompatibility. The bilosome-loaded HPMC gel formulation exhibited desirable physicochemical properties, sustained drug release, and excellent cytocompatibility, making it a promising vehicle for topical delivery of ACIN. Further anti-inflammatory and in vivo studies are recommended to confirm its potential for topical or anti-inflammatory applications.

Indexed as

AcemetacinBilosomesBox-Behnken designHydrogelsTopical drug delivery

Identifiers

PMID41622218
PMCPMC12927240

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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.