Evidence map›Paper›PMID 39757603›Full record

ArticleAnti-inflammatory & anti-allergy agents in medicinal chemistry2025

Formulation, Characterization and Cytotoxic Effect of Indomethacin-loaded Nanoparticles.

Kaan Yalcınkaya, Behiye Senel, Evrim Akyıl

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Article in Anti-inflammatory & anti-allergy agents in medicinal chemistry, 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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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

3 authors.

Kaan YalcınkayaDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Anadolu University, Eskişehir, Turkey.ORCID 0000-0002-4921-0231
Behiye SenelDepartment of Pharmaceutical Biotechnology, Faculty of Pharmacy, Anadolu University, Eskişehir, Turkey.ORCID 0000-0001-9747-8307
Evrim AkyılDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Anadolu University, Eskişehir, Turkey.ORCID 0000-0002-7979-0089

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIndomethacin (IND), classified as class 2 in the Biopharmaceutical Classification System (BCS), has emerged as an anti-inflammatory agent with low solubility and high permeability. Widely used in the treatment of various diseases, such as rheumatoid arthritis and ankylosing spondylitis, this drug is well-known for its adverse effects, particularly in the stomach, and a short biological half-life, which is around 1.5-2 hours.

objectivesThe aim of this study was to overcome the challenges of low solubility, short half-life, and serious side effects occurring with the use of IND-loaded formulations of Solid Lipid Nanoparticles (SLNs) and Polymeric Nanoparticles (PNPs).

methodsFor PNPs, emulsification/solvent evoporation method was employed, and for SLNs, the hot homogenizaton method was applied. Eudragit

resultsBoth PNP and SLN formulations' zeta potential, particle size, and PDI results indicated the formulations to have good stability. Encapsulation efficiency values were obtained as desired. Drug-excipient compatibility was proved using DSC, FT-IR, and 1H NMR. In vitro dissolution results have proven both formulations to have longer release than pure indomethacin. In the MTT analysis of indomethacin application for 24 and 48 hours, a linear correlation was observed between drug concentration and cell viability, and it was determined that the PNP formulation exhibited fewer toxic effects among the formulations. This has proven the PNP nanocarrier as safer for normal cells.

conclusionIND-loaded PNP and SLN formulations have been successfully prepared in this work and they have achieved drug release in the intestine and prolonged the release duration.

Indexed as

Anti-Inflammatory Agents, Non-SteroidalIndomethacinNanoparticlesCell SurvivalDrug CompoundingHumansLipidsParticle SizeSolubilityAnti-Inflammatory Agents, Non-SteroidalIndomethacinLipidsdynasan®116.homogenizationIndomethacinnanoprecipitationpolymeric nanoparticlessolid lipid nanoparticles

Identifiers

PMID39757603
PMCPMC12606602

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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.