Evidence map›Paper›PMID 40205488›Full record

ArticleBMC pharmacology & toxicology2025

Modified diatom-based ocular suspension for sustained diclofenac sodium delivery: a novel drug carrier approach.

Ramin Ghasemishayan, Dorsa Jalaei, Faramarz Dobakhti

Erratum issuedAbstract 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. An erratum has been issued. Not yet cited 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

5 · Who and what money

Authors and funding

3 authors.

Ramin GhasemishayanRadiology Department, Paramedical Faculty, Tabriz University of Medical Sciences, Tabriz, Iran.
Dorsa JalaeiSchool of Pharmacy, Zanjan University of Medical Sciences, Zanjan, Iran.
Faramarz DobakhtiSchool of Pharmacy, Zanjan University of Medical Sciences, Zanjan, Iran. fdobakhti@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeOphthalmic drugs typically last only around 15 minutes due to rapid elimination from tear flow, with only about 2% absorption, while the rest may enter the nasal mucosa, potentially causing systemic side effects. Diatoms, with properties like unique structure, abundance, low cost, heat resistance, non-toxicity, and easy access, present a promising solution for sustained drug delivery. This study aimed to prepare and evaluate an ocular suspension of diclofenac sodium loaded onto modified diatoms.

methodsDiatoms were modified with aluminum sulfate solution, followed by loading of diclofenac sodium. Characteristics of diatoms before and after modification-particle size, surface charge, and drug loading-were analyzed using electron microscopy, FTIR (Fourier Transform Infrared Spectroscopy), XRD (X-ray Diffraction), and elemental mapping. BET (Brunauer-Emmett-Teller (Surface Area Analysis) testing provided adsorption data, while DSC (Differential Scanning Calorimetry) assessed thermal properties. An in vitro release study using a dialysis bag in artificial tear fluid examined drug release over 8 hours. Drug content was determined by spectrophotometry, and cytotoxicity on MDA-MB-231 and HEP-G2 cell lines was evaluated at different diatom concentrations.

resultsSEM (Scanning Electron Microscopy) imaging showed no topographic changes post-modification. BET and XRD analyses confirmed drug loading and structural stability, while FTIR indicated involvement of carboxylate groups. TGA and DSC showed stable thermal properties. Elemental mapping confirmed increased surface elements and high drug loading. Modified diatoms showed sustained drug release and no significant cytotoxicity differences.

conclusionModified diatoms demonstrated higher drug loading and sustained release, indicating their potential for safe and effective ocular drug delivery. Further studies are recommended to confirm these findings.

Indexed as

Anti-Inflammatory Agents, Non-SteroidalDiatomsDiclofenacDrug CarriersAdministration, OphthalmicCell Line, TumorCell SurvivalDelayed-Action PreparationsDrug Delivery SystemsDrug LiberationHumansParticle SizeSuspensionsAnti-Inflammatory Agents, Non-SteroidalDelayed-Action PreparationsDiclofenacDrug CarriersSuspensionsDiatomiteDiclofenac sodiumOcular drug deliveryOcular formulationPorous-silicaSustained release

Identifiers

PMID40205488
PMCPMC11983991

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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.