Evidence map›Paper›PMID 37896270›Full record

ArticlePharmaceutics2023

Nanoemulsions as a Promising Carrier for Topical Delivery of Etodolac: Formulation Development and Characterization.

Samet Özdemir, Burcu Üner, Alptuğ Karaküçük, Burak Çelik, Engin Sümer, Çetin Taş

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 18% of its field
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

6 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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  6. 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

6 authors at 5 institutions in 2 countries.

Samet ÖzdemirDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Istanbul Health and Technology University, 34445 Istanbul, Turkey.ORCID 0000-0001-6212-2706
Burcu ÜnerDepartment of Administrative and Pharmaceutical Sciences, University of Health Science and Pharmacy in St. Louis, St. Louis, MO 63110, USA.
Alptuğ KaraküçükDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Ankara Medipol University, 06050 Ankara, Turkey.
Burak ÇelikDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Bezmialem Vakif University, 34093 Istanbul, Turkey.
Engin SümerExperimental Research Center (YUDETAM), Faculty of Medicine, Yeditepe University, 34755 Istanbul, Turkey.ORCID 0000-0002-9228-7963
Çetin TaşDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Yeditepe University, 34755 Istanbul, Turkey.
Yeditepe University · TRBezmiâlem Vakıf Üniversitesi · TRIstanbul Health and Technology UniversityIstanbul Medipol University · TRUniversity of Health Sciences and Pharmacy · US

Funding

Scientific and Technological Research Council of Turkey 221S147
6 · The paper itself

Abstract

This research primarily focuses on the development of innovative topical nanoemulsions for etodolac, aimed at surmounting its inherent limitations. The preparation of etodolac nanoemulsions is accomplished through a combination of high shear homogenization and ultrasonication methods. The optimization of the formulation components is systematically conducted using the design of experiments methodology. The droplet size (DS), polydispersity index (PDI), and zeta potential (ZP) of the optimized formulation were assessed using the differential light scattering (DLS) technique. Surface morphology examinations were conducted using electron microscopy, while interactions between excipients and the drug were analyzed through FTIR analysis. Additionally, in vitro release and ex vivo permeability studies were carried out. Furthermore, anti-inflammatory activity was evaluated in the context of a carrageenan-induced paw edema model in rats. The DS, PDI, and ZP of the optimal formulation were 163.5 nm, 0.141, and -33.1 mV, respectively. The in vitro release profile was assessed as a sustained release by following a non-Fickian drug transport. The flux of etodolac nanoemulsions and coarse dispersions were 165.7 ± 11.7 µg/cm

Indexed as

etodolacnanoemulsionspaw edemapermeationtopical drug delivery

Identifiers

PMID37896270
PMCPMC10610052
OpenAlexW4387879172

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.