Evidence map›Paper›PMID 39289408›Full record

ArticleScientific reports2024

Follicular mediated etodolac phosalosomal gel for contact dermatitis alleviation, insights from optimization to in-vivo appraisal.

Noha Khalifa Abo Aasy, Doaa Ragab, Marwa Ahmed Sallam, Kadria A Elkhodairy

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

4 authors.

Noha Khalifa Abo AasyDepartment of Industrial Pharmacy, Faculty of Pharmacy, Alexandria University, 1 Khartoum Square, Azarita, Post Office, P.O. Box 21521, Alexandria, Egypt. noha.abouassy@alexu.edu.eg.ORCID http://orcid.org/0000-0003-4348-0318
Doaa RagabDepartment of Industrial Pharmacy, Faculty of Pharmacy, Alexandria University, 1 Khartoum Square, Azarita, Post Office, P.O. Box 21521, Alexandria, Egypt.
Marwa Ahmed SallamDepartment of Industrial Pharmacy, Faculty of Pharmacy, Alexandria University, 1 Khartoum Square, Azarita, Post Office, P.O. Box 21521, Alexandria, Egypt.
Kadria A ElkhodairyDepartment of Industrial Pharmacy, Faculty of Pharmacy, Alexandria University, 1 Khartoum Square, Azarita, Post Office, P.O. Box 21521, Alexandria, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite its long history as a preferential cyclooxygenase-2 inhibitor, the topical application of etodolac in inflammatory disorders does not achieve the desired clinical efficiency because of its poor water solubility and poor skin permeation. In the ongoing study, phosalosomes were designed to mitigate the etodolac drawbacks and to enhance its skin localization. Hyaluronic acid was utilized to prepare a dermal gel for the alleviation of skin inflammation. Etodolac loaded hyaluronic acid phosalosomal gel had a sustainable release profile and 10.59-fold enhanced skin retention compared to free etodolac, with boosted skin tolerability on histopathological examination after acute and chronic applications. Confocal laser microscopy imaging indicated that the etodolac amounts accumulated in the liver and kidney following dermal application were 29 and 5.7-fold lower than those following the systemic dose, respectively. For in vivo studies, etodolac loaded hyaluronic acid phosalosomal gel presented superior anti-oedemic and significant anti-nociception potential. The promising homogenous localization highlighted its potential for the delivery of lipophilic drugs for the targeted treatment of other localized skin disorders.

Indexed as

Dermatitis, ContactEtodolacGelsHyaluronic AcidLiposomesAdministration, CutaneousAnimalsFemaleMaleMiceRatsSkinSkin AbsorptionEtodolacGelsHyaluronic AcidLiposomesAnti-inflammatoryContact dermatitis, PhosalosomesHyaluronic acidNociceptionSkin irritation

Identifiers

PMID39289408
PMCPMC11408589

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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.