Evidence map›Paper›PMID 40006508›Full record

ArticlePharmaceutics2025

Development of

Krisztina Bodnár, Boglárka Papp, Dávid Sinka, Pálma Fehér, Zoltán Ujhelyi, István Lekli, Richárd Kajtár, Fruzsina Nacsa, Ildikó Bácskay, Liza Józsa

Abstract read
In one paragraph

Article in Pharmaceutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. RSC advances · 2026
    Article
  2. Article
  3. Article
  4. 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

10 authors.

Krisztina BodnárDepartment of Pharmaceutical Technology, Faculty of Pharmacy, University of Debrecen, 4032 Debrecen, Hungary.
Boglárka PappDepartment of Pharmaceutical Technology, Faculty of Pharmacy, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0009-0005-1750-4496
Dávid SinkaDepartment of Pharmaceutical Technology, Faculty of Pharmacy, University of Debrecen, 4032 Debrecen, Hungary.
Pálma FehérDepartment of Pharmaceutical Technology, Faculty of Pharmacy, University of Debrecen, 4032 Debrecen, Hungary.
Zoltán UjhelyiDepartment of Pharmaceutical Technology, Faculty of Pharmacy, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0000-0001-9724-0614
István LekliDoctoral School of Pharmaceutical Sciences, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0000-0002-0992-4176
Richárd KajtárDoctoral School of Pharmaceutical Sciences, University of Debrecen, 4032 Debrecen, Hungary.
Fruzsina NacsaMEDITOP Pharmaceutical Ltd., Pilisborosjeno Ady Endre Street 1, 2097 Pilisborosjeno, Hungary.ORCID 0009-0005-0064-6180
Ildikó BácskayDepartment of Pharmaceutical Technology, Faculty of Pharmacy, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0000-0001-8663-2890
Liza JózsaDepartment of Pharmaceutical Technology, Faculty of Pharmacy, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0000-0001-5835-5304

Funding

National Research, Development and Innovation Office 2022-1.2.2-TÉT-IPARI-UZ-2022-00006National Research, Development and Innovation Office TKP2021-EGA-18
6 · The paper itself

Abstract

BACKGROUND/

objectivesThe present study focused on the formulation and evaluation of novel topical systems containing

methodsThe formulations were characterized for droplet size, zeta potential, polydispersity index (PDI), encapsulation efficacy, and stability. The composition exhibiting the most favorable characteristics, with particle sizes falling within the nanoscale range, was incorporated into a cream and a gel, which were compared for their textural properties, carnosol penetration, biocompatibility and efficacy.

resultsRelease studies conducted using Franz diffusion cells demonstrated that the SNEDDS-based cream achieved up to 80% carnosol release, outperforming gels. The 2,2-diphenyl-1-picrylhydrazyl (DPPH) test and enzyme-linked immunosorbent assays (ELISA) showed strong efficacy, with an in vivo carrageenan-induced rat paw edema model revealing that the SNEDDS-based cream significantly reduced inflammation.

conclusionsThese findings highlight the potential of SNEDDS-enhanced topical formulations in improving therapeutic outcomes. Further research is warranted to confirm their long-term safety and efficacy.

Indexed as

anti-inflammatory effectantioxidant effectdermal drug deliverySalvia officinalisSNEDDS

Identifiers

PMID40006508
PMCPMC11858885

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.