Evidence map›Paper›PMID 42518428›Full record

ArticleACS omega2026

Impact of Menthol Concentration on Ketoprofen Permeation and Photostability in Compounded Topical Preparations in a Pentravan Base.

Urszula Adamiak-Giera, Michał Gackowski, Damian Malinowski, Tomasz Osmałek, Bozena Michniak-Kohn, Mateusz Kurzawski, Anna Machoy-Mokrzyńska, Monika Białecka

Abstract read
In one paragraph

Article in ACS omega, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Urszula Adamiak-GieraDepartment of Pharmacokinetics and Therapeutic Drug Monitoring, Pomeranian Medical University in Szczecin, Szczecin 70-111, Poland.ORCID https://orcid.org/0000-0002-6032-1661
Michał GackowskiPoznan University of Medical Sciences, Chair and Department of Pharmaceutical Technology, Poznań 60-806, Poland.
Damian MalinowskiDepartment of Pharmacokinetics and Therapeutic Drug Monitoring, Pomeranian Medical University in Szczecin, Szczecin 70-111, Poland.
Tomasz OsmałekPoznan University of Medical Sciences, Chair and Department of Pharmaceutical Technology, Poznań 60-806, Poland.
Bozena Michniak-KohnCenter for Dermal Research and Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854, United States.
Mateusz KurzawskiLaboratory of Pharmacodynamics, Pomeranian Medical University in Szczecin, Szczecin 71-899, Poland.
Anna Machoy-MokrzyńskaDepartment of Experimental and Clinical Pharmacology, Pomeranian Medical University in Szczecin, Szczecin 70-111, Poland.
Monika BiałeckaDepartment of Pharmacokinetics and Therapeutic Drug Monitoring, Pomeranian Medical University in Szczecin, Szczecin 70-111, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTopical nonsteroidal anti-inflammatory drugs provide localized pain relief while reducing the risk of systemic adverse effects. Menthol is frequently used in topical formulations both as an analgesic agent and as a penetration enhancer.

objectiveThis study evaluated the effect of menthol concentration on ketoprofen permeation through Strat-M membranes and photostability in compounded topical formulations based on a Pentravan vehicle. RESEARCH DESIGN AND

methodsSemisolid formulations containing ketoprofen, lidocaine hydrochloride, and increasing concentrations of menthol were prepared using the Pentravan base. In vitro permeation experiments were performed using Franz diffusion cells with Strat-M membranes as a screening model. Ketoprofen concentrations were determined using UHPLC analysis. Photostability under UVA exposure (0-200 Wh/m

resultsKetoprofen permeation increased with increasing menthol concentration. After 12 h, the cumulative amount detected in the acceptor phase ranged from 194.9 μg for the menthol-free formulation to 475.9 μg for the formulation containing 10% menthol. Photostability studies showed formulation-dependent degradation profiles. The menthol-free formulation retained the highest proportion of ketoprofen during UVA exposure, whereas the menthol-containing formulation and the commercial product showed more pronounced drug degradation.

conclusionMenthol enhanced ketoprofen permeation in the applied in vitro model while also influencing the drug's photodegradation behavior under UVA exposure, highlighting the importance of formulation composition in compounded topical preparations.

Identifiers

PMID42518428
PMCPMC13382757

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.