Evidence map›Paper›PMID 41900067›Full record

ArticleMolecules (Basel, Switzerland)2026

Amaranth Oil for Dermatologic Conditions: Inflammation Control and Cytotoxicity Assessment in Skin-Related Cell Models-Preliminary Study.

Paweł Paśko, Agnieszka Galanty, Ewelina Prochownik, Alma Leticia Martinez-Ayala, Alma Chu-Martínez, Pitipong Thobunluepop, Danail Pavlov, Aviva Friedman-Ezra, Shela Gorinstein

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 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

9 authors.

Paweł PaśkoDepartment of Food Chemistry and Nutrition, Jagiellonian University Medical College, 30-688 Kraków, Poland.ORCID 0000-0002-4821-4492
Agnieszka GalantyDepartment of Pharmacognosy, Jagiellonian University Medical College, 30-688 Kraków, Poland.ORCID 0000-0001-5636-8646
Ewelina ProchownikDepartment of Food Chemistry and Nutrition, Jagiellonian University Medical College, 30-688 Kraków, Poland.ORCID 0000-0001-7848-4787
Alma Leticia Martinez-AyalaCentro de Desarrollo de Productos Bióticos, Instituto Politécnico Nacional, Yautepec 62731, Morelos, Mexico.ORCID 0000-0001-9875-4086
Alma Chu-MartínezCentro de Desarrollo de Productos Bióticos, Instituto Politécnico Nacional, Yautepec 62731, Morelos, Mexico.ORCID 0000-0002-4531-8229
Pitipong ThobunluepopDepartment of Agronomy, Faculty of Agriculture, Kasetsart University, Chatuchak, Bangkok 10900, Thailand.ORCID 0000-0001-6592-5141
Danail PavlovLaboratory of Nutrigenomics, Functional Foods and Nutraceuticals, Department of Biochemistry, Molecular Medicine and Nutrigenomics, Faculty of Pharmacy, Medical University of Varna, 9002 Varna, Bulgaria.ORCID 0000-0001-7382-2054
Aviva Friedman-EzraInstitute for Drug Research, School of Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem 9112001, Israel.ORCID 0000-0001-6443-6813
Shela GorinsteinInstitute for Drug Research, School of Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem 9112001, Israel.ORCID 0000-0002-0621-8305

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amaranth oil (AMO) and its topical formulation enriched with rose oil (AMOR) were evaluated for anti-inflammatory and cytotoxic properties in skin-relevant models. Two complementary inflammation models were used to assess immunomodulatory potential, (i) LPS-stimulated macrophages and (ii) TNF-α/IFN-γ-stimulated immortalized HaCaT keratinocytes, while cytotoxicity and selectivity were tested on human HaCaT keratinocytes and melanoma cell lines (A375, HTB140). GC-MS and FTIR analyses were performed to confirm the presence of key bioactive compounds (squalene, fatty acids, phenolics). AMOR showed significantly higher polyphenol and palmitic acid content than AMO. In both inflammation models, AMOR more effectively reduced IL-6, IL-1β, and TNF-α release. Cytotoxicity assays revealed that both oils were safe for normal keratinocytes, while selectively cytotoxic to melanoma cells, with AMOR demonstrating greater potency (IC

Indexed as

Anti-Inflammatory AgentsInflammationPlant OilsSkinCell LineCell Line, TumorCell SurvivalHaCaT CellsHumansKeratinocytesMacrophagesAnti-Inflammatory AgentsPlant Oilsamaranth oilcytotoxicityfood for skinhuman serum albumin bindinginflammationrose oilskinskin cancertopical use

Identifiers

PMID41900067
PMCPMC13029062

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.