ArticleAAPS PharmSciTech2026
Topical 915-3985 MHz Microwave Sweep-Assisted Retention of Nanoemulsified α-Tocopherol for Dermatitis Treatment.
Article in AAPS PharmSciTech, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Being more lipophilic than tocotrienol, tocopherol is anticipated to diffuse into/through skin more than tocotrienol. Microwave sweep treatment of skin may porosify the anatomy and render indifferent permeability regardless of vitamin E lipophilicity. This study explores the microwave sweep (915 to 3985 MHz) impact on skin transport behaviour of nanoemulsified α-tocopherol against nanoemulsified γ-tocotrienol. Physicochemical properties of nanoemulsions and their skin delivery and anti-dermatitis activities were evaluated. Pre-treating skin with 915-3985 MHz microwave sweep formed cavities along epidermal-dermal gradient to retain nanoemulsified α-tocopherol at the expense of skin permeation. In comparison to nanoemulsified γ-tocotrienol, the nanoemulsified α-tocopherol was characterized by higher skin permeation and lower skin retention profiles. The high permeation profile of α-tocopherol was ascribed to facilitated transport by the nanoemulsified structure, higher lipidic character and lower negative zeta potential magnitude undergoing lower skin-nanoemulsion electrostatic repulsion. A higher skin permeation capacity of nanoemulsified α-tocopherol was translated to reduced skin retention and dermatitis healing capacity with reference to transepidermal water loss, skin thickness, suppressive rate, morphology and histological profiles. A high nanoemulsified vitamin E retention in skin, as a function of therapeutic chemistry and microwave sweep, was partly essential to promote the recovery of skin from dermatitis-like inflammation.
Indexed as
Identifiers
41709030What OpenQuestion holds
Registered trials
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.