Benefits
Helps Support Skin Elasticity
Dermaval® is positioned as a skin-from-within nutricosmetic that helps maintain elastin integrity by inhibiting elastase activity associated with oxidative and glycemic stress, which may support a firmer, more elastic skin appearance over time.
Provides Polyphenol Antioxidant Support
The blended fruit and herbal concentrates deliver a broad mix of anthocyanins, betacyanins, catechins, and flavonoids, which contribute to overall antioxidant defense and help neutralize reactive oxygen species generated by sun, pollution, and high-glycemic meals.
May Support a Youthful Complexion
By targeting enzymes that break down structural skin proteins like elastin and collagen, Dermaval® is formulated to support skin smoothness, suppleness, and a youthful look as part of an inside-out beauty regimen.
Convenient Low-Dose Beauty Blend
Standardized to deliver meaningful polyphenol activity at just 50 mg, Dermaval® fits easily into capsules, gummies, drink mixes, and skin-focused multivitamins without contributing significant calories or flavor.
Mechanism of action
Human Neutrophil Elastase Inhibition
In vitro and acute human work indicates that Dermaval® polyphenols inhibit HNE, a serine protease that cleaves elastin in the dermal extracellular matrix during inflammation and after glucose challenges.
Reactive Oxygen Species Quenching
Anthocyanins, betacyanins, and catechins in the blend donate electrons to free radicals generated by UV exposure and metabolic stress, supporting cellular redox balance in skin and circulating cells.
AGE-Related Skin Stress Modulation
By blunting the post-meal HNE spike that follows glucose intake, the blend is theorized to limit one downstream pathway by which dietary sugar can contribute to elastin breakdown and skin aging.
Clinical trials
Randomized, double-blind, crossover trial; single 50 mg dose of Dermaval® or placebo before a glucose challenge
20 healthy adult volunteers
A single 50 mg dose of the polyphenol blend significantly blunted the glucose-induced rise in circulating human neutrophil elastase activity at 60 and 120 minutes post-ingestion compared with placebo, supporting the proposed elastin-sparing mechanism.