GoldCosmetica® Platinum Night 14/1 is a high-end cosmetic additive composed of pure platinum powder with embedded platinum leaves (1×1 mm). It is formulated for incorporation into night creams, serums, or masks to support skin rejuvenation.
Application – Designed for evening use in leave-on products (serums, creams, masks) to complement the skin’s natural nighttime repair cycle.
Platinum Night — Scientific Summary
Platinum Night is an active ingredient designed for incorporation into cosmetic formulations at a concentration of 416 mg platinum powder and 416 mg platinum leaf squares (1 × 1 mm) per 1000 ml. Within the field, it is regarded as a well-respected ingredient known for its consistent quality and reproducible performance. When used at the recommended concentrations, Platinum Night primarily supports biological processes associated with skin tightening, improved elasticity, and increased dermal density.
Functional profile
• Mode of action — Acts as a topical active that supports dermal matrix organization and mechanical firmness.
• Primary effects — Skin tightening; enhancement of elasticity; dermal density increase.
• Onset and visibility — Effects are formulation- and usage-dependent; measurable improvements are typically evaluated through biomechanical testing and imaging in controlled studies.
Formulation compatibility and sensory impact
Platinum Night is compatible with common cosmetic bases and does not alter the core physico-chemical properties of the carrier formulation (such as viscosity, emulsion stability, pH, or the performance of other active ingredients). At recommended use levels, its only notable sensory/visual effect is a subtle, homogeneous grayish tint, which is dose-dependent.
Quality and application notes
• Quality — Manufactured to consistent purity standards and accepted by formulators for reliable incorporation.
• Recommended use — incorporate at a concentration of 416 mg platinum powder + 416 mg platinum leaf squares (1 × 1 mm) per 1000 ml. Validate performance within the target formulation; confirm color acceptance in final packaging.
• Testing — Standard in vitro and in vivo assessments are recommended for evaluating tightening, elasticity (e.g., cutometer), and dermal density (e.g., ultrasound or confocal imaging) to substantiate formulation-specific claims.