Matrixyl
/ Synthetic palmitoylated pentapeptide; INCI 'Palmitoyl Pentapeptide-4'; collagen-stimulating cosmetic peptideALIAS · Matrixyl (trade — Sederma) · Palmitoyl Pentapeptide-4 (INCI) · Pal-KTTKS
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Tier 4 by the schema's clinical-evidence ladder, but the most-studied of the palmitoyl cosmetic peptides. Multiple topical-efficacy and dermatology-research papers (Robinson 2005 in International Journal of Cosmetic Science; Watson 2009 cosmeceutical review in British Journal of Dermatology) discuss the ingredient. None are Phase 3 pharmaceutical trials in the regulatory sense.
Pal-KTTKS is the palmitoylated form of the matrikine pentapeptide KTTKS, a fragment of the C-terminal propeptide of type I procollagen. The unconjugated KTTKS pentapeptide stimulates extracellular matrix synthesis (collagen I, collagen III, fibronectin) in cultured dermal fibroblasts; palmitoylation at the N-terminus increases lipophilicity and is intended to improve passive penetration through the stratum corneum when applied topically.
Tier 4. Robinson 2005 (Int J Cosmet Sci) reported a 12-week split-face topical study of Pal-KTTKS in a moisturiser base versus vehicle; the active arm produced greater improvement in fine lines and skin roughness scores by image analysis. Watson 2009 (Br J Dermatol) reviewed Pal-KTTKS in the broader cosmeceutical-peptide context and discussed the pro-collagen-fragment matrikine rationale.
Topical application has been broadly tolerated in published cosmetic-trial settings; no consistent safety signal at typical formulation concentrations (around 3 ppm to a few hundred ppm). No systemic exposure data, which is consistent with the topical small-molecule regulatory framework rather than a clinical safety database.
Regulatory status
- FDA status:
- Not FDA-approved
Most published data on Pal-KTTKS come from industry-collaborated dermatology research; independent academic replication is relatively limited. Effect sizes are modest and image-analysis-driven rather than histological in most clinical-grade studies.