Matrixyl

Matrixyl (palmitoyl pentapeptide-4) is a synthetic lipopeptide that stimulates collagen, collagen IV, and hyaluronic acid synthesis in skin fibroblasts. It is researched for its wound-healing and anti-wrinkle properties.

Matrixyl is a lipopeptide consisting of a palmitic acid chain linked to a pentapeptide sequence (KTTKS). It is one of the most studied cosmetic peptides, discovered through research into wound healing acceleration and wrinkle formation.

Overview

Matrixyl was discovered through two branches of dermatological research: the search for substances that accelerate wound healing and the study of what causes wrinkles. The active peptide sequence KTTKS is derived from the procollagen I C-terminal propeptide, which acts as a feedback signal to stimulate new collagen production. The palmitoyl group was added to enhance skin penetration and bioavailability. In clinical studies, Matrixyl has demonstrated the ability to significantly increase collagen synthesis, collagen IV synthesis, and hyaluronic acid production in skin fibroblasts, leading to measurable reduction in wrinkle depth.

Mechanism of Action

Matrixyl functions as a matrikine -- a peptide fragment of extracellular matrix proteins that signals cells to produce new matrix components. The KTTKS sequence mimics a fragment of type I procollagen, activating fibroblasts through interaction with cell surface receptors involved in matrix remodeling. This stimulates production of collagen types I and IV, fibronectin, and hyaluronic acid. The palmitoyl chain facilitates penetration through the stratum corneum, allowing the peptide to reach the dermal layer where fibroblasts reside. By upregulating matrix synthesis, Matrixyl helps counteract the natural decline in collagen production associated with aging Katayama et al. (1993).

Reconstitution Calculator

Reconstitution Calculator

Calculate your peptide dosing

Draw Volume
0.100mL
Syringe Units
10units
Concentration
2,500mcg/mL
Doses / Vial
20doses
Vial Total
5mg
Waste / Vial
0mcg
Syringe Cap.
100units · 1mL
How to reconstitute
Gather & prepare
1/6Gather & prepare

Set up a clean workspace with all supplies ready.

1.Wash hands thoroughly, put on disposable gloves
2.Your 5mg peptide vial (lyophilized powder)
3.Bacteriostatic water (you'll need 2mL)
4.A 3–5mL syringe with 21–25 gauge needle for reconstitution
5.Alcohol swabs (70% isopropyl)
Use bacteriostatic water (0.9% benzyl alcohol) for multi-dose vials. Sterile water is only safe for single-use.
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$0.00per dose
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Store 2-8°C30 day shelf lifeSwirl gentlyFor research purposes only

Research

In Vitro ECM Stimulation

Fibroblast culture studies established that Pal-KTTKS stimulates procollagen I synthesis at concentrations as low as 1 ppm. Dose-response analysis showed a bell-shaped curve, with optimal stimulation in the 1-10 ppm range. At these concentrations, fibronectin production increased by 117% and collagen synthesis by approximately 350% relative to untreated controls, as reported in Sederma's technical documentation.

Formulation and Stability

Pal-Pentapeptide-4 is stable in typical cosmetic formulations at pH 5.0-6.5. The palmitoyl chain provides adequate emulsion compatibility while maintaining skin penetration. Studies indicate that oil-in-water emulsion bases optimize delivery compared to aqueous solutions or anhydrous formulations.

Matrixyl Evolution

The success of the original Matrixyl led Sederma to develop subsequent generations of the technology. Matrixyl 3000 combined Palmitoyl Tripeptide-1 with Palmitoyl Tetrapeptide-7, adding anti-inflammatory activity to the collagen-stimulating effect. Matrixyl Synthe'6 (Palmitoyl Tripeptide-38) was later introduced to target hyaluronic acid and collagen VI synthesis. Matrixyl Morphomics followed, targeting the adipocyte-fibroblast axis. Each generation built on the matrikine signal peptide concept pioneered by the original Pal-KTTKS.

Clinical Wrinkle Reduction (Robinson et al.)

The landmark study by Robinson et al. (2005) evaluated palmitoyl pentapeptide-4 in a double-blind, placebo-controlled trial. Ninety-three women applied either a Matrixyl-containing moisturizer or vehicle control twice daily to the face for 12 weeks. Profilometric analysis of silicone replicas demonstrated statistically significant reductions in wrinkle depth and roughness parameters in the treatment group. Improvements were noted as early as 4 weeks, with progressive benefit through 12 weeks.

Cosmetic Peptide Landscape

Lintner et al. (2009) reviewed the cosmetic peptide field and positioned Pal-KTTKS as the benchmark signal peptide against which newer entries are compared. The review noted that Matrixyl's clinical evidence base was stronger than most competing peptides at the time of publication.

Wound Healing

Similar to copper peptides, Matrixyl stimulates the lower layers of the skin to heal themselves, accelerating wound closure. Fibroblasts are responsible for knitting together wounds, but with aging they progressively lose the capacity for collagen production. By stimulating fibroblast activity and matrix protein synthesis, Matrixyl helps restore the extracellular environment necessary for efficient wound repair.

Skin Matrix Remodeling

Matrixyl stimulates the "matrix" layers of the skin, primarily collagen and fibronectin. When stimulated, fibroblasts produce more collagen. Loss of collagen leads to thinning skin and wrinkling of newly inelastic skin. The peptide promotes remodeling of the dermal extracellular matrix, helping to restore skin thickness and elasticity that diminish with age.

Collagen Stimulation and Anti-Wrinkle Effects

In clinical studies, Matrixyl has been shown to:

  • Increase overall collagen synthesis by up to 117%
  • Increase collagen IV synthesis by up to 327%
  • Increase hyaluronic acid synthesis by up to 267%

Deep wrinkles were reduced by approximately half, while smaller wrinkles and fine lines sometimes faded completely. Every participant in the study showed noticeable improvement within two weeks Robinson et al. (2005). When combined with other peptides, the results are further enhanced.

Safety Profile

Matrixyl has an excellent safety profile consistent with topical cosmetic peptides. As it is applied topically and acts locally in the skin, systemic exposure is minimal. No significant adverse effects have been reported in clinical studies. The peptide is non-irritating, non-sensitizing, and compatible with a wide range of cosmetic formulations. It does not affect melanin production or cause pigmentation changes. Long-term topical use has not been associated with any safety concerns in published research.

Pharmacokinetic Profile

Half-life
Not established

Quick Start

Route
Topical

Molecular Structure

2D Structure
Matrixyl molecular structure
Molecular Properties
Formula
C39H75N7O10
Weight
802.05 Da
CAS
214047-00-4
PubChem CID
11696273
Exact Mass
365.0760 Da
LogP
2.6
TPSA
139 Ų
H-Bond Donors
2
H-Bond Acceptors
7
Rotatable Bonds
3
Complexity
564
Identifiers (SMILES, InChI)
InChI
InChI=1S/C17H11N5O5/c23-17(15-7-8-18-27-15)19-11-3-1-10(2-4-11)16-20-13-6-5-12(22(25)26)9-14(13)21(16)24/h1-9,24H,(H,19,23)
InChIKeyJDACYFZSJPUBKV-UHFFFAOYSA-N

Research Protocols

topical

Palmitoylation of the N-terminal lysine residue was introduced to enhance lipophilicity and improve skin penetration, transforming an otherwise poorly absorbed hydrophilic peptide into a topically effective cosmetic active.

GoalDoseFrequency
General Research ProtocolSee literatureTwice daily

Interactions

Peptide Interactions

Retinoids (Tretinoin, Retinol)synergistic

Matrixyl stimulates collagen I, III, and fibronectin synthesis via TGF-beta signaling, while retinoids enhance collagen production through RAR/RXR receptor activation and reduce MMP-mediated degradation. The two pathways are complementary, and their combination has shown enhanced anti-wrinkle effects in cosmeceutical studies. (Robinson et al., 2005, Int J Cosmet Sci)

Frequently Asked Questions

References (6)

  1. [4]
    Lintner et al Peptides and proteins in personal care Int. J. Cosmet. Sci. (2009)
  2. [5]
  3. [6]
  4. [7]
  5. [1]
    Katayama et al *J J. Biol. Chem. (1993)
  6. [2]
    Robinson et al *Int Int. J. Cosmet. Sci. (2005)
Updated 2026-03-08Reviewed by Tides Research Team3 citationsSources: peptide-wiki-mdx, pubchem, peptide-wiki-mdx-v2

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