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Matrixyl (Pal-KTTKS)

Research Use
Also known as Palmitoyl Pentapeptide-4, Pal-KTTKS

Get a source-linked, educational explanation from this profile.

Complete Research Guide

Open each section for the available evidence. Gaps are stated rather than inferred.

Overview

Matrixyl (Pal-KTTKS) is listed as beauty / topical collagen stimulator.

  • •Wrinkles
  • •Dermal collagen support

Regulatory status: Cosmetic ingredient (global).

Structure & Properties

Compound: Matrixyl (Pal-KTTKS); also known as Palmitoyl Pentapeptide-4, Pal-KTTKS.

Pharmacologic class: Beauty / Topical Collagen Stimulator.

Known delivery routes: Topical.

Sequence, molecular weight, salt form, and excipient details are formulation-specific and are not listed unless verified by a manufacturer or laboratory COA.

How It Works

Lipidated pentapeptide derived from procollagen I C-terminus — signals fibroblasts to upregulate collagen I, III, and fibronectin synthesis.

  • •Reduced fine lines
  • •Improved skin density
  • •Well tolerated
Human Research

Evidence grade: Clinical RCT (Limited)

Clinical RCT (Limited). Multiple split-face cosmetic RCTs.

Laboratory Research

Multiple split-face cosmetic RCTs

Preclinical findings describe biological plausibility, not proven benefit in people. Animal and laboratory doses do not translate directly to human use.

Processing & Interactions

Timing and exposure

Topical, 1–2× daily (AM and/or PM). Layer under moisturizer. Avoid same-application vitamin C or strong acids.

Potential interactions and combinations to avoid

  • •Concurrent same-time strong acids/retinoids — separate by 12 hrs

Absorption, half-life, metabolism, and clearance can vary by formulation and route. Use prescribing information when an approved product exists.

Safety & Precautions

Known or reported risks

  • •Mild irritation (rare)
  • •Slow onset (8–12 weeks)

Contraindications

  • •Active dermatitis on application site
  • •Broken, infected, sunburned, or actively inflamed skin
  • •Concurrent prescription retinoid, chemical peel, or laser resurfacing without dermatologic guidance
  • •Known copper sensitivity or Wilson's disease (copper-carrier peptides)
  • •Eczema, rosacea, or perioral dermatitis in active flare
  • •Not FDA-approved for human therapeutic use — no verified purity, sterility, or potency standards
  • •Immunocompromised or transplant patients (unverified sterility and immunogenicity risk)
  • •Concurrent participation in drug-tested sport (WADA prohibited or non-cleared substance)
  • •Known hypersensitivity or prior reaction to this compound or any excipient/diluent
  • •Pregnancy, attempting conception, or breastfeeding unless prescribed and monitored by a physician
  • •Children and adolescents with open growth plates (unless under specialist endocrine care)
  • •Active or recently treated malignancy without oncology clearance
  • •Use without a confirmed diagnosis, baseline labs, and licensed clinical supervision

Unknown long-term toxicity should be assumed where controlled human data are limited. Seek urgent care for a severe or unexpected reaction.

Administration & Studied Formulations

Reference range: 3–5% in topical formulation

Frequency: 1–2× daily

Cycling: Continuous topical use.

Topical

Cosmetic anti-aging.

Serum (3–5% Matrixyl 3000 or Synthe'6). Apply to clean skin AM and PM under moisturizer.

Dosing information is educational context, not a personal recommendation. Approved products must follow their label and prescriber instructions.

Applications & Related Therapies

Potentially complementary measures

  • •Argireline (AM), GHK-Cu (opposite time of day)

Clinical use should account for diagnosis, approved alternatives, nutrition, activity, sleep, rehabilitation, current medicines, and appropriate monitoring.

Cases, Considerations & Ethics

Decision framework: establish the clinical goal, confirm evidence quality and legal status, screen contraindications and interactions, compare approved alternatives, define monitoring and stopping criteria, and use shared decision-making with a licensed clinician.

Case evidence: individual reports cannot establish safety or effectiveness and should not outweigh controlled trials.

Ethics: informed consent should distinguish established care from experimental use, disclose uncertainty and cost, avoid overstated claims, and never substitute research products for medically necessary care.

What is Matrixyl (Pal-KTTKS)?

In plain words

Matrixyl is a short chain of five amino acids, the building blocks of proteins, linked to a fatty acid and used in skin-care products. It can signal skin cells to make more collagen and other proteins that help support skin structure. Researchers study it for reducing wrinkles and supporting skin collagen, but human trial evidence is limited. Mild skin irritation can occur.

Technical definition

Matrixyl (Pal-KTTKS), also called palmitoyl pentapeptide-4, is a lipidated signaling peptide composed of palmitic acid linked to the five-amino-acid sequence lysine–threonine–threonine–lysine–serine, derived from the C-terminal region of type I procollagen. It signals dermal fibroblasts to increase synthesis of collagen types I and III and fibronectin, although a specific receptor has not been firmly established. It is used internationally as a cosmetic ingredient and is not an FDA-approved drug.

Function

Primary
Wrinkles · Dermal collagen support
Mechanism
Lipidated pentapeptide derived from procollagen I C-terminus — signals fibroblasts to upregulate collagen I, III, and fibronectin synthesis.
Evidence
Clinical RCT (Limited)
Research
Multiple split-face cosmetic RCTs

Dosing

Range
3–5% in topical formulation
Frequency
1–2× daily
Route
Topical

Recommended Time of Day

Topical, morning and evening skincare routine.

See “Timing & Interactions” below for full fasted/fed circumstances, what to avoid combining, and what pairs well.

Administration & Technique

Topical
Cosmetic anti-aging.
DeviceSerum (3–5% Matrixyl 3000 or Synthe'6).
TechniqueApply to clean skin AM and PM under moisturizer.

Injection & Application Sites

Front
Back
Topical
  • Face / neck (topical) — Clean dry skin, AM and PM, before moisturizer.

Diagram is a general illustration, not a medical instruction. Rotate sites every injection, keep 1 in (2.5 cm) between recent sites, and avoid scars, moles, bruises and the navel area.

Cycling

Continuous topical use.

Timing & Interactions

When to take
Topical, 1–2× daily (AM and/or PM). Layer under moisturizer. Avoid same-application vitamin C or strong acids.
Do not combine with
  • ·Concurrent same-time strong acids/retinoids — separate by 12 hrs
Complements
  • ·Argireline (AM), GHK-Cu (opposite time of day)

Storage & Reconstitution

Powder (Pre-Reconstitution)
Lyophilized powder: refrigerate 2–8°C for up to 24 months, or freeze at –20°C for extended storage. Keep sealed, desiccated, and protected from light.
After Reconstitution
After reconstitution with bacteriostatic water, refrigerate at 2–8°C and use within 28 days. Discard if cloudy, discolored, or precipitated.
Notes
Do not freeze after reconstitution — freeze/thaw cycles degrade most peptides.
Full BAC water & reconstitution guide →How to read a COA →

Reconstitution Calculator

Concentration
2.50 mg/mL
Volume per dose
0.100 mL
Insulin syringe
10.0 units (U-100)

1 mL = 100 units on a standard U-100 insulin syringe. Draw to the nearest 0.5 unit and confirm dosing with a clinician before injection.

Your Notes

Your Notes

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Benefits

  • ·Reduced fine lines
  • ·Improved skin density
  • ·Well tolerated

Risks

  • ·Mild irritation (rare)
  • ·Slow onset (8–12 weeks)

Contraindications

  • ·Active dermatitis on application site
  • ·Broken, infected, sunburned, or actively inflamed skin
  • ·Concurrent prescription retinoid, chemical peel, or laser resurfacing without dermatologic guidance
  • ·Known copper sensitivity or Wilson's disease (copper-carrier peptides)
  • ·Eczema, rosacea, or perioral dermatitis in active flare
  • ·Not FDA-approved for human therapeutic use — no verified purity, sterility, or potency standards
  • ·Immunocompromised or transplant patients (unverified sterility and immunogenicity risk)
  • ·Concurrent participation in drug-tested sport (WADA prohibited or non-cleared substance)
  • ·Known hypersensitivity or prior reaction to this compound or any excipient/diluent
  • ·Pregnancy, attempting conception, or breastfeeding unless prescribed and monitored by a physician
  • ·Children and adolescents with open growth plates (unless under specialist endocrine care)
  • ·Active or recently treated malignancy without oncology clearance
  • ·Use without a confirmed diagnosis, baseline labs, and licensed clinical supervision

Regulatory

Cosmetic ingredient (global)

Veterinary Use (Pets)

No established veterinary protocol for Matrixyl (Pal-KTTKS). Consult a licensed veterinarian before considering off-label use in any species.

Full veterinary reference →

Functional Groups

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Educational reference only. Not medical advice. Consult a qualified clinician before starting any peptide protocol.

Non-FDA-approved peptides are for research use only. Not for human or animal consumption.