
GHK-Cu (glycyl-L-histidyl-L-lysine copper complex) is a naturally occurring human tripeptide that forms a stable complex with copper(II). It was first isolated from human plasma during studies comparing the biological activity of young plasma (ages 20–25) against older plasma (ages 50–70) on hepatic tissue function. Researchers observed that younger plasma more effectively preserved tissue health — specifically by suppressing fibrinogen synthesis — and traced this protective activity to the tripeptide GHK.
| Component | Detail |
|---|---|
| GHK-Cu (Copper Tripeptide) | 15 mg lyophilized powder per vial |
| Reconstitution diluent | Bacteriostatic water for injection, 6 mL |
| Working concentration | 2.5 mg/mL post-reconstitution |
| Prescribed dose | 20 units (0.20 mL) = 500 mcg per injection |




GHK-Cu is used in integrative, anti-aging, and regenerative medicine as an adjunct peptide therapy. It does not replace conventional dermatological treatment, wound care, or oncological management. Clinical contexts in which providers incorporate GHK-Cu include:
Skin Aging and Rejuvenation: Reduction of fine lines, wrinkles, and skin laxity; improvement of firmness, elasticity, and clarity; smoothing of rough or textured skin; reduction of photodamage, mottled hyperpigmentation, sunspots, and lesions.
Wound Healing: Acceleration of healing in chronic or slow-healing wounds, post-procedural skin recovery, and repair of the skin's protective barrier proteins.
Hair and Scalp: Support for hair follicle health and follicular regeneration, particularly in the context of age-related thinning.
Gastrointestinal and Mucosal Repair: Support for healing of stomach and intestinal lining in conditions involving mucosal compromise.
Bone and Connective Tissue: Stimulation of collagen and GAG synthesis relevant to bone density and connective tissue integrity.
Systemic Anti-Aging and Inflammation Management: Reduction of chronic systemic inflammation, oxidative stress, and fibrinogen burden in patients with elevated cardiovascular or metabolic risk profiles.
Neurological Support: Adjunct use in protocols targeting age-associated cognitive decline, as part of neuroprotective programming; human data is preliminary.
All applications are off-label and investigational. Providers should discuss the experimental nature of GHK-Cu injectable therapy with patients before initiating treatment.
Prescribed dose: 20 units (0.20 mL = 500 mcg) per injection Frequency: Once daily Route: Subcutaneous injection Recommended timing: Evening administration, to align with circadian-driven repair and regenerative activity during sleep Typical cycle: Provider-directed; commonly 4–12 weeks
Reconstitution Instructions:
Allow the lyophilized vial to reach room temperature before handling.
Draw 6 mL of bacteriostatic water into the provided syringe.
Insert the needle into the vial and inject the diluent slowly down the inner wall of the vial — do not inject directly onto the powder cake.
Gently swirl to dissolve. Do not shake — agitation can degrade peptide integrity.
The reconstituted solution should be clear. Do not use if cloudy, discolored, or particulate matter is visible.
Withdraw 20 units (0.20 mL) for each daily injection.
Swab the injection site with an alcohol wipe and allow to dry before injecting.
Administer subcutaneously in the abdomen or upper thigh. Rotate injection sites with each dose.
This compound has not been approved by the FDA for any therapeutic indication. All clinical use is investigational. Long-term safety data from large-scale human trials is not established.
Contraindications and Caution:
Active malignancy: GHK-Cu's gene-modulating and angiogenic activity warrants caution in patients with active cancer. While preclinical data suggests GHK-Cu helps restore normal apoptosis in cancer cells, its use in oncology settings should be coordinated with the treating oncologist.
Copper metabolism disorders (Wilson's disease): GHK-Cu delivers bioavailable copper. Patients with impaired copper metabolism should not use this compound without specialist supervision.
Pregnancy and breastfeeding: Safety data is absent. Use is not recommended.
Pediatric use: Not studied in patients under 18. Safety and dosing are unknown.
Benzyl alcohol sensitivity: The bacteriostatic water diluent contains benzyl alcohol (0.9%). Patients with known benzyl alcohol sensitivity should not use this formulation.
Potential Side Effects: GHK-Cu has a well-established safety profile in topical applications and a favorable reported profile in injectable use. The following have been noted:
Injection site reactions: mild redness, bruising, or transient discomfort
Temporary skin flushing or warmth, consistent with local vasodilatory effects
Mild headache, reported occasionally
Transient fatigue during initial treatment days
Serious adverse effects have not been documented in available reports at therapeutic doses.
Contact your provider immediately if you experience: persistent or worsening injection site reaction, signs of systemic allergic response (hives, difficulty breathing, facial swelling), unusual neurological symptoms, or any symptoms that concern you.
Formal drug interaction studies for injectable GHK-Cu have not been conducted. The following considerations apply based on mechanism:
Copper-chelating agents (D-penicillamine, trientine): Agents used to reduce copper load in conditions such as Wilson's disease would directly antagonize GHK-Cu activity by chelating the copper component. Concomitant use is contraindicated without specialist guidance.
Antioxidant supplementation: High-dose exogenous antioxidants (e.g., high-dose vitamin C, NAC) may theoretically interact with the copper-mediated redox modulation central to GHK-Cu's mechanism. Clinical significance at standard supplemental doses is not established.
Immunosuppressants: GHK-Cu modulates immune and inflammatory gene expression; interactions with systemic immunosuppressive therapy cannot be excluded. Use in immunocompromised patients requires individualized provider evaluation.
No significant interactions with commonly prescribed peptide therapies, hormones, or compounded medications have been identified in available literature.
Before reconstitution (lyophilized vial):
Refrigerate at 36°F – 46°F (2°C – 8°C)
Protect from light; store in original packaging
Do not freeze
Use before labeled expiration date
After reconstitution (bacteriostatic water):
Refrigerate at 36°F – 46°F (2°C – 8°C)
Use within 28 days of reconstitution
Keep vial capped and away from direct light
Discard if solution becomes cloudy, discolored, or shows visible particulate matter

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