cat. no. GHK-CU
GHK-Cu
Copper-binding tripeptide (Gly-His-Lys complexed with Cu2+) - a naturally occurring human plasma peptide produced synthetically for cosmetic, wound-care and research use
also: Copper Tripeptide-1 / Glycyl-L-Histidyl-L-Lysine Copper(II) / Cu-GHK / Copper Peptide
At a glance
What it is
GHK-Cu is a tiny naturally occurring piece of protein - three amino acids (glycine, histidine, lysine) - that grabs a copper ion and carries it into tissue. The body makes it naturally, and blood levels fall with age, from roughly 200 ng/mL around age 20 down to about 80 ng/mL by 60, which is part of why it got tied to anti-aging research in the first place. Once copper is delivered, GHK-Cu switches on a large set of genes involved in tissue repair, and it directly prompts fibroblasts (the cells that build skin) to make more collagen, elastin and other structural matrix, while also helping clear out damaged matrix through controlled enzyme activity. That build-and-remodel combination is why it shows up in wound-healing research (faster wound contraction and granulation tissue in animal studies) and in skincare (creams and serums aimed at fine lines and skin density). The strongest, most repeated evidence is topical: cosmetic-science and skin-penetration studies where GHK-Cu is applied to skin and shown to form a copper depot in tissue that lingers well after it clears from blood. Injectable use is a different picture - popular in peptide communities for skin, hair and recovery goals, but that dosing is extrapolated from lab cell-culture data rather than human injection trials, and a 2024 academic review notes FDA flagged compounded injectable GHK-Cu for a safety-risk review. Treat topical and injectable GHK-Cu as two separate evidence pictures under one name.
Dose ranges
Study-backed ranges carry a source you can open. Community ranges are widely reported but not clinically established - treat them as what people do, not as advice.
In vitro human skin penetration/retention study, dermatomed skin, diffusion cells (topical)
study0.68 % aqueous solution
single application, measured over 48 hours
Human dermal fibroblast cell-culture studies (mechanistic - not a finished topical product dose)
study1-10 nM
single in vitro incubation
Preclinical intra-articular injection (mouse study)
study0.3 mg/mL
per injection, per study protocol
Cosmetic/skincare formulation inclusion rate (topical serums, creams - industry guidance)
community0.05-0.1 % w/w
formulated into a daily-use product
Community-reported human injectable self-dosing (skin, hair, recovery goals)
community1.7-3 mg/day
daily, subcutaneous, commonly cycled 8 weeks on / 8 weeks off
Reconstitution & storage
Vendor convention, not a manufacturer or clinical standard - no FDA-approved GHK-Cu drug product exists. A common chart uses 2 mL bacteriostatic water across 50/100/200 mg vials (about 25/50/100 mg/mL). Let the vial reach room temperature, direct the water at the inside wall rather than the powder, and swirl gently rather than shaking. Refrigerate immediately after mixing.
Lyophilized
Vendor/community guidance: keep sealed powder cold and dark. Cited stability is roughly 12-18 months refrigerated (2-8C), 18-24 months frozen at -20C, up to about 3 years at -80C, and only 2-4 months at room temperature. The copper ion is photochemically light-sensitive and the peptide chain can be degraded by UV, so vendors recommend amber vials or a dark box even for brief handling.
Reconstituted
Vendor/community guidance: refrigerate at 2-8C; commonly cited stability is about 28-30 days with bacteriostatic water, or within 24 hours if mixed with plain sterile water instead. Avoid freezing reconstituted solution - community sources warn ice crystals can shear the peptide bonds apart.
Common stacks
Interactions & cautions
No human drug-interaction trials exist for GHK-Cu - what follows is reasoned pharmacology and secondary regulatory reporting, not clinical guidance. Because GHK-Cu's job is delivering bioavailable copper into tissue, combining it with copper-chelation therapy (penicillamine, trientine, or similar drugs used for Wilson's disease or copper overload) is a direct pharmacological conflict - one delivers copper, the other is designed to strip it out - so anyone on chelation therapy or with a diagnosed copper-handling disorder should avoid it and check with their doctor first; this is basic toxicology reasoning, not a documented GHK-Cu-specific interaction study. A 2024 narrative review (Yale Journal of Biology and Medicine) reports that FDA placed GHK-Cu on a list of bulk drug substances flagged for significant safety risk in compounding, citing immunogenicity and impurity concerns specific to the injectable route - note that FDA's compounding bulks lists are revised periodically and a direct fetch of FDA's own list page 404'd for us, so this should be read as the 2024 review's characterization rather than a live regulatory lookup. Topical/cosmetic GHK-Cu has decades of reported use with no adverse effects noted in a 2018 review, though individual skin irritation is always possible with any active cosmetic ingredient. It is not FDA-approved as a drug for any indication or route.
Questions people ask
Does the research on GHK-Cu apply to injecting it, or only to putting it on skin?
Mostly to skin. Nearly all of the controlled study data we could verify - cell-culture collagen studies, animal wound-healing work, and the human skin-penetration research - used topical application. Injectable GHK-Cu is popular in peptide communities but its dosing is extrapolated from lab data, not from human injection trials, so treat the two routes as separate evidence pictures.
Why do different sites list such different half-life numbers for GHK-Cu?
Because no single human study has nailed it down. The two most thorough peer-reviewed reviews we checked neither report a half-life value. Community and vendor sites cite anywhere from about 30 to 105 minutes without pointing to a source study. What is better documented is that topical GHK-Cu forms a copper depot in skin tissue that outlasts however long it circulates in blood.
Can I use GHK-Cu if I have Wilson's disease or another copper-handling condition?
This needs a doctor's input, not a peptide vendor's advice. GHK-Cu's entire job is delivering bioavailable copper into tissue, which runs directly against the goal of copper-chelation therapy and copper-overload conditions. There is no GHK-Cu-specific study on this - it is straightforward toxicology reasoning, not documented clinical data.
Is injectable GHK-Cu FDA-approved or backed by clinical trials?
No. There is no FDA-approved GHK-Cu drug product for any route. A 2024 academic review reported that FDA had flagged GHK-Cu on a list of bulk substances with significant compounding safety risk, citing immunogenicity and impurity concerns for the injectable form specifically - though these compounding lists are revised periodically, so check current status with a pharmacist rather than relying on any single snapshot, including this one.
What is the 'GLOW stack' people mention with GHK-Cu?
It's a vendor-marketed combination of GHK-Cu with BPC-157 and TB-500, sold as a bundle aimed at skin, healing and recovery together. Each peptide has its own separate research base; we could not find a dedicated clinical trial on the three combined, so treat the pairing as a community/vendor convention rather than a studied protocol.
Sources
- [1]Regenerative and Protective Actions of the GHK-Cu Peptide in the Light of the New Gene Data PMID 29986520reviewDescribes GHK-Cu stimulating collagen, glycosaminoglycan and decorin synthesis and modulating MMP/TIMP activity, reports human plasma GHK falling from about 200 ng/mL at age 20 to 80 ng/mL by age 60, and states decades of cosmetic use show no adverse effects; it does not report a half-life value.
- [2]GHK Peptide as a Natural Modulator of Multiple Cellular Pathways in Skin Regeneration PMID 26236730reviewReports GHK-Cu activates TGF-beta and integrin signaling in fibroblasts, stimulates collagen/dermatan sulfate/chondroitin sulfate/decorin at 1-10 nM in fibroblast studies, reduces TNF-alpha-induced IL-6, and penetrates the stratum corneum; states no half-life is reported in the review.
- [3]Local and Systemic Peptide Therapies for Soft Tissue Regeneration: A Narrative Review PMID 39351323reviewStates topical GHK improved wound contraction and granulation tissue formation in full-thickness rabbit wounds while reducing TNF-alpha, MMP-2 and MMP-9, cites a 0.3 mg/mL GHK-Cu dose used in mouse intra-articular injection studies, and reports GHK-Cu was placed on an FDA list of bulk drug substances flagged for significant compounding safety risk, citing immunogenicity and impurity concerns for the injectable route.
- [4]Human skin retention and penetration of a copper tripeptide in vitro as function of skin layer towards anti-inflammatory therapy PMID 20703511studyIn vitro human skin diffusion-cell study using a 0.68% aqueous GHK-Cu solution found a permeability coefficient of 2.43x10^-4 cm/h through dermatomed skin, with 136.2 mcg/cm2 of copper permeating and 82 mcg/cm2 retained in tissue as a depot over 48 hours.
- [5]GHK-Cu Reconstitution: 50mg + 2mL ChartcommunityVendor/community guide reporting common 50/100/200 mg vial sizes reconstituted with 2 mL bacteriostatic water, a swirl-not-shake technique, immediate refrigeration at 2-8C, and about 28 days of stability once mixed.
- [6]GHK-Cu Dosage Chart: Injectable ProtocolcommunityStates injectable GHK-Cu dosing (roughly 1.7-3 mg/day subcutaneous, commonly 8 weeks on / 8 weeks off) is entirely community-developed and extrapolated from cell-culture bioactivity data, explicitly noting injectable GHK-Cu has no human trials, unlike topical use.
- [7]Copper Tripeptide-1 (GHK-Cu): The Premier Anti-Aging Ingredient for Skincare FormulatorscommunityIngredient-manufacturer guidance recommending 0.05-0.1% w/w as a typical starting inclusion rate for GHK-Cu in cosmetic formulations, to be stored in cool, dark conditions.
- [8]GHK-Cu Storage Guide: Temperature, Shelf Life & HandlingcommunityVendor storage guide reporting lyophilized GHK-Cu stability of about 12-18 months refrigerated (2-8C), 18-24 months frozen at -20C, and up to 3 years at -80C; reconstituted solution about 28-30 days refrigerated; and that UV light and the copper ion's photochemical sensitivity require dark or amber-vial storage.
- [9]GHK-Cu: Copper Content, Half-Life & Skin Repair ResearchcommunityCommunity pharmacokinetics reference listing an approximate 105-minute plasma half-life without attributing it to a specific study, alongside a note that topical application produces prolonged tissue retention versus plasma clearance.
What we could not verify
examine.com returned 403 (no reachable GHK-Cu page) and is not cited. A direct fetch of FDA's 'Certain Bulk Drug Substances...Significant Safety Risks' list page 404'd, so the FDA compounding-flag claim is sourced only through a secondary 2024 review (PMC11426299) and not confirmed against fda.gov's current live list - compounding categories are revised periodically (community sources reference an April 2026 revision removing some peptides), so treat GHK-Cu's regulatory status as unconfirmed-current rather than settled. mdpi.com/2079-9284/5/2/29 (Skin Regenerative and Anti-Cancer Actions of Copper Peptides) and medsci.org/v22p4175.htm both failed to load (403/404) and are not cited despite looking relevant. A Walsh Medical Media PDF describing a GHK-Cu facial-cream trial with MMP/TIMP and wrinkle-parameter data would not extract as readable text, so its specific numbers are omitted rather than guessed. A widely-repeated claim of a 2015 'Clinical, Cosmetic and Investigational Dermatology' trial in 71 photodamaged women, and a separate claim of a '2023 safety review of 12 studies/512 participants' citing 4.2% transient redness, both appeared only inside AI-generated web-search summaries with no page we could independently fetch and verify - both are deliberately excluded rather than cited secondhand. No confirmed, study-attributed human half-life exists; the 105-minute figure and the 30-60 minute range seen elsewhere are both vendor/community claims with no primary study attribution we could locate.