GHK-Cu 1%

Licensed practices only

Glycyl-L-histidyl-L-lysine copper(II) complex

Format
Scalp Solution
Spec
30 mL
Sourcing
A 503A pharmacy licensed by its state Board of Pharmacy

Back to Hair and Scalp Formulations

Available Formulations

Compounded to order by our 503A pharmacy partner; not a dosing recommendation. Beyond-use dates are assigned at compounding and printed on each label, and the shortest applicable limit governs.

Available strengths, sizes, beyond-use dates and per-fill limits
Strength & sizeBeyond-use dateQuantity per fill
Solution 30 mL35 daysMax 1 unit
Compounding standard
USP <795>, non-sterile
Pricing
Available on verified account approval

Molecular structure

Two-dimensional chemical structure of GHK-Cu, as depicted by PubChem
GHK-Cu, two-dimensional structure (PubChem CID 139035031). [1]

Mechanism & Physiological Role

Endogenous tripeptide-copper complex studied in skin remodeling, angiogenesis, hair-follicle biology and matrix metalloproteinase modulation.

Clinical & Research Applications

Topical formulations discussed in dermatologic research on hair-follicle biology and dermal repair. Preclinical literature reports activity in the hair-follicle stem-cell niche and dermal collagen deposition.

Biosynthesis, Handling & Sourcing

GHK is a tripeptide, glycyl-L-histidyl-L-lysine, and almost nothing studied about it concerns the free peptide. Its N-terminal amine, the adjacent peptide nitrogen and the imidazole side chain of the histidine together form a square-planar coordination site with high affinity for copper(II), and it is that complex, written GHK-Cu, which the literature describes. Formulating the peptide without accounting for the metal produces a different substance from the one the published work studied.

The mechanistic literature is largely about matrix turnover rather than about growth. Work reporting modulation of matrix metalloproteinase expression in wound models is now several decades old and has not been substantially revisited, while copper is separately described as a required cofactor for lysyl oxidase, the enzyme that cross-links collagen and elastin. Read together those describe a molecule investigated in the context of remodelling existing matrix, which is a narrower and better supported statement than most marketing copy about copper peptides makes. More recent work has moved toward coordination chemistry and delivery rather than toward new mechanism.

Formulation is where a copper peptide is most easily got wrong, and it is the part a practice can actually inspect. The complex is pH-sensitive and dissociates outside a fairly narrow window; chelating agents common in cosmetic bases will compete for the copper; and reducing agents, ascorbic acid among them, will reduce copper(II) to copper(I) and change the species entirely. A blue-tinted solution is the visible sign that the complex is intact, so a scalp preparation that has lost its color has told you something. These are non-sterile preparations compounded under USP General Chapter 795 with a beyond-use date assigned at preparation.

Most of what is published is in vitro and animal work, with human data concentrated in small dermatologic studies rather than in controlled scalp trials, and the literature on the hair-follicle niche specifically remains preclinical. Nothing on this page is a statement that any preparation is suitable for a given patient. Compounded medications are not FDA-approved finished drug products.

Peer-Reviewed References

Figure sources

  1. [1]PubChem CID 139035031, GHK-Cu. National Center for Biotechnology Information, PubChem. Public domain.

Ready to add GHK-Cu 1% to your protocol?

Compounded formulations are dispensed by our 503A pharmacy partner, licensed by the Texas State Board of Pharmacy, under a valid patient-specific prescription. Prefer a formal quote? Request formulation-specific pricing instead.