Product Overview

GHK-Cu

GHK-Cu (glycyl-L-histidyl-L-lysine copper) is an endogenous tripeptide–copper complex with broad regenerative and reparative properties. GHK is present in plasma, saliva, and urine, but levels decline with age. GHK-Cu forms via high-affinity binding of GHK to copper(II), a physiologically relevant process for wound healing and skin regeneration.[1–4]

Mechanism of Action & Cellular Effects

  • Modulates skin-regeneration pathways: stimulates collagen, elastin, glycosaminoglycan, and decorin; regulates MMPs and their inhibitors.[1][5–7]
  • Promotes dermal fibroblast/keratinocyte proliferation and migration, enhances angiogenesis (VEGF activation), and recruits immune/endothelial cells to injury sites.[1][3–5][8–10]
  • Anti-inflammatory/antioxidant: suppresses free radicals, thromboxane, and pro-inflammatory cytokines; increases SOD and vasodilation.[3][11]
  • Gene modulation: up-/down-regulates thousands of human genes involved in DNA repair, proteasome activation, and suppression of tissue-destructive/cancer-promoting genes.[2][5][11]

Clinical & Translational Evidence

  • Accelerates healing in skin, hair follicles, GI tract, bone, and other tissues in animal and human studies.[1][3–6][8–10]
  • In aged skin: improves tightness, elasticity, density, firmness; reduces fine lines, wrinkles, photodamage, and hyperpigmentation.[1][3][12]
  • Increases integrin expression and p63 positivity in keratinocytes → supports stem-cell survival and barrier repair.[4][12]
  • Advanced delivery (nanoengineered/liposomal) enhances stability, bioactivity, and wound-healing efficacy.[8–10]
  • Protective effects in models of liver injury, GI ulcers, and bone healing; under investigation for skin inflammation, COPD, and metastatic colon cancer.[1–5]

Safety & Tolerability

  • Long history of safe use in wound care and skincare with no significant adverse effects in clinical/preclinical studies.[1][11][12]

Summary: GHK-Cu (100 mg) is a multifunctional peptide–copper complex that accelerates wound healing, drives tissue regeneration, reduces inflammation/oxidative stress, and broadly shifts gene expression toward a reparative phenotype—supporting uses across dermatology, regenerative medicine, and potential systemic applications.[1–12]

References

  1. Pickart L, Vasquez-Soltero JM, Margolina A. Biomed Res Int. 2015:648108.
  2. Pickart L, Vasquez-Soltero JM, Margolina A. Biomed Res Int. 2014:151479.
  3. Pickart L. J Biomater Sci Polym Ed. 2008;19(8):969-88.
  4. Kang YA, Choi HR, Na JI, et al. Arch Dermatol Res. 2009;301(4):301-6.
  5. Pickart L, Margolina A. Int J Mol Sci. 2018;19(7):E1987.
  6. Siméon A, Wegrowski Y, Bontemps Y, Maquart FX. J Invest Dermatol. 2000;115(6):962-8.
  7. Siméon A, Emonard H, Hornebeck W, Maquart FX. Life Sci. 2000;67(18):2257-65.
  8. Lee S, Lee SM, Lee SH, et al. Acta Biomater. 2023;172:159-174.
  9. Castro VIB, Araújo AR, Reis RL, et al. ACS Appl Mater Interfaces. 2025;17(8):11624-11633.
  10. Wang X, Liu B, Xu Q, et al. Wound Repair Regen. 2017;25(2):270-278.
  11. Pickart L, Vasquez-Soltero JM, Margolina A. Oxid Med Cell Longev. 2012:324832.
  12. He B, Wang F, Qu L. Front Pharmacol. 2023;14:1267765.

ALL ARTICLES AND PRODUCT INFORMATION PROVIDED ON THIS WEBSITE ARE FOR INFORMATIONAL AND EDUCATIONAL PURPOSES ONLY. The products offered on this website are furnished for in-vitro studies only. In-vitro studies (Latin: in glass) are performed outside of the body. These products are not medicines or drugs and have not been approved by the FDA to prevent, treat or cure any medical condition, ailment or disease. Bodily introduction of any kind into humans or animals is strictly forbidden by law.