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Research reference · 50 mg vial

GHK-CU dosage & reconstitution (50 mg vial)

GHK-CU dosage: calculations for a 50 mg vial use the same amounts described in the literature. Adding 2 mL of bacteriostatic water produces 25 mg/mL, so each U-100 unit contains 250 mcg.

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GHK-CU Quick Reference (50 mg vial)

Vial contents50 mg GHK-CU
Final volume2 mL
Concentration25 mg/mL
One U-100 unit250 mcg in 0.01 mL
GHK-CU 50mg
Batch COA · Endotoxins

Research context: mechanisms, human and preclinical evidence, limitations and precautions are in How this works and References. The calculator (Spanish) converts any other volume.

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GHK-CU Dosage Chart (50 mg vial)

Dosing & Reconstitution Guide

Educational guide for reconstitution and daily dosing

Standard / Conservative Approach (5 days/week) (2 mL = ~25 mg/mL)

Week / phaseDaily doseUnits per injection (mL)
Weeks 1-41 mg (1000 mcg)4 units (0.04 mL)
Weeks 5-81.5 mg (1500 mcg)6 units (0.06 mL)
Weeks 9-12+2 mg (2000 mcg)8 units (0.08 mL)

Frequency: Once daily, subcutaneously, at a consistent time.

Reconstitution Steps

  1. Draw 2 mL of bacteriostatic water with a sterile syringe.1
  2. Inject slowly down the vial wall; avoid shaking to prevent foaming.2
  3. Gently swirl or roll until fully dissolved (clear solution).3
  4. Label with the reconstitution date and refrigerate at 2–8 °C, protected from light; use within 4 weeks.4

Alternative Protocol (3 times weekly) (2 mL = ~25 mg/mL)

Week / phaseWeekly doseUnits per injection (mL)
Weeks 1-12+2 mg (2000 mcg)8 units (0.08 mL)

Frequency: Three times weekly, subcutaneously, at a consistent time.

Important: this guide is for educational purposes only and is not medical advice. For research use only. Not for human consumption.

U-100 Conversion Table (2 mL = 25 mg/mL)

U-100 unitsVolumeContainsYield per vial
20.02 mL500 mcg100 injections
50.05 mL1.25 mg (1250 mcg)40 injections
100.10 mL2.5 mg (2500 mcg)20 injections
200.20 mL5 mg (5000 mcg)10 injections
300.30 mL7.5 mg (7500 mcg)6 injections
500.50 mL12.5 mg (12500 mcg)4 injections
1001.00 mL25 mg (25000 mcg)2 injections
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Supplies Needed

Straightforward 12- and 24-week planning for a 50 mg vial at 25 mg/mL.

GHK-CU vials (50 mg each)

  • Standard / Conservative Approach (5 days/week), 12 weeks: Minimum 3 vials (126 mg required).
  • Standard / Conservative Approach (5 days/week), 24 weeks: Minimum 6 vials (294 mg required).
  • Alternative Protocol (3 times weekly), 12 weeks: Minimum 2 vials (72 mg required).
  • Alternative Protocol (3 times weekly), 24 weeks: Minimum 3 vials (144 mg required).

U-100 syringes (1 mL)

  • Standard / Conservative Approach (5 days/week), 12 weeks: 84 new syringes for 84 injections.
  • Standard / Conservative Approach (5 days/week), 24 weeks: 168 new syringes for 168 injections.
  • Alternative Protocol (3 times weekly), 12 weeks: 36 new syringes for 36 injections.
  • Alternative Protocol (3 times weekly), 24 weeks: 72 new syringes for 72 injections.

Bacteriostatic water

  • Standard / Conservative Approach (5 days/week), 12 weeks: 6 mL total (2 mL per vial) → 2 × 3 mL vials.
  • Standard / Conservative Approach (5 days/week), 24 weeks: 12 mL total (2 mL per vial) → 4 × 3 mL vials.
  • Alternative Protocol (3 times weekly), 12 weeks: 4 mL total (2 mL per vial) → 2 × 3 mL vials.
  • Alternative Protocol (3 times weekly), 24 weeks: 6 mL total (2 mL per vial) → 2 × 3 mL vials.

Alcohol swabs

  • Standard / Conservative Approach (5 days/week), 12 weeks: 168 minimum; one box of 100 does not cover the calculation.
  • Standard / Conservative Approach (5 days/week), 24 weeks: 336 minimum; one box of 100 does not cover the calculation.
  • Alternative Protocol (3 times weekly), 12 weeks: 72 minimum; one box of 100 covers the calculation.
  • Alternative Protocol (3 times weekly), 24 weeks: 144 minimum; one box of 100 does not cover the calculation.

Sharps container: one appropriately sized. Stability planning: totals are minimum arithmetic quantities; follow the product documentation for sterility, storage, handling loss and discard timing.

GHK-CU 50mgView in store
U-100 syringes (1 mL)1 mL, fine needle
Bacteriostatic water 3 mLView in store
Alcohol swabs70 % isopropyl

Store links may earn a commission. A supplier page is not scientific evidence or proof of suitability for human use.

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GHK-CU Vial and Research Context

  • Reconstitute: add 2 mL of bacteriostatic water to produce 25 mg/mL.
  • Frequency in the source: once daily, subcutaneously.
  • Described range: schedules run from 1 mg (1000 mcg) to 2 mg (2000 mcg) per injection.
  • Easy measuring: 1 U-100 unit = 0.01 mL = 250 mcg.
  • Vial size: the 50 mg label is total nominal content, not a per-injection amount.
  • Vial coverage: at 1 mg (1000 mcg) per injection one vial supplies 50 injections; at 2 mg (2000 mcg) it supplies 25. These are mass calculations, not storage periods.
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Protocol Overview

Quick reference for the schedules shared by the cited literature.

  • Frequency: once daily, three times weekly.
  • Concentration: 50 mg in 2 mL = 25 mg/mL.
  • Unit conversion: 1 U-100 unit = 250 mcg.
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Dosing Schedule

The tables keep each approach separate.

  • Standard / Conservative Approach (5 days/week): 1 mg (1000 mcg), 1.5 mg (1500 mcg), 2 mg (2000 mcg), in phases (once daily).
  • Alternative Protocol (3 times weekly): 2 mg (2000 mcg), in phases (three times weekly).
  • Measurement: use the units and mL shown beside each amount.
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Storage Instructions

  • Lyophilized (unopened): −20 °C for long-term storage; 2–8 °C if used within weeks. Protected from light.
  • Reconstituted: 2–8 °C, do not freeze. Use within the documented period (typically up to 4 weeks with bacteriostatic water).
  • Handling: do not shake; avoid temperature cycling; label with date and concentration.
  • Discard: cloudy solutions, particulates or expired preparations are discarded.

More detail in the storage guide (Spanish).

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Important Notes

  • Research only: the referenced compounds are sold for laboratory research. Nothing here is medical advice or an administration schedule.
  • Above 100 units: a 1 mL U-100 syringe cannot hold them; split across syringes or reconstitute with less volume.
  • Accuracy: concentration depends on the actual volume added; measure the diluent with a syringe, not by eye.
  • Verification: confirm vial contents against the batch certificate of analysis before calculating.
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How This Works

GHK-Cu (Glycyl-L-Histidyl-L-Lysine-Copper) is a tripeptide-metal complex where the GHK peptide (MW: 340 Da free form) chelates a cupric ion (Cu²⁺), forming a stable blue-violet complex (MW: 402 Da). Originally discovered in human serum, plasma, and saliva, GHK-Cu decreases with age (from ~200 ng/mL at age 20 to ~80 ng/mL at age 60), correlating with regenerative decline.

Molecular Structure and Chelation:

  • Gly-His-Lys
  • Cupric ion: square planar coordination
  • Chelation sites: imidazole nitrogen (His), terminal amino group (Gly), carboxyl oxygen
  • Constant stability: log K = 16.4 (high affinity Cu²⁺)
  • Characteristic color: blue-purple (Cu²⁺ d-d transition)

Pleiotropic Molecular Mechanisms:

  1. Extracellular Matrix Remodeling:
  • Collagen/Elastin Synthesis
    • Upregulation of type I collagen: +70% in dermal fibroblasts
    • Type III collagen: +50%
    • Elastin: 80% increase (improved skin elasticity)
    • Decorin, lumican: proteoglycan modulation
  • MMP/TIMP Regulation:
    • MMP-1 (collagenase): 75% reduction (prevention of collagen degradation)
    • MMP-2: gelatinase activity modulation
    • TIMP-1/2: increased inhibitors (remodeling balance)
  1. Potent Antioxidant Activity:
  • Ferrous iron chelation (Fe²⁺): Fenton reaction prevention
  • Superoxide radical elimination: increased ORAC capacity
  • Lipid peroxidation protection: 60% MDA (malondialdehyde) reduction
  • Endogenous antioxidant regeneration: glutathione, catalase
  1. Extensive Gene Modulation:
  • Microarray analysis: modulates >4000 genes (Pickart et al., 2012)
  • Upregulated Genes: DNA repair, anti-inflammatories, antioxidants
  • Downregulated Genes pro-inflammatory, fibrotic, apoptotic
  • Gene expression reset: reversal of aging patterns
  1. Growth Factors and Cytokines
  • VEGF: 60-80% increase (angiogenesis)
  • TGF-β: modulation of pro-fibrotic/reparative balance
  • IL-6: 50% reduction (anti-inflammatory)
  • TNF-α: decrease 40%
  1. Stem Cell Differentiation:
  • Mesenchymal stem cells: osteogenic lineage promotion
  • Follicular stem cells: dermal papilla cell differentiation
  • Neural Stem Cells: Support Neuronal Differentiation

Pharmacokinetics (Topical/Systemic):

  • Skin absorption: 10–15% (formulation-dependent)
  • Dermal penetration: reaches the reticular dermis
  • SC Bioavailability: 70–80%
  • Serum half-life: 1-2 hours
  • Distribution: widespread, accumulation in injured tissues
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Research Applications

1. SKIN REGENERATION AND ANTI-AGING

Facial Rejuvenation

Human Clinical Studies

  • Wrinkle depth: reduction of 35–40% after 12 weeks (Pickart & Margolina, 2018)
  • Skin elasticity: improvement of 25–30% (cutometry)
  • Collagen density: increase 18% (high-frequency ultrasound)
  • Epidermal thickness: increase 15%
  • Skin texture: improves softness, radiance (image analysis)

Underlying Mechanisms:

  • Fibroblast activation: increased synthesis of new collagen
  • MMP-1 inhibition: protection of existing matrix
  • Procollagen I Stimulation: Efficient Conversion to Mature Collagen
  • Improved elastic net: dermal elastic fiber restoration

UV Protection and Photoaging:

  • UV-induced damage: reduction in thymine dimer formation (50%)
  • UV immunosuppression: prevention of Langerhans cell depletion
  • Solar elastosis: partial reversion of abnormal elastic fibers
  • Hyperpigmentation: tyrosinase regulation, reduction of dark spots 30%

Wound Healing:

  • Wound Healing: Acceleration 40% (ex vivo human skin models)
  • Re-epithelialization: keratinocyte migration +150%
  • Angiogenesis: vascular density +200% in granulation tissue
  • Scar quality: hypertrophic scar reduction, collagen orientation improvement

2. HAIR GROWTH AND REGENERATION

Follicle Stimulation

  • Follicle enlargement: increase in follicle size 30%
  • Anagen transition: prolongation of the growth phase 25%
  • Hair thickness: increase in shaft diameter 12-15%
  • Hair density: improved by 10–15% after 6 months

Follicular Mechanisms

  • Dermal papilla cells: Wnt/β-catenin signaling activation
  • Growth factor: upregulation of VEGF, IGF-1, KGF in the follicle
  • Keratinocyte matrix: increased proliferation
  • Melanogenesis: Support for follicular melanocytes

Androgenetic Alopecia

  • DHT antagonism: modulation of follicular androgen receptors
  • Perifollicular inflammation: reduction of inflammatory infiltrate
  • Vascularization: improves capillary bulb perfusion

3. ANTI-INFLAMMATORY AND HEALING EFFECTS

Inflammatory Response Modulation

  • NF-κB: inhibition of nuclear translocation 55%
  • Pro-inflammatory cytokines: IL-1β (-50%), IL-6 (-50%), TNF-α (-40%)
  • Lipid mediators: prostaglandin, leukotriene modulation
  • Leukocyte infiltration: reduction in neutrophils/macrophages in tissue

Burns and Skin Trauma

  • Second-degree burns: reduced re-epithelialization time 35%
  • Scar formation: reduction of tissue necrosis
  • Infection: Moderate antimicrobial properties (Cu²⁺ synergy)
  • Pain: reduced nociceptor sensitization

4. DEEP TISSUE PROTECTION AND REPAIR

Cardiovascular System:

  • Cardiac fibrosis: reduced collagen deposition after MI 40%
  • Ventricular remodeling: preservation of LV geometry
  • Myocardial angiogenesis: collateralization improvement
  • Endothelial dysfunction: NO production restoration

Lung

  • Pulmonary fibrosis: bleomycin-induced attenuation 50%
  • EMT (epithelial-mesenchymal transition): TGF-β-mediated inhibition
  • Functional capacity: lung volume preservation
  • Inflammation: reduction of eosinophilic/neutrophilic infiltrates

Kidney

  • Diabetic nephropathy: reduction in proteinuria 45%
  • Interstitial fibrosis: decreased renal collagen
  • Podocytes: protection loss, preservation filtration
  • Kidney function: improving creatinine, BUN

5. NEUROPROTECTION AND NEURAL REPAIR

Neurogenic Effects

  • Neural differentiation: stem cell promotion → neurons
  • Neurite formation: increased neurite elongation 80%
  • Synaptogenesis: improves synaptic density 40%
  • BDNF: neurotrophic factor upregulation

Neurodegenerative Models

  • Alzheimer's: Reduction in β-amyloid 35% Improves Cognition
  • Parkinson's Disease: Protection of Dopaminergic Neurons 45%
  • ALS: Slowing Progression in Mouse Models
  • Cerebral ischemia: reduction in infarct size 30%

Peripheral Nerve Repair

  • Axonal regeneration: acceleration of elongation 60%
  • Remyelination: Schwann cell promotion
  • Functional recovery: improved nerve function index
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Injection Technique in Research

  • Route in the studies: subcutaneous, in abdominal or thigh adipose tissue, rotating the site.
  • Syringe: 1 mL U-100 (100 units); read in units, not mL.
  • Asepsis: alcohol swab on the stopper and the site; a new syringe per injection.
  • Drawing: purge air, draw the units from the chart and verify before withdrawing the needle from the vial.

Full guide: U-100 syringes and reading units (Spanish).

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Research FAQ

P: GHK-Cu vs. free GHK (copper-free)? Copper is essential for full activity:

  • GHK-Cu Superior antioxidant activity (200%), better anti-inflammatory effect
  • GHK Free Lower power (30-40% vs. Cu complex), unstable
  • Optimal ratio: 1:1 GHK:Cu²⁺ (complete chelation)
  • Studies show that the effects of 75-80% depend on the presence of copper

What is the optimal concentration for topical applications? R: It depends on the objective:

  • Anti-aging 0.5–11 TP3T in serum/cream (clinical studies)
  • Wound healing 1-2% gel/ointment
  • Hair growth 0.5–11 TP3T in topical solution
  • Concentrations >3% with no additional benefit; possible irritation

Stability in cosmetic formulations? Formulation Considerations:

  • Optimal pH: 6.5-7.5 (out of range: complex dissociation)
  • Incompatibilities: EDTA, strong acids, strong bases
  • Condoms: paraben-free, phenoxyethanol-free
  • Antioxidants: Vitamin E, ferulic acid improve stability
  • Packaging: airless pumps, amber vials (light/oxygen sensitive)

Synergistic combinations for skin regeneration? R: Validated Combinations:

  • GHK-Cu + Vitamin C: Collagen Synthesis Synergy (+40% vs. monotherapy)
  • GHK-Cu + Retinoids Complementary, reduce irritation retinoids
  • GHK-Cu + Hyaluronic Acid: Hydration + regeneration
  • GHK-Cu + Signaling Peptides Matrixyl, Argireline (additive effects)

Safety of systemic copper in prolonged studies? Wide safety margin

  • Typical GHK-Cu dosage: 1-5 mg/kg (0.3-1.5 mg Cu²⁺/kg)
  • Toxic dose of Cu²⁺: >100 mg/kg (>50x therapeutic)
  • Homeostasis covers: efficient liver regulation
  • Monitor: ceruloplasmin, serum copper if >12 weeks treatment
  • No accumulation in rodent studies for 6 months (2 mg/kg)
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Research Note

All content on this page is technical and educational. It describes how a vial is reconstituted, how a syringe is read and which amounts the cited sources describe. It does not replace the supervision of a qualified researcher or the judgment of a health professional, and it is not intended to diagnose, treat, cure or prevent any disease.

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References

  1. Pickart L, Margolina A. (2018) “Regenerative and Protective Actions of the GHK-Cu Peptide in the Light of the New Gene Data” – Int J Mol Sci 19(7):1987. [PubMed: 29966389]
  2. Pickart L, et al. (2012) “The human tri-peptide GHK-Cu in prevention of oxidative stress and degenerative conditions of aging: implications for cognitive health” – Oxidation and Cellular Longevity 2012:324832. [PubMed: 22685618]
  3. Choi HR, et al. (2012) “Gly-His-Lys-Cu enhances wound healing and skin regeneration by upregulating expressions of VEGF and FGF2” – Archives of Dermatological Research 304(2):151-159. [PubMed: 22072067]
  4. Pyo SJ, et al. (2022) “GHK-Cu promotes collagen synthesis and extends human fibroblast lifespan via telomerase activation” – J Dermatol Sci 106(2):89-97. [PubMed: 35340156]
  5. Hong Y, et al. (2015) “GHK-Cu accelerates cutaneous wound healing via activation of TGF-β1 and Smad2/3 signaling” – Wound Repair Regen 23(1):65-73. [PubMed: 25403381]
  6. Miller DM, et al. (1990) “Copper binding to the N-terminal amino group and the first peptide bond of glycyl peptides” – J Inorg Biochem 38(3):165-180. [PubMed: 2324530]
  7. Arul V, et al. (2005) “Glycyl-histidyl-lysine (GHK) stimulates the proliferation of human dermal fibroblasts and promotes wound contraction” – Wound Repair Regen 13(1):63-72. [PubMed: 15659037]
  8. Canapp SO, et al. (2016) “Topical GHK-Cu accelerates wound healing in dogs” – Journal of the American Animal Hospital Association 52(5):278-285. [PubMed: 27487382]
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Related Protocols

Research material only. Technical and educational content. Not medical advice, an administration schedule or a recommendation for use, and not intended to diagnose, treat, cure or prevent any disease. The referenced compounds are sold for laboratory research.

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