原料辞典検索/copper-tripeptide-1/COPPER TRIPEPTIDE-1
Tier 1 Monograph · SSOT 15 FieldsRaw .md (GEO) ↗
ペプチド・タンパク質 (Peptide)

COPPER TRIPEPTIDE-1

標準 INCI 準拠: COPPER TRIPEPTIDE-1
皮膚コンディショニング剤
[EU CosIng Official Definition] Copper Tripeptide-1 is a copper complex of Tripeptide-1
結論先行 エグゼクティブ規制・安全性ファクトボックスAEO / GEO CITATION ANCHOR

化粧品における COPPER TRIPEPTIDE-1 のグローバル配合基準と処方特性とは?

COPPER TRIPEPTIDE-1(CAS番号: N/A)は、化粧品処方において主に皮膚コンディショニング剤として配合される原料です。日本厚労省/JCIA(規制なし)、韓国MFDS(規制なし)、欧州CosIng(規制なし)など6大法域の法定基準下で管理され、通常 0.01–0.2%(適正安定域 pH 5.5–7)で処方されます。

7大トラック 国別・用途別 公式全成分表示名称マトリクス

各国公的告示原典のみ収録 · 機械翻訳・任意音訳ゼロ
7-Track Official Statutory Label Names for COPPER TRIPEPTIDE-1
法域・規制トラック公式全成分表示名称ワンクリックコピー
① 韓国 (MFDS 化粧品標準名称)COPPER TRIPEPTIDE-1 (KR MFDS Registered)
② 韓国旧名称履歴 (301 リダイレクト)Former KR Nomenclature Redirect Active—
③ 欧州連合 (EU CosIng EC 1223/2009)COPPER TRIPEPTIDE-1
④ 米国一般化粧品 (US PCPC / MoCRA INCI)COPPER TRIPEPTIDE-1
⑤ 米国 FDA OTC モノグラフ有効成分名— (米国 OTC 対象外 / 一般化粧品原料)—
⑥ 中国 (NMPA IECIC 標準中国語名称)三肽-1 铜
⑦ 日本化粧品表示名称 / 医薬部外品外原規名称 (JCIA / MHLW)COPPER TRIPEPTIDE-1 (標準INCI参照 · 任意カタカナ音訳排除)

Layer 1 — 6大法域 法定配合上限および規制ステータス

Layer 1 Statutory Regulatory Limits Across 6 Regions for COPPER TRIPEPTIDE-1
法域規制ステータス配合上限制限条件および一次法源出典
韓国 (MFDS)規制なしGMP公的化粧品原料目録収載 (GMP基準内使用)
欧州 (EU)規制なしGMP公的化粧品原料目録収載 (GMP基準内使用)
米国 (FDA)規制なしGMP公的化粧品原料目録収載 (GMP基準内使用)
中国 (NMPA)配合可能GMPIECIC Entry #5807
日本 (MHLW)規制なしGMP公的化粧品原料目録収載 (GMP基準内使用)
ASEAN (ACD)規制なしGMP公的化粧品原料目録収載 (GMP基準内使用)

Layer 2 — 毒性・安全性評価上限 (US CIR / EU SCCS / CN IECIC)

「欧州 SCCS 安全性評価上限」は消費者安全科学委員会が安全域 (MoS≥100) と判定した毒性学的上限であり、「米国 CIR 市販製品最大報告濃度」および「中国 IECIC 最高歴史使用量」は市販製品における最大実績濃度です。

Layer 2 Toxicological & Historical Safe Use Concentrations for COPPER TRIPEPTIDE-1
安全性評価基準適用範囲・用途安全濃度範囲判定結果および文献参照
中国 IECIC 最高歴史使用量leave_on≤ 0.5%安全判定 (MoS≥100)NMPA IECIC (2025) Entry 05915 (2025)
中国 IECIC 最高歴史使用量rinse_off≤ 0.2%安全判定 (MoS≥100)NMPA IECIC (2025) Entry 05915 (2025)
⚠️ 参考用案内 (免責事項): 本辞典の成分名・規制上限・処方ガイドは研究開発の参考用です。法改正の時差やデータの誤記・漏れがあり得るため、実際の処方・ラベル表示・届出前には必ず管轄当局の最新告示原文をご確認ください。本情報の利用により生じた問題について運営主体は法的責任を負いません。
Interactive Quartile Box-Plot (Min–Q1–Median–Q3–Max)

Layer 3 Formulation Concentration Box-Plot vs. Statutory Limit

Aqueous Serum / Ampoulen=38
Min 0.01% · Q1 0.02% · Median 0.05% · Q3 0.1% · Max 0.2%
Emulsion / Creamn=35
Min 0.01% · Q1 0.02% · Median 0.05% · Q3 0.1% · Max 0.2%
Aqueous Serum / Ampoule — Copper-delivering matrikine peptide for collagen remodeling & anti-inflammation (GHK-Cu)
Verified Source: Pickart et al. PubMed GHK-Cu Monograph & CN IECIC (pubmed) · Active Peptide · Vincience · Corum
Typical Median: 0.05%

Layer 3 — 剤形別通常配合濃度 (四分位数 n≥5) & 物理化学・相溶性ガイド

Layer 3 Formulation Concentration Quartiles by Product Category for COPPER TRIPEPTIDE-1
剤形グループMin – Q1 – Median – Q3 – Max (%)処方役割・作用機序Source ID
剤形群 A — 水성化粧水・美容液・アンプル0.01% · 0.02% · 0.05% · 0.1% · 0.2%Copper-delivering matrikine peptide for collagen remodeling & anti-inflammation (GHK-Cu)Pickart et al. PubMed GHK-Cu Monograph & CN IECIC
剤形群 B — 乳液・エマルジョン・クリーム0.01% · 0.02% · 0.05% · 0.1% · 0.2%Dermal remodeling & barrier repair peptidePubMed GHK-Cu Studies & CN IECIC
Cutaneous Permeation Science (500 Dalton Rule)MW: 403.92 Da · LogP: -4.5

Stratum Corneum Penetration Depth & Bio-Spicule Transdermal Delivery

Stratum Corneum (Brick & Mortar Barrier · 10–20 µm)500 Da Molecular Weight Cutoff BarrierViable Epidermis (Keratinocytes & Melanocytes · 50–100 µm)Target for Brightening (Tyrosinase/Melanosome) & Barrier LipidsPapillary Dermis (Fibroblasts & ECM Collagen · 150–300 µm)Target for Collagen I/III Synthesis, Peptides, PDRN & ExosomesEpidermal Passive Permeation (<500 Da)
Molecular Weight & LogP Permeation Diagnosis
Low Molecular Weight (403.92 Da ≤ 500 Da) — Passive Permeation Feasible

Under passive topical application, molecules diffuse tortuously through intercellular lipids. Hydrophilic compounds >500 Da remain primarily on the outer stratum corneum.

Estimated Target Depth
40–90 µm
Optimal Delivery System
Polyol Enhancer / Serum
Colloid Interface, pH Spectrum & Thermal Stability

pH Stability Window (0–14), Thermal Limit & HLB Colloidal Phase Behavior

Freely soluble in water (imparts natural royal blue color)
Optimal Formulation pH Stability Window (0–14)pH 5.5 – 7.0
0245.5791114

Outside pH 5.5–7, risk of hydrolysis, viscosity loss, or ionic dissociation increases.

Maximum Thermal Processing Limit (°C)≤ 45°C
25°C45°C60°C75°C85°C100°C

Thermolabile active: Must be added during post-emulsification Cool-down Phase (<40–45°C).

HLB Scale (0–20) & Colloidal Micelle / Lamellar Phase Simulator
O/W Oil-in-Water Micelle Emulsion (Lotion / Cream)
HLB 11.5
W/O (3–6)Lamellar (8–10.5)O/W Emulsion (11–15)Solubilizer (15–19)O/W Droplet
Biochemical Signaling & Mechanism Pathway

Cellular & Molecular Target Mechanism Flow

1. Epidermal Interaction→ Upregulation / Activation
Intercellular Lipid & Hydration Matrix
→
TEWL Reduction & Barrier Conditioning
2. Homeostasis Modulation⊣ Inhibition / Blockade
Oxidative Stress (ROS) & Irritant Cascade
⊣
Cutaneous Soothing & Homeostasis
Formulation Ontology Radial Graph

Interactive Synergy Pairings (Solid) & Incompatibility Warnings (Dashed)

+ SODIUM HYALURONATE+ PANTHENOL+ ECTOIN+ HYDROXYETHYLCELLUL…+ HYDROLYZED SPONGE✕ CRITICAL INCOMPATIBI…✕ CRITICAL INCOMPATIBI…COPPER TRIPEPTIDE-1
Interactive Node Guide

Click any green synergy node to jump directly to its monograph, or click a red dashed node to inspect the chemical incompatibility mechanism.

代表商品名参考 (商標法第90条第1項第2号 記述的表示)
Prezatide Copper AcetateGHK-Cu Pure Powder

商品名は研究者がグレードを識別するための参考表記であり、各商標権は原メーカーに帰属します。

学術・毒性・処方統合モノグラフ

Tier 1 Synthesis

本原料に紐づく NIH PubMed 査読付き論文アブストラクトおよび公的毒性評価報告書のみに基づいて作成された学術要約です。

■ [1. Chemical Identity & International Labeling Nomenclature] - INCI Name: COPPER TRIPEPTIDE-1 | CAS No.: N/A | EC No.: N/A - Origin: PEPTIDE | Functions: Skin Conditioning - Physicochemical Profile: Formula C14H22CuN6O4 | MW 403.92 g/mol | LogP -4.5 | Ionic Nature: cationic | PubChem CID 9941957 - Official Regional Label Names: US [COPPER TRIPEPTIDE-1] · EU [COPPER TRIPEPTIDE-1] · CN [三肽-1 铜] · JP [-] · JP Quasi-Drug [-] ■ [2. Dermatological Mechanism of Action & Functional Role] - Naturally occurring matrikine tripeptide-copper complex (GHK-Cu) that delivers bioavailable Cu2+ into dermal cells. Upregulates superoxide dismutase (SOD), lysyl oxidase, Type I collagen, decorin, and glycosaminoglycan synthesis while modulating wound-healing and anti-inflammatory gene networks. ■ [3. Global 6-Jurisdiction Regulatory Status & Safety Limits (Layer 1 & Layer 2)] - Regional Summary: KR: NONE | EU: NONE | US: NONE | CN: ALLOWED | JP: NONE | ASEAN: NONE (CN IECIC (2025) Entry No. 5807 (三肽-1 铜)) - No specific Annex prohibition or numeric restriction across the 6 major jurisdictions (Permitted under general GMP safety assessment). - Official Safety & Historical Use Concentration (Layer 2): CN_IECIC_2025 (cn_iecic_max, leave_on): Max 0.5% / CN_IECIC_2025 (cn_iecic_max, rinse_off): Max 0.2% ■ [4. Formulation Dosage Guide by Product Category (Layer 3-A)] - [aqueous_serum] Typical range: 0.01 ~ 0.2% (Median 0.05%, Ref: Pickart et al. PubMed GHK-Cu Monograph & CN IECIC) — Copper-delivering matrikine peptide for collagen remodeling & anti-inflammation (GHK-Cu) - [emulsion_cream] Typical range: 0.01 ~ 0.2% (Median 0.05%, Ref: PubMed GHK-Cu Studies & CN IECIC) — Dermal remodeling & barrier repair peptide ■ [5. Formulation Engineering, Stability & Incompatibility Matrix (Layer 3-B)] - Addition Phase: Final Cool-down Phase (< 40°C) - Optimal pH Range: pH 5.5 ~ 7.0 | Max Process Temp: Max 45°C | Electrolyte Tolerance: LOW - Incompatibility / Caution: CRITICAL INCOMPATIBILITY 1: Never use with chelating agents (Disodium EDTA, Sodium Phytate, Caprylhydroxamic Acid), which strip Cu2+ from the peptide, turning the blue solution green/brown and deactivating it - Incompatibility / Caution: CRITICAL INCOMPATIBILITY 2: Incompatible with Ascorbic Acid, strong acids (AHA/BHA, pH < 5.0), and Carbomer; formulate at pH 5.5~7.0 using non-ionic thickeners (HEC, Sclerotium Gum) - Synergy Pairings: SODIUM HYALURONATE, PANTHENOL, ECTOIN, HYDROXYETHYLCELLULOSE, HYDROLYZED SPONGE | Reference Trade Names: Prezatide Copper Acetate, GHK-Cu Pure Powder ■ [6. Peer-Reviewed Literature & Official Compendia Evidence] - PMID 42193036 (2026, Curr Issues Mol Biol): Multi-Target Restoration of Dermal Elastic Fibers Through Elastin Upregulation, Elastase Suppression, and Scaffold Reinf - PMID 41001334 (2025, Cureus): Efficacy and Safety Assessment of ThriveCo Scar Fader Gel With Scarcede™ in the Treatment of Skin Scars - PMID 39449909 (2024, Cureus): An Assessment of the Safety, Efficacy, and Tolerability of a Novel Scalp Treatment Regimen Combining a Hydroxy Acid-Base

関連査読付き学術論文 (NIH PubMed) (9)

Multi-Target Restoration of Dermal Elastic Fibers Through Elastin Upregulation, Elastase Suppression, and Scaffold Reinforcement [PMID: 42193036 · 2026]
Ye S, Kang S, Jeong ET, Jun SH, Kang NG · Curr Issues Mol Biol (2026)

Elastic fibers are key components of the skin extracellular matrix and are essential for maintaining skin integrity and elasticity. During skin aging, particularly photoaging, elastic fiber integrity is progressively compromised by increased elastase activity and the downregulation of elastin and scaffold-related gene expression. Therefore, effective strategies to preserve elastic fiber function should address not only elastin synthesis but also enzymatic degradation and scaffold integrity. In this study, we investigated a multitarget approach to restoring the elastic fiber network by modulating elastin production, elastase activity, and scaffold protein expression. We found that Copper Tripeptide-1 enhanced elastin expression and secretion, ethyl ferulate inhibited elastase activity, and cedrol promoted scaffold-related gene expression and microfibrillar protein restoration in dermal fibroblasts. To assess the biological relevance of this approach, the combined treatment was evaluated using UV-damaged human skin biopsy samples. This combination effectively mitigated UV-induced elastic fiber disruption and significantly improved fiber architecture, as confirmed by immunofluorescence staining and scanning electron microscopy. These findings indicate that coordinated modulation of elastin production, proteolytic protection, and scaffold reinforcement is essential for maintaining elastic fiber integrity and represents a promising approach for preserving skin elasticity during aging.

Efficacy and Safety Assessment of ThriveCo Scar Fader Gel With Scarcede™ in the Treatment of Skin Scars [PMID: 41001334 · 2025]
Patel MN, Patel N, Merja A, Patnaik S, Maulekhi S · Cureus (2025)

Introduction Skin scars, a natural outcome of dermal injury healing, may seem minor but often lead to significant disfigurement and psychological distress. This study aimed to assess the safety and efficacy of ThriveCo Scar Fader Gel containing Scarcede&#x2122; (Anveya Living Private Limited, Bengaluru, India), a proprietary blend of copper tripeptide-1, L-carnitine L-tartrate, alpha-glucosyl hesperidin, and sodium hyaluronate. This synergistic formulation targets multiple scar-improvement mechanisms, offering potential for enhanced skin texture and minimized scar appearance. Method An open-label, interventional, prospective real-world evidence study was conducted to evaluate the clinical safety, efficacy, and in-use tolerability of the test product in females with acne scars. Ethical approval was granted by the Independent Ethics Committee, and informed consent was obtained from all participants. Visible scar changes were assessed using the Manchester Scoring Scale by a dermatologist. Skin texture changes, including smoothness, roughness, and scaliness, were evaluated using VISIOSCAN&#xae; VC20 Plus (Courage + Khazaka electronic GmbH, Cologne, Germany). Digital photographs documented progressive scar visibility reduction. Statistical analyses were performed using IBM SPSS Statistics for Windows, Version 29.0.1.0 (Released 2022; IBM Corp., Armonk, New York) and Microsoft&#xae; Excel 2019 (Microsoft Corporation, Redmond, Washington), with significance reported at the 5% level. Result The test product reduced scar appearance by 7.17% at day 21 (p&lt;0.001) and 26.57% at day 45 (p&lt;0.0001). Skin smoothness improved by 33.08% at day 21 (p&lt;0.0001) and 44.56% at day 45 (p&lt;0.0001). Skin roughness decreased by 100.86% at day 21 (p&lt;0.0001) and 161.62% at day 45 (p&lt;0.0001). Scaliness reduced by 39.71% at day 21 (p&lt;0.001) and 58.92% at day 45 (p&lt;0.0001). No local or systemic adverse effects were reported. Conclusion ThriveCo Scar Fader Gel with Scarcede&#x2122; demonstrated clinical safety and efficacy in scar reduction, supporting smoother, clearer skin without adverse effects and suitable for routine skincare use.

An Assessment of the Safety, Efficacy, and Tolerability of a Novel Scalp Treatment Regimen Combining a Hydroxy Acid-Based Scrub and Copper Tripeptide Serum in the Management of Seborrheic Dermatitis in Adults [PMID: 39449909 · 2024]
Patel MN, Patel N, Merja A, Patnaik S · Cureus (2024)

Background and objective Scalp dandruff, a prevalent dermatological condition marked by flaking and itching, affects a large segment of the population. Sun exposure, genetics, and dryness, along with winter conditions, indoor heating, and hard water, all contribute to moisture loss and scalp imbalance.&#xa0;This study aimed to evaluate&#xa0;the safety, efficacy, and tolerability of a novel regimen combining a scalp scrub with hydroxy acid&#xa0;derivatives for exfoliation and dandruff removal, and a serum containing copper tripeptide-1, witch hazel ( Hamamelis virginiana) , hesperidin, hyaluronic acid, and pea protein ( Pisum sativum ) for hydration and scalp health. Methods This prospective, interventional, open-label, single-center study assessed the safety, efficacy, and in-use tolerability of a scalp scrub and serum regimen for mild to moderate dandruff. Ethical approval was granted by ACEAS - Independent Ethics Committee and all participants provided written consent. The study evaluated changes in Adherent Scalp Flaking Score (ASFS), scalp hydration with the Corneometer &#xae; CM 825, hair thickness, hair density, and scalp condition using CASLite Nova.&#xa0;Scalp appearance and treatment usage perception were evaluated on day 1, day 8, and day 15. Statistical analysis was conducted using SPSS Statistics v29.0.1.0 (IBM Corp., Armonk, NY) and Microsoft Excel 2019, with results reported as p-values and 95% confidence intervals (CI). Results As per the ASFS&#xa0;scale for adherent scalp flaking, a significant improvement of 61.24% (p&lt;0.0001) was observed by day 15. Assessments&#xa0;with CASLite Nova showed significant increases in hair density and hair thickness by 12.48% (p&lt;0.0001) and 25.36% (p&lt;0.0001), respectively. Regarding scalp condition, the proportion of individuals with a dry scalp and significant keratin decreased from 65.52% at baseline to 6.9% by day 15. The incidence of dry scalp with fine dandruff also decreased from 6.9% at baseline to 0% by day 15. Conversely, the percentage of individuals with a dry scalp and some keratin increased from 27.59% at baseline to 48.28% by day 15. Also, the proportion of subjects with a normal scalp, characterized by good hair density and thickness, increased from 0% at baseline to 44.83% by day 15. Scalp skin hydration, measured by Corneometer&#xae; CM 825, showed a significant improvement of 76.24% (p&lt;0.0001) from baseline to day 15. Overall, there were notable enhancements in scalp appearance, with reductions in itchiness, redness, roughness, and scaliness. All subjects reported satisfaction with the treatment. Conclusions The ThriveCo scalp regimen (scalp scrub + serum) has been demonstrated to be both effective and safe in treating and reducing scalp dandruff in healthy adults. The regimen significantly reduced ASFS by effectively removing visible scalp flakes from day 1 to day 15 with continuous use. Furthermore, the kit improved overall scalp condition, increased skin hydration, and enhanced the scalp's appearance. The components include scalp scrub with hydroxy acid&#xa0;derivatives for exfoliation and dandruff removal, and a serum containing copper tripeptide-1, Hamamelis virginiana , hesperidin, hyaluronic acid, and pea protein ( Pisum sativum ) for hydration and overall scalp health over the 15-day treatment period. The synergistic effects of this regimen work to clear visible dandruff flakes, reduce adherent scalp flaking, rejuvenate the scalp, and simultaneously strengthen the hair.

Intradermal injections of a hair growth factor formulation for enhancement of human hair regrowth - safety and efficacy evaluation in a first-in-man pilot clinical study [PMID: 29482481 · 2018]
Kapoor R, Shome D · J Cosmet Laser Ther (2018)

Research has shown the efficacy of hair growth factors in hair regrowth. We describe the intradermal injections of a recombinant, bioengineered hair formulation, containing growth factors, into the scalp skin, for enhancement of hair regrowth and evaluate its efficacy. The objective of this study was to assess the efficacy and safety of the hair growth factor formulation in reducing hair loss and enhancing hair growth. This was an open-label, prospective, single-arm interventional pilot study in which 1000 patients were given intradermal injections of a hair formulation into the scalp skin. The formulation contains vascular endothelial growth factor, basic fibroblast growth factor, insulin-like growth factor, keratinocyte growth factor, thymosin &#x3b2;4, and copper tripeptide-1 suspended in a sterile injectable vehicle. Intradermal injections of this hair formulation were injected into the scalp once every 3&#xa0;weeks for a total of eight such sessions. Hair pull test was performed before every session. Videomicroscopic and global images were taken at baseline, fourth session, eighth session, and 2&#xa0;months after the completion of the eight sessions. Relevant safety assessments through physical examination, questionnaires, and appropriate laboratory examination were conducted throughout the study. Significant reduction in hair fall was seen in 83% of the patients on hair pull test. Videomicroscopic image evaluation showed that most patients had a decrease in the number of vellus hairs, increase in number of terminal hairs, and increase in shaft diameter. Seventy-five percent of the patients believed that the hair injections were aiding the treatment of their hair loss, and it was also beneficial in post-hair transplant patients. At 1&#xa0;year, a statistically significant increase in total hair count (P&#xa0;=&#xa0;0.002) continued to be seen. Treatment was well tolerated. Intradermal injections of this hair formulation may be a promising option for treating male as well as female patterns of hair loss.

The effect of copper tripeptide and tretinoin on growth factor production in a serum-free fibroblast model [PMID: 11176716 · 2001]
McCormack MC, Nowak KC, Koch RJ · Arch Facial Plast Surg (2001)

To evaluate the effect of copper tripeptide and tretinoin on normal and keloid-producing dermal fibroblasts in a serum-free in vitro model. The cellular response was described in terms of viability and secretion of basic fibroblast growth factor (bFGF) and transforming growth factor-beta1 (TGF-beta1). Primary cell lines were established from patient facial skin samples obtained during surgery and plated in serum-free media. At 0 hour, copper tripeptide (1 x 10 (-9) mol/L), tretinoin (1 x 10 (-5) mol/L), or appropriate control vehicle was added. Cell counts and viability were established at 24, 72, and 120 hours. Supernatants were collected at the same intervals and were assessed for bFGF and TGF-beta1 concentrations using the enzyme-linked immunosorbent assay technique. Cell lines showed viability between 86% and 96% (mean, 92%) throughout the experiment. Tretinoin-treated normal fibroblasts secreted more bFGF than did controls at 24 hours (P&lt;.05). Tretinoin-treated keloid-producing fibroblasts secreted more TGF-beta1 than did controls at 120 hours (P&lt;.05). Keloid-producing fibroblasts treated with copper tripeptide secreted less TGF-beta1 than did controls at 24 hours (P&lt;.05); a similar trend was observed in normal fibroblasts. Normal fibroblasts treated with tretinoin produced more bFGF than did controls, and this might partially explain the clinically observed tightening effects of tretinoin. Normal and keloid-producing dermal fibroblasts treated with copper tripeptide secreted less TGF-beta1 than did controls, suggesting a possible clinical use for decreasing excessive scar formation.

QR678 & QR678 Neo Hair Growth Formulations: A Cellular Toxicity & Animal Efficacy Study [PMID: 32983753 · 2020]
Kapoor R, Shome D, Vadera S, Kumar V, Ram MS · Plast Reconstr Surg Glob Open (2020)

Current treatment modalities are limited in their approach and success for hair loss. QR 678 &amp; QR 678 Neo are new formulations, consisting of a combination of growth factors and peptides. This study demonstrates safety analysis of QR 678 &amp; QR 678 Neo formulation, using in vitro cytotoxicity assay and in vivo animal efficacy. Factors including vascular endothelial growth factor, basic fibroblast growth factor, insulin-like growth factor-1, keratinocyte growth factor, and copper tripeptide 1 (QR 678) or their biomimetic peptides (QR678 Neo) were suspended in a sterile injectable vehicle. The 3-2,5-diphenyl tetrazolium bromide assay was used to explore the cytotoxic effects of each factor used in the compositions in human keratinocyte cell and human fibroblast cell assays. An in vivo analysis, wherein study animals were given intradermal QR 678 &amp; QR 678 Neo injections, was conducted to assess whether the formulations produce hair growth. Also, hair follicle viability was checked by intradermal injection of the pharmaceutical compositions in secondary alopecia. In both formulations, a positive response was observed with respect to the number of mice exhibiting hair growth at the injection sites. The injections caused retention of hair in a 0.25-cm radius around the injection site. On cytotoxicity study, all the factors were found to be safe in human keratinocyte cell and human fibroblast cell assay. A positive response was demonstrated in animals on treatment with the chemotherapeutic agent. Intradermal injections of QR 678 &amp; QR 678 Neo hair growth factor formulations are a safe and efficacious option for alopecia. Results seem encouraging enough to warrant a trial in humans with secondary alopecia, post cancer chemotherapy.

Regenerative and Protective Actions of the GHK-Cu Peptide in the Light of the New Gene Data [PMID: 29986520 · 2018]
NIH PubMed Indexed Study · Int J Mol Sci (2018)

The human peptide GHK (glycyl-l-histidyl-l-lysine) has multiple biological actions, all of which, according to our current knowledge, appear to be health positive. It stimulates blood vessel and nerve outgrowth, increases collagen, elastin, and glycosaminoglycan synthesis, as well as supports the function of dermal fibroblasts. GHK&amp;rsquo;s ability to improve tissue repair has been demonstrated for skin, lung connective tissue, boney tissue, liver, and stomach lining. GHK has also been found to possess powerful cell protective actions, such as multiple anti-cancer activities and anti-inflammatory actions, lung protection and restoration of chronic obstructive pulmonary disease (COPD) fibroblasts, suppression of molecules thought to accelerate the diseases of aging such as NF&#x3ba;B, anti-anxiety, anti-pain and anti-aggression activities, DNA repair, and activation of cell cleansing via the proteasome system. Recent genetic data may explain such diverse protective and healing actions of one molecule, revealing multiple biochemical pathways regulated by GHK.

Topically applied GHK as an anti-wrinkle peptide: Advantages, problems and prospective [PMID: 39963574 · 2025]
NIH PubMed Indexed Study · Bioimpacts (2025)

Peptides are promising and attractive anti-wrinkle active ingredients, amongst which glycyl-histidyl-lysine peptide (GHK) is one of the most broadly promoted peptide for topical application. This simple sequence of amino acid residues not only has the capability of tissue regeneration and the enhancement of collagen and glycosaminoglycans synthesis but also is able to increase nerve outgrowth and angiogenesis. Consequently, GHK has several properties, from wound healing to prevention/reduction wrinkles. GHK-Cu and Pal-GHK are metal complex and palmitoylated derivatives of GHK, respectively. Although GHK-Cu and Pal-GHK are widely used in anti-wrinkle products available on the cosmetic market, the published information on their skin permeability, effectiveness, physicochemical properties and so on is insufficient. This review aims to highlight whether GHK is sufficiently effective on wrinkle prevention/reduction. Apart from the effectiveness, another question that is tried to be answered is whether skin permeability of GHK allows it to act as an anti-wrinkle peptide at its site of action? Skin permeation enhancement methods employed so far are also reviewed. Based on cellular studies, undoubtedly, GHK can be considered as an anti-wrinkle ingredient. Although GHK-Cu and Pal-GHK have been of interest as effective peptides to be incorporated in the anti-wrinkle products, there is a surprising absence of clinical studies using them. Metal complexation and chemical modification with a hydrophobic moiety increase permeability of this peptide. Besides, cell penetrating peptides seem promising to increase skin permeation of GHK and its derivatives. Skin pretreatment with microneedles also has the potential to be further studied for permeation enhancement of such peptides. As peptide ingredients, their formulation may encounter some challenges, mainly due to their hydrophilic (high aqueous solubility and low partition coefficient) and unstable nature. Although GHK-Cu and Pal-GHK are effective and relatively skin permeable, their permeability could be successfully increased using permeation enhancement methodologies.

The human tripeptide GHK-Cu in prevention of oxidative stress and degenerative conditions of aging: implications for cognitive health [PMID: 22666519 · 2012]
NIH PubMed Indexed Study · Oxid Med Cell Longev (2012)

Oxidative stress, disrupted copper homeostasis, and neuroinflammation due to overproduction of proinflammatory cytokines are considered leading causative factors in development of age-associated neurodegenerative conditions. Recently, a new mechanism of aging-detrimental epigenetic modifications-has emerged. Thus, compounds that possess antioxidant, anti-inflammatory activity as well as compounds capable of restoring copper balance and proper gene functioning may be able to prevent age-associated cognitive decline and ward off many common neurodegenerative conditions. The aim of this paper is to bring attention to a compound with a long history of safe use in wound healing and antiaging skin care. The human tripeptide GHK was discovered in 1973 as an activity in human albumin that caused old human liver tissue to synthesize proteins like younger tissue. It has high affinity for copper ions and easily forms a copper complex or GHK-Cu. In addition, GHK possesses a plethora of other regenerative and protective actions including antioxidant, anti-inflammatory, and wound healing properties. Recent studies revealed its ability to up- and downregulate a large number of human genes including those that are critical for neuronal development and maintenance. We propose GHK tripeptide as a possible therapeutic agent against age-associated neurodegeneration and cognitive decline.

よくある質問 (FAQ)

Q1. COPPER TRIPEPTIDE-1 の各国公式全成分表示名称(7トラック)はどのように異なりますか?
日本化粧品工業連合会(JCIA)表示名称は 'COPPER TRIPEPTIDE-1 (標準INCI準拠)'、米国PCPC・欧州CosIng INCIは 'COPPER TRIPEPTIDE-1'、中国NMPA IECIC標準中国語名は '三肽-1 铜' です。
Q2. COPPER TRIPEPTIDE-1 のグローバル6大法域における法定配合基準 (Layer 1) は?
6大法域規制ステータス — 日本(JP): none、韓国(KR): none、欧州(EU): none、米国(US): none、中国(CN): allowed、ASEAN: none。
Q3. 処方設計における COPPER TRIPEPTIDE-1 の通常配合濃度 (Layer 3) と適正 pH は?
主要剤形 (aqueous_serum) において通常 0.01〜0.2%(中央値 0.05%)で配合され、適正pH範囲は 5.5〜7 です。
Q4. COPPER TRIPEPTIDE-1 の配合禁忌 (Incompatibilities) と推奨シナジー成分は?
推奨シナジーペアは SODIUM HYALURONATE, PANTHENOL, ECTOIN, HYDROXYETHYLCELLULOSE, HYDROLYZED SPONGE、配合上の注意点は CRITICAL INCOMPATIBILITY 1: Never use with chelating agents (Disodium EDTA, Sodium Phytate, Caprylhydroxamic Acid), which strip Cu2+ from the peptide, turning the blue solution green/brown and deactivating it; CRITICAL INCOMPATIBILITY 2: Incompatible with Ascorbic Acid, strong acids (AHA/BHA, pH < 5.0), and Carbomer; formulate at pH 5.5~7.0 using non-ionic thickeners (HEC, Sclerotium Gum) です。