原料词典检索/copper-tripeptide-1/COPPER TRIPEPTIDE-1
Tier 1 Monograph · SSOT 15 FieldsRaw .md (GEO) ↗
多肽与蛋白 (Peptide)

COPPER TRIPEPTIDE-1

中国 NMPA《已使用化妆品原料目录 (IECIC)》标准中文名: 三肽-1 铜 (序号 #5807)
皮肤调理剂
[EU CosIng Official Definition] Copper Tripeptide-1 is a copper complex of Tripeptide-1
核心法规与安全结论 (Executive Fact Box)AEO / GEO CITATION ANCHOR

化妆品中 三肽-1 铜 (COPPER TRIPEPTIDE-1) 的全球法规限值与配方应用标准是什么?

三肽-1 铜(标准 INCI: COPPER TRIPEPTIDE-1,CAS 号: N/A)是化妆品配方中主要用作皮肤调理剂的核心成分。受中国 NMPA(已使用/准用)、韩国 MFDS(未列管)及欧盟 CosIng(未列管)等 6 大法域法定标准监管,常规建议添加量为 0.01–0.2%(最佳稳定窗口 pH 5.5–7)。

全球 7 轨官方全成分标签名称对照表

严格采用各国政府官方目录原名 · 严禁机器翻译
7-Track Official Statutory Label Names for COPPER TRIPEPTIDE-1
法域与监管轨道官方公告全成分标准名称一键复制
① 韩国 (MFDS 化妆品标准名称)COPPER TRIPEPTIDE-1 (KR MFDS Registered)
② 韩国旧名称历史 (301 重定向)Former KR Nomenclature Redirect Active—
③ 欧盟 (EU CosIng EC 1223/2009)COPPER TRIPEPTIDE-1
④ 美国普通化妆品 (US PCPC / MoCRA INCI)COPPER TRIPEPTIDE-1
⑤ 美国 OTC 防晒/祛痘专论活性物名称 (FDA OTC)— (非美国 OTC 专论活性成分 / 普通化妆品原料)—
⑥ 中国 (NMPA《已使用化妆品原料目录 IECIC》标准中文名)三肽-1 铜
⑦ 日本普通化妆品 / 医药部外品 (JCIA / MHLW)COPPER TRIPEPTIDE-1 (标准 INCI 参照)

Layer 1 — 全球 6 大法域法定限值与监管状态

Layer 1 Statutory Regulatory Limits Across 6 Regions for COPPER TRIPEPTIDE-1
法域监管状态法定限值适用条件与法定依据来源
韩国 (MFDS)未列管GMP已列入官方化妆品原料目录 (按 GMP 规范使用)
欧盟 (EU)未列管GMP已列入官方化妆品原料目录 (按 GMP 规范使用)
美国 (FDA)未列管GMP已列入官方化妆品原料目录 (按 GMP 规范使用)
中国 (NMPA)已使用/准用GMPIECIC Entry #5807
日本 (MHLW)未列管GMP已列入官方化妆品原料目录 (按 GMP 规范使用)
东盟 (ACD)未列管GMP已列入官方化妆品原料目录 (按 GMP 规范使用)

Layer 2 — 毒理评估与历史最高使用量 (CN IECIC / US CIR / EU SCCS)

“欧盟 SCCS 安全评估上限”代表消费者安全科学委员会判定安全边际 (MoS≥100) 的毒理阈值;“美国 CIR 市售最高报告浓度”与“中国 IECIC 最高历史使用量”代表已上市化妆品的最高实际使用浓度。

Layer 2 Toxicological & Historical Safe Use Concentrations for COPPER TRIPEPTIDE-1
安全评估依据适用范围与剂型评估浓度范围评估结论与文献档案
中国 IECIC 最高历史使用量leave_on≤ 0.5%安全判定 (MoS≥100)NMPA IECIC (2025) Entry 05915 (2025)
中国 IECIC 最高历史使用量rinse_off≤ 0.2%安全判定 (MoS≥100)NMPA IECIC (2025) Entry 05915 (2025)
⚠️ 仅供参考 (免责声明): 本词典中的原料名称、法规限值与配比指南仅供研发参考。鉴于法规修订时差或潜在数据误差,实际配方设计、标签印制及备案前请务必核实主管部门最新官方公告原文;因使用本词典信息产生的任何问题,运营方概不承担法律责任。
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 — 剂型常规配比指南与理化配伍性

Layer 3 Formulation Concentration Quartiles by Product Category for COPPER TRIPEPTIDE-1
剂型分类Min – Q1 – Median – Q3 – Max (%)配方作用与机理Source ID
剂型组 A — 水剂爽肤水 / 精华液 / 安瓶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
剂型组 B — 乳液 / 面霜 (O/W · W/O)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.

代表性商品名参考 (商标法第90条第1款第2项说明性标示)
Prezatide Copper AcetateGHK-Cu Pure Powder

商品名仅供配方师识别原料规格参考,商标权归各原厂商所有。

学术与毒理综合摘要

Tier 1 Synthesis

本综述严格基于与该原料关联的 NIH PubMed 同行评审文献摘要及官方毒理学评估档案编写。

■ [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

关联同行评审文献 (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.

常见问题解答 (FAQ)

Q1. 三肽-1 铜 (COPPER TRIPEPTIDE-1) 在全球 7 大法域的官方全成分标签名称是什么?
中国 NMPA《已使用化妆品原料目录 (IECIC)》标准中文名为 '三肽-1 铜',美国 PCPC 与欧盟 CosIng 标准 INCI 为 'COPPER TRIPEPTIDE-1',日本 JCIA 表示名称为 'COPPER TRIPEPTIDE-1'。
Q2. 三肽-1 铜 (COPPER TRIPEPTIDE-1) 在中、韩、欧、美、日、东盟的法定监管状态 (Layer 1) 如何?
6 大法域监管汇总 — 中国(CN): allowed,韩国(KR): none,欧盟(EU): none,美国(US): none,日本(JP): none,东盟(ASEAN): none。
Q3. 三肽-1 铜 (COPPER TRIPEPTIDE-1) 的常规配方添加量 (Layer 3) 与最佳稳定 pH 窗口是多少?
在代表性剂型 (aqueous_serum) 中常规添加量为 0.01%–0.2%(中位数 0.05%),最佳稳定 pH 范围为 5.5–7。
Q4. 三肽-1 铜 (COPPER TRIPEPTIDE-1) 有哪些配伍禁忌 (Incompatibilities) 与协同增效组合?
推荐协同组合包括 SODIUM HYALURONATE, PANTHENOL, ECTOIN, HYDROXYETHYLCELLULOSE, HYDROLYZED SPONGE;配伍禁忌注意: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)。