Caffeoyl Tripeptide-35 is a chemical compound, a synthetic tripeptide enriched with a coffee derivative, caffeic acid, known for its many beneficial skin functions.

Synthetic peptides can be generated as copies of protein fragments by incorporating non-proteinogenic amino acids and modified so as to also increase the proteolytic stability of the molecules. Peptides are used in the development of therapeutic drugs (1) because of their antimicrobial activity (2), their bioactive interest (3).

What it is used for and where

Caffeoyl Tripeptide-35 is utilized in cosmetic formulations for its outstanding antioxidant properties, which help neutralize free radicals and prevent oxidative damage to the skin. It also acts as a chelating agent, binding heavy metals and reducing their ability to cause stress and damage to the skin. Moreover, it protects the skin from the harmful effects of UV rays, functioning as a UV filter that helps prevent sunburn and premature aging. This peptide is especially useful in sunscreen creams, protective lotions, and anti-aging products, offering comprehensive protection to keep the skin healthy and resilient.

Cosmetics - INCI Functions

• Antioxidant agent. Ingredient that counteracts oxidative stress and prevents cellular damage. Free radicals, pathological inflammatory processes, reactive nitrogen species, and reactive oxygen species are responsible for the aging process and many diseases caused by oxidation.
• Chelating agent. Has the function of preventing unstable reactions and improving the bioavailability of chemical components within a product; it removes calcium and magnesium cations that can cause cloudiness in clear liquids.
• Skin protective. Creates a protective barrier on the skin to defend it from harmful substances, irritants, allergens, and pathogens that can cause various inflammatory conditions. These products can also improve the natural skin barrier, and in most cases more than one is needed to achieve an effective result.
• UV filter. This is the defining ingredient in sunscreens that can attenuate solar ultraviolet (UV) radiation, which is a high risk factor for the development of skin cancer, erythema, and photoaging. 

Chemical Industrial Synthesis Process

• Reagent selection. Reagents, including the three amino acids that make up the tripeptide and caffeic acid, are carefully selected for purity and reactivity.
• Solid-phase peptide synthesis (SPPS). Using solid-phase peptide synthesis, the three amino acids are sequentially coupled starting from the C-terminal amino acid attached to a solid resin.
• Caffeic acid coupling. After the tripeptide synthesis, caffeic acid is coupled to the N-terminus of the peptide via a peptide coupling reaction.
• Cleavage and deprotection. The complete peptide is released from the resin, and protective groups are removed using an appropriate cleavage mixture.
• Purification. The crude peptide is purified via reverse-phase chromatography to remove impurities and unreacted reaction products.
• Quality control. The purified product is analyzed using high-performance liquid chromatography (HPLC) and mass spectrometry to ensure correct peptide sequence and purity.
• Formulation. Finally, the peptide is formulated with other cosmetic ingredients to create a stable and effective final product.

References_____________________________________________________________________

(1) Myšková A, Sýkora D, Kuneš J, Maletínská L. Lipidization as a tool toward peptide therapeutics. Drug Deliv. 2023 Dec;30(1):2284685. doi: 10.1080/10717544.2023.2284685. 

Abstract. Peptides, as potential therapeutics continue to gain importance in the search for active substances for the treatment of numerous human diseases, some of which are, to this day, incurable. As potential therapeutic drugs, peptides have many favorable chemical and pharmacological properties, starting with their great diversity, through their high affinity for binding to all sort of natural receptors, and ending with the various pathways of their breakdown, which produces nothing but amino acids that are nontoxic to the body. Despite these and other advantages, however, they also have their pitfalls. One of these disadvantages is the very low stability of natural peptides. They have a short half-life and tend to be cleared from the organism very quickly. Their instability in the gastrointestinal tract, makes it impossible to administer peptidic drugs orally. To achieve the best pharmacologic effect, it is desirable to look for ways of modifying peptides that enable the use of these substances as pharmaceuticals. There are many ways to modify peptides. Herein we summarize the approaches that are currently in use, including lipidization, PEGylation, glycosylation and others, focusing on lipidization. We describe how individual types of lipidization are achieved and describe their advantages and drawbacks. Peptide modifications are performed with the goal of reaching a longer half-life, reducing immunogenicity and improving bioavailability. In the case of neuropeptides, lipidization aids their activity in the central nervous system after the peripheral administration. At the end of our review, we summarize all lipidized peptide-based drugs that are currently on the market.

(2) Nguyen HLT, Trujillo-Paez JV, Umehara Y, Yue H, Peng G, Kiatsurayanon C, Chieosilapatham P, Song P, Okumura K, Ogawa H, Ikeda S, Niyonsaba F. Role of Antimicrobial Peptides in Skin Barrier Repair in Individuals with Atopic Dermatitis. Int J Mol Sci. 2020 Oct 14;21(20):7607. doi: 10.3390/ijms21207607.

Abstract. Atopic dermatitis (AD) is a common chronic inflammatory skin disease that exhibits a complex interplay of skin barrier disruption and immune dysregulation. Patients with AD are susceptible to cutaneous infections that may progress to complications, including staphylococcal septicemia. Although most studies have focused on filaggrin mutations, the physical barrier and antimicrobial barrier also play critical roles in the pathogenesis of AD. Within the physical barrier, the stratum corneum and tight junctions play the most important roles. The tight junction barrier is involved in the pathogenesis of AD, as structural and functional defects in tight junctions not only disrupt the physical barrier but also contribute to immunological impairments. Furthermore, antimicrobial peptides, such as LL-37, human b-defensins, and S100A7, improve tight junction barrier function. Recent studies elucidating the pathogenesis of AD have led to the development of barrier repair therapy for skin barrier defects in patients with this disease. This review analyzes the association between skin barrier disruption in patients with AD and antimicrobial peptides to determine the effect of these peptides on skin barrier repair and to consider employing antimicrobial peptides in barrier repair strategies as an additional approach for AD management.

(3) Stephanopoulos N. Peptide-Oligonucleotide Hybrid Molecules for Bioactive Nanomaterials. Bioconjug Chem. 2019 Jul 17;30(7):1915-1922. doi: 10.1021/acs.bioconjchem.9b00259. Epub 2019 May 28. PMID: 31082220.

Abstract. Peptides and oligonucleotides are two of the most interesting molecular platforms for making bioactive materials. Peptides provide bioactivity that can mimic that of proteins, whereas oligonucleotides like DNA can be used as scaffolds to immobilize other molecules with nanoscale precision. In this Topical Review, we discuss covalent conjugates of peptides and DNA for creating bioactive materials that can interface with cells. In particular, we focus on two areas. The first is multivalent presentation of peptides on a DNA scaffold, both linear assemblies and more complex nanostructures. The second is the reversible tuning of the extracellular environment-like ligand presentation, stiffness, and hierarchical morphology-in peptide-DNA biomaterials. These examples highlight the potential for creating highly potent materials with benefits not possible with either molecule alone, and we outline a number of future directions and applications for peptide-DNA conjugates.