KPV - 10ml/100mg - Spray

ADVANCED DELIVERY SYSTEM - CELL PENETRATING PEPTIDE TECHNOLOGY 

This product utilizes advanced delivery technology incorporating calibrated cell-penetrating peptide (CPP) systems. The formulation is engineered to support efficient and targeted intracellular delivery of active ingredients, contributing to enhanced transport performance and bioavailability.

SPECIFICATIONS

Product Code: KPV100S

Sequence: Lys-Pro-Val

Molecular Formula: C16H30N4O4

Molecular Weight: 342.43 g/mol

CAS: 67727-97-3

Purity: Technical / Research Grade ≥98%

Other details: No TFA Salt

Form: Liquid Solution

Color: Clear / Slightly opalescent

Total Content: 10 mL / 100 mg

Concentration: 10 mg/mL

Approximate Sprays per Bottle: ~82

Approximate Peptide per Spray: ~1.22 mg

Vehicle / Carrier System: Proprietary carrier system

Storage Temperature: 4°C (Do not freeze)

Source: Synthetic

Safety classification: Standard handling

DESCRIPTION

KPV is the C-terminal peptide fragment of alpha-melanocyte-stimulating hormone (α-MSH). The peptide KPV, composed of lysine, proline, and valine, has been extensively studied in experimental and preclinical settings for its role in modulating inflammatory processes. Ongoing research has focused on KPV in studies related to inflammatory bowel disease and other inflammation-associated conditions. Evidence from laboratory and animal models suggests that KPV exhibits anti-inflammatory activity in multiple biological systems, including the central nervous system, gastrointestinal tract, lungs, cardiovascular system, and joint tissues.

One of the most significant findings emerging from KPV research is its association with reduced intestinal inflammatory signaling. In mouse models of inflammatory bowel disease, KPV has demonstrated reductions in inflammatory cell infiltration, myeloperoxidase (MPO) activity, and histological markers of inflammation. Animals receiving KPV exhibited faster recovery patterns and increases in body weight compared to placebo-treated controls. Additional research has shown associations with reduced tumor necrosis factor alpha (TNF-α) levels and accelerated mucosal repair processes.

Experimental data indicate that KPV can inhibit nuclear factor kappa B (NF-κB) and mitogen-activated protein kinase (MAPK), both central mediators of inflammatory signaling cascades. In comparative studies, animals treated with KPV displayed reduced colonic inflammatory infiltration and preservation of normal colon length relative to untreated controls.

Research led by Didier Merlin demonstrated that KPV enters small intestinal epithelial cells via the PepT1 transporter, which is upregulated during inflammatory states. This mechanism may explain why KPV shows greater activity in inflamed tissue and minimal effects under normal physiological conditions.

Early studies conducted in 1984 showed anti-inflammatory and antipyretic properties in rabbit models, although with lower potency compared to intact α-MSH. Unlike α-MSH, KPV does not induce skin pigmentation, which has positioned it as a preferred fragment for research exploring anti-inflammatory mechanisms without pigmentation-related effects.

α-MSH and related peptides demonstrate anti-inflammatory activity across multiple experimental disease models, including fever, dermatitis, vasculitis, fibrosis, arthritis, and inflammation affecting the eyes, brain, lungs, and gastrointestinal system. While α-MSH generally shows stronger overall activity, KPV preserves a substantial portion of its anti-inflammatory profile without pigmentation effects.

Research suggests that KPV may influence innate immune responses and inhibit the growth of microorganisms such as Staphylococcus aureus and Candida albicans at physiological concentrations. Importantly, experimental observations indicate that KPV does not suppress host immune defense mechanisms.

Unlike α-MSH, KPV does not appear to exert its activity via classical melanocortin receptor pathways. Studies in mouse models have shown that inhibition of MC3 and MC4 receptors does not block the anti-inflammatory actions of KPV, supporting the involvement of alternative signaling mechanisms.

Animal studies have demonstrated that KPV can be administered via multiple routes, including oral, subcutaneous, peripheral, central, and transdermal delivery, providing flexibility in experimental research design.

REFERENCES

All observations described above originate from in vitro systems, animal studies, or other preclinical experimental models. They are intended solely to support basic research into molecular, cellular, and physiological mechanisms and do not imply therapeutic, diagnostic, or preventive applications in humans or animals.

T. Brzoska et al., “Terminal signal: anti-inflammatory effects of α-melanocyte-stimulating hormone related peptides beyond the pharmacophore” [PubMed]

G. Dalmasso et al., “PepT1-mediated tripeptide KPV uptake reduces intestinal inflammation” [PubMed]

K. Pawar et al., “Transdermal Iontophoretic Delivery of Lysine-Proline-Valine (KPV) Peptide Across Microporated Human Skin” [PubMed]

M. E. Hiltz et al., “Antiinflammatory activity of a COOH-terminal fragment of the neuropeptide alpha-MSH” [PubMed]

T. Brzoska et al., “Alpha-melanocyte-stimulating hormone and related tripeptides: antiinflammatory and protective effects in vitro and in vivo” [PubMed]

S. J. Getting et al., “Dissection of the Anti-Inflammatory Effect of the Core and C-Terminal (KPV) -Melanocyte-Stimulating Hormone Peptides” [Journal of Pharmacology and Experimental Therapeutics]

B. Xiao et al., “Orally Targeted Delivery of Tripeptide KPV via Hyaluronic Acid-Functionalized Nanoparticles Efficiently Alleviates Ulcerative Colitis” [PubMed]

K. Kannengiesser et al., “Melanocortin-derived tripeptide KPV has anti-inflammatory potential in murine models of inflammatory bowel disease” [Inflammatory Bowel Diseases]

T. A. Luger et al., “alpha-MSH related peptides: a new class of anti-inflammatory and immunomodulating drugs” [PubMed]

DISCLAIMER

This product is intended for laboratory research and development use only. These studies are performed outside of the body. This product is not a medicine or drug and has not been approved by the FDA or EMA 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. This product should only be handled by licensed, qualified professionals.

All product information provided on this website is for informational and educational purposes only.