NanoActive™ Xantho 

 

PURIPHARM CO. LTD.

NanoActive™ Xantho

The Multi-Pathway Hop Bioactive for Skin & Scalp Longevity

INCI NAME — HUMULUS LUPULUS EXTRACT

Powered by PURISOME® Liposome Delivery Technology

XANTHOHUMOL · C21H22O5 · A PRENYLATED CHALCONE FROM HUMULUS LUPULUS

02 · POSITIONING

More Than a Botanical Antioxidant

From Hops to High-Performance Beauty Science

Xanthohumol is a prenylated chalcone naturally present in hops (Humulus lupulus L.) that connects several major biological pathways underlying visible skin aging, uneven tone, redness, blemish-prone skin and scalp stress.

NanoActive™ Xantho brings this multi-pathway biology into modern cosmetic formulation through advanced liposome delivery.

01|Oxidative Defense:multi-ROS and singlet-oxygen quenching capacity

02|Inflammation Control:modulation of NF-κB-driven inflammatory signaling

03|Tone Optimization:keratinocyte–melanocyte stress communication

04|Matrix Preservation:MMP and elastase inhibition, structural protein support

05|Blemish Ecosystem Support:microbial, oxidative and inflammatory balance

06|Scalp Homeostasis:a healthier foundation for scalp and hair

03 · PRODUCT PROFILE

NanoActive™ Xantho at a Glance

A Clean Technical Profile — Confirmed Information Only

Item:Product

Confirmed information:NanoActive™ Xantho

Item:INCI name

Confirmed information:HUMULUS LUPULUS EXTRACT

Item:Botanical source

Confirmed information:Humulus lupulus L.

Item:Signature bioactive

Confirmed information:Xanthohumol

Item:Bioactive family

Confirmed information:Prenylated chalcones

Item:Technology platform

Confirmed information:NanoActive™ · PURISOME® Liposome Delivery

Item:Application fields

Confirmed information:Skin Care + Scalp & Hair Care

Core Cosmetic Positioning

Antioxidant · Soothing · Tone-Evening · Anti-Aging · Blemish Care · Scalp Care

One botanical molecule. Multiple interconnected pathways of skin and scalp aging.

04 · THE MOLECULE

Xanthohumol: A Distinctive Prenylated Chalcone

Botanical Origin. Molecular Precision.

Xanthohumol combines the radical-scavenging chemistry of a polyphenol with a prenylated molecular architecture that supports interactions with lipid-rich biological environments.

Prenyl side chain: affinity for lipid-rich biological environments. Polyphenolic chalcone core: radical-scavenging chemistry.

Humulus lupulus L.: the cone of the hop plant, a natural reservoir of prenylated chalcones.

Reported Biological Activities

Reported biological activity:Antioxidant

Description:Multi-ROS defense

Reported biological activity:Antimicrobial

Description:Broad Gram-positive activity

Reported biological activity:Anti-inflammatory

Description:NF-κB pathway modulation

Reported biological activity:Pigmentation-modulating

Description:Multi-level tone pathways

Reported biological activity:ECM-protective

Description:MMP and elastase inhibition

Kołodziejczak A, et al. Int J Mol Sci. 2024;25:11938. · Oledzka E. Int J Mol Sci. 2024;25:3398.

05 · DELIVERY SCIENCE

Why Advanced Delivery Matters

Great biology meets a formulation challenge: NanoActive™ technology translates a lipophilic botanical active into a formulation-friendly format.

PURISOME® liposome concept—xanthohumol positioned within the phospholipid bilayer

Native xanthohumol:Highly lipophilic chalcone

NanoActive™ Xantho:Liposome-based incorporation strategy

Native xanthohumol:Poor aqueous solubility

NanoActive™ Xantho:Improved dispersion concept

Native xanthohumol:Challenging dispersion in water-rich cosmetic systems

NanoActive™ Xantho:Protection within a lipid-compatible microenvironment

Native xanthohumol:Delivery depends strongly on formulation environment

NanoActive™ Xantho:Designed for modern skin and scalp formulations

Native xanthohumol:

NanoActive™ Xantho:A rational route to unlock a hydrophobic botanical active

Published research has investigated xanthohumol delivery using nanoliposomes, nanoparticles, solid lipid nanoparticles, microemulsions and other nanocarrier systems. Liposome-based delivery is a rational formulation strategy for sophisticated skin and scalp care systems.

Oledzka E. Int J Mol Sci. 2024;25:3398. · Khatib N, et al. J Food Process Preserv. 2019;43:e14075. · Harish V, et al. Pharmaceutics. 2022;14:2403.

06 · MECHANISM MAP

One Active, Multiple Beauty Pathways

A Systems Approach to Skin & Scalp Longevity

A systems approach to skin and scalp longevity

Pathway:ROS / singlet oxygen

Reported direction:Quenched ↓

Pathway:NF-κB inflammatory signaling

Reported direction:Modulated ↓

Pathway:GM-CSF / melanocyte activation

Reported direction:Suppressed ↓

Pathway:MMPs + elastase

Reported direction:Inhibited ↓

Pathway:Collagen · elastin · fibrillin

Reported direction:Supported ↑

Pathway:Acne-associated microbial pressure

Reported direction:Reduced ↓

Visible Outcomes

More resilient-looking skin · reduced appearance of redness · more even-looking tone · firmer, smoother appearance · blemish-prone skin support · healthier scalp environment.

07 · ANTIOXIDANT EVIDENCE

Antioxidant Performance Beyond Conventional Benchmarks

Exceptional Defense Against Multiple Reactive Oxygen Species

Total ORAC — Published Assay

Total ORAC: xanthohumol 4.20, green tea catechin reference 4.20, vitamin C 1.40, vitamin E 0.75

Xanthohumol delivered approximately 3× the total ORAC value of vitamin C and more than 5× that of vitamin E in this assay system.

Singlet Oxygen Absorbance Capacity — SOAC

SOAC sample:Xanthohumol

Vitamin E equivalents:14.1

SOAC sample:Green tea catechin reference

Vitamin E equivalents:1.8

SOAC sample:Vitamin E

Vitamin E equivalents:1.0

Why Singlet Oxygen Matters

Lipid oxidation · squalene peroxidation · photo-oxidative stress · inflammatory amplification · visible aging.

Yamaguchi N, Satoh-Yamaguchi K, Ono M. Phytomedicine. 2009;16:369–376. DOI: 10.1016/j.phymed.2008.12.021.

08 · INFLAMMATION CONTROL

Breaking the Oxidative–Inflammatory Loop

Calm the Signals That Accelerate Visible Aging

Xanthohumol—Interrupts the Cascade

Environmental / UV stress→ROS generation→TLR4 / MD2—NF-κB activation

→TNF-α · IL-1β · IL-6 · IL-12 · NO→Redness · irritation · ECM degradation · uneven appearance

Published Evidence

Suppression of NF-κB-related inflammatory signaling; reduced IL-12 production; reduced nitric oxide production; modulation of TNF-α, IL-1β and IL-6 signaling; and reduced chronic inflammatory response in experimental skin models.

Designed to help move stressed skin from inflammatory reactivity toward visible equilibrium.

Cho Y-C, et al. Int Immunopharmacol. 2010;10:556–561. · Philips N, et al. Anti-Inflamm Anti-Allergy Agents Med Chem. 2010;9:142–149. · Kołodziejczak A, et al. Int J Mol Sci. 2024;25:11938.

09 · TONE SCIENCE|GM-CSF

Interrupting Keratinocyte-to-Melanocyte Stress Signaling

GM-CSF—A Distinctive Skin-Stress Target

UV and chemical stress activate epidermal keratinocytes→Stressed keratinocytes release GM-CSF→Melanocyte activation and stress-associated pigmentation signaling

Reduction of Stress-Induced GM-CSF Release—In Vitro

PMA-induced stress −48%; UVB-induced stress −21%

Stress model:PMA-induced stress

With xanthohumol:52% of control, a 48% reduction

Positive-control context:57% reduction

Stress model:UVB-induced stress

With xanthohumol:79% of control, a 21% reduction

Positive-control context:45% reduction

Targeting the communication between stressed keratinocytes and melanocytes.

Patent-reported keratinocyte data: WO2010044076.

10 · TONE SCIENCE|EX VIVO

Ex Vivo Human Skin: Keeping the UV Stress Signal Near Baseline

A Compelling Keratinocyte–Melanocyte Story

Study element:Model

Detail:Human skin explants

Study element:Donor panel

Detail:n=6 donors

Study element:Skin phototype

Detail:Phototype III

Study element:Stress induction

Detail:UVA + UVB challenge

Active melanocytes: baseline 5.6, UVAB 10.5, UVAB + xanthohumol approximately basal

Endpoint:GM-CSF release

Baseline:5.35 pg/mL

UVAB:approximately 4× baseline

UVAB + xanthohumol:6.95 pg/mL

Endpoint:Active melanocytes

Baseline:5.6

UVAB:10.5

UVAB + xanthohumol:approximately basal

Xanthohumol helped disconnect UV stress from melanocyte activation.

Patent-reported ex vivo human skin data: WO2010044076.

11 · TONE SCIENCE|MULTI-LEVEL

More Than Tyrosinase: Multi-Level Tone Optimization

Target Pigmentation Across the Epidermal Signaling Network

01|Signal—GM-CSF stress-signal control:reduced keratinocyte-driven melanocyte activation following UV stress

02|Synthesis—melanogenic enzyme modulation:published mushroom tyrosinase studies demonstrate potent inhibition of L-tyrosine and L-DOPA oxidation

03|Transfer—reduced melanocyte dendricity:reported decrease in dendrite number and length, potentially reducing pigment transfer

04|Clearance—melanosome clearance:published cell studies indicate enhanced melanosome degradation in keratinocytes

From pigment signaling to pigment transfer and clearance—a multi-level approach to visible tone uniformity.

Goenka S, Simon SR. Biochem Biophys Rep. 2021;26:100955. · Kołodziejczak A, et al. Int J Mol Sci. 2024;25:11938. · WO2010044076.

12 · HUMAN EVIDENCE

Human Use Data: Visible Tone Evening in 8 Weeks

Patent-Reported Human Cosmetic Study

Study Design

25 female subjects; mean age 34.1 ± 6.1 years; phototypes III–IV; twice-daily application for 8 weeks; test cream containing 3% P1 xanthohumol preparation, equivalent to 22.5 ppm xanthohumol. Measurements included L*, ITA°, redness a* and pigmented-spot morphology.

Result:Objective brightness / ITA° criteria

Finding:68–72% of subjects demonstrated improvement after 8 weeks

Result:Pigmented spot area

Finding:−12.6% after 8 weeks

Result:Visible redness

Finding:Significantly reduced after 8 weeks

Visible tone uniformity backed by human cosmetic-use data.

Patent-reported human-use data: WO2010044076. Not proprietary NanoActive™ Xantho clinical testing.

13 · MATRIX LONGEVITY

Defending the Youthful Extracellular Matrix

Protect What Gives Skin Its Strength and Elasticity

Matrix Synthesis ⇌ Matrix Degradation

Slows degradation:Inhibits MMP-1, MMP-2, MMP-8, MMP-9 and elastase

Supports structural renewal:Published fibroblast data report increased biosynthesis of collagen I, III and V, elastin, fibrillin-1 and fibrillin-2

Slows degradation:MMP-1 inhibition: 91% at 100 µg/mL MMP-8 inhibition: 99% at 100 µg/mL

Supports structural renewal:Structural proteins associated with skin strength and elasticity

Slows degradation:Reported IC50: MMP-1 20.5 µg/mL; MMP-8 16.8 µg/mL

Supports structural renewal:

Dual-action matrix strategy—slow degradation while supporting structural renewal.

Yamaguchi N, et al. Phytomedicine. 2009;16:369–376. · Philips N, et al. J Cosmet Sci. 2010;61:125–132.

14 · BLEMISH CARE

A Multi-Target Active for Blemish-Prone Skin

Beyond Antibacterial: Rebalancing the Blemish Ecosystem

Target:Microbial pressure

Direction:Acne-associated bacteria ↓

Target:Oxidative stress

Direction:ROS and singlet oxygen ↓

Target:Inflammatory signaling

Direction:COX-2 / PGE2 / IL-1β / TNF-α-associated pathways ↓

Target:Matrix stress

Direction:MMP-driven collagen degradation ↓

Published MIC Values—µg/mL

MIC values: C. acnes 3 µg/mL; S. aureus 1; S. epidermidis 3; S. pyogenes 1

Organism:C. acnes

Published MIC, µg/mL:3

Organism:S. aureus

Published MIC, µg/mL:1

Organism:S. epidermidis

Published MIC, µg/mL:3

Organism:S. pyogenes

Published MIC, µg/mL:1

Cutibacterium acnes was reported as Propionibacterium acnes in the original study.

Antioxidant + antimicrobial + inflammation-modulating + matrix-protective activity in one botanical platform.

Yamaguchi N, et al. Phytomedicine. 2009;16:369–376.

15 · SCALP & HAIR CARE

Scalp-First Hair Care

Healthy-Looking Hair Starts with Scalp Homeostasis

Scalp and follicular microenvironment—oxidative, sebum and microbial stress signals

01|Oxidative-Stress Defense:helps counter environmental and photo-oxidative stress affecting the scalp

02|Scalp Comfort:supports modulation of inflammatory signaling associated with visible redness and discomfort

03|Sebum Environment Support:hop and xanthohumol literature supports sebum-conscious cosmetic concepts

04|Microbial-Balance-Oriented Care:broad activity against relevant Gram-positive microorganisms supports scalp-purifying concepts

05|Follicular Environment Protection:helps maintain a healthier biochemical environment around the scalp and follicular opening

A scalp-first active for stronger skin foundations and healthier-looking hair.

WO2010044076 describes topical xanthohumol applications for improving the overall condition of skin and scalp.

16 · APPLICATIONS

Formulation & Application Opportunities

From High-Performance Facial Care to Advanced Scalp Systems

Skin Care:Antioxidant serums; tone-evening essences; anti-aging concentrates

Scalp & Hair Care:Scalp serums; scalp tonics; scalp essences

Skin Care:Blemish-prone skin serums; post-stress soothing products; redness-care formulations

Scalp & Hair Care:Sebum-conscious scalp care; sensitive-scalp formulas; anti-pollution scalp care

Skin Care:Urban defense / anti-pollution care; after-sun skin care

Scalp & Hair Care:Premium shampoos; conditioners; leave-on scalp treatments

Skin Care:Eye and facial care; premium night-repair products

Scalp & Hair Care:Hair-density appearance support concepts*

*Based on scalp health.

Suitable for development across sophisticated leave-on and rinse-off skin and scalp formats.

17 · THE NANOACTIVE™ XANTHO ADVANTAGE

One Active. Six Strategic Beauty Territories.

01|Antioxidant Shield:multi-ROS and singlet-oxygen defense

02|Redness & Comfort:multi-pathway inflammatory-signaling modulation

03|Even-Tone Science:GM-CSF, melanocyte activation, pigment transport and melanosome pathways

04|Matrix Longevity:MMP / elastase inhibition plus structural-protein support

05|Blemish Ecosystem:antimicrobial, antioxidant, inflammatory and matrix approach

06|Scalp Homeostasis:oxidative, inflammatory, sebum and microbial-environment support

Multi-Pathway Botanical Intelligence, Delivered by Liposome Science.

NanoActive™ Xantho transforms the biological versatility of hop-derived xanthohumol into a modern active platform for next-generation skin and scalp care.

18 · EVIDENCE BASE

Selected Scientific References

Human & Ex Vivo Evidence · Primary Mechanistic Data · High-Quality Reviews

01|Yamaguchi N, Satoh-Yamaguchi K, Ono M. In vitro evaluation of antibacterial, anticollagenase, and antioxidant activities of hop components addressing acne vulgaris.Phytomedicine.2009;16:369–376. DOI: 10.1016/j.phymed.2008.12.021.

02|Philips N, Samuel M, Arena R, et al. Direct inhibition of elastase and matrix metalloproteinases and stimulation of biosynthesis of fibrillar collagens, elastin, and fibrillins by xanthohumol.J Cosmet Sci.2010;61:125–132.

03|Cho YC, You SK, Kim HJ, et al. Xanthohumol inhibits IL-12 production and reduces chronic allergic contact dermatitis.Int Immunopharmacol.2010;10:556–561.

04|Goenka S, Simon SR. Depigmenting effect of xanthohumol from hop extract in MNT-1 human melanoma cells and normal human melanocytes.Biochem Biophys Rep.2021;26:100955.

05|Kołodziejczak A, Dziedzic M, Algiert-Zielińska B, et al. A Novel Look at Mechanisms and Applications of Xanthohumol in Dermatology and Cosmetology.Int J Mol Sci.2024;25:11938. DOI: 10.3390/ijms252211938.

06|Oledzka E. Xanthohumol—A Miracle Molecule with Biological Activities: A Review of Biodegradable Polymeric Carriers and Naturally Derived Compounds for Its Delivery.Int J Mol Sci.2024;25:3398. DOI: 10.3390/ijms25063398.

07|Gerhäuser C. Broad spectrum antiinfective potential of xanthohumol from hop in comparison with activities of other hop constituents and metabolites.Mol Nutr Food Res.2005;49:827–831.

08|WO2010044076. Cosmetic and topical uses of xanthohumol, including skin brightening, reduction of skin redness and GM-CSF-related mechanisms.

Evidence hierarchy: human / ex vivo cosmetic evidence → primary peer-reviewed mechanistic data → high-quality scientific reviews.

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