NanoActive™ SA

NanoActive™ SA Nano-encapsulated Salicylic Acid

Precision purification, from pores to scalp

NEXT-GENERATION SALICYLIC ACID DELIVERY

NanoActive™ SA | Nano-encapsulated Salicylic Acid

Precision purification, from pores to scalp

Powered by PURISOME® FlexVes™ Liposome Technology

INCI: Salicylic Acid

POSITIONING

Proven salicylic acid efficacy × advanced nanoliposomal delivery

NanoActive™ SA combines the well-established biological value of salicylic acid with PuriPharm’s proprietary nano-delivery platform, offering a more formulation-friendly, skin-compatible and targeted solution for modern cosmetic formulations.

Classic salicylic acid, scientifically validated

Keratin renewal and normalized desquamationComedolytic action and follicular decongestionSebum and blemish management

PURISOME® nanoliposomal delivery

Water-phase friendlyControlled, sustained deliveryPotential for follicular targeting

Face care · Body care · Scalp and hair care

MODERN SKIN & SCALP CHALLENGES

Oily skin and scalp: persistent, recurring concerns

Recurring concerns

01 Visibly enlarged pores02 Excess keratin buildup03 Blackheads and whiteheads04 Rough, uneven texture05 Shine and dullness06 Recurrent pore congestion07 Scalp oil and adherent flakes

What determines the appearance of visible pores?

Keratin buildup within folliclesLevel of sebum productionStructural visibility of follicular openingsSkin surface texture

Pore appearance = keratin × sebum × structure × texture

Pore concerns are multifactorial. This limits purely astringent approaches and provides a clear scientific entry point for actives that manage keratinization.

THE CLASSIC ACTIVE

Salicylic acid: an enduring classic in skin science

Salicylic Acid · C₇H₆O₃

INCI: Salicylic AcidType: aromatic hydroxy acid (BHA), pKa ≈ 3.0Properties: lipophilic, with affinity for sebum-rich and follicular environments; limited solubility in water at room temperature.

01 Aromatic hydroxy-acid structure

The benzene ring and ortho hydroxyl and carboxyl groups determine its distinctive physicochemical behavior.

02 Lipophilicity

Unlike water-soluble AHAs, it can enter sebum-rich follicular environments.

03 Affinity for the pilosebaceous unit

It can act where comedones and blemishes originate.

04 Activity within the stratum corneum

It acts on connections between corneocytes without requiring deep penetration.

Its molecular properties give salicylic acid a distinctive role in pore and follicular care.

MECHANISM 01 · DESMOLYTIC ACTION

Mechanism 1: desmolysis regulates cohesion rather than “dissolving keratin”

Modern skin science holds that salicylic acid disrupts intercellular connections and reduces corneocyte cohesion, allowing abnormally accumulated keratin to shed in an orderly manner rather than simply “dissolving keratin.”

Densely accumulated stratum corneum

Reduced corneocyte cohesion

Normalized desquamation

Smoother skin surface

Formulation relevance: Desmolysis rather than aggressive peeling supports keratin management with a lower burden. This biology underpins applications for oily skin, pores, blemishes and the scalp.

MECHANISM 02 · COMEDOLYTIC ACTION

Mechanism 2: comedolytic action along the follicular pathway

Comedone formation cascade

Hyperkeratinization

Follicular opening blockage

Microcomedone

Blackhead / whitehead

Inflammatory lesion

① Normalized desquamation

Corrects hyperkeratinization at the follicular opening and reduces blockage at its source.

② Lipophilic penetration

Moves through the sebum-rich environment into the follicle instead of remaining on the surface.

③ Reduced cellular buildup

Decreases abnormal accumulation of keratinocytes within the follicle.

④ Comedolysis

Helps clear established blockages and improve blackheads and whiteheads.

Effective comedone management depends on keratinization within the follicle, not only surface cleansing. Salicylic acid’s lipophilicity gives it this distinctive position.

Mechanism review: Arif T. Clin Cosmet Investig Dermatol. 2015;8:455–461.

MECHANISM 03 · INFLAMMATION & BLEMISH BIOLOGY

Mechanism 3: the inflammatory dimension of acne biology

Inflammation is present throughout acne development, including the invisible microcomedone stage. Blemish care therefore should not begin only after lesions become visible.

Published literature reports that salicylic acid modulates multiple inflammation-related pathways, including arachidonic-acid metabolism and inflammatory signaling. Together with its desmolytic and comedolytic actions, this supports both purification and stabilization.

Sebum production + abnormal keratinization

Changed follicular microenvironment

Microbial involvement

Amplified inflammatory cascade

Erythema, papules and post-acne marks

Salicylic acid intervenes at several upstream points: keratinization, the follicular environment and inflammation.

These mechanism-level statements reflect literature consensus and explain ingredient-level biological relevance. They do not constitute pharmaceutical treatment claims.

Mechanism review: Arif T. Clin Cosmet Investig Dermatol. 2015;8:455–461.

CLINICAL EVIDENCE 01 · ASIAN ACNE STUDY

30% salicylic acid peel: a 12-week study in Asian patients with acne

35

Asian participants

Mild to moderate

Facial acne

30%

Salicylic acid peel

Every 2 weeks

One treatment

12 weeks

Observation period

77.1%

Reported moderate or good improvement

  • Significant reduction in inflammatory lesions
  • Significant reduction in non-inflammatory lesions
  • Significant decrease in overall acne severity
  • No statistically significant worsening in stratum-corneum hydration, surface lipids, skin pH or TEWL

Lee HS, Kim IH. Salicylic acid peels for the treatment of acne vulgaris in Asian patients. Dermatol Surg. 2003;29:1196–1199.

This is published clinical evidence for salicylic acid, not a finished-product efficacy trial of NanoActive™ SA.

CLINICAL EVIDENCE 02 · COMEDONE COUNT

Mean facial comedone count fell by approximately 75% over 10 weeks

Statistical significance

p = 0.001

Study information

Participants: 16 Japanese patientsSystem: 30% salicylic acid in PEGFrequency: once every 2 weeksDuration: 10 weeks

Mean count decreased from 39.3 at baseline to 9.2 at Week 10, with continued improvement throughout follow-up.

Hashimoto Y, et al. Salicylic acid peels in polyethylene glycol vehicle for the treatment of comedogenic acne in Japanese patients. Dermatol Surg. 2008;34:276–279.

Published evidence for a 30% salicylic acid–PEG peel, not a finished-product efficacy trial of NanoActive™ SA.

POST-ACNE MARKS · UNEVEN TONE

From acne to post-acne marks: a framework for managing pigmentation

How salicylic acid can improve uneven tone

① Normalize exfoliation: accelerate surface renewal

② Remove pigment-containing corneocytes: lift superficial deposited pigment

③ Improve acne-related inflammation: reduce conditions that promote new marks

A more even-looking skin tone

Salicylic acid is not a tyrosinase inhibitor. Its tone-related value comes from the combined effects of keratin renewal and inflammation management, not direct inhibition of melanin synthesis.

Comparative clinical evidence

30% salicylic acid vs 30% glycolic acidMild-to-moderate acne with post-inflammatory hyperpigmentation (PIH)

Study findings

Both peel regimens improved PIH; the salicylic acid group showed better tolerability in this study; relevant to combined acne and post-acne-mark concerns.

The literature also documents salicylic acid use in superficial peels for melasma and photo-induced uneven tone.

Reference: Arif T. Clin Cosmet Investig Dermatol. 2015;8:455–461.

TEXTURE & PHOTOAGING

Beyond blemish care: keratin renewal and younger-looking texture

Controlled keratin renewal can address not only blemishes, but also surface features associated with aging and photodamage:

  • Roughness and grainy texture
  • Dullness and loss of radiance
  • Fine surface lines
  • Uneven texture
  • Visible signs of photoaging

Change from baseline with a sodium salicylate formulation

Evidence boundary: The study tested a sodium salicylate formulation, not free salicylic acid. Histology also indicated increases in fibrillin and procollagen I. The findings support salicylate/exfoliation biology and are not direct clinical evidence for NanoActive™ SA.

Merinville E, et al. Three clinical studies showing the anti-aging benefits of sodium salicylate in human skin. J Cosmet Dermatol. 2010;9:174–184. Wrinkle depth and skin roughness decreased significantly at Weeks 4 and 8.

THE FORMULATION PARADOX

The challenge with salicylic acid is delivery, not efficacy

Salicylic acid has limited solubility in water at room temperature. Traditional clear aqueous products often rely on ethanol, glycols, surfactant solubilization, partial neutralization and precise pH management, creating a persistent trade-off between efficacy and formulation elegance.

Traditional free-salicylic-acid formulation pathway

Salicylic acid powder

Solvent system

Partial neutralization

pH adjustment

Trade-offs in crystallization, irritation and sensory profile

Each step solves one problem while introducing another compromise.

NanoActive™ SA technology pathway

NanoActive™ SA

Pre-engineered nano-delivery

Easy incorporation into the aqueous phase

Controlled active delivery · formulation freedom

The carrier addresses solubility so formulators regain design flexibility. Delivery technology is the dividing line in modernizing salicylic acid.

FREE ACID & pH

The free-acid state determines effective delivery

Salicylic Acid ⇌ Salicylate− + H+

Molecular form (free acid)  Ionic form (salicylate)

pH < pKa

Free acid predominates, with a greater tendency to penetrate.

pKa ≈ 3.0

Key reference point for the ionization equilibrium.

pH > pKa

The salt form predominates, increasing water solubility.

01 Molecular and ionic forms

They differ in solubility, partition coefficient and skin penetration.

02 pH determines equilibrium

Small pH adjustments can change the free-acid fraction in the same formulation.

03 Carrier and pH jointly affect penetration

The formulation itself is part of salicylic acid performance.

04 Cost of conventional neutralization

Higher water solubility comes with a changed effective free-acid fraction.

PURISOME® Technology proposition: A nanocarrier environment supports effective salicylic acid delivery while improving formulation compatibility and reducing reliance on high solvent levels and complex neutralization strategies.

THE PURIPHARM RESPONSE

NanoActive™ SA: PuriPharm’s technology response

NanoActive™ SANano-encapsulated salicylic acidINCI: Salicylic AcidPowered by PURISOME® FlexVes™ Liposome Technology

Maintains an effective free-acid state

The carrier environment protects the effective form of salicylic acid.

Aqueous formulation compatibility

Disperses stably and incorporates easily into aqueous systems.

Potential for clear formulations

Supports modern formats such as clear serums and gels.

Reduced solvent dependence

Reduces the need for large amounts of ethanol or polyols.

Controlled delivery

Gradual release produces more even exposure.

Improved skin comfort

A sustained-release approach supports a better user experience.

Potential for follicular targeting

Follicular reservoir effect and localized enrichment.

Face and scalp applications

One platform supports multiple use cases.

This is a redesigned delivery pathway for salicylic acid, not merely salicylic acid placed inside a carrier.

THE TECHNOLOGY PLATFORM

PURISOME® FlexVes™ Liposome Technology

PuriPharm’s proprietary advanced nanoliposomal platform uses skin-compatible phospholipid bilayer vesicles.

Cross-sectional schematic: amphiphilic phospholipids self-assemble into a bilayer that encapsulates or associates with the active.

01 Improved formulation compatibility

A water-dispersed format bypasses the solubility bottleneck.

02 Controlled, sustained release

Carrier association releases the active gradually through interfacial processes.

03 Lower potential for localized irritation

Avoids sudden skin contact with a high concentration of free acid.

04 Improved deposition and delivery

Skin-compatible lipids promote active deposition in the target region.

Hereafter referred to as PURISOME® Technology. Its four delivery advantages support the same goal: bringing the active to the intended site at an appropriate rate.

DELIVERY MECHANISM

PURISOME® FlexVes™: a redesigned salicylic acid delivery pathway

Schematic: larger particles remain on the surface because they cannot pass through intercellular gaps, while smaller nanocarriers can move along these gaps and release the active.

01 Interaction with stratum-corneum lipids

Skin-compatible phospholipids approach intercellular lipids.

02 Gradual release

The active is progressively released from the carrier interface.

03 Follicular deposition

The carrier moves along the follicular pathway and enriches the target region.

Nanoscale delivery · skin-compatible lipids · controlled release · improved compatibility · follicular-delivery potential · better sensory profile

The schematic follows standard pharmaceutics models of phospholipid bilayer vesicle interactions with skin.

FOLLICULAR TARGETING

Follicular targeting and the follicular-reservoir concept

Nanoparticles vs free drug: a, stratum-corneum surface; b, enrichment in the follicular infundibulum; c, migration deeper along the follicle.

Particles deposit in the follicular infundibulum and diffuse into surrounding tissue.

Follicular targeting · follicular reservoir · localized enrichment

  • Blackheads and comedones
  • Oily pores
  • Scalp buildup
  • Keratin buildup within follicles

Statements about follicular targeting and reservoirs are based on the PURISOME® Technology platform’s delivery concept and are consistent with existing NanoActive™ platform data.

Left image adapted from Prow TW, et al. Nanoparticles and microparticles for skin drug delivery. Adv Drug Deliv Rev. 2011;63:470–491.

CONTROLLED RELEASE & SKIN COMFORT

From concentration peaks to gradual release

Traditional free salicylic acid

Rapid local exposure produces a concentration peak, with potential stinging and irritation.

NanoActive™ SA

Carrier-associated delivery supports gradual release, more even local exposure and potential for improved comfort.

Nanocarrier occlusion effectSmaller particles and a higher number of carriers per unit area can form a denser lipid film on the skin surface. This may improve stratum-corneum hydration, promote active penetration and reduce water loss, adding another mechanistic basis for efficacy with comfort.

FOR FORMULATORS

Making salicylic acid easier to formulate and use

  1. Easy incorporation and process-friendly handling
  2. Suitable for aqueous systems
  3. Potential for transparent and clear formulations
  4. Reduced dependence on high ethanol levels
  5. Less need for aggressive solubilization strategies
  6. Compatible with serums, gels, cleansers and scalp formats
  7. Can be added at low temperature, depending on the process
Process and compatibility guidance Details
Suggested use level Approximately 1–5%
Addition method Add at low temperature
Compatibility note Avoid combining with divalent or trivalent metal ions

Based on historical PuriPharm technical materials. If this information differs from the latest product TDS, follow the current TDS.

Formulation freedom is itself a product advantage.

APPLICATION MAP

One application map, from face to scalp

FACE

Anti-acne serumPore-refining serumKeratin-regulating tonerCleanserClear gelMoisturizer for oily skinBlemish care

BODY

Body acne sprays and lotionsKeratosis pilaris careExfoliating body washCare for rough areas

SCALP & HAIR

Anti-dandruff shampooShampoo for oily scalpScalp serumScalp exfoliating treatmentScalp-cleansing products

One technology platform supports three major application areas: face, body and scalp.

SCALP & HAIR 01 · SCALP BIOLOGY

From facial pores to scalp follicles

Persistent scalp concerns

01 Scalp keratin buildup02 Excess scalp oil03 Adherent flakes04 Buildup at follicular openings05 Scalp cleanliness and freshness06 Disrupted scalp-renewal rhythm

Why salicylic acid suits scalp care

Desmolytic action: softens and removes corneocytes adhering to the scalp surface.Reduced surface buildup: addresses adherent layers formed by oil and keratin.Clearer follicular openings: lipophilicity supports entry along the sebum-rich environment.Improved appearance of oily scalp: a fresher scalp and lighter-feeling roots.

Scalp follicles present a problem structurally analogous to facial pores. Scalp care is another application of the same keratin biology, not merely an extension of facial care.

SCALP & HAIR 02 · DANDRUFF CARE

Scalp purification and dandruff care

Biology of dandruff

Dandruff is associated with abnormal desquamation of the stratum corneum.Malassezia plays an important role in dandruff biology.Effective management should address flake control, microbial factors and overall scalp condition.

Scalp positioning of NanoActive™ SA

① Desmolytic scalp active② Scalp-flake removal③ Oily-scalp care④ Follicular cleansing⑤ Supporting ingredient in anti-dandruff shampoo systems

Scientific boundary: salicylic acid should not be claimed as a standalone antifungal ingredient. In multi-ingredient anti-dandruff systems, it contributes keratin management and flake control.

Suggested formats: anti-dandruff shampoo · shampoo for oily scalp · scalp serum · scalp treatment liquid · scalp exfoliating treatment · pre-shampoo scalp care

Dandruff systems require multiple complementary mechanisms. NanoActive™ SA addresses the keratin and flake-control component.

COMPARISON

Traditional salicylic acid vs NanoActive™ SA

Dimension Traditional salicylic acid NanoActive™ SA
Aqueous formulation difficulty High: limited water solubility Low: easy dispersion and incorporation in water
Crystallization risk Potential precipitation and crystallization Carrier encapsulation lowers risk
Solvent dependence Often requires high levels of ethanol or polyols Dependence substantially reduced
pH management Precise control changes the free-acid fraction A more flexible formulation window
Delivery profile Rapid release and local concentration peak Gradual release and more even exposure
Skin comfort Stinging possible at high concentration Sustained-release approach with comfort potential
Clear-formulation capability Limited Supports clear, transparent formulations
Follicular delivery Relies on compensating formulation engineering Potential for follicular targeting and reservoir deposition
Dosage-form flexibility Limited selection Serums, gels, cleansers and scalp formats
Fit for scalp applications Dual challenge of solubilization and irritation Aqueous-friendly and suited to modern scalp formats

VALUE PROPOSITION

NanoActive™ SA: a four-dimensional value proposition

EFFICACY|Classic salicylic acid, multidimensional purification

Peer-reviewed literature supports the combined mechanisms of keratin renewal, comedolysis and inflammation modulation.

DELIVERY|PURISOME® nanoliposomal delivery

Skin-compatible phospholipid bilayer vesicles carry the active and support follicular targeting and reservoir deposition.

COMFORT|Sustained-release concept for a better experience

Gradual release smooths concentration peaks and troughs, adding comfort potential to efficacy.

FORMULATION|Aqueous-friendly with greater design freedom

From serums to shampoos, the platform enables salicylic acid formats that were previously difficult to formulate.

Evidence for efficacy, technology for delivery, attention to experience and room for formulation.

REFERENCES

References and evidence grading

Published literature cited in this presentation

  1. Lee HS, Kim IH. Salicylic acid peels for the treatment of acne vulgaris in Asian patients. Dermatol Surg. 2003;29:1196–1199.
  2. Hashimoto Y, et al. Salicylic acid peels in polyethylene glycol vehicle for the treatment of comedogenic acne in Japanese patients. Dermatol Surg. 2008;34:276–279.
  3. Arif T. Salicylic acid as a peeling agent: a comprehensive review. Clin Cosmet Investig Dermatol. 2015;8:455–461.
  4. Merinville E, et al. Three clinical studies showing the anti-aging benefits of sodium salicylate in human skin. J Cosmet Dermatol. 2010;9:174–184.

Clinical evidence for salicylic acid

References [1] and [2]: 30% peel systems, not finished-product studies.

Evidence for a salicylate derivative

Reference [4]: sodium salicylate, supporting the biological pathway.

Mechanism and review literature

Reference [3]: exfoliation, comedolysis and skin-tone applications.

None of the published references cited here constitutes a finished-product efficacy trial of NanoActive™ SA.

NANOACTIVE™ SA

Making classic salicylic acid more suitable for next-generation formulations

Powered by PURISOME® FlexVes™ Liposome Technology

PuriPharm Co. Ltd.

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