NanoActive™Retinal – Bakuchiol 纳米包裹视黄醛-补骨脂酚

NanoActive™Retinal – Bakuchiol

Nano-Encapsulated Retinal–Bakuchiol

Dual-Pathway Retinoid Renewal · Nano-Delivery Technology

INCI NAME — RETINAL, BAKUCHIOL

PuriPharm Co. Ltd. · Technical Marketing Presentation

02 · RETINOID CARE — THE NEXT CHAPTER

Retinoid Care Is Entering Its Next Stage

Retinoids remain the most evidence-supported active family for managing skin photoaging. The questions facing brands and formulators have moved beyond whether a formula contains a retinoid to four more fundamental issues: Can the active be converted efficiently? Can it remain stable? Can consumers sustain long-term use? Does the formula provide sufficient design freedom?

Core question Explanation
01 Efficacy Retinoids must be converted to retinoic acid to act; the conversion pathway determines the speed and intensity of activity.
02 Stability High activity comes with sensitivity to light and oxygen; active retention during shelf life and in-formula is essential.
03 Tolerance Irritation determines adherence, and adherence determines whether long-term benefits can be realized.
04 Formulation Dosage form, sensory profile and system compatibility define the space for product differentiation.

The next-stage answer: advanced actives × complementary mechanisms × nano delivery.

03 · PRODUCT OVERVIEW

NanoActive™ Retinal-Bakuchiol

Identity Information
Product name Nano-Encapsulated Retinal–Bakuchiol
INCI name Retinal, Bakuchiol
Technology platform NanoActive™ nano-encapsulation and delivery system
Application settings Dual use across skin care and scalp care
01 Biology: Retinal is the direct precursor of retinoic acid; one oxidation step drives advanced retinoid biology.
02 Synergy: Bakuchiol supports retinol-like gene expression, antioxidant defense, inflammatory modulation, extracellular-matrix biology and skin homeostasis.
03 Delivery: NanoActive™ improves protection, dispersion, formulation suitability and delivery performance for sensitive actives.

This is not a simple ingredient blend. It is a next-generation dual-pathway renewal platform integrating high-efficiency renewal, complementary mechanisms, nano delivery and both skin and scalp applications.

04 · 01 · BIOLOGY — RETINAL

Why Retinal: Closer to the Active EndpointRetinyl esters → Retinol → Retinal → Retinoic acid

Metabolic node Description
Retinyl esters Storage form; hydrolyzed to retinol.
Retinol Requires a rate-limiting oxidation step to form retinal.
Retinal An advanced cosmetic retinoid that requires only one oxidation step to form retinoic acid.
Retinoic acid The active retinoid endpoint; a drug active not permitted as a cosmetic ingredient.
Key advantage Data and significance
Approximately 3× biological activity Bypassing retinol’s first rate-limiting oxidation step gives retinal approximately three times the retinoid biological activity of retinol.
At least 11× faster conversion Conversion of retinal to retinoic acid is estimated to be more than 11 times faster than the retinol pathway and occurs in both differentiated and undifferentiated keratinocytes.

Retinal is the direct precursor of retinoic acid—an advanced retinoid positioned closer to the active endpoint.

Siegenthaler G, Saurat JH, Ponec M. Biochem J. 1990;268(2):371–378. | Brown A, et al. Dermatol Ther (Heidelb). 2023;13(10):2299–2317.

05 · 01 · BIOLOGY — ADVANCED RETINOID BIOLOGY

One Oxidation Step Directly Drives Classical Retinoid SignalingRetinal → one-step oxidation → retinoic acid → RAR/RXR nuclear receptors → target-gene transcription → visible epidermal and dermal renewal

01 Retinal undergoes one oxidation step inside keratinocytes to form retinoic acid.
02 Retinoic acid binds nuclear RAR receptors and forms heterodimers with RXR.
03 RAR-RXR binds promoter regions and regulates target genes involved in skin biology.
04 The result is visible renewal across both the epidermis and dermis.
Level Biological effects
Epidermis Accelerated epidermal renewal; regulation of keratinocyte differentiation; increased epidermal thickness; upregulation of RA-activity markers such as CRABP-II; regulation of barrier- and hydration-related genes; improved desquamation, texture refinement and tone uniformity.
Dermis Support for fibroblast function and extracellular-matrix remodeling; new collagen deposition; inhibition of UV-induced MMP-related matrix degradation; restoration of the elastic-fiber network; visible outcomes in wrinkles, texture, laxity and photoaging pigmentation.

A complete retinoid-biology pathway drives systematic renewal from the epidermis to the dermis.

Saurat JH, et al. J Invest Dermatol. 1994;103(6):770–774. | Fisher GJ, et al. Nature. 1996;379(6563):335–339. | Xiao JH, et al. J Biol Chem. 1995;270(7):3001–3010.

06 · 01 · BIOLOGY — EPIDERMIS TO DERMIS

Retinal: From Epidermal Renewal to Dermal RemodelingEpidermis: renewal, differentiation, thickness and texture; Dermis: fibroblasts, collagen, elastic fibers, ECM and MMP management

Evidence Finding
Human study: epidermis and elasticity After one year of 0.05% retinaldehyde, high-resolution ultrasound and rheological measurements showed significant increases in epidermal thickness and skin elasticity (p < 0.01), with a trend toward increased dermal thickness.
Ex vivo: repair of UVA damage In a UVA-photodamaged human skin model, two weeks of 0.05% retinaldehyde restored elastic fibers and collagen to levels close to non-photodamaged skin.
Biological effects in human skin Topical retinaldehyde induced typical retinoid effects, including epidermal thickening and CRABP-II expression, while maintaining good tolerance.

Metabolic position → retinoid biology → epidermal renewal → ECM/collagen/elastin support → visible human outcomes: one complete evidence chain.

Diridollou S, et al. Dermatology. 1999;199(Suppl 1):37–41. | Boisnic S, et al. Dermatology. 1999;199(Suppl 1):43–48. | Saurat JH, et al. J Invest Dermatol. 1994;103(6):770–774.

07 · 01 · CLINICAL EVIDENCE — PHOTOAGING

Human Photoaging: Improvement Comparable to Retinoic Acid

Study design Details
Randomized controlled study n=125; 18 weeks; optical profilometry; 0.05% retinaldehyde (n=40) versus 0.05% retinoic acid (n=40) versus vehicle (n=45).
Dimension Result
Efficacy: comparable Both actives significantly reduced wrinkles and skin roughness; no statistically significant efficacy difference was observed between retinaldehyde and retinoic acid. An open study (n=32, four months) also found clear reductions in surface roughness and coarse wrinkles.
Tolerance: better Local irritation was more frequent with retinoic acid and affected adherence. Retinaldehyde caused fewer local adverse reactions and supported better long-term adherence. Comparable efficacy plus better tolerance forms retinal’s core value proposition.

In photoaged human skin, 0.05% retinaldehyde delivered wrinkle and roughness improvements comparable to 0.05% retinoic acid while maintaining significantly better local tolerance.

Creidi P, et al. J Am Acad Dermatol. 1998;39(6):960–965. | Creidi P, Humbert P. Dermatology. 1999;199(Suppl 1):49–52. | Mukherjee S, et al. Clin Interv Aging. 2006;1(4):327–348.

08 · 01 · CLINICAL EVIDENCE — LONG-TERM

Elasticity, Skin Thickness and Long-Term Performance

One-Year Instrumental Study: 0.05% Retinaldehyde

n=21 in the retinaldehyde group versus n=19 in the emollient-control group; high-resolution ultrasound plus echorheometry; measurements at baseline and one year.

01 Temporal epidermal thickness increased significantly versus control (p < 0.01).
02 Skin elasticity improved significantly versus control using suction rheology (p < 0.01).
03 Dermal thickness showed an increasing trend, while skin stiffness showed a decreasing trend.
04 Tolerance remained good throughout, supporting long-term daily use.

Increase in Dermal Thickness with a Non-Ablative Laser Regimen

Randomized double-blind study (n=16); 0.05% retinaldehyde versus vehicle for three months.

Diridollou S, et al. Dermatology. 1999;199(Suppl 1):37–41. | Mordon data cited in Mukherjee S, et al. Clin Interv Aging. 2006;1(4):327–348.

09 · 01 · TOLERANCE PROFILE

High Activity Does Not Have to Mean High Irritation

In long-term clinical use, all three reaction rates were significantly lower with retinaldehyde; between-group analysis p < 0.0001.

Setting Finding
Maximized conditions Retinol and retinaldehyde showed similarly low irritation potential, while retinoic acid was significantly more irritating (p < 0.05). Laser Doppler confirmed an irritant effect for RA but not for ROL/RAL (p = 0.001).
Long-term clinical conditions Retinaldehyde demonstrated clear retinoid biological activity, while rates of erythema, scaling and burning/pruritus were significantly lower than with retinoic acid.
Product implication Efficacy and user experience can coexist, supporting sustained use and repurchase in premium retinoid products.

Fluhr JW, et al. Dermatology. 1999;199(Suppl 1):57–60. | Sachsenberg-Studer EM. Dermatology. 1999;199(Suppl 1):61–63.

10 · 02 · SYNERGY — BAKUCHIOL

Why Bakuchiol

Bakuchiol is a plant-derived molecule with retinol-like gene-expression effects and multi-pathway skin activity. It is more than a natural retinol alternative; it represents an independent multi-pathway biology.

Feature Description
Source and class Derived from the seeds and leaves of Psoralea corylifolia; a meroterpene phenol.
Structure and function Chemically dissimilar to retinoids but functionally analogous to retinol.
Mechanism Does not directly engage the RAR receptor pathway, helping explain its gentler tolerance profile.
Use pattern No reported photosensitivity; suitable for morning and evening use.

Retinol-like gene expression, collagen and ECM support, antioxidant defense, inflammatory-signal modulation, skin homeostasis and barrier support, and pigment management

Antioxidant defense × inflammatory modulation × ECM support × homeostasis maintenance form a second renewal pathway beyond retinal.

Chaudhuri RK, Bojanowski K. Int J Cosmet Sci. 2014;36(3):221–230.

11 · 02 · SYNERGY — GENE EXPRESSION & COLLAGEN

Bakuchiol: Retinol-Like Gene Expression × ECM Support

Evidence dimension Finding
Collagen expression Human dermal fibroblast model; ELISA; untreated control set at 100%; 10 μg/mL. Bakuchiol exceeded retinol for Collagen I and IV expression and was comparable for Collagen III.
Gene-expression profile DNA microarray analysis in a full-thickness reconstructed skin model showed highly similar overall regulation by bakuchiol and retinol, including upregulation of COL1A2, COL4A6, COL9A2, COL17A1, HAS3 and hydration-related AQP3.
Non-classical RA pathway No effect on RA receptor genes such as RARB and RARG, suggesting action through non-classical retinoic-acid signaling and supporting a gentler irritation profile.
12-week human study 0.5% bakuchiol significantly improved fine lines and wrinkles, pigmentation, elasticity, firmness and overall photodamage without the adverse effects commonly associated with retinol therapy.

Chaudhuri RK, Bojanowski K. Int J Cosmet Sci. 2014;36(3):221–230. | Brown A, et al. Dermatol Ther (Heidelb). 2023;13(10):2299–2317.

12 · 02 · BAKUCHIOL — HUMAN EVIDENCE

Comparable Efficacy to 0.5% Retinol with Better Tolerance

Study design: prospective, randomized, double-blind study; n=44; 12 weeks; 0.5% bakuchiol twice daily versus 0.5% retinol once daily; high-resolution facial imaging plus blinded dermatologist grading.

Tolerance difference Description
Retinol More facial scaling and stinging were reported.
Bakuchiol Suitable for morning and evening use, with no reported photosensitivity; offers wider design space for sensitive skin and higher-frequency use.

Head-to-head human evidence shows that bakuchiol was comparable to 0.5% retinol for both wrinkles and pigmentation, with better tolerance.

Dhaliwal S, et al. Br J Dermatol. 2019;180(2):289–296. | Draelos ZD, et al. J Drugs Dermatol. 2020;19(12):1181–1183.

13 · 03 · COMPLEMENTARY BIOLOGY

Two Actives, Two Complementary Biological Systems

Dimension Retinal Bakuchiol Complementary value
Core pathway Direct precursor of retinoic acid → classical RAR retinoid signaling Retinol-like transcriptional response via a non-classical RA pathway Dual-pathway coverage without full overlap
Epidermal action Epidermal renewal, keratinocyte differentiation and epidermal thickness Barrier and homeostasis support; enhancement of differentiation-related genes Renewal plus homeostasis
ECM/collagen Fibroblast function, new collagen deposition and MMP inhibition Collagen I/III/IV expression and ECM support Synthesis promotion × degradation management
Oxidation/inflammation Management of photoaging-related matrix degradation ROS defense and inflammatory-signal modulation A protective environment for high-efficiency activity
Pigment/blemish-prone skin Depigmenting activity, keratinization renewal and C. acnes inhibition Pigmentation improvement and blemish-prone skin support Multi-target clarity and tone management
Tolerance Significantly better than retinoic acid Better than 0.5% retinol in a head-to-head study Long-term-use friendliness for premium products

One pathway is a high-efficiency engine operating through classical RAR signaling; the other is a multi-pathway support system for homeostasis—Retinal × Bakuchiol complementary biology.

14 · 03 · DUAL-PATHWAY RENEWAL

Dual-Pathway Renewal: A More Complete Renewal LogicClassical RAR signaling from retinal plus multi-pathway homeostasis support from bakuchiol

Retinal pathway Bakuchiol pathway
One-step oxidation to retinoic acid Plant-derived meroterpene phenol
RAR-RXR heterodimer and target-gene transcription Retinol-like transcriptional response plus antioxidant and inflammatory modulation; non-classical RA pathway, NF-κB and ROS defense
Epidermal renewal, keratinocyte differentiation, ECM remodeling, collagen homeostasis and MMP management Skin homeostasis, barrier support, ECM support, photoaging defense and pigment management

Dual-pathway retinoid renewal: epidermal renewal · ECM support · oxidative defense · homeostasis maintenance.

15 · 03 · RETINAL + BAKUCHIOL — COMBINED HUMAN EVIDENCE

Combined-System Human Study: Multidimensional Signals in 28 Days

Study design: open-label proof of concept; n=32 women, 65.6% with sensitive skin; once nightly for 28 days; a complex containing 0.1% liposomal retinal plus bakuchiol, with Vigna aconitifolia extract, niacinamide and melatonin.

01 100% of subjects showed a reduction in crow’s-feet count; all 32 of 32 participants improved.
02 Good tolerance: no significant changes in erythema or burning/stinging; no participant, including those with sensitive skin, needed to alter the once-daily regimen.
03 Methods: Cutometer® for firmness R0 and elasticity R2, Primos®-CR for wrinkles and VISIA®-CR for tone; D0–D28 change from baseline; *p<0.05, ***p<0.001.

Note: These data describe the complete active system containing retinal plus bakuchiol and do not isolate the individual contribution of either ingredient.

Brown A, et al. Dermatol Ther (Heidelb). 2023;13(10):2299–2317.

16 · 03 · FROM EFFICACY TO MECHANISM

From Human Efficacy to Molecular Mechanism

01 Enhanced gene expression: In a full-thickness reconstructed human skin model, adding bakuchiol to 0.1% retinal further enhanced retinal’s regulation of keratinocyte-differentiation genes CASP14, KRT14 and TP63 and barrier genes FLG, CDSN and CLDN1. Several changes exceeded the 0.05% retinoic-acid control.
02 No increase in irritation potential: In a reconstructed human epidermis model, ET50 remained >24 hours for both 0.1% retinal alone and retinal + bakuchiol + Vigna aconitifolia extract, maintaining gentleness while improving performance.
03 Mechanistic interpretation: Bakuchiol upregulated CRABP-II and genes related to retinol metabolism, supporting efficient RA signaling and providing a complementary mechanistic explanation for combined-system efficacy.

Ex Vivo UV-Photodamaged Skin Model: Combined System

Marker Change
CRABP-II expression +68%
Hyaluronic acid +71% versus UV-exposed skin
Procollagen I +33%
Degraded collagen −46% by CHP staining
MMP-1 expression −36%
Total collagen +16%, fully preventing UV-induced loss

Scientific boundary: the evidence demonstrates multidimensional efficacy and complementary mechanisms for the combined system; it does not prove strict pharmacological synergy between the two ingredients.

Brown A, et al. Dermatol Ther (Heidelb). 2023;13(10):2299–2317.

17 · 04 · DELIVERY — THE FORMULATION CHALLENGE

Why Nano Delivery Is Needed

Retinal: high activity, high sensitivity Bakuchiol: the dispersion challenge of a lipophilic molecule
Oxidation-sensitive aldehyde structure Lipophilic and naturally incompatible with high-water systems
Light-sensitive, with activity loss under illumination Application and dispersion challenges in high-water systems
Storage-stability challenges Formula uniformity requires technical support
Free active is vulnerable to the formulation environment System compatibility requires optimization

High activity does not automatically equal high performance. An active must be protected, dispersed and delivered before efficacy can be realized in a formula. NanoActive™ encapsulation is designed for sensitive actives.

18 · 04 · DELIVERY — NANOACTIVE™ TECHNOLOGY

Nano-Encapsulation Converts High Activity into High PerformanceNano-carriers encapsulate retinal and bakuchiol across protection, dispersion, delivery and formulation performance

01 Protection: Isolates and protects sensitive actives, reducing direct exposure to light, oxygen and the formulation environment.
02 Dispersion: Improves the dispersion and uniformity of lipophilic actives in high-water systems and optimizes compatibility.
03 Delivery: Supports even delivery and distribution of actives on the skin.
04 Performance: Improves development flexibility across serums, emulsions, gels and other modern formats—converting high activity into high formulation performance.

19 · 04 · FREE ACTIVE vs NANO-ENCAPSULATED

Free Active vs Nano-Encapsulated

Free active NanoActive™ encapsulation system
Light/oxygen/formulation environment: direct exposure to degradation factors Active encapsulation: retinal and bakuchiol loaded into nano-carriers
Activity loss during storage and shelf life Protection from light, oxygen and the formulation environment
Dispersion challenge and limited uniformity in high-water systems Stable and uniform distribution in high-water systems
Restricted delivery, reduced performance and narrower dosage-form choice Uniform delivery and greater design freedom across serums, emulsions, gels and other modern formats

Specific technical parameters such as particle size, encapsulation efficiency, release profile and stability are subject to the PuriPharm product technical documents (TDS/COA).

20 · 05 · APPLICATION — SKIN PERFORMANCE

Wrinkles · Firmness · Elasticity · Renewal

01 Wrinkles and photoaging: RAR-driven epidermal renewal and dermal remodeling; a retinal + bakuchiol system reduced wrinkle count by 43.2% in 28 days (p<0.001); retinaldehyde produced wrinkle and roughness improvement comparable to retinoic acid in an n=125 randomized trial.
02 Firmness and elasticity: Support for Collagen I/III, elastin, ECM and MMP management; after 28 days, elasticity increased 13.9% (p<0.001) and firmness increased 5.6% (p<0.05); one year of 0.05% retinaldehyde significantly improved skin elasticity (p<0.01).
03 Epidermal renewal: Regulation of keratinocyte differentiation and renewal, increased epidermal thickness (p<0.01), and improved texture and radiance—the mechanistic basis for night renewal and Skin Longevity products.
04 Tone improvement: Retinal depigmenting activity and epidermal renewal plus bakuchiol-associated pigment improvement in 59% of subjects; tone uniformity increased 7.0% after 28 days (p<0.05).

Brown A, et al. Dermatol Ther (Heidelb). 2023;13(10):2299–2317. | Diridollou S, et al. Dermatology. 1999;199(Suppl 1):37–41. | Sorg O, et al. Dermatology. 2013;227(3):231–237. | Dhaliwal S, et al. Br J Dermatol. 2019;180(2):289–296.

21 · 05 · APPLICATION — ANTIOXIDANT · BLEMISH-PRONE SKIN

Antioxidant Defense and Blemish-Prone Skin Microenvironment ManagementUV/pollution → ROS → oxidative stress → inflammatory signaling → increased MMP → collagen degradation; bakuchiol supports ROS defense, inflammatory modulation and MMP management

A Distinct Antibacterial Dimension of Retinal

01 In vivo: daily 0.05% retinaldehyde reduced median viable C. acnes density by 10² log/cm² after two weeks; vehicle had no effect.
02 Comedolytic and keratinization-renewal activity was observed in an animal model.
03 Bakuchiol antioxidant and inflammatory-modulating activity supports blemish-prone skin care.
04 Cosmetic language: clarity, balance, keratin renewal, blemish-prone skin care and microenvironment management.

Pechère M, et al. Dermatology. 1999;199(Suppl 1):29–31. | Fort-Lacoste L, et al. Dermatology. 1999;199(Suppl 1):33–35. | Chaudhuri RK, Bojanowski K. Int J Cosmet Sci. 2014;36(3):221–230.

22 · 06 · SKIN & SCALP LONGEVITY

From Skin Longevity to Scalp Longevity

The scalp is an extension of facial skin. The same biology that drives facial renewal—epidermal turnover, barrier homeostasis, oxidative-stress management and ECM support—also applies to the scalp and follicular microenvironment.

Skin Longevity → Scalp Longevity → Follicular Microenvironment

Setting Core biology
Facial skin Renewal, ECM, tone and homeostasis
Scalp Keratinization renewal, barrier, ROS and inflammatory microenvironment
Follicular microenvironment Epithelial homeostasis and perifollicular ECM
01 Scalp aging involves declining barrier function, accumulated oxidative stress and changes in the follicular microenvironment, sharing a mechanistic framework with facial photoaging.
02 The dual-pathway logic of retinoid biology and antioxidant support naturally extends to scalp-renewal applications.
03 The NanoActive™ delivery system supports dispersion and delivery in lightweight scalp-serum formats.

Positioning: Scalp Longevity Active System | Scalp Longevity Serum | Advanced Scalp Renewal | Skin & Scalp Longevity

23 · 06 · SCALP & FOLLICLE BIOLOGY

Scalp Renewal and Follicular Microenvironment SupportScalp epidermis, dermal/follicular zone and follicular microenvironment

Level Support direction
Scalp epidermis Keratinization renewal, scalp barrier and homeostasis
Dermal/follicular zone Follicular epithelium, perifollicular ECM and sebaceous glands
Follicular microenvironment ROS management, inflammatory signaling and environmental stress
01 Retinoid biology and the follicle: Retinoic-acid synthesis is localized to specific regions of the follicle and sebaceous gland, including the stem-cell microenvironment. Precisely regulated RA levels are essential to follicular epithelial homeostasis.
02 Oxidative stress and scalp aging: Oxidative stress is an important driver of scalp and hair aging. Bakuchiol’s antioxidant and inflammatory-modulating properties provide protective support for the perifollicular microenvironment.
03 Product positioning: Focuses on the scalp-care environment and biological support—scalp renewal, barrier maintenance and follicular microenvironment management—without drug-like hair-growth or anti-hair-loss claims.

Everts HB. Biochim Biophys Acta. 2012;1821(1):222–229. | Trüeb RM. Int J Trichology. 2009;1(1):6–14. | Trüeb RM. Int J Cosmet Sci. 2015;37(Suppl 2):25–30.

24 · 07 · APPLICATION MAP

Multi-Setting Applications

Face Eye Scalp & Hair
Advanced anti-aging serumsNight-renewal serumsLine-smoothing serumsFirming creamsSkin Longevity productsPhotoaging careTone-radiance careBlemish-prone skin care Eye serumsLine-smoothing eye creamsCrow’s-feet managementIn the combined-system study, 100% of subjects showed fewer crow’s feet after 28 days Scalp serumsAnti-aging scalp serumsScalp Longevity SerumHair Vitality SerumNight scalp careFollicular microenvironment care

Premium concepts: Retinoid Cycling | Skin Longevity | Scalp Longevity | Healthy Aging | Preventive Aging | Night Renewal

25 · THE PLATFORM

A Next-Generation Dual-Pathway Retinoid Renewal PlatformAdvanced retinal biology + complementary multi-pathway bakuchiol activity + NanoActive™ nano delivery

Platform value Description
Performance One oxidation step to RAR signaling, supported by a complete human-efficacy evidence chain.
Complementary biology Retinol-like gene expression × antioxidant defense × homeostasis support.
Delivery Protection, dispersion and delivery convert high activity into high formulation performance.
Skin + scalp applications A platform spanning both Skin Longevity and Scalp Longevity.

NanoActive™ Retinal-Bakuchiol: Retinoid performance, redefined.

PuriActives® and NanoActive™ are trademarks of PuriPharm Co., Ltd. This material is intended solely for technical communication concerning cosmetic ingredients.

26 · SCIENTIFIC REFERENCES

Scientific References

01 Siegenthaler G, Saurat JH, Ponec M. Retinol and retinal metabolism. Relationship to the state of differentiation of cultured human keratinocytes. Biochem J. 1990;268(2):371–378.
02 Saurat JH, et al. Topical retinaldehyde on human skin: biologic effects and tolerance. J Invest Dermatol. 1994;103(6):770–774.
03 Creidi P, et al. Profilometric evaluation of photodamage after topical retinaldehyde and retinoic acid treatment. J Am Acad Dermatol. 1998;39(6):960–965.
04 Creidi P, Humbert P. Clinical use of topical retinaldehyde on photoaged skin. Dermatology. 1999;199(Suppl 1):49–52.
05 Diridollou S, et al. Efficacy of topical 0.05% retinaldehyde in skin aging by ultrasound and rheological techniques. Dermatology. 1999;199(Suppl 1):37–41.
06 Boisnic S, et al. Repair of UVA-induced elastic fiber and collagen damage by 0.05% retinaldehyde cream in an ex vivo human skin model. Dermatology. 1999;199(Suppl 1):43–48.
07 Pechère M, et al. Antibacterial activity of retinaldehyde against Propionibacterium acnes. Dermatology. 1999;199(Suppl 1):29–31.
08 Fort-Lacoste L, et al. Comedolytic effect of topical retinaldehyde in the rhino mouse model. Dermatology. 1999;199(Suppl 1):33–35.
09 Fluhr JW, et al. Tolerance profile of retinol, retinaldehyde and retinoic acid under maximized and long-term clinical conditions. Dermatology. 1999;199(Suppl 1):57–60.
10 Sachsenberg-Studer EM. Tolerance of topical retinaldehyde in humans. Dermatology. 1999;199(Suppl 1):61–63.
11 Mukherjee S, et al. Retinoids in the treatment of skin aging: an overview of clinical efficacy and safety. Clin Interv Aging. 2006;1(4):327–348.
12 Sorg O, et al. The potential depigmenting activity of retinaldehyde. Dermatology. 2013;227(3):231–237.
13 Kwon HS, et al. Efficacy and safety of retinaldehyde 0.1% and 0.05% creams used to treat photoaged skin: a randomized double-blind controlled trial. J Cosmet Dermatol. 2018;17(3):471–476.
14 Chaudhuri RK, Bojanowski K. Bakuchiol: a retinol-like functional compound revealed by gene expression profiling and clinically proven to have anti-aging effects. Int J Cosmet Sci. 2014;36(3):221–230.
15 Dhaliwal S, et al. Prospective, randomized, double-blind assessment of topical bakuchiol and retinol for facial photoageing. Br J Dermatol. 2019;180(2):289–296.
16 Brown A, et al. Natural retinol analogs potentiate the effects of retinal on aged and photodamaged skin: results from in vitro to clinical studies. Dermatol Ther (Heidelb). 2023;13(10):2299–2317.
17 Draelos ZD, et al. Clinical evaluation of a nature-based bakuchiol anti-aging moisturizer for sensitive skin. J Drugs Dermatol. 2020;19(12):1181–1183.
18 Fisher GJ, et al. Molecular basis of sun-induced premature skin ageing and retinoid antagonism. Nature. 1996;379(6563):335–339.
19 Everts HB. Endogenous retinoids in the hair follicle and sebaceous gland. Biochim Biophys Acta. 2012;1821(1):222–229.
20 Trüeb RM. Oxidative stress in ageing of hair. Int J Trichology. 2009;1(1):6–14.

 

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