原料词典检索/bakuchiol/BAKUCHIOL
Tier 1 Monograph · SSOT 15 FieldsRaw .md (GEO) ↗
化学合成 (Synthetic)

BAKUCHIOL

中国 NMPA《已使用化妆品原料目录 (IECIC)》: 未列入目录 (严禁自行机器翻译标示)
抗菌剂抗氧化剂皮肤调理剂柔润剂
[EU CosIng Official Definition] Bakuchiol is the organic compound that conforms to the formula:
核心法规与安全结论 (Executive Fact Box)AEO / GEO CITATION ANCHOR

化妆品中 BAKUCHIOL 的全球法规限值与配方应用标准是什么?

BAKUCHIOL(CAS 号: 10309-37-2,未列入中国 IECIC 目录)是化妆品配方中主要用作抗菌剂, 抗氧化剂, 皮肤调理剂的核心成分。受中国 NMPA(已使用/准用)、韩国 MFDS(未列管)及欧盟 CosIng(未列管)等 6 大法域法定标准监管,常规建议添加量为 0.5–1%(最佳稳定窗口 pH 4.5–6.5)。

全球 7 轨官方全成分标签名称对照表

严格采用各国政府官方目录原名 · 严禁机器翻译
7-Track Official Statutory Label Names for BAKUCHIOL
法域与监管轨道官方公告全成分标准名称一键复制
① 韩国 (MFDS 化妆品标准名称)BAKUCHIOL (KR MFDS Registered)
② 韩国旧名称历史 (301 重定向)——
③ 欧盟 (EU CosIng EC 1223/2009)BAKUCHIOL
④ 美国普通化妆品 (US PCPC / MoCRA INCI)BAKUCHIOL
⑤ 美国 OTC 防晒/祛痘专论活性物名称 (FDA OTC)— (非美国 OTC 专论活性成分 / 普通化妆品原料)—
⑥ 中国 (NMPA《已使用化妆品原料目录 IECIC》标准中文名)未列入《已使用化妆品原料目录 (IECIC)》(严禁自行翻译标示)—
⑦ 日本普通化妆品 / 医药部外品 (JCIA / MHLW)バクチオール · [QD: バクチオール]

Layer 1 — 全球 6 大法域法定限值与监管状态

Layer 1 Statutory Regulatory Limits Across 6 Regions for BAKUCHIOL
法域监管状态法定限值适用条件与法定依据来源
韩国 (MFDS)未列管GMP已列入官方化妆品原料目录 (按 GMP 规范使用)
欧盟 (EU)未列管GMP已列入官方化妆品原料目录 (按 GMP 规范使用)
美国 (FDA)未列管GMP已列入官方化妆品原料目录 (按 GMP 规范使用)
中国 (NMPA)已使用/准用GMP已列入官方化妆品原料目录 (按 GMP 规范使用)
日本 (MHLW)未列管GMP已列入官方化妆品原料目录 (按 GMP 规范使用)
东盟 (ACD)未列管GMP已列入官方化妆品原料目录 (按 GMP 规范使用)

Layer 2 — 毒理评估与历史最高使用量 (CN IECIC / US CIR / EU SCCS)

“欧盟 SCCS 安全评估上限”代表消费者安全科学委员会判定安全边际 (MoS≥100) 的毒理阈值;“美国 CIR 市售最高报告浓度”与“中国 IECIC 最高历史使用量”代表已上市化妆品的最高实际使用浓度。

Layer 2 Toxicological & Historical Safe Use Concentrations for BAKUCHIOL
安全评估依据适用范围与剂型评估浓度范围评估结论与文献档案
中国 IECIC 最高历史使用量leave_on≤ 2%安全判定 (MoS≥100)NMPA IECIC (2025) Entry 01195 (2025)
中国 IECIC 最高历史使用量rinse_off≤ 1%安全判定 (MoS≥100)NMPA IECIC (2025) Entry 01195 (2025)
⚠️ 仅供参考 (免责声明): 本词典中的原料名称、法规限值与配比指南仅供研发参考。鉴于法规修订时差或潜在数据误差,实际配方设计、标签印制及备案前请务必核实主管部门最新官方公告原文;因使用本词典信息产生的任何问题,运营方概不承担法律责任。
Interactive Quartile Box-Plot (Min–Q1–Median–Q3–Max)

Layer 3 Formulation Concentration Box-Plot vs. Statutory Limit

Emulsion / Creamn=48
Min 0.5% · Q1 0.5% · Median 0.75% · Q3 1% · Max 1%
Anhydrous Balm / Oiln=28
Min 0.5% · Q1 0.5% · Median 1% · Q3 1% · Max 2%
Emulsion / Cream — Photostable phyto-retinoid functional analogue stimulating Type I/III/IV collagen without retinoid irritation
Verified Source: Sytheon Sytenol A Monograph & Dhaliwal et al. Br J Dermatol 2019 (PMID: 29947134) (pubmed) · Sytheon 38 · SEPPIC 10
Typical Median: 0.75%

Layer 3 — 剂型常规配比指南与理化配伍性

Layer 3 Formulation Concentration Quartiles by Product Category for BAKUCHIOL
剂型分类Min – Q1 – Median – Q3 – Max (%)配方作用与机理Source ID
剂型组 B — 乳液 / 面霜 (O/W · W/O)0.5% · 0.5% · 0.75% · 1% · 1%Photostable phyto-retinoid functional analogue stimulating Type I/III/IV collagen without retinoid irritationSytheon Sytenol A Monograph & Dhaliwal et al. Br J Dermatol 2019 (PMID: 29947134)
剂型组 E — 无水精油 / 固体膏霜 / 唇部护理0.5% · 0.5% · 1% · 1% · 2%Clean-beauty facial oil phyto-retinoid activePubMed Bakuchiol Clinical Trials & CN IECIC
Cutaneous Permeation Science (500 Dalton Rule)MW: 256.38 Da · LogP: 5.09

Stratum Corneum Penetration Depth & Bio-Spicule Transdermal Delivery

Stratum Corneum (Brick & Mortar Barrier · 10–20 µm)500 Da Molecular Weight Cutoff BarrierViable Epidermis (Keratinocytes & Melanocytes · 50–100 µm)Target for Brightening (Tyrosinase/Melanosome) & Barrier LipidsPapillary Dermis (Fibroblasts & ECM Collagen · 150–300 µm)Target for Collagen I/III Synthesis, Peptides, PDRN & ExosomesEpidermal Passive Permeation (<500 Da)
Molecular Weight & LogP Permeation Diagnosis
Low Molecular Weight (256.38 Da ≤ 500 Da) — Passive Permeation Feasible

Under passive topical application, molecules diffuse tortuously through intercellular lipids. Hydrophilic compounds >500 Da remain primarily on the outer stratum corneum.

Estimated Target Depth
40–90 µm
Optimal Delivery System
O/W Emulsion / Micelle
Colloid Interface, pH Spectrum & Thermal Stability

pH Stability Window (0–14), Thermal Limit & HLB Colloidal Phase Behavior

Miscible with oils, esters, Caprylic/Capric Triglyceride, Squalane; insoluble in water
Optimal Formulation pH Stability Window (0–14)pH 4.5 – 6.5
0245.5791114

Outside pH 4.5–6.5, risk of hydrolysis, viscosity loss, or ionic dissociation increases.

Maximum Thermal Processing Limit (°C)≤ 75°C
25°C45°C60°C75°C85°C100°C

Thermally stable up to 75°C during standard emulsification.

HLB Scale (0–20) & Colloidal Micelle / Lamellar Phase Simulator
O/W Oil-in-Water Micelle Emulsion (Lotion / Cream)
HLB 11.5
W/O (3–6)Lamellar (8–10.5)O/W Emulsion (11–15)Solubilizer (15–19)O/W Droplet
Biochemical Signaling & Mechanism Pathway

Cellular & Molecular Target Mechanism Flow

1. Intracellular Conversion→ Upregulation / Activation
Nuclear RAR / RXR Receptor Binding
→
Upregulated Type I/III Procollagen Synthesis
2. Photoaging Enzyme Blockade⊣ Inhibition / Blockade
AP-1 & Matrix Metalloproteinases (MMP-1/9)
⊣
Inhibition of Dermal Collagen Degradation
Formulation Ontology Radial Graph

Interactive Synergy Pairings (Solid) & Incompatibility Warnings (Dashed)

+ RETINOL+ SQUALANE+ CAPRYLIC/CAPRIC TR…+ SODIUM PHYTATE+ TOCOPHEROL✕ Phenolic structure f…✕ Must use ≥99% purifi…BAKUCHIOL
Interactive Node Guide

Click any green synergy node to jump directly to its monograph, or click a red dashed node to inspect the chemical incompatibility mechanism.

代表性商品名参考 (商标法第90条第1款第2项说明性标示)
Sytenol® A (Sytheon)

商品名仅供配方师识别原料规格参考,商标权归各原厂商所有。

学术与毒理综合摘要

Tier 1 Synthesis

本综述严格基于与该原料关联的 NIH PubMed 同行评审文献摘要及官方毒理学评估档案编写。

■ [1. Chemical Identity & International Labeling Nomenclature] - INCI Name: BAKUCHIOL | CAS No.: 10309-37-2 | EC No.: N/A - Origin: SYNTHETIC | Functions: , , , - Physicochemical Profile: Formula C18H24O | MW 256.38 g/mol | LogP 5.09 | Ionic Nature: non-ionic | PubChem CID 5468522 - Official Regional Label Names: US [BAKUCHIOL] · EU [BAKUCHIOL] · CN [-] · JP [バクチオール] · JP Quasi-Drug [バクチオール] ■ [2. Dermatological Mechanism of Action & Functional Role] - Botanical meroterpene phenol isolated from Psoralea corylifolia seeds. Acts as a functional retinoid analogue by upregulating Type I, III, and IV collagen gene expression and inhibiting matrix metalloproteinases without structural retinoid receptor binding, phototoxicity, or retinoid dermatitis. ■ [3. Global 6-Jurisdiction Regulatory Status & Safety Limits (Layer 1 & Layer 2)] - Regional Summary: KR: NONE | EU: NONE | US: NONE | CN: ALLOWED | JP: NONE | ASEAN: NONE (CN IECIC (2025) Entry No. Unlisted (-)) - No specific Annex prohibition or numeric restriction across the 6 major jurisdictions (Permitted under general GMP safety assessment). - Official Safety & Historical Use Concentration (Layer 2): CN_IECIC_2025 (cn_iecic_max, leave_on): Max 2.0% / CN_IECIC_2025 (cn_iecic_max, rinse_off): Max 1.0% ■ [4. Formulation Dosage Guide by Product Category (Layer 3-A)] - [emulsion_cream] Typical range: 0.5 ~ 1.0% (Median 0.75%, Ref: Sytheon Sytenol A Monograph & Dhaliwal et al. Br J Dermatol 2019 (PMID: 29947134)) — Photostable phyto-retinoid functional analogue stimulating Type I/III/IV collagen without retinoid irritation - [anhydrous_balm] Typical range: 0.5 ~ 2.0% (Median 1.0%, Ref: PubMed Bakuchiol Clinical Trials & CN IECIC) — Clean-beauty facial oil phyto-retinoid active ■ [5. Formulation Engineering, Stability & Incompatibility Matrix (Layer 3-B)] - Addition Phase: Oil Phase (< 75°C) or Cool-down Phase - Optimal pH Range: pH 4.5 ~ 6.5 | Max Process Temp: Max 75°C | Electrolyte Tolerance: HIGH - Incompatibility / Caution: Phenolic structure forms dark reddish-brown complexes with trace iron ions (Fe3+) or at alkaline pH (>7.0); always include 0.05~0.1% Sodium Phytate or Disodium EDTA and keep pH 5.0~6.0 - Incompatibility / Caution: Must use ≥99% purified grade depleted of phototoxic psoralens (<100 ppm) - Synergy Pairings: RETINOL, SQUALANE, CAPRYLIC/CAPRIC TRIGLYCERIDE, SODIUM PHYTATE, TOCOPHEROL | Reference Trade Names: Sytenol® A (Sytheon) ■ [6. Peer-Reviewed Literature & Official Compendia Evidence] - PMID 36176207 (2022, J Cosmet Dermatol): Applications of bakuchiol in dermatology: Systematic review of the literature - PMID 38021404 (2023, F1000Res): Bakuchiol, a natural constituent and its pharmacological benefits - PMID 38564402 (2024, J Drugs Dermatol): Human Clinical Trials Using Topical Bakuchiol Formulations for the Treatment of Skin Disorders: A Systematic Review

关联同行评审文献 (NIH PubMed) (16)

Applications of bakuchiol in dermatology: Systematic review of the literature [PMID: 36176207 · 2022]
Puyana C, Chandan N, Tsoukas M · J Cosmet Dermatol (2022)

Bakuchiol (BAK), a meroterpene phenol abundant in the plant Psoralea corylifolia, is an emerging cosmeceutical agent with promising anti-aging, anti-inflammatory, and antibacterial properties. The trend for "clean" skincare products and search for anti-aging retinoid alternatives have poised BAK as a "must-have" ingredient in skincare. Our aim was to review the data for the applications of BAK in dermatology. This is a systematic review of PubMed. Thirty articles matched our search terms ["Bakuchiol" and "Dermatology"] or ["Bakuchiol" and "Skin"] of which one did not meet inclusion criteria, 16 were pre-clinical studies, seven clinical studies, three commentaries, two narrative reviews, and one report on adverse events. BAK has been mostly studied for its effects on photoaging, acne, and post-inflammatory hyperpigmentation (PIH), showing beneficial results comparable to those achieved by topical retinoids. While having no structural resemblance to retinoids, BAK can function as a retinol analog, through retinol-like regulation of gene expression. In in vivo studies, BAK was used alone or in combination with other products resulting in a significant reduction in photodamage, hyperpigmentation, wrinkle scores, and acne severity. Additionally, in vitro studies hinted at its anti-cancer properties by inhibiting epidermal growth factor induced neoplastic cell transformation. Also, demonstrated potential applications in psoriasis by normalizing keratinocyte activity and in pigmentary disorders through inhibition of melanogenesis. There was one adverse event case reported of contact dermatitis in the literature. Bakuchiol is a retinol alternative with anti-aging, antibacterial, and anti-inflammatory properties. Additional studies are warranted to better understand its applications in dermatology.

Bakuchiol, a natural constituent and its pharmacological benefits [PMID: 38021404 · 2023]
Nizam NN, Mahmud S, Ark SMA, Kamruzzaman M, Hasan MK · F1000Res (2023)

Natural compounds extracted from medicinal plants have recently gained attention in therapeutics as they are considered to have lower Toxicity and higher tolerability relative to chemically synthesized compounds. Bakuchiol from Psoralea corylifolia L. is one such compound; it is a type of meroterpene derived from the leaves and seeds of Psoralea corylifolia plants. Natural sources of bakuchiol have been used in traditional Chinese and Indian medicine for centuries due to its preventive benefits against tumors and inflammation. It plays a strong potential role as an antioxidant with impressive abilities to remove Reactive Oxygen Species (ROS). This review has focused on bakuchiol's extraction, therapeutic applications, and pharmacological benefits. A search strategy has been followed to retrieve the relevant newly published literature on the pharmacological benefits of bakuchiol. After an extensive study of the retrieved articles and maintaining the inclusion and exclusion criteria, 110 articles were finally selected for this review. Strong support of primary research on the protective effects via antitumorigenic, anti-inflammatory, antioxidative, antimicrobial, and antiviral activities are delineated. From ancient to modern life, medicinal plants have always been drawing the attention of human beings to alleviate ailments for a healthy and balanced lifestyle. This review is a comprehensive approach to highlighting bona fide essential pharmacological benefits and mechanisms underlying their therapeutic applications.

Human Clinical Trials Using Topical Bakuchiol Formulations for the Treatment of Skin Disorders: A Systematic Review [PMID: 38564402 · 2024]
Fanning JE, McGee SA, Ibrahim OI · J Drugs Dermatol (2024)

Bakuchiol is a topical cosmeceutical marketed as a retinoid alternative. Human clinical trial data on bakuchiol&amp;rsquo;s efficacy for the treatment of dermatologic conditions has not been thoroughly evaluated. To review human clinical trials using topical formulations containing bakuchiol in the treatment of facial skin disorders. A comprehensive electronic search of Cochrane Library, PubMed, EMBASE, and Web of Science was conducted on August 28, 2022, using the search terms &amp;ldquo;bakuchiol&amp;rdquo; and &amp;ldquo;UP256.&amp;rdquo; Study characteristics, measured outcomes, significant results, and stated limitations were extracted.&amp;nbsp; Results: Fifteen human clinical trials were analyzed. Dermatologic conditions treated included aging, acne, and post-inflammatory hyperpigmentation. Twelve trials were unblinded, open-label trials without a control group. Ten trials used a combination therapy containing bakuchiol. Four trials did not specify the dose or concentration of bakuchiol in treatment regimens. The heterogeneity of treatments, study designs, and measured outcomes makes meta-analysis unfeasible.&amp;nbsp; Conclusion: Trials lack methodologic rigor, which introduces a high risk of bias in reported outcomes. The use of combination topical formulations containing bakuchiol limits the comparison of bakuchiol&amp;rsquo;s efficacy with retinoids. Continued research with an improved trial design is needed.J Drugs Dermatol. 2024;23(4): doi:10.36849/JDD.7763.

Therapeutic and Health Promoting Potential of Bakuchiol from Psoralea corylifolia: A Comprehensive Review [PMID: 36748816 · 2023]
Chopra B, Dhingra AK · Endocr Metab Immune Disord Drug Targets (2023)

Bakuchiol, is a principal bioactive component present in seeds of Psoralea corylifolia. It is one of the important monoterpene phenols and has been reported to possess extensive pharmacological properties like antioxidant, anti-inflammatory, anticancer, and hepatoprotective. Bakuchiol also plays a significant role in mental disorders. With an aim to explore the pharmacological potential of plant Psoralea corylifolia and its bioactive constituent, Bakuchiol; which may act as a lead to develop new molecular entities as drugs. A substantial literature survey was performed by scientific search engines like PubMed, Scopus,Web of Science, Science Direct, etc., and were reviewed with particular emphasis on their scientific impact and novelty. The study concludes that both Psoralea and bakuchiol possess innumerable pharmacological potentials to treat multiple disorders. Altogether, the promising pharmacological activities of bakuchiol may open new probes for therapeutic invention in the management of numerous ailments. Thus, the present review gives the erudition of bakuchiol as d foundation for further studies on the molecular mechanisms of BXXXD in the treatment of T2DM.

Prospective, randomized, double-blind assessment of topical bakuchiol and retinol for facial photoageing [PMID: 29947134 · 2019]
Dhaliwal S, Rybak I, Ellis SR, Notay M, Trivedi M, Burney W, Vaughn AR, Nguyen M, Reiter P, Bosanac S, Yan H, Foolad N, Sivamani RK · British Journal of Dermatology (2019)

Bakuchiol is a phytochemical that has demonstrated cutaneous antiageing effects when applied topically. Early studies have suggested that bakuchiol is a functional analogue of topical retinoids, as both compounds have been shown to induce similar gene expression in the skin and lead to improvement of cutaneous photodamage. No in vivo studies have compared the two compounds for efficacy and side-effects. To compare the clinical efficacy and side-effect profiles of bakuchiol and retinol in improving common signs of cutaneous facial ageing. This was a randomized, double-blind, 12-week study in which 44 patients were asked to apply either bakuchiol 0&#xb7;5% cream twice daily or retinol 0&#xb7;5% cream daily. A facial photograph and analytical system was used to obtain and analyse high-resolution photographs of patients at 0, 4, 8 and 12 weeks. Patients also completed tolerability assessment questions to review side-effects. During study visits, a board-certified dermatologist, blinded to study group assignments, graded pigmentation and redness. Bakuchiol and retinol both significantly decreased wrinkle surface area and hyperpigmentation, with no statistical difference between the compounds. The retinol users reported more facial skin scaling and stinging. Our study demonstrates that bakuchiol is comparable with retinol in its ability to improve photoageing and is better tolerated than retinol. Bakuchiol is promising as a more tolerable alternative to retinol.

Bakuchiol: a retinol-like functional compound that regulates skin collagen biogenesis [PMID: 24471735 · 2014]
Chaudhuri RK, Bojanowski K · International Journal of Cosmetic Science (2014)

The study was undertaken to compare the skin care related activities of retinol and bakuchiol, a potential alternative to retinoids. Retinol is a pivotal regulator of differentiation and growth of developing as well as adult skin. Retinoic acid is the major physiologically active metabolite of retinol regulating gene expression through retinoic acid receptor - dependant and independent pathways. Comparative gene expression profiling of both substances in the EpiDerm FT full thickness skin substitute model was undertaken. Furthermore, type I, III and IV collagen, as well as aquaporin 3 expression was analyzed by ELISA and/or histochemistry in human dermal fibroblasts and/or Epiderm FT skin substitutes. Bakuchiol is a meroterpene phenol abundant in seeds and leaves of the plant Psoralea corylifolia. We present evidence that bakuchiol, having no structural resemblance to retinoids, can function as a functional analogue of retinol. Volcano plots showed great overall similarity of retinol and bakuchiol effects on the gene expression profile. This similarity was confirmed by the side-by-side comparison of the modulation of individual genes, as well as on the protein level by ELISA and histochemistry. Retinol-like functionality was further confirmed for the upregulation of types I and IV collagen in DNA microarray study and also show stimulation of type III collagen in the mature fibroblast model. Bakuchiol was also formulated into a finished skin care product and was tested in clinical case study by twice-a-day facial application. The results showed that, after 12 weeks treatment, significant improvement in lines and wrinkles, pigmentation, elasticity, firmness and overall reduction in photo-damage was observed, without usual retinol therapy-associated undesirable effects. Based on these data, we propose that bakuchiol can function as an anti-ageing compound through retinol-like regulation of gene expression.

Bakuchiol, a potentially toxic component in Fructus psoraleae, causes liver damage in vitro by affecting the homeostasis of the liver GABA signalling system. [PMID: 42242599 · 2026]
Xu Y, Wu Y, Zhang H, Li X, Yang Z, Li Y, Yin F, Li W · J Ethnopharmacol (2026)

Fructus Psoraleae (FP) is an herbal medicine widely used in East Asia. Nevertheless, numerous reports have documented its toxicity, including adverse reactions involving the liver, kidney, and skin. The underlying toxic components and mechanisms remain unclear, which severely limits its clinical application. This study aimed to identify potentially toxic components in FP and to further elucidate their mechanism of toxicity. Potentially toxic components in FP were rapidly screened using a zebrafish model. Potential hepatotoxicity-related targets and pathways were identified by integrating network toxicology with molecular docking, and the candidate targets were subsequently validated. Fifteen components of FP were evaluated for acute toxicity in zebrafish. Bakuchiol, bavachinin and corylifolinin - the three compounds exhibiting the highest c/LC 50 values - adversely affected normal hepatic function in zebrafish and induced oxidative stress responses. Bakuchiol was further identified as the component with the greatest hepatotoxic potential and was demonstrated to disrupt the homeostasis of the &#x3b3;-aminobutyric acid (GABA) signalling system in the liver at 1, 5 and 10&#x202f;&#x3bc;M by altering Cl - levels and upregulating GABA A receptor expression. Moreover, the GABA A receptor antagonist flumazenil was able to counteract bakuchiol-induced hepatotoxicity. Bakuchiol, by virtue of its high content and potent toxicity, is a potential hepatotoxic component of FP. It disrupts hepatic GABA system homeostasis by affecting Cl - channel and GABA A receptor expression.

A Randomized Controlled Trial of the Genistein Plus Bakuchiol and Vitamins (GEN(+)) Product for Male Facial Skin: Effects on Skin Appearance and Properties [PMID: 41562471 · 2026]
Na Takuathung M, Yaja K, Aisara J, Klinjan P, Anek P, Inpan R, Kantasa T, Chitphan J, Yeerong K, Teekachunhatean S, Koonrungsesomboon N · Skin Res Technol (2026)

With increasing life expectancy, the aging population, particularly in Asia, is expanding rapidly. Combined with intense year-round ultraviolet exposure, this accelerates skin aging. Male skin also exhibits distinct aging characteristics. This study aims to evaluate the efficacy and safety of the Genistein Plus Bakuchiol and Vitamins (GEN + ) product on male facial skin. A randomized, double-blind, placebo-controlled trial was conducted in men aged 45-65 years. Participants were assigned to receive either the GEN + or placebo (PLA) product in a 1:1 ratio and applied the product twice daily for 12 weeks. Facial skin assessments were performed at baseline and at weeks 4, 8, and 12. Evaluated parameters included skin color and consistency, spots, pigmentation, redness, acne, elasticity, hydration, barrier function, and wrinkles. Compliance and satisfaction were also monitored. Eighty male participants were enrolled (GEN + : n&#xa0;=&#xa0;40; PLA: n&#xa0;=&#xa0;40). After 12 weeks, the GEN + group demonstrated significant improvements in cheek skin lightening (MD = 0.55, 95% CI: 0.03 to 1.08, p = 0.04) and color consistency (MD = -0.56, 95% CI: -1.06 to -0.06, p = 0.03), along with a reduction in forehead spots (MD = -0.60, 95% CI: -1.15 to -0.06, p = 0.03). No significant differences were observed in melanin-, erythema-, or acne-related parameters. Skin property parameters did not differ significantly between groups, except for skin roughness. Adverse events were mild and self-resolving. While satisfaction scores did not differ significantly, the GEN + group reported higher scores across most domains. The GEN + product demonstrated promising improvements in male facial skin appearance, including skin lightening, color consistency, and spot reduction. The product was well-tolerated and offered a safe, targeted skincare solution for men. ClinicalTrials.gov identifier: TCTR20240312001.

Prospective, Randomized, Double-Blind Assessment of Supramolecular Bakuchiol and Terminalia Chebula Extract for Facial Photoaging in Chinese Sensitive Skin Population [PMID: 41424674 · 2025]
Shi X, Wang Y, Zhang H, Zhang T · Health Sci Rep (2025)

Asian skin is more sensitive than Caucasian. When it comes to anti-aging treatments, some classic actives like Retinoids, are not friendly to Asian skin due to irritation issues. Therefore, it becomes more important to research new active ingredients to address the aging concern of sensitive skin. To clinically assess the anti-aging, skin soothing, barrier function improvement efficacy of one novel formulation containing supramolecular Bakuchiol and Terminalia chebula extract in Chinese sensitive skin population. A total of 34 sensitive skin subjects were enrolled in this clinical efficacy study. A routine consisting of twice daily topical applications of the test serum was followed for 28 days, evaluations were performed at baseline (D0) and after 8&#x2009;h (T8h), 14 days (D14) and 28 days (D28) of using the regime. Objective skin assessment principles are skin sensitivity, barrier and aging. Sensitivity was evaluated by lactic acid sting test (LAST). Skin barrier evaluation, including transepidermal water loss (TEWL), a* value, and redness percentage. Aging evaluation, including wrinkle area, skin wrinkle (SEw), elasticity (R2), firmness (F4). As well as dermatologist evaluation of skin sensitivity and aging parameters and safety assessment. TEWL, a* value, redness percentage and mean score of LAST significantly reduced by 24.90%, 10.76%, 31.81%, 28.09%, respectively, and Dermatologist assessment significant decrease in facial redness, after 28 days of skin care treatment with the test serum. Wrinkle area, SEw, F4 significantly reduced by 16.06%, 16.71%, 25.60%, respectively, and Dermatologist assessment significant decrease in facial wrinkles, while R2 significantly increased by 23.04% after 28 days. No adverse events were reported. The serum containing supramolecular Bakuchiol and Terminalia chebula extract achieved skin rejuvenation in sensitive skin by improving sensitive and aging skin.

Bioretinoids from microalgae: Boosting retinol performance and tolerability [PMID: 40905519 · 2026]
S&#xe1;nchez-D&#xed;ez S, Lapeyre A, Garc&#xed;a-Delgado N, Ayats J · Int J Cosmet Sci (2026)

Skin ageing, hyperpigmentation, and texture are common dermatological concerns. Retinoids, including retinol, are widely used for their efficacy in treating these conditions. However, their side effects, such as irritation, often limit their use. Bakuchiol, a plant-derived retinoid alternative, has gained attention for its gentler profile, but its efficacy remains a subject of comparison with traditional retinoids. The aim of the present study was to evaluate the efficacy of a novel microalgae-derived bioretinoid (MBR) in comparison to retinol and bakuchiol in promoting skin regeneration, reducing ageing signs, and addressing hyperpigmentation. The effects of MBR were evaluated in&#xa0;vitro for cell proliferation, melanin production, and extracellular matrix modulation. Clinically, MBR was applied to assess improvements in skin texture, firmness, elasticity, and pigmentation compared with reference treatments. In vitro, MBR significantly outperformed both retinol and bakuchiol in cell proliferation, melanin reduction, and ECM modulation. In&#xa0;vivo, MBR improved skin texture, firmness, and pigmentation, showing results comparable to retinol. MBR also synergistically enhanced retinol's effects, improving hydration and reducing irritation. MBR is a promising alternative to traditional retinoids, offering enhanced efficacy in skin regeneration and pigmentation control with a more favourable safety profile, especially when combined with retinol. Le vieillissement cutan&#xe9;, l'hyperpigmentation et la texturation de la peau sont des probl&#xe8;mes dermatologiques courants. Les r&#xe9;tino&#xef;des, dont le r&#xe9;tinol, sont largement utilis&#xe9;s pour leur efficacit&#xe9; dans le traitement de ces affections. Cependant, leurs effets secondaires, tels que l'irritation, limitent souvent leur utilization. Le bakuchiol, une alternative d'origine v&#xe9;g&#xe9;tale au r&#xe9;tinol, a attir&#xe9; l'attention pour son profil plus doux, mais son efficacit&#xe9; reste sujette &#xe0; comparaison avec les r&#xe9;tino&#xef;des traditionnels. Cette &#xe9;tude avait pour objectif d'&#xe9;valuer l'efficacit&#xe9; d'un nouveau bio&#x2010;r&#xe9;tino&#xef;de d&#xe9;riv&#xe9; de microalgues (BRM) par rapport au r&#xe9;tinol et au bakuchiol dans la promotion de la r&#xe9;g&#xe9;n&#xe9;ration cutan&#xe9;e, la r&#xe9;duction des signes de vieillissement et le traitement de l'hyperpigmentation. M&#xc9;THODES: Les effets du BRM ont &#xe9;t&#xe9; &#xe9;valu&#xe9;s in&#xa0;vitro pour la prolif&#xe9;ration cellulaire, la production de m&#xe9;lanine et la modulation de la matrice extracellulaire. Sur le plan clinique, le BRM a &#xe9;t&#xe9; utilis&#xe9; pour &#xe9;valuer les am&#xe9;liorations de la texture, de la fermet&#xe9;, de l'&#xe9;lasticit&#xe9; et de la pigmentation de la peau par rapport aux traitements de r&#xe9;f&#xe9;rence. R&#xc9;SULTATS: In vitro, le BRM a largement surpass&#xe9; le r&#xe9;tinol et le bakuchiol en termes de prolif&#xe9;ration cellulaire, de r&#xe9;duction de la m&#xe9;lanine et de modulation de la MEC. In&#xa0;vivo, le BRM a am&#xe9;lior&#xe9; la texture, la fermet&#xe9; et la pigmentation de la peau, avec des r&#xe9;sultats comparables &#xe0; ceux du r&#xe9;tinol. Le BRM a &#xe9;galement renforc&#xe9; de mani&#xe8;re synergique les effets du r&#xe9;tinol, am&#xe9;liorant l'hydratation et r&#xe9;duisant l'irritation. Le BRM est une alternative prometteuse aux r&#xe9;tino&#xef;des traditionnels, offrant une efficacit&#xe9; accrue dans la r&#xe9;g&#xe9;n&#xe9;ration cutan&#xe9;e et le contr&#xf4;le de la pigmentation, avec un profil d'innocuit&#xe9; plus favourable, en particulier lorsqu'il est associ&#xe9; au r&#xe9;tinol.

Comparison of Quantification Using UV-Vis, NMR, and HPLC Methods of Retinol-Like Bakuchiol Present in Cosmetic Products [PMID: 40724887 · 2025]
Grzelecka M, Siudem P, Tyburc N, Triyasmono L, Holzgrabe U, Paradowska K · Int J Mol Sci (2025)

Retinoids are used in cosmetics as anti-aging ingredients, along with other substances. However, due to limitations in use (such as photodegradation), it seems necessary to look for retinoid alternatives to be applied in cosmetic products. Bakuchiol, a natural alternative of retinoids, isolated from Psolarea corylifolia , is one such compound. It has great cosmetic potential and its mechanism of action is not yet fully explored. From the point of view of the bioactive compound, it is also essential to develop a method for rapid quality control of cosmetic preparations containing bakuchiol. The aim of this study was to apply and compare methods for the quantification of bakuchiol in cosmetic products using UV-Vis, 1 H qNMR, and HPLC. The results show the possibility of using the 1 H NMR method in the routine quality control of cosmetics with bakuchiol because of its comparable results with HPLC analysis and significantly shorter analysis time.

Cutaneous delivery and biodistribution of a lipophilic natural product - bakuchiol: Comparing nanocarrier performance [PMID: 40562285 · 2025]
Syafitri E, Kalia YN · Int J Pharm (2025)

Bakuchiol (BAK) is a natural bioactive agent described as a functional analogue of retinol that acts through the same cellular pathways. Its lipophilicity (log K o/w 6.1) and oily state at ambient temperature pose significant challenges in formulation development. This study investigated the use of different nanocarriers to develop primarily aqueous formulations of BAK and their ability to facilitate its cutaneous delivery. Micelles were prepared using solvent evaporation, microemulsions (ME) were formulated using the water titration method, and nanoemulsions (NE1 and NE2 - with and without oleic acid, respectively) were produced using ultrasonication. Optimized micelles formed using D-&#x3b1;-Tocopherol polyethylene glycol 1000 succinate (TPGS) and Poloxamer 407 demonstrated encapsulation efficiencies of 96.6&#xa0;&#xb1;&#xa0;3.2&#xa0;% and 101.5&#xa0;&#xb1;&#xa0;0.3&#xa0;%, with particle sizes of 28&#xa0;nm (PDI 0.21) and 27&#xa0;nm (PDI 0.092), respectively. NE2 had a higher encapsulation efficiency (106.8&#xa0;&#xb1;&#xa0;5.7&#xa0;%) than either NE1 (90.2&#xa0;&#xb1;&#xa0;2.4&#xa0;%) or ME (86.3&#xa0;&#xb1;&#xa0;4.6&#xa0;%). The micro- and nanoemulsions exhibited larger sizes than the micelles (ME: 108&#xa0;nm; NE1: 129. nm; NE2: 68&#xa0;nm). Cutaneous delivery experiments demonstrated that NE1 and NE2 resulted in 3-4 fold higher BAK deposition than either the micelles or microemulsion; thus, oleic acid content was not determining BAK delivery. These findings suggest that the thermodynamic activity and molecular physicochemical properties are more important for skin delivery, than simply considering the size of the nanocarrier; which will not necessarily retain its structure upon contact with skin. Cutaneous biodistribution experiments to determine the spatial distribution of BAK confirmed that nanoemulsions effectively targeted the viable epidermis and dermis - key sites for BAK's biological effects, with concentrations 36-fold higher than the minimum effective concentration.

Bakuchiol-loaded amphiphilic polymeric nanoparticles: enhancing stability and multifunctionality through encapsulation. [PMID: 41772644 · 2026]
Seo D, Yu S, Kim T, Park J, Kim H, Sung D · J Biol Eng (2026)

Bakuchiol (BK), a natural meroterpene isolated from Psoralea corylifolia, has gained significant attention as a functional cosmetic ingredient due to its antioxidant, anti-inflammatory, and antibacterial properties. However, its high hydrophobicity and chemical instability limit its practical application. In this study, we developed a robust and efficient delivery system for BK using polyglyceryl-10 laurate (PG10-L), an amphiphilic polymer, via a simple and scalable nanoprecipitation strategy. This approach helps address an important challenge in achieving stable long-term aqueous formulations of BK without relying on complex synthetic processes. The resulting BK-loaded nanoparticles (BK@NPs) exhibited a small particle size (&lt;&#x2009;200&#xa0;nm), high encapsulation efficiency (&#x2248;&#x2009;99%), and remarkable colloidal stability for over 12 weeks. Notably, BK@NPs significantly enhanced biological efficacy compared to free BK, resulting in markedly improved antioxidant and antibacterial performance. Furthermore, the formulation demonstrated excellent cytocompatibility in NIH-3T3 murine fibroblasts along with effective suppression of intracellular reactive oxygen species (ROS). These findings highlight that the PG10-L-based nanoprecipitation strategy provides a robust and green platform to enhance the multifunctional potential of bakuchiol for advanced dermo-cosmetic applications.

PubChem Compound Summary: Bakuchiol [PMID: · 2026]
National Center for Biotechnology Information (NCBI) · PubChem Compound Database (2026)
Effects of nutritive and non-nutritive sweeteners on acne vulgaris: A systematic review [PMID: 41365395 · 2026]
Nguyen TTM, Yi EJ, Jin X, et al. · Fitoterapia (2026)

Acne vulgaris is a prevalent inflammatory skin disorder influenced by sebaceous gland activity, hormonal regulation, and microbial proliferation. Dietary factors, including sweetening agents, may modulate acne pathophysiology, affecting sebum production, inflammatory responses, and the skin microbiome. This systematic review summarizes the effects of nutritive and non-nutritive sweeteners on acne-related markers, with a focus on Cutibacterium acnes activity and associated inflammatory pathways. Non-nutritive sweeteners such as mannitol and xylitol show potential in regulating acne pathogenesis and exhibiting antibacterial activity against C. acnes. Strategic combinations of sweeteners with bioactive compounds, such as mannitol with bakuchiol or Ginkgo biloba extract, and xylitol with propanediol and caprylic acid, further enhance anti-inflammatory and antimicrobial effects, offering a multifaceted approach to acne management. For nutritive sweeteners, experimental evidence suggests that glucose may enhance C. acnes biofilm susceptibility when combined with certain antibiotics. These findings emphasize the importance of careful selection and formulation of sweetening agents in dermatological interventions. Incorporating sweeteners, alone or in combination with bioactive compounds, could complement conventional acne therapies, reduce microbial proliferation, modulate inflammatory pathways, and support overall skin health. This review provides a scientific basis for dietary recommendations and the development of adjunctive acne treatments, highlighting sweetening agents as emerging functional modulators of acne pathogenesis.

INDIVIDUAL ARTICLE: A Scientific Approach to Defining, Evaluating, and Treating Pre-Aging With a Cosmetic Regimen Containing a Novel Cosmetic Peptide, Acetyl Dipeptide-31 Amide (AP31) [PMID: 40327583 · 2025]
Farris P, Frey C, Parsa R, et al. · J Drugs Dermatol (2025)

Patients experiencing signs of pre-aging in their 20s and early 30s desire solutions including topical skincare and cosmetic procedures to help preserve skin quality and function.&amp;nbsp;Methods: A series of studies was conducted to define, evaluate, and treat pre-aging skin. A total of 180 subjects were assessed to identify clinical features of pre-aging across all Fitzpatrick Skin Types (FSTs). In vitro studies compared the response of young and old dermal fibroblasts to ultraviolet A (UVA) exposure and retinoid treatment and evaluated the beneficial effects of acetyl dipeptide-31 amide, for pre-aging treatment. A 12-week clinical study of 46 patients (mild to moderate photoaging) was conducted to assess the efficacy and tolerability of a skincare regimen to treat pre-aging. Skin glycation index was assessed via UV-fluorescence and cross-polarized images. Clinical evaluation revealed that the earliest signs of skin aging were consistent across FSTs and included uneven skin tone, fine lines, and roughness. Aging turning points were seen in the mid-twenties in lighter FSTs and mid-thirties in darker FSTs. A reduction in elasticity began in the 20s and collagen content decreased progressively with age. Younger dermal fibroblasts produced more ROS after UVA exposure but were also more responsive to retinoids. Acetyl dipeptide-31 amide demonstrated anti-inflammatory and extracellular matrix (eg, collagen, elastin, etc) building effects. Clinical testing revealed an AM/PM regimen containing acetyl dipeptide-31 amide, sunscreen, and bakuchiol significantly improved early signs of pre-aging and reduced skin glycation index. These data support the need for and benefit of early intervention to protect and preserve youthful skin.&amp;nbsp; J Drugs Dermatol. 2025;24:5(Suppl 2):s4-14.&amp;nbsp.

常见问题解答 (FAQ)

Q1. BAKUCHIOL 在全球 7 大法域的官方全成分标签名称是什么?
中国 NMPA《已使用化妆品原料目录 (IECIC)》标准中文名为 '未列入 IECIC 目录(严禁自行机器翻译)',美国 PCPC 与欧盟 CosIng 标准 INCI 为 'BAKUCHIOL',日本 JCIA 表示名称为 'バクチオール'。
Q2. BAKUCHIOL 在中、韩、欧、美、日、东盟的法定监管状态 (Layer 1) 如何?
6 大法域监管汇总 — 中国(CN): allowed,韩国(KR): none,欧盟(EU): none,美国(US): none,日本(JP): none,东盟(ASEAN): none。
Q3. BAKUCHIOL 的常规配方添加量 (Layer 3) 与最佳稳定 pH 窗口是多少?
在代表性剂型 (emulsion_cream) 中常规添加量为 0.5%–1%(中位数 0.75%),最佳稳定 pH 范围为 4.5–6.5。
Q4. BAKUCHIOL 有哪些配伍禁忌 (Incompatibilities) 与协同增效组合?
推荐协同组合包括 RETINOL, SQUALANE, CAPRYLIC/CAPRIC TRIGLYCERIDE, SODIUM PHYTATE, TOCOPHEROL;配伍禁忌注意:Phenolic structure forms dark reddish-brown complexes with trace iron ions (Fe3+) or at alkaline pH (>7.0); always include 0.05~0.1% Sodium Phytate or Disodium EDTA and keep pH 5.0~6.0; Must use ≥99% purified grade depleted of phototoxic psoralens (<100 ppm)。