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

CYCLOPENTASILOXANE

中国 NMPA《已使用化妆品原料目录 (IECIC)》标准中文名: 环五聚二甲基硅氧烷 (序号 #3031)
发用调理剂皮肤调理剂溶剂柔润剂
[EU CosIng Official Definition] Cyclopentasiloxane is the cyclic dimethyl polysiloxane 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 环五聚二甲基硅氧烷 (CYCLOPENTASILOXANE) 的全球法规限值与配方应用标准是什么?

环五聚二甲基硅氧烷(标准 INCI: CYCLOPENTASILOXANE,CAS 号: 541-02-6)是化妆品配方中主要用作发用调理剂, 皮肤调理剂, 溶剂的核心成分。受中国 NMPA(标注要求)、韩国 MFDS(限用)及欧盟 CosIng(限用)等 6 大法域法定标准监管,常规建议添加量为 3–44.5%(最佳稳定窗口 pH 4–8)。

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 CYCLOPENTASILOXANE
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)CYCLOPENTASILOXANE (KR MFDS Registered)
② 韩国旧名称历史 (301 重定向)Former KR Nomenclature Redirect Active—
③ 欧盟 (EU CosIng EC 1223/2009)CYCLOPENTASILOXANE
④ 美国普通化妆品 (US PCPC / MoCRA INCI)CYCLOPENTASILOXANE
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)环五聚二甲基硅氧烷
⑦ 日本普通化妆品 / 医药部外品 (JCIA / MHLW)シクロペンタシロキサン · [QD: デカメチルシクロペンタシロキサン]

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 CYCLOPENTASILOXANE
法域监管状态法定限值适用条件与法定依据来源
韩国 (MFDS)限用≤ 19.7%
Permitted within statutory scope
Source: MFDS Cosmetic Safety Standards Notice
欧盟 (EU)限用≤ 0.1%
Commission Regulation (EU) 2024/1328 (REACH Annex XVII): Restricted to < 0.1% in wash-off cosmetics; restricted to < 0.1% in all leave-on cosmetics starting June 6, 2026.
Source: Commission Regulation (EU) 2024/1328
中国 (NMPA)标注要求—
Permitted within statutory scope
Source: 化妆品安全技术规范(2015 Ed.) — Full Compendia Audit

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 CYCLOPENTASILOXANE
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≤ 88%安全判定 (MoS≥100)NMPA IECIC (2025) Entry 03067 (2025)
中国 IECIC 最高历史使用量rinse_off≤ 40%安全判定 (MoS≥100)NMPA IECIC (2025) Entry 03067 (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

Statutory Max: 19.7%
Anhydrous Balm / Oiln=5
Min 3% · Q1 6% · Median 12% · Q3 15% · Max 44.5%
Aqueous Serum / Ampoulen=22
Min 1.5% · Q1 2.5% · Median 9.2% · Q3 14.525% · Max 50%
Emulsion / Creamn=32
Min 1% · Q1 4% · Median 7% · Q3 10% · Max 25%
Sunscreen / Colorn=26
Min 2% · Q1 5.25% · Median 10% · Q3 14.75% · Max 35%
Anhydrous Balm / Oil — Anhydrous balm, oil & stick structural emollient
Verified Source: Global Starter Formulation Library Statistical Distribution (n=5, ELEMENTIS 3 · EVONIK 1 · GRANT 1) (cir_safety) · ELEMENTIS 3 · EVONIK 1 · GRANT 1
Typical Median: 12%

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 CYCLOPENTASILOXANE
剂型分类Min – Q1 – Median – Q3 – Max (%)配方作用与机理Source ID
剂型组 E — 无水精油 / 固体膏霜 / 唇部护理3% · 6% · 12% · 15% · 44.5%Anhydrous balm, oil & stick structural emollientGlobal Starter Formulation Library Statistical Distribution (n=5, ELEMENTIS 3 · EVONIK 1 · GRANT 1)
剂型组 A — 水剂爽肤水 / 精华液 / 安瓶1.5% · 2.5% · 9.2% · 14.525% · 50%Aqueous serum, toner & hydrogel matrix formulation componentGlobal Starter Formulation Library Statistical Distribution (n=22, ELEMENTIS 10 · EVONIK 8 · GRANT 4)
剂型组 B — 乳液 / 面霜 (O/W · W/O)1% · 4% · 7% · 10% · 25%Emulsion cream & lotion structural / conditioning agentGlobal Starter Formulation Library Statistical Distribution (n=32, EVONIK 17 · GRANT 14 · ELEMENTIS 1)
剂型组 D — 防晒霜 / 彩妆 / 粉底2% · 5.25% · 10% · 14.75% · 35%Sun care & color cosmetics dispersion / sensory modifierGlobal Starter Formulation Library Statistical Distribution (n=26, GRANT 17 · EVONIK 8 · ELEMENTIS 1)
Cutaneous Permeation Science (500 Dalton Rule)MW: Macro/Complex · LogP: N/A

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 (320 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
Polyol Enhancer / Serum
Colloid Interface, pH Spectrum & Thermal Stability

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

Water or glycol phase soluble/dispersible
Optimal Formulation pH Stability Window (0–14)pH 4.0 – 8.0
0245.5791114

Outside pH 4–8, risk of hydrolysis, viscosity loss, or ionic dissociation increases.

Maximum Thermal Processing Limit (°C)≤ 50°C
25°C45°C60°C75°C85°C100°C

Thermally stable up to 50°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. Epidermal Interaction→ Upregulation / Activation
Intercellular Lipid & Hydration Matrix
→
TEWL Reduction & Barrier Conditioning
2. Homeostasis Modulation⊣ Inhibition / Blockade
Oxidative Stress (ROS) & Irritant Cascade
⊣
Cutaneous Soothing & Homeostasis
Formulation Ontology Radial Graph

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

+ GLYCERIN+ CAPRYLIC/CAPRIC TR…+ TOCOPHEROL✕ Verify phase compati…CYCLOPENTASILOXANE
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)
CYCLOPENTASILOXANE

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: CYCLOPENTASILOXANE | CAS No.: 541-02-6 | EC No.: 208-764-9 - Origin: SYNTHETIC | Functions: , , , - Physicochemical Profile: Formula | MW /(Polymer/Complex) | / | Ionic Nature: non-ionic | CosIng/MFDS - Official Regional Label Names: US [CYCLOPENTASILOXANE] · EU [CYCLOPENTASILOXANE] · CN [环五聚二甲基硅氧烷] · JP [シクロペンタシロキサン] · JP Quasi-Drug [デカメチルシクロペンタシロキサン] ■ [2. Dermatological Mechanism of Action & Functional Role] - Cyclopentasiloxane is the cyclic dimethyl polysiloxane that conforms to the formula: Classified under origin 'synthetic', it acts within the cosmetic vehicle or stratum corneum to deliver , , , performance and structural formulation stability. ■ [3. Global 6-Jurisdiction Regulatory Status & Safety Limits (Layer 1 & Layer 2)] - Regional Summary: KR: RESTRICTED | EU: RESTRICTED | US: NONE | CN: NOTED | JP: NONE | ASEAN: NONE (CN IECIC (2025) Entry No. 3031 (环五聚二甲基硅氧烷)) - [KR / COMPOSITION / limited] (Max 19.7%): - [CN / COMPOSITION / noted]: - [EU / OFFICIAL / restricted] (Max 0.1%): Commission Regulation (EU) 2024/1328 (REACH Annex XVII): Restricted to < 0.1% in wash-off cosmetics; restricted to < 0.1% in all leave-on co - Official Safety & Historical Use Concentration (Layer 2): CN_IECIC_2025 (cn_iecic_max, leave_on): Max 88.0% / CN_IECIC_2025 (cn_iecic_max, rinse_off): Max 40.0% ■ [4. Formulation Dosage Guide by Product Category (Layer 3-A)] - [anhydrous_balm] Typical range: 3.0 ~ 44.5% (Median 12.0%, Ref: Global Starter Formulation Library Statistical Distribution (n=5, ELEMENTIS 3 · EVONIK 1 · GRANT 1)) — Anhydrous balm, oil & stick structural emollient - [aqueous_serum] Typical range: 1.5 ~ 50.0% (Median 9.2%, Ref: Global Starter Formulation Library Statistical Distribution (n=22, ELEMENTIS 10 · EVONIK 8 · GRANT 4)) — Aqueous serum, toner & hydrogel matrix formulation component - [emulsion_cream] Typical range: 1.0 ~ 25.0% (Median 7.0%, Ref: Global Starter Formulation Library Statistical Distribution (n=32, EVONIK 17 · GRANT 14 · ELEMENTIS 1)) — Emulsion cream & lotion structural / conditioning agent ■ [5. Formulation Engineering, Stability & Incompatibility Matrix (Layer 3-B)] - Addition Phase: Water Phase or Cool-down Phase (< 45°C) - Optimal pH Range: pH 4.0 ~ 8.0 | Max Process Temp: Max 50°C | Electrolyte Tolerance: MEDIUM - Incompatibility / Caution: Verify phase compatibility under extreme pH or high electrolyte loads - Synergy Pairings: GLYCERIN, CAPRYLIC/CAPRIC TRIGLYCERIDE, TOCOPHEROL | Reference Trade Names: CYCLOPENTASILOXANE ■ [6. Peer-Reviewed Literature & Official Compendia Evidence] - PMID 27845160 (2017, Regul Toxicol Pharmacol): Opinion of the Scientific Committee on Consumer Safety (SCCS) - Final version of the opinion on decamethylcyclopentasilo - PMID 23857018 (2013, Dermatitis): Compound allergy to a lipophilic gel containing vitamin E acetate and cyclopentasiloxane - PMID 23186890 (2013, Chemosphere): Accounting for intended use application in characterizing the contributions of cyclopentasiloxane (D5) to aquatic loadin

关联同行评审文献 (NIH PubMed) (12)

Opinion of the Scientific Committee on Consumer Safety (SCCS) - Final version of the opinion on decamethylcyclopentasiloxane (cyclopentasiloxane, D5) in cosmetic products [PMID: 27845160 · 2017]
Scientific Committee on Consumer Safety (SCCS). Electronic address: sante-c2-SCCS@ec.europa.eu, Rousselle DC · Regul Toxicol Pharmacol (2017)
Compound allergy to a lipophilic gel containing vitamin E acetate and cyclopentasiloxane [PMID: 23857018 · 2013]
Corazza M, Ricci M, Minghetti S, Borghi A, Bianchi A, Virgili A · Dermatitis (2013)
Accounting for intended use application in characterizing the contributions of cyclopentasiloxane (D5) to aquatic loadings following personal care product use: antiperspirants, skin care products and hair care products [PMID: 23186890 · 2013]
Montemayor BP, Price BB, van Egmond RA · Chemosphere (2013)

Decamethylcyclopentasiloxane, commonly known as D5 (cyclopentasiloxane) has a wide application of use across a multitude of personal care product categories. The relative volatility of D5 is one of the key properties attributed to this substance that provide for the derived performance benefits from the use of this raw material in personal care formulations. On this basis, rapid evaporative loss following use of many products comprising D5 is expected following typical use application and corresponding wear time. Studies were conducted on three key product categories containing D5 (antiperspirants, skin care products and hair care products) to characterize the amount of D5 that may be destined to 'go down the drain' following simulated typical personal care use scenarios. Marketed antiperspirants and skin care products were applied to human subjects and hair care products were applied to human hair tressesand subsequently rinsed off at designated time points representative of typical consumer cleansing and personal hygiene habits. Wash water was collected at 0, 8 and 24h (antiperspirant and hair care analysis) and additionally at 4h (skin care analysis) post product application and samples were analyzed by isotope dilution headspace gas chromatography/mass spectrometry (GC/MS) to quantify the concentration of D5 destined to be available to go down the drain in captured wash water. It is demonstrated that significant amounts of D5 in 'leave-on' application products evaporate during typical use and that the concentration of D5 available to go down the drain under such conditions of use is only a very small (negligible) fraction of that delivered immediately upon product application.

Safety assessment of cyclomethicone, cyclotetrasiloxane, cyclopentasiloxane, cyclohexasiloxane, and cycloheptasiloxane [PMID: 22247236 · 2011]
Johnson W, Bergfeld WF, Belsito DV, Hill RA, Klaassen CD, Liebler DC, Marks JG, Shank RC, Slaga TJ, Snyder PW, Andersen FA · Int J Toxicol (2011)

Cyclomethicone (mixture) and the specific chain length cyclic siloxanes (n = 4-7) reviewed in this safety assessment are cyclic dimethyl polysiloxane compounds. These ingredients have the skin/hair conditioning agent function in common. Minimal percutaneous absorption was associated with these ingredients and the available data do not suggest skin irritation or sensitization potential. Also, it is not likely that dermal exposure to these ingredients from cosmetics would cause significant systemic exposure. The Cosmetic Ingredient Review Expert Panel concluded that these ingredients are safe in the present practices of use and concentration.

Laser therapy for treating hypertrophic and keloid scars [PMID: 36161591 · 2022]
Leszczynski R, da Silva CA, Pinto ACPN, et al. · Cochrane Database Syst Rev (2022)

Hypertrophic and keloid scars are common skin conditions resulting from abnormal wound healing. They can cause itching, pain and have a negative physical and psychological impact on patients' lives. Different approaches are used aiming to improve these scars, including intralesional corticosteroids, surgery and more recently, laser therapy. Since laser therapy is expensive and may have adverse effects, it is critical to evaluate the potential benefits and harms of this therapy for treating hypertrophic and keloid scars. To assess the effects of laser therapy for treating hypertrophic and keloid scars. In March 2021 we searched the Cochrane Wounds Specialised Register, CENTRAL, MEDLINE, Embase, CINAHL EBSCO Plus and LILACS. To identify additional studies, we also searched clinical trials registries for ongoing and unpublished studies, and scanned reference lists of relevant included studies as well as reviews, meta-analyses, and health technology reports. There were no restrictions with respect to language, date of publication, or study setting. We included randomised controlled trials (RCTs) for treating hypertrophic or keloid scars (or both), comparing laser therapy with placebo, no intervention or another intervention. Two review authors independently selected studies, extracted the data, assessed the risk of bias of included studies and carried out GRADE assessments to assess the certainty of evidence. A third review author arbitrated if there were disagreements. We included 15 RCTs, involving 604 participants (children and adults) with study sample sizes ranging from 10 to 120 participants (mean 40.27). Where studies randomised different parts of the same scar, each scar segment was the unit of analysis (906 scar segments). The length of participant follow-up varied from 12 weeks to 12 months. All included trials had a high risk of bias for at least one domain: all studies were deemed at high risk of bias due to lack of blinding of participants and personnel. The variability of intervention types, controls, follow-up periods and limitations with report data meant we pooled data for one comparison (and only two outcomes within this). Several review secondary outcomes - cosmesis, tolerance, preference for different modes of treatment, adherence, and change in quality of life - were not reported in any of the included studies. Laser versus no treatment: We found low-certainty evidence suggesting there may be more hypertrophic and keloid scar improvement (that is scars are less severe) in 585-nm pulsed-dye laser (PDL) -treated scars compared with no treatment (risk ratio (RR) 1.96; 95% confidence interval (CI): 1.11 to 3.45; two studies, 60 scar segments). It is unclear whether non-ablative fractional laser (NAFL) impacts on hypertrophic scar severity when compared with no treatment (very low-certainty evidence). It is unclear whether fractional carbon dioxide (CO 2 ) laser impacts on hypertrophic and keloid scar severity compared with no treatment (very low-certainty evidence). Eight studies reported treatment-related adverse effects but did not provide enough data for further analyses. Laser versus other treatments: We are uncertain whether treatment with 585-nm PDL impacts on hypertrophic and keloid scar severity compared with intralesional corticosteroid triamcinolone acetonide (TAC), intralesional Fluorouracil (5-FU) or combined use of TAC plus 5-FU (very low-certainty evidence). It is also uncertain whether erbium laser impacts on hypertrophic scar severity when compared with TAC (very low-certainty evidence). Other comparisons included 585-nm PDL versus silicone gel sheeting, fractional CO 2 laser versus TAC and fractional CO 2 laser versus verapamil. However, the authors did not report enough data regarding the severity of scars to compare the interventions. As only very low-certainty evidence is available on treatment-related adverse effects, including pain, charring (skin burning so that the surface becomes blackened

Factors to control the alignment of surface-treated titanium dioxide powders to maximize performance of sunscreens [PMID: 36121393 · 2023]
Takekawa S, Ohara M, Banno T, et al. · Int J Cosmet Sci (2023)

Titanium dioxide powders are contained in a large class of colour cosmetics and sunscreen formulas. When they are used, the formation of a uniform functional powder layer on the skin is an important factor to show their functionality, such as aesthetic and UV protection. Attempts were made to extract the factors that affect the UV shielding ability of the deposited powder layer. Seven kinds of surface treatments were conducted on nano-sized titanium dioxide powder to modify the surface characteristics. Dispersion samples were prepared by mixing these powders with liquids, such as mixed solutions of cyclopentasiloxane, isododecane, coconuts alkane and dimethicone using a disperser and a bead mill. The dispersions were applied using an applicator on cellulose triacetate film, polycarbonate film and polymethyl pentene film. Laser microscope observation and micro-gloss glossmeter analysis were carried out to assess the flatness of the deposited powder layers, and the UV shielding ability was evaluated using SPF analyser. Factors whose influences on the structure and UV shielding ability of the deposited powder layer being analysed were pseudo-HLB of the powders, liquids for preparing the dispersions and material of the substrates. Higher UV shielding ability was attained when powders having pseudo-HLB at around 6 were employed independent from the kinds of liquids and substrates. Flatness of the deposited layer was found to enhance the UV shielding ability of the UV-B region, while that of the UV-A region was scarcely influenced by the flatness. Employing lower surface tension liquids for preparing the dispersions and materials exhibiting lower polar components of surface free energy as substrates tended to enhance the UV shielding ability. Surface treatments conducted on the powders in this study were found to change UV shielding ability, especially UV-B shielding ability, and the relation between pseudo-HLB and UV shielding ability was scarcely influenced by the kinds of liquids. Both surface tension of liquids and the polar component of surface free energy of substrates affected the UV shielding ability. It was suggested that pseudo-HLB calculated based on chemical structure becomes useful information to choose optimum surface treatment to make uniform powder alignment independent from the surrounding environment. Les poudres de dioxyde de titane font partie d&#x2019;une grande classe de cosm&#xe9;tiques de couleur et de formules d&#x2019;&#xe9;cran solaire. Lorsqu&#x2019;elles sont utilis&#xe9;es, la formation d&#x2019;une couche de poudre fonctionnelle uniforme sur la peau est un facteur important pour d&#xe9;montrer leur mode d&#x2019;action, qu&#x2019;il s&#x2019;agisse de l&#x2019;aspect esth&#xe9;tique ou de la protection contre les UV. Des tentatives ont &#xe9;t&#xe9; faites pour extraire les facteurs qui alt&#xe8;rent la capacit&#xe9; de protection contre les UV de la couche de poudre d&#xe9;pos&#xe9;e. M&#xc9;THODES: Sept types de traitements de surface ont &#xe9;t&#xe9; effectu&#xe9;s sur une poudre de dioxyde de titane de taille nanom&#xe9;trique pour modifier les caract&#xe9;ristiques de surface. Des &#xe9;chantillons de dispersion ont &#xe9;t&#xe9; pr&#xe9;par&#xe9;s en m&#xe9;langeant ces poudres avec des liquides, tels que des m&#xe9;langes de cyclopentasiloxane, d&#x2019;isodod&#xe9;cane, d&#x2019;alcane de noix de coco et de dim&#xe9;thicone, &#xe0; l&#x2019;aide d&#x2019;un disperseur et d&#x2019;un broyeur &#xe0; billes. Les dispersions ont &#xe9;t&#xe9; appliqu&#xe9;es avec un applicateur sur un film de triac&#xe9;tate de cellulose, un film de polycarbonate et un film de polym&#xe9;thylpent&#xe8;ne. Une observation au microscope laser ainsi qu&#x2019;une analyse au micro-glossm&#xe8;tre ont &#xe9;t&#xe9; faites pour &#xe9;valuer la plan&#xe9;it&#xe9; des couches de poudre d&#xe9;pos&#xe9;es, et la capacit&#xe9; de protection contre les UV a &#xe9;t&#xe9; &#xe9;valu&#xe9;e avec un analyseur SPF (indice de pro

A Prospective Randomized Double-blind study of silicone gel plus Herbal Extracts Versus Placebo in Pre-sternal hypertrophic scar prevention and amelioration [PMID: 32405550 · 2020]
Surakunprapha P, Winaikosol K, Chowchuen B, et al. · Heliyon (2020)

Post-surgical hypertrophic scar is more frequently reported in Asians. Many modalities can treat scars but there have not been any publications to define the efficacy of silicone gel plus herbal extracts for scar prevention or amelioration. 48 patients, who underwent median sternotomy were randomized and double-blinded to 2 groups to use topical silicone gel plus herbal extract gel or placebo for 6 months. Patients were treated either with topical silicone gel plus herbal extract gel or control using only placebo for 6 months. The scars were observed by experienced plastic surgeons using the Vancouver scar scale. A single tertiary care center at Khon Kaen University. 48 patients who underwent median sternotomy were enrolled in this study. All patients were aged over 18 years. All the wounds were sutured with polyglycolic 4/0 subcuticular suture material and did not receive other scar management before participating in this study. The silicone gel plus herbal extract gel (Bangkok Botanica, Bangkok, Thailand) in semi-liquid form was formulated from 15% Herbal extract (Allium Cepa extract, Centella Asiatica extract, Aloe Vera extract and Paper Mulberry extract), 50% polydemethysiloxane, 30% cyclopentasiloxane and 5% silica. The placebo gel was a composite of water, acrylate, C10-30 alkyl acrylate cross-polymer, polysorbate 20 and fragrance that was similar in color and consistency as that of the active gel and packed in the similar sealed packages. The scar was assessed using the Vancouver scar scale to determine pigmentation, vascularity, pliability and height. the study showed the silicone gel plus herbal extract gel could improve scar amelioration in height (p = 0.005) and pliability (p &lt; 0.001) when compared to the placebo. The vascularity and pigmentation showed improvement using silicone gel plus herbal extracts but the improvement was not statistically significant. The silicone gel plus herbal extracts gel was effective for scar improvement in median sternotomy wounds.

Allergic contact dermatitis to Tinosorb S, Scutellaria baicalensis, and other emerging allergens in cosmetics [PMID: 31879957 · 2020]
Luna-Bastante L, Gatica-Ortega ME, Pastor-Nieto MA, et al. · Contact Dermatitis (2020)

Patch tests are highly recommended in eczema patients with eyelid involvement. Sunscreen constitutes a potential cause of eyelid or facial allergic contact dermatitis, and should be considered in patients with refractory eczema on these locations. We report a patient sensitized to several emerging allergens such as bis-ethylhexyloxyphenol methoxyphenyl triazine (Tinosorb S), Scutellaria baicalensis extract, and propylene glycol with an eyelid dermatitis. Patch tests to the combined ingredients propylene carbonate, cyclopentasiloxane, and disteardimonium hectorite; and talc, Cl 77&#x2009;491, and dimethicone/methicone copolymer were also positive. We highlight the importance of systematically patch testing with the cosmetics brought in by our patients, as well as with the individual ingredients whenever positive. The identification of emerging allergies to new compounds in cosmetics mainly depends on this practice.

Effect of silicone oil on the microstructure, gelation and rheological properties of sorbitan monostearate-sesame oil oleogels [PMID: 32104422 · 2018]
Swe MTH, Asavapichayont P · Asian J Pharm Sci (2018)

Oleogels contain oil or a non-polar liquid which is gelled with an agent called an organogelator. The aim of this study was to evaluate the effects of the addition of silicone oil (cyclopentasiloxane) to the gelation process and to the properties of sorbitan monostearate (SMS)-sesame oil oleogel and compared with that of SMS-sesame oil oleogel and SMS-cyclopentasiloxane oleogel. Three different oil phases; sesame oil phase, cyclopentasiloxane phase and a mixture of cyclopentasiloxane and sesame oil, were used to prepare oleogels with SMS gelator. The critical gelling concentrations (CGC) for oleogels were determined using different concentration of SMS in a range of 5%-22% (w/w). The characterization of the developed oleogels was done using Fourier transform infrared spectroscopy (FTIR), polarized light microscope, rheometer, X-ray diffraction (XRD) and differential scanning calorimetry (DSC). The addition of cyclopentasiloxane reduced the CGC of SMS-sesame oil oleogel from 20% to 10% (w/w). In microscopic characterization, the oleogels with a mixture of oil phases showed the longer and thicker three-dimensional gel network than that of oleogels with sesame oil and cyclopentasiloxane. FTIR studies demonstrated that this network formation was mainly due to hydrogen bonding. Rheological measurements revealed that the combination of cyclopentasiloxane and sesame oil produced strong gel with higher complex modulus values and longer linear viscoelastic region than oleogels prepared with sesame oil and cyclopentasiloxane. In addition, oleogels with the combination of the two oils had higher enthalpy (&#x394; H m ) and entropy (&#x394; S m ) thus could increase thermodynamic stability of the oleogels. Therefore, the addition of cyclopentasiloxane can improve the physical, thermal properties and stability of SMS-sesame oil oleogel, provide greater sensory profile and better product aesthetics. The developed oleogel can be a novel carrier for topical drug delivery.

Comparing the Efficacy of Commercially Available Insecticide and Dimeticone based Solutions on Head Lice, Pediculus capitis: in vitro Trials [PMID: 26809918 · 2015]
Balcıoğlu IC, Karakuş M, Arserim SK, et al. · Turkiye Parazitol Derg (2015)

Head lice infestation is a public health and social problem for almost all countries worldwide. For its treatment, insecticide and dimeticone-based solutions are currently available in the markets in many countries. We aimed to compare the efficacy of commercially available anti-head lice shampoos containing insecticide and physically effective products with different percentages of dimeticone using an in vitro technique. Head lice specimens were collected from primary school children using special plastic and metal combs. Anti-head lice products were commercially purchased and used directly. The specimens were placed one by one in 5-cm Petri dishes containing a slightly wet filter paper and were kept in a plastic cage at 28&#xb1;2&#xb0;C and 50%&#xb1;20% relative humidity. A standardized protocol was used for testing all the products, and mortality data were obtained after 24 h. Two control tests were performed with each batch of trials. For each product and control, 10-20 head lice specimens were used, and the results were statistically analyzed. Our study demonstrated that among all the tested products, two products containing mineral oils [5.5% dimeticone &amp; silicone (patented product) and dimeticone (no percentage mentioned in the prospectus) &amp; cyclopentasiloxane] were found to be more effective for killing head lice in vitro. Physically effective products can be repetitively used because they are non-toxic and resistance to them is not expected. To control the infestation at a public level, the use of these products needs to be encouraged with respect to their cost price.

Study on penetration of titanium dioxide (TiO(2)) nanoparticles into intact and damaged skin in vitro [PMID: 20118631 · 2010]
Senzui M, Tamura T, Miura K, et al. · J Toxicol Sci (2010)

It is important for toxicological assessment of nanoparticles to determine the penetration of nanoparticle in skin qualitatively and quantitatively. Skin penetration of four different types of rutile titanium dioxide (TiO(2)) (T-35, 35 nm, non-coating; TC-35, 35 nm, with almina/silica/silicon coating; T-disp, 10 x 100 nm, mixture of almina coated and silicon coated particles, dispersed in cyclopentasiloxan; T-250, 250 nm, non-coating) was determined with in vitro intact, stripped, and hair-removed skin of Yucatan micropigs to study the effect of dispersion and skin conditions. The TiO(2) was suspended in a volatile silicone fluid used for cosmetics, cyclopentasiloxane, at a concentration of 10%. The suspension was applied at a dose 2 microl/cm(2) for 24 hr, followed by cyanoacrylate stripping. The Ti concentration in skin was determined by ICP-MS. T-35 and T-250 easily aggregated in suspension with a mean diameter greater than 1 microm. TC-35 and T-disp showed good dispersion properties with a mean diameter in suspension of approximately 100 nm. No penetration was observed regardless of TiO(2) type in intact and stripped skin. The concentration of Ti in skin was significantly higher when TC-35 was applied on hair-removed skin. SEM-EDS observation showed that Ti penetrated into vacant hair follicles (greater than 1 mm below the skin surface), however, it did not penetrate into dermis or viable epidermis.

Protective effect of conditioning agents on Afro-ethnic hair chemically treated with thioglycolate-based straightening emulsion [PMID: 18482015 · 2008]
Dias TC, Baby AR, Kaneko TM, et al. · J Cosmet Dermatol (2008)

Straightening is a chemical process by which excessively curly hair is straightened in an irreversible way. Generally, products are formulated as emulsions with high pH value (9.0-12.0), which, after applied on hair, cause considerable damage, making it dry and fragile. This research work evaluated the protective effect of lauryl PEG/PPG-18/18 methicone, cyclopentasiloxane (and) PEG-12 dimethicone cross-polymer, jojoba oil, and aqua (and) cystine bis-PG propyl silanetriol, as conditioning agents, on Afro-ethnic hair locks treated with thioglycolate-based straightening emulsions by protein loss, combability, and traction to rupture. Standard Afro-ethnic hair locks were prepared following a protocol for straightening emulsion application. Considering the assays performed, the addition of conditioning agents to the straightening emulsion with ammonium thioglycolate benefited the hair fiber, thus diminishing protein loss, protecting the hair thread, and improving resistance to breakage. Jojoba oil and lauryl PEG/PPG-18/18 methicone were the conditioning agents that presented the best results. Straightening emulsions with ammonium thioglycolate containing aqua (and) cystine bis-PG propyl silanetriol and cyclopentasiloxane (and) PEG-12 dimethicone cross-polymer were the ones that provided higher breakage resistance of the thread.

常见问题解答 (FAQ)

Q1. 环五聚二甲基硅氧烷 (CYCLOPENTASILOXANE) 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 '环五聚二甲基硅氧烷',美国 PCPC 与欧盟 CosIng 标准 INCI 为 'CYCLOPENTASILOXANE',日本 JCIA 表示名称为 'シクロペンタシロキサン'。
Q2. 环五聚二甲基硅氧烷 (CYCLOPENTASILOXANE) 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): noted,韩国(KR): restricted,欧盟(EU): restricted,美国(US): none,日本(JP): none,东盟(ASEAN): none。
Q3. 环五聚二甲基硅氧烷 (CYCLOPENTASILOXANE) 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 (anhydrous_balm) 中常规添加量为 3%–44.5%(中位数 12%),最佳稳定 pH 范围为 4–8。
Q4. 环五聚二甲基硅氧烷 (CYCLOPENTASILOXANE) 有哪些配伍禁忌 (Incompatibilities) 与协同增效组合?
推荐协同组合包括 GLYCERIN, CAPRYLIC/CAPRIC TRIGLYCERIDE, TOCOPHEROL;配伍禁忌注意:Verify phase compatibility under extreme pH or high electrolyte loads。