원료 사전 탐색/propanediol/PROPANEDIOL
Tier 1 Monograph · SSOT 15 FieldsRaw .md (GEO) ↗
합성 (Synthetic)

PROPANEDIOL

식약처 한글 표준명: 프로판다이올
용제점도조절제
[식약처 공정서 기원 및 정의] 이 원료는 다음의 구조를 갖는 유기화합물이다.
[EU CosIng Official Definition] Propanediol is the organic compound that conforms to the formula
결론 선행 Executive Regulatory & Safety Fact BoxAEO / GEO CITATION ANCHOR

화장품에서 프로판다이올 (PROPANEDIOL)의 글로벌 배합 한도와 핵심 효능·처방 기준은 무엇인가요?

프로판다이올(표준 INCI: PROPANEDIOL, CAS 번호: 504-63-2)은 화장품 처방에서 주로 용제, 점도조절제 목적으로 배합되는 핵심 원료입니다. 한국 식약처(미규제) 및 유럽 CosIng(미규제) 등 6대 권역 법정 기준 하에 관리되며, 통상 2–15%(적정 pH 2–12) 범위에서 안정적으로 처방됩니다.

7대 갈래 국가별·용도별 공식 전성분 라벨 표기명 매트릭스

각국 1차 법원 고시 정본 · 기계번역·임의 음차 0건
7-Track Official Statutory Label Names for PROPANEDIOL
국가·규제 트랙공식 고시 전성분 표기명원클릭 복사
① 한국 (MFDS 화장품 한글 표준명)프로판다이올
② 한국 구명칭 (개정 전 이력 · 301 리다이렉트)프로판디올
③ 유럽 (EU CosIng EC 1223/2009)PROPANEDIOL
④ 미국 일반화장품 (US PCPC / MoCRA INCI)PROPANEDIOL
⑤ 미국 OTC (FDA Active Ingredient Monograph)— (비-OTC 일반 화장품 원료)—
⑥ 중국 (NMPA IECIC 표준 중문명)1,3-丙二醇
⑦ 일본 일반화장품 / 의약부외품 (JCIA / MHLW)プロパンジオール · [QD: 1,3-プロパンジオール]

Layer 1 — 글로벌 6대 권역 법정 배합 한도 및 규제 상태

Layer 1 Statutory Regulatory Limits Across 6 Regions for PROPANEDIOL
권역규제 상태배합 한도제한 조건 및 1차 법원 출처
한국 (MFDS)미규제GMP공식 화장품 원료 목록 등재 (GMP 기준 사용)
유럽 (CosIng)미규제GMP공식 화장품 원료 목록 등재 (GMP 기준 사용)
미국 (FDA/CIR)미규제GMP공식 화장품 원료 목록 등재 (GMP 기준 사용)
중국 (NMPA)등재·허용GMPIECIC Entry #6
일본 (MHLW)미규제GMP공식 화장품 원료 목록 등재 (GMP 기준 사용)
아세안 (ACD)미규제GMP공식 화장품 원료 목록 등재 (GMP 기준 사용)

Layer 2 — 독성·안전성 평가 한도 (US CIR · EU SCCS MoS≥100 · CN IECIC 최고역사사용량)

「SCCS 안전 판정 상한」은 유럽 소비자안전과학위원회가 안전역(MoS≥100)으로 판정한 상한이며, 「CIR 시판 보고 농도」와 「중국 IECIC 최고역사사용량」은 실제 시판 제품에 보고된 최대 농도입니다.

Layer 2 Toxicological & Historical Safe Use Concentrations for PROPANEDIOL
안전성 평가 기준적용 부위·유형안전 농도 범위판정 결과 및 문헌 번호
중국 IECIC 최고역사사용량leave_on≤ 50%안전 판정(MoS≥100)NMPA IECIC (2025) Entry 00006 (2025)
중국 IECIC 최고역사사용량rinse_off≤ 40%안전 판정(MoS≥100)NMPA IECIC (2025) Entry 00006 (2025)
⚠️ 참조용 안내 (법적 면책 공지): 이 사전의 성분명·규제 한도·배합 가이드는 연구·개발 참조용으로만 제공됩니다. 각국 고시 개정 시차나 데이터 오기·누락이 있을 수 있으므로, 실제 제품 처방·라벨 표기·인허가 전에는 반드시 관할 기관(식약처 등)의 최신 공식 고시 원문을 직접 확인하시기 바라며, 본 사전의 정보를 잘못 사용하여 발생하는 문제에 대해 운영 주체는 법적 책임을 지지 않습니다.
제형군별 사분위수(Min–Q1–Median–Q3–Max) 분포 그래프

Layer 3 제형군별 통상 배합 농도(%) 레인지 & Layer 1 법정 한도 대조

수성 토너·세럼·앰플n=146
Min 2% · Q1 3% · Median 5% · Q3 8% · Max 15%
O/W · W/O 에멀전·크림n=168
Min 2% · Q1 3% · Median 5% · Q3 7% · Max 12%
자외선차단·색조n=11
Min 2% · Q1 3.5% · Median 4% · Q3 6.45% · Max 55.5%
수성 토너·세럼·앰플 — 옥수수 발효 유래 천연(ISO 16128 100%) 보습제·용제 및 경피 흡수 촉진
공식 검증 원천: CovationBio Zemea Propanediol TDS & CIR Assessment (cir_safety) · CovationBio 68 · Evonik 46 · SEPPIC 32
권장 중앙값: 5%

Layer 3 — 제형군별 통상 배합 농도(n≥5 사분위수) & 물리화학·상용성 가이드

Layer 3 Formulation Concentration Quartiles by Product Category for PROPANEDIOL
제형군 분류Min – Q1 – Median – Q3 – Max (%)처방 역할 및 기전Source ID
제형군 A — 수성 토너 · 세럼 · 고농축 앰플2% · 3% · 5% · 8% · 15%옥수수 발효 유래 천연(ISO 16128 100%) 보습제·용제 및 경피 흡수 촉진CovationBio Zemea Propanediol TDS & CIR Assessment
제형군 B — 유화 로션 · 에멀전 · 크림 (O/W · W/O)2% · 3% · 5% · 7% · 12%클린뷰티 에멀전 보습 및 방부 부스팅Zemea Propanediol Technical Monograph
제형군 D — 자외선차단제(선크림) · 색조 · 파운데이션2% · 3.5% · 4% · 6.45% · 55.5%선케어·색조 메이크업 분산 안정화 및 발림성 조절Global Starter Formulation Library Statistical Distribution (n=11, GRANT 11)
피부 투과 과학 시각화 (Bos & Meinardi 500 Dalton Rule)MW: 76.09 Da · LogP: -1.04

각질층 장벽 투과 깊이 & 바이오 스피큘 경피전달(DDS) 시뮬레이션

각질층 (Stratum Corneum · 10~20 µm)500 Dalton 장벽 (고분자·친수성 성분 차단)생존 표피층 (Viable Epidermis · 50~100 µm)멜라닌세포 · 각질형성세포 타깃 (미백·장벽·턴오버)진피 유두층 (Papillary Dermis · 150~300 µm)섬유아세포 콜라겐 I/III · 엘라스틴 · PDRN 재생 타깃표피~상부 진피 확산 (<500 Da)
분자량(MW) & 친유성(LogP) 투과 판정
저분자 영역 (76.09 Da ≤ 500 Da) — 각질층 수동 확산 가능

단독 도포 시 각질층 세포간 지질(Brick & Mortar) 경로를 통해 확산됩니다. 500 Dalton 이상 친수성 분자는 각질층 표면에 주로 머물러 보습·보호막 역할을 수행합니다.

예상 도달 깊이
40–90 µm
권장 전달 시스템
Polyol Enhancer / Serum
계면화학 · pH · 열역학 공정 시각화

pH 안정성 스펙트럼(0~14) · 가열 한계 게이지 · HLB 콜로이드 상거동

Miscible with water, ethanol, glycols
적정 처방 pH 안전 윈도우 (pH 0 ~ 14 스펙트럼)pH 2.0 – 12.0
0245.5791114

권장 구간 밖(pH < 2 또는 pH > 12)에서는 가수분해·점도 저하·이온 탈리 위험이 증가합니다.

공정 가열 한계 온도 (Max Process Temp)≤ 90°C
25°C45°C60°C75°C85°C100°C

최대 90°C 가열 공정에서 열적 안정성이 유지됩니다.

계면활성·유화 HLB 스펙트럼 (0 ~ 20) & 미셀/액정 배열 시뮬레이터
O/W 수중유형 미셀 에멀전 (수분 크림·로션)
HLB 11.5
W/O (3–6)Lamellar (8–10.5)O/W Emulsion (11–15)Solubilizer (15–19)O/W Droplet
생화학 신호전달 경로 (Biochemical Pathway Map)

세포·분자 타깃 작용 기전 플로우 다이어그램

1. 각질층·표피 작용→ 촉진·활성 (Activation)
각질층 세포간 지질 & 수분 결합 네트워크
→
경피수분손실(TEWL) 억제 및 피부결 개선
2. 염증 매개체 조절⊣ 억제·차단 (Inhibition)
외부 자극 유도 산화 스트레스(ROS) 및 사이토카인
⊣
피부 진정 및 항상성 유지
처방 온톨로지 네트워크 그래프

권장 시너지(🟢 실선) & 배합 금기·주의(🔴 점선) 인터랙티브 관계도

+ GLYCERIN+ FERULIC ACID+ SALICYLIC ACID+ ASCORBIC ACID✕ 석유계 프로필렌글라이콜(Propyle…PROPANEDIOL
노드 인터랙션 가이드

🟢 초록색 시너지 원료 노드를 클릭하면 해당 원료 모노그래프로 즉시 이동하며, 🔴 붉은색 점선 노드를 클릭하면 화학적 상충(석출·변색·실활) 메커니즘을 표시합니다.

대표 상용명 참고 (상표법 제90조 제1항 제2호 설명적 표기)
Zemea® Propanediol

상용명 표기는 상표법 제90조 제1항 제2호에 의거하여 연구원에게 원료 등급·규격을 설명하기 위한 참고용이며, 각 상표의 권리는 해당 원료사에 귀속됩니다.

학술·독성·제형 종합 요약 (Tier 1~3 탄력 요약)

Tier 1 Synthesis

이 원료에 매칭된 PubMed 동료심사 논문 초록과 공인 독성 보고서만으로 작성된 학술 요약입니다.

■ [1. 화학적 정체성 및 규격 (Chemical Identity & Standard Nomenclature)] - 표준명: 프로판다이올 | INCI: PROPANEDIOL | CAS No.: 504-63-2 | EC No.: 207-997-3 - 기원 및 분류: SYNTHETIC | 주요 기능: 용제, 점도조절제 - 물리화학 스펙: 분자식 C3H8O2 | 분자량 76.09 g/mol | LogP -1.04 | 이온성: non-ionic | PubChem CID 10442 - 7대 권역 공식 라벨 표기: KR [프로판다이올] · EU [PROPANEDIOL] · US [PROPANEDIOL] · CN [1,3-丙二醇] · JP [プロパンジオール] · JP의약부외품 [1,3-プロパンジオール] ■ [2. 피부과학적 작용 기전 및 제형 내 역할 (Mechanism of Action & Function)] - 이 원료는 다음의 구조를 갖는 유기화합물이다. 물리화학적 분류상 기원(synthetic)에 기반하여 피부 장벽 및 제형 매트릭스 내에서 고유한 기능(용제, 점도조절제)을 수행하며, 계면 안정화·보습·피부 컨디셔닝 또는 유효성분 전달에 기여합니다. ■ [3. 글로벌 6대 권역 법정 규제 및 안전성 한도 (Layer 1 & Layer 2 Regulatory Matrix)] - 6개국 요약: KR: NONE | EU: NONE | US: NONE | CN: ALLOWED | JP: NONE | ASEAN: NONE (중국 IECIC(2025) 등재번호 6 (1,3-丙二醇)) - 6대 주요 권역(KR·EU·US·CN·JP·ASEAN) 별도 배합금지/특수제한 고시 없음 (GMP 일반 안전 기준 내 배합 허용). - 공인 안전성·역사적 사용 농도(Layer 2): CN_IECIC_2025 (cn_iecic_max, leave_on): 최대 50.0% / CN_IECIC_2025 (cn_iecic_max, rinse_off): 최대 40.0% ■ [4. 제형군별 통상 배합 가이드 (Layer 3-A Formulation Dosage Guide)] - [aqueous_serum] 권장 범위: 2.0 ~ 15.0% (중앙값 5.0%, 근거: CovationBio Zemea Propanediol TDS & CIR Assessment) — 옥수수 발효 유래 천연(ISO 16128 100%) 보습제·용제 및 경피 흡수 촉진 - [emulsion_cream] 권장 범위: 2.0 ~ 12.0% (중앙값 5.0%, 근거: Zemea Propanediol Technical Monograph) — 클린뷰티 에멀전 보습 및 방부 부스팅 - [sun_color] 권장 범위: 2.0 ~ 55.5% (중앙값 4.0%, 근거: Global Starter Formulation Library Statistical Distribution (n=11, GRANT 11)) — 선케어·색조 메이크업 분산 안정화 및 발림성 조절 ■ [5. 연구원 공정 설계 · 안정성 · 배합 금기 (Layer 3-B Process & Compatibility)] - 투입 공정(Phase): Water Phase - 적정 pH 구간: pH 2.0 ~ 12.0 | 공정 내열 온도: 최대 90°C | 전해질(염) 내성: HIGH - 배합 주의/금기: 석유계 프로필렌글라이콜(Propylene Glycol, 1,2-PDO) 대비 피부 감작성·따가움이 현저히 적고 살리실산·아젤라산·페룰릭애씨드의 뛰어난 공용매로 작동 - 시너지 추천 원료: GLYCERIN, FERULIC ACID, SALICYLIC ACID, ASCORBIC ACID | 참고 상용 원료명: Zemea® Propanediol ■ [6. 학술 논문 및 공인 문헌 근거 (Peer-Reviewed Literature & Compendia)] - PMID 41831283 (2026, J Chromatogr B Analyt Technol Biomed Life Sci): Screening natural deep eutectic solvent-based extraction to analyze illegal skin-whitening ingredients in cosmetics usin - PMID 41796369 (2026, Microb Cell Fact): Cometabolic regulation of glucose and glycerol to enhance 1,3-propanediol yield by Clostridium butyricum - PMID 41321210 (2026, Int J Cosmet Sci): Cosmetic creams with caprylic acid-based Natural Eutectic Solvents: Stability, rheology and user perception

근거 동료심사 학술 논문 (미국 NIH PubMed) (12)

Screening natural deep eutectic solvent-based extraction to analyze illegal skin-whitening ingredients in cosmetics using HPLC and LC-MS/MS [PMID: 41831283 · 2026]
Park CG, Kim YK, Kim HK, Kim HS, Han KM · J Chromatogr B Analyt Technol Biomed Life Sci (2026)

Despite regulatory bans on hazardous substances such as hydroquinone, glucocorticoids, and retinoids, these compounds are still detected in cosmetic products, underscoring the need for reliable analytical methods. This study evaluated four sample preparation approaches for detecting banned ingredients: ultrasound-assisted extraction (UAE), "Quick, Easy, Cheap, Effective, Rugged, Safe" (QuEChERS), solid-phase extraction (SPE), and natural deep eutectic solvents (NaDESs). High-performance liquid chromatography with diode array detection (HPLC-DAD) revealed low recoveries for QuEChERS and SPE. In contrast, NaDESs prepared with choline chloride (ChCl) or betaine as hydrogen bond acceptors (HBAs) and 1,3-propanediol as a hydrogen bond donor (HBD) achieved significantly higher recoveries. In particular the ChCl-1,3-propanediol NaDES (1:4&#xa0;M ratio) provided recoveries of 83.96-105.45%. UAE using methanol yielded comparable recoveries (91.29-106.81%), but the NaDES approach was more environmentally sustainable due to reduced organic solvent use. Method validation following International Conference on Harmonization (ICH) guidelines confirmed acceptable sensitivity (limit of detection: 0.27-1.59&#xa0;&#x3bc;g/mL; limit of quantification: 0.81-4.81&#xa0;&#x3bc;g/mL), recovery, linearity, precision, and accuracy. Target analytes were further verified using liquid chromatography-tandem mass spectrometry. These results demonstrate the feasibility of applying green solvents in cosmetic analysis and highlight a sustainable, effective method for detecting banned skin-whitening agents.

Cometabolic regulation of glucose and glycerol to enhance 1,3-propanediol yield by Clostridium butyricum [PMID: 41796369 · 2026]
Wang L, Sun Y, Xiu Z · Microb Cell Fact (2026)

BACKGROUND: 1,3-Propanediol (PDO) is a high value-added product with significant potential for application and development in various industries including textiles, cosmetics, food, and chemicals. Microbial fermentation for 1,3-PDO production has advantage over chemical synthesis in response to environmental and energy challenges. In view of the complexity and benefits of biometabolic synthesis, there is a necessity to enhance the yield of 1,3-PDO to glycerol by means of co-substrates, whilst concomitantly reducing the cost of production. RESULTS: In this study, the efficiency and cost-effectiveness of 1,3-PDO synthesis by Clostridium butyricum DL07 were improved through elucidating the regulatory mechanism of glucose-glycerol cometabolism and optimizing the ratio of co-substrates. Among the screened co-substrates, glucose emerged as the optimal choice for enhancing the yield and concentration of 1,3-PDO synthesized from glycerol. If the molar ratio of glucose to glycerol was 0.51&#xa0;mol/mol, the 1,3-PDO yield reached 0.90&#xa0;mol/mol in the co-substrate fermentation. Real-time quantitative PCR revealed that the dha operon expression was affected by glucose on inhibition of GDH (dhaD) and phasically upregulation of PDOR activity (dhaT). Stoichiometric analysis combined with further optimization of the different feeding strategies increased the 1,3-PDO yield to the highest level of fed-batch fermentation (0.86&#xa0;mol/mol) reported to date for natural strains. The material cost analysis demonstrated that the co-substrate strategy reduced raw material cost by 13&#x2013;20%. CONCLUSIONS: This study presents an investigation into the synthesis of 1,3-PDO through cometabolism in C. butyricum DL07. The research elucidates the synergistic impact of co-substrate ratios and temporal regulation on the synthesis of 1,3-PDO. Moreover, it offers a theoretical basis and a practical approach for achieving cost-effective and efficient industrial production.

Cosmetic creams with caprylic acid-based Natural Eutectic Solvents: Stability, rheology and user perception [PMID: 41321210 · 2026]
Verger A, Grard R, Pradel C, Perse X, Bouderbala S, Despres A, Boudesocque-Delaye L, Munnier E · Int J Cosmet Sci (2026)

This study investigates the impact of hydrophobic Natural Eutectic Solvents (NES) on the physicochemical and sensory characteristics of cosmetic creams. The aim is to assess their potential as innovative, sustainable ingredients introduced directly into the oily phase of an oil-in-water emulsion prior to emulsification. Four NES formulations, composed of natural components such as caprylic acid, lauric acid, menthol and 1,3-propanediol were incorporated at 10% wt. into a COSMOS-compliant cream chassis. The resulting creams were evaluated for physical stability using static multiple light scattering (Turbiscan&#xae;), rheological behaviour via shear and oscillatory tests, and sensory attributes through a trained panel. Among the four NES-containing creams, three formulations demonstrated satisfactory physical stability over 30&#x2009;days under accelerated ageing conditions. Menthol-based NES induced phase separation, correlating with increased droplet size and higher Turbiscan Stability Index values. All creams exhibited shear-thinning behaviour, with viscosity profiles and yield stress varying depending on NES composition. Sensory analysis revealed that NES significantly influenced key attributes such as odour intensity, spreading, pick-up and firmness. Hydrophobic NES can be successfully integrated into the internal phase of cosmetic creams, influencing both their structural and sensory properties. These findings highlight their potential as multifunctional and eco-friendly ingredients in cosmetic formulation, supporting the development of more sustainable, more performant skincare products. Cette &#xe9;tude examine l&#x2018;impact des solvants eutectiques naturels (Natural Eutectic Solvents, NES) hydrophobes sur les caract&#xe9;ristiques physicochimiques et sensorielles des cr&#xe8;mes cosm&#xe9;tiques. L&#x2018;objectif est d&#x2018;&#xe9;valuer leur potentiel en tant qu&#x2018;ingr&#xe9;dients innovants et durables introduits directement dans la phase huileuse d&#x2018;une &#xe9;mulsion huile dans l&#x2018;eau avant l&#x2018;&#xe9;mulsification. M&#xc9;THODES: Quatre formulations de NES, constitu&#xe9;es de composants naturels tels que l&#x2018;acide caprylique, l&#x2018;acide laurique, le menthol et le 1,3&#x2010;propanediol, ont &#xe9;t&#xe9; incorpor&#xe9;es &#xe0; 10&#x2009;% en poids dans un ch&#xe2;ssis de cr&#xe8;me conforme &#xe0; COSMOS. La stabilit&#xe9; physique des cr&#xe8;mes r&#xe9;sultantes a &#xe9;t&#xe9; &#xe9;valu&#xe9;e &#xe0; l&#x2018;aide d&#x2018;une diffusion statique de lumi&#xe8;re multiple (Turbiscan&#xae;), le comportement rh&#xe9;ologique par des tests de cisaillement et d&#x2018;oscillation, et les attributs sensoriels par le biais d&#x2018;un comit&#xe9; d&#x2018;&#xe9;valuation form&#xe9;. R&#xc9;SULTATS: Parmi les quatre cr&#xe8;mes contenant des NES, trois formulations ont d&#xe9;montr&#xe9; une stabilit&#xe9; physique satisfaisante sur 30&#x2009;jours dans des conditions de vieillissement acc&#xe9;l&#xe9;r&#xe9;es. Les NES &#xe0; base de menthol ont induit une s&#xe9;paration de phase, corr&#xe9;l&#xe9;e &#xe0; une taille de gouttelettes accrue et &#xe0; des valeurs plus &#xe9;lev&#xe9;es de l&#x2018;indice de stabilit&#xe9; de Turbiscan. Toutes les cr&#xe8;mes ont montr&#xe9; un comportement de rh&#xe9;ofluidification, avec des profils de viscosit&#xe9; et des contraintes de rendement variables en fonction de la composition en NES. L&#x2018;analyse sensorielle a r&#xe9;v&#xe9;l&#xe9; que les NES influen&#xe7;aient de mani&#xe8;re significative des caract&#xe9;ristiques cl&#xe9;s telles que l&#x2018;intensit&#xe9; des odeurs, la propagation, la r&#xe9;cup&#xe9;ration et la fermet&#xe9;. Les NES hydrophobes peuvent &#xea;tre int&#xe9;gr&#xe9;s avec succ&#xe8;s dans la phase interne des cr&#xe8;mes cosm&#xe9;tiques, influen&#xe7;ant &#xe0; la fois leurs propri&#xe9;t&#xe9;s structurelles et sensorielles. Ces r&#xe9;sultats soulignent leur potentiel en tant qu&#x2018;ingr&#xe9;dients multifo

Design and mechanistic insights of diacylglycerol-based microemulsions for enhanced transdermal delivery: experimental optimization and molecular dynamics simulation [PMID: 41205530 · 2026]
Zou S, Ai H, Xie P, Lee YY, Huang Y, Pei HS, Xu M, Wang Y, Zhang Z · J Colloid Interface Sci (2026)

A diacylglycerol (DAG)-based microemulsion system was designed and optimized for efficient transdermal delivery. Pseudo-ternary phase diagrams and D-optimal mixture design identified the optimal formulation (6.23&#xa0;% DAG oil, 21.41&#xa0;% RH-40, 18.09&#xa0;% 1,3-propanediol, and 54.27&#xa0;% water), yielding a transparent and stable microemulsion with a droplet size of 24.43&#xa0;nm and infinite dilution capacity. The amphiphilic structure of DAG expanded the one-phase microemulsion region and reduced surfactant demand. Physicochemical evaluations confirmed excellent stability under centrifugation, thermal stress, and long-term storage. Molecular dynamics simulations showed that DAG molecules stabilized droplets at the oil-water interface, whereas triacylglycerol clusters destabilized and dispersed, underscoring the structural advantage of DAG. These nanoscale behaviors translated into superior delivery performance: in vitro studies confirmed that DAG-based microemulsions enhanced the drug transdermal permeation by 2.50-fold and increased dermal retention nearly 3.0-fold compared with oil solutions. Confocal imaging further demonstrated intact droplet penetration across skin layers. This work highlight the amphiphilic advantage of DAG in stabilizing microemulsions and facilitating dermal delivery of lipophilic bioactives, offering a promising route for safe, effective, and surfactant-efficient delivery platforms.

Sustainable Olive Pomace Extracts for Skin Barrier Support [PMID: 40870985 · 2025]
Ri&#xe9;ffel RC, Agostini L, Rodrigues NP, Berlitz SJ, Marczak LDF, K&#xfc;lkamp-Guerreiro IC · Pharmaceutics (2025)

Background : Olive pomace, a byproduct of olive oil production, represents approximately 85% of the processed material and poses environmental risks when improperly discarded. Its composition is rich in polyphenols with potential for cosmetic use, especially in skin barrier care. Objective : To develop a natural extract rich in antioxidants from olive pomace using sustainable solvents (water and 1,3-propanediol) for skin barrier support. Methods : The phenolic composition and in vitro biological activities of the extracts were analyzed. Results : The extracts demonstrated a reducing capacity (15 to 33 mg GAE/g) and flavonoid content (4 to 5 mg QE/g). In addition, their antioxidant capacity was proven through the inhibition of the DPPH radical (7% to 91%) and ABTS (7% to 95%) and the reduction in oxidation in the beta-carotene/linoleic acid system (6% to 35%), presenting results superior to those of tocopherol acetate. The hydroxytyrosol and oleuropein compounds, ranging from 28 to 54 and 51 to 85 &#xb5;g/mL, respectively, were quantified via HPLC. The extract with the highest levels of hydroxytyrosol and oleuropein was analyzed via UHPLC-QqTOF-MS, and 33 compounds were identified. This extract showed antiglycation activity (24% to 40%). The incorporation of this extract into a cosmetic emulsion resulted in sufficient antioxidant capacity to replace tocopherol acetate. Conclusions : The use of effective extraction techniques and nontoxic solvents ensures the sustainability and safety of the extract for application as a natural cosmetic ingredient, aiming to promote the health and integrity of the skin barrier.

Antioxidant and Photoprotective Activities of Viola philippica Polyol Extracts [PMID: 40722988 · 2025]
Li J, Ma J, Li Y, Luo L, Zhang W, Tian Y, Tian Y, Li Y, Wang Z, Wu M · Antioxidants (Basel) (2025)

Viola philippica (VP), a traditional Chinese medicinal herb widely used for its antibacterial and antioxidant properties, has recently garnered attention for its potential in skin photoprotection. VP was extracted using glycerol (GLY), 1,3-propanediol (PDO), and 1,3-butanediol (BDO) at concentrations of 30%, 60%, and 90% ( w / w ) to evaluate its antioxidant and UV-protective properties. The total phenolic content (TPC) and total flavonoid content (TFC) of the nine extracts ranged from 34.73 to 71.45 mg GAEs/g and from 26.68 to 46.68 mg REs/g, respectively, with the highest TPC observed in 90% PDO and the highest TFC in 60% GLY. Antioxidant assays revealed IC 50 values of 0.49-1.26 mg/mL (DPPH), 0.10-0.19 mg/mL (ABTS), and 1.58-460.95 mg/mL (OH). Notably, the 60% GLY, 30% PDO, and 90% PDO extracts demonstrated notable protective effects against UVB-induced cell damage, reducing intracellular ROS levels and preventing DNA damage. RNA-seq analysis revealed that the protective effects were associated with the modulation of key molecular pathways, including neutrophil extracellular trap formation and TNF, IL-17, and HIF-1 signaling. These findings suggest that Viola philippica polyol extracts, particularly those using 60% GLY, 30% PDO, and 90% PDO, have promising potential for skin photoprotection and could be utilized as natural antioxidants in cosmetic formulations.

Multifunctional natural herbal extracts Lamiophlomis rotata (Benth.) Kudo composite gel for infected wounds healing [PMID: 41687221 · 2026]
Yi X, Xiong S, Tuo W, et al. · Colloids Surf B Biointerfaces (2026)

Wounds are susceptible to persistent infections and chronic inflammation, which can significantly impeding the healing process.Lamiophlomis rotata (Benth.) Kudo(LR), a traditional Tibetan medicine, is known for its efficacy in treating injuries, contusions, and skin ulcers. Existing LR-related formulations such as capsules and patches are primarily used for pain relief and cannot provide an optimal environment for infected wounds, thereby limiting their healing potential. In this study, we successfully extracted an extract of LR and confirmed its strong antibacterial activity, supporting its use in infected wound management. A gel matrix was developed using carbomer 940 (CP940) as the base, along with glycerol, 1,2-propanediol, and other excipients. The LR was incorporated into this matrix to obtain Lamiophlomis rotata (Benth.) Kudo gel (LR Gel). Rheological experiments characterized the adhesion and mechanical strength of LR Gel, confirming that it possesses sufficient adhesive force and mechanical strength to tightly adhere to and protect the wound site. Animal experiments showed that LR Gel effectively modulates immune activity and significantly promotes healing in a rat model of infectious full-thickness skin defects. These findings indicate that the LR Gel can prevent wound infection and secondary damage, offering a safe and efficient treatment for infected wounds with promising clinical application.

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.

Green extraction of poplar type propolis: ultrasonic extraction parameters and optimization via response surface methodology [PMID: 41029725 · 2025]
Popova M, Trusheva B, Chimshirova R, et al. · BMC Chem (2025)

Optimizing the extraction of natural products is an important step to obtain products rich in bioactive compounds with less energy use and costs. The aim of this study was to optimize the ultrasonic extraction process of poplar type propolis with natural deep eutectic solvent (NADES) citric acid:1,2-propanediol 1:4 (CAPD 1:4). Based on preliminary experiments, the extraction parameters solvent to solid ratio, temperature, and time were found to have a strong positive effect on the extraction of phenolic compounds, and they were further optimized by response surface methodology (RSM) via the Box-Behnken design (BBD). Solvent to solid ratio of 30 mL/g, ultrasonication time of 39&#xa0;min and temperature of 65&#xa0;&#xb0;C were determined as optimum conditions for the highest values of total phenolic content (TPC, 290.35&#xa0;mg/g), total flavones and flavonols content (TFC, 89.48&#xa0;mg/g) and radical scavenging activity (31.89%RSA). The optimized extract was analyzed by gas chromatography-mass spectrometry (GC-MS) and a high relative content of valuable propolis constituents was found such as pinocembrin, 3-acetylpinobanksin, chrysin, galangin and phenethyl caffeate (CAPE). The results provide knowledge about optimal conditions for the development of a greener extract of poplar type propolis rich in valuable bioactive compounds with potential application in cosmetic, nutraceutical and pharmaceutical industries.

Facile Evaporation-Stamping Technique for Stimuli-Responsive Biopolymer-Supported Eutectogels Containing Opal Micropatterns [PMID: 40824633 · 2025]
Kalidindi S, Zackin AK, Alsaedi MK, et al. · ACS Appl Mater Interfaces (2025)

Biopolymer-supported deep eutectic solvent (DES)-based gels, also known as eutectogels, have emerged as promising alternatives to hydrogels and ionic-liquid-based gels for multiple applications in stretchable electronics and sensors due to many key advantages including their high ionic conductivity, tensile toughness, easy handling, simple synthesis, low cost, biocompatibility, and ultralow volatility. Particularly, gelatin-supported 1,2-propanediol (PD)-based eutectogels containing water have shown promise due to their hydrogel-like properties. They have low modulus values and biofriendly components, making them "skin-like" materials. They are optically transparent, which makes them ideal as user-friendly visual devices. Incorporation of color-tunable micropatterned opal structures into these novel gelatin-supported eutectogels enables the preparation of user-friendly, mechanically resilient, and stimuli-responsive materials for many applications via a simple color change. In this work, we utilize a simple and robust evaporative deposition-stamping technique to prepare eutectogels containing opal micropatterns to overcome limitations in existing fabrication techniques such as photolithography and soft lithography that suffer from costly equipment, harsh radical polymerization, and multistep processing and/or reliance on external forces. First, uniform and color-tunable opal micropatterns are formed via simple evaporative deposition. Scanning electron microscopy (SEM) images show the formation of a uniform hexagonal packing throughout the opal micropatterns. Next, the opal micropatterns are successfully transferred into gelatin-supported PD eutectogels via a simple hand-stamping technique to form opal eutectogels having uniform opal micropatterns due to the eutectogels' adhesive and mechanically resilient nature without the need for costly equipment. Photographs and dark-field optical micrographs, in combination with wavelength spectra measurements, illustrate the reliable nature of our simple evaporation-stamping method. Finally, sandwich eutectogels that fully encapsulate the opal micropatterns were produced by simply adding a secondary eutectogel layer to the top, yielding a reversible optical response to mechanical stimuli. We envision that this simple, reliable, and robust evaporation-stamping technique can be readily extended to manufacture biocompatible and user-friendly visual monitoring devices.

Design of fipronil and praziquantel drops using hydroxypropyl methyl cellulose E5 with superior release and penetration [PMID: 40669624 · 2025]
Huang S, Xiao X, Li J · Int J Biol Macromol (2025)

The design of a superior release and penetration of fipronil (FPN) and praziquantel (PZQ) drops holds significant importance in the simultaneous deworming of pets both in vitro and in vivo. Herein, the application of 1,2-propanediol, azone, hydroxypropyl methyl cellulose E5 (HPMC E5) and anhydrous ethanol as osmotic promoters was investigated, with the primary objective of enhancing the drug's release and permeability. Dosages of 1,2-propanediol, azone, HPMC E5 and anhydrous ethanol were screened based on in vitro drug release and transdermal testing. The optimal prescription for the FPN and PZQ drops was obtained by using 9-11&#xa0;% 1,2-propylene glycol, 69-70&#xa0;% anhydrous ethanol, and 0.1-0.15&#xa0;% HPMC E5. The addition of HPMC E5 can increase the in vitro cumulative release of drops and improve drug penetration into the skin. The optimal PZQ and FPN drops presented safe skin irritation, and should be stored away from strong light and high temperature.

Efficacy of a topical polyphenol-based formulation in palmoplantar psoriasis: an observational study [PMID: 40631809 · 2026]
Amato S, Dattola A, Bennardo L, et al. · Dermatol Reports (2026)

This single-arm observational study evaluated the efficacy and safety of a novel topical formulation containing a complex mixture of polyphenols (CMP) - a proprietary blend rich in oleocanthal and oleuropein aglycone (each &gt;60%), along with hydroxytyrosol and other extra virgin olive oil (EVOO)-derived polyphenols - combined with triticum vulgare germ (TVG) oil, betaine, propanediol, and tocopheryl acetate in patients with mild palmoplantar psoriasis (PPP). Twenty participants (aged 20-55) applied the formulation twice daily for 8 days, with assessments conducted on days 0 (baseline), 5, and 8. Participants underwent a 60-day follow-up to assess the durability of benefits and potential late-onset adverse events. Clinical evaluations measured lesion extent, keratinization, inflammation, desquamation, and infiltration. A patient-reported questionnaire evaluated quality of life (QoL) and symptom burden. By day 8, the mean lesion extent had decreased by approximately 40%, inflammation had improved by about 50%, and desquamation had resolved fully in most cases. Patient-reported outcomes improved alongside clinical measures. At day 60, these improvements persisted in 85% of participants, and no adverse events emerged. The formulation's mechanism of action is hypothesized to involve the concerted antioxidant and anti-inflammatory activities of polyphenols (oleocanthal, oleuropein aglycone, and hydroxytyrosol) in synergy with TVG oil's supportive lipid matrix and other excipients. These findings suggest that EVOO-derived polyphenols formulated in TVG oil may serve as a valuable adjunct for managing PPP with good tolerability and sustained benefits.

자주 묻는 질문 (AEO 스니펫 최적화 FAQ)

Q1. 프로판다이올 (PROPANEDIOL)의 국가별 공식 전성분 표기명은 어떻게 다른가요?
한국 식약처 표준명은 '프로판다이올', 미국 PCPC 및 유럽 CosIng INCI 표기는 'PROPANEDIOL', 중국 NMPA IECIC 표준명은 '1,3-丙二醇', 일본 화장품 표시명칭은 'プロパンジオール'입니다.
Q2. 프로판다이올의 글로벌 6대 권역 법정 배합 한도(Layer 1)는 무엇인가요?
한국(KR: none), 유럽(EU: none), 미국(US: none), 중국(CN: allowed), 일본(JP: none), 아세안(ASEAN: none) 고시 기준을 준수하여 처방해야 합니다.
Q3. 제형 설계 시 프로판다이올의 통상 배합 농도(Layer 3)와 적정 pH는 얼마인가요?
대표 제형군(aqueous_serum) 기준 통상 2~15%(권장 중앙값 5%) 범위로 투입하며, 적정 pH는 2~12입니다.
Q4. 프로판다이올 배합 시 주의해야 할 상용성 금기(Incompatibilities)와 시너지 성분은 무엇인가요?
주요 권장 시너지 조합은 GLYCERIN, FERULIC ACID, SALICYLIC ACID, ASCORBIC ACID이며, 배합 주의사항은 석유계 프로필렌글라이콜(Propylene Glycol, 1,2-PDO) 대비 피부 감작성·따가움이 현저히 적고 살리실산·아젤라산·페룰릭애씨드의 뛰어난 공용매로 작동입니다.