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Characterization and topical delivery of phenylethyl resorcinol / Y. Zhang in INTERNATIONAL JOURNAL OF COSMETIC SCIENCE, Vol. 41, N° 5 (10/2019)
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Titre : Characterization and topical delivery of phenylethyl resorcinol Type de document : texte imprimé Auteurs : Y. Zhang, Auteur ; B. C. Sil, Auteur ; C.-P. Kung, Auteur ; J. Hadgraft, Auteur ; M. Heinrich, Auteur ; B. Sinko, Auteur ; M. E. Lane, Auteur Année de publication : 2019 Article en page(s) : p. 479-488 Note générale : Bibliogr. Langues : Anglais (eng) Catégories : Caractérisation
Cuirs et peaux de porcs
Etude in vitro
Peau humaine
Phényléthyle résorcinolIndex. décimale : 668.5 Parfums et cosmétiques Résumé : - OBJECTIVE : Phenylethyl resorcinol (PR) has been used widely in the personal care industry as a novel skin lightening ingredient. Surprisingly, there is only limited information describing the physicochemical properties of this active. Therefore, the primary objective of this study was to perform a comprehensive characterization of PR. A secondary objective was to investigate the delivery of this molecule to mammalian skin.
- METHODS : Phenylethyl resorcinol was characterized using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and nuclear magnetic resonance (NMR). A new high-performance liquid chromatographic (HPLC) method for analysis of PR was developed and validated. The log P (octanol water partition coefficient), value, solubility and short-term stability of PR in a series of vehicles were also determined using HPLC. The evaporation of the selected vehicles was examined using dynamic vapour sorption (DVS). The permeation profiles of PR were investigated under finite dose conditions in porcine and human skin.
- RESULTS : The melting point of PR was determined to be 79.13°C and the measured log P (octanol water partition coefficient) at 21 °C was 3.35 ± 0.03. The linearity of the HPLC analytical method was confirmed with an r2 value of 0.99. Accuracy of the method was evaluated by average recovery rates at three tested concentrations, and the values ranged from 99 to 106%. The limit of detection (LOD) and limit of quantification (LOQ) were 0.19 and 0.57 µg mL-1 , respectively. The solubility of PR in PG, DMI, glycerol was within the range of 367 to 877 mg mL-1 . The stability of PR in tested solvents was also confirmed by the 72 h stability studies. From the DVS studies, 70-125% of applied formulations were recovered at 24 h. The permeation through porcine skin at 24 h ranged from 4 to 13 µg cm-2 , while the corresponding amounts of PR delivered through human skin were 2 to 10 µg cm-2.
- CONCLUSION : The physicochemical properties of PR confirm it is suitable for dermal delivery. In this study, propylene glycol was the most promising vehicle for PR delivery to human skin. Future work will expand the range of vehicles studied and explore the percutaneous absorption from more complex formulations.Note de contenu : - MATERIALS AND METHODS : Materials - Nuclear Magnetic Resonance (NMR) - Thermal analysis - Dynamic vapour sorption studies and preparation of PR solutions - UV, HPLC analysis and method validation - The log P (octanol water partition coefficient), solubility and stability determination - In vitro permeation studies and mass balance studies - Statistical analysis
- RESULTS AND DISCUSSION : NMR - Thermal analysis - DVS results - UV, HPLC analysis and method validation - The log P (octanol water partition coefficient), solubility and stability determination - Permeation studiesDOI : 10.1111/ics.12565 En ligne : https://drive.google.com/file/d/1Me87OFDtFowEaJzTmQyrSF9j0M3NqAH7/view?usp=drive [...] Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=33215
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