Microemulsion system for topical delivery of thai mango seed kernel extract: development, physicochemical characterisation and ex vivo skin permeation studies
- Molecules. 2014 Oct 24;19(11):17107-29. doi: 10.3390/molecules191117107.
- 1. Department of Pharmacy, Faculty of Pharmacy, Mahidol University, 447 Sri-Ayuthaya Road, Rajathevi, Bangkok 10400, Thailand. [email protected].
- 2. EA 4169 "Fonctions Normales et Pathologiques de la Barrière Cutanée", Laboratoire de Recherche et Développement de Pharmacie Galénique Industrielle, ISPB-Faculté de Pharmacie, Université Claude Bernard Lyon-I, 8 Avenue Rockefeller, F-69373 Lyon Cedex 08, France. [email protected].
- 3. EA 4169 "Fonctions Normales et Pathologiques de la Barrière Cutanée", Laboratoire de Recherche et Développement de Pharmacie Galénique Industrielle, ISPB-Faculté de Pharmacie, Université Claude Bernard Lyon-I, 8 Avenue Rockefeller, F-69373 Lyon Cedex 08, France. [email protected].
- 4. Department of Pharmacognosy and Pharmaceutical Botany, Faculty of Pharmaceutical Sciences, Chulalongkorn University, 254 Payathai Road, Pathumwan, Bangkok 10330, Thailand. [email protected].
- 5. Department of Pharmacy, Faculty of Pharmacy, Mahidol University, 447 Sri-Ayuthaya Road, Rajathevi, Bangkok 10400, Thailand. [email protected].
A microemulsion system containing Thai mango seed kernel extract (MSKE, cultivar "Fahlun") was developed and characterised for the purpose of topical skin delivery. The MSKE-loaded microemulsions were prepared by using the spontaneous emulsification method. Isopropyl myristate (IPM) was selected as the oil phase. A polyoxyethylene sorbitan monooleate and sorbitan monododecanoate (1:1, w/w) system was used as the surfactant phase; an aqueous mixture of different cosurfactants (absolute ethanol, 96.3% v/v ethanol, 1-propanol, 2-propanol or 1,2-propanediol) at a weight ratio of 1:1 was used as the aqueous phase. Among the cosurfactants studied, the 1-propanol aqueous mixture had the largest microemulsion region (48.93%) in the pseudo-ternary phase diagram. Microemulsions containing 1% MSKE demonstrated good physicochemical stability during a six-month study period at 25 ± 2 °C/60% ± 5% RH. The ex vivo skin permeation study demonstrated that the microemulsions exhibited a potent skin enhancement effect allowing MSKE to penetrate skin layers up to 60-fold higher compared with the control. Neither skin irritation nor skin corrosion was observed in ex vivo studies. The present study revealed that IPM-based microemulsion systems may be promising carriers to enhance skin penetration and delivering MSKE for topical treatment.
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Cat. No.Product NameDescriptionTargetResearch Area
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Research Areas: Others