Ethosomes of Phenylethyl Resorcinol as Vesicular Delivery System for Skin Lightening Applications
Ethosome formulations containing phenylethyl resorcinol (PR) were developed. The formulation was produced from 0.5% w/v PR, 0.5% w/v cholesterol from lanolin, 3% w/v L-α-phosphatidylcholine from soybean, 30% v/v absolute ethanol, and water up to 100% v/v. It was characterized by a vesicular size of...
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Online Access: | http://dx.doi.org/10.1155/2017/8310979 |
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doaj-9bb4cf4aa6014628b13a6b0f751b38db2020-11-24T22:47:40ZengHindawi LimitedBioMed Research International2314-61332314-61412017-01-01201710.1155/2017/83109798310979Ethosomes of Phenylethyl Resorcinol as Vesicular Delivery System for Skin Lightening ApplicationsTunyaluk Limsuwan0Prapaporn Boonme1Pasarat Khongkow2Thanaporn Amnuaikit3Department of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Songkhla 90112, ThailandDepartment of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Songkhla 90112, ThailandInstitute of Biomedical Engineering, Faculty of Medicine, Prince of Songkla University, Songkhla 90112, ThailandDepartment of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Songkhla 90112, ThailandEthosome formulations containing phenylethyl resorcinol (PR) were developed. The formulation was produced from 0.5% w/v PR, 0.5% w/v cholesterol from lanolin, 3% w/v L-α-phosphatidylcholine from soybean, 30% v/v absolute ethanol, and water up to 100% v/v. It was characterized by a vesicular size of 389 nm, low polydispersity index of 0.266, zeta potential of −34.19±0.44 mV, high PR entrapment efficiency of 71%, and good stability on storage at 4 and 30°C at 75% RH for 4 months. In vitro studies using pig skin revealed that permeation coefficient of PR from ethosomes was significantly higher than that from liposomes. In vitro retention profiles showed that PR accumulation in pig skin following application of ethosome formulations was 7.4-, 3.3-, and 1.8-fold higher than that achieved using liposomes, 20% propylene glycol solution, and 30% hydroethanolic solution, respectively. An inhibition value of around 80% was measured for antityrosinase activity of PR in pig skin. Consistently, ethosomes exhibited higher tyrosinase inhibition activity and melanin content reduction when compared to other formulations in B16 melanoma cells. Ethosomes did not cause acute dermal irritation in albino rabbits. These findings demonstrate that ethosomes are capable of delivering PR into the skin efficiently and hold promise for topical application of skin lightening products.http://dx.doi.org/10.1155/2017/8310979 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tunyaluk Limsuwan Prapaporn Boonme Pasarat Khongkow Thanaporn Amnuaikit |
spellingShingle |
Tunyaluk Limsuwan Prapaporn Boonme Pasarat Khongkow Thanaporn Amnuaikit Ethosomes of Phenylethyl Resorcinol as Vesicular Delivery System for Skin Lightening Applications BioMed Research International |
author_facet |
Tunyaluk Limsuwan Prapaporn Boonme Pasarat Khongkow Thanaporn Amnuaikit |
author_sort |
Tunyaluk Limsuwan |
title |
Ethosomes of Phenylethyl Resorcinol as Vesicular Delivery System for Skin Lightening Applications |
title_short |
Ethosomes of Phenylethyl Resorcinol as Vesicular Delivery System for Skin Lightening Applications |
title_full |
Ethosomes of Phenylethyl Resorcinol as Vesicular Delivery System for Skin Lightening Applications |
title_fullStr |
Ethosomes of Phenylethyl Resorcinol as Vesicular Delivery System for Skin Lightening Applications |
title_full_unstemmed |
Ethosomes of Phenylethyl Resorcinol as Vesicular Delivery System for Skin Lightening Applications |
title_sort |
ethosomes of phenylethyl resorcinol as vesicular delivery system for skin lightening applications |
publisher |
Hindawi Limited |
series |
BioMed Research International |
issn |
2314-6133 2314-6141 |
publishDate |
2017-01-01 |
description |
Ethosome formulations containing phenylethyl resorcinol (PR) were developed. The formulation was produced from 0.5% w/v PR, 0.5% w/v cholesterol from lanolin, 3% w/v L-α-phosphatidylcholine from soybean, 30% v/v absolute ethanol, and water up to 100% v/v. It was characterized by a vesicular size of 389 nm, low polydispersity index of 0.266, zeta potential of −34.19±0.44 mV, high PR entrapment efficiency of 71%, and good stability on storage at 4 and 30°C at 75% RH for 4 months. In vitro studies using pig skin revealed that permeation coefficient of PR from ethosomes was significantly higher than that from liposomes. In vitro retention profiles showed that PR accumulation in pig skin following application of ethosome formulations was 7.4-, 3.3-, and 1.8-fold higher than that achieved using liposomes, 20% propylene glycol solution, and 30% hydroethanolic solution, respectively. An inhibition value of around 80% was measured for antityrosinase activity of PR in pig skin. Consistently, ethosomes exhibited higher tyrosinase inhibition activity and melanin content reduction when compared to other formulations in B16 melanoma cells. Ethosomes did not cause acute dermal irritation in albino rabbits. These findings demonstrate that ethosomes are capable of delivering PR into the skin efficiently and hold promise for topical application of skin lightening products. |
url |
http://dx.doi.org/10.1155/2017/8310979 |
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