Vesicular carriers containing phenylethyl resorcinol for topical delivery system; liposomes, transfersomes and invasomes

Topical administration of phenylethyl resorcinol (PR) has attracted much attention as skin lightening agent with potent anti-tyrosinase activity. Two novel types of elastic carriers were developed to overcome the limitation of PR as topical delivery by increasing the solubility, stability and decrea...

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Main Authors: Thanaporn Amnuaikit, Tunyaluk Limsuwan, Pasarat Khongkow, Prapaporn Boonme
Format: Article
Language:English
Published: Elsevier 2018-09-01
Series:Asian Journal of Pharmaceutical Sciences
Online Access:http://www.sciencedirect.com/science/article/pii/S1818087617308619
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author Thanaporn Amnuaikit
Tunyaluk Limsuwan
Pasarat Khongkow
Prapaporn Boonme
author_facet Thanaporn Amnuaikit
Tunyaluk Limsuwan
Pasarat Khongkow
Prapaporn Boonme
author_sort Thanaporn Amnuaikit
collection DOAJ
description Topical administration of phenylethyl resorcinol (PR) has attracted much attention as skin lightening agent with potent anti-tyrosinase activity. Two novel types of elastic carriers were developed to overcome the limitation of PR as topical delivery by increasing the solubility, stability and decreasing skin irritation compared to conventional liposomes. In addition, it also promotes skin penetration of PR to reach deep skin layer at the target site. The lead formulations were obtained from the invasomes containing 1% (w/v) d-limonene mixed with 10% (v/v) absolute ethanol as the skin enhancer, and transfersomes containing 15% (w/w) sodium deoxycholate (SDC) as edge activator. All formulations gave a vesicle size < 500 nm, polydispersity index (PDI) < 0.3, high zeta potential, entrapment efficiency > 50%, and good stability on storage at 30 °C at 75% RH for 4 months. Transfersomes have a lower degree of deformability (6.63%) than invasomes (25.26%). In contrast, the liposomes as rigid vesicles do not show a deformable property. This characteristic affects the skin permeation, and thus, transfersomes with high elastic property provided a significantly higher cumulative amount, steady state flux (Jss) and permeability coefficient (Kp) compared to other formulations. However, in vitro PR accumulation in full-thickness newborn pig skin demonstrated that the application of elastic carrier formulations gave significantly higher accumulation than liposomes, and gave anti-tyrosinase activity up to 80%. These results are straightforwardly related to the results of cellular level study. Transfersomes and invasomes showed higher tyrosinase inhibition activity and melanin content reduction when compared to liposomes in B16 melanoma cells. In addition, acute irritation test in rabbits confirmed that these formulations are safe for skin application. Therefore, elastic vesicle carriers have the efficiency to deliver PR into the deep skin in both quantity and effectiveness which are better than conventional liposomes and appropriate for a skin lightening product. Keywords: Phenylethyl resorcinol, Transfersomes, Invasomes, Tyrosinase inhibition
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spelling doaj.art-bf846fd4ee1c4ef389661cf83cca5c332022-12-21T19:41:06ZengElsevierAsian Journal of Pharmaceutical Sciences1818-08762018-09-01135472484Vesicular carriers containing phenylethyl resorcinol for topical delivery system; liposomes, transfersomes and invasomesThanaporn Amnuaikit0Tunyaluk Limsuwan1Pasarat Khongkow2Prapaporn Boonme3Department of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Songkhla 90112, Thailand; Corresponding author. Department of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Songkhla 90112, Thailand. Tel.: +66896588838.Department 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, Thailand; Nanotec-PSU Center of Excellence on Drug Delivery System, Songkhla 90112, ThailandTopical administration of phenylethyl resorcinol (PR) has attracted much attention as skin lightening agent with potent anti-tyrosinase activity. Two novel types of elastic carriers were developed to overcome the limitation of PR as topical delivery by increasing the solubility, stability and decreasing skin irritation compared to conventional liposomes. In addition, it also promotes skin penetration of PR to reach deep skin layer at the target site. The lead formulations were obtained from the invasomes containing 1% (w/v) d-limonene mixed with 10% (v/v) absolute ethanol as the skin enhancer, and transfersomes containing 15% (w/w) sodium deoxycholate (SDC) as edge activator. All formulations gave a vesicle size < 500 nm, polydispersity index (PDI) < 0.3, high zeta potential, entrapment efficiency > 50%, and good stability on storage at 30 °C at 75% RH for 4 months. Transfersomes have a lower degree of deformability (6.63%) than invasomes (25.26%). In contrast, the liposomes as rigid vesicles do not show a deformable property. This characteristic affects the skin permeation, and thus, transfersomes with high elastic property provided a significantly higher cumulative amount, steady state flux (Jss) and permeability coefficient (Kp) compared to other formulations. However, in vitro PR accumulation in full-thickness newborn pig skin demonstrated that the application of elastic carrier formulations gave significantly higher accumulation than liposomes, and gave anti-tyrosinase activity up to 80%. These results are straightforwardly related to the results of cellular level study. Transfersomes and invasomes showed higher tyrosinase inhibition activity and melanin content reduction when compared to liposomes in B16 melanoma cells. In addition, acute irritation test in rabbits confirmed that these formulations are safe for skin application. Therefore, elastic vesicle carriers have the efficiency to deliver PR into the deep skin in both quantity and effectiveness which are better than conventional liposomes and appropriate for a skin lightening product. Keywords: Phenylethyl resorcinol, Transfersomes, Invasomes, Tyrosinase inhibitionhttp://www.sciencedirect.com/science/article/pii/S1818087617308619
spellingShingle Thanaporn Amnuaikit
Tunyaluk Limsuwan
Pasarat Khongkow
Prapaporn Boonme
Vesicular carriers containing phenylethyl resorcinol for topical delivery system; liposomes, transfersomes and invasomes
Asian Journal of Pharmaceutical Sciences
title Vesicular carriers containing phenylethyl resorcinol for topical delivery system; liposomes, transfersomes and invasomes
title_full Vesicular carriers containing phenylethyl resorcinol for topical delivery system; liposomes, transfersomes and invasomes
title_fullStr Vesicular carriers containing phenylethyl resorcinol for topical delivery system; liposomes, transfersomes and invasomes
title_full_unstemmed Vesicular carriers containing phenylethyl resorcinol for topical delivery system; liposomes, transfersomes and invasomes
title_short Vesicular carriers containing phenylethyl resorcinol for topical delivery system; liposomes, transfersomes and invasomes
title_sort vesicular carriers containing phenylethyl resorcinol for topical delivery system liposomes transfersomes and invasomes
url http://www.sciencedirect.com/science/article/pii/S1818087617308619
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AT pasaratkhongkow vesicularcarrierscontainingphenylethylresorcinolfortopicaldeliverysystemliposomestransfersomesandinvasomes
AT prapapornboonme vesicularcarrierscontainingphenylethylresorcinolfortopicaldeliverysystemliposomestransfersomesandinvasomes