Nanoemulsions as vehicles for transdermal delivery of glycyrrhizin

The present investigation aims to evaluate an isotropic and thermodynamically stable nanoemulsion formulation for transdermal delivery of glycyrrhizin (GZ), with minimum surfactant and cosurfactant (Smix) concentrations that could improve its solubility, permeation enhancement, and stability. Pseudo...

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Main Authors: Ranjit Kumar Harwansh, Kartik Chandra Patra, Surendra Kumar Pareta, Jagadish Singh, Mohammed Akhlaquer Rahman
Format: Article
Language:English
Published: Universidade de São Paulo 2011-12-01
Series:Brazilian Journal of Pharmaceutical Sciences
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502011000400014
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spelling doaj-0d9091f18517493f9d59e5ac14fcc0182020-11-25T00:04:40ZengUniversidade de São PauloBrazilian Journal of Pharmaceutical Sciences1984-82502175-97902011-12-0147476977810.1590/S1984-82502011000400014Nanoemulsions as vehicles for transdermal delivery of glycyrrhizinRanjit Kumar HarwanshKartik Chandra PatraSurendra Kumar ParetaJagadish SinghMohammed Akhlaquer RahmanThe present investigation aims to evaluate an isotropic and thermodynamically stable nanoemulsion formulation for transdermal delivery of glycyrrhizin (GZ), with minimum surfactant and cosurfactant (Smix) concentrations that could improve its solubility, permeation enhancement, and stability. Pseudo-ternary phase diagrams were developed and various nanoemulsion formulations were prepared using soyabean oil as oil, Span 80, Brij 35 as a surfactant and isopropyl alcohol as a cosurfactant. Nanoemulsion formulations that passed the thermodynamic stability tests were characterized for pH, viscosity and droplet size using a transmission electron microscopy. The transdermal ability of glycyrrhizin through human cadaver skin was determined using Franz diffusion cells. The in vitro skin permeation profile of the optimized nanoemulsion formulation (NE2) was compared to that of conventional gel. A significant increase in permeability parameters such as steady-state flux (Jss) and permeability coefficient (Kp) was observed in the optimized nanoemulsion formulation (NE2), which consisted of 1% wt/wt of mono ammonium glycyrrhizinate (MAG), 32.4% Span 80, 3.7% Brij 35, 10% isopropyl alcohol, 46.5% soyabean oil and 6.4% distilled water. No obvious skin irritation was observed for the studied nanoemulsion formulation (NE2) or the gel. The results indicated that nanoemulsions are promising vehicles for transdermal delivery of glycyrrhizin through human cadaver skin, without the use of additional permeation enhancers, because excipients of nanoemulsions act as permeation enhancers themselves.<br>O objetivo da investigação é avaliar uma nanoemulsão isotrópica termodinamicamente estável para a administração transdérmica da glicirrizina (GZ), com concentrações mínimas de tensoativo e co-tensoativo (Smix), que poderiam melhorar a sua solubilidade, a permeação e a estabilidade. Os diagramas pseudo-ternários de fase foram desenvolvidos e diversas nanoemulsões foram preparadas com óleo de soja como óleo, Span 80, Brij 35 como tensoativos e álcool isopropílico como co-tensoativo. As nanoemulsões que passaram por testes de estabilidade termodinâmica foram caracterizadas por pH, viscosidade, tamanho de gota e microscopia eletrônica de transmissão. A capacidade transdérmica da glicirrizina em passar através da pele de cadáver humano foi determinada por células de difusão de Franz. O perfil in vitro de permeação cutânea da formulação otimizada (NE2) foi comparada com a de gel convencional. Observou-se aumento significativo nos parâmetros de permeabilidade, como fluxo de equilíbrio (JSS) e coeficiente de permeabilidade (Kp) na formulação otimizado (NE2), que consistiu de 1% wt/wt de monoglicirrizinato de amônio (MAG), 32,4% de Span 80, 3,7% de Brij 35, 10% de álcool isopropílico, 46,5% de óleo de soja e 6,4% de água destilada. Não se observou irritação óbvia da pele para as nanoemulsões estudadas (NE2) ou de gel. Os resultados indicaram que nanoemulsões são promissores veículos para a administração transdérmica de glicirrizina através da pele de cadáveres humanos, sem o uso adicional de promotor de permeação, porque excipientes de nanoemulsões atuam como promotores de permeação.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502011000400014NanoemulsãoNanoemulsãoGlicirrizinaNanoemulsão isotrópicaAnti-inflamatóriosTensoativosPermeaçãoPermeaçãoNanoemulsionsNanoemulsionsGlycyrrhizinIsotropic nanoemulsion formulationAnti-inflammatoriesSurfactantsPermeationPermeation
collection DOAJ
language English
format Article
sources DOAJ
author Ranjit Kumar Harwansh
Kartik Chandra Patra
Surendra Kumar Pareta
Jagadish Singh
Mohammed Akhlaquer Rahman
spellingShingle Ranjit Kumar Harwansh
Kartik Chandra Patra
Surendra Kumar Pareta
Jagadish Singh
Mohammed Akhlaquer Rahman
Nanoemulsions as vehicles for transdermal delivery of glycyrrhizin
Brazilian Journal of Pharmaceutical Sciences
Nanoemulsão
Nanoemulsão
Glicirrizina
Nanoemulsão isotrópica
Anti-inflamatórios
Tensoativos
Permeação
Permeação
Nanoemulsions
Nanoemulsions
Glycyrrhizin
Isotropic nanoemulsion formulation
Anti-inflammatories
Surfactants
Permeation
Permeation
author_facet Ranjit Kumar Harwansh
Kartik Chandra Patra
Surendra Kumar Pareta
Jagadish Singh
Mohammed Akhlaquer Rahman
author_sort Ranjit Kumar Harwansh
title Nanoemulsions as vehicles for transdermal delivery of glycyrrhizin
title_short Nanoemulsions as vehicles for transdermal delivery of glycyrrhizin
title_full Nanoemulsions as vehicles for transdermal delivery of glycyrrhizin
title_fullStr Nanoemulsions as vehicles for transdermal delivery of glycyrrhizin
title_full_unstemmed Nanoemulsions as vehicles for transdermal delivery of glycyrrhizin
title_sort nanoemulsions as vehicles for transdermal delivery of glycyrrhizin
publisher Universidade de São Paulo
series Brazilian Journal of Pharmaceutical Sciences
issn 1984-8250
2175-9790
publishDate 2011-12-01
description The present investigation aims to evaluate an isotropic and thermodynamically stable nanoemulsion formulation for transdermal delivery of glycyrrhizin (GZ), with minimum surfactant and cosurfactant (Smix) concentrations that could improve its solubility, permeation enhancement, and stability. Pseudo-ternary phase diagrams were developed and various nanoemulsion formulations were prepared using soyabean oil as oil, Span 80, Brij 35 as a surfactant and isopropyl alcohol as a cosurfactant. Nanoemulsion formulations that passed the thermodynamic stability tests were characterized for pH, viscosity and droplet size using a transmission electron microscopy. The transdermal ability of glycyrrhizin through human cadaver skin was determined using Franz diffusion cells. The in vitro skin permeation profile of the optimized nanoemulsion formulation (NE2) was compared to that of conventional gel. A significant increase in permeability parameters such as steady-state flux (Jss) and permeability coefficient (Kp) was observed in the optimized nanoemulsion formulation (NE2), which consisted of 1% wt/wt of mono ammonium glycyrrhizinate (MAG), 32.4% Span 80, 3.7% Brij 35, 10% isopropyl alcohol, 46.5% soyabean oil and 6.4% distilled water. No obvious skin irritation was observed for the studied nanoemulsion formulation (NE2) or the gel. The results indicated that nanoemulsions are promising vehicles for transdermal delivery of glycyrrhizin through human cadaver skin, without the use of additional permeation enhancers, because excipients of nanoemulsions act as permeation enhancers themselves.<br>O objetivo da investigação é avaliar uma nanoemulsão isotrópica termodinamicamente estável para a administração transdérmica da glicirrizina (GZ), com concentrações mínimas de tensoativo e co-tensoativo (Smix), que poderiam melhorar a sua solubilidade, a permeação e a estabilidade. Os diagramas pseudo-ternários de fase foram desenvolvidos e diversas nanoemulsões foram preparadas com óleo de soja como óleo, Span 80, Brij 35 como tensoativos e álcool isopropílico como co-tensoativo. As nanoemulsões que passaram por testes de estabilidade termodinâmica foram caracterizadas por pH, viscosidade, tamanho de gota e microscopia eletrônica de transmissão. A capacidade transdérmica da glicirrizina em passar através da pele de cadáver humano foi determinada por células de difusão de Franz. O perfil in vitro de permeação cutânea da formulação otimizada (NE2) foi comparada com a de gel convencional. Observou-se aumento significativo nos parâmetros de permeabilidade, como fluxo de equilíbrio (JSS) e coeficiente de permeabilidade (Kp) na formulação otimizado (NE2), que consistiu de 1% wt/wt de monoglicirrizinato de amônio (MAG), 32,4% de Span 80, 3,7% de Brij 35, 10% de álcool isopropílico, 46,5% de óleo de soja e 6,4% de água destilada. Não se observou irritação óbvia da pele para as nanoemulsões estudadas (NE2) ou de gel. Os resultados indicaram que nanoemulsões são promissores veículos para a administração transdérmica de glicirrizina através da pele de cadáveres humanos, sem o uso adicional de promotor de permeação, porque excipientes de nanoemulsões atuam como promotores de permeação.
topic Nanoemulsão
Nanoemulsão
Glicirrizina
Nanoemulsão isotrópica
Anti-inflamatórios
Tensoativos
Permeação
Permeação
Nanoemulsions
Nanoemulsions
Glycyrrhizin
Isotropic nanoemulsion formulation
Anti-inflammatories
Surfactants
Permeation
Permeation
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502011000400014
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AT surendrakumarpareta nanoemulsionsasvehiclesfortransdermaldeliveryofglycyrrhizin
AT jagadishsingh nanoemulsionsasvehiclesfortransdermaldeliveryofglycyrrhizin
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