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Novel Gel Microemulsion as Topical Drug Delivery System for Curcumin in Dermatocosmetics
Gel microemulsion combines the advantages of the microemulsion, which can encapsulate, protect and deliver large quantities of active ingredients, and the gel, which is so appreciated in the cosmetic industry. This study aimed to develop and characterize new gel microemulsions suitable for topical c...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8067601/ https://www.ncbi.nlm.nih.gov/pubmed/33916981 http://dx.doi.org/10.3390/pharmaceutics13040505 |
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author | Scomoroscenco, Cristina Teodorescu, Mircea Raducan, Adina Stan, Miruna Voicu, Sorina Nicoleta Trica, Bodgan Ninciuleanu, Claudia Mihaela Nistor, Cristina Lavinia Mihaescu, Catalin Ionut Petcu, Cristian Cinteza, Ludmila Otilia |
author_facet | Scomoroscenco, Cristina Teodorescu, Mircea Raducan, Adina Stan, Miruna Voicu, Sorina Nicoleta Trica, Bodgan Ninciuleanu, Claudia Mihaela Nistor, Cristina Lavinia Mihaescu, Catalin Ionut Petcu, Cristian Cinteza, Ludmila Otilia |
author_sort | Scomoroscenco, Cristina |
collection | PubMed |
description | Gel microemulsion combines the advantages of the microemulsion, which can encapsulate, protect and deliver large quantities of active ingredients, and the gel, which is so appreciated in the cosmetic industry. This study aimed to develop and characterize new gel microemulsions suitable for topical cosmetic applications, using grape seed oil as the oily phase, which is often employed in pharmaceuticals, especially in cosmetics. The optimized microemulsion was formulated using Tween 80 and Plurol(®) Diisostearique CG as a surfactant mix and ethanol as a co-solvent. Three different water-soluble polymers were selected in order to increase the viscosity of the microemulsion: Carbopol(®) 980 NF, chitosan, and sodium hyaluronate salt. All used ingredients are safe, biocompatible and biodegradable. Curcumin was chosen as a model drug. The obtained systems were physico-chemically characterized by means of electrical conductivity, dynamic light scattering, polarized microscopy and rheometric measurements. Evaluation of the cytotoxicity was accomplished by MTT assay. In the final phase of the study, the release behavior of Curcumin from the optimized microemulsion and two gel microemulsions was evaluated. Additionally, mathematical models were applied to establish the kinetic release mechanism. The obtained gel microemulsions could be effective systems for incorporation and controlled release of the hydrophobic active ingredients. |
format | Online Article Text |
id | pubmed-8067601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80676012021-04-25 Novel Gel Microemulsion as Topical Drug Delivery System for Curcumin in Dermatocosmetics Scomoroscenco, Cristina Teodorescu, Mircea Raducan, Adina Stan, Miruna Voicu, Sorina Nicoleta Trica, Bodgan Ninciuleanu, Claudia Mihaela Nistor, Cristina Lavinia Mihaescu, Catalin Ionut Petcu, Cristian Cinteza, Ludmila Otilia Pharmaceutics Article Gel microemulsion combines the advantages of the microemulsion, which can encapsulate, protect and deliver large quantities of active ingredients, and the gel, which is so appreciated in the cosmetic industry. This study aimed to develop and characterize new gel microemulsions suitable for topical cosmetic applications, using grape seed oil as the oily phase, which is often employed in pharmaceuticals, especially in cosmetics. The optimized microemulsion was formulated using Tween 80 and Plurol(®) Diisostearique CG as a surfactant mix and ethanol as a co-solvent. Three different water-soluble polymers were selected in order to increase the viscosity of the microemulsion: Carbopol(®) 980 NF, chitosan, and sodium hyaluronate salt. All used ingredients are safe, biocompatible and biodegradable. Curcumin was chosen as a model drug. The obtained systems were physico-chemically characterized by means of electrical conductivity, dynamic light scattering, polarized microscopy and rheometric measurements. Evaluation of the cytotoxicity was accomplished by MTT assay. In the final phase of the study, the release behavior of Curcumin from the optimized microemulsion and two gel microemulsions was evaluated. Additionally, mathematical models were applied to establish the kinetic release mechanism. The obtained gel microemulsions could be effective systems for incorporation and controlled release of the hydrophobic active ingredients. MDPI 2021-04-07 /pmc/articles/PMC8067601/ /pubmed/33916981 http://dx.doi.org/10.3390/pharmaceutics13040505 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Scomoroscenco, Cristina Teodorescu, Mircea Raducan, Adina Stan, Miruna Voicu, Sorina Nicoleta Trica, Bodgan Ninciuleanu, Claudia Mihaela Nistor, Cristina Lavinia Mihaescu, Catalin Ionut Petcu, Cristian Cinteza, Ludmila Otilia Novel Gel Microemulsion as Topical Drug Delivery System for Curcumin in Dermatocosmetics |
title | Novel Gel Microemulsion as Topical Drug Delivery System for Curcumin in Dermatocosmetics |
title_full | Novel Gel Microemulsion as Topical Drug Delivery System for Curcumin in Dermatocosmetics |
title_fullStr | Novel Gel Microemulsion as Topical Drug Delivery System for Curcumin in Dermatocosmetics |
title_full_unstemmed | Novel Gel Microemulsion as Topical Drug Delivery System for Curcumin in Dermatocosmetics |
title_short | Novel Gel Microemulsion as Topical Drug Delivery System for Curcumin in Dermatocosmetics |
title_sort | novel gel microemulsion as topical drug delivery system for curcumin in dermatocosmetics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8067601/ https://www.ncbi.nlm.nih.gov/pubmed/33916981 http://dx.doi.org/10.3390/pharmaceutics13040505 |
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