Enhancement of physicochemical properties of nanocolloidal carrier loaded with cyclosporine for topical treatment of psoriasis: in vitro diffusion and in vivo hydrating action

Siti Hajar Musa,1 Mahiran Basri,1 Hamid Reza Fard Masoumi,1 Norashikin Shamsudin,2 Norazlinaliza Salim1 1Department of Chemistry, Faculty of Science, 2Department of Medicine, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Malaysia Abstract: Psoriasis is a chronic auto...

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Autores principales: Musa SH, Basri M, Fard Masoumi HR, Shamsudin N, Salim N
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Publicado: Dove Medical Press 2017
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spelling oai:doaj.org-article:fea8305e5e10482ca579bd1695c5b2982021-12-02T01:11:29ZEnhancement of physicochemical properties of nanocolloidal carrier loaded with cyclosporine for topical treatment of psoriasis: in vitro diffusion and in vivo hydrating action1178-2013https://doaj.org/article/fea8305e5e10482ca579bd1695c5b2982017-03-01T00:00:00Zhttps://www.dovepress.com/enhancement-of-physicochemical-properties-of-nanocolloidal-carrier-loa-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Siti Hajar Musa,1 Mahiran Basri,1 Hamid Reza Fard Masoumi,1 Norashikin Shamsudin,2 Norazlinaliza Salim1 1Department of Chemistry, Faculty of Science, 2Department of Medicine, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Malaysia Abstract: Psoriasis is a chronic autoimmune disease that cannot be cured. It can however be controlled by various forms of treatment, including topical, systemic agents, and phototherapy. Topical treatment is the first-line treatment and favored by most physicians, as this form of therapy has more patient compliance. Introducing a nanoemulsion for transporting cyclosporine as an anti-inflammatory drug to an itchy site of skin disease would enhance the effectiveness of topical treatment for psoriasis. The addition of nutmeg and virgin coconut-oil mixture, with their unique properties, could improve cyclosporine loading and solubility. A high-shear homogenizer was used in formulating a cyclosporine-loaded nanoemulsion. A D-optimal mixture experimental design was used in the optimization of nanoemulsion compositions, in order to understand the relationships behind the effect of independent variables (oil, surfactant, xanthan gum, and water content) on physicochemical response (particle size and polydispersity index) and rheological response (viscosity and k-value). Investigation of these variables suggests two optimized formulations with specific oil (15% and 20%), surfactant (15%), xanthan gum (0.75%), and water content (67.55% and 62.55%), which possessed intended responses and good stability against separation over 3 months’ storage at different temperatures. Optimized nanoemulsions of pH 4.5 were further studied with all types of stability analysis: physical stability, coalescence-rate analysis, Ostwald ripening, and freeze–thaw cycles. In vitro release proved the efficacy of nanosize emulsions in carrying cyclosporine across rat skin and a synthetic membrane that best fit the Korsmeyer–Peppas kinetic model. In vivo skin analysis towards healthy volunteers showed a significant improvement in the stratum corneum in skin hydration. Keywords: cyclosporine, nanoemulsion, mixture experimental design, psoriasis, Ostwald ripening, Franz diffusion cell, transepidermal water lossMusa SHBasri MFard Masoumi HRShamsudin NSalim NDove Medical PressarticleCiclosporinnanoemulsionmixture experimental designpsoriasisOstwald ripeningFranz-diffusion celltransepidermal water lossMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 12, Pp 2427-2441 (2017)
institution DOAJ
collection DOAJ
language EN
topic Ciclosporin
nanoemulsion
mixture experimental design
psoriasis
Ostwald ripening
Franz-diffusion cell
transepidermal water loss
Medicine (General)
R5-920
spellingShingle Ciclosporin
nanoemulsion
mixture experimental design
psoriasis
Ostwald ripening
Franz-diffusion cell
transepidermal water loss
Medicine (General)
R5-920
Musa SH
Basri M
Fard Masoumi HR
Shamsudin N
Salim N
Enhancement of physicochemical properties of nanocolloidal carrier loaded with cyclosporine for topical treatment of psoriasis: in vitro diffusion and in vivo hydrating action
description Siti Hajar Musa,1 Mahiran Basri,1 Hamid Reza Fard Masoumi,1 Norashikin Shamsudin,2 Norazlinaliza Salim1 1Department of Chemistry, Faculty of Science, 2Department of Medicine, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Malaysia Abstract: Psoriasis is a chronic autoimmune disease that cannot be cured. It can however be controlled by various forms of treatment, including topical, systemic agents, and phototherapy. Topical treatment is the first-line treatment and favored by most physicians, as this form of therapy has more patient compliance. Introducing a nanoemulsion for transporting cyclosporine as an anti-inflammatory drug to an itchy site of skin disease would enhance the effectiveness of topical treatment for psoriasis. The addition of nutmeg and virgin coconut-oil mixture, with their unique properties, could improve cyclosporine loading and solubility. A high-shear homogenizer was used in formulating a cyclosporine-loaded nanoemulsion. A D-optimal mixture experimental design was used in the optimization of nanoemulsion compositions, in order to understand the relationships behind the effect of independent variables (oil, surfactant, xanthan gum, and water content) on physicochemical response (particle size and polydispersity index) and rheological response (viscosity and k-value). Investigation of these variables suggests two optimized formulations with specific oil (15% and 20%), surfactant (15%), xanthan gum (0.75%), and water content (67.55% and 62.55%), which possessed intended responses and good stability against separation over 3 months’ storage at different temperatures. Optimized nanoemulsions of pH 4.5 were further studied with all types of stability analysis: physical stability, coalescence-rate analysis, Ostwald ripening, and freeze–thaw cycles. In vitro release proved the efficacy of nanosize emulsions in carrying cyclosporine across rat skin and a synthetic membrane that best fit the Korsmeyer–Peppas kinetic model. In vivo skin analysis towards healthy volunteers showed a significant improvement in the stratum corneum in skin hydration. Keywords: cyclosporine, nanoemulsion, mixture experimental design, psoriasis, Ostwald ripening, Franz diffusion cell, transepidermal water loss
format article
author Musa SH
Basri M
Fard Masoumi HR
Shamsudin N
Salim N
author_facet Musa SH
Basri M
Fard Masoumi HR
Shamsudin N
Salim N
author_sort Musa SH
title Enhancement of physicochemical properties of nanocolloidal carrier loaded with cyclosporine for topical treatment of psoriasis: in vitro diffusion and in vivo hydrating action
title_short Enhancement of physicochemical properties of nanocolloidal carrier loaded with cyclosporine for topical treatment of psoriasis: in vitro diffusion and in vivo hydrating action
title_full Enhancement of physicochemical properties of nanocolloidal carrier loaded with cyclosporine for topical treatment of psoriasis: in vitro diffusion and in vivo hydrating action
title_fullStr Enhancement of physicochemical properties of nanocolloidal carrier loaded with cyclosporine for topical treatment of psoriasis: in vitro diffusion and in vivo hydrating action
title_full_unstemmed Enhancement of physicochemical properties of nanocolloidal carrier loaded with cyclosporine for topical treatment of psoriasis: in vitro diffusion and in vivo hydrating action
title_sort enhancement of physicochemical properties of nanocolloidal carrier loaded with cyclosporine for topical treatment of psoriasis: in vitro diffusion and in vivo hydrating action
publisher Dove Medical Press
publishDate 2017
url https://doaj.org/article/fea8305e5e10482ca579bd1695c5b298
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