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Combination of calcipotriol and methotrexate in nanostructured lipid carriers for topical delivery

The combination of calcipotriol with methotrexate can strengthen the topical therapy for psoriasis. The aim of the present study was to evaluate the potential of nanostructured lipid carriers (NLCs) loaded with lipophilic calcipotriol and hydrophilic methotrexate as topical therapy. NLCs composed of...

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Autores principales: Lin, Yin-Ku, Huang, Zih-Rou, Zhuo, Rou-Zi, Fang, Jia-You
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841490/
https://www.ncbi.nlm.nih.gov/pubmed/20309398
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author Lin, Yin-Ku
Huang, Zih-Rou
Zhuo, Rou-Zi
Fang, Jia-You
author_facet Lin, Yin-Ku
Huang, Zih-Rou
Zhuo, Rou-Zi
Fang, Jia-You
author_sort Lin, Yin-Ku
collection PubMed
description The combination of calcipotriol with methotrexate can strengthen the topical therapy for psoriasis. The aim of the present study was to evaluate the potential of nanostructured lipid carriers (NLCs) loaded with lipophilic calcipotriol and hydrophilic methotrexate as topical therapy. NLCs composed of Precirol ATO 5 with various amounts of squalene as the liquid lipid were prepared. The particle size, surface charge, molecular environment, drug permeation, and skin irritation of the carriers were assessed. Hyperproliferative skin was also used as a permeation barrier in this study. It was found that variations in the Precirol(®)/squalene ratio had profound effects on the physicochemical characteristics of the NLCs. The range of particle size of the NLC preparations was 270 to 320 nm, with vehicles containing a higher Precirol amount exhibiting a larger diameter. NLCs with a higher Precirol/squalene ratio also showed greater polarity in their molecular environment. Calcipotriol-loaded NLC systems provided drug fluxes of 0.62 to 1.08 μg/cm(2)/h, which were slightly higher or comparable to the 30% ethanol vehicle (control, 0.72 μg/cm(2)/h). The methotrexate amount permeating the skin was 2.4 to 4.4-times greater using NLCs compared to that with the control. Dual drug-loaded NLCs exhibited reduced skin permeation of calcipotriol but not methotrexate. The in vivo topical delivery examined by confocal laser scanning microscopy (CLSM) showed a good correlation with the in vitro results. These two drugs with extremely different polarities can successfully be combined in NLCs. Results suggest that NLCs may have the potential to serve as delivery carriers for antipsoriatic drugs because of enhanced drug permeation and limited skin irritation.
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spelling pubmed-28414902010-03-22 Combination of calcipotriol and methotrexate in nanostructured lipid carriers for topical delivery Lin, Yin-Ku Huang, Zih-Rou Zhuo, Rou-Zi Fang, Jia-You Int J Nanomedicine Original Research The combination of calcipotriol with methotrexate can strengthen the topical therapy for psoriasis. The aim of the present study was to evaluate the potential of nanostructured lipid carriers (NLCs) loaded with lipophilic calcipotriol and hydrophilic methotrexate as topical therapy. NLCs composed of Precirol ATO 5 with various amounts of squalene as the liquid lipid were prepared. The particle size, surface charge, molecular environment, drug permeation, and skin irritation of the carriers were assessed. Hyperproliferative skin was also used as a permeation barrier in this study. It was found that variations in the Precirol(®)/squalene ratio had profound effects on the physicochemical characteristics of the NLCs. The range of particle size of the NLC preparations was 270 to 320 nm, with vehicles containing a higher Precirol amount exhibiting a larger diameter. NLCs with a higher Precirol/squalene ratio also showed greater polarity in their molecular environment. Calcipotriol-loaded NLC systems provided drug fluxes of 0.62 to 1.08 μg/cm(2)/h, which were slightly higher or comparable to the 30% ethanol vehicle (control, 0.72 μg/cm(2)/h). The methotrexate amount permeating the skin was 2.4 to 4.4-times greater using NLCs compared to that with the control. Dual drug-loaded NLCs exhibited reduced skin permeation of calcipotriol but not methotrexate. The in vivo topical delivery examined by confocal laser scanning microscopy (CLSM) showed a good correlation with the in vitro results. These two drugs with extremely different polarities can successfully be combined in NLCs. Results suggest that NLCs may have the potential to serve as delivery carriers for antipsoriatic drugs because of enhanced drug permeation and limited skin irritation. Dove Medical Press 2010 2010-03-09 /pmc/articles/PMC2841490/ /pubmed/20309398 Text en © 2010 Lin et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Lin, Yin-Ku
Huang, Zih-Rou
Zhuo, Rou-Zi
Fang, Jia-You
Combination of calcipotriol and methotrexate in nanostructured lipid carriers for topical delivery
title Combination of calcipotriol and methotrexate in nanostructured lipid carriers for topical delivery
title_full Combination of calcipotriol and methotrexate in nanostructured lipid carriers for topical delivery
title_fullStr Combination of calcipotriol and methotrexate in nanostructured lipid carriers for topical delivery
title_full_unstemmed Combination of calcipotriol and methotrexate in nanostructured lipid carriers for topical delivery
title_short Combination of calcipotriol and methotrexate in nanostructured lipid carriers for topical delivery
title_sort combination of calcipotriol and methotrexate in nanostructured lipid carriers for topical delivery
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841490/
https://www.ncbi.nlm.nih.gov/pubmed/20309398
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