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Self-Assembled Cubic Liquid Crystalline Nanoparticles for Transdermal Delivery of Paeonol

BACKGROUND: The aim of this study was to optimize the preparation method for self-assembled glyceryl monoolein-based cubosomes containing paeonol and to characterize the properties of this transdermal delivery system to improve the drug penetration ability in the skin. MATERIAL/METHODS: In this stud...

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Autores principales: Li, Jian-Chun, Zhu, Na, Zhu, Jin-Xiu, Zhang, Wen-Jing, Zhang, Hong-Min, Wang, Qing-Qing, Wu, Xiao-Xiang, Wang, Xiu, Zhang, Jin, Hao, Ji-Fu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632989/
https://www.ncbi.nlm.nih.gov/pubmed/26517086
http://dx.doi.org/10.12659/MSM.894484
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author Li, Jian-Chun
Zhu, Na
Zhu, Jin-Xiu
Zhang, Wen-Jing
Zhang, Hong-Min
Wang, Qing-Qing
Wu, Xiao-Xiang
Wang, Xiu
Zhang, Jin
Hao, Ji-Fu
author_facet Li, Jian-Chun
Zhu, Na
Zhu, Jin-Xiu
Zhang, Wen-Jing
Zhang, Hong-Min
Wang, Qing-Qing
Wu, Xiao-Xiang
Wang, Xiu
Zhang, Jin
Hao, Ji-Fu
author_sort Li, Jian-Chun
collection PubMed
description BACKGROUND: The aim of this study was to optimize the preparation method for self-assembled glyceryl monoolein-based cubosomes containing paeonol and to characterize the properties of this transdermal delivery system to improve the drug penetration ability in the skin. MATERIAL/METHODS: In this study, the cubic liquid crystalline nanoparticles loaded with paeonol were prepared by fragmentation of glyceryl monoolein (GMO)/poloxamer 407 bulk cubic gel by high-pressure homogenization. We evaluated the Zeta potential of these promising skin-targeting drug-delivery systems using the Malvern Zeta sizer examination, and various microscopies and differential scanning calorimetry were also used for property investigation. Stimulating studies were evaluated based on the skin irritation reaction score standard and the skin stimulus intensity evaluation standard for paeonol cubosomes when compared with commercial paeonol ointment. In vitro tests were performed on excised rat skins in an improved Franz diffusion apparatus. The amount of paeonol over time in the in vitro penetration and retention experiments both was determined quantitatively by HPLC. RESULTS: Stimulating studies were compared with the commercial ointment which indicated that the paeonol cubic liquid crystalline nanoparticles could reduce the irritation in the skin stimulating test. Thus, based on the attractive characteristics of the cubic crystal system of paeonol, we will further exploit the cosmetic features in the future studies. CONCLUSIONS: The transdermal delivery system of paeonol with low-irritation based on the self-assembled cubic liquid crystalline nanoparticles prepared in this study might be a promising system of good tropical preparation for skin application.
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spelling pubmed-46329892015-11-16 Self-Assembled Cubic Liquid Crystalline Nanoparticles for Transdermal Delivery of Paeonol Li, Jian-Chun Zhu, Na Zhu, Jin-Xiu Zhang, Wen-Jing Zhang, Hong-Min Wang, Qing-Qing Wu, Xiao-Xiang Wang, Xiu Zhang, Jin Hao, Ji-Fu Med Sci Monit Animal Study BACKGROUND: The aim of this study was to optimize the preparation method for self-assembled glyceryl monoolein-based cubosomes containing paeonol and to characterize the properties of this transdermal delivery system to improve the drug penetration ability in the skin. MATERIAL/METHODS: In this study, the cubic liquid crystalline nanoparticles loaded with paeonol were prepared by fragmentation of glyceryl monoolein (GMO)/poloxamer 407 bulk cubic gel by high-pressure homogenization. We evaluated the Zeta potential of these promising skin-targeting drug-delivery systems using the Malvern Zeta sizer examination, and various microscopies and differential scanning calorimetry were also used for property investigation. Stimulating studies were evaluated based on the skin irritation reaction score standard and the skin stimulus intensity evaluation standard for paeonol cubosomes when compared with commercial paeonol ointment. In vitro tests were performed on excised rat skins in an improved Franz diffusion apparatus. The amount of paeonol over time in the in vitro penetration and retention experiments both was determined quantitatively by HPLC. RESULTS: Stimulating studies were compared with the commercial ointment which indicated that the paeonol cubic liquid crystalline nanoparticles could reduce the irritation in the skin stimulating test. Thus, based on the attractive characteristics of the cubic crystal system of paeonol, we will further exploit the cosmetic features in the future studies. CONCLUSIONS: The transdermal delivery system of paeonol with low-irritation based on the self-assembled cubic liquid crystalline nanoparticles prepared in this study might be a promising system of good tropical preparation for skin application. International Scientific Literature, Inc. 2015-10-30 /pmc/articles/PMC4632989/ /pubmed/26517086 http://dx.doi.org/10.12659/MSM.894484 Text en © Med Sci Monit, 2015 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License
spellingShingle Animal Study
Li, Jian-Chun
Zhu, Na
Zhu, Jin-Xiu
Zhang, Wen-Jing
Zhang, Hong-Min
Wang, Qing-Qing
Wu, Xiao-Xiang
Wang, Xiu
Zhang, Jin
Hao, Ji-Fu
Self-Assembled Cubic Liquid Crystalline Nanoparticles for Transdermal Delivery of Paeonol
title Self-Assembled Cubic Liquid Crystalline Nanoparticles for Transdermal Delivery of Paeonol
title_full Self-Assembled Cubic Liquid Crystalline Nanoparticles for Transdermal Delivery of Paeonol
title_fullStr Self-Assembled Cubic Liquid Crystalline Nanoparticles for Transdermal Delivery of Paeonol
title_full_unstemmed Self-Assembled Cubic Liquid Crystalline Nanoparticles for Transdermal Delivery of Paeonol
title_short Self-Assembled Cubic Liquid Crystalline Nanoparticles for Transdermal Delivery of Paeonol
title_sort self-assembled cubic liquid crystalline nanoparticles for transdermal delivery of paeonol
topic Animal Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632989/
https://www.ncbi.nlm.nih.gov/pubmed/26517086
http://dx.doi.org/10.12659/MSM.894484
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