Preparation of redispersible liposomal dry powder using an ultrasonic spray freeze-drying technique for transdermal delivery of human epithelial growth factor

Fei Yin,1 Shiyan Guo,2 Yong Gan,2 Xinxin Zhang21Department of Pharmacy, Liaoning Cancer Hospital and Institute, Shenyang, 2Shanghai Institute of Materia Medica, Chinese Academy of Science, Shanghai, People's Republic of ChinaAbstract: In this work, an ultrasonic spray freeze-drying (USFD) t...

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Autores principales: Yin F, Guo S, Gan Y, Zhang X
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Publicado: Dove Medical Press 2014
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spelling oai:doaj.org-article:8350895f14d545cab0f272ddaa78274c2021-12-02T02:44:08ZPreparation of redispersible liposomal dry powder using an ultrasonic spray freeze-drying technique for transdermal delivery of human epithelial growth factor1178-2013https://doaj.org/article/8350895f14d545cab0f272ddaa78274c2014-03-01T00:00:00Zhttp://www.dovepress.com/preparation-of-redispersible-liposomal-dry-powder-using-an-ultrasonic--a16293https://doaj.org/toc/1178-2013 Fei Yin,1 Shiyan Guo,2 Yong Gan,2 Xinxin Zhang21Department of Pharmacy, Liaoning Cancer Hospital and Institute, Shenyang, 2Shanghai Institute of Materia Medica, Chinese Academy of Science, Shanghai, People's Republic of ChinaAbstract: In this work, an ultrasonic spray freeze-drying (USFD) technique was used to prepare a stable liposomal dry powder for transdermal delivery of recombinant human epithelial growth factor (rhEGF). Morphology, particle size, entrapment efficiency, in vitro release, and skin permeability were systematically compared between rhEGF liposomal dry powder prepared using USFD and that prepared using a conventional lyophilization process. Porous and spherical particles with high specific area were produced under USFD conditions. USFD effectively avoided formation of ice crystals, disruption of the bilayer structure, and drug leakage during the liposome drying process, and maintained the stability of the rhEGF liposomal formulation during storage. The reconstituted rhEGF liposomes prepared from USFD powder did not show significant changes in morphology, particle size, entrapment efficiency, or in vitro release characteristics compared with those of rhEGF liposomes before drying. Moreover, the rhEGF liposomal powder prepared with USFD exhibited excellent enhanced penetration in ex vivo mouse skin compared with that for powder prepared via conventional lyophilization. The results suggest that ultrasonic USFD is a promising technique for the production of stable protein-loaded liposomal dry powder for application to the skin.Keywords: spray freeze-drying, recombinant human epithelial growth factor, liposomes, skin permeability, transdermal drug deliveryYin FGuo SGan YZhang XDove Medical PressarticleMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol 2014, Iss Issue 1, Pp 1665-1676 (2014)
institution DOAJ
collection DOAJ
language EN
topic Medicine (General)
R5-920
spellingShingle Medicine (General)
R5-920
Yin F
Guo S
Gan Y
Zhang X
Preparation of redispersible liposomal dry powder using an ultrasonic spray freeze-drying technique for transdermal delivery of human epithelial growth factor
description Fei Yin,1 Shiyan Guo,2 Yong Gan,2 Xinxin Zhang21Department of Pharmacy, Liaoning Cancer Hospital and Institute, Shenyang, 2Shanghai Institute of Materia Medica, Chinese Academy of Science, Shanghai, People's Republic of ChinaAbstract: In this work, an ultrasonic spray freeze-drying (USFD) technique was used to prepare a stable liposomal dry powder for transdermal delivery of recombinant human epithelial growth factor (rhEGF). Morphology, particle size, entrapment efficiency, in vitro release, and skin permeability were systematically compared between rhEGF liposomal dry powder prepared using USFD and that prepared using a conventional lyophilization process. Porous and spherical particles with high specific area were produced under USFD conditions. USFD effectively avoided formation of ice crystals, disruption of the bilayer structure, and drug leakage during the liposome drying process, and maintained the stability of the rhEGF liposomal formulation during storage. The reconstituted rhEGF liposomes prepared from USFD powder did not show significant changes in morphology, particle size, entrapment efficiency, or in vitro release characteristics compared with those of rhEGF liposomes before drying. Moreover, the rhEGF liposomal powder prepared with USFD exhibited excellent enhanced penetration in ex vivo mouse skin compared with that for powder prepared via conventional lyophilization. The results suggest that ultrasonic USFD is a promising technique for the production of stable protein-loaded liposomal dry powder for application to the skin.Keywords: spray freeze-drying, recombinant human epithelial growth factor, liposomes, skin permeability, transdermal drug delivery
format article
author Yin F
Guo S
Gan Y
Zhang X
author_facet Yin F
Guo S
Gan Y
Zhang X
author_sort Yin F
title Preparation of redispersible liposomal dry powder using an ultrasonic spray freeze-drying technique for transdermal delivery of human epithelial growth factor
title_short Preparation of redispersible liposomal dry powder using an ultrasonic spray freeze-drying technique for transdermal delivery of human epithelial growth factor
title_full Preparation of redispersible liposomal dry powder using an ultrasonic spray freeze-drying technique for transdermal delivery of human epithelial growth factor
title_fullStr Preparation of redispersible liposomal dry powder using an ultrasonic spray freeze-drying technique for transdermal delivery of human epithelial growth factor
title_full_unstemmed Preparation of redispersible liposomal dry powder using an ultrasonic spray freeze-drying technique for transdermal delivery of human epithelial growth factor
title_sort preparation of redispersible liposomal dry powder using an ultrasonic spray freeze-drying technique for transdermal delivery of human epithelial growth factor
publisher Dove Medical Press
publishDate 2014
url https://doaj.org/article/8350895f14d545cab0f272ddaa78274c
work_keys_str_mv AT yinf preparationofredispersibleliposomaldrypowderusinganultrasonicsprayfreezedryingtechniquefortransdermaldeliveryofhumanepithelialgrowthfactor
AT guos preparationofredispersibleliposomaldrypowderusinganultrasonicsprayfreezedryingtechniquefortransdermaldeliveryofhumanepithelialgrowthfactor
AT gany preparationofredispersibleliposomaldrypowderusinganultrasonicsprayfreezedryingtechniquefortransdermaldeliveryofhumanepithelialgrowthfactor
AT zhangx preparationofredispersibleliposomaldrypowderusinganultrasonicsprayfreezedryingtechniquefortransdermaldeliveryofhumanepithelialgrowthfactor
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