Corneal permeation properties of a charged lipid nanoparticle carrier containing dexamethasone
Junfeng Ban, Yan Zhang, Xin Huang, Guanghan Deng, Dongzhi Hou, Yanzhong Chen, Zhufen Lu Guangdong Provincial Key Laboratory of Advanced Drug Delivery Systems, Guangdong Pharmaceutical University, Guangzhou, People’s Republic of China Abstract: Drug delivery carriers can maintain effectiv...
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doaj-96f7e2ffba3b45399c0be152f298e2022020-11-25T00:47:25ZengDove Medical PressInternational Journal of Nanomedicine1178-20132017-02-01Volume 121329133931362Corneal permeation properties of a charged lipid nanoparticle carrier containing dexamethasoneBan JZhang YHuang XDeng GHHou DZChen YZLu ZFJunfeng Ban, Yan Zhang, Xin Huang, Guanghan Deng, Dongzhi Hou, Yanzhong Chen, Zhufen Lu Guangdong Provincial Key Laboratory of Advanced Drug Delivery Systems, Guangdong Pharmaceutical University, Guangzhou, People’s Republic of China Abstract: Drug delivery carriers can maintain effective therapeutic concentrations in the eye. To this end, we developed lipid nanoparticles (L/NPs) in which the surface was modified with positively charged chitosan, which engaged in hydrogen bonding with the phospholipid membrane. We evaluated in vitro corneal permeability and release characteristics, ocular irritation, and drug dynamics of modified and unmodified L/NPs in aqueous humor. The size of L/NPs was uniform and showed a narrow distribution. Corneal permeation was altered by the presence of chitosan and was dependent on particle size; the apparent permeability coefficient of dexamethasone increased by 2.7 and 1.8 times for chitosan-modified and unmodified L/NPs, respectively. In conclusion, a chitosan-modified system could be a promising method for increasing the ocular bioavailability of unmodified L/NPs by enhancing their retention time and permeation into the cornea. These findings provide a theoretical basis for the development of effective drug delivery systems in the treatment of ocular disease. Keywords: ocular drug delivery system, local bioavailability, dexamethasone, eye drop administrationhttps://www.dovepress.com/corneal-permeation-properties-of-a-charged-lipid-nanoparticle-carrier--peer-reviewed-article-IJNocular drug delivery systemlocal bioavailabilitydexamethasoneeye drop administration |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ban J Zhang Y Huang X Deng GH Hou DZ Chen YZ Lu ZF |
spellingShingle |
Ban J Zhang Y Huang X Deng GH Hou DZ Chen YZ Lu ZF Corneal permeation properties of a charged lipid nanoparticle carrier containing dexamethasone International Journal of Nanomedicine ocular drug delivery system local bioavailability dexamethasone eye drop administration |
author_facet |
Ban J Zhang Y Huang X Deng GH Hou DZ Chen YZ Lu ZF |
author_sort |
Ban J |
title |
Corneal permeation properties of a charged lipid nanoparticle carrier containing dexamethasone |
title_short |
Corneal permeation properties of a charged lipid nanoparticle carrier containing dexamethasone |
title_full |
Corneal permeation properties of a charged lipid nanoparticle carrier containing dexamethasone |
title_fullStr |
Corneal permeation properties of a charged lipid nanoparticle carrier containing dexamethasone |
title_full_unstemmed |
Corneal permeation properties of a charged lipid nanoparticle carrier containing dexamethasone |
title_sort |
corneal permeation properties of a charged lipid nanoparticle carrier containing dexamethasone |
publisher |
Dove Medical Press |
series |
International Journal of Nanomedicine |
issn |
1178-2013 |
publishDate |
2017-02-01 |
description |
Junfeng Ban, Yan Zhang, Xin Huang, Guanghan Deng, Dongzhi Hou, Yanzhong Chen, Zhufen Lu Guangdong Provincial Key Laboratory of Advanced Drug Delivery Systems, Guangdong Pharmaceutical University, Guangzhou, People’s Republic of China Abstract: Drug delivery carriers can maintain effective therapeutic concentrations in the eye. To this end, we developed lipid nanoparticles (L/NPs) in which the surface was modified with positively charged chitosan, which engaged in hydrogen bonding with the phospholipid membrane. We evaluated in vitro corneal permeability and release characteristics, ocular irritation, and drug dynamics of modified and unmodified L/NPs in aqueous humor. The size of L/NPs was uniform and showed a narrow distribution. Corneal permeation was altered by the presence of chitosan and was dependent on particle size; the apparent permeability coefficient of dexamethasone increased by 2.7 and 1.8 times for chitosan-modified and unmodified L/NPs, respectively. In conclusion, a chitosan-modified system could be a promising method for increasing the ocular bioavailability of unmodified L/NPs by enhancing their retention time and permeation into the cornea. These findings provide a theoretical basis for the development of effective drug delivery systems in the treatment of ocular disease. Keywords: ocular drug delivery system, local bioavailability, dexamethasone, eye drop administration |
topic |
ocular drug delivery system local bioavailability dexamethasone eye drop administration |
url |
https://www.dovepress.com/corneal-permeation-properties-of-a-charged-lipid-nanoparticle-carrier--peer-reviewed-article-IJN |
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