Dexamethasone distribution characteristic following controllable continuous sub-tenon drug delivery in rabbit
Drug delivery systems are required to be safe, minimally invasive and effectively delivery drug to the target tissues. But delivery drugs to the eye has not yet satisfied this need. Here, we focused on examining the distribution of dexamethasone (DEX) in ocular and plasmic samples following controll...
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doaj-888e17696df340bdb0e13c497352a9dd2020-11-25T03:27:17ZengTaylor & Francis GroupDrug Delivery1071-75441521-04642017-01-0124181882410.1080/10717544.2017.13245311324531Dexamethasone distribution characteristic following controllable continuous sub-tenon drug delivery in rabbitXuetao Huang0Manqiang Peng1Yezhen Yang2Yiqin Duan3Kuanshu Li4Shaogang Liu5Changhua Ye6Ding Lin7Changsha Aier Hospital, Aier School of Ophthalmology, Central South UniversityChangsha Aier Hospital, Aier School of Ophthalmology, Central South UniversityChangsha Aier Hospital, Aier School of Ophthalmology, Central South UniversityChangsha Aier Hospital, Aier School of Ophthalmology, Central South UniversityChangsha Aier Hospital, Aier School of Ophthalmology, Central South UniversityAdvanced Research Center, Central South UniversityChangsha Aier Hospital, Aier School of Ophthalmology, Central South UniversityChangsha Aier Hospital, Aier School of Ophthalmology, Central South UniversityDrug delivery systems are required to be safe, minimally invasive and effectively delivery drug to the target tissues. But delivery drugs to the eye has not yet satisfied this need. Here, we focused on examining the distribution of dexamethasone (DEX) in ocular and plasmic samples following controllable continuous sub-Tenon drug delivery (CCSDD) of dexamethasone disodium phosphate (DEXP) in rabbit, and to compare that with two traditional routes: subconjunctival injection and intravenous injection. The DEX concentration was analyzed by Shimadzu LC–MS 2010 system. In CCSDD group, during observed 24 h, the mean DEX level in collected samples from highest to lowest following in order: sclera, cornea, retina/choroid, iris, plasma, aqueous humor, lens and vitreous body. In ocular solid tissue, the DEX level in posterior segment is higher than in anatomic corresponding anterior segment, but it is opposite in ocular fluid tissue. High levels of DEX were maintained at 12 h in the ocular tissue immediately after the administration. Even at 24 h, the mean DEX concentration was 31.72 ng/ml and 22.40 ng/ml in aqueous and vitreous, respectively. In CCSDD group, the ocular DEX exposure (AUC0-24) is much higher and plasma exposure is much less than IV group, and it is also similar in SC group except iris. The amount of DEX levels are markedly increased in ocular tissues but it yield lower plasma levels indicating reduction of systemic absorption by CCSDD. Thus, CCSDD is an effective method of delivering DEX into anterior and posterior segment of the eye.http://dx.doi.org/10.1080/10717544.2017.1324531drug deliverydexamethasonetopical administrationocular tissuerabbit eyesub-tenon infusiondrug distribution |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Xuetao Huang Manqiang Peng Yezhen Yang Yiqin Duan Kuanshu Li Shaogang Liu Changhua Ye Ding Lin |
spellingShingle |
Xuetao Huang Manqiang Peng Yezhen Yang Yiqin Duan Kuanshu Li Shaogang Liu Changhua Ye Ding Lin Dexamethasone distribution characteristic following controllable continuous sub-tenon drug delivery in rabbit Drug Delivery drug delivery dexamethasone topical administration ocular tissue rabbit eye sub-tenon infusion drug distribution |
author_facet |
Xuetao Huang Manqiang Peng Yezhen Yang Yiqin Duan Kuanshu Li Shaogang Liu Changhua Ye Ding Lin |
author_sort |
Xuetao Huang |
title |
Dexamethasone distribution characteristic following controllable continuous sub-tenon drug delivery in rabbit |
title_short |
Dexamethasone distribution characteristic following controllable continuous sub-tenon drug delivery in rabbit |
title_full |
Dexamethasone distribution characteristic following controllable continuous sub-tenon drug delivery in rabbit |
title_fullStr |
Dexamethasone distribution characteristic following controllable continuous sub-tenon drug delivery in rabbit |
title_full_unstemmed |
Dexamethasone distribution characteristic following controllable continuous sub-tenon drug delivery in rabbit |
title_sort |
dexamethasone distribution characteristic following controllable continuous sub-tenon drug delivery in rabbit |
publisher |
Taylor & Francis Group |
series |
Drug Delivery |
issn |
1071-7544 1521-0464 |
publishDate |
2017-01-01 |
description |
Drug delivery systems are required to be safe, minimally invasive and effectively delivery drug to the target tissues. But delivery drugs to the eye has not yet satisfied this need. Here, we focused on examining the distribution of dexamethasone (DEX) in ocular and plasmic samples following controllable continuous sub-Tenon drug delivery (CCSDD) of dexamethasone disodium phosphate (DEXP) in rabbit, and to compare that with two traditional routes: subconjunctival injection and intravenous injection. The DEX concentration was analyzed by Shimadzu LC–MS 2010 system. In CCSDD group, during observed 24 h, the mean DEX level in collected samples from highest to lowest following in order: sclera, cornea, retina/choroid, iris, plasma, aqueous humor, lens and vitreous body. In ocular solid tissue, the DEX level in posterior segment is higher than in anatomic corresponding anterior segment, but it is opposite in ocular fluid tissue. High levels of DEX were maintained at 12 h in the ocular tissue immediately after the administration. Even at 24 h, the mean DEX concentration was 31.72 ng/ml and 22.40 ng/ml in aqueous and vitreous, respectively. In CCSDD group, the ocular DEX exposure (AUC0-24) is much higher and plasma exposure is much less than IV group, and it is also similar in SC group except iris. The amount of DEX levels are markedly increased in ocular tissues but it yield lower plasma levels indicating reduction of systemic absorption by CCSDD. Thus, CCSDD is an effective method of delivering DEX into anterior and posterior segment of the eye. |
topic |
drug delivery dexamethasone topical administration ocular tissue rabbit eye sub-tenon infusion drug distribution |
url |
http://dx.doi.org/10.1080/10717544.2017.1324531 |
work_keys_str_mv |
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