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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Main Authors: Xuetao Huang, Manqiang Peng, Yezhen Yang, Yiqin Duan, Kuanshu Li, Shaogang Liu, Changhua Ye, Ding Lin
Format: Article
Language:English
Published: Taylor & Francis Group 2017-01-01
Series:Drug Delivery
Subjects:
Online Access:http://dx.doi.org/10.1080/10717544.2017.1324531
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spelling 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
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