Delivery of antisense oligonucleotide to the cornea by iontophoresis

被引:51
作者
Berdugo, M
Valamanesh, F
Andrieu, C
Klein, C
Benezra, D
Courtois, Y
Behar-Cohen, F
机构
[1] Assoc Claude Bermond, INSERM, U450, IFR58, F-75006 Paris, France
[2] Rothschild Ophthalmol Fdn, Paris, France
[3] Hadassah Hebrew Hosp Univ, Jerusalem, Israel
来源
ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT | 2003年 / 13卷 / 02期
关键词
D O I
10.1089/108729003321629647
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We wished to evaluate the potential of iontophoresis to promote the delivery of antisense oligonucleotides (ODN) directed at the vascular endothelial growth factor (VEGF)-R2 receptor (KDR/Flk) to the cornea of the rat eye. Fluorescence (CY5)-labeled ODNs in phosphate-buffered saline (PBS) (20 muM) were locally administered to rat eyes, and their fate within the anterior segment was studied. Thirty-four male, 5-week-old Wistar rats were used for all experiments. The rats were divided in four groups. In group I (12 rats, 12 eyes), the ODNs (20 muM) were delivered by iontophoresis (300 muA for 5 minutes) using a specially designed corneal applicator. In group II (12 rats, 12 eyes), the ODNs (20 muM) were delivered using the same applicator, but no electrical current was applied. In group III (6 rats, 6 eyes), a corneal neovascular reaction was induced prior to the application of ODNs (20 muM), and iontophoresis electrical current was delivered as for group I rats. Group IV (4 rats, 4 eyes) received ODN (60 muM) iontophoresis application (300 muA for 5 minutes) and were used for ODN integrity studies. The animals were killed 5 minutes, 90 minutes, and 24 hours after a single ODN application and studied. Topically applied ODNs using the same iontophoresis applicator but without current do not penetrate the cornea and remain confined to the superficial epithelial layer. ODNs delivered with transcorneoscleral iontophoresis penetrate into all corneal layers and are also detected in the iris. In corneas with neovascularization, ODNs were particularly localized within the vascular endothelial cells of the stroma. ODNs extracted from eye tissues 24 hours after iontophoresis remained unaltered. The iontophoresis current did not cause any detectable ocular damage under these conditions. Iontophoresis promotes the delivery of ODNs to the anterior segment of the eye, including all corneal layers. Iontophoresis of ODNs directed at VEGF-R2 may be used for the design of specific antiangiogenic strategy in diseases of the cornea.
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页码:107 / 114
页数:8
相关论文
共 26 条
[1]   PHARMACOKINETICS, BIODISTRIBUTION, AND STABILITY OF OLIGODEOXYNUCLEOTIDE PHOSPHOROTHIOATES IN MICE [J].
AGRAWAL, S ;
TEMSAMANI, J ;
TANG, JY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (17) :7595-7599
[2]  
Amano S, 1998, INVEST OPHTH VIS SCI, V39, P18
[3]   Induction of gene into the rabbit eye by iontophoresis: Preliminary report [J].
Asahara, T ;
Shinomiya, K ;
Naito, T ;
Shiota, H .
JAPANESE JOURNAL OF OPHTHALMOLOGY, 2001, 45 (01) :31-39
[4]  
Bayever E, 1993, Antisense Res Dev, V3, P383
[5]  
Behar-Cohen F, 2001, J FR OPHTALMOL, V24, P319
[6]  
Behar-Cohen FF, 1998, INVEST OPHTH VIS SCI, V39, P897
[7]   Iontophoresis of dexamethasone in the treatment of endotoxin-induced-uveitis in rats [J].
BeharCohen, FF ;
Parel, JM ;
Pouliquen, Y ;
ThillayeGoldenberg, B ;
Goureau, O ;
Heydolph, S ;
Courtois, Y ;
DeKozak, Y .
EXPERIMENTAL EYE RESEARCH, 1997, 65 (04) :533-545
[8]  
Belfort R, 2002, AM J OPHTHALMOL, V133, P467
[9]  
BENNETT MR, 1995, J DRUG DEV CLIN PR, V7, P225
[10]   Comparison of the ocular distribution of a model oligonucleotide after topical instillation in rabbits of conventional and new dosage forms [J].
Bochot, A ;
Mashhour, B ;
Puisieux, F ;
Couvreur, P ;
Fattal, E .
JOURNAL OF DRUG TARGETING, 1998, 6 (04) :309-313