Ocular drug delivery targeted by iontophoresis in the suprachoroidal space using a microneedle

被引:87
|
作者
Jung, Jae Hwan [1 ]
Chiang, Bryce [2 ,3 ,4 ]
Grossniklaus, Hans E. [5 ]
Prausnitz, Mark R. [1 ,2 ,3 ]
机构
[1] Georgia Inst Technol, Sch Chem & Biomol Engn, Atlanta, GA 30332 USA
[2] Georgia Tech, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30332 USA
[3] Emory Univ, Georgia Inst Technol, Atlanta, GA 30332 USA
[4] Emory Univ, Sch Med, Atlanta, GA 30322 USA
[5] Emory Univ, Sch Med, Dept Ophthalmol, Atlanta, GA 30322 USA
基金
美国国家卫生研究院;
关键词
Iontophoresis; Microneedle; Ocular drug delivery; Posterior segment; Suprachoroidal injection; Targeted drug delivery; COULOMB-CONTROLLED IONTOPHORESIS; POSTERIOR SEGMENT; TRANSSCLERAL IONTOPHORESIS; TRIAMCINOLONE ACETONIDE; INTRAVITREAL INJECTION; RABBIT EYE; IN-VIVO; HYDROGEL; MODEL; NANOPARTICLES;
D O I
10.1016/j.jconrel.2018.03.001
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Treatment of many posterior-segment ocular indications would benefit from improved targeting of drug delivery to the back of the eye. Here, we propose the use of iontophoresis to direct delivery of negatively charged nanoparticles through the suprachoroidal space (SCS) toward the posterior pole of the eye. Injection of nanoparticles into the SCS of the rabbit eye ex vivo without iontophoresis led to a nanoparticle distribution mostly localized at the site of injection near the limbus and < 15% of nanoparticles delivered to the most posterior region of SCS (> 9 mm from the limbus). Iontophoresis using a novel microneedle-based device increased posterior targeting with > 30% of nanoparticles in the most posterior region of SCS. Posterior targeting increased with increasing iontophoresis current and increasing application time up to 3 min, but further increasing to 5 min was not better, probably due to the observed collapse of the SCS within 5 min after injection ex vivo. Reversing the direction of iontophoretic flow inhibited posterior targeting, with just similar to 5% of nanoparticles reaching the most posterior region of SCS. In the rabbit eye in vivo, iontophoresis at 0.14 mA for 3 min after injection of a 100 mu L suspension of nanoparticles resulted in similar to 30% of nanoparticles delivered to the most posterior region of the SCS, which was consistent with ex vivo findings. The procedure was well tolerated, with only mild, transient tissue effects at the site of injection. We conclude that iontophoresis in the SCS using a microneedle has promise as a method to target ocular drug delivery within the eye, especially toward the posterior pole.
引用
收藏
页码:14 / 22
页数:9
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