Division of Clinical Cell Therapy, United Centers for Advanced Research and Translational Medicine (ART), Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Japan.
Department of Finemechanics, Graduate School of Engineering, Tohoku University, 6-6-01 Aramaki, Aoba-ku, Sendai 980-8579, Japan.
Eur J Pharm Biopharm. 2019 Mar;136:184-191. doi: 10.1016/j.ejpb.2019.01.024. Epub 2019 Jan 25.
Continuous drug administration with better adherence to treatment and less invasive procedures is important in treating retinal diseases such as age-related macular disease. In this study, we report a drug-refillable device consisting of a silicone reservoir and an injectable gelatin/chitosan gel (iGel). The silicone reservoir was fabricated with polydimethylsiloxane (PDMS) using a computer-aided design and manufacturing to have micropores at a releasing side for uniaxial release to the sclera. A stainless steel wire and sheet were combined in the side and bottom of the reservoir to ensure flexibility and to fit on the curvature of the eyeball and prevent irritation to the sclera through the bottom of the reservoir. The drug was injected and formulated in the reservoir by in situ crosslinking of gelatin/chitosan gel with the crosslinker; 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride. The in vitro release study using fluorescein molecules showed that the release rate from encapsulated iGel in the reservoir was slower than that from the original iGel. After reinjecting the iGel into the reservoir, the same release profile as the first injection was observed. The reservoir containing iGel was placed on the sclera of a rabbit and the distribution of 150 kDa fluorescein isothiocyanate-dextran (FD150) in the retina and choroid/retinal pigment epithelium (choroid/RPE) was studied. The cryosections showed that FD150 was observed in the choroid/RPE. Homogenates of the retina and choroid/RPE showed fluorescence during 12 weeks implantation, indicating the drug could be delivered to the retina by using the device. The drug filling was successful into the reservoir implanted on the sclera through the conjunctiva by using a needle. In conclusion, the refillable drug delivery device is a promising tool to administer drugs long-term by reinjection with less invasiveness to intraocular tissues.
持续给药,提高治疗依从性,减少侵入性操作,这对于治疗年龄相关性黄斑病变等视网膜疾病非常重要。在本研究中,我们报告了一种由硅树脂储液器和可注射明胶/壳聚糖凝胶(iGel)组成的药物可再填充装置。硅树脂储液器是使用计算机辅助设计和制造技术,由聚二甲基硅氧烷(PDMS)制成的,在释放侧具有微孔,用于向巩膜进行单轴释放。不锈钢丝和薄片组合在储液器的侧面和底部,以确保其灵活性,并适应眼球的曲率,防止储液器底部对巩膜造成刺激。药物通过明胶/壳聚糖凝胶与交联剂 1-乙基-3-(3-二甲基氨基丙基)碳二亚胺盐酸盐的原位交联注入并配制在储液器中。使用荧光分子进行的体外释放研究表明,从储液器中包裹的 iGel 中释放的速度比原始 iGel 慢。将 iGel 重新注入储液器后,观察到与第一次注射相同的释放曲线。将装有 iGel 的储液器放置在兔子的巩膜上,研究视网膜和脉络膜/视网膜色素上皮(脉络膜/RPE)中 150kDa 荧光素异硫氰酸酯-葡聚糖(FD150)的分布。冷冻切片显示 FD150 存在于脉络膜/RPE 中。视网膜和脉络膜/RPE 的匀浆在植入 12 周时显示荧光,表明该装置可将药物递送到视网膜。通过使用结膜上的针头成功地将药物填充到植入巩膜上的储液器中。总之,这种可再填充的药物输送装置是一种很有前途的工具,通过再次注射,可以长期、低侵入性地向眼内组织输送药物。