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TAK-593 眼用乳剂治疗年龄相关性黄斑变性的潜力。

Potential of TAK-593 Ophthalmic Emulsion for the Treatment of Age-Related Macular Degeneration.

机构信息

Research and Development Division, Senju Pharmaceutical Co., Ltd.

Department of Bioscience and Bioinformatics, Kyushu Institute of Technology.

出版信息

Biol Pharm Bull. 2023 Jul 1;46(7):921-928. doi: 10.1248/bpb.b23-00066. Epub 2023 May 11.

DOI:10.1248/bpb.b23-00066
PMID:37164692
Abstract

Intravitreal injection therapy of anti-vascular endothelial growth factor (VEGF) antibody or steroids is the mainstream for patients with age-related macular degeneration (AMD). However, since intravitreal injection is invasive administration, side effects such as endophthalmitis are major problems. In this study, we selected eye drops as a non-invasive treatment method, and aimed to develop eye drops that can deliver TAK-593 (VEGF receptor tyrosine kinase inhibitor) to the posterior segment of the eye. Since TAK-593 is a poorly water-soluble drug, the TAK-593 emulsion was formulated. The solubility of TAK-593 in various oils was measured, and the oil used for the emulsion was selected. Furthermore, viscosity enhancers were added to the emulsion in order to improve the drug delivery into the eye. As viscosity enhancer, xanthan gum was selected based on the properties and the viscosity of the emulsion. The delivery of TAK-593 to the posterior eye was increased by the formulation concentration and the addition of viscosity enhancers. In the laser-induced choroidal neovascularization model, TAK-593 emulsion eye drops showed the same angiogenesis-suppression efficacy as anti-VEGF antibody intravitreal injection. From these results, it was revealed that TAK-593 with an effective drug concentration can be delivered to the posterior eye by non-invasive eye drop administration.

摘要

抗血管内皮生长因子 (VEGF) 抗体或类固醇的玻璃体内注射疗法是治疗年龄相关性黄斑变性 (AMD) 的主流方法。然而,由于玻璃体内注射是一种有创的给药方式,因此眼内炎等副作用是主要问题。在这项研究中,我们选择滴眼剂作为非侵入性治疗方法,旨在开发可将 TAK-593(VEGF 受体酪氨酸激酶抑制剂)递送至眼后段的滴眼剂。由于 TAK-593 是一种水溶性较差的药物,因此我们配制了 TAK-593 乳剂。测量了 TAK-593 在各种油中的溶解度,并选择了用于乳剂的油。此外,为了改善药物向眼内的递送,向乳剂中添加了增粘剂。作为增粘剂,根据乳剂的性质和粘度选择了黄原胶。通过制剂浓度和添加增粘剂来增加 TAK-593 向眼后段的递送。在激光诱导脉络膜新生血管化模型中,TAK-593 乳剂滴眼剂显示出与玻璃体内注射抗 VEGF 抗体相同的血管生成抑制效果。从这些结果可以看出,通过非侵入性滴眼剂给药可以将具有有效药物浓度的 TAK-593 递送至眼后段。

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