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选择性向视网膜细胞递送药物:生物障碍和途径
Eva Ramsay1, Tatu Lajunen2, Madhushree Bhattacharya1
1Drug Research Programme, Division of Pharmaceutical Biosciences, Faculty of Pharmacy, University of Helsinki, 00014 University of Helsinki, Finland.
概括
开发有针对性的视网膜药物输送系统对于治疗眼睛疾病至关重要. 未来的战略将利用细胞特异性传递的生物机制,改善生物可用性和治疗结果.
科学领域:
- 眼科和制药科学 眼科和制药科学
- 生物医学工程 生物医学工程
背景情况:
- 由于解剖学和生理学障碍,视网膜药物输送面临重大挑战,限制了治疗疗效.
- 目前的静脉注射为小分子提供了有限的持续时间,对蛋白质和基因疗法等生物制剂的生物可用性较差.
- 现有的输送系统缺乏细胞特异性和细胞内向性,阻碍了现代生物药物的输送.
结论:
- 选择性视网膜药物递送技术尚不发达,但非常可行,特别是在局部眼部施用时.
- 有针对性的治疗可以克服目前生物可用性和作用持续时间的局限性.
- 这一重点审查为未来细胞特异性视网膜药物递送系统的生物机制提供了洞察力.
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