并行传输
纳米载体
视网膜
视网膜
眼球后段
核酸
细胞生物学
血-视网膜屏障
药物输送
体内
生物
眼底(子宫)
紧密连接
全身给药
材料科学
生物物理学
药理学
纳米技术
眼科
内分泌学
生物化学
医学
神经科学
磁导率
生物技术
糖尿病
糖尿病性视网膜病变
膜
作者
Sheng Wang,Yanhan Liu,Wenjuan Xiao,Qiuxue Yi,Mengmeng Jiang,Ruiyan Guo,Lu Song,Min Li,Fan Li,Danli Shi,Lingyi Zhao,Weiyi Huang,Xiaolei Zuo,Xiuhai Mao
标识
DOI:10.1021/acsami.2c18042
摘要
Designing an ocular drugs delivery system that can permeate the outer blood-retinal barrier (oBRB) is crucial for the microinvasive or noninvasive treatment of ocular fundus diseases. However, due to the lack of a nanocarrier that can maintain structure and composition at the oBRB, only intravitreal injection at the eyeball can deliver therapeutics directly to the ocular fundus via paracellular and intercellular routes, despite the intraocular operations risks. Here, we demonstrated tetrahedral framework nucleic acids (tFNAs) can penetrate the oBRB and deliver therapeutic nucleic acids to the retina of the rat eye in vivo following subconjunctival injection. We also discovered that tFNAs were transported via a paracellular route across the intercellular tight junctions at the oBRB. The histology analysis for ocular layers indicated that individual and aptamer/doxorubicin-loaded tFNAs penetrated all layers of the posterior segment of the eyeball to reach the innermost retina and persisted for over 3 days with minimal systemic biodistribution. We expect that the programmability and penetrability of tFNAs will provide a promising method for drug delivery across oBRB and long-term sustenance at the target site via periocular administration to various tissues.
科研通智能强力驱动
Strongly Powered by AbleSci AI