Department of Electronics Engineering, College of Engineering, Pusan National University, Busan, Republic of Korea.
Medical Device Development Center, Daegu-Gyeongbuk Medical Innovation Foundation (K-MEDI Hub), Daegu, Republic of Korea.
Transl Vis Sci Technol. 2024 May 1;13(5):5. doi: 10.1167/tvst.13.5.5.
The blood-retinal barrier (BRB) restricts the delivery of intravenous therapeutics to the retina, necessitating innovative approaches for treating retinal disorders. This study sought to explore the potential of focused ultrasound (FUS) to non-invasively deliver intravenously administered gold nanoparticles (AuNPs) across the BRB. FUS-BRB modulation can offer a novel method for targeted retinal therapy.
AuNPs of different sizes and shapes were characterized, and FUS parameters were optimized to permeate the BRB without causing retinal damage in a rodent model. The delivery of 70-kDa dextran and AuNPs to the retinal ganglion cell (RGC) layer was visualized using confocal and two-photon microscopy, respectively. Histological and statistical analyses were conducted to assess the effectiveness and safety of the procedure.
FUS-BRB modulation resulted in the delivery of dextran and AuNPs to the RGC and inner nuclear layer. Smaller AuNPs reached the retinal layers to a greater extent than larger ones. The delivery of dextran and AuNPs across the BRB with FUS was achieved without significant retinal damage.
This investigation provides the first evidence, to our knowledge, of FUS-mediated AuNP delivery across the BRB, establishing a foundation for a targeted and non-invasive approach to retinal treatment. The results contribute to developing promising non-invasive therapeutic strategies in ophthalmology to treat retinal diseases.
Modifying the BRB with ultrasound offers a targeted and non-invasive delivery strategy of intravenous therapeutics to the retina.
血视网膜屏障(BRB)限制了静脉内治疗药物向视网膜的输送,因此需要创新的方法来治疗视网膜疾病。本研究旨在探索聚焦超声(FUS)在不破坏视网膜的情况下将静脉内给予的金纳米颗粒(AuNPs)经 BRB 递送至视网膜的潜力。FUS-BRB 调制为靶向视网膜治疗提供了一种新方法。
对不同大小和形状的 AuNPs 进行了表征,并优化了 FUS 参数,以在啮齿动物模型中渗透 BRB 而不会造成视网膜损伤。使用共聚焦和双光子显微镜分别可视化 70-kDa 葡聚糖和 AuNPs 向视网膜神经节细胞(RGC)层的递送。进行了组织学和统计学分析,以评估该程序的有效性和安全性。
FUS-BRB 调制导致葡聚糖和 AuNPs 递送至 RGC 和内核层。与较大的 AuNPs 相比,较小的 AuNPs 更能到达视网膜层。FUS 介导的 AuNP 穿过 BRB 的递送不会引起明显的视网膜损伤。
本研究首次提供了 FUS 介导的 AuNP 穿过 BRB 的递送至视网膜的证据,为靶向和非侵入性的视网膜治疗方法奠定了基础。研究结果有助于开发有前途的眼科非侵入性治疗策略,以治疗视网膜疾病。
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