Investigative Ophthalmology & Visual Science Cover Image for Volume 65, Issue 7
June 2024
Volume 65, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2024
Silicon nanoneedles for sustained treatment of choroidal neovascularization
Author Affiliations & Notes
  • Yannis Mantas Paulus
    Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, Michigan, United States
  • Phuc Nguyen
    Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, Michigan, United States
  • Jinheon Jeong
    Weldon School of Biomedical Engineering, Purdue University, West Lafayette, Indiana, United States
  • Junsang Lee
    Weldon School of Biomedical Engineering, Purdue University, West Lafayette, Indiana, United States
  • Chi Hwan Lee
    Weldon School of Biomedical Engineering, Purdue University, West Lafayette, Indiana, United States
  • Footnotes
    Commercial Relationships   Yannis Paulus None; Phuc Nguyen None; Jinheon Jeong None; Junsang Lee None; Chi Hwan Lee None
  • Footnotes
    Support  NIH NEI 1R01EY033000, 1R01EY03432, Department of Defense CDMRP HT9425-23-10179, Fight for Sight- International Retinal Research Foundation FFSGIA16002, Alcon Research Institute Young Investigator Grant, unrestricted departmental support from Research to Prevent Blindness
Investigative Ophthalmology & Visual Science June 2024, Vol.65, 3990. doi:
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    • Get Citation

      Yannis Mantas Paulus, Phuc Nguyen, Jinheon Jeong, Junsang Lee, Chi Hwan Lee; Silicon nanoneedles for sustained treatment of choroidal neovascularization. Invest. Ophthalmol. Vis. Sci. 2024;65(7):3990.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : Choroidal neovascularization (CNV) is a major cause of vision loss and blindness in wet macular degeneration. To treat CNV, intravitreal anti-vascular endothelial growth factor therapy (VEGF) such as bevacizumab (BEV) are often utilized, but these treatments require frequent invasive administration and can carry a risk of endophthalmitis. To improve the treatment efficiency, reduce the treatment burden, and reduce the side-effects and invasiveness, the current study describes a novel treatment of CNV using miniature biodegradable silicon nanoneedles (SiNNs) fabricated on a tear-soluble contact lens.

Methods : The SiNNs were encapsulated with BEV (BEV@SiNNs) and used as drug carriers for long-term, sustained drug delivery. BEV@SiNNs were evaluated on a New Zealand rabbit CNV model (n = 7) after approval from the University of Michigan IACUC. To generate CNV, subretinal injection of Matrigel (20 μL) and VEGF (7.5 μL, 100 μg/mL) was performed using a 30G Hamilton needle. A contact lens was inserted subconjunctivally on the posterior sclera 3 days after CNV creation and monitored by color fundus photography, OCT, and fluorescein angiography (FA) before and at 1, 3, 7, 14, and 28 days and then monthly for up to 7 months post-treatment.

Results : BEV@SiNNs resulted in long-term, sustained reduction in mean FA CNV leakage intensity for at least 7 months. There was a rapid 45% reduction in CNV within 1 week. CNV continued to gradually reduce further to an 80% reduction in CNV by 4 months that was persistent to 7 months (Figure, red line). Control CNV did not have a significant change in CNV over 7 months (Figure, blue line). Rabbits were comfortable on the grimace scale, and no complications occurred with treatment in any animals. OCT showed normal retinal morphology and layers.

Conclusions : SiNNs are an efficient drug delivery platform technology for long-term (at least 7 month), sustained treatment of CNV in this rabbit model.

This abstract was presented at the 2024 ARVO Annual Meeting, held in Seattle, WA, May 5-9, 2024.

 

Fluorescein angiography CNV mean leakage intensity evaluated longitudinally over 7 months after BEV@SiNNs (red) and control (blue) demonstrating a significant 80% reduction in CNV that persisted to 7 months with BEV@SiNNs. No change in CNV was noted in controls.

Fluorescein angiography CNV mean leakage intensity evaluated longitudinally over 7 months after BEV@SiNNs (red) and control (blue) demonstrating a significant 80% reduction in CNV that persisted to 7 months with BEV@SiNNs. No change in CNV was noted in controls.

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