Ophthalmic Tethered Gold Yarnball‐Mediated Retained Drug Delivery for Eye Fundus Disease Treatment

Author:

Chou Shih‐Jie12,Yang Yi‐Ping12,Chiang Min‐Ren3,Chen Chih‐Ying12,Lai Henkie Isahwan Ahmad Mulyadi124,Lin Yi‐Ying12,Wu You‐Ren12,Wang I‐Chieh12,Yarmishyn Aliaksandr A.12,Chiou Guang‐Yuh56,Lin Tai‐Chi78,Hwang De‐Kuang78,Chen Shih‐Jen78,Chien Yueh12,Hu Shang‐Hsiu3ORCID,Chiou Shih‐Hwa1289

Affiliation:

1. Department of Medical Research Taipei Veterans General Hospital Taipei 112201 Taiwan

2. Institute of Pharmacology College of Medicine National Yang Ming Chiao Tung University Taipei 112304 Taiwan

3. Department of Biomedical Engineering and Environmental Sciences National Tsing Hua University Hsinchu 300044 Taiwan

4. Department of Medical Sciences, Faculty of Health Sciences University College of MAIWP International Kuala Lumpur 68100 Malaysia

5. Department of Biological Science and Technology National Yang Ming Chiao Tung University Hsinchu 300093 Taiwan

6. Center for Intelligent Drug Systems and Smart Bio‐Devices National Yang Ming Chiao Tung University Hsinchu 300093 Taiwan

7. Department of Ophthalmology Taipei Veterans General Hospital Taipei 112201 Taiwan

8. School of Medicine National Yang Ming Chiao Tung University Taipei 112304 Taiwan

9. Genomic Research Center Academia Sinica Taipei 115024 Taiwan

Abstract

Eye fundus diseases, such as retinal degenerative diseases, which lead to blindness in ≈12% of individuals aged >65 years, cause permanent damage to retinal cells. The antioxidant quercetin (QC) is promising for the effective treatment of eye fundus diseases; however, its poor solubility and low retention rate often limit its clinical application. Herein, an in situ ophthalmic tethered gold yarnball (GY) that doubles as an ocular retention agent and QC reservoir to overcome low fundus drug retention is developed. After intravitreal injection, QC@GYs enhance retinal cell leakage and internal limiting membrane permeability, facilitating the partial penetration of QC@GYs into the intraretinal tissue. The combination of retina‐tethered QC@GY and first‐level sustained release reduces macular degeneration in vivo by effectively regulating oxidative stress. Furthermore, the sustained release of QC preserves the viability of retinal pigment epithelium cells, reduces apoptosis, and suppresses drusen formation. This preservation of retinal morphology and function maximizes the therapeutic impact while minimizing the need for frequent intraocular administration. Overall, the ophthalmic tethered GY platform is a versatile tool for retinal drug delivery for the treatment of eye fundus diseases.

Funder

National Science and Technology Council

Publisher

Wiley

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