# DNA Nanoflower LYTACs Enable Efficient VEGF Degradation and Verteporfin Loading for Combined Therapy of Wet Age‐Related Macular Degeneration

**Authors:** Mengxuan Li, Yan Yue, Sijin Wu, Xinyu He, Jiayi Song, Shuwen Ma, Haokun Zhang, Chenyu Xu, Song Chen, Yanming Huang, Songbo Xie, Hua Yan

PMC · DOI: 10.1002/advs.202515852 · Advanced Science · 2026-01-28

## TL;DR

A new DNA-based treatment combines VEGF degradation and photodynamic therapy to effectively treat wet age-related macular degeneration with fewer side effects.

## Contribution

The novel DNA nanoflower integrates VEGF degradation and photodynamic therapy for combined treatment of wAMD.

## Key findings

- The DNA nanoflower effectively degrades extracellular VEGF in the lesion area.
- NF@VER generates reactive oxygen species under near-infrared light to induce endothelial cell death.
- The combined therapy blocks VEGF-induced CNV in vivo without noticeable side effects.

## Abstract

Wet age‐related macular degeneration (wAMD), characterized by pathological choroidal neovascularization (CNV), is a leading cause of irreversible vision loss in the elderly. The current standard treatment—anti‐vascular endothelial growth factor (VEGF) therapy—effectively manages neovascularization in many patients. However, some experience suboptimal responses, and frequent intravitreal injections raise safety concerns. Photodynamic therapy is another effective option for treating wAMD, but it can lead to an increase in reactive VEGF after the procedure, resulting in CNV recurrence. In response to these challenges, we propose an integrated approach that combines a DNA nanoflower VEGF degrader with photodynamic therapy. The DNA nanoflower consists of numerous aptamer‐based lysosome‐targeted chimaera (LYTAC) units, which drive extracellular VEGF in the lesion area to the lysosome for degradation. Simultaneously, the DNA nanoflower acts as a carrier for verteporfin (VER), a clinically used photosensitizer. The resulting nanoflower, named NF@VER, generates reactive oxygen species under near‐infrared light to induce endothelial cell death. These combined effects on endothelial cells effectively block VEGF‐induced CNV in vivo, without causing noticeable side effects. Overall, this innovative approach presents a precise and effective strategy for treating wAMD, reducing the risk of VEGF reactivation‐induced CNV recurrence, and minimizing the systemic side effects associated with photodynamic therapy.

An integrated approach that combines a DNA nanoflower VEGF degrader with photodynamic therapy is developed for the treatment of wet age‐related macular degeneration, which reduces the risk of VEGF reactivation‐induced CNV recurrence and minimizes the systemic side effects associated with photodynamic therapy.

## Linked entities

- **Proteins:** VEGFA (vascular endothelial growth factor A)
- **Diseases:** wet age-related macular degeneration (MONDO:0005417), choroidal neovascularization (MONDO:0810000)

## Full-text entities

- **Genes:** VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}
- **Diseases:** Wet Age-Related Macular Degeneration (MESH:D057135), CNV (MESH:D020256), vision loss (MESH:D014786)
- **Chemicals:** VER (MESH:D000077362), reactive oxygen species (MESH:D017382), NF@VER (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13042913/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC13042913/full.md

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Source: https://tomesphere.com/paper/PMC13042913