# Azobenzene-bridged ionizable amphiphilic Janus glycosides for light-controlled, single-component and organ-modulable pDNA delivery

**Authors:** Zhaoxin Wang, Gonzalo Rivero-Barbarroja, Juan M. Benito, Stéphane Maisonneuve, Itziar Vélaz, Inmaculada Juárez-Gonzálvez, María J. Garrido, Conchita Tros de Ilarduya, Carmen Ortiz Mellet, Juan Xie, José M. García Fernández

PMC · DOI: 10.1038/s42004-026-01920-z · 2026-02-05

## TL;DR

Researchers developed light-sensitive DNA delivery carriers that can change their behavior with light, allowing precise control over where and when DNA is delivered in the body.

## Contribution

The novel contribution is the design of azobenzene-bridged glycosides that enable light-controlled DNA delivery with organ-specific targeting.

## Key findings

- Light-induced photoisomerization alters nanocomplex properties and transfection outcomes in different cell types.
- O-glycosides shift gene expression from liver to lung upon light exposure, while S-glycosides target the spleen.
- All formulations showed high cell viability across tested cell lines and macrophages.

## Abstract

Stimuli-responsive supramolecular systems enable spatiotemporal control of nucleic acid (NA) delivery. To achieve precise and programmable vectors, we designed azobenzene-bridged ionizable amphiphilic Janus glycosides (IAJGs) as single-component, light-responsive DNA carriers. These glucopyranose-based dimers undergo reversible E/Z photoisomerization while forming stable nanocomplexes with plasmid DNA (pDNA). Photoisomerization alters nanocomplex size, surface charge, and internal order, resulting in distinct transfection outcomes. In vitro, O- and S-glycoside derivatives displayed isomer-dependent activity across COS-7, HepG2, and RAW264.7 cells, with pronounced switching effects specially in macrophages. In vivo, systemic administration revealed organ-selective responses: O-glycosides shifted expression from liver to lung upon E → Z conversion, whereas S-glycosides favored spleen targeting. All formulations maintained high cell viability. These results highlight photoswitchable IAJGs as structurally defined vectors for adjustable control over NA delivery and organ tropism.

Stimuli-responsive supramolecular systems offer innovative solutions for precise nucleic acid delivery, addressing the need for spatiotemporal control. Here, the authors develop azobenzene-bridged ionizable amphiphilic Janus glycosides as light-responsive DNA carriers, demonstrating reversible photoisomerization that modulates transfection outcomes and organ targeting.

## Linked entities

- **Chemicals:** azobenzene (PubChem CID 2272), glucopyranose (PubChem CID 5793)

## Full-text entities

- **Chemicals:** E (MESH:D004540), S-glycosides (MESH:D006027), Azobenzene (MESH:C009850), Janus (-)

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12982485/full.md

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Source: https://tomesphere.com/paper/PMC12982485