# One-Pot Anodic Electrodeposition of Dual-Cation-Crosslinked Sodium Alginate/Carboxymethyl Chitosan Interpenetrating Hydrogel with Vessel-Mimetic Heterostructures

**Authors:** Xuli Li, Yuqing Qu, Yong Zhang, Pei Chen, Siyu Ding, Miaomiao Nie, Kun Yan, Shefeng Li

PMC · DOI: 10.3390/jfb16070235 · Journal of Functional Biomaterials · 2025-06-26

## TL;DR

This study creates a new type of hydrogel with layered structures that mimic blood vessels, using a one-step electrochemical process.

## Contribution

A novel one-pot anodic electrodeposition method is introduced to fabricate dual-cation-crosslinked, vessel-mimetic hydrogels with tailored mechanical and antibacterial properties.

## Key findings

- The hydrogels show rapid growth rates and excellent mechanical strength.
- They exhibit strong antibacterial performance and can be customized for biomedical applications.
- The method allows scalable production of multilayered tubular hydrogels for artificial vessels and organ interfaces.

## Abstract

This study develops a one-pot anodic templating electrodeposition strategy using dual-cation-crosslinking and interpenetrating networks, coupled with pulsed electrical signals, to fabricate a vessel-mimetic multilayered tubular hydrogel. Typically, the anodic electrodeposition is performed in a mixture of sodium alginate (SA) and carboxymethyl chitosan (CMC), with the ethylenediaminetetraacetic acid calcium disodium salt hydrate (EDTA·Na2Ca) incorporated to provide a secondary ionic crosslinker (i.e., Ca2+) and modulate the cascade reaction diffusion process. The copper wire electrodes serve as templates for electrochemical oxidation and enable a copper ion (i.e., Cu2+)-induced tubular hydrogel coating formation, while pulsed electric fields regulate layer-by-layer deposition. The dual-cation-crosslinked interpenetrating hydrogels (CMC/SA-Cu/Ca) exhibit rapid growth rates and tailored mechanical strength, along with excellent antibacterial performance. By integrating the unique pulsed electro-fabrication with biomimetic self-assembly, this study addresses challenges in vessel-mimicking structural complexity and mechanical compatibility. The approach enables scalable production of customizable multilayered hydrogels for artificial vessel grafts, smart wound dressings, and bioengineered organ interfaces, demonstrating broad biomedical potential.

## Linked entities

- **Chemicals:** carboxymethyl chitosan (PubChem CID 71306969), ethylenediaminetetraacetic acid calcium disodium salt hydrate (PubChem CID 6096880), copper (PubChem CID 23978), Cu2+ (PubChem CID 27099), Ca2+ (PubChem CID 271)

## Full-text entities

- **Chemicals:** Cu (MESH:D003300), SA (MESH:D000464), Ca2+ (-), CMC (MESH:C514968), Ca (MESH:D002118)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12294871/full.md

## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12294871/full.md

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Source: https://tomesphere.com/paper/PMC12294871