Sustainable DNA-polysaccharide hydrogels as recyclable bioplastics

  • Yujie KE
  • , Kai LAN
  • , Jing Yi WONG
  • , Hongfang LU
  • , Shujun GAO
  • , Keunhyuk RYU
  • , Feng CHEN
  • , Wei Wei LOH
  • , Zhili DONG
  • , Jason Y. C. LIM
  • , Zhaogang DONG
  • , Xi CHEN*
  • , Itamar WILLNER*
  • , Yuwei HU*
  • *Corresponding author for this work

Research output: Journal PublicationsJournal Article (refereed)peer-review

1 Citation (Scopus)

Abstract

Traditional petrochemical-derived plastics are challenging to recycle and degrade, and the existing (re)process methods are organic solvent-based and/or energy-intensive, resulting in significant environmental contamination and greenhouse gas emissions. This study presents a sustainable bioplastic material characterized by multi-closed-loop recyclability and water (re)processability. The bioplastics are derived from abundant polysaccharide sources of dextran, alginic acid, carboxymethyl cellulose, and DNA of plant and living organism waste. The process involves chemical oxidation of polysaccharides to produce aldehyde-functionalized derivatives, which subsequently form reversible imine covalent bonds with amine groups in DNA. This reaction yields water-processable polysaccharide/DNA crosslinked hydrogels, serving as raw materials for producing sustainable bioplastics. The bioplastic products exhibit (bio)degradability and recyclability, enabling aqueous recovery of the hydrogel constituents through plastic hydrolysis and the natural biodegradability of DNA and polysaccharides. These products demonstrate excellent resistance to organic solvents, self-healing, scalability, and effective processing down to nanometer scales, underscoring their potential for broad and versatile applications. The work provides potential pathways for advancing sustainable and environmentally friendly bioplastic materials.
Original languageEnglish
Article number7467
JournalNature Communications
Volume16
Early online date12 Aug 2025
DOIs
Publication statusPublished - Dec 2025

Bibliographical note

Publisher Copyright:
© The Author(s) 2025.

Funding

The research is supported by A*STAR (CDF, C210112014, to Y.H.), and Science and Engineering Research Council (CRF, UIBR, KIMR220901Asercrf, to Y.H.), Singapore. Y.K. acknowledges the support of start-up fund, faculty research grant (SISFRG2513), and the Lam Woo Research Fund (LWP20039) from Lingnan University, Hong Kong. Z.G.D. would like to acknowledge the funding support from National Research Foundation via Quantum Engineering Programme 2.0 (Award No. NRF2021-QEP2-03-P09).

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