Hiring in life sciences? Share your open positions with our professional community. Read more Close

Advertisement

Liquid Gallium Nanozyme Coatings Enable Sustained Nitric Oxide Generation With Antioxidant and Anti-Inflammatory Functions.

Created on 13 Aug 2026

Authors

Franco Centurion, Kang Lin, Shu Geng, Siti Nur Asyura Adzlan, Qingqing Fan, Federico Mazur, Ravindra Kokate, Priyank Kumar, Christina Cortez-Jugo, Frank Caruso, Rona Chandrawati

Published in

Advanced science (Weinheim, Baden-Wurttemberg, Germany). Pages e77143. Aug 13, 2026. Epub Aug 13, 2026.

Abstract

Artificial nanozymes, defined as nanomaterials that mimic enzyme-like catalytic activity, emerge as adaptable tools for biomedical applications by uniting catalytic activity with structural stability and chemical versatility. Here, we introduce liquid gallium (Ga) as a catalytic center for nitric oxide (NO) generation and demonstrate its translation into a multifunctional coating. Ga nanoparticles were stabilized with tannic acid (TA) and embedded into a TA-zirconium (TA-Zr4+) metal-phenolic network (MPN), producing robust, substrate-independent films. Ga catalyzed the decomposition of S-nitrosothiols (RSNOs) through electron transfer, enabling NO generation from both model donors such as S-nitrosoglutathione (GSNO) and endogenous precursors in human umbilical vein endothelial cells (HUVECs), with activity retained over multiple cycles. The TA-Zr4+ framework stabilized the coatings and contributed intrinsic antioxidant and anti-inflammatory activities, resulting in a platform that amplified therapeutic outcomes. Functionally, the coatings displayed tunable NO generation, enhanced intracellular NO levels in HUVECs by ∼48%, reduced pro-inflammatory cytokines TNF-α and IL-6 by ∼35% and ∼40%, respectively, under LPS stimulation, and supported endothelial biocompatibility. Together, these findings establish liquid Ga as an efficient catalyst for NO generation and present a design strategy that advances implant coatings from conventional NO donor-based systems toward active, regenerative, and multifunctional therapeutic interfaces.

PMID:
42591068
Bibliographic data and abstract were imported from PubMed on 13 Aug 2026.

Read full publication at:
Please sign in to see all details.

Advertisement

Stats

  • Community rating n/a 0 votes
  • Reviewers' rating n/a 0 votes
  • Your rating

1-terrible, 9-excellent. How would you rate this publication? Sign in in to submit your rating.

  • Recommendations n/a n/a positive of 0 vote(s)
  • Views 3
  • Comments 0

Recommended by

  • No recommendations yet.

Post a comment

You need to be signed in to post comments. You can sign in here.

Comments

There are no comments yet.

Advertisement