Related Experiment Video
Updated: Jun 13, 2025

10:16
Electroactive Polymer Nanoparticles Exhibiting Photothermal Properties
Published on: January 8, 2016
13.9K
Cu(II)-Organic Coordination Polymer Networks for Persistent Nitric Oxide Release in Tumor Therapy
Hyejoong Jeong1, Na Kyung Kim2, Daehwan Park2,3
1Research Institute of Advanced Materials (RIAM), Seoul National University, Seoul 08826, Republic of Korea.
Biomacromolecules
|September 16, 2024
Summary
This study introduces a novel copper-organic polymer film that sustainably releases nitric oxide (NO). This NO release effectively reprograms immune cells, showing promise for advanced cancer immunotherapy treatments.
Area of Science:
- Biomaterials Science
- Immunology
- Nanotechnology
Background:
- Nitric oxide (NO) is crucial for immune regulation, particularly in polarizing macrophages to the M1 phenotype, which is beneficial for cancer immunotherapy.
- Developing materials for sustained NO delivery is essential for enhancing therapeutic efficacy.
Purpose of the Study:
- To create a robust copper-organic coordination polymer network for sustained nitric oxide (NO) release.
- To investigate the potential of this material as an anticancer patch for macrophage polarization.
Main Methods:
- A dual-interaction process involving complexation and cross-linking was used to construct the polymer network from 4-((6-(acryloyloxy)hexyl)oxy)benzoic acid (BA) and Cu(II) ions.
- The polymer film's ability to release NO from S-nitrosoglutathione was assessed over 90 days in a physiological environment.
- The effect of released NO on macrophage polarization (M0 and M2 to M1) was evaluated.
Main Results:
- The developed BA-Cu polymer network demonstrated robust structure and sustained NO release for over 90 days.
- The released NO effectively polarized both resting (M0) and tumor-associated (M2) macrophages towards the proinflammatory M1 phenotype.
- The material exhibited significant physiological stability.
Conclusions:
- The BA-Cu polymer films offer a stable platform for sustained NO delivery.
- These films show potential as anticancer patches by continuously promoting antitumoral macrophages through NO-mediated M1 polarization.

