Sonosensitizer-Functionalized Graphene Nanoribbons for Adhesion Blocking and Sonodynamic Ablation of Ovarian Cancer Spheroids
Related Experiment Video
Updated: Nov 4, 2025

Surface-enhanced Resonance Raman Scattering Nanoprobe Ratiometry for Detecting Microscopic Ovarian Cancer via Folate Receptor Targeting
Published on: March 25, 2019
Hak Rae Lee1, Dae Woo Kim2, Victoria O Jones1
1Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, MN, 55455, USA.
Abstract:
Advanced stage ovarian cancer is challenging to treat due to widespread seeding of tumor spheroids throughout the mesothelial lining of the peritoneal cavity. In this work, a therapeutic strategy using graphene nanoribbons (GNR) functionalized with 4-arm polyethylene glycol (PEG) and chlorin e6 (Ce6), a sonosensitizer, to target metastatic ovarian cancer spheroids is reported. GNR-PEG-Ce6 adsorbs onto the spheroids and disrupts their adhesion to extracellular matrix proteins or LP-9 mesothelial cells. Furthermore, for spheroids that do adhere, GNR-PEG-Ce6 delays spheroid disaggregation and spreading as well as mesothelial clearance, key metastatic processes following adhesion. Owing to the sonodynamic effects of Ce6 and its localized delivery via the biomaterial, GNR-PEG-Ce6 can kill ovarian cancer spheroids adhered to LP-9 cell monolayers when combined with mild ultrasound irradiation. The interaction with GNR-PEG-Ce6 also loosens cell-cell adhesions within the spheroids, rendering them more susceptible to treatment with the chemotherapeutic agents cisplatin and paclitaxel, which typically have difficulty in penetrating ovarian cancer spheroids. Thus, this material can facilitate effective chemotherapeutic and sonodynamic combination therapies. Finally, the adhesion inhibiting and sonodynamic effects of GNR-PEG-Ce6 are also validated with tumor spheroids derived from the ascites fluid of ovarian cancer patients, providing evidence of the translational potential of this biomaterial approach.
Insights
This study introduces graphene nanoribbons (GNR) functionalized with polyethylene glycol (PEG) and chlorin e6 (Ce6) to treat ovarian cancer spheroids. This novel therapeutic agent inhibits metastasis and enhances chemotherapy and sonodynamic treatments.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Oncology
Background:
- Advanced ovarian cancer is difficult to treat due to widespread peritoneal metastasis.
- Ovarian cancer spheroids resist conventional therapies and promote disease spread.
Purpose of the Study:
- To develop a targeted therapeutic agent for metastatic ovarian cancer spheroids.
- To evaluate the efficacy of graphene nanoribbons (GNR) functionalized with polyethylene glycol (PEG) and chlorin e6 (Ce6) in inhibiting spheroid adhesion and enhancing treatment outcomes.
Main Methods:
- GNR-PEG-Ce6 was synthesized and characterized.
- The agent's effect on ovarian cancer spheroid adhesion to mesothelial cells and extracellular matrix was assessed.
- Sonodynamic therapy and combination chemotherapy (cisplatin, paclitaxel) efficacy were evaluated in vitro.
- Experiments were validated using patient-derived ascites tumor spheroids.
Main Results:
- GNR-PEG-Ce6 effectively inhibited spheroid adhesion and spreading.
- Localized sonodynamic therapy with GNR-PEG-Ce6 eradicated adhered spheroids.
- The agent sensitized spheroids to cisplatin and paclitaxel by loosening cell-cell adhesions.
- Therapeutic effects were confirmed in patient-derived spheroids.
Conclusions:
- GNR-PEG-Ce6 is a promising biomaterial for targeting ovarian cancer metastasis.
- This approach facilitates effective combination therapy, integrating sonodynamic and chemotherapeutic strategies.
- The findings demonstrate significant translational potential for treating advanced ovarian cancer.

