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Focal therapies such as hyperthermia have been successfully used to treat solid localized tumors; however, they are not easily applied to cancers that may present in a disseminated form such as ovarian cancer. To address this need, iron oxide (IO) particles were incorporated into microporous poly(caprolactone) scaffolds previously shown to recruit disseminating cancer cells. Under an alternating magnetic field, IO-loaded scaffolds exhibited heating and killed ID8 ovarian cancer cells in vitro. After implantation in the intraperitoneal cavity of mice, IO-loaded scaffolds became infiltrated with tissue after 6–7 weeks, and infiltrated cells were successfully treated ex vivo. Finally, IO-loaded scaffolds noninvasively killed infiltrated cells in vivo as evidenced by decreases in number of nuclei. These studies demonstrate the promising use of IO-loaded scaffolds as a tool for noninvasive hyperthermia, which could be an innovative modality for treatment of disseminated cancers.
Bibliographical noteFunding Information:
The authors would like to thank Colleen Forster for histological training and assistance, Stephen O'Flanagan, Victoria Granger, and Brandon Burbach for assistance with animal studies, Vinayak Rajesh for assistance with scaffold fabrication, and Michael Etheridge for assistance with the magnetic field probe. Parts of this work were carried out in the Characterization Facility, University of Minnesota, which receives partial support from the National Science Foundation through the MRSEC program.
- iron oxide
How much support was provided by MRSEC?
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4/1/19 → 3/31/22
Project: Research project