Intratumoral iron oxide nanoparticle hyperthermia and radiation cancer treatment

P. J. Hoopes; R. R. Strawbridge; U. J. Gibson; Q. Zeng; Z. E. Pierce; M. Savellano; J. A. Tate; J. A. Ogden; I. Baker; R. Ivkov; A. R. Foreman

doi:10.1117/12.706302

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13 February 2007 Intratumoral iron oxide nanoparticle hyperthermia and radiation cancer treatment

P. J. Hoopes, R. R. Strawbridge, U. J. Gibson, Q. Zeng, Z. E. Pierce, M. Savellano, J. A. Tate, J. A. Ogden, I. Baker, R. Ivkov, A. R. Foreman

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Proceedings Volume 6440, Thermal Treatment of Tissue: Energy Delivery and Assessment IV; 64400K (2007) https://doi.org/10.1117/12.706302
Event: SPIE BiOS, 2007, San Jose, California, United States

Abstract

The potential synergism and benefit of combined hyperthermia and radiation for cancer treatment is well established, but has yet to be optimized clinically. Specifically, the delivery of heat via external arrays /applicators or interstitial antennas has not demonstrated the spatial precision or specificity necessary to achieve appropriate a highly positive therapeutic ratio. Recently, antibody directed and possibly even non-antibody directed iron oxide nanoparticle hyperthermia has shown significant promise as a tumor treatment modality. Our studies are designed to determine the effects (safety and efficacy) of iron oxide nanoparticle hyperthermia and external beam radiation in a murine breast cancer model. Methods: MTG-B murine breast cancer cells (1 x 106) were implanted subcutaneous in 7 week-old female C3H/HeJ mice and grown to a treatment size of 150 mm3 +/- 50 mm3. Tumors were then injected locally with iron oxide nanoparticles and heated via an alternating magnetic field (AMF) generator operated at approximately 160 kHz and 400 - 550 Oe. Tumor growth was monitored daily using standard 3-D caliper measurement technique and formula. specific Mouse tumors were heated using a cooled, 36 mm diameter square copper tube induction coil which provided optimal heating in a 1 cm wide region in the center of the coil. Double dextran coated 80 nm iron oxide nanoparticles (Triton Biosystems) were used in all studies. Intra-tumor, peri-tumor and rectal (core body) temperatures were continually measured throughout the treatment period. Results: Preliminary in vivo nanoparticle-AMF hyperthermia (167 KHz and 400 or 550 Oe) studies demonstrated dose responsive cytotoxicity which enhanced the effects of external beam radiation. AMF associated eddy currents resulted in nonspecific temperature increases in exposed tissues which did not contain nanoparticles, however these effects were minor and not injurious to the mice. These studies also suggest that iron oxide nanoparticle hyperthermia is more effective than non-nanoparticle tumor heating techniques when similar thermal doses are applied. Initial electron and light microscopy studies of iron oxide nanoparticle and AMF exposed tumor cells show a rapid uptake of particles and acute cytotoxicity following AMF exposure.

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P. J. Hoopes, R. R. Strawbridge, U. J. Gibson, Q. Zeng, Z. E. Pierce, M. Savellano, J. A. Tate, J. A. Ogden, I. Baker, R. Ivkov, and A. R. Foreman "Intratumoral iron oxide nanoparticle hyperthermia and radiation cancer treatment", Proc. SPIE 6440, Thermal Treatment of Tissue: Energy Delivery and Assessment IV, 64400K (13 February 2007); https://doi.org/10.1117/12.706302

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