DocumentCode :
2391798
Title :
Nanoparticle enhanced thermal therapies
Author :
Shenoi, Mithun M. ; Anderson, J. Kyle ; Bischof, John C.
Author_Institution :
Biomed. Eng. Dept., Univ. of Minnesota, Minneapolis, MN, USA
fYear :
2009
fDate :
3-6 Sept. 2009
Firstpage :
1979
Lastpage :
1982
Abstract :
Thermal therapies such as hyperthermia, radiofrequency ablation, cryoablation, etc. have shown great potential and are gaining increasing clinical acceptance in the treatment of solid tumors. However, these treatment modalities are limited by the size of tumor that can be treated, incomplete tumor kill, and damage to adjacent normal tissues. To address these limitations, the concept of adjuvant-assisted thermal therapies has been proposed and tested to enhance the tumor destructive effects of thermal therapies. CYT-6091, a pegylated colloidal gold nanoparticle containing TNF-alpha bound to its surface, has been extensively investigated in our lab as an adjuvant to enhance thermal therapies. This paper describes our investigations of nanoparticle enhanced thermal therapies in various preclinical and translational models of solid tumors.
Keywords :
cancer; colloids; gold; hyperthermia; nanoparticles; radiofrequency heating; surgery; tumours; adjuvant-assisted thermal therapy; cryoablation; hyperthermia; nanoparticle enhanced thermal therapy; pegylated colloidal gold nanoparticle; preclinical model; radiofrequency ablation; solid tumor treatment; translational model; tumor destructive effect; Animals; Female; Fibrosarcoma; Gold Colloid; Hyperthermia, Induced; Mammary Neoplasms, Experimental; Mice; Mice, Inbred A; Nanoparticles; Neoplasms; Sarcoma, Experimental; Tumor Necrosis Factor-alpha;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Engineering in Medicine and Biology Society, 2009. EMBC 2009. Annual International Conference of the IEEE
Conference_Location :
Minneapolis, MN
ISSN :
1557-170X
Print_ISBN :
978-1-4244-3296-7
Electronic_ISBN :
1557-170X
Type :
conf
DOI :
10.1109/IEMBS.2009.5333447
Filename :
5333447
Link To Document :
بازگشت