
Proceedings Paper
Selective nanoparticle-directed photothermal ablation of the canine prostateFormat | Member Price | Non-Member Price |
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Paper Abstract
This study adapted AuroLase® Therapy, previously reported for the treatment of brain tumors, to the treatment of
prostate disease by 1) using normal canine prostate in vivo, directly injected with a solution of nanoparticles as a
proxy for prostate tumor and, 2) developing an appropriate laser dosimetry for prostate which is which is subablative
in native prostate while simultaneously producing photothermal coagulation in prostate tissue containing
therapeutic nanoshells.
Healthy, mixed-breed hound dogs were given surgical laparotomies during which nanoshells were injected directly
into one or both prostate hemispheres. Laser energy was delivered percutaneously to the parenchyma of the prostate
along 1-5 longitudinal tracts via a liquid-cooled optical fiber catheter terminated with a 1-cm isotropic diffuser after
which the incision was closed and sutured using standard surgical techniques. The photothermal lesions were
permitted to resolve for up to 8 days, after which each animal was euthanized, necropsied, and the prostate taken for
histopathological analysis.
We developed a laser dosimetry which is sub- to marginally ablative in native prostate and simultaneously ablative
of prostate tissue containing nanoshells which would indicate a viable means of treating tumors of the prostate
which are known from other studies to accumulate nanoshells. Secondly, we determined that multiple laser
treatments of nanoshell-containing prostate tissue could be accomplished while sparing the urethra and prostate
capsule thermal damage. Finally, we determined that the extent of damage zone radii correlate positively with
nanoshell concentration, and negatively to the length of time between nanoshell injection and laser treatment.
Paper Details
Date Published: 23 February 2011
PDF: 9 pages
Proc. SPIE 7901, Energy-based Treatment of Tissue and Assessment VI, 790116 (23 February 2011); doi: 10.1117/12.879824
Published in SPIE Proceedings Vol. 7901:
Energy-based Treatment of Tissue and Assessment VI
Thomas P. Ryan, Editor(s)
PDF: 9 pages
Proc. SPIE 7901, Energy-based Treatment of Tissue and Assessment VI, 790116 (23 February 2011); doi: 10.1117/12.879824
Show Author Affiliations
Jon A. Schwartz, Nanospectra Biosciences, Inc. (United States)
Roger E. Price, Baylor College of Medicine (United States)
Kelly L. Gill-Sharp, Nanospectra Biosciences, Inc. (United States)
Krystina L. Sang, Nanospectra Biosciences, Inc. (United States)
Roger E. Price, Baylor College of Medicine (United States)
Kelly L. Gill-Sharp, Nanospectra Biosciences, Inc. (United States)
Krystina L. Sang, Nanospectra Biosciences, Inc. (United States)
Jennifer D. Khorchani, Nanospectra Biosciences, Inc. (United States)
J. Donald Payne, Nanospectra Biosciences, Inc. (United States)
Bradford S. Goodwin, The Univ. of Texas Health Science Ctr. at Houston (United States)
J. Donald Payne, Nanospectra Biosciences, Inc. (United States)
Bradford S. Goodwin, The Univ. of Texas Health Science Ctr. at Houston (United States)
Published in SPIE Proceedings Vol. 7901:
Energy-based Treatment of Tissue and Assessment VI
Thomas P. Ryan, Editor(s)
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