Photodynamic therapy of prostate cancer by means of 5-aminolevulinic acid-induced protoporphyrin IX - In vivo experiments on the dunning rat tumor model
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vor 20 Jahren
Objective: In order to expand the use of photodynamic therapy (PDT)
in the treatment of prostate carcinoma (PCA), the aim of this study
was to evaluate PDT by means of 5-aminolevulinic acid
(5-ALA)-induced protoporphyrin IX ( PPIX) in an in vivo tumor
model. Methods: The model used was the Dunning R3327 tumor. First
of all, the pharmacokinetics and the localization of PPIX were
obtained using fluorescence measurement techniques. Thereafter, PDT
using 150 mg 5-ALA/kg b.w.i.v. was performed by homogenous
irradiation of the photosensitized tumor (diode laser lambda = 633
nm). The tumors necrosis was determined histopathologically.
Results: The kinetics of PPIX fluorescence revealed a maximum
intensity in the tumor tissue within 3 and 4.5 h post-application
of 5-ALA. At this time, specific PPIX fluorescence could be
localized selectively in the tumor cells. The PDT-induced necrosis
(n = 18) was determined to be 94 B 12% (range 60-100%), while the
necrosis of the controls ( n = 12) differs significantly (p <
0.01), being less than 10%. Conclusion: These first in vivo results
demonstrate the effective potential of 5-ALA-mediated PDT on PCA in
an animal model. Copyright (C) 2004 S. Karger AG, Basel.
in the treatment of prostate carcinoma (PCA), the aim of this study
was to evaluate PDT by means of 5-aminolevulinic acid
(5-ALA)-induced protoporphyrin IX ( PPIX) in an in vivo tumor
model. Methods: The model used was the Dunning R3327 tumor. First
of all, the pharmacokinetics and the localization of PPIX were
obtained using fluorescence measurement techniques. Thereafter, PDT
using 150 mg 5-ALA/kg b.w.i.v. was performed by homogenous
irradiation of the photosensitized tumor (diode laser lambda = 633
nm). The tumors necrosis was determined histopathologically.
Results: The kinetics of PPIX fluorescence revealed a maximum
intensity in the tumor tissue within 3 and 4.5 h post-application
of 5-ALA. At this time, specific PPIX fluorescence could be
localized selectively in the tumor cells. The PDT-induced necrosis
(n = 18) was determined to be 94 B 12% (range 60-100%), while the
necrosis of the controls ( n = 12) differs significantly (p <
0.01), being less than 10%. Conclusion: These first in vivo results
demonstrate the effective potential of 5-ALA-mediated PDT on PCA in
an animal model. Copyright (C) 2004 S. Karger AG, Basel.
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