英文誌(2004-)
Original Article(原著)
(0033 - 0044)
Study of the Mechanisms of Drug Excitationin Sonodynamic Therapy: Direct Measurement of the Acoustic Cavitation-Induced Luminescence of Photosensitizers
Noboru TAKAHASHI1, Hiroshi UENOHARA2, Keigo SASAKI1, Takashi YOSHIMOTO1
1Department of Neurosurgery, Tohoku University School of Medicine, 2Department of Neurosurgery, Sendai National Hospital
キーワード : Daunorubicin, Doxycycline, Hematoporphyrin, SDT, Sonoluminescence
The cell-damaging effects of the combined use of ultrasound and any of various drugs (sonodynamic
therapy [SDT]) has been investigated for use as a new modality for the treatment of malignant
tumor. The mechanisms of the ultrasound-induced drug excitation remains unclear, however.
Because we were interested in the fact that many sensitizers that can be excited by ultrasound have
been used as photosensitizers, we investigated the luminescence phenomenon observed when certain
drugs, known as photosensitizers, including hematoporphyrin (HP), daunorubicin (DNR), and
doxycycline (DOXY), were excited by ultrasound.
Saline and solutions of these photosensitizers were sonicated at 361 kHz and 1.0 W/cm2, and their
luminescence spectra were measured in a wavelength range of 250 to 750 nm using a spectrometer with
0. 5-nm resolution. The sonoluminescence curve of saline peaked at about 415 nm and had a gently
sloping tail on the longer-wavelength side. Although solutions of the sensitizers examined had
luminescence spectra similar to those of the sonoluminescence of saline at low concentrations, every
sensitizer showed a decrease in some component of its absorption region as its concentration
increased. A decrease in light intensity was observed at around 380 nm for HP, around 490 nm for
DNR, and around 360 nm for DOXY. Namely, the sonoluminescence of saline was absorbed by
these drugs as excitation light. These results suggest, therefore, that sonoluminescence contributed to
the ultrasonic excitation of these drugs, causing indirect photodynamic excitation.
Moreover, when concentration was increased, DOXY showed afluorescence peak at about 510
nm, which was stronger in intensity than the sonoluminescence of saline. This indicated that other
mechanisms associated with acoustic cavitation are involved along with photodynamic excitation
produced by sonoluminescence in drug excitation by ultrasound.