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Evaluation the Effect of Sonodynamic Therapy with 5-Aminolevulinic Acid and Sodium Fluorescein by Preclinical Animal Study.
Huang, Chiung-Yin; Li, Jui-Chin; Chen, Ko-Ting; Lin, Ya-Jui; Feng, Li-Ying; Liu, Hao-Li; Wei, Kuo-Chen.
  • Huang CY; Neuroscience Research Center, Chang Gung Memorial Hospital, Taoyuan 33305, Taiwan.
  • Li JC; Neuroscience Research Center, Chang Gung Memorial Hospital, Taoyuan 33305, Taiwan.
  • Chen KT; Department of Neurosurgery, New Taipei Municipal TuCheng Hospital, New Taipei 236017, Taiwan.
  • Lin YJ; Neuroscience Research Center, Chang Gung Memorial Hospital, Taoyuan 33305, Taiwan.
  • Feng LY; Department of Neurosurgery, Chang Gung Memorial Hospital, Taoyuan 33305, Taiwan.
  • Liu HL; School of Medicine, Chang Gung University, Taoyuan 33302, Taiwan.
  • Wei KC; Neuroscience Research Center, Chang Gung Memorial Hospital, Taoyuan 33305, Taiwan.
Cancers (Basel) ; 16(2)2024 Jan 05.
Article en En | MEDLINE | ID: mdl-38254744
ABSTRACT
Sonodynamic therapy (SDT) is a novel tumor treatment that combines biosafe sonosensitizers and noninvasive focused ultrasound to eradicate solid tumors. Sonosensitizers such as 5-aminolevulinic acid and fluorescein have great potential in tumor treatment. Here, rodent subcutaneous and brain tumor models were used to evaluate the treatment effect of both 5-ALA- and fluorescein-mediated SDT. The subcutaneous tumor growth rates of both SDT groups were significantly inhibited compared with that of the control groups. For intracranial tumors, 5-ALA-SDT treatment significantly inhibited brain tumor growth, while fluorescein-SDT exerted no therapeutic effect in animals. The distribution of fluorescein in the brain tumor region underwent further assessment. Seven days post tumor implantation, experimental animals received fluorescein and were sacrificed for brain specimen collection. Analysis of the dissected brains revealed no fluorescence signals, indicating an absence of fluorescein accumulation in the early-stage glioma tissue. These data suggest that the fluorescein-SDT treatment response is closely related to the amount of accumulated fluorescein. This study reports the equivalent effects of 5-ALA and fluorescein on the treatment of somatic tumors. For orthotopic brain tumor models, tumor vascular permeability should be considered when choosing fluorescein as a sonosensitizer. In conclusion, both fluorescein and 5-ALA are safe and effective SDT sonosensitizers, and the tumor microenvironment and pathologic type should be considered in the selection of adequate sonosensitizers.
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