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Sonodynamic therapy on chemically induced mammary tumor: pharmacokinetics, tissue distribution and sonodynamically induced antitumor effect of gallium-porphyrin complex ATX-70.

Abstract
Sonodynamically induced antitumor effect of a gallium porphyrin complex, ATX-70 was evaluated on a chemically induced mammary tumor in Sprague-Dawley rats. The timing of 24 h after the administration of ATX-70 was chosen for ultrasonic exposure, based on pharmacokinetic analysis of ATX-70 concentrations in the tumor, plasma, skin, and muscle. At an ATX-70 dose not less than 2.5 mg/kg and at a free-field ultrasonic intensity not less than 3 W/cm(2), the synergistic effect between ATX-70 administration and ultrasonic exposure on the tumor growth inhibition was significant. These results suggest that ATX-70 is a potential sonosensitizer for sonodynamic treatment of spontaneous mammary tumors.
AuthorsNagahiko Yumita, Nobuo Okuyama, Kazuaki Sasaki, Shin-Ichiro Umemura
JournalCancer chemotherapy and pharmacology (Cancer Chemother Pharmacol) Vol. 60 Issue 6 Pg. 891-7 (Nov 2007) ISSN: 0344-5704 [Print] Germany
PMID17426974 (Publication Type: Journal Article)
Chemical References
  • Antineoplastic Agents
  • Photosensitizing Agents
  • Porphyrins
  • ATX 70
  • 9,10-Dimethyl-1,2-benzanthracene
Topics
  • 9,10-Dimethyl-1,2-benzanthracene
  • Animals
  • Antineoplastic Agents (administration & dosage, pharmacokinetics, pharmacology)
  • Area Under Curve
  • Combined Modality Therapy
  • Drug Screening Assays, Antitumor
  • Female
  • Mammary Neoplasms, Experimental (chemically induced, therapy)
  • Photosensitizing Agents (administration & dosage, pharmacokinetics, pharmacology)
  • Porphyrins (administration & dosage, pharmacokinetics, pharmacology)
  • Rats
  • Rats, Sprague-Dawley
  • Time Factors
  • Tissue Distribution
  • Ultrasonic Therapy

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