نمایش مختصر رکورد

dc.contributor.authorBarati, Amir Hoshangen_US
dc.contributor.authorMokhtari-Dizaji, Manijheen_US
dc.contributor.authorMozdarani, Hosseinen_US
dc.contributor.authorBathaie, Seyedeh Zahraen_US
dc.contributor.authorMohammad Hassan, Zahiren_US
dc.contributor.authorKazemnejad, Anoshirvanen_US
dc.date.accessioned1399-07-09T07:33:13Zfa_IR
dc.date.accessioned2020-09-30T07:33:13Z
dc.date.available1399-07-09T07:33:13Zfa_IR
dc.date.available2020-09-30T07:33:13Z
dc.date.issued2009-03-01en_US
dc.date.issued1387-12-11fa_IR
dc.date.submitted2008-08-05en_US
dc.date.submitted1387-05-15fa_IR
dc.identifier.citationBarati, Amir Hoshang, Mokhtari-Dizaji, Manijhe, Mozdarani, Hossein, Bathaie, Seyedeh Zahra, Mohammad Hassan, Zahir, Kazemnejad, Anoshirvan. (2009). Treatment of Murine Tumor Models of Breast Adenocarcinoma by Continuous Dual-Frequency Ultrasound. Iranian Journal of Medical Physics, 6(1), 1-12. doi: 10.22038/ijmp.2009.7385en_US
dc.identifier.issn2345-3672
dc.identifier.urihttps://dx.doi.org/10.22038/ijmp.2009.7385
dc.identifier.urihttp://ijmp.mums.ac.ir/article_7385.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/324213
dc.description.abstract<strong>Introduction:</strong> Acoustic transient cavitation is the primary mechanism of sonochemical reaction and has potential use for tumor treatment. In this study, the <em>in vivo </em>anti-tumor effect of simultaneous dual-frequency ultrasound at low-level intensity (I<sub>SATA </sub>< 6 W/cm<sup>2</sup>) was investigated in a spontaneous murine model of breast adenocarcinoma in Balb/c mice. <br/><strong>Materials and Methods:</strong> Forty tumor bearing mice were divided into four groups (10 in each group). The treated groups received 15 or 30 minutes of combined dual-frequency ultrasound in continuous mode (1 MHz<sub>con </sub>+ 150 kHz<sub>con</sub>) respectively. The control and the sham groups contained the untreated mice. The tumor growth delay parameters including tumor volume, relative tumor volume, T<sub>5</sub> and T<sub>2</sub> (the needed time for each tumor to reach 5 and 2 times the initial tumor volume, respectively), survival period and percent of tumor growth inhibition ratio were measured on different days after treatment. <br/><strong>Results:</strong> The results showed that the 30 min treatment was effective in tumor growth delay and percent of tumor growth inhibitory ratio compared to the sham and the control groups. The tumor volume growth and relative volume of tumors in the same treated group showed an anti-tumor effect relative to the sham and the control groups. There was a significant difference in tumor volume growth between this 30 min treatment group and the sham group 12 days after treatment (p-value <0.05). The mean of the survival period for animals in the 30 min treatment group was 16% more than the control group. The percent of tumor growth inhibition in the 30 and 15 min treatment groups were 23% and 20% respectively, showing a statistically significant difference. <br/><strong>Conclusion:</strong> Sonodynamic therapy with combined dual–frequency ultrasound in progressive wave mode can be useful in cancer therapy.en_US
dc.format.extent651
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherMashhad University of Medical Sciencesen_US
dc.relation.ispartofIranian Journal of Medical Physicsen_US
dc.relation.isversionofhttps://dx.doi.org/10.22038/ijmp.2009.7385
dc.subjectSonodynamic therapyen_US
dc.subjectLow-levelen_US
dc.subjectTransient cavitationen_US
dc.subjectBreast Canceren_US
dc.subjectMedical Physicsen_US
dc.subjectSound and Ultrasounden_US
dc.titleTreatment of Murine Tumor Models of Breast Adenocarcinoma by Continuous Dual-Frequency Ultrasounden_US
dc.typeTexten_US
dc.typeOriginal Paperen_US
dc.contributor.departmentPh.D., Medical Physics Dept., Tarbiat Modares University, Tehran, Iran.en_US
dc.contributor.departmentProfessor, Medical Physics Dept., Tarbiat Modares University, Tehran, Iran.en_US
dc.contributor.departmentProfessor, Medical Genetics Dept., Tarbiat Modares University, Tehran, Iran.en_US
dc.contributor.departmentAssociate Professor, Clinical Biochemistry Dept., Tarbiat Modares University, Tehran, Iran.en_US
dc.contributor.departmentAssociate Professor, Immunology Dept., Tarbiat Modares University, Tehran, Iran.en_US
dc.contributor.departmentAssociate Professor, Biostatistics Dept., Tarbiat Modares University, Tehran, Iran.en_US
dc.citation.volume6
dc.citation.issue1
dc.citation.spage1
dc.citation.epage12
nlai.contributor.orcid0000-0003-1598-2038


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