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Analysis of Boron Distribution In Vivo for Boron Neutron Capture Therapy using Two Different Boron Compounds by Secondary Ion Mass Spectrometry
Yokoyama, K., Miyatake, S-I., Kajimoto, Y., Kawabata, S., Doi, A., Yoshida, T., Okabe, M., Kirihata, M., Ono, K. and Kuroiwa, T. Analysis of Boron Distribution In Vivo for Boron Neutron Capture Therapy using Two Different Boron Compounds by Secondary Ion Mass Spectrometry. Radiat. Res. 167, 102–109...
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Published in: | Radiation research 2007-01, Vol.167 (1), p.102-109 |
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creator | Yokoyama, Kunio Miyatake, Shin-Ichi Kajimoto, Yoshinaga Kawabata, Shinji Doi, Atsushi Yoshida, Toshiko Okabe, Motonori Kirihata, Mitsunori Ono, Koji Kuroiwa, Toshihiko |
description | Yokoyama, K., Miyatake, S-I., Kajimoto, Y., Kawabata, S., Doi, A., Yoshida, T., Okabe, M., Kirihata, M., Ono, K. and Kuroiwa, T. Analysis of Boron Distribution In Vivo for Boron Neutron Capture Therapy using Two Different Boron Compounds by Secondary Ion Mass Spectrometry. Radiat. Res. 167, 102–109 (2007). The efficiency of boron neutron capture therapy (BNCT) for malignant gliomas depends on the selective and absolute accumulation of 10B atoms in tumor tissues. Only two boron compounds, BPA and BSH, currently can be used clinically. However, the detailed distributions of these compounds have not been determined. Here we used secondary ion mass spectrometry (SIMS) to determine the histological distribution of 10B atoms derived from the boron compounds BSH and BPA. C6 tumor-bearing rats were given 500 mg/kg of BPA or 100 mg/kg of BSH intraperitoneally; 2.5 h later, their brains were sectioned and subjected to SIMS. In the main tumor mass, BPA accumulated heterogeneously, while BSH accumulated homogeneously. In the peritumoral area, both BPA and BSH accumulated measurably. Interestingly, in this area, BSH accumulated distinctively in a diffuse manner even 800 μm distant from the interface between the main tumor and normal brain. In the contralateral brain, BPA accumulated measurably, while BSH did not. In conclusion, both BPA and BSH each have advantages and disadvantages. These compounds are considered to be essential as boron delivery agents independently for clinical BNCT. There is some rationale for the simultaneous use of both compounds in clinical BNCT for malignant gliomas. |
doi_str_mv | 10.1667/RR0501.1 |
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Analysis of Boron Distribution In Vivo for Boron Neutron Capture Therapy using Two Different Boron Compounds by Secondary Ion Mass Spectrometry. Radiat. Res. 167, 102–109 (2007). The efficiency of boron neutron capture therapy (BNCT) for malignant gliomas depends on the selective and absolute accumulation of 10B atoms in tumor tissues. Only two boron compounds, BPA and BSH, currently can be used clinically. However, the detailed distributions of these compounds have not been determined. Here we used secondary ion mass spectrometry (SIMS) to determine the histological distribution of 10B atoms derived from the boron compounds BSH and BPA. C6 tumor-bearing rats were given 500 mg/kg of BPA or 100 mg/kg of BSH intraperitoneally; 2.5 h later, their brains were sectioned and subjected to SIMS. In the main tumor mass, BPA accumulated heterogeneously, while BSH accumulated homogeneously. In the peritumoral area, both BPA and BSH accumulated measurably. Interestingly, in this area, BSH accumulated distinctively in a diffuse manner even 800 μm distant from the interface between the main tumor and normal brain. In the contralateral brain, BPA accumulated measurably, while BSH did not. In conclusion, both BPA and BSH each have advantages and disadvantages. These compounds are considered to be essential as boron delivery agents independently for clinical BNCT. 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Analysis of Boron Distribution In Vivo for Boron Neutron Capture Therapy using Two Different Boron Compounds by Secondary Ion Mass Spectrometry. Radiat. Res. 167, 102–109 (2007). The efficiency of boron neutron capture therapy (BNCT) for malignant gliomas depends on the selective and absolute accumulation of 10B atoms in tumor tissues. Only two boron compounds, BPA and BSH, currently can be used clinically. However, the detailed distributions of these compounds have not been determined. Here we used secondary ion mass spectrometry (SIMS) to determine the histological distribution of 10B atoms derived from the boron compounds BSH and BPA. C6 tumor-bearing rats were given 500 mg/kg of BPA or 100 mg/kg of BSH intraperitoneally; 2.5 h later, their brains were sectioned and subjected to SIMS. In the main tumor mass, BPA accumulated heterogeneously, while BSH accumulated homogeneously. In the peritumoral area, both BPA and BSH accumulated measurably. Interestingly, in this area, BSH accumulated distinctively in a diffuse manner even 800 μm distant from the interface between the main tumor and normal brain. In the contralateral brain, BPA accumulated measurably, while BSH did not. In conclusion, both BPA and BSH each have advantages and disadvantages. These compounds are considered to be essential as boron delivery agents independently for clinical BNCT. There is some rationale for the simultaneous use of both compounds in clinical BNCT for malignant gliomas.</description><subject>Animals</subject><subject>Atoms</subject><subject>Boron</subject><subject>Boron - therapeutic use</subject><subject>Boron compounds</subject><subject>Boron Compounds - therapeutic use</subject><subject>Boron neutron capture therapy</subject><subject>Boron Neutron Capture Therapy - methods</subject><subject>Brain - metabolism</subject><subject>Brain neoplasms</subject><subject>Brain Neoplasms - radiotherapy</subject><subject>Cell Line, Tumor</subject><subject>Glioma</subject><subject>Glioma - metabolism</subject><subject>Glioma - radiotherapy</subject><subject>Histology</subject><subject>Ions</subject><subject>Male</subject><subject>Mass Spectrometry</subject><subject>Microscopes</subject><subject>Neoplasm Transplantation</subject><subject>Neurons</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>REGULAR ARTICLES</subject><subject>Space life sciences</subject><subject>Time Factors</subject><subject>Tumors</subject><issn>0033-7587</issn><issn>1938-5404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqFkc1u3CAUhVHVqpmklfIAUcWqysYJGDB4mU7_RkpTKZlma4GBhGgMLuBWfoq-conGarqpurq6Ot8998IB4BijM9w0_Pz6GjGEz_AzsMItERWjiD4HK4QIqTgT_AAcpvSASo-b9iU4wLzGlGG0Ar8uvNzNySUYLHwXYvDwvUs5OjVlV5qNh7fuR4A2xEW-MlN-rGs55ikauL03UY4znJLzd3D7MxQDa000Pi8T6zCMYfI6QTXDG9MHr2Wc4aZIX2RK8GY0fbEcTI7zK_DCyl0yr5d6BL59_LBdf64uv37arC8uK0UamiuGbdMjyVHNWkqkEFhrShgSColWEcwFUlxbLButSG05xy3luhe6prrtGSJH4O3ed4zh-2RS7gaXerPbSW_ClLpG0PJF5P9g3bKGipoV8HQP9jGkFI3txuiG8tAOo-4xpW6fUocL-mbxnNRg9BO4xFKAkz3wkHKIf3SKa075XzcpF4I3_170G0F1ots</recordid><startdate>200701</startdate><enddate>200701</enddate><creator>Yokoyama, Kunio</creator><creator>Miyatake, Shin-Ichi</creator><creator>Kajimoto, Yoshinaga</creator><creator>Kawabata, Shinji</creator><creator>Doi, Atsushi</creator><creator>Yoshida, Toshiko</creator><creator>Okabe, Motonori</creator><creator>Kirihata, Mitsunori</creator><creator>Ono, Koji</creator><creator>Kuroiwa, Toshihiko</creator><general>Radiation Research Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>200701</creationdate><title>Analysis of Boron Distribution In Vivo for Boron Neutron Capture Therapy using Two Different Boron Compounds by Secondary Ion Mass Spectrometry</title><author>Yokoyama, Kunio ; Miyatake, Shin-Ichi ; Kajimoto, Yoshinaga ; Kawabata, Shinji ; Doi, Atsushi ; Yoshida, Toshiko ; Okabe, Motonori ; Kirihata, Mitsunori ; Ono, Koji ; Kuroiwa, Toshihiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b364t-51f6c0a7025943a881dd43508b089b31780b7df1a6db32f771947dc8d24d9c503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Atoms</topic><topic>Boron</topic><topic>Boron - therapeutic use</topic><topic>Boron compounds</topic><topic>Boron Compounds - therapeutic use</topic><topic>Boron neutron capture therapy</topic><topic>Boron Neutron Capture Therapy - methods</topic><topic>Brain - metabolism</topic><topic>Brain neoplasms</topic><topic>Brain Neoplasms - radiotherapy</topic><topic>Cell Line, Tumor</topic><topic>Glioma</topic><topic>Glioma - metabolism</topic><topic>Glioma - radiotherapy</topic><topic>Histology</topic><topic>Ions</topic><topic>Male</topic><topic>Mass Spectrometry</topic><topic>Microscopes</topic><topic>Neoplasm Transplantation</topic><topic>Neurons</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>REGULAR ARTICLES</topic><topic>Space life sciences</topic><topic>Time Factors</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yokoyama, Kunio</creatorcontrib><creatorcontrib>Miyatake, Shin-Ichi</creatorcontrib><creatorcontrib>Kajimoto, Yoshinaga</creatorcontrib><creatorcontrib>Kawabata, Shinji</creatorcontrib><creatorcontrib>Doi, Atsushi</creatorcontrib><creatorcontrib>Yoshida, Toshiko</creatorcontrib><creatorcontrib>Okabe, Motonori</creatorcontrib><creatorcontrib>Kirihata, Mitsunori</creatorcontrib><creatorcontrib>Ono, Koji</creatorcontrib><creatorcontrib>Kuroiwa, Toshihiko</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Radiation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yokoyama, Kunio</au><au>Miyatake, Shin-Ichi</au><au>Kajimoto, Yoshinaga</au><au>Kawabata, Shinji</au><au>Doi, Atsushi</au><au>Yoshida, Toshiko</au><au>Okabe, Motonori</au><au>Kirihata, Mitsunori</au><au>Ono, Koji</au><au>Kuroiwa, Toshihiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of Boron Distribution In Vivo for Boron Neutron Capture Therapy using Two Different Boron Compounds by Secondary Ion Mass Spectrometry</atitle><jtitle>Radiation research</jtitle><addtitle>Radiat Res</addtitle><date>2007-01</date><risdate>2007</risdate><volume>167</volume><issue>1</issue><spage>102</spage><epage>109</epage><pages>102-109</pages><issn>0033-7587</issn><eissn>1938-5404</eissn><abstract>Yokoyama, K., Miyatake, S-I., Kajimoto, Y., Kawabata, S., Doi, A., Yoshida, T., Okabe, M., Kirihata, M., Ono, K. and Kuroiwa, T. Analysis of Boron Distribution In Vivo for Boron Neutron Capture Therapy using Two Different Boron Compounds by Secondary Ion Mass Spectrometry. Radiat. Res. 167, 102–109 (2007). The efficiency of boron neutron capture therapy (BNCT) for malignant gliomas depends on the selective and absolute accumulation of 10B atoms in tumor tissues. Only two boron compounds, BPA and BSH, currently can be used clinically. However, the detailed distributions of these compounds have not been determined. Here we used secondary ion mass spectrometry (SIMS) to determine the histological distribution of 10B atoms derived from the boron compounds BSH and BPA. C6 tumor-bearing rats were given 500 mg/kg of BPA or 100 mg/kg of BSH intraperitoneally; 2.5 h later, their brains were sectioned and subjected to SIMS. In the main tumor mass, BPA accumulated heterogeneously, while BSH accumulated homogeneously. In the peritumoral area, both BPA and BSH accumulated measurably. Interestingly, in this area, BSH accumulated distinctively in a diffuse manner even 800 μm distant from the interface between the main tumor and normal brain. In the contralateral brain, BPA accumulated measurably, while BSH did not. In conclusion, both BPA and BSH each have advantages and disadvantages. These compounds are considered to be essential as boron delivery agents independently for clinical BNCT. There is some rationale for the simultaneous use of both compounds in clinical BNCT for malignant gliomas.</abstract><cop>United States</cop><pub>Radiation Research Society</pub><pmid>17214510</pmid><doi>10.1667/RR0501.1</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Atoms Boron Boron - therapeutic use Boron compounds Boron Compounds - therapeutic use Boron neutron capture therapy Boron Neutron Capture Therapy - methods Brain - metabolism Brain neoplasms Brain Neoplasms - radiotherapy Cell Line, Tumor Glioma Glioma - metabolism Glioma - radiotherapy Histology Ions Male Mass Spectrometry Microscopes Neoplasm Transplantation Neurons Rats Rats, Wistar REGULAR ARTICLES Space life sciences Time Factors Tumors |
title | Analysis of Boron Distribution In Vivo for Boron Neutron Capture Therapy using Two Different Boron Compounds by Secondary Ion Mass Spectrometry |
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