Uptake and retention of the photosensitizer mono-l-asparthyl chlorine e6 in experimental malignant glioma
The objective of the study was to investigate the potential of mono- l -aspartyl chlorine e6 (NPe6), a water-soluble photosensitizer derived from chlorophyll, for use in photodynamic diagnosis (PDD) of malignant brain tumor. A C6 glioma cell line was transplanted in the SD rat brain to create a brai...
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description | The objective of the study was to investigate the potential of mono-
l
-aspartyl chlorine e6 (NPe6), a water-soluble photosensitizer derived from chlorophyll, for use in photodynamic diagnosis (PDD) of malignant brain tumor. A C6 glioma cell line was transplanted in the SD rat brain to create a brain tumor model. Five days after transplantation, NPe6 was administrated via the tail vein at concentrations ranging from 1.25 to 10 mg/kg; then the skull was opened in the rat brain, the site of tumor transplant was irradiated with a diode laser beam at 664 nm, and the time-course intensity and distribution of emerging fluorescence were observed. Furthermore, the correlation between fluorescence distribution and histopathological findings was investigated in the removed brain. Fluorescence was observed in the site of brain tumor transplant from 5 min after injection, and stable fluorescence was recognized at the site until 4 h after administration. No differences were noted in fluorescence intensity at NPe6 doses of 2.5 mg/kg or more; therefore, it was possible to estimate the optimal dose range. Fluorescence distribution had a clear correlation with tumor cell density, and it was possible to capture the margin of tumor cell invasion with fluorescence. The photosensitizer NPe6 is capable of assessing tumor cell density in malignant glioma tissue in terms of differences in fluorescence intensity. The usefulness of PDD using 5-aminoleveulinic acid during surgery for malignant glioma has been recognized in recent years. The results of the present study suggested the potential of NPe6 as a promising photosensitizer for use in PDD for accurate grasp of the extent of removal during the course of malignant glioma surgery. |
doi_str_mv | 10.1007/s10103-007-0469-3 |
format | Article |
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-aspartyl chlorine e6 (NPe6), a water-soluble photosensitizer derived from chlorophyll, for use in photodynamic diagnosis (PDD) of malignant brain tumor. A C6 glioma cell line was transplanted in the SD rat brain to create a brain tumor model. Five days after transplantation, NPe6 was administrated via the tail vein at concentrations ranging from 1.25 to 10 mg/kg; then the skull was opened in the rat brain, the site of tumor transplant was irradiated with a diode laser beam at 664 nm, and the time-course intensity and distribution of emerging fluorescence were observed. Furthermore, the correlation between fluorescence distribution and histopathological findings was investigated in the removed brain. Fluorescence was observed in the site of brain tumor transplant from 5 min after injection, and stable fluorescence was recognized at the site until 4 h after administration. No differences were noted in fluorescence intensity at NPe6 doses of 2.5 mg/kg or more; therefore, it was possible to estimate the optimal dose range. Fluorescence distribution had a clear correlation with tumor cell density, and it was possible to capture the margin of tumor cell invasion with fluorescence. The photosensitizer NPe6 is capable of assessing tumor cell density in malignant glioma tissue in terms of differences in fluorescence intensity. The usefulness of PDD using 5-aminoleveulinic acid during surgery for malignant glioma has been recognized in recent years. The results of the present study suggested the potential of NPe6 as a promising photosensitizer for use in PDD for accurate grasp of the extent of removal during the course of malignant glioma surgery.</description><subject>Animals</subject><subject>Brain cancer</subject><subject>Brain Neoplasms - diagnosis</subject><subject>Cell Line, Tumor</subject><subject>Dentistry</subject><subject>Fluorescence</subject><subject>Glioma - diagnosis</subject><subject>Lasers</subject><subject>Male</subject><subject>Medical diagnosis</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Neoplasm Transplantation</subject><subject>Optical Devices</subject><subject>Optics</subject><subject>Original Article</subject><subject>Pharmaceuticals</subject><subject>Photonics</subject><subject>Photosensitizing Agents - pharmacokinetics</subject><subject>Porphyrins - pharmacokinetics</subject><subject>Quantum Optics</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><issn>0268-8921</issn><issn>1435-604X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kU2LFDEQhoMo7rj6A7xI8KCnaKqTTjpHWfyCBS8ueAvpTPVM1u6kTTKw6683wwwogkIgBfXUE1IvIc-BvwHO9dsCHLhgrWRcKsPEA7IBKXqmuPz2kGx4pwY2mA4uyJNSbjkHrUA8JhegNRdC9BsSbtbqviN1cUszVow1pEjTROse6bpPNRWMJdTwEzNdUkxsZq6sLtf9_Uz9fk45RKSoaIgU71bMYWkSN9PFzWEXXax0N4e0uKfk0eTmgs_O9yW5-fD-69Undv3l4-erd9fMS6UrE2i0Gr0EMNxM4HDECbjRWo-T8HKQXva663oYTe-cnwRsuXOdh14PSvqtuCSvT941px8HLNUuoXicZxcxHYrVUihQQgyNfPVfUpmuM0MHDXz5F3ibDjm2X1gwQztcHm1wgnxOpWSc7Np24fK9BW6PcdlTXPZYHuOyos28OIsP44Lb3xPnfBrQnYDSWnGH-Y-X_2n9BZ6RoIo</recordid><startdate>20080701</startdate><enddate>20080701</enddate><creator>Matsumura, Hiroyuki</creator><creator>Akimoto, Jiro</creator><creator>Haraoka, Jo</creator><creator>Aizawa, Katsuo</creator><general>Springer-Verlag</general><general>Springer Nature B.V</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>3V.</scope><scope>7QO</scope><scope>7RV</scope><scope>7SP</scope><scope>7U5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H8D</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>L7M</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20080701</creationdate><title>Uptake and retention of the photosensitizer mono-l-asparthyl chlorine e6 in experimental malignant glioma</title><author>Matsumura, Hiroyuki ; Akimoto, Jiro ; Haraoka, Jo ; Aizawa, Katsuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c467t-3e976bc411909f1aebef109777bf3c484c4572251b95aacf31d0aa2c157864cd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Brain cancer</topic><topic>Brain Neoplasms - diagnosis</topic><topic>Cell Line, Tumor</topic><topic>Dentistry</topic><topic>Fluorescence</topic><topic>Glioma - diagnosis</topic><topic>Lasers</topic><topic>Male</topic><topic>Medical diagnosis</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Neoplasm Transplantation</topic><topic>Optical Devices</topic><topic>Optics</topic><topic>Original Article</topic><topic>Pharmaceuticals</topic><topic>Photonics</topic><topic>Photosensitizing Agents - pharmacokinetics</topic><topic>Porphyrins - pharmacokinetics</topic><topic>Quantum Optics</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matsumura, Hiroyuki</creatorcontrib><creatorcontrib>Akimoto, Jiro</creatorcontrib><creatorcontrib>Haraoka, Jo</creatorcontrib><creatorcontrib>Aizawa, Katsuo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Electronics & Communications Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Aerospace Database</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Lasers in medical science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matsumura, Hiroyuki</au><au>Akimoto, Jiro</au><au>Haraoka, Jo</au><au>Aizawa, Katsuo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Uptake and retention of the photosensitizer mono-l-asparthyl chlorine e6 in experimental malignant glioma</atitle><jtitle>Lasers in medical science</jtitle><stitle>Lasers Med Sci</stitle><addtitle>Lasers Med Sci</addtitle><date>2008-07-01</date><risdate>2008</risdate><volume>23</volume><issue>3</issue><spage>237</spage><epage>245</epage><pages>237-245</pages><issn>0268-8921</issn><eissn>1435-604X</eissn><coden>LMSCEZ</coden><abstract>The objective of the study was to investigate the potential of mono-
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-aspartyl chlorine e6 (NPe6), a water-soluble photosensitizer derived from chlorophyll, for use in photodynamic diagnosis (PDD) of malignant brain tumor. A C6 glioma cell line was transplanted in the SD rat brain to create a brain tumor model. Five days after transplantation, NPe6 was administrated via the tail vein at concentrations ranging from 1.25 to 10 mg/kg; then the skull was opened in the rat brain, the site of tumor transplant was irradiated with a diode laser beam at 664 nm, and the time-course intensity and distribution of emerging fluorescence were observed. Furthermore, the correlation between fluorescence distribution and histopathological findings was investigated in the removed brain. Fluorescence was observed in the site of brain tumor transplant from 5 min after injection, and stable fluorescence was recognized at the site until 4 h after administration. No differences were noted in fluorescence intensity at NPe6 doses of 2.5 mg/kg or more; therefore, it was possible to estimate the optimal dose range. Fluorescence distribution had a clear correlation with tumor cell density, and it was possible to capture the margin of tumor cell invasion with fluorescence. The photosensitizer NPe6 is capable of assessing tumor cell density in malignant glioma tissue in terms of differences in fluorescence intensity. The usefulness of PDD using 5-aminoleveulinic acid during surgery for malignant glioma has been recognized in recent years. The results of the present study suggested the potential of NPe6 as a promising photosensitizer for use in PDD for accurate grasp of the extent of removal during the course of malignant glioma surgery.</abstract><cop>London</cop><pub>Springer-Verlag</pub><pmid>17703335</pmid><doi>10.1007/s10103-007-0469-3</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Brain cancer Brain Neoplasms - diagnosis Cell Line, Tumor Dentistry Fluorescence Glioma - diagnosis Lasers Male Medical diagnosis Medicine Medicine & Public Health Neoplasm Transplantation Optical Devices Optics Original Article Pharmaceuticals Photonics Photosensitizing Agents - pharmacokinetics Porphyrins - pharmacokinetics Quantum Optics Rats Rats, Sprague-Dawley |
title | Uptake and retention of the photosensitizer mono-l-asparthyl chlorine e6 in experimental malignant glioma |
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