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Water-Solubilization of P(V) and Sb(V) Porphyrins and Their Photobiological Application
Porphyrins have been widely utilized as biochemical and biological functional chromophores which can operate under visible-light irradiation. Water-soluble porphyrins have been used as the drug for photodynamic therapy (PDT) and photodynamic inactivation (PDI). Although usual water-solubilization of...
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Published in: | International journal of photoenergy 2015-01, Vol.2015 (2015), p.1-12 |
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creator | Yasuda, Masahide Hirakawa, Kazutaka Shiragami, Tsutomu Matsumoto, Jin |
description | Porphyrins have been widely utilized as biochemical and biological functional chromophores which can operate under visible-light irradiation. Water-soluble porphyrins have been used as the drug for photodynamic therapy (PDT) and photodynamic inactivation (PDI). Although usual water-solubilization of porphyrins has been achieved by an introduction of an ionic group such as ammonium, pyridinium, sulfonate, phosphonium, or carboxyl to porphyrin ring, we proposed the preparation of water-soluble P and Sb porphyrins by modification of axial ligands. Alkyl (type A), ethylenedioxy (type E), pyridinium (type P), and glucosyl groups (type G) were introduced to axial ligands of Sb and P porphyrins to achieve water-solubilization of Sb porphyrin and P porphyrins. Here, we review their water-soluble P and Sb porphyrins from the standpoints of preparation, bioaffinity, and photosensitized inactivation. |
doi_str_mv | 10.1155/2015/148964 |
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Water-soluble porphyrins have been used as the drug for photodynamic therapy (PDT) and photodynamic inactivation (PDI). Although usual water-solubilization of porphyrins has been achieved by an introduction of an ionic group such as ammonium, pyridinium, sulfonate, phosphonium, or carboxyl to porphyrin ring, we proposed the preparation of water-soluble P and Sb porphyrins by modification of axial ligands. Alkyl (type A), ethylenedioxy (type E), pyridinium (type P), and glucosyl groups (type G) were introduced to axial ligands of Sb and P porphyrins to achieve water-solubilization of Sb porphyrin and P porphyrins. Here, we review their water-soluble P and Sb porphyrins from the standpoints of preparation, bioaffinity, and photosensitized inactivation.</description><identifier>ISSN: 1110-662X</identifier><identifier>EISSN: 1687-529X</identifier><identifier>DOI: 10.1155/2015/148964</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Antimony ; Aqueous solutions ; Biochemistry ; Biological ; Chromophores ; Inactivation ; Ligands ; Molecular weight ; Photodynamic therapy ; Porphyrins ; Rings (mathematics)</subject><ispartof>International journal of photoenergy, 2015-01, Vol.2015 (2015), p.1-12</ispartof><rights>Copyright © 2015 Jin Matsumoto et al.</rights><rights>Copyright © 2015 Jin Matsumoto et al. Jin Matsumoto et al. 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Water-soluble porphyrins have been used as the drug for photodynamic therapy (PDT) and photodynamic inactivation (PDI). Although usual water-solubilization of porphyrins has been achieved by an introduction of an ionic group such as ammonium, pyridinium, sulfonate, phosphonium, or carboxyl to porphyrin ring, we proposed the preparation of water-soluble P and Sb porphyrins by modification of axial ligands. Alkyl (type A), ethylenedioxy (type E), pyridinium (type P), and glucosyl groups (type G) were introduced to axial ligands of Sb and P porphyrins to achieve water-solubilization of Sb porphyrin and P porphyrins. Here, we review their water-soluble P and Sb porphyrins from the standpoints of preparation, bioaffinity, and photosensitized inactivation.</description><subject>Antimony</subject><subject>Aqueous solutions</subject><subject>Biochemistry</subject><subject>Biological</subject><subject>Chromophores</subject><subject>Inactivation</subject><subject>Ligands</subject><subject>Molecular weight</subject><subject>Photodynamic therapy</subject><subject>Porphyrins</subject><subject>Rings (mathematics)</subject><issn>1110-662X</issn><issn>1687-529X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqF0c9LHTEQB_CltFCxnnovC73YltX83uQoUq0g-MBH9RYm2cQXiZttsg_Rv948t5TSS3OZYfjwTcI0zUeMjjDm_JggzI8xk0qwN80eFrLvOFG3b2uPMeqEILfvm4NSgkGM9QxTKfaamxuYXe6uU9yaEMMzzCGNbfLt6vDnlxbGob02u26V8rR5ymEsr8P1xoXcrjZpTiakmO6ChdieTFOszS7iQ_POQyzu4Hfdb9Zn39enP7rLq_OL05PLDjgRc0cx89iLgQ126IFLj4y3RnGhvFDWW0QtcOoZJQpbQ40ZBuY4pVI6b6Cn-83FEjskuNdTDg-Qn3SCoF8HKd9pyHOw0WlpMDXcOlnvY_XUCrxXAlFCwQGuWYdL1pTTr60rs34IxboYYXRpWzQWfa-oYoRX-vkfep-2eawfrYpzQhDBrKpvi7I5lZKd__NAjPRuZXq3Mr2srOqvi96EcYDH8B_8acGuEufhLywE7SV9AXo5nhk</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Yasuda, Masahide</creator><creator>Hirakawa, Kazutaka</creator><creator>Shiragami, Tsutomu</creator><creator>Matsumoto, Jin</creator><general>Hindawi Publishing Corporation</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7TB</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>KR7</scope><scope>L6V</scope><scope>L7M</scope><scope>M7S</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>DOA</scope></search><sort><creationdate>20150101</creationdate><title>Water-Solubilization of P(V) and Sb(V) Porphyrins and Their Photobiological Application</title><author>Yasuda, Masahide ; 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Water-soluble porphyrins have been used as the drug for photodynamic therapy (PDT) and photodynamic inactivation (PDI). Although usual water-solubilization of porphyrins has been achieved by an introduction of an ionic group such as ammonium, pyridinium, sulfonate, phosphonium, or carboxyl to porphyrin ring, we proposed the preparation of water-soluble P and Sb porphyrins by modification of axial ligands. Alkyl (type A), ethylenedioxy (type E), pyridinium (type P), and glucosyl groups (type G) were introduced to axial ligands of Sb and P porphyrins to achieve water-solubilization of Sb porphyrin and P porphyrins. Here, we review their water-soluble P and Sb porphyrins from the standpoints of preparation, bioaffinity, and photosensitized inactivation.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><doi>10.1155/2015/148964</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antimony Aqueous solutions Biochemistry Biological Chromophores Inactivation Ligands Molecular weight Photodynamic therapy Porphyrins Rings (mathematics) |
title | Water-Solubilization of P(V) and Sb(V) Porphyrins and Their Photobiological Application |
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