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Volumn 222, Issue 1, 2011, Pages 228-235

Carboxylate modified benzylidene cyclopentanone dyes for one- and two-photon excited photodynamic therapy

Author keywords

Benzylidene cyclopentanone; Photodynamic therapy; Two photon absorption; Water lipid amphipathy

Indexed keywords


EID: 80051790613     PISSN: 10106030     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jphotochem.2011.06.002     Document Type: Article
Times cited : (28)

References (38)
  • 2
    • 33645718814 scopus 로고    scopus 로고
    • Water-soluble bis(imidazolylporphyrin) self-assemblies with large two-photon absorption cross sections as potential agents for photodynamic therapy
    • K. Ogawa, H. Hasegawa, Y. Inaba, Y. Kobuke, H. Inouye, Y. Kanemitsu, E. Kohno, T. Hirano, S. Ogura, and I. Okura Water-soluble bis(imidazolylporphyrin) self-assemblies with large two-photon absorption cross sections as potential agents for photodynamic therapy J. Med. Chem. 49 2006 2276 2283
    • (2006) J. Med. Chem. , vol.49 , pp. 2276-2283
    • Ogawa, K.1    Hasegawa, H.2    Inaba, Y.3    Kobuke, Y.4    Inouye, H.5    Kanemitsu, Y.6    Kohno, E.7    Hirano, T.8    Ogura, S.9    Okura, I.10
  • 3
    • 33646249161 scopus 로고    scopus 로고
    • Simultaneous two-photon excitation of photofrin in relation to photodynamic therapy
    • A. Karotki, M. Khurana, J.R. Lepock, and B.C. Wilson Simultaneous two-photon excitation of photofrin in relation to photodynamic therapy Photochem. Photobiol. 82 2006 443 452
    • (2006) Photochem. Photobiol. , vol.82 , pp. 443-452
    • Karotki, A.1    Khurana, M.2    Lepock, J.R.3    Wilson, B.C.4
  • 5
    • 0742271396 scopus 로고    scopus 로고
    • Research advances in the use of tetrapyrrolic photosensitizers for photodynamic therapy
    • DOI 10.1016/j.jphotobiol.2003.10.002, PII S1011134403001507
    • E.S. Nyman, and P.H. Hynninen Research advances in the use of tetrapyrrolic photosensitizers for photodynamic therapy J. Photochem. Photobiol. B: Biol. 73 2004 1 28 (Pubitemid 38145763)
    • (2004) Journal of Photochemistry and Photobiology B: Biology , vol.73 , Issue.1-2 , pp. 1-28
    • Nyman, E.S.1    Hynninen, P.H.2
  • 6
    • 4043107044 scopus 로고    scopus 로고
    • The present and future role of photodynamic therapy in cancer treatment
    • DOI 10.1016/S1470-2045(04)01529-3, PII S1470204504015293
    • S.B. Brown, E.A. Brown, and I. Walker The present and future role of photodynamic therapy in cancer treatment Lancet Oncol. 5 2004 497 508 (Pubitemid 39069400)
    • (2004) Lancet Oncology , vol.5 , Issue.8 , pp. 497-508
    • Brown, S.B.1    Brown, E.A.2    Walker, I.3
  • 7
    • 34548181645 scopus 로고    scopus 로고
    • Quantitative in vitro demonstration of two-photon photodynamic therapy using Photofrin® and Visudyne®
    • DOI 10.1111/j.1751-1097.2007.00185.x
    • M. Khurana, H.A. Collins, A. Karotki, H.L. Anderson, D.T. Cramb, and B.C. Wilson Quantitative in vitro demonstration of two-photon photodynamic therapy using photofrin and visudyne Photochem. Photobiol. 83 2007 1441 1448 (Pubitemid 350132612)
    • (2007) Photochemistry and Photobiology , vol.83 , Issue.6 , pp. 1441-1448
    • Khurana, M.1    Collins, H.A.2    Karotki, A.3    Anderson, H.L.4    Cramb, D.T.5    Wilson, B.C.6
  • 8
    • 58149176735 scopus 로고    scopus 로고
    • New two-photon activated photodynamic therapy sensitizers induce xenograft tumor regressions after near-IR laser treatment through the body of the host mouse
    • J.R. Starkey, A.K. Rebane, M.A. Drobizhev, F.-Q. Meng, A.-J. Gong, A. Elliott, K. McInnerney, and C.W. Spangler New two-photon activated photodynamic therapy sensitizers induce xenograft tumor regressions after near-IR laser treatment through the body of the host mouse Clin. Cancer Res. 14 2008 6564 6573
    • (2008) Clin. Cancer Res. , vol.14 , pp. 6564-6573
    • Starkey, J.R.1    Rebane, A.K.2    Drobizhev, M.A.3    Meng, F.-Q.4    Gong, A.-J.5    Elliott, A.6    McInnerney, K.7    Spangler, C.W.8
  • 10
    • 0030774313 scopus 로고    scopus 로고
    • An in vivo quantitative structure-activity relationship for a congeneric series of pyropheophorbide derivatives as photosensitizers for photodynamic therapy
    • B.W. Henderson, D.A. Bellnier, W.R. Greco, A. Sharma, R.K. Pandey, L.A. Vaughan, K.R. Weishaupt, and T.J. Dougherty An in vivo quantitative structure-activity relationship for a congeneric series of pyropheophorbide derivatives as photosensitizers for photodynamic therapy Cancer Res. 57 1997 4000 4007 (Pubitemid 27427689)
    • (1997) Cancer Research , vol.57 , Issue.18 , pp. 4000-4007
    • Henderson, B.W.1    Bellnier, D.A.2    Greco, W.R.3    Sharma, A.4    Pandey, R.K.5    Vaughan, L.A.6    Weishaupt, K.R.7    Dougherty, T.J.8
  • 13
    • 65949095886 scopus 로고    scopus 로고
    • Design of two-photon absorbing materials for molecular optical memory and photodynamic therapy
    • K. Ogawa, and Y. Kobuke Design of two-photon absorbing materials for molecular optical memory and photodynamic therapy Org. Biomol. Chem. 7 2009 2241 2246
    • (2009) Org. Biomol. Chem. , vol.7 , pp. 2241-2246
    • Ogawa, K.1    Kobuke, Y.2
  • 16
    • 68249104176 scopus 로고    scopus 로고
    • A new series of quadrupolar type two-photon absorption chromophores bearing 11, 12-dibutoxydibenzo[a,c]-phenazine bridged amines: Their applications in two-photon fluorescence imaging and two-photon photodynamic therapy
    • M. Velusamy, J.Y. Shen, J.T. Lin, Y.C. Lin, C.C. Hsieh, C.H. Lai, M.L. Ho, Y.C. Chen, P.T. Chou, and J.K. Hsiao A new series of quadrupolar type two-photon absorption chromophores bearing 11, 12-dibutoxydibenzo[a,c]-phenazine bridged amines: Their applications in two-photon fluorescence imaging and two-photon photodynamic therapy Adv. Funct. Mater. 19 2009 2388 2397
    • (2009) Adv. Funct. Mater. , vol.19 , pp. 2388-2397
    • Velusamy, M.1    Shen, J.Y.2    Lin, J.T.3    Lin, Y.C.4    Hsieh, C.C.5    Lai, C.H.6    Ho, M.L.7    Chen, Y.C.8    Chou, P.T.9    Hsiao, J.K.10
  • 17
    • 43549108812 scopus 로고    scopus 로고
    • Recent advances in two-photon photodynamic therapy
    • DOI 10.2174/187152008783961860
    • K. Ogawa, and Y. Kobuke Recent advances in two-photon photodynamic therapy Anticancer Agents Med. Chem. 8 2008 269 279 (Pubitemid 351761432)
    • (2008) Anti-Cancer Agents in Medicinal Chemistry , vol.8 , Issue.3 , pp. 269-279
    • Ogawa, K.1    Kobuke, Y.2
  • 18
    • 0344442315 scopus 로고    scopus 로고
    • An Outline of the Hundred-Year History of PDT
    • J. Moan, and Q. Peng An outline of the hundred-year history of PDT Anticancer Res. 23 2003 3591 3600 (Pubitemid 37474301)
    • (2003) Anticancer Research , vol.23 , Issue.5 A , pp. 3591-3600
    • Moan, J.1    Peng, Q.2
  • 20
    • 33745699004 scopus 로고    scopus 로고
    • Multibranched benzylidene cyclopentanone dyes with large two-photon absorption cross-sections
    • DOI 10.1039/b604695a
    • J. Wu, Y.X. Zhao, X. Li, M.Q. Shi, F.P. Wu, and X.Y. Fang Multibranched benzylidene cyclopentanone dyes with large two-photon absorption cross-sections New J. Chem. 30 2006 1098 1103 (Pubitemid 44000946)
    • (2006) New Journal of Chemistry , vol.30 , Issue.7 , pp. 1098-1103
    • Wu, J.1    Zhao, Y.2    Li, X.3    Shi, M.4    Wu, F.5    Fang, X.6
  • 21
    • 53349123107 scopus 로고    scopus 로고
    • Novel benzylidene cyclopentanone dyes for two-photon photopolymerization
    • J.Q. Xue, Y.X. Zhao, J. Wu, and F.P. Wu Novel benzylidene cyclopentanone dyes for two-photon photopolymerization J. Photochem. Photobiol. A: Chem. 195 2008 261 266
    • (2008) J. Photochem. Photobiol. A: Chem. , vol.195 , pp. 261-266
    • Xue, J.Q.1    Zhao, Y.X.2    Wu, J.3    Wu, F.P.4
  • 22
    • 34548689875 scopus 로고    scopus 로고
    • Two-photon absorption property and photopolymerization sensitizing efficiency of asymmetrical benzylidene cyclopentanone dyes
    • DOI 10.1016/j.dyepig.2007.01.007, PII S0143720807000174
    • J. Wu, M.Q. Shi, Y.X. Zhao, and F.P. Wu Two-photon absorption property and photopolymerization sensitizing efficiency of asymmetrical benzylidene cyclopentanone dyes Dyes Pigments 76 2008 690 695 (Pubitemid 47412959)
    • (2008) Dyes and Pigments , vol.76 , Issue.3 , pp. 690-695
    • Wu, J.1    Shi, M.2    Zhao, Y.3    Wu, F.4
  • 24
    • 33745725079 scopus 로고    scopus 로고
    • Syntheses of novel asymmetric cyclopentanone dyes and measurement of two-photon absorption cross-section
    • T. Wang, F.P. Wu, and M.Q. Shi Syntheses of novel asymmetric cyclopentanone dyes and measurement of two-photon absorption cross-section Chem. Res. Chin. Univ. 19 2003 470 473
    • (2003) Chem. Res. Chin. Univ. , vol.19 , pp. 470-473
    • Wang, T.1    Wu, F.P.2    Shi, M.Q.3
  • 25
    • 0020954536 scopus 로고
    • Fluorescence quantum yields of some rhodamine dyes
    • DOI 10.1016/0022-2313(82)90045-X
    • R.F. Kubin, and A.N. Fletcher Fluorescence quantum yields of some rhodamine dyes J. Lumin. 27 1982 455 462 (Pubitemid 13505734)
    • (1983) Journal of Luminescence , vol.27 , Issue.4 , pp. 455-462
    • Kubin, R.F.1    Fletcher, A.N.2
  • 26
    • 50749135933 scopus 로고
    • Photosensitization by anticancer agents. 12. Perylene quinonoid pigments, a novel type of singlet oxygen sensitizer
    • Z.J. Diwu, and J.W. Lown Photosensitization by anticancer agents. 12. Perylene quinonoid pigments, a novel type of singlet oxygen sensitizer J. Photochem. Photobiol. A: Chem. 64 1992 273 287
    • (1992) J. Photochem. Photobiol. A: Chem. , vol.64 , pp. 273-287
    • Diwu, Z.J.1    Lown, J.W.2
  • 27
    • 0033212287 scopus 로고    scopus 로고
    • A compilation of singlet oxygen yields from biologically relevant molecules
    • R.W. Redmond, and J.N. Gamlin A compilation of singlet oxygen yields from biologically relevant molecules Photchem. Photobiol. 70 1999 391 475 (Pubitemid 129555813)
    • (1999) Photochemistry and Photobiology , vol.70 , Issue.4 , pp. 391-475
    • Redmond, R.W.1    Gamlin, J.N.2
  • 28
    • 0030532990 scopus 로고    scopus 로고
    • Measurement of two-photon excitation cross sections of molecular fluorophores with data from 690 to 1050 nm
    • C. Xu, and W.W. Webb Measurement of two-photon excitation cross sections of molecular fluorophores with data from 690 to 1050 nm J. Opt. Soc. Am. B 13 1996 481 491
    • (1996) J. Opt. Soc. Am. B , vol.13 , pp. 481-491
    • Xu, C.1    Webb, W.W.2
  • 29
    • 0024395179 scopus 로고
    • Determination of octanol/water partition coefficients for hydrophobic organic chemicals with the 'slow-stirring' method
    • J. De Bruijn, F. Busser, W. Seinen, and J. Hermens Determination of octanol/water partition coefficients for hydrophobic organic chemicals with the 'slow-stirring' method Environ. Toxicol. Chem. 8 1989 499 512 (Pubitemid 19160260)
    • (1989) Environmental Toxicology and Chemistry , vol.8 , Issue.6 , pp. 499-512
    • De Bruijn, J.1    Busser, F.2    Seinen, W.3    Hermens, J.4
  • 30
    • 13844269030 scopus 로고    scopus 로고
    • Polyethylenimine with acid-labile linkages as a biodegradable gene carrier
    • DOI 10.1016/j.jconrel.2004.11.008, PII S016836590400567X
    • Y.H. Kim, J.H. Park, M. Lee, Y.H. Kim, T.G. Park, and S.W. Kim Polyethylenimine with acid-labile linkages as a biodegradable gene carrier J. Control. Release 103 2005 209 219 (Pubitemid 40248573)
    • (2005) Journal of Controlled Release , vol.103 , Issue.1 , pp. 209-219
    • Kim, Y.H.1    Park, J.H.2    Lee, M.3    Kim, Y.-H.4    Park, T.G.5    Kim, S.W.6
  • 31
    • 1242269267 scopus 로고    scopus 로고
    • Intramolecular Charge Transfer with the Planarized 4-Aminobenzonitrile 1-tert-Butyl-6-cyano-1,2,3,4-tetrahydroquinoline (NTC6)
    • K.A. Zachariasse, S.I. Druzhinin, W. Bosch, and R. Machinek Intramolecular charge transfer with the planarized 4-aminobenzonitrile 1-tert-butyl-6-cyano-1,2,3,4-tetrahydroquinoline (NTC6) J. Am. Chem. Soc. 126 2004 1705 1715 (Pubitemid 38222755)
    • (2004) Journal of the American Chemical Society , vol.126 , Issue.6 , pp. 1705-1715
    • Zachariasse, K.A.1    Druzhinin, S.I.2    Bosch, W.3    Machinek, R.4
  • 32
    • 0006275640 scopus 로고    scopus 로고
    • Intramolecular charge transfer and photoisomerization of 2-(p-dimethylaminostyryl)benzoxazole: A new fluorescent probe
    • T.A. Fayed Intramolecular charge transfer and photoisomerization of 2-(p-dimethylaminostyryl)benzoxazole: a new fluorescent probe J. Photochem. Photobiol. A: Chem. 121 1999 17 25
    • (1999) J. Photochem. Photobiol. A: Chem. , vol.121 , pp. 17-25
    • Fayed, T.A.1
  • 33
    • 0031344013 scopus 로고    scopus 로고
    • Photophysical properties of squaraine derivatives: Evidence for charge separation
    • C. Cornelissen-Gude, W. Rettig, and R. Lapouyade Photophysical properties of squaraine derivatives: evidence for charge separation J. Phys. Chem. A 101 1997 9673 9677 (Pubitemid 127617207)
    • (1997) Journal of Physical Chemistry A , vol.101 , Issue.50 , pp. 9673-9677
    • Cornelissen-Gude, C.1    Rettig, W.2    Lapouyade, R.3
  • 34
    • 33947292939 scopus 로고
    • Viscosity dependence of fluorescence quantum yields
    • S. Sharafy, and K.A. Muszkat Viscosity dependence of fluorescence quantum yields J. Am. Chem. Soc. 93 1971 4119 4125
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 4119-4125
    • Sharafy, S.1    Muszkat, K.A.2
  • 35
    • 0031148463 scopus 로고    scopus 로고
    • Photophysical and photobiological processes in the photodynamic therapy of tumours
    • DOI 10.1016/S1011-1344(96)07428-3, PII S1011134496074283
    • M. Ochsner Photophysical and photobiological processes in the photodynamic therapy of tumours J. Photochem. Photobiol. B: Biol. 39 1997 1 18 (Pubitemid 27285576)
    • (1997) Journal of Photochemistry and Photobiology B: Biology , vol.39 , Issue.1 , pp. 1-18
    • Ochsner, M.1
  • 36
    • 0002289244 scopus 로고
    • Type i and type II mechanisms of photodynamic action
    • C.S. Foote Type I and type II mechanisms of photodynamic action ACS Symp. Ser. 339 1987 22 38
    • (1987) ACS Symp. Ser. , vol.339 , pp. 22-38
    • Foote, C.S.1
  • 37
    • 0029999114 scopus 로고    scopus 로고
    • - and OH) during the photosensitization of a water-soluble perylenequinone derivative
    • - and OH) during the photosensitization of a water-soluble perylenequinone derivative J. Photochem. Photobiol. B: Biol. 33 1996 51 59
    • (1996) J. Photochem. Photobiol. B: Biol. , vol.33 , pp. 51-59
    • Hu, Y.Z.1    Jiang, L.J.2
  • 38
    • 8644243613 scopus 로고
    • Partition coefficients and their uses
    • A. Leo, C. Hansch, and D. Elkins Partition coefficients and their uses Chem. Rev. 71 1971 525 616
    • (1971) Chem. Rev. , vol.71 , pp. 525-616
    • Leo, A.1    Hansch, C.2    Elkins, D.3


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