메뉴 건너뛰기




Volumn 19, Issue 9, 2014, Pages 13282-13304

Elucidation of the relationships between H-bonding patterns and excited state dynamics in cyclovalone

Author keywords

Curcuminoid; Cyclovalone; Fluorescence; H bonding; Infrared and UV Vis absorption; Photodegradation; Photosensitizer

Indexed keywords

CURCUMIN; CYCLOVALONE; PHOTOSENSITIZING AGENT; SINGLET OXYGEN; SUPEROXIDE;

EID: 84908123191     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules190913282     Document Type: Article
Times cited : (14)

References (57)
  • 1
    • 0037026270 scopus 로고    scopus 로고
    • Studies of curcumin and curcuminoids. XXVII. Cyclodextrin complexation: Solubility, chemical and photochemical stability
    • Tønnesen, H. H.; Màsson, M.; Loftsson, T. Studies of curcumin and curcuminoids. XXVII. Cyclodextrin complexation: Solubility, chemical and photochemical stability. Int. J. Pharm. 2002, 244, 127-135.
    • (2002) Int. J. Pharm. , vol.244 , pp. 127-135
    • Tønnesen, H.H.1    Màsson, M.2    Loftsson, T.3
  • 2
    • 85054433476 scopus 로고    scopus 로고
    • Patir, H. Prophylactic administration of curcumin abates the incidence of hypobaric hypoxia induced pulmonary edema in rats: A molecular approach
    • Sagi, S. S. K.; Mathew, T.; Patir, H. Prophylactic administration of curcumin abates the incidence of hypobaric hypoxia induced pulmonary edema in rats: A molecular approach. J. Pulm. Respir. Med. 2014, 4, 1000164.
    • (2014) J. Pulm. Respir. Med. , vol.4 , pp. 1000164
    • Sagi, S.S.K.1    Mathew, T.2
  • 4
    • 84908126638 scopus 로고    scopus 로고
    • Nanocurcumin attenuates inflammation by decreasing Toll-like receptor 2 and 4 expression and activity and promoting an anti-inflammatory macrophage phenotype
    • Chen, X.; Chenna, V.; Maitra, A.; Devaraj, S. Nanocurcumin attenuates inflammation by decreasing Toll-like receptor 2 and 4 expression and activity and promoting an anti-inflammatory macrophage phenotype. FASEB J. 2014, 28(Suppl.), 830-822.
    • (2014) FASEB J. , vol.28 , pp. 830-822
    • Chen, X.1    Chenna, V.2    Maitra, A.3    Devaraj, S.4
  • 6
    • 45849115079 scopus 로고    scopus 로고
    • Antioxidant and radical scavenging properties of curcumin
    • Ak, T.; Gulcin, I. Antioxidant and radical scavenging properties of curcumin. Chem.-Biol. Interact. 2008, 174, 27-37.
    • (2008) Chem.-Biol. Interact. , vol.174 , pp. 27-37
    • Ak, T.1    Gulcin, I.2
  • 8
    • 33645787817 scopus 로고    scopus 로고
    • Antioxidant activities of curcumin, demethoxycurcumin and bisdemethoxycurcumin
    • Jayaprakasha, G. K.; Rao, L. J.; Sakarian, K. K. Antioxidant activities of curcumin, demethoxycurcumin and bisdemethoxycurcumin. Food Chem. 2006, 98, 720-724.
    • (2006) Food Chem. , vol.98 , pp. 720-724
    • Jayaprakasha, G.K.1    Rao, L.J.2    Sakarian, K.K.3
  • 9
    • 84891613383 scopus 로고    scopus 로고
    • The molecular basis for the pharmacokinetics and pharmacodynamics of curcumin and its metabolites in relation to cancer
    • Heger, M.; van Golen, R. F.; Michel, M. C. The molecular basis for the pharmacokinetics and pharmacodynamics of curcumin and its metabolites in relation to cancer. Pharmacol. Rev. 2014, 66, 222-307.
    • (2014) Pharmacol. Rev. , vol.66 , pp. 222-307
    • Heger, M.1    Van Golen, R.F.2    Michel, M.C.3
  • 10
    • 0036080207 scopus 로고    scopus 로고
    • The molecular mechanisms for the antitumorigenic effect of curcumin
    • Leu, T. H.; Maa, M. C. The molecular mechanisms for the antitumorigenic effect of curcumin. Curr. Med. Chem. 2002, 2, 357-370.
    • (2002) Curr. Med. Chem. , vol.2 , pp. 357-370
    • Leu, T.H.1    Maa, M.C.2
  • 11
    • 0042169007 scopus 로고    scopus 로고
    • Molecular mechanisms of curcumin-induced cyclotoxicity: Induction of apoptosis through generation of reactive oxygen species, down-regulation of Bcl-XL and IAP, the release of cytochrome c and inhibition of Akt
    • Woo, J.; Kim, Y.; Choi, Y.; Kim, D.; Lee, K.; Bae, J. H.; Chang, D. S.; Jeong, Y. J.; Lee, Y. H.; Park, J.; et al. Molecular mechanisms of curcumin-induced cyclotoxicity: Induction of apoptosis through generation of reactive oxygen species, down-regulation of Bcl-XL and IAP, the release of cytochrome c and inhibition of Akt. Carcinogenesis 2003, 24, 1199-1208.
    • (2003) Carcinogenesis , vol.24 , pp. 1199-1208
    • Woo, J.1    Kim, Y.2    Choi, Y.3    Kim, D.4    Lee, K.5    Bae, J.H.6    Chang, D.S.7    Jeong, Y.J.8    Lee, Y.H.9    Park, J.10
  • 12
    • 4544383470 scopus 로고    scopus 로고
    • Curcumin impairs tumor suppressor p53 function in colon cancer cells
    • Moos, P. J.; Edes, K.; Mullally, J.; Fitzpatrick, J. Curcumin impairs tumor suppressor p53 function in colon cancer cells. Carcinogenesis 2004, 25, 1611-1617.
    • (2004) Carcinogenesis , vol.25 , pp. 1611-1617
    • Moos, P.J.1    Edes, K.2    Mullally, J.3    Fitzpatrick, J.4
  • 13
    • 34547451145 scopus 로고    scopus 로고
    • Curcumin labels amyloid pathology in vivo, disrupts existing plaques, and partially restores distorted neurites in an Alzheimer mouse model
    • Garcia-Alloza, M.; Borrelli, L. A.; Rozkalne, A.; Hyman, B. T.; Bacskai, B. J. Curcumin labels amyloid pathology in vivo, disrupts existing plaques, and partially restores distorted neurites in an Alzheimer mouse model. J. Neurochem. 2007, 102, 1095-1104.
    • (2007) J. Neurochem. , vol.102 , pp. 1095-1104
    • Garcia-Alloza, M.1    Borrelli, L.A.2    Rozkalne, A.3    Hyman, B.T.4    Bacskai, B.J.5
  • 16
    • 5444265248 scopus 로고    scopus 로고
    • A theoretical investigation on intramolecular hydrogen-atom transfer in curcumin
    • Kong, L.; Priyadarsini, K. I.; Zhang, H. Y. A theoretical investigation on intramolecular hydrogen-atom transfer in curcumin. J. Mol. Struct. Theochem 2004, 685, 111-116.
    • (2004) J. Mol. Struct. Theochem , vol.685 , pp. 111-116
    • Kong, L.1    Priyadarsini, K.I.2    Zhang, H.Y.3
  • 17
    • 34548058841 scopus 로고    scopus 로고
    • Curcumin, demethoxycurcumin, bisdemethoxycurcumin, tetrahydrocurcumin and turmerones differentially regulate anti-inflammatory anti-proliferative responses through a ROS-independent mechanism
    • Sandur, S. K.; Pandey, M. K.; Sung, B.; Ahn, K. S.; Murakami, A.; Sethi, G.; Limtrakul, P.; Badmaev, V.; Aggarwal, B. B. Curcumin, demethoxycurcumin, bisdemethoxycurcumin, tetrahydrocurcumin and turmerones differentially regulate anti-inflammatory anti-proliferative responses through a ROS-independent mechanism. Carcinogenesis 2007, 28, 1765-1773.
    • (2007) Carcinogenesis , vol.28 , pp. 1765-1773
    • Sandur, S.K.1    Pandey, M.K.2    Sung, B.3    Ahn, K.S.4    Murakami, A.5    Sethi, G.6    Limtrakul, P.7    Badmaev, V.8    Aggarwal, B.B.9
  • 19
    • 0001617853 scopus 로고
    • Structural studies of curcuminoids. I. The crystal structure of curcumin
    • Tønnesen, H. H.; Karlsen, J.; Mostad, A. Structural studies of curcuminoids. I. The crystal structure of curcumin. Acta Chem. Scand. B 1982, 36, 475-479.
    • (1982) Acta Chem. Scand. B , vol.36 , pp. 475-479
    • Tønnesen, H.H.1    Karlsen, J.2    Mostad, A.3
  • 20
    • 33646186813 scopus 로고    scopus 로고
    • Structure-radical scavenging activity relationships of phenolic compounds from traditional Chinese medical plants
    • Cai, Y. Z.; Sun, M.; Xing, J.; Luo, Q.; Corke, H. Structure-radical scavenging activity relationships of phenolic compounds from traditional Chinese medical plants. Life Sci. 2006, 78, 2872-2888.
    • (2006) Life Sci. , vol.78 , pp. 2872-2888
    • Cai, Y.Z.1    Sun, M.2    Xing, J.3    Luo, Q.4    Corke, H.5
  • 21
    • 31344440514 scopus 로고    scopus 로고
    • Curcumin and its analogues as potent inhibitors of low density lipoprotein oxidation: H-atom abstraction from the phenolic groups and possible involvement of the 4-hydroxy-3-methoxyphenil groups
    • Chen, W. F.; Deng, S. L.; Zhou, B.; Yang, L.; Liu, Z. L. Curcumin and its analogues as potent inhibitors of low density lipoprotein oxidation: H-atom abstraction from the phenolic groups and possible involvement of the 4-hydroxy-3-methoxyphenil groups. Free Radic. Biol. Med. 2006, 40, 526-535.
    • (2006) Free Radic. Biol. Med. , vol.40 , pp. 526-535
    • Chen, W.F.1    Deng, S.L.2    Zhou, B.3    Yang, L.4    Liu, Z.L.5
  • 22
    • 33846066817 scopus 로고    scopus 로고
    • Comparative antioxidant activities of curcumin and its demethoxy and hydrogenated derivatives
    • Somparn, P.; Phisalaphong, C.; Nakornchai, S.; Unchern, S.; Morales, N. P. Comparative antioxidant activities of curcumin and its demethoxy and hydrogenated derivatives. Biol. Pharm. Bull. 2007, 30, 74-78.
    • (2007) Biol. Pharm. Bull. , vol.30 , pp. 74-78
    • Somparn, P.1    Phisalaphong, C.2    Nakornchai, S.3    Unchern, S.4    Morales, N.P.5
  • 23
    • 34247880427 scopus 로고    scopus 로고
    • Curcuminoids, curcumin, and demethoxycurcumin reduce lead-induced memory deficits in male wistar rats
    • Dairam, A.; Limson, J. L.; Watkins, G. M.; Antunes, E.; Daya, S. Curcuminoids, curcumin, and demethoxycurcumin reduce lead-induced memory deficits in male wistar rats. J. Agric. Food Chem. 2007, 55, 1039-1044.
    • (2007) J. Agric. Food Chem. , vol.55 , pp. 1039-1044
    • Dairam, A.1    Limson, J.L.2    Watkins, G.M.3    Antunes, E.4    Daya, S.5
  • 25
    • 0023183657 scopus 로고
    • Studies on curcumin and curcuminoids IX: Investigation of the photobiological activity of curcumin using bacterial indicator systems
    • Tønnesen, H. H.; de Vries, H.; Karlsen, J.; van Henegouwen, G. B. Studies on curcumin and curcuminoids IX: Investigation of the photobiological activity of curcumin using bacterial indicator systems. J. Pharm. Sci. 1987, 76, 371-373.
    • (1987) J. Pharm. Sci. , vol.76 , pp. 371-373
    • Tønnesen, H.H.1    Vries, H.2    Karlsen, J.3    Van Henegouwen, G.B.4
  • 26
    • 74949087264 scopus 로고    scopus 로고
    • Photokilling of bacteria by curcumin in different aqueous preparations. Studies on curcumin and curcuminoids
    • Haukvik, T.; Bruzell, E.; Kristensen, S.; Tønnesen, H. H. Photokilling of bacteria by curcumin in different aqueous preparations. Studies on curcumin and curcuminoids. XXXVII. Pharmazie 2009, 64, 666-673.
    • (2009) Pharmazie , vol.64 , pp. 666-673
    • Haukvik, T.1    Bruzell, E.2    Kristensen, S.3    Tønnesen, H.H.4
  • 27
    • 77955870855 scopus 로고    scopus 로고
    • Photokilling of bacteria by curcumin in selected polyethylene glycol 400 (PEG 400) preparations studies on curcumin and curcuminoids XLI
    • Haukvik, T.; Bruzell, E.; Kristensen, S.; Tønnesen, H. H. Photokilling of bacteria by curcumin in selected polyethylene glycol 400 (PEG 400) preparations studies on curcumin and curcuminoids XLI. Pharmazie 2010, 65, 600-606.
    • (2010) Pharmazie , vol.65 , pp. 600-606
    • Haukvik, T.1    Bruzell, E.2    Kristensen, S.3    Tønnesen, H.H.4
  • 28
    • 78650038681 scopus 로고    scopus 로고
    • Formulation and bacterial phototoxicity of curcumin loaded alginate foams for wound applications studies on curcumin and curcumioids
    • Hegge, A. B.; Andersen, T.; Melvik, J. E.; Bruzell, E.; Kristensen, S.; Tønnesen, H. H. Formulation and bacterial phototoxicity of curcumin loaded alginate foams for wound applications studies on curcumin and curcumioids. XLII. J. Pharm. Sci. 2011, 100, 174-185.
    • (2011) J. Pharm. Sci. , vol.100 , pp. 174-185
    • Hegge, A.B.1    Andersen, T.2    Melvik, J.E.3    Bruzell, E.4    Kristensen, S.5    Tønnesen, H.H.6
  • 29
    • 79953301826 scopus 로고    scopus 로고
    • A Screening for antibacterial phototoxic effects of curcumin derivatives studies on curcumin and curcuminoids. XLIII
    • Haukvik, T.; Bruzell, E.; Kristensen, S.; Tønnesen, H. H. A Screening for antibacterial phototoxic effects of curcumin derivatives studies on curcumin and curcuminoids. XLIII. Pharmazie 2011, 66, 69-77.
    • (2011) Pharmazie , vol.66 , pp. 69-77
    • Haukvik, T.1    Bruzell, E.2    Kristensen, S.3    Tønnesen, H.H.4
  • 30
    • 84857500592 scopus 로고    scopus 로고
    • Impact of curcumin supersaturation in antibacterial photodynamic therapy (aPDT)-Effect of cyclodextrin type and amount, studies on curcumin and curcuminoids XLV
    • Hegge, A. B.; Nielsen, T. T.; Larsen, K. L.; Bruzell, E.; Tønnesen, H. H. Impact of curcumin supersaturation in antibacterial photodynamic therapy (aPDT)-Effect of cyclodextrin type and amount, studies on curcumin and curcuminoids XLV. J. Pharm. Sci. 2012, 101, 1524-1537.
    • (2012) J. Pharm. Sci. , vol.101 , pp. 1524-1537
    • Hegge, A.B.1    Nielsen, T.T.2    Larsen, K.L.3    Bruzell, E.4    Tønnesen, H.H.5
  • 31
    • 84861890028 scopus 로고    scopus 로고
    • Photoinactivation of Staphylococcus epidermidis biofilms and suspensions by the hydrophobic photosensitizer curcumin-Effect of selected nanocarrier. Studies on curcumin and curcuminoides XLVII
    • Hegge, A. B.; Bruzell, E.; Kristensen, S.; Tønnesen, H. H. Photoinactivation of Staphylococcus epidermidis biofilms and suspensions by the hydrophobic photosensitizer curcumin-Effect of selected nanocarrier. Studies on curcumin and curcuminoides XLVII. Eur. J. Pharm. Sci. 2012, 47, 65-74.
    • (2012) Eur. J. Pharm. Sci. , vol.47 , pp. 65-74
    • Hegge, A.B.1    Bruzell, E.2    Kristensen, S.3    Tønnesen, H.H.4
  • 32
    • 84876730009 scopus 로고    scopus 로고
    • The influence of Pluronics on dark cytotoxicity, photocytotoxicity, localization and uptake of curcumin in cancer cells. Studies on curcumin and curcuminoids XLIX
    • Singh, R.; Kristensen, S.; Tønnesen, H. H.; Berg, K. The influence of Pluronics on dark cytotoxicity, photocytotoxicity, localization and uptake of curcumin in cancer cells. Studies on curcumin and curcuminoids XLIX. Photochem. Photobiol. Sci. 2013, 12, 559-575.
    • (2013) Photochem. Photobiol. Sci. , vol.12 , pp. 559-575
    • Singh, R.1    Kristensen, S.2    Tønnesen, H.H.3    Berg, K.4
  • 33
    • 84871923748 scopus 로고    scopus 로고
    • Solid dispersions for preparation of phototoxic supersaturated solutions for antimicrobial photodynamic therapy (aPDT). Studies on curcumin and curcuminoids L
    • Hegge, A. B.; Vukicevic, M.; Bruzell, E.; Kristensen, S.; Tønnesen, H. H. Solid dispersions for preparation of phototoxic supersaturated solutions for antimicrobial photodynamic therapy (aPDT). Studies on curcumin and curcuminoids L. Eur. J. Pharm. Biopharm. 2013, 83, 95-105.
    • (2013) Eur. J. Pharm. Biopharm. , vol.83 , pp. 95-105
    • Hegge, A.B.1    Vukicevic, M.2    Bruzell, E.3    Kristensen, S.4    Tønnesen, H.H.5
  • 35
    • 22944488591 scopus 로고    scopus 로고
    • Studies on curcumin and curcuminoids. XXIX. Photoinduced cytotoxicity of curcumin in selected aqueous preparations
    • Bruzell, E.; Morisbak, E.; Tønnesen, H. H. Studies on curcumin and curcuminoids. XXIX. Photoinduced cytotoxicity of curcumin in selected aqueous preparations. Photochem. Photobiol. Sci. 2005, 4, 523-530.
    • (2005) Photochem. Photobiol. Sci. , vol.4 , pp. 523-530
    • Bruzell, E.1    Morisbak, E.2    Tønnesen, H.H.3
  • 39
    • 84862235747 scopus 로고    scopus 로고
    • Photophysical properties of dimethoxycurcumin and bis-dehydroxycurcumin
    • Nardo, L.; Andreoni, A.; Bondani, M.; Màsson, M.; Tønnesen, H. H. Photophysical properties of dimethoxycurcumin and bis-dehydroxycurcumin. J. Fluorescence 2012, 22, 597-608.
    • (2012) J. Fluorescence , vol.22 , pp. 597-608
    • Nardo, L.1    Andreoni, A.2    Bondani, M.3    Màsson, M.4    Tønnesen, H.H.5
  • 40
    • 84866599550 scopus 로고    scopus 로고
    • Excited-state dynamics of bis-dehydroxycurcumin carboxylic acid, a water-soluble derivative of the photosensitizer curcumin
    • Nardo, L.; Maspero, A.; Selva, M.; Bondani, M.; Palmisano, G.; Ferrari, E.; Saladini, M. Excited-state dynamics of bis-dehydroxycurcumin carboxylic acid, a water-soluble derivative of the photosensitizer curcumin. J. Phys. Chem. A 2012, 116, 9321-9330.
    • (2012) J. Phys. Chem. A , vol.116 , pp. 9321-9330
    • Nardo, L.1    Maspero, A.2    Selva, M.3    Bondani, M.4    Palmisano, G.5    Ferrari, E.6    Saladini, M.7
  • 41
    • 33947434999 scopus 로고
    • Absorption Spectra of Certain α, β-Unsaturated Ketones, including Benzal Compounds
    • French, H. S.; Holden, M. G. T. Absorption Spectra of Certain α, β-Unsaturated Ketones, including Benzal Compounds. J. Am. Chem. Soc. 1945, 67, 1239-1242.
    • (1945) J. Am. Chem. Soc. , vol.67 , pp. 1239-1242
    • French, H.S.1    Holden, M.G.T.2
  • 42
    • 0001008861 scopus 로고
    • The dipole moments, spectra and structure of some new 2-phenyl-, 2-benzyl-, 2-(p-halobenzy1idene) - and 2, 6-Bis-(p-halobenzy1idene)-cyclohexanones
    • Huitric, A. C.; Kumler, W. D. The dipole moments, spectra and structure of some new 2-phenyl-, 2-benzyl-, 2-(p-halobenzy1idene) - and 2, 6-Bis-(p-halobenzy1idene)-cyclohexanones. J. Am. Chem. Soc. 1956, 78, 614-622.
    • (1956) J. Am. Chem. Soc. , vol.78 , pp. 614-622
    • Huitric, A.C.1    Kumler, W.D.2
  • 43
    • 0142069725 scopus 로고
    • Electronic absorption spectra of some diarylidene-cyclopentanones and-cyclohexanones
    • Issa, R. M.; Etaiw, S. H.; Issa, I. M.; El-Shafie, A. K. Electronic absorption spectra of some diarylidene-cyclopentanones and-cyclohexanones. Acta Chim. (Budapest) 1976, 89, 381-391.
    • (1976) Acta Chim. (Budapest) , vol.89 , pp. 381-391
    • Issa, R.M.1    Etaiw, S.H.2    Issa, I.M.3    El-Shafie, A.K.4
  • 44
    • 0142040168 scopus 로고    scopus 로고
    • Electronic absorption and fluorescence properties of 2, 5-diarylidene-cyclopentanones
    • Connors, R. E.; Ucak-Astarlioglu, M. G. Electronic absorption and fluorescence properties of 2, 5-diarylidene-cyclopentanones. J. Phys. Chem. A 2003, 107, 7684-7691.
    • (2003) J. Phys. Chem. A , vol.107 , pp. 7684-7691
    • Connors, R.E.1    Ucak-Astarlioglu, M.G.2
  • 45
    • 25844461511 scopus 로고    scopus 로고
    • Absorption and fluorescence of 2, 5-diarylidenecyclopentanones in acidic media: Evidence for excited-state proton transfer
    • Ucak-Astarlioglu, M. G.; Connors, R. E. Absorption and fluorescence of 2, 5-diarylidenecyclopentanones in acidic media: Evidence for excited-state proton transfer. J. Phys. Chem. A 2005, 109, 8275-8279.
    • (2005) J. Phys. Chem. A , vol.109 , pp. 8275-8279
    • Ucak-Astarlioglu, M.G.1    Connors, R.E.2
  • 47
    • 15144355755 scopus 로고    scopus 로고
    • Geometrically and conformationally restrained cinnamoyl compounds as inhibitors of HIV-1 integrase: Synthesis, biological evaluation, and molecular modeling
    • Artico, M.; di Santo, R.; Costi, R.; Novellino, E.; Greco, G.; Massa, S.; Tramontano, E.; Marongiu, M. E.; de Montis, A.; la Colla, P. Geometrically and conformationally restrained cinnamoyl compounds as inhibitors of HIV-1 integrase: Synthesis, biological evaluation, and molecular modeling. J. Med. Chem. 1998, 41, 3948-3960.
    • (1998) J. Med. Chem. , vol.41 , pp. 3948-3960
    • Artico, M.1    Di Santo, R.2    Costi, R.3    Novellino, E.4    Greco, G.5    Massa, S.6    Tramontano, E.7    Marongiu, M.E.8    Montis, A.9    Colla, P.10
  • 48
    • 0041573625 scopus 로고
    • Linear solvation energy relationships. 23. A comprehensive collection of the solvatochromic parameters, πz.ast;, a, and, β, and some methods for simplifying the generalized solvatochromic equation
    • Kamlet, M. J.; Abboud, J. L. M.; Abraham, M. H.; Taft, R. W. Linear solvation energy relationships. 23. A comprehensive collection of the solvatochromic parameters, πz.ast;, a, and, β, and some methods for simplifying the generalized solvatochromic equation. J. Org. Chem. 1983, 48, 2877-2887.
    • (1983) J. Org. Chem. , vol.48 , pp. 2877-2887
    • Kamlet, M.J.1    Abboud, J.L.M.2    Abraham, M.H.3    Taft, R.W.4
  • 50
    • 84962433171 scopus 로고    scopus 로고
    • Theoretical study on physicochemical properties of curcumin
    • Shen, L.; Ji, H. F. Theoretical study on physicochemical properties of curcumin. Spectrochim. Acta A 2007, 67, 619-623.
    • (2007) Spectrochim. Acta A , vol.67 , pp. 619-623
    • Shen, L.1    Ji, H.F.2
  • 51
    • 36849117004 scopus 로고
    • Spin orbit coupling and the radiationless processes in nitrogen heterocyclics
    • El Sayed, M. A. Spin orbit coupling and the radiationless processes in nitrogen heterocyclics. J. Chem. Phys. 1963, 38, 2834-2838.
    • (1963) J. Chem. Phys. , vol.38 , pp. 2834-2838
    • El Sayed, M.A.1
  • 52
    • 77955556510 scopus 로고    scopus 로고
    • Time-domain evaluation of drug-solvent interactions of the photosensitizers TPCS2a and TPPS2a as part of physicochemical characterization
    • Lilletvedt, M.; Tønnesen, H. H.; Høgset, A.; Kristensen, S.; Nardo, L. Time-domain evaluation of drug-solvent interactions of the photosensitizers TPCS2a and TPPS2a as part of physicochemical characterization. J. Photochem. Photobiol. A Chem. 2010, 214, 40-47.
    • (2010) J. Photochem. Photobiol. A Chem. , vol.214 , pp. 40-47
    • Lilletvedt, M.1    Tønnesen, H.H.2    Høgset, A.3    Kristensen, S.4    Nardo, L.5
  • 54
    • 79959258921 scopus 로고    scopus 로고
    • The photostability and fluorescence properties of diphenylisobenzofuran
    • Zhang, X.-F.; Li, X. The photostability and fluorescence properties of diphenylisobenzofuran. J. Lumin. 2011, 131, 2263-2266.
    • (2011) J. Lumin. , vol.131 , pp. 2263-2266
    • Zhang, X.-F.1    Li, X.2
  • 55
    • 29244444522 scopus 로고    scopus 로고
    • Fluorescence probes used for detection of reactive oxygen species
    • Gomes, A.; Fernandes, E.; Lima, J. L. F. C. Fluorescence probes used for detection of reactive oxygen species. J. Biochem. Biophys. Methods 2005, 65, 45-80.
    • (2005) J. Biochem. Biophys. Methods , vol.65 , pp. 45-80
    • Gomes, A.1    Fernandes, E.2    Lima, J.L.F.C.3
  • 57
    • 70349663514 scopus 로고    scopus 로고
    • Standardization of kinetic studies of photodegradation reactions
    • Tønnesen, H. H., Ed.; CRC Press: Boca Raton, FL, USA
    • Moore, D. E. Standardization of kinetic studies of photodegradation reactions. In Photostability of Drugs and Drug Formulations; Tønnesen, H. H., Ed.; CRC Press: Boca Raton, FL, USA, 2004; pp. 49-53.
    • (2004) Photostability of Drugs and Drug Formulations , pp. 49-53
    • Moore, D.E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.