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Volumn 33, Issue 8, 2014, Pages 1809-1816

Experimental and theoretical insights into photochemical transformation kinetics and mechanisms of aqueous propylparaben and risk assessment of its degradation products

Author keywords

Ecotoxicology assessment; Endocrine disruptors; Environmental transformation; Parabens; Photoenhanced toxicity

Indexed keywords

DEGRADATION; DETOXIFICATION; EXCITED STATES; PARABENS; PHOTOLYSIS; PROPYLPARABEN; RISK ASSESSMENT; TOXICITY;

EID: 84904437064     PISSN: 07307268     EISSN: 15528618     Source Type: Journal    
DOI: 10.1002/etc.2632     Document Type: Article
Times cited : (26)

References (40)
  • 2
    • 77953535993 scopus 로고    scopus 로고
    • Development of a thermal desorption-gas chromatography-mass spectrometry method for determining personal care products in air
    • Ramirez N, Marce RM, Borrull F. 2010. Development of a thermal desorption-gas chromatography-mass spectrometry method for determining personal care products in air. J Chromatogr A 1217:4430-4438.
    • (2010) J Chromatogr A , vol.1217 , pp. 4430-4438
    • Ramirez, N.1    Marce, R.M.2    Borrull, F.3
  • 3
    • 7044264201 scopus 로고    scopus 로고
    • Determination of estrogenic activity by LYES-assay (yeast estrogen screen-assay assisted by enzymatic digestion with lyticase)
    • Schultis T, Metzger JW. 2004. Determination of estrogenic activity by LYES-assay (yeast estrogen screen-assay assisted by enzymatic digestion with lyticase). Chemosphere 57:1649-1655.
    • (2004) Chemosphere , vol.57 , pp. 1649-1655
    • Schultis, T.1    Metzger, J.W.2
  • 4
    • 78650545102 scopus 로고    scopus 로고
    • Direct and indirect photolysis of sulfamethoxazole and trimethoprim in wastewater treatment plant effluent
    • Ryan CC, Tan DT, Arnold WA. 2011. Direct and indirect photolysis of sulfamethoxazole and trimethoprim in wastewater treatment plant effluent. Water Res 45:1280-1286.
    • (2011) Water Res , vol.45 , pp. 1280-1286
    • Ryan, C.C.1    Tan, D.T.2    Arnold, W.A.3
  • 5
    • 33747833410 scopus 로고    scopus 로고
    • UV excimer lamp irradiation of fibroblasts: The influence on antioxidant homeostasis
    • Erofeev MV, Kieft IE, Sosnin EA, Stoffels E. 2006. UV excimer lamp irradiation of fibroblasts: The influence on antioxidant homeostasis. IEEE T Plasma Sci 34:1359-1364.
    • (2006) IEEE T Plasma Sci , vol.34 , pp. 1359-1364
    • Erofeev, M.V.1    Kieft, I.E.2    Sosnin, E.A.3    Stoffels, E.4
  • 6
    • 83555166090 scopus 로고    scopus 로고
    • Photosensitised oxidation of a water pollutant using sulphonated porphyrin
    • Gmurek M, Miller JS. 2012. Photosensitised oxidation of a water pollutant using sulphonated porphyrin. Chem Pap 66:120-128.
    • (2012) Chem Pap , vol.66 , pp. 120-128
    • Gmurek, M.1    Miller, J.S.2
  • 8
    • 71549117088 scopus 로고    scopus 로고
    • Characterization of the transient species generated in the photoexcitation of benzoic acid, 2-hydroxy-, 2-D-ribofuranosylhydrazide
    • Wang M, Cheng LL, Zhu H, Li K, Wu QS, Yao SD, Wang SL. 2009. Characterization of the transient species generated in the photoexcitation of benzoic acid, 2-hydroxy-, 2-D-ribofuranosylhydrazide. J Photochem Photobiol A 208:104-109.
    • (2009) J Photochem Photobiol A , vol.208 , pp. 104-109
    • Wang, M.1    Cheng, L.L.2    Zhu, H.3    Li, K.4    Wu, Q.S.5    Yao, S.D.6    Wang, S.L.7
  • 12
    • 84904429982 scopus 로고    scopus 로고
    • SWizard program. University of Ottawa, Ottawa, Canada. [cited 2014 March 13]. Available from
    • Gorelsky SI. 2010. SWizard program. University of Ottawa, Ottawa, Canada. [cited 2014 March 13]. Available from: http://www.sg-chem.net/.
    • (2010)
    • Gorelsky, S.I.1
  • 14
    • 84860426892 scopus 로고    scopus 로고
    • Biodegradation and detoxification of bisphenol A with one newly-isolated strain Bacillus sp GZB: Kinetics, mechanism and estrogenic transition
    • Li GY, Zu L, Wong PK, Hui XP, Lu Y, Xiong JK, An TC. 2012. Biodegradation and detoxification of bisphenol A with one newly-isolated strain Bacillus sp GZB: Kinetics, mechanism and estrogenic transition. Bioresource Technol 114:224-230.
    • (2012) Bioresource Technol , vol.114 , pp. 224-230
    • Li, G.Y.1    Zu, L.2    Wong, P.K.3    Hui, X.P.4    Lu, Y.5    Xiong, J.K.6    An, T.C.7
  • 15
    • 78650414975 scopus 로고    scopus 로고
    • Photochemical fate of atorvastatin (lipitor) in simulated natural waters
    • Razavi B, Ben Abdelmelek S, Song W, O'Shea KE, Cooper WJ. 2011. Photochemical fate of atorvastatin (lipitor) in simulated natural waters. Water Res 45:625-631.
    • (2011) Water Res , vol.45 , pp. 625-631
    • Razavi, B.1    Ben Abdelmelek, S.2    Song, W.3    O'Shea, K.E.4    Cooper, W.J.5
  • 16
    • 0037149191 scopus 로고    scopus 로고
    • Balance of the deactivation channels of the first excited singlet state of phenols: Effect of alkyl substitution, sterical hindrance, and solvent polarity
    • Hermann R, Mahalaxmi GR, Jochum T, Naumov S, Brede O. 2002. Balance of the deactivation channels of the first excited singlet state of phenols: Effect of alkyl substitution, sterical hindrance, and solvent polarity. J Phys Chem A 106:2379-2389.
    • (2002) J Phys Chem A , vol.106 , pp. 2379-2389
    • Hermann, R.1    Mahalaxmi, G.R.2    Jochum, T.3    Naumov, S.4    Brede, O.5
  • 19
    • 0034284416 scopus 로고    scopus 로고
    • Comparison of high-performance liquid chromatography and capillary zone electrophoresis for the determination of parabens in a cosmetic product
    • Labat L, Kummer E, Dallet P, Dubost JP. 2000. Comparison of high-performance liquid chromatography and capillary zone electrophoresis for the determination of parabens in a cosmetic product. J Pharmaceut Biomed 23:763-769.
    • (2000) J Pharmaceut Biomed , vol.23 , pp. 763-769
    • Labat, L.1    Kummer, E.2    Dallet, P.3    Dubost, J.P.4
  • 20
    • 0030621215 scopus 로고    scopus 로고
    • Aromatic carbonyl compounds as aqueous-phase photochemical sources of hydrogen peroxide in acidic sulfate aerosols, fogs, and clouds. 1. Non-phenolic methoxybenzaldehydes and methoxyacetophenones with reductants (phenols)
    • Anastasio C, Faust BC, Rao CJ. 1996. Aromatic carbonyl compounds as aqueous-phase photochemical sources of hydrogen peroxide in acidic sulfate aerosols, fogs, and clouds. 1. Non-phenolic methoxybenzaldehydes and methoxyacetophenones with reductants (phenols). Environ Sci Technol 31:218-232.
    • (1996) Environ Sci Technol , vol.31 , pp. 218-232
    • Anastasio, C.1    Faust, B.C.2    Rao, C.J.3
  • 21
    • 34548546614 scopus 로고    scopus 로고
    • Inhibition of humic substances mediated photooxygenation of furfuryl alcohol by 2,4,6-trimethylphenol. Evidence for reactivity of the phenol with humic triplet excited states
    • Halladja S, Ter Halle A, Aguer JP, Boulkamh A, Richard C. 2007. Inhibition of humic substances mediated photooxygenation of furfuryl alcohol by 2, 4, 6-trimethylphenol. Evidence for reactivity of the phenol with humic triplet excited states. Environ Sci Technol 41:6066-6073.
    • (2007) Environ Sci Technol , vol.41 , pp. 6066-6073
    • Halladja, S.1    Ter Halle, A.2    Aguer, J.P.3    Boulkamh, A.4    Richard, C.5
  • 23
    • 13944282536 scopus 로고    scopus 로고
    • Aqueous photochemistry of triclosan: Formation of 2,4-dichlorophenol, 2,8-dichlorodibenzo-p-dioxin, and oligomerization products
    • Latch DE, Packer JL, Stender BL, VanOverbeke J, Arnold WA, McNeill K. 2005. Aqueous photochemistry of triclosan: Formation of 2, 4-dichlorophenol, 2, 8-dichlorodibenzo-p-dioxin, and oligomerization products. Environ Toxicol Chem 24:517-525.
    • (2005) Environ Toxicol Chem , vol.24 , pp. 517-525
    • Latch, D.E.1    Packer, J.L.2    Stender, B.L.3    VanOverbeke, J.4    Arnold, W.A.5    McNeill, K.6
  • 24
    • 0001078755 scopus 로고
    • The photolysis (lambda=254 nm) of tyrosine in aqueous solutions in the absence and presence of oxygen. The reaction of tyrosine with singlet oxygen
    • Jin FM, Leitich J, vonSonntag C. 1995. The photolysis (lambda=254 nm) of tyrosine in aqueous solutions in the absence and presence of oxygen. The reaction of tyrosine with singlet oxygen. J Photochem Photobiol A 92:147-153.
    • (1995) J Photochem Photobiol A , vol.92 , pp. 147-153
    • Jin, F.M.1    Leitich, J.2    vonSonntag, C.3
  • 25
    • 0037107499 scopus 로고    scopus 로고
    • Aqueous photodegradation of polycyclic aromatic hydrocarbons
    • Fasnacht MP, Blough NV. 2002. Aqueous photodegradation of polycyclic aromatic hydrocarbons. Environ Sci Technol 36:4364-4369.
    • (2002) Environ Sci Technol , vol.36 , pp. 4364-4369
    • Fasnacht, M.P.1    Blough, N.V.2
  • 27
    • 77957347770 scopus 로고    scopus 로고
    • Quantum chemical investigation and experimental verification on the aquatic photochemistry of the sunscreen 2-phenylbenzimidazole-5-sulfonic acid
    • Zhang SY, Chen JW, Qiao XL, Ge LK, Cai XY, Na GS. 2010. Quantum chemical investigation and experimental verification on the aquatic photochemistry of the sunscreen 2-phenylbenzimidazole-5-sulfonic acid. Environ Sci Technol 44:7484-7490.
    • (2010) Environ Sci Technol , vol.44 , pp. 7484-7490
    • Zhang, S.Y.1    Chen, J.W.2    Qiao, X.L.3    Ge, L.K.4    Cai, X.Y.5    Na, G.S.6
  • 28
    • 0000553829 scopus 로고
    • Transfer of triplet state energy in fluid solutions. 3. Reversible energy transfer
    • Sandros K. 1964. Transfer of triplet state energy in fluid solutions. 3. Reversible energy transfer. Acta Chem Scand 18:2355-2374.
    • (1964) Acta Chem Scand , vol.18 , pp. 2355-2374
    • Sandros, K.1
  • 29
    • 0032052529 scopus 로고    scopus 로고
    • New trends in photobiology (invited review): Photosensitizing drugs containing the benzophenone chromophore
    • Boscá F, Miranda MA. 1998. New trends in photobiology (invited review): Photosensitizing drugs containing the benzophenone chromophore. J Photochem Photobiol B 43:1-26.
    • (1998) J Photochem Photobiol B , vol.43 , pp. 1-26
    • Boscá, F.1    Miranda, M.A.2
  • 30
    • 0001649158 scopus 로고    scopus 로고
    • Generation, characterization, and deprotonation of phenol radical cations
    • Gadosy TA, Shukla D, Johnston LJ. 1999. Generation, characterization, and deprotonation of phenol radical cations. J Phys Chem A 103:8834-8839.
    • (1999) J Phys Chem A , vol.103 , pp. 8834-8839
    • Gadosy, T.A.1    Shukla, D.2    Johnston, L.J.3
  • 31
    • 0037461696 scopus 로고    scopus 로고
    • Radical-induced oxidative transformation of quinoline
    • Nicolaescu AR, Wiest O, Kamat PV. 2003. Radical-induced oxidative transformation of quinoline. J Phys Chem A 107:427-433.
    • (2003) J Phys Chem A , vol.107 , pp. 427-433
    • Nicolaescu, A.R.1    Wiest, O.2    Kamat, P.V.3
  • 32
    • 78650177681 scopus 로고    scopus 로고
    • In situ photoelectrocatalytic generation of bactericide for instant inactivation and rapid decomposition of Gram-negative bacteria
    • Li GY, Liu XL, Zhang HM, An TC, Zhang SQ, Carroll AR, Zhao HJ. 2011. In situ photoelectrocatalytic generation of bactericide for instant inactivation and rapid decomposition of Gram-negative bacteria. J Catal 277:88-94.
    • (2011) J Catal , vol.277 , pp. 88-94
    • Li, G.Y.1    Liu, X.L.2    Zhang, H.M.3    An, T.C.4    Zhang, S.Q.5    Carroll, A.R.6    Zhao, H.J.7
  • 33
    • 80054993941 scopus 로고    scopus 로고
    • Kinetic effects of increased proton transfer distance on proton-coupled oxidations of phenol-amines
    • Markle TF, Rhile IJ, Mayer JM. 2011. Kinetic effects of increased proton transfer distance on proton-coupled oxidations of phenol-amines. J Am Chem Soc 133:17341-17352.
    • (2011) J Am Chem Soc , vol.133 , pp. 17341-17352
    • Markle, T.F.1    Rhile, I.J.2    Mayer, J.M.3
  • 34
    • 67650531124 scopus 로고    scopus 로고
    • Light-induced oxidation of tryptophan and histidine. Reactivity of aromatic n-heterocycles toward triplet-excited flavins
    • Huvaere K, Skibsted LH. 2009. Light-induced oxidation of tryptophan and histidine. Reactivity of aromatic n-heterocycles toward triplet-excited flavins. J Am Chem Soc 131:8049-8060.
    • (2009) J Am Chem Soc , vol.131 , pp. 8049-8060
    • Huvaere, K.1    Skibsted, L.H.2
  • 35
    • 33845556122 scopus 로고
    • Laser flash-photolysis study of the reactions of carbonyl triplets with phenols and photochemistry of para-hydroxypropiophenone
    • Das PK, Encinas MV, Scaiano JC. 1981. Laser flash-photolysis study of the reactions of carbonyl triplets with phenols and photochemistry of para-hydroxypropiophenone. J Am Chem Soc 103:4154-4162.
    • (1981) J Am Chem Soc , vol.103 , pp. 4154-4162
    • Das, P.K.1    Encinas, M.V.2    Scaiano, J.C.3
  • 36
    • 0001462148 scopus 로고
    • Mechanism of aromatic hydroxylation in the Fenton and related reactions-one-electron oxidation and the NIH shift
    • Kurata T, Watanabe Y, Katoh M, Sawaki Y. 1988. Mechanism of aromatic hydroxylation in the Fenton and related reactions-one-electron oxidation and the NIH shift. J Am Chem Soc 110:7472-7478.
    • (1988) J Am Chem Soc , vol.110 , pp. 7472-7478
    • Kurata, T.1    Watanabe, Y.2    Katoh, M.3    Sawaki, Y.4
  • 37
    • 0347812894 scopus 로고    scopus 로고
    • Mechanisms of the aqueous photodegradation of polycyclic aromatic hydrocarbons
    • Fasnacht MP, Blough NV. 2003. Mechanisms of the aqueous photodegradation of polycyclic aromatic hydrocarbons. Environ Sci Technol 37:5767-5772.
    • (2003) Environ Sci Technol , vol.37 , pp. 5767-5772
    • Fasnacht, M.P.1    Blough, N.V.2
  • 38
    • 43049128918 scopus 로고    scopus 로고
    • Photocatalytic degradation of non-steroidal anti-inflammatory drugs with TiO2 and simulated solar irradiation
    • Mendez-Arriaga F, Esplugas S, Gimenez J. 2008. Photocatalytic degradation of non-steroidal anti-inflammatory drugs with TiO2 and simulated solar irradiation. Water Res 42:585-594.
    • (2008) Water Res , vol.42 , pp. 585-594
    • Mendez-Arriaga, F.1    Esplugas, S.2    Gimenez, J.3
  • 39
    • 17044392658 scopus 로고    scopus 로고
    • Safety assessment of esters of p-hydroxybenzoic acid (parabens)
    • Soni MG, Carabin IG, Burdock GA. 2005. Safety assessment of esters of p-hydroxybenzoic acid (parabens). Food Chem Toxicol 43:985-1015.
    • (2005) Food Chem Toxicol , vol.43 , pp. 985-1015
    • Soni, M.G.1    Carabin, I.G.2    Burdock, G.A.3


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