Photochemistry of dihydrobiopterin in aqueous solution
Dihydrobiopterin (H2Bip) and its oxidized analogue, biopterin (Bip), accumulate in the skin of patients suffering from vitiligo, a chronic depigmentation disorder in which the protection against UV radiation fails. The photochemistry of H2Bip was studied in neutral aqueous solutions upon UV-A irradi...
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2010
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| Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_14770520_v8_n4_p800_Vignoni http://hdl.handle.net/20.500.12110/paper_14770520_v8_n4_p800_Vignoni |
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paper:paper_14770520_v8_n4_p800_Vignoni2023-06-08T16:18:07Z Photochemistry of dihydrobiopterin in aqueous solution Anaerobic conditions Aqueous solutions Autocatalytic Biological implications Biopterin Electrospray ionization mass spectrometry Enzymatic methods Irradiation time Neutral aqueous solution Oxidation of H Photochemical process Photodimerization Photoproducts Room temperature Singlet excited state UV radiation UV/vis spectrophotometry Dimers Electrospray ionization Excited states Hydrogels Hydrogen peroxide Irradiation Mass spectrometry Molecular mass Oxidation Radiation protection Solutions Ultraviolet radiation Photochemical reactions 7,8-dihydrobiopterin biopterin dihydrobiopterin drug derivative hydrogen peroxide oxygen water article chemistry high performance liquid chromatography human methodology oxidation reduction reaction photochemistry solution and solubility ultraviolet spectrophotometry Biopterin Chromatography, High Pressure Liquid Humans Hydrogen Peroxide Oxidation-Reduction Oxygen Pharmaceutical Solutions Photochemistry Solutions Spectrophotometry, Ultraviolet Water Dihydrobiopterin (H2Bip) and its oxidized analogue, biopterin (Bip), accumulate in the skin of patients suffering from vitiligo, a chronic depigmentation disorder in which the protection against UV radiation fails. The photochemistry of H2Bip was studied in neutral aqueous solutions upon UV-A irradiation (320-400 nm) at room temperature. The photochemical reactions were followed by UV/vis spectrophotometry, HPLC and enzymatic methods for hydrogen peroxide (H2O2) determination. Photoproducts were analyzed by means of electrospray ionization mass spectrometry. Under anaerobic conditions, excitation of H2Bip leads to the formation of at least two isomeric dimers with molecular masses equal to exactly twice the molecular mass of the reactant. This reaction takes place from the singlet excited state of the reactant. To the best of our knowledge, this is the first time that the photodimerization of a dihydropterin is reported. In the presence of air, the dimers are again the main photoproducts at the beginning of the reaction, but a small proportion of the reactant is converted into Bip. As the reaction proceeds and enough Bip accumulates in the solution, a photosensitized process starts, where Bip photoinduces the oxidation of H2Bip to Bip, and H 2O2 is formed. As a consequence, the rates of H 2Bip consumption and Bip formation increase as a function of irradiation time, resulting in an autocatalytic photochemical process. In this process, Bip in its triplet excited state reacts with the ground state of H 2Bip. The mechanisms involved are analyzed and the biological implications of the results are discussed. © The Royal Society of Chemistry 2010. 2010 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_14770520_v8_n4_p800_Vignoni http://hdl.handle.net/20.500.12110/paper_14770520_v8_n4_p800_Vignoni |
| institution |
Universidad de Buenos Aires |
| institution_str |
I-28 |
| repository_str |
R-134 |
| collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
| topic |
Anaerobic conditions Aqueous solutions Autocatalytic Biological implications Biopterin Electrospray ionization mass spectrometry Enzymatic methods Irradiation time Neutral aqueous solution Oxidation of H Photochemical process Photodimerization Photoproducts Room temperature Singlet excited state UV radiation UV/vis spectrophotometry Dimers Electrospray ionization Excited states Hydrogels Hydrogen peroxide Irradiation Mass spectrometry Molecular mass Oxidation Radiation protection Solutions Ultraviolet radiation Photochemical reactions 7,8-dihydrobiopterin biopterin dihydrobiopterin drug derivative hydrogen peroxide oxygen water article chemistry high performance liquid chromatography human methodology oxidation reduction reaction photochemistry solution and solubility ultraviolet spectrophotometry Biopterin Chromatography, High Pressure Liquid Humans Hydrogen Peroxide Oxidation-Reduction Oxygen Pharmaceutical Solutions Photochemistry Solutions Spectrophotometry, Ultraviolet Water |
| spellingShingle |
Anaerobic conditions Aqueous solutions Autocatalytic Biological implications Biopterin Electrospray ionization mass spectrometry Enzymatic methods Irradiation time Neutral aqueous solution Oxidation of H Photochemical process Photodimerization Photoproducts Room temperature Singlet excited state UV radiation UV/vis spectrophotometry Dimers Electrospray ionization Excited states Hydrogels Hydrogen peroxide Irradiation Mass spectrometry Molecular mass Oxidation Radiation protection Solutions Ultraviolet radiation Photochemical reactions 7,8-dihydrobiopterin biopterin dihydrobiopterin drug derivative hydrogen peroxide oxygen water article chemistry high performance liquid chromatography human methodology oxidation reduction reaction photochemistry solution and solubility ultraviolet spectrophotometry Biopterin Chromatography, High Pressure Liquid Humans Hydrogen Peroxide Oxidation-Reduction Oxygen Pharmaceutical Solutions Photochemistry Solutions Spectrophotometry, Ultraviolet Water Photochemistry of dihydrobiopterin in aqueous solution |
| topic_facet |
Anaerobic conditions Aqueous solutions Autocatalytic Biological implications Biopterin Electrospray ionization mass spectrometry Enzymatic methods Irradiation time Neutral aqueous solution Oxidation of H Photochemical process Photodimerization Photoproducts Room temperature Singlet excited state UV radiation UV/vis spectrophotometry Dimers Electrospray ionization Excited states Hydrogels Hydrogen peroxide Irradiation Mass spectrometry Molecular mass Oxidation Radiation protection Solutions Ultraviolet radiation Photochemical reactions 7,8-dihydrobiopterin biopterin dihydrobiopterin drug derivative hydrogen peroxide oxygen water article chemistry high performance liquid chromatography human methodology oxidation reduction reaction photochemistry solution and solubility ultraviolet spectrophotometry Biopterin Chromatography, High Pressure Liquid Humans Hydrogen Peroxide Oxidation-Reduction Oxygen Pharmaceutical Solutions Photochemistry Solutions Spectrophotometry, Ultraviolet Water |
| description |
Dihydrobiopterin (H2Bip) and its oxidized analogue, biopterin (Bip), accumulate in the skin of patients suffering from vitiligo, a chronic depigmentation disorder in which the protection against UV radiation fails. The photochemistry of H2Bip was studied in neutral aqueous solutions upon UV-A irradiation (320-400 nm) at room temperature. The photochemical reactions were followed by UV/vis spectrophotometry, HPLC and enzymatic methods for hydrogen peroxide (H2O2) determination. Photoproducts were analyzed by means of electrospray ionization mass spectrometry. Under anaerobic conditions, excitation of H2Bip leads to the formation of at least two isomeric dimers with molecular masses equal to exactly twice the molecular mass of the reactant. This reaction takes place from the singlet excited state of the reactant. To the best of our knowledge, this is the first time that the photodimerization of a dihydropterin is reported. In the presence of air, the dimers are again the main photoproducts at the beginning of the reaction, but a small proportion of the reactant is converted into Bip. As the reaction proceeds and enough Bip accumulates in the solution, a photosensitized process starts, where Bip photoinduces the oxidation of H2Bip to Bip, and H 2O2 is formed. As a consequence, the rates of H 2Bip consumption and Bip formation increase as a function of irradiation time, resulting in an autocatalytic photochemical process. In this process, Bip in its triplet excited state reacts with the ground state of H 2Bip. The mechanisms involved are analyzed and the biological implications of the results are discussed. © The Royal Society of Chemistry 2010. |
| title |
Photochemistry of dihydrobiopterin in aqueous solution |
| title_short |
Photochemistry of dihydrobiopterin in aqueous solution |
| title_full |
Photochemistry of dihydrobiopterin in aqueous solution |
| title_fullStr |
Photochemistry of dihydrobiopterin in aqueous solution |
| title_full_unstemmed |
Photochemistry of dihydrobiopterin in aqueous solution |
| title_sort |
photochemistry of dihydrobiopterin in aqueous solution |
| publishDate |
2010 |
| url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_14770520_v8_n4_p800_Vignoni http://hdl.handle.net/20.500.12110/paper_14770520_v8_n4_p800_Vignoni |
| _version_ |
1768543150012366848 |