Studies on the photostability and in vitro phototoxicity of Labetalol

被引:30
作者
Andrisano, V
Ballardini, R
Hrelia, P
Cameli, N
Tosti, A
Gotti, R
Cavrini, V
机构
[1] Univ Bologna, Dipartimento Sci Farmaceut, I-40126 Bologna, Italy
[2] CNR, Ist FRAE, I-40129 Bologna, Italy
[3] Univ Bologna, Dipartimento Farmacol, I-40126 Bologna, Italy
[4] Univ Bologna, Dermatol Clin, I-40126 Bologna, Italy
关键词
labetalol; photostability; phototoxicity; photomutagenicity; photoproducts; UVA-UVB radiation;
D O I
10.1016/S0928-0987(00)00218-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The purpose of this study was to obtain information on the photochemical and phototoxic properties of Labetalol, a beta-blocker drug. Preliminary information on the drug photoreactivity was achieved using a flow system with a photochemical reactor on-line with a diode array detection system. Photophysical and photochemical investigations on the drug were performed in aqueous solutions at different pH values using spectrophotometric and fluorimetric methods; the photodegradation quantum yield was found to be 2.7x10(-3) at pH 5.8 and 1.5x10(-2) at pH 11.5. Forced photodegradation of labetalol solutions under exposure to UVA-UVB radiations (xenon are lamp) was monitored by reversed-phase liquid chromatography. The main photodegradation products were isolated and characterized by NMR and mass spectrometry; labetalol was found to give 3-amino-1-phenylbutane and salicylamide-4-carboxaldehyde as the main photoproducts. Preliminary phototoxic testings on human keratinocyte cultures were performed evaluating the viability of the cells by the neutral-red uptake assay; mutagenic and photomutagenicity tests were also carried out based on Salmonella typhimurium strains. As a result, labetalol was found to be photolabile, mainly in alkaline medium, but evidences of significant phototoxic and photomutagenic effects by the drug were not observed. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:495 / 504
页数:10
相关论文
共 29 条
[1]  
ALBINI A, 1998, DRUGS PHOTOCHEMISTRY, P1
[2]   Photodegradation studies on Atenolol by liquid chromatography [J].
Andrisano, V ;
Gotti, R ;
Leoni, A ;
Cavrini, V .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1999, 21 (04) :851-857
[3]  
[Anonymous], 1997, ADV DRUG RES, DOI [DOI 10.1016/S0065-2490(97)80014-7, 10.1016/S0065-2490(97)80014-7]
[4]  
[Anonymous], 1998, DRUGS PHOTOCHEMISTRY, DOI DOI 10.1039/9781847550712-00247
[5]   Use of dermal equivalent and skin equivalent models for identifying phototoxic compounds in vitro [J].
Augustin, C ;
Collombel, C ;
Damour, O .
PHOTODERMATOLOGY PHOTOIMMUNOLOGY & PHOTOMEDICINE, 1997, 13 (1-2) :27-36
[6]  
CHATENAT A, 1993, MUTAT RES, V292, P241
[7]   The use of human keratinocytes in the EU/COLIPA international in vitro phototoxicity test validation study and the ECVAM/COLIPA study on UV filter chemicals [J].
Clothier, R ;
Willshaw, A ;
Cox, H ;
Garle, M ;
Bowler, H ;
Combes, R .
ATLA-ALTERNATIVES TO LABORATORY ANIMALS, 1999, 27 (02) :247-259
[8]   EPISKIN - AN IN-VITRO MODEL FOR THE EVALUATION OF PHOTOTOXICITY AND SUNSCREEN PHOTOPROTECTIVE PROPERTIES [J].
COHEN, C ;
DOSSOU, KG ;
ROUGIER, A ;
ROGUET, R .
TOXICOLOGY IN VITRO, 1994, 8 (04) :669-671
[9]   FLUORESCENCE YIELDS OF AROMATIC COMPOUNDS [J].
DAWSON, WR ;
WINDSOR, MW .
JOURNAL OF PHYSICAL CHEMISTRY, 1968, 72 (09) :3251-&
[10]   DEVELOPMENT OF ASSAYS FOR THE DETECTION OF PHOTOMUTAGENICITY OF CHEMICALS DURING EXPOSURE TO UV-LIGHT .1. ASSAY DEVELOPMENT [J].
DEAN, SW ;
LANE, M ;
DUNMORE, RH ;
RUDDOCK, SP ;
MARTIN, CN ;
KIRKLAND, DJ ;
LOPRIENO, N .
MUTAGENESIS, 1991, 6 (05) :335-341