Evaluation of UV-radiation induced singlet oxygen generation potential of selected drugs

被引:11
作者
Pandey, R
Mehrotra, S [1 ]
Ray, RS
Joshi, PC
Hans, RK
机构
[1] Dr RML Avadh Univ, Dept Biochem, Faizabad 224001, Uttar Pradesh, India
[2] Ind Toxicol Res Ctr, Photobiol Div, Lucknow 226001, Uttar Pradesh, India
[3] Rensselaer Polytech Inst, Dept Chem, Cogswell Lab, Troy, NY 12180 USA
关键词
ultraviolet radiation; singlet oxygen; drugs; quenchers;
D O I
10.1081/DCT-120003261
中图分类号
O6 [化学];
学科分类号
0703 [化学];
摘要
Photosensitization reaction of drugs leading to the formation of reactive oxygen species under ultraviolet radiation (UVR) can cause tissue injury, resulting in damage to various cellular macromolecules. The aim of this study was to determine the singlet oxygen generation potential of some commonly used antibiotics so that due precautions can be exercised to minimize their photosensitizing action and oxidative stress potential. The selected antibiotics were examined for their ability to produce singlet oxygen (O-1(2)) under artificial UVA (320-400 nm). Singlet oxygen generation of various screened antibiotics under UVA is of the following order:Nalidixic acid > Amphotericin-B > Cephradine > Cefazolin > Nafcillin > Cephalothin > Ampicillin > Cephalexin > Puromycin > Kanamycin > Lincomycin > Tetracycline > Nystatin > Gentamicin sulphate. Nalidixic acid, the most potent generator of O-1(2) among the screened antibiotics, was selected to carry out further studies. Certain specific quenchers Of O-1(2) such as P-carotene, 1,4-diazabicyclo[2.2.2] octane (DABCO), and sodium azide (NaN3) accorded significant inhibition in the production of O-1(2). The results suggest that precautions are necessary to avoid ultraviolet radiation after the intake of photoreactive drugs, especially in tropical countries such as India. These findings are significant because UVB radiation is reportedly increasing on earth surface in part due to depletion of stratospheric ozone layer. The selected drugs are commonly used for the treatment of various diseases. Thus. the synergistic action of both can lead to undesirable phototoxic responses.
引用
收藏
页码:215 / 225
页数:11
相关论文
共 45 条
[1]
Effect of pyridone carboxylic acid anti-microbials on the generation of reactive oxygen species in vitro [J].
Akamatsu, H ;
Niwa, Y ;
Sasaki, H ;
Matoba, Y ;
Asada, Y ;
Horio, T .
JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, 1996, 24 (04) :345-351
[2]
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
[3]
FOOTE CS, 1972, TETRAHEDRON LETT, P45
[4]
CROSS-LINKING OF LENS CRYSTALLINS IN A PHOTODYNAMIC SYSTEM - A PROCESS MEDIATED BY SINGLET OXYGEN [J].
GOOSEY, JD ;
ZIGLER, JS ;
KINOSHITA, JH .
SCIENCE, 1980, 208 (4449) :1278-1280
[5]
PHOTOSENSITIZED DEGRADATION OF DNA BY DAUNOMYCIN [J].
GRAY, PJ ;
PHILLIPS, DR ;
WEDD, AG .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1982, 36 (01) :49-57
[6]
Light-dependent generation of reactive oxygen species in cell culture media [J].
Grzelak, A ;
Rychlik, B ;
Baptosz, G .
FREE RADICAL BIOLOGY AND MEDICINE, 2001, 30 (12) :1418-1425
[7]
HARBER LC, 1989, PHOTOSENSITIVITY DIS, P169
[8]
HARBER LC, 1989, PHOTOSENSITIVITY DIS, P160
[9]
HASAN T, 1984, J INVEST DERMATOL, V83, P1793
[10]
THE ROLE OF ACTIVE OXYGEN (O-1(2) AND O-2.-) INDUCED BY CRUDE COAL-TAR AND ITS INGREDIENTS USED IN PHOTOCHEMOTHERAPY OF SKIN DISEASES [J].
JOSHI, PC ;
PATHAK, MA .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1984, 82 (01) :67-73