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磺酰胺类口服降糖药和利尿剂的光降解产物在体外无光毒性。

Photodegradation products of sulphonamide-derived oral antidiabetics and diuretics are not phototoxic in vitro.

作者信息

Selvaag E, Thune P

机构信息

Department of Dermatology, Ullevaal Hospital, University of Oslo, Norway.

出版信息

Photodermatol Photoimmunol Photomed. 1996 Apr;12(2):79-83. doi: 10.1111/j.1600-0781.1996.tb00179.x.

DOI:10.1111/j.1600-0781.1996.tb00179.x
PMID:8897593
Abstract

The oral antidiabetics glibenclamide and glipizide, and the diuretics bendroflumethiazide and furosemide, all sulphonamide derived drugs, were investigated in vitro for phototoxic properties. Irradiation with broad-band UV induced phototoxic inhibition of colony forming ability in cell cultures. During irradiation, the substances lost one absorption maximum in the UVA region, demonstrated by UV spectroscopy. These findings correlate well with the UV applied, the action spectrum being in the UVA region. Photoproducts detected during and after irradiation showed a decomposition of the substances due to ionization and fragmentation. Incubation of these preirradiated drugs with the cell cultures revealed no phototoxic effects.

摘要

对口服抗糖尿病药物格列本脲和格列吡嗪以及利尿剂苄氟噻嗪和呋塞米这几种均为磺酰胺衍生药物进行了体外光毒性特性研究。用宽带紫外线照射可诱导细胞培养物中集落形成能力的光毒性抑制。在照射过程中,通过紫外光谱法证明这些物质在UVA区域失去了一个吸收最大值。这些发现与所施加的紫外线密切相关,作用光谱在UVA区域。照射期间和照射后检测到的光产物显示出这些物质因电离和碎片化而分解。将这些预先照射过的药物与细胞培养物一起孵育未显示出光毒性作用。

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Photodegradation products of sulphonamide-derived oral antidiabetics and diuretics are not phototoxic in vitro.磺酰胺类口服降糖药和利尿剂的光降解产物在体外无光毒性。
Photodermatol Photoimmunol Photomed. 1996 Apr;12(2):79-83. doi: 10.1111/j.1600-0781.1996.tb00179.x.
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Phototoxicity to diuretics and antidiabetics in the cultured keratinocyte cell line HaCaT: evaluation by clonogenic assay and single cell gel electrophoresis Comet assay).培养的角质形成细胞系HaCaT对利尿剂和抗糖尿病药物的光毒性:通过克隆形成试验和单细胞凝胶电泳彗星试验进行评估
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Photodegradation and phototoxicity studies of furosemide. Involvement of singlet oxygen in the photoinduced hemolysis and lipid peroxidation.呋塞米的光降解和光毒性研究。单线态氧在光诱导溶血和脂质过氧化中的作用。
J Photochem Photobiol B. 1998 Mar;42(3):219-25. doi: 10.1016/s1011-1344(98)00074-8.

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