血卟啉衍生物对培养的人角质形成细胞的光动力毒性。

Molecular toxicology Pub Date : 1987-09-01
H Kappus, C Reinhold, M Artuc
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引用次数: 0

摘要

培养的人角质形成细胞能够吸收用于肿瘤光动力化疗的血卟啉衍生物(HPDs)。在没有光线的情况下,HPDs对角质形成细胞没有细胞毒性作用。然而,在可见光照射后,通过中性红色摄取测定,HPDs诱导了立即的细胞毒性。另一方面,通过蛋白质估计测量的细胞附着不受影响。当细胞用HPDs处理和光照射后,再培养72小时,它们部分失去了附着在胶原蛋白表面的能力。在HPDs和光照作用下,72 h后仍附着的大部分细胞不再存活。所有测量的参数取决于所用HPDs的细胞内浓度(7-50 ng/10(5)个细胞)和照射时间(0-30 min)。这些结果表明,人角质形成细胞是研究光动力活性药物细胞毒性作用的良好模型。此外,角化细胞在HPDs和光照造成的损伤后无法恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Photodynamic toxicity of hematoporphyrin derivatives to human keratinocytes in culture.

Human keratinocytes in culture were able to take up hematoporphyrin derivatives (HPDs) used during photodynamic chemotherapy of tumors. In the absence of light, HPDs showed no cytotoxic effects to keratinocytes. However, after irradiation with visible light, HPDs induced immediate cytotoxicity as measured by the neutral red uptake assay. On the other hand, cell attachment as measured by protein estimation was not affected. When the cells treated with HPDs and irradiated with light were cultured for a further 72 h, they partially lost their ability to attach to the collagen surface. Most of the cells remaining attached after 72 h were no longer viable following treatment with HPDs and light. All parameters measured depended on the intracellular concentration of HPDs used (7-50 ng/10(5) cells) and the time of irradiation (0-30 min). These results suggest that human keratinocytes are a good model to study cytotoxic effects of photodynamically active drugs. Further, keratinocytes were unable to recover after damage caused by HPDs and light.

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