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辐射增效剂SR 4233(WIN 59075)每日给小鼠给药的毒理学

Toxicology of daily administration to mice of the radiation potentiator SR 4233 (WIN 59075).

作者信息

Spiegel J F, Spear M A, Brown J M

机构信息

Department of Radiation Oncology, Stanford University School of Medicine, CA 94305-5468.

出版信息

Radiother Oncol. 1993 Jan;26(1):79-81. doi: 10.1016/0167-8140(93)90031-3.

DOI:10.1016/0167-8140(93)90031-3
PMID:8438092
Abstract

We have investigated the feasibility of administration of an effective dose of the hypoxic cytotoxin, SR 4233, Monday-Friday daily for 6 weeks. From a thorough hematological, histopathological and clinical chemistry evaluation throughout the course and during a 3-week recovery period, we conclude that daily administration of a radiopotentiating dose of SR 4233 in mice is well tolerated and that bone marrow suppression is likely to be the dose-limiting toxicity.

摘要

我们研究了在周一至周五每天给予有效剂量的低氧细胞毒素SR 4233,持续6周的可行性。通过在整个疗程以及3周恢复期内进行全面的血液学、组织病理学和临床化学评估,我们得出结论,在小鼠中每日给予放射增敏剂量的SR 4233耐受性良好,骨髓抑制可能是剂量限制性毒性。

相似文献

1
Toxicology of daily administration to mice of the radiation potentiator SR 4233 (WIN 59075).辐射增效剂SR 4233(WIN 59075)每日给小鼠给药的毒理学
Radiother Oncol. 1993 Jan;26(1):79-81. doi: 10.1016/0167-8140(93)90031-3.
2
Phase I trial of the hypoxic cell cytotoxin tirapazamine with concurrent radiation therapy in the treatment of refractory solid tumors.
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Assessment of micronucleus induction in SCCVII cells treated with bioreductive agents, WIN 59075 (SR 4233) and mitomycin C, under aerobic and hypoxic conditions.在有氧和缺氧条件下,评估用生物还原药物WIN 59075(SR 4233)和丝裂霉素C处理的SCCVII细胞中的微核诱导情况。
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[Evaluation of the toxicity of tirapazamine plus cisplatin in a mouse tumor model].[替拉扎明联合顺铂在小鼠肿瘤模型中的毒性评估]
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Comparison of the enhancement of tumor responses to fractionated irradiation by SR 4233 (tirapazamine) and by nicotinamide with carbogen.比较SR 4233(替拉扎明)和烟酰胺联合碳合气对分次照射肿瘤反应增强作用的研究。
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Muscle cramping in phase I clinical trials of tirapazamine (SR 4233) with and without radiation.在有或无放疗情况下进行的替拉扎明(SR 4233)一期临床试验中的肌肉痉挛。
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Acute lesions in rats caused by 3-amino-1,2,4-benzotriazine-1,4-dioxide (SR 4233) or nitromin: a comparison with rates of reduction in microsomal systems from target organs.3-氨基-1,2,4-苯并三嗪-1,4-二氧化物(SR 4233)或硝米芬在大鼠体内引起的急性损伤:与靶器官微粒体系统的还原率比较
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引用本文的文献

1
The effect of tirapazamine (SR-4233) alone or combined with chemotherapeutic agents on xenografted human tumours.替拉扎明(SR-4233)单独或与化疗药物联合应用对人异种移植肿瘤的作用。
Br J Cancer. 1996 Jun;73(12):1480-5. doi: 10.1038/bjc.1996.280.
2
SR 4233 (tirapazamine): a new anticancer drug exploiting hypoxia in solid tumours.SR 4233(替拉扎明):一种利用实体瘤缺氧特性的新型抗癌药物。
Br J Cancer. 1993 Jun;67(6):1163-70. doi: 10.1038/bjc.1993.220.