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新型放射增敏剂Ro 03-8799在人体中的药代动力学。

The pharmacokinetics of a new radiosensitiser, Ro 03-8799 in humans.

作者信息

Allen J G, Dische S, Lenox-Smith I, Malcolm S L, Saunders M I

出版信息

Eur J Clin Pharmacol. 1984;27(4):483-9. doi: 10.1007/BF00549599.

Abstract

A new hypoxic cell radiosensitiser, Ro 03-8799 has been administered intravenously to human volunteers and its kinetic parameters derived from plasma and urine data. Good penetration of drug into tumour tissue is found, consistent with its large volume of distribution. The plasma clearance of this compound is rapid due to high metabolic and renal clearances. These parameters combine to produce an elimination half-life of 5.6 h, approximately half that of misonidazole, a well studied radiosensitiser. It is hoped that this decrease in total body exposure will also reduce the cumulative toxicity seen when misonidazole is administered repeatedly.

摘要

一种新型低氧细胞放射增敏剂Ro 03-8799已通过静脉注射给予人类志愿者,并根据血浆和尿液数据得出其动力学参数。发现该药物对肿瘤组织有良好的穿透性,这与其较大的分布容积一致。由于高代谢清除率和肾清除率,该化合物的血浆清除迅速。这些参数共同作用产生了5.6小时的消除半衰期,约为已得到充分研究的放射增敏剂米索硝唑半衰期的一半。人们希望全身暴露的这种降低也将减少重复给予米索硝唑时所见的累积毒性。

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