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In Vitro Study of the Enzymatic and Nonenzymatic Conjugation of Treosulfan with Glutathione

机译:硫磷与谷胱甘肽的酶促和非酶促结合的体外研究

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摘要

Background and ObjectivesTreosulfan (dihydroxybusulfan), licensed for the treatment of ovarian carcinoma, is investigated in clinical trials as a myeloablative agent for conditioning prior to hematopoietic stem cell transplantation. Clinical experience shows that treosulfan exhibits lower organ toxicity than busulfan, including hepatotoxicity. Elimination of busulfan primarily via enzymatic conjugation with glutathione (GSH) in the liver is considered to be the main cause of the drug’s hepatotoxicity and interpatient clearance variability. It is believed that treosulfan undergoes no hepatic metabolism but empirical evidence is lacking. The aim of this kinetic study was to verify if treosulfan is capable of conjugating with GSH.
机译:背景和目的在临床试验中已研究了用于治疗卵巢癌的获许可的硫丹(dihydroxybusulfan),作为一种造血干细胞移植前的调理清髓剂。临床经验表明,硫代硫丹比白硫丹具有更低的器官毒性,包括肝毒性。主要通过肝脏中谷胱甘肽(GSH)的酶促结合消除白消安被认为是该药物肝毒性和患者间清除率差异的主要原因。据认为,硫丹没有肝代谢,但缺乏经验证据。该动力学研究的目的是验证硫代硫丹是否能够与GSH结合。

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