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采用液相色谱法研究吉西他滨和2',2'-二氟脱氧尿苷在人血浆中的药代动力学。

Investigation of the pharmacokinetics of gemcitabine and 2',2'-difluorodeoxyuridine in human plasma by liquid chromatography.

作者信息

Yilmaz Bilal, Kadioğlu Yücel Yaşar, Aksoy Yilmaz

机构信息

Department of Analytical Chemistry, Faculty of Pharmacy, Atatürk University, 25240, Erzurum, Turkey.

出版信息

Anal Biochem. 2004 Sep 15;332(2):234-7. doi: 10.1016/j.ab.2004.05.059.

Abstract

Gemcitabine (2',2'-difluorodeoxycytidine, dFdC) is a difluorine-substituted deoxycytidine analogue that has demonstrated antitumor activity against solid tumors. The pharmacokinetics of dFdC and its metabolite, 2',2'-difluorodeoxyuridine (dFdU) have been studied; however, their disposition has never been evaluated in a patient with bladder cancer. A patient with bladder cancer was treated with dFdC 1000 mg/m(2) over a 30min period. The patient received a dFdC infusion once per week for 3 weeks followed by a rest week. Serial plasma samples were obtained prior to, during, and after completion of the infusion for determination of dFdC and dFdU concentrations. dFdC and dFdU concentrations were measured using normal-phase high-performance liquid chromatography and one-compartment open model methods. Maximum plasma concentrations (C(max)) and area under the plasma concentration-time curve for dFdC and dFdU were 24.5 microg/ml and 11200 microg/Lh, 49.1 microg/ml and 272,800 microg/Lh, respectively.

摘要

吉西他滨(2',2'-二氟脱氧胞苷,dFdC)是一种二氟取代的脱氧胞苷类似物,已显示出对实体瘤的抗肿瘤活性。已对dFdC及其代谢产物2',2'-二氟脱氧尿苷(dFdU)的药代动力学进行了研究;然而,从未在膀胱癌患者中评估过它们的处置情况。一名膀胱癌患者在30分钟内接受了1000 mg/m(2)的dFdC治疗。该患者每周接受一次dFdC输注,共3周,随后休息1周。在输注前、输注期间和输注完成后采集系列血浆样本,以测定dFdC和dFdU浓度。使用正相高效液相色谱法和一室开放模型方法测量dFdC和dFdU浓度。dFdC和dFdU的最大血浆浓度(C(max))以及血浆浓度-时间曲线下面积分别为24.5μg/ml和11200μg/Lh、49.1μg/ml和272,800μg/Lh。

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