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尿中葡萄糖醛酸测量的意义及其在紫杉醇治疗中的应用。

Significance of urinary glucaric acid measurement and its application to paclitaxel therapy.

作者信息

Morimoto Shigefumi, Koda Toshiki, Suidzu Tomoki, Uranishi Ryunosuke, Shono Yoshiharu, Akiyama Isao, Shimizu Kumiyo, Fujita Yoshikazu, Hasegawa Kenji, Tabuse Katsuyoshi

机构信息

Dept. of Pharmacy, Osaka Minami Medical Center, National Hospital Organization.

出版信息

Gan To Kagaku Ryoho. 2009 Nov;36(11):1857-61.

Abstract

Individual variations in P-450 activity affect the in vivo pharmacokinetics as well as the efficacy and side effect of drugs. It is proposed that urinary glucaric acid (GA) level may indirectly represent P-450 activity and may therefore be an indicator of P- 450 activity in the clinical setting. However, no standard method has been developed so far. Metabolism of paclitaxel (PTX), an anticancer drug, is mediated by P-450. If P-450 activity could be predicted by measuring urinary GA level during PTX administration and individual blood PTX concentration could be inferred, urinary GA level would be a potent tool to predict the efficacy and side effects of the drug. We therefore measured the urinary GA levels of patients on antiepileptics that are suggested to induce P-450 and those of control subjects, to determine whether urinary GA level could be an indicator of P-450 activity. Then, we examined the relationship between urinary GA level and blood PTX concentration and looked into the possibility of predicting pharmacokinetics based on the relationship between urinary GA level and area under the blood concentration-time curve (AUC). The means+/-S. D. of urinary [(GA level)/(Cr level) x 10] levels of 16 patients on antiepileptic medication and 24 control subjects were 0. 98 mg/mL+/-0. 91 and 0. 19 mg/mL+/-0. 07, respectively. The urinary GA levels of patients on antiepileptic medication were significantly higher than those of control subjects. On the other hand, the relationship between AUC and urinary GA levels in eight patients on PTX showed that AUC tended to become large when urinary GA levels were low. The above results reveal that measuring urinary GA level by the easy and noninvasive way of urine collection would enable us to predict P-450 activity and infer blood PTX concentration.

摘要

细胞色素P - 450活性的个体差异会影响药物的体内药代动力学以及疗效和副作用。有人提出,尿中葡萄糖醛酸(GA)水平可能间接反映细胞色素P - 450活性,因此可能是临床环境中细胞色素P - 450活性的一个指标。然而,目前尚未开发出标准方法。抗癌药物紫杉醇(PTX)的代谢由细胞色素P - 450介导。如果在PTX给药期间通过测量尿GA水平能够预测细胞色素P - 450活性,并能推断个体血液中PTX浓度,那么尿GA水平将成为预测该药物疗效和副作用的有力工具。因此,我们测量了服用被认为可诱导细胞色素P - 450的抗癫痫药物的患者以及对照受试者的尿GA水平,以确定尿GA水平是否可以作为细胞色素P - 450活性的指标。然后,我们研究了尿GA水平与血液PTX浓度之间的关系,并探讨了基于尿GA水平与血药浓度 - 时间曲线下面积(AUC)之间的关系预测药代动力学的可能性。16例服用抗癫痫药物的患者和24例对照受试者的尿[(GA水平)/(肌酐水平)×10]水平的均值±标准差分别为0.98 mg/mL±0.91和0.19 mg/mL±0.07。服用抗癫痫药物患者的尿GA水平显著高于对照受试者。另一方面,8例接受PTX治疗患者的AUC与尿GA水平之间的关系表明,当尿GA水平较低时,AUC往往会变大。上述结果表明,通过简单且无创的尿液收集方式测量尿GA水平,能够使我们预测细胞色素P - 450活性并推断血液PTX浓度。

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