首页> 美国卫生研究院文献>Journal of Young Pharmacists : JYP >Estimation of plasma levels of warfarin and 7-hydroxy warfarin by high performance liquid chromatography in patients receiving warfarin therapy
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Estimation of plasma levels of warfarin and 7-hydroxy warfarin by high performance liquid chromatography in patients receiving warfarin therapy

机译:高效液相色谱法评估接受华法林治疗的患者的华法林和7-羟基华法林的血浆水平

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摘要

Warfarin is one of the most commonly prescribed oral anticoagulant for prevention of thromboembolic events. The effect of this drug is measured by monitoring prothrombin time expressed as International Normalized Ratio (INR). In some cases, however, the measurement of plasma concentration of warfarin was emphasized. In the present study, reversed phase high performance liquid chromatography (HPLC) was used to estimate the plasma drug levels. A total of 185 patients were enrolled in this study. Five milliliter of venous blood was collected using sodium EDTA tubes for pharmacokinetic analysis. Solid phase extraction was used to recover the warfarin and it's metabolite from plasma using isopropanol and potassium phosphate buffer (40:60) mobile phase. Warfarin, 7-hydroxy warfarin and carbamazepine (internal standard) were separated on a C18 column and had the retention time 3.6 min, 2.9 min and 5.9 min, respectively. The assay was linear in warfarin concentration ranges of 0.1–5 μg/ml. The extraction recovery was found to be ≃85%. The mean plasma concentrations of warfarin and 7-hydroxy warfarin were found to be 3.47 ± 1.87 (SD) μg/ml, 1.25 ± 0.81 (SD) μg/ml, respectively. Through the present study the plasma concentrations of warfarin, 7-hydroxy warfarin and their metabolic ratio was determined. The assay was sensitive to follow warfarin pharmacokinetics in a patient with warfarin therapy for 3 months and above.
机译:华法林是预防血栓栓塞事件最常用的口服抗凝药之一。通过监测凝血酶原时间(以国际标准化比率(INR)表示)来衡量该药物的效果。然而,在某些情况下,强调了华法林的血浆浓度测量。在本研究中,反相高效液相色谱法(HPLC)用于估计血浆药物水平。本研究共纳入185名患者。使用EDTA钠试管收集5毫升静脉血进行药代动力学分析。固相萃取用于通过异丙醇和磷酸钾缓冲液(40:60)流动相从血浆中回收华法林及其代谢产物。华法林,7-羟基华法林和卡马西平(内标)在C18色谱柱上分离,保留时间分别为3.6分钟,2.9分钟和5.9分钟。该测定在华法林浓度范围为0.1–5μg/ ml时呈线性。发现提取回收率为≃85%。华法林和7-羟基华法林的平均血浆浓度分别为3.47±1.87(SD)μg/ ml,1.25±0.81(SD)μg/ ml。通过本研究确定了华法林,7-羟基华法林的血浆浓度及其代谢率。该测定对华法林治疗3个月及以上的患者遵循华法林药代动力学很敏感。

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