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液相色谱-串联质谱法同时定量测定大鼠干血斑中的比索洛尔、雷米普利拉、普萘洛尔和咪达唑仑。

Liquid chromatography-tandem mass spectrometry method for simultaneous quantification of bisoprolol, ramiprilat, propranolol and midazolam in rat dried blood spots.

作者信息

Cvan Trobec Katja, Trontelj Jurij, Springer Jochen, Lainscak Mitja, Kerec Kos Mojca

机构信息

University Clinic of Respiratory and Allergic Diseases Golnk, Pharmacy Department, Golnik 36, 4204 Golnik, Slovenia.

University of Ljubljana, Faculty of Pharmacy, Askerceva 7, 1000 Ljubljana, Slovenia.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2014 May 1;958:29-35. doi: 10.1016/j.jchromb.2014.03.009. Epub 2014 Mar 15.

Abstract

Dried blood spot (DBS) sampling represents a suitable method for pharmacokinetic studies in rats, particularly if serial sampling is needed. To study the pharmacokinetics of drugs in a rat heart failure (HF) model, we developed and validated a method for the simultaneous determination of bisoprolol, ramiprilat, propranolol and midazolam in DBS samples. Bisoprolol and ramipril are widely used in the treatment of HF, and midazolam and propranolol are markers of hepatic metabolism, which can be altered in HF. A 20μL sample of rat blood was pipetted onto Whatman 903 Protein Saver Card and allowed to dry. The whole spot was excised and 300μL of solvent (methanol with 10% ultrapure water and 0.1% formic acid) was added. After mixing and incubating the sample in an ultrasonic bath, a mixture of isotopically labeled internal standards was added. After centrifugation, the extracts were cleaned on an Ostro™ plate and analyzed using liquid chromatography-tandem mass spectroscopy. The method was successfully validated. No significant interference was observed in the retention times of analytes or internal standards. The intraday and interday accuracy and precision were within a ±15% interval. The method was linear in the range 5-250μg/L and the lower limit of quantification was 5μg/L for all four analytes. The absolute matrix effect ranged from 98.7% for midazolam to 121% for ramiprilat. The recovery was lowest for ramiprilat and highest for propranolol. Samples were stable at all tested temperatures. The method has been used successfully in a real-time pharmacokinetic study in rats.

摘要

干血斑(DBS)采样是大鼠药代动力学研究的一种合适方法,特别是在需要进行连续采样时。为了研究大鼠心力衰竭(HF)模型中药物的药代动力学,我们开发并验证了一种同时测定DBS样品中比索洛尔、雷米普利拉、普萘洛尔和咪达唑仑的方法。比索洛尔和雷米普利广泛用于治疗HF,而咪达唑仑和普萘洛尔是肝代谢标志物,在HF中可能会发生改变。将20μL大鼠血液样本移液到Whatman 903蛋白保存卡上,使其干燥。切下整个血斑,加入300μL溶剂(含10%超纯水和0.1%甲酸的甲醇)。在超声浴中混合并孵育样品后,加入同位素标记内标混合物。离心后,提取物在Ostro™ 板上进行净化,并使用液相色谱-串联质谱进行分析。该方法成功得到验证。在分析物或内标的保留时间上未观察到明显干扰。日内和日间准确度和精密度在±15%区间内。该方法在5-250μg/L范围内呈线性,所有四种分析物的定量下限均为5μg/L。绝对基质效应范围从咪达唑仑的98.7%到雷米普利拉的121%。雷米普利拉的回收率最低,普萘洛尔的回收率最高。样品在所有测试温度下均稳定。该方法已成功用于大鼠的实时药代动力学研究。

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