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采用 LC-HRMS 对干血斑样本中的阿替洛尔进行定量测定:评估用药依从性的潜在方法。

Quantitative determination of atenolol in dried blood spot samples by LC-HRMS: a potential method for assessing medication adherence.

机构信息

Leicester School of Pharmacy, Faculty of Health and Life Sciences, De Montfort University, Leicester LE1 9BH, UK.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2012 May 15;897:72-9. doi: 10.1016/j.jchromb.2012.04.013. Epub 2012 Apr 16.

Abstract

The use of blood spot collection cards was investigated as a means of obtaining small volume samples for the quantification of therapeutic drugs for assessing medication adherence. A liquid chromatography-high resolution TOF mass spectrometry (LC-HRMS) method, based on the measurement at the accurate mass to charge ratio of the target analyte, was used to ensure specificity for atenolol in the dried blood spot (DBS) samples. A working method was developed and validated. For the preparation of DBS samples whole blood spiked with analyte was used to produce 30 μl blood spots on specimen collection cards. A 5mm disc was cut from the dried blood spot and extracted using methanol:water (60:40, v/v) containing the internal standard, atenolol-d(7). Extracts were vortexed, sonicated and then centrifuged. Gradient chromatographic elution was achieved using an Ascentis Express C18 100mm×2.1mm column and a mobile phase flow rate of 0.2 ml/min and the column oven temperature at 30 °C. MS detection was carried out in electrospray positive ion mode for target ions at accurate mass m/z 267.1703 for atenolol and 274.2143 for the IS. Drug extraction efficiency from spiked blood spots was demonstrated to be 96±5% and the drug was stable in DBS for at least 10 weeks. The developed LC-HRMS method was linear within the tested calibration range of 25-1500 ng/ml and validation showed the accuracy (relative error) and precision (coefficient of variation) values were within the pre-defined limits of ≤ 5% at all concentrations with a limit of quantification of 25 ng/ml. Factors with potential to affect drug quantification measurements such as the matrix effects, volume of blood applied onto the collection card and effect of different sampling cards were investigated. The developed LC-HRMS method was applied to blood spots on sampling card taken from adult healthy volunteers previously administered a 50mg atenolol tablet and a DBS concentration-time profile was obtained for atenolol. Requiring only a micro volume (30 μl) blood sample for analysis, the developed DBS based assay has the potential to assess patient adherence to atenolol.

摘要

采集血斑作为获取小体积样本的方法,用于定量治疗药物以评估药物依从性。研究了一种基于液相色谱-高分辨飞行时间质谱(LC-HRMS)的方法,该方法基于目标分析物的精确质量电荷比进行测量,以确保在干血斑(DBS)样品中特异地检测到阿替洛尔。建立并验证了工作方法。为了制备 DBS 样品,用含分析物的全血在标本采集卡上制备 30μl 血斑。从干燥的血斑上切下 5mm 圆片,用含内标阿替洛尔-d(7)的甲醇:水(60:40,v/v)提取。提取液涡旋、超声处理后离心。使用 Ascentis Express C18 100mm×2.1mm 柱和 0.2ml/min 的流动相流速实现梯度洗脱,柱箱温度为 30°C。采用电喷雾正离子模式进行 MS 检测,目标离子的精确质量 m/z 为 267.1703 的阿替洛尔和内标 274.2143 的阿替洛尔-d(7)。从加标血斑中提取药物的效率证明为 96±5%,且药物在 DBS 中至少稳定 10 周。所建立的 LC-HRMS 方法在 25-1500ng/ml 的测试校准范围内呈线性,验证结果表明,在所有浓度下,准确度(相对误差)和精密度(变异系数)值均在≤5%的预定范围内,定量下限为 25ng/ml。考察了可能影响药物定量测量的因素,如基质效应、采集卡上施加的血量以及不同采样卡的影响。该方法应用于先前给予 50mg 阿替洛尔片的成年健康志愿者的采样卡上的血斑,获得了阿替洛尔的 DBS 浓度-时间曲线。该方法仅需 30μl 微量血液样本进行分析,具有评估阿替洛尔患者依从性的潜力。

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