Quantification of the Plasma Concentration of Vadadustat by High-Performance Liquid Chromatography with Ultraviolet Detection and Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry.

IF 2.8 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY
Satoshi Yokoyama, Junichi Nakagawa, Michiko Shimada, Kayo Ueno, Masahiro Ishiyama, Norio Nakamura, Hirofumi Tomita, Takenori Niioka
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引用次数: 0

Abstract

Background: An inexpensive, simple, and accurate plasma concentration measurement system is needed to actively conduct pharmacokinetic and pharmacodynamic analyses of vadadustat, hypoxia-inducible factor-prolyl hydroxylase inhibitor, in clinical settings. In this study, the authors aimed to develop a method for measuring vadadustat in human plasma that could be applied for therapeutic drug monitoring using high-performance liquid chromatography with ultraviolet detection (HPLC-UV) in a clinical setting.

Methods: Plasma samples (100 μL) were pretreated with acetonitrile using butyl paraoxybenzoate as an internal standard. Chromatographic separation was performed on a SunShell PFP C18 column (2.6 μm, 4.6 mm × 150 mm). The mobile phase consisted of (A) 20 mM of phosphate buffer (pH 2.4) and (B) acetonitrile (60:40, v/v), delivered isocratically at a flow rate of 1 mL/min. The analytes were detected by UV absorbance at a wavelength of 220 nm, and the column temperature was 40°C. To evaluate the applicability of HPLC-UV in a clinical setting, blood samples were collected at 19 time points from 7 patients who had been taking vadadustat.

Results: The calibration curve was linear over the concentration range of 0.2-150 mcg/mL (R2 > 0.99). Intra-assay and interassay accuracy, precision, and stability met the Food and Drug Administration recommendations. The vadadustat plasma concentrations of patients analyzed using the current HPLC-UV method were almost equal to those measured using ultra-performance liquid chromatography-tandem mass spectrometry (mean difference: 0.13 mcg/mL). Large variability in the dose-adjusted plasma concentrations of vadadustat at 12 hours after administration was observed between patients (coefficient of variation = 57.6%).

Conclusions: This HPLC-UV method is a simple, accurate quantification method for evaluating plasma concentrations in patients taking vadadustat in a clinical setting.

利用高效液相色谱-紫外检测法和超高效液相色谱-串联质谱法对伐杜司他的血浆浓度进行定量分析
背景:为了在临床中积极开展低氧诱导因子-脯氨酰羟化酶抑制剂伐杜司他的药代动力学和药效学分析,需要一种廉价、简单、准确的血浆浓度测量系统。在本研究中,作者旨在开发一种测定人血浆中伐杜司他的方法,该方法可在临床环境中使用高效液相色谱-紫外检测法(HPLC-UV)进行治疗药物监测:血浆样品(100 μL)经乙腈预处理,以对氧苯甲酸丁酯为内标。采用 SunShell PFP C18 色谱柱(2.6 μm,4.6 mm × 150 mm)进行色谱分离。流动相包括 (A) 20 mM 磷酸盐缓冲液(pH 2.4)和 (B) 乙腈(60:40, v/v),以 1 mL/min 的流速等压流动。分析物通过波长为 220 nm 的紫外吸收检测,色谱柱温度为 40°C。为了评估 HPLC-UV 在临床环境中的适用性,在 19 个时间点采集了 7 名服用伐杜司他的患者的血液样本:校准曲线在 0.2-150 微克/毫升的浓度范围内呈线性关系(R2 > 0.99)。测定内和测定间的准确度、精密度和稳定性均符合食品药品管理局的建议。使用目前的高效液相色谱-紫外法分析的患者血浆中的伐杜司他浓度与使用超高效液相色谱-串联质谱法测定的浓度几乎相等(平均差异:0.13 微克/毫升)。用药 12 小时后,经剂量调整后的血浆中伐杜司他浓度在不同患者之间存在较大差异(变异系数 = 57.6%):该高效液相色谱-紫外法是一种简单、准确的定量方法,可用于评估临床中服用伐杜司他的患者的血浆浓度。
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来源期刊
Therapeutic Drug Monitoring
Therapeutic Drug Monitoring 医学-毒理学
CiteScore
5.00
自引率
8.00%
发文量
213
审稿时长
4-8 weeks
期刊介绍: Therapeutic Drug Monitoring is a peer-reviewed, multidisciplinary journal directed to an audience of pharmacologists, clinical chemists, laboratorians, pharmacists, drug researchers and toxicologists. It fosters the exchange of knowledge among the various disciplines–clinical pharmacology, pathology, toxicology, analytical chemistry–that share a common interest in Therapeutic Drug Monitoring. The journal presents studies detailing the various factors that affect the rate and extent drugs are absorbed, metabolized, and excreted. Regular features include review articles on specific classes of drugs, original articles, case reports, technical notes, and continuing education articles.
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