不同干燥条件下容量吸收微采样(VAMS)采集的人血中乙酰水杨酸的稳定性

IF 1.1 Q4 PHARMACOLOGY & PHARMACY Translational and Clinical Pharmacology Pub Date : 2022-03-01 DOI:10.12793/tcp.2022.30.e5
S. Moon, Song Han, Y. Kwak, Min-Gul Kim
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引用次数: 2

摘要

乙酰水杨酸(ASA)是全球市场上最常用的药物之一,某些患者有中毒风险。然而,监测血液药物浓度通常需要经常去医院就诊;因此,通过在家中进行血液采样来增加以患者为中心的需求没有得到满足。体积吸收微采样(VAMS)是一种无需静脉穿刺即可收集均匀准确体积血液的设备,可供不在医院的患者使用;但是由于ASA易于水解并且不能将稳定试剂添加到VAMS样品中,因此必须开发提高样品稳定性的方法。本研究的目的是确定VAMS收集的ASA样品不稳定的原因,并评估提高样品稳定性的方法。使用液相色谱-串联质谱法(LC-MS/MS)分析全血中ASA的浓度。将用VAMS收集的样品保存在不同的干燥条件下(干燥器、加压、氮气和家用真空封口机),并与通过常规静脉取样收集的对照样品进行比较。当VAMS样品在室温下干燥时,ASA的回收率约为对照的31%,而在湿度控制条件下的VAMS样品显示出超过85%的回收率。我们的研究结果表明,足够的湿度控制水平对于确保ASA样品的稳定性至关重要,这种湿度控制也可以在家中使用家用真空密封器实现,从而能够进行以患者为中心的临床试验。
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Stability of acetylsalicylic acid in human blood collected using volumetric absorptive microsampling (VAMS) under various drying conditions
Acetylsalicylic acid (ASA) is one of the most commonly used medications in global market, with a risk of intoxication in certain patients. However, monitoring blood drug concentration often requires frequent hospital visits; hence there is an unmet need to increase patient-centricity by conducting blood sampling at home. Volumetric absorptive microsampling (VAMS) is a device that allows collection of homogenous and accurate volume of blood without venipuncture, and can be utilized by patients who are not in hospital settings; but because ASA is prone to hydrolysis and stabilizing reagents cannot be added to VAMS samples, a way to improve sample stability must be developed. The objective of this study was to identify the cause of instability with ASA samples collected by VAMS, and to evaluate ways to improve sample stability. A liquid chromatography with tandem mass spectrometry (LC-MS/MS) was used for analysis of ASA concentration in whole blood. Samples collected with VAMS were kept under different drying conditions (desiccator, pressurized, nitrogen gas and household vacuum sealer) and were compared to the control samples collected by conventional venous sampling. The recovery of ASA was about 31% of the control when VAMS sample was dried at room temperature, whereas VAMS samples under humidity controlled conditions showed more than 85% of recovery. Our results suggest that adequate level of humidity control was critical to ensure sample stability of ASA, and this humidity control could also be achieved at home using household vacuum sealer, thus enabling patient-centric clinical trials to be conducted.
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来源期刊
Translational and Clinical Pharmacology
Translational and Clinical Pharmacology Medicine-Pharmacology (medical)
CiteScore
1.60
自引率
11.10%
发文量
17
期刊介绍: Translational and Clinical Pharmacology (Transl Clin Pharmacol, TCP) is the official journal of the Korean Society for Clinical Pharmacology and Therapeutics (KSCPT). TCP is an interdisciplinary journal devoted to the dissemination of knowledge relating to all aspects of translational and clinical pharmacology. The categories for publication include pharmacokinetics (PK) and drug disposition, drug metabolism, pharmacodynamics (PD), clinical trials and design issues, pharmacogenomics and pharmacogenetics, pharmacometrics, pharmacoepidemiology, pharmacovigilence, and human pharmacology. Studies involving animal models, pharmacological characterization, and clinical trials are appropriate for consideration.
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