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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >UHPLC-MS/MS method with protein precipitation extraction for the simultaneous quantification of ten antihypertensive drugs in human plasma from resistant hypertensive patients
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UHPLC-MS/MS method with protein precipitation extraction for the simultaneous quantification of ten antihypertensive drugs in human plasma from resistant hypertensive patients

机译:UHPLC-MS / MS方法结合蛋白质沉淀提取物同时定量抗药性高血压患者血浆中的十种降压药

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Today the management of resistant hypertension is a critical health problem: the main difficulty on this field is the discrimination of cases of poor therapeutic adherence from cases of real resistance. This gives rise to the need of high throughput and reliable quantification methods for the Therapeutic Drug Monitoring (TDM) of antihypertensive drugs. The aim of this work was the development and validation of a UHPLC-Tandem mass spectrometry assay for this application and its use in plasma from patients with resistant hypertension. The novelty of this method resides in the ability to simultaneously quantify a wide panel of antihypertensive drugs: amlodipine, atenolol, clonidine, chlortalidone, doxazosin, hydrochlorothiazide, nifedipine, olmesartan, ramipril and telmisartan. Moreover, this method stands out for its simplicity and cheapness, resulting feasible for clinical routine. Both standards and quality controls were prepared in human plasma. After the addition of internal standard, each sample underwent protein precipitation with acetonitrile and was then dried. Extracts were resuspended in water:acetonitrile 90:10(0.05% formic acid) and then injected into the chromatographic system. Chromatographic separation was performed on an Acquity (R) UPLC HSS T3 1.8 mu m 2.1 x 150mm column, with a gradient of water and acetonitrile, both added with 0.05% formic acid.
机译:如今,抗药性高血压的管理已成为一个关键的健康问题:该领域的主要困难是将治疗依从性差的病例与真正的抗药性加以区分。这就需要对抗高血压药物的治疗药物监测(TDM)具有高通量和可靠的定量方法。这项工作的目的是开发和验证用于此应用的UHPLC-串联质谱分析及其在耐药性高血压患者血浆中的使用。该方法的新颖之处在于能够同时对多种降压药进行定量:氨氯地平,阿替洛尔,可乐定,氯噻酮,多沙唑嗪,氢氯噻嗪,硝苯地平,奥美沙坦,雷米普利和替米沙坦。此外,该方法以其简单和便宜而著称,因此对于临床常规可行。在人血浆中制备了标准品和质量控制品。添加内标后,将每个样品用乙腈进行蛋白沉淀,然后干燥。将萃取液重悬于水:乙腈90:10(0.05%甲酸)中,然后注入色谱系统。色谱分离是在Acquity(R)UPLC HSS T3 1.8微米2.1 x 150mm色谱柱上进行的,用水和乙腈进行梯度洗脱,均加入0.05%的甲酸。

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