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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 >Validation of a method for the simultaneous quantification of chloroquine, desethylchloroquine and primaquine in plasma by HPLC-DAD
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Validation of a method for the simultaneous quantification of chloroquine, desethylchloroquine and primaquine in plasma by HPLC-DAD

机译:HPLC-DAD法同时测定血浆中氯喹,去乙基氯喹和伯氨喹的方法的验证

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One of the most important aspects regarding the therapeutic efficacy of antimalarials is its quantification in biologic fluids. The detection and measurement of antimalarial drug levels is important for demonstrating (1) adequate absorption of the drug being given, (2) compliance in taking the full regimen required for treatment and (3) the level of drug in the blood at any time during the test period that parasites reappear. There is a lack of validated methods that simultaneously quantify different antimalarials administered at the same time, such as the use of chloroquine (CQ) and primaquine (PQ) in infections caused by Plasmodium vivax. In this study, a bioanalytical method was validated for the simultaneous quantification of primaquine (PQJ, chloroquine (CQ) and desethylchloroquine (DSCQ) in human plasma using liquid-liquid extraction and high performance liquid chromatography with a diode array detector (HPLC-DAD). The PQ was evaluated over a concentration range of 100-3000 nM and the CQand DSCQ was evaluated over a concentration range of 20-2000 nM. The selectivity of the method was verified by checking for interference by commonly used antimalarials and plasma samples. The accuracy and precision of the method was assessed for drugs spiked into human plasma and recoveries of 83.7%, 92.3%, and 76.5% were obtained for CQ, DSCQ, and PQ, respectively. The applicability of this method was also demonstrated with blood samples from patients with vivax malaria that received combination CQ plus PQ treatment. The simultaneous detection and accurate measurement of CQ, DSCQ, and PQ. levels in human plasma provides an important and economical method for validating and monitoring sensitivity/resistance of P. vivax to more common treatment regimen.
机译:关于抗疟疾治疗功效的最重要方面之一是其在生物体液中的定量。检测和测量抗疟药的水平对于证明(1)所吸收的药物的充分吸收,(2)遵从治疗所需的完整方案的依从性和(3)在此期间的任何时间血液中的药物水平很重要寄生虫再次出现的测试时期。缺乏同时量化同时施用的不同抗疟药的经过验证的方法,例如在间日疟原虫引起的感染中使用氯喹(CQ)和伯氨喹(PQ)。在这项研究中,验证了一种生物分析方法,可同时使用液-液萃取和带有二极管阵列检测器(HPLC-DAD)的高效液相色谱法同时定量测定人血浆中的伯氨喹(PQJ,氯喹(CQ)和去乙基氯喹(DSCQ))在100-3000 nM的浓度范围内评估PQ,在20-2000 nM的浓度范围内评估CQ和DSCQ。通过检查常用抗疟药和血浆样品的干扰来验证方法的选择性。该方法对加标到人血浆中的药物的准确性和精密度进行了评估,CQ,DSCQ和PQ的回收率分别为83.7%,92.3%和76.5%,并且还从来自美国的血液样本中证明了该方法的适用性。间质性疟疾患者接受CQ加PQ联合治疗,同时检测和准确测量人血浆中CQ,DSCQ和PQ的水平提供了重要的验证和监测间日疟原虫对更常见治疗方案的敏感性/耐药性的经济方法。

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