A SENSITIVE LC-MS/MS ASSAY FOR THE QUANTIFICATION OF METHADONE AND ITS METABOLITES IN DRIED BLOOD SPOTS: COMPARISON WITH PLASMA.

IF 2.8 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY Therapeutic Drug Monitoring Pub Date : 2020-02-01 DOI:10.1097/FTD.0000000000000674
B. Davari, Nidhi Kotecha, C. Clavijo, J. Thomas, Rachael Rzasa-Lynn, J. Galinkin, U. Christians, C. Sempio
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引用次数: 5

Abstract

INTRODUCTION Methadone, a synthetic narcotic, is widely used both in adults and children for pain control, and as a replacement drug in opioid use disorder to prevent craving and withdrawal. To support clinical pharmacokinetic trials in neonates, infants, and children, the authors developed and validated a novel, automated, highly sensitive liquid chromatography-electrospray-tandem mass spectrometry ionization (LC-ESI-MS/MS) method for the quantification of methadone and its metabolites, 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) and 2-ethyl-5-methyl-3,3-diphenylpyraline (EMDP), in samples collected as dried blood spots (DBS). METHODS Blood was spiked with different concentrations of methadone, EDDP and EMDP and blood drops were applied to filter paper cards. Punches of 6.4 mm were removed from the cards and 600 µL of protein precipitation solution (methanol/0.2M ZnSO4, 7:3, v/v) containing the internal standards (methadone-d9 and EDDP-d5) at a concentration of 1 μg/L was added. The extracts were analyzed using LC-ESI-MS/MS in combination with online extraction. The mass spectrometer was run in the positive multiple reaction monitoring mode and the total run time was 3.2 min. RESULTS For the DBS, the assay has a lower limit of quantification of 0.1 μg/L for methadone, EDDP and EMDP. The range of reliable response for methadone for the ion transition m/z = 310.2→265.1 was 0.1-100 µg/L and for the ion transition m/z = 310.2→223.1 5-1000 µg/L. For EDDP, on the range of reliable response for the ion transition m/z = 278.2→234.3 was 0.1-100 µg/L and for the ion transition m/z = 278.2→186.1 5-1000 µg/L. The calibration range for EMDP was 0.1-100 μg/L. Accuracy (85-115 %) and imprecision (< 15 %) met predefined acceptance criteria. DISCUSSION This assay allows for the measurement of small volume blood samples without the need for an intravenous blood draw and thus, it is suitable for pharmacokinetics studies and therapeutic drug monitoring in pediatric patients.
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一种灵敏的LC-MS/MS测定干燥血斑中美沙酮及其代谢产物的方法:与血浆的比较。
简介美沙酮是一种合成麻醉剂,广泛用于成人和儿童的疼痛控制,并作为阿片类药物使用障碍的替代药物,预防渴求和戒断。为了支持新生儿、婴儿和儿童的临床药代动力学试验,作者开发并验证了一种新的、自动化的、高灵敏度的液相色谱-电喷雾串联质谱电离(LC-ESI-MS/MS)方法,用于定量美沙酮及其代谢物,2-亚乙基-1,5-二甲基-3,3-二苯基吡咯烷(EDDP)和2-乙基-5-甲基-3,4-二苯基吡喃啉(EMDP)。方法在血液中掺入不同浓度的美沙酮、EDDP和EMDP,并在滤纸卡上滴血。从卡片上取下6.4 mm的冲头,并加入600µL的蛋白质沉淀溶液(甲醇/0.2M ZnSO4,7:3,v/v),该溶液含有浓度为1μg/L的内标物(美沙酮-d9和EDDP-d5)。使用LC-ESI-MS/MS结合在线提取对提取物进行分析。质谱仪在正多重反应监测模式下运行,总运行时间为3.2分钟。RESULTS对于DBS,美沙酮、EDDP和EMDP的定量下限为0.1μg/L。美沙酮对离子跃迁的可靠响应范围m/z=310.2→265.1为0.1-100µg/L,离子跃迁m/z=310.2→223.1 5-1000µg/L。对于EDDP,在离子跃迁的可靠响应范围内,m/z=278.2→234.3为0.1-100µg/L,离子跃迁m/z=278.2→186.1 5-1000µg/L。EMDP的校准范围为0.1-100μg/L。准确度(85-115%)和不准确度(<15%)符合预定义的验收标准。讨论这种测定方法可以测量小体积血液样本,而无需静脉抽血,因此适用于儿科患者的药代动力学研究和治疗药物监测。
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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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