B. Davari, Nidhi Kotecha, C. Clavijo, J. Thomas, Rachael Rzasa-Lynn, J. Galinkin, U. Christians, C. Sempio
{"title":"A SENSITIVE LC-MS/MS ASSAY FOR THE QUANTIFICATION OF METHADONE AND ITS METABOLITES IN DRIED BLOOD SPOTS: COMPARISON WITH PLASMA.","authors":"B. Davari, Nidhi Kotecha, C. Clavijo, J. Thomas, Rachael Rzasa-Lynn, J. Galinkin, U. Christians, C. Sempio","doi":"10.1097/FTD.0000000000000674","DOIUrl":null,"url":null,"abstract":"INTRODUCTION\nMethadone, 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).\n\n\nMETHODS\nBlood 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.\n\n\nRESULTS\nFor 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.\n\n\nDISCUSSION\nThis 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.","PeriodicalId":23052,"journal":{"name":"Therapeutic Drug Monitoring","volume":" ","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2020-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1097/FTD.0000000000000674","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Therapeutic Drug Monitoring","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1097/FTD.0000000000000674","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICAL LABORATORY TECHNOLOGY","Score":null,"Total":0}
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.
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.