A quantitative method was developed and validated for rapid and sensitive analysis of cimetidine in human plasma. The method involved the use of liquid chromatography (LC) coupled with atmospheric pressure chemical ionization (APCI) and selected reaction monitoring (SRM) mass spectrometry (MS). A ci
A comprehensive LC-MS-based quantitative analysis of fentanyl-like drugs in plasma and urine
✍ Scribed by Sarah Cooreman; Christa Deprez; Frank Martens; Jan Van Bocxlaer; Kathleen Croes
- Book ID
- 102441693
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 214 KB
- Volume
- 33
- Category
- Article
- ISSN
- 1615-9306
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Fentanyl, norfentanyl, alfentanil, sufentanil, remifentanil and 3‐methylfentanyl are potent, short‐acting, synthetic narcotic analgesics that are not revealed in standard opiate immunoassays. In this article, a fully validated analytical method for the determination of these fentanyl‐type compounds in plasma and urine is presented, consisting of a liquid–liquid extraction followed by a LC‐MS/MS analysis using electrospray ionisation in the positive ionisation mode. Fentanyl‐d~5~ and norfentanyl‐d~5~ were used as internal standards. The lower LOQ in plasma and urine was 0.1 ng/mL for fentanyl, norfentanyl, alfentanil, remifentanil and 3‐methylfentanyl, and 0.2 ng/mL for sufentanil. The method proved linear over a concentration range of 0.2–50 ng/mL for sufentanil and 0.1–50 ng/mL for all other analytes, with correlation coefficients of 0.998 or better. The analytical procedure showed excellent selectivity and precision (all CVs below 15%) for all analytes. Accuracy was good, except for sufentanil, where deviations of more than 15% from nominal concentrations were observed. No matrix effects were observed, and stability of stock and internal standard solutions was within acceptability limits.
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