Quantification of ropivacaine and its major metabolites in human urine samples utilizing microextraction in a packed syringe automated with liquid chromatography-tandem mass spectrometry (MEPS-LC-MS/MS) The determination of ropivacaine and its major metabolites in urine was performed using microext
Quantitative analysis of methadone in human urine samples by microextraction in packed syringe-gas chromatography-mass spectrometry (MEPS-GC-MS)
✍ Scribed by Aziza El-Beqqali; Mohamed Abdel-Rehim
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 664 KB
- Volume
- 30
- Category
- Article
- ISSN
- 1615-9306
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A method for the simultaneous analysis of methadone in urine samples by microextraction in a packed syringe online with GC‐MS (MEPS‐GC‐MS) is described. The new method reduced the sample handling and the detection limit by two‐ to seven‐fold compared to published methods. Using a quantitation method based on the calculation of analyte concentration by comparison to an internal standard, we were able to measure methadone levels consistent with values reported for healthy individuals. The intra‐assay precisions (RSD) of the method using quality control (QC) samples at three different concentration levels were about 11–14% (n = 6). The interassay precisions (RSD) were 11–15% for methadone in urine samples (n = 18). The accuracy varied from 89 to 109% for intra‐assay (n = 6), and 97 to 107% for inter‐assay (n = 18). The regression correlation coefficients (r^2^) were over 0.99 in all experiments.
📜 SIMILAR VOLUMES
## Abstract A new technique for sample preparation on‐line with liquid chromatographic/tandem mass spectrometric (LC/MS/MS) assay was developed. Microextraction in a packed syringe (MEPS) is a new miniaturized, solid‐phase extraction technique that can be connected on‐line to gas or liquid chromato
A method for assay of urinary dhydroxymelatonin, the major metabolite of the pineal hormone melatonin is described. After addition of an internal standard of deuterated 6hydroxymelatonin sulfate, human mine was hydrolyzed enzymatically and free dhydroxymelatonin extracted, reacted to form a stable t