Results are given for a more sensitive screening procedure for non-steroidal anti-inflammatory drugs using GC-MS-MS. By monitoring a selected characteristic reaction for each drug very low detection limits are reached even in a difficult biological matrix such as equine urine. Detection down to 5 ng
Direct determination of non-steroidal anti-inflammatory drugs by column-switching LC–MS
✍ Scribed by Koichi Suenami; Lee Wah Lim; Toyohide Takeuchi; Yasuhide Sasajima; Kiyohito Sato; Yuji Takekoshi; Susumu Kanno
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 484 KB
- Volume
- 29
- Category
- Article
- ISSN
- 1615-9306
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✦ Synopsis
A method for determination of 16 non-steroidal anti-inflammatory drugs (NSAIDs) in human plasma samples without time-consuming sample pre-treatments was developed. The system consisted of two pumps for mobile phase delivery, a six-port switching valve, a pre-column (Oasis HLB Cartridge Column), and a reversed phase analytical column (COSMOSIL 3C18-MS-II). The analytes were trapped on the precolumn and subsequently separated on the analytical column. The present method allowed on-line sample clean-up and enrichment, leading to improved sensitivity without any tedious sample preparation. The recoveries of NSAIDs from human plasma by column-switching were greater than 72.6%. The total analysis time for a single analytical run was approximately 11 min. The detection limits of NSAIDs were 0.0025 to 0.2 microg/mL using the selected ion monitoring mode.
📜 SIMILAR VOLUMES
Direct serum injection methods are described for the HPLC determination of selected non-steroidal anti-inflammatory drugs (NSAIDS) on restricted access media (RAM) columns, using either a Pinkerton (ISRP) or semi-permeable surface (SPS) column. Twenty microlitres of a filtered serum sample was injec
## Abstract The gas chromatography/mass spectrometric assay method was developed for the determination of 13 non‐steroidal anti‐inflammatory drugs (NSAIDs) in river water. Extraction was achieved by a liquid‐phase extraction procedure using methylene chloride. The extract was reacted for 30 min at
Buffer: 50 mM ammonium acetate-13.75 mM ammonia in water (1) or in methanol (2). Voltage: À25 kV in (1) and 25 kV in (2). Temperature: 25°C; wavelength: 280 nm; capillary: uncoated fused capillary (44 cm; 50 mm i.d.).