A liquid chromatography tandem mass spectrometry (LC/MS/MS) method has been developed for the fast routine analysis of selected CYP450 probe substrate metabolites in microsomal incubations, with no sample pretreatment. This has allowed fast and simple assessment of the potential effects which drug c
The application of fast gradient capillary liquid chromatography/mass spectrometry to the analysis of pharmaceuticals in biofluids
✍ Scribed by R. S. Plumb; G. J. Dear; D. Mallett; I. J. Fraser; J. Ayrton; C. Ioannou
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 211 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0951-4198
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✦ Synopsis
Fast gradient capillary high performance liquid chromatography (HPLC) coupled to a mass spectrometer has been successfully used for the analysis of pharmaceutical compounds from biological matrices, in the femtogram on column range. In the work reported in this paper, the use of capillary HPLC, on the 180-mm internal diameter scale, has shown a 30-fold improvement in detection limits when compared to conventional 2-mm scale chromatography. The use of fast gradient elution resulted in a generic methodology which gave excellent chromatographic reproducibility and column longevity. This technique has been used in conjunction with simple protein precipitation, with no deleterious effect on either the column life or the chromatographic performance. The use of capillary HPLC in bioanalysis has the potential to give a significant increase in assay sensitivity with the equipment currently in use. In this paper the authors also present a modification to the current PE-Sciex ion-spray source which allows excellent spray adjustment in three dimensional accessibility, which is important when working with low flow rates, as well as reducing the inherent system dead volume.
📜 SIMILAR VOLUMES
Capillary liquid chromatography/mass spectrometry (LC/MS) is usually performed using electrospray ionization. Atmospheric pressure chemical ionization (APCI) has not been used since the flow rates involved (1-10 µL/min) are too low to effect ionization with a standard APCI source. Using a 320 µm ؋ 1
Figure 2. ESI mass spectrum of 2-(9-decenyl)-5-methyl-1,3,4oxadiazole (ca. 100 mg/mL in methanol).