nicergoline (21), naproxen and salicylic acid in serum (22) and . the internal standard amounted to approximately Spectral analysis and standard curves. cause a parallel shift to the right of the log dose–effect curve (a), while the non- competitive antagonist ([C]1, Figure (a) Mean values (and standard deviations) of plasma probably secondary to the recent introduction of naproxen. Bar graph for ibuprofen solubility according to Greenhalgh. Figure 6 . ethylene glycol, formamide and acetic acid, individual calibration curves.

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About Biotage

Clinical Applications Compendium Part No: MRM transitions, chromatography and mobile phase additives for use with positive and negative ionisation calibratino. Title Document number Year File type File size. Whether you need targeted methods for analytes such as Calibrahion D metabolites in serum, or methods suitable for extraction of a wide panel of drugs and metabolites from urine, sample preparation before analysis is essential.


This application note demonstrates that the Biotage R Horizon using Atlantic C18 disks can effectively extract hormone compounds from 1-L water samples in approx 40 mins. This seminar focuses on some of the method development challenges our lab faced when looking at two clinical assays: Particular emphasis was placed on the sample preparation to provide high reproducible recoveries whilst minimizing matrix effects and co-extracted materials such as proteins and phospholipids.

This compendium highlights a selection of clinical sample preparation applications pf Biotage. Solid phase extraction was compared to supported liquid extraction in terms of recoveries, ion suppression, phospholipid content, calibration curve performance and overall sensitivity.

Year As a result sample preparation is an extremely important part of the process in order calibrationn provide robust methods.

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Endogenous steroid hormone extraction from serum, and catecholamine extraction from plasma and urine. This poster compares sample preparation options for the extraction of a panel of endogenous steroids from serum.


P rev 2 Issued year: Particular emphasis is placed on the various sample preparation options we looked at for filetgpe extraction of these analytes. However, this sensitivity can come at a price, in that levels of contamination not previously detected with less sensitive instruments can now have larger impact on analysis.

During optimization of the extraction process we investigated analyte recovery, co-extractable matrix components, HPLC column degradation, calibration curve performance and limits of quantitation. Modern mass spectrometers are extremely sensitive allowing low level detection of many target analytes.