Discovery stage pharmacokinetics using dried blood spots.

Early in the discovery stage, the measurement of drug candidates in biological fluids as a function time provides important information used in decision making for lead optimization. The detection methodology primarily used is liquid chromatography coupled to triple quadrupole mass spectrometry (LC-MS). Sample preparation is an important aspect of these experiments and robotic-based automation is commonly used. The often overlooked aspect of these experiments is the sample collection itself. Typically, several hundred microliters of whole blood is collected and the plasma fraction separated for each time-point. The plasma is then transferred to an appropriate vessel for subsequent aliquoting and processing. We describe a method for performing discovery stage pharmacokinetic analysis using whole blood dried onto filter paper. The use of dried blood spots is a well established technique for neo-natal screening, and its application to early screening of drug candidates proves to be robust, reliable and reproducible.

[1]  T. Olah,et al.  Quantitation of the 5HT1D agonists MK-462 and sumatriptan in plasma by liquid chromatography-atmospheric pressure chemical ionization mass spectrometry. , 1996, Journal of chromatography. A.

[2]  A P Watt,et al.  Higher throughput bioanalysis by automation of a protein precipitation assay using a 96-well format with detection by LC-MS/MS. , 2000, Analytical chemistry.

[3]  Å. Jansson,et al.  High-performance liquid chromatographic method for the determination of quinine and 3-hydroxyquinine in blood samples dried on filter paper. , 2003, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[4]  A. Hattersley,et al.  Development of a bloodspot assay for insulin. , 2001, Clinica chimica acta; international journal of clinical chemistry.

[5]  D. Phillips,et al.  Effect of lot-to-lot variability in filter paper on the quantification of thyroxin, thyrotropin, and phenylalanine in dried-blood specimens. , 1988, Clinical chemistry.

[6]  R. Plumb,et al.  Optimisation and routine use of generic ultra-high flow-rate liquid chromatography with mass spectrometric detection for the direct on-line analysis of pharmaceuticals in plasma. , 1998, Journal of chromatography. A.

[7]  M. Lemnge,et al.  High‐Performance Liquid Chromatography Determination of Dapsone, Monoacetyldapsone, and Pyrimethamine in Filter Paper Blood Spots , 1995, Therapeutic drug monitoring.

[8]  M. Green,et al.  High-performance liquid chromatographic assay for the simultaneous determination of sulfadoxine and pyrimethamine from whole blood dried onto filter paper. , 2002, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[9]  T. Olah,et al.  A direct technique for the simultaneous determination of 10 drug candidates in plasma by liquid chromatography-atmospheric pressure chemical ionization mass spectrometry interfaced to a Prospekt solid-phase extraction system. , 1997, Journal of pharmaceutical and biomedical analysis.

[10]  R. Guthrie,et al.  A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS. , 1963, Pediatrics.

[11]  M. Jacob,et al.  Screening blood spots for inborn errors of metabolism by electrospray tandem mass spectrometry with a microplate batch process and a computer algorithm for automated flagging of abnormal profiles. , 1997, Clinical chemistry.

[12]  D. Brambilla,et al.  Quantitation of Human Immunodeficiency Virus Type 1 RNA in Plasma by Using Blood Dried on Filter Paper , 1998, Journal of Clinical Microbiology.

[13]  J. Henion,et al.  Liquid-liquid extraction in the 96-well plate format with SRM LC/MS quantitative determination of methotrexate and its major metabolite in human plasma. , 1999, Analytical chemistry.

[14]  E. Gunter,et al.  Evaluation of factors influencing precision in the analysis of samples taken from blood spots on filter paper. , 1995, Clinical and laboratory haematology.

[15]  W. Watkins,et al.  Measurement of physiological concentrations of dapsone and its monoacetyl metabolite: a miniaturised assay for liquid or filter paper-absorbed samples. , 1996, Journal of chromatography. B, Biomedical applications.

[16]  K. Bateman,et al.  Reduction of animal usage by serial bleeding of mice for pharmacokinetic studies: application of robotic sample preparation and fast liquid chromatography-mass spectrometry. , 2001, Journal of chromatography. B, Biomedical sciences and applications.