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WHAWB129243

QIAcard FTA DMPK Cards

FTA DMPK-C card, 4 sample areas per card, pack of 100 cards

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Synonym(s):
QIAcard FTA DMPK-C (100), whatman dmpk, whatman fta
NACRES:
NB.22

material

white

manufacturer/tradename

Qiagen WB129243

packaging

pack of 100 cards

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This Item
WHAWB129241WHAWB129242WHAWB120412
QIAcard™ FTA™ DMPK Cards FTA DMPK-C card, 4 sample areas per card, pack of 100 cards

WHAWB129243

QIAcard FTA DMPK Cards

QIAcard™ FTA™ DMPK Cards FTA DMPK-A card, 4 sample areas per card, pack of 100 cards

WHAWB129241

QIAcard FTA DMPK Cards

QIAcard™ FTA™ DMPK Cards FTA DMPK-B card, 4 sample areas per card, pack of 100 cards

WHAWB129242

QIAcard FTA DMPK Cards

manufacturer/tradename

Qiagen WB129243

manufacturer/tradename

Qiagen WB129241

manufacturer/tradename

Qiagen WB129242

manufacturer/tradename

Qiagen WB120412

packaging

pack of 100 cards

packaging

pack of 100 cards

packaging

pack of 100 cards

packaging

pkg of 25 cards

General description

Drug Metabolism (DM) Pharmacokinetic (PK) studies provide crucial insight into the way drug candidates behave in the body. These studies are a critical step in drug development.

QIAcard FTA DMPK Cards for Drug Metabolism Pharmacokinetics enable microvolume sampling with only 10 to 20 µl per sample and are designed for use with blood samples. The cards can also be used with colorless samples such as plasma, cerebrospinal fluid and urine.

QIAcard FTA DMPK-A contains impregnated chemicals enabling protein denaturation to inactivate endogenous enzymes. Cell lysis releases endogenous cellular materials onto card. Stabilization of DNA allows resampling of blood spot for pharmacogenomics. Impregnated chemicals may interfere with mass spectrometry detection e.g. ion suppression.

Features and Benefits

  • DBS microvolume sampling requires only 10—20 μl per sample.
  • Consistent data are obtained through more serial sampling from individual animals.
  • Less reliance on composite data.
  • The 3-step DBS procedure is more straightforward than the cumbersome centrifugation, isolation and clean-up of plasma.
  • Conveys greater analyte stability through on-substrate clean-up, especially for enzyme-sensitive compounds.
  • Room temperature stability saves on cost of dry ice shipments and allows remote sampling.

Other Notes

Analysis is primarily with HPLC or UHPLC followed by MS/MS detection, direct desorption MS techniques such as DESI. Methanol or aqueous/organic mixtures have been shown to work well for small molecules and aqueous buffers are recommended for proteins. Select a good solvent for the analyte while maintaining compatibility with the HPLC conditions to be used. The choice of DMPK card depends on many factors such as the analyte chemical structure, extraction solvent and analysis workflow.

Field of Use : For internal research use only

Legal Information

FTA is a trademark of Qiagen Group
QIAcard is a trademark of Qiagen Group

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Customers Also Viewed

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Neil Spooner et al.
Analytical chemistry, 81(4), 1557-1563 (2009-01-22)
A novel approach has been developed for the quantitative determination of circulating drug concentrations in clinical studies using dried blood spots (DBS) on paper, rather than conventional plasma samples. A quantitative bioanalytical HPLC-MS/MS assay requiring small blood volumes (15 microL)
Matthew Barfield et al.
Analytical chemistry, 83(1), 118-124 (2010-12-09)
A novel approach has been developed for the quantitative determination of circulating drug concentrations in clinical studies using dried plasma spots (DPS) on paper substrates, rather than conventional plasma samples. A quantitative bioanalytical high-pressure liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) assay

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