Agilent Determination of Fluvastatin in Plasma Using the Agilent 6410B Triple Quadrupole LC/MS System and Agilent 1200 S

This Application Note describes a rapid and sensitive method for quantification of fluvastatin in plasma using the Agilent 1200 Series Rapid Resolution Liquid Chromatography (RRLC) system and the Agilent 6410 Triple Quadrupole LC/MS system. Sample preparation was carried out by a simple protein precipitation step. Atorvastatin at 40 ng/mL was used as the internal standard. The developed method had a short run time of two minutes and was found to be linear in the concentration range of 0.5 ng/mL to 200 ng/mL. The limit of detection (LOD) of the method is 0.2 ng/mL, or 1 pg on-column.


Agilent Determination of Fluvastatin in Plasma Using the Agilent 6410B Triple Quadrupole LC/MS System and Agilent 1200 S - cover page
Brand
Agilent
Document type
Application Note
Language
English
Pages
4
File format
PDF
File size
204 KB
Published
02 July, 2012
Updated
30 September, 2023
MD5 checksum
EAA86F9A37A7E2D0EE8BA7D1B5E67588

About this manual

This document details an analytical method developed by Agilent Technologies to quantify fluvastatin in human plasma. The method utilizes the Agilent 6410B Triple Quadrupole LC/MS system coupled with the Agilent 1200 Series Rapid Resolution Liquid Chromatography (RRLC) system. Sample preparation involves a simple protein precipitation step using acetonitrile, followed by centrifugation and reconstitution.

What's inside

  • Abstract
  • Introduction
  • Experimental
  • LC/MS/MS instrumentation
  • Sample preparation
  • Results and discussion
  • Conclusion

Frequently asked questions

What is the run time for this analysis method?

The developed method has a short run time of two minutes.

How much plasma sample volume is required for preparation?

Fluvastatin and the internal standard were spiked into 250 µL of plasma.

What concentration was used for the internal standard atorvastatin?

The internal standard concentration was maintained at 40 ng/mL.

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