Agilent 6410 Quantitative Analysis of Water-Soluble B-Vitamins in Cereal Using Rapid Resolution LC/MS/MS Application Not

Agilent 6410 Triple Quadrupole Mass Spectrometer (QQQ) is used to analyze several water-soluble B-vitamin compounds in breakfast cereal, including thiamine, riboflavin, pyridoxine, vitamin B12, pantothenic acid, biotin, and niacinamide, which are present at relatively high levels. A simple gradient elution is carried out on a Rapid Resolution High Throughput SB-Aq column (particle size 1.8 µm). All compounds elute in less than 7.5 minutes, and with the exception of pyridoxine, good linearity over more than three orders of magnitude, from 0.5 to 500 ppb, is demonstrated with good peak area reproducibility at the 0.5 ppb level, which is the lowest level of quantitation considered.


Agilent 6410 Quantitative Analysis of Water-Soluble B-Vitamins in Cereal Using Rapid Resolution LC/MS/MS Application Not - cover page
Brand
Agilent
Document type
Application Note
Language
English
Pages
12
File format
PDF
File size
1.7 MB
Published
12 June, 2012
Updated
30 September, 2023
MD5 checksum
2F1FD3D202C1E8184617D35F16991660

About this manual

The document details a quantitative analysis method for eight water-soluble B-vitamin compounds (Thiamine, Pantothenic acid, Pyridoxine, Nicotinic acid, Nicotinamide, Cyanocobalamin, Folic acid, and Riboflavin) in breakfast cereal. The method utilizes an Agilent 6410 Triple Quadrupole Mass Spectrometer coupled with an Agilent 1200 Series liquid chromatography system.

What's inside

  • Abstract
  • Introduction
  • Sample Preparation
  • LC/ MS Method Details
  • Results and Discussion

Frequently asked questions

What is the lowest concentration level demonstrated for quantitation in this method?

The method demonstrates good peak area reproducibility at 0.5 ppb, which is considered the lowest level of quantitation.

How long does it take for all compounds to elute using this method?

All compounds elute in less than 7.5 minutes with a simple gradient elution.

What is the run-to-run cycle time for screening and quantitation?

The method allows for screening and quantitation with a run-to-run cycle time as low as 10 minutes.

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