Agilent 1290 Infinity LC 6530 Q-TOF Metabolite Identification Application Note

This Application Note describes the rapid separation of metabolites generated from in-vitro experiments using the Agilent 1290 Infinity LC system. It also explains the fast acquisition of TOF mass spectra using Agilent 6530 Accurate-Mass Quadrupole Time-of-Flight LC/MS systems. The software-assisted identification of main metabolites from in-vitro experiments using Agilent MassHunter Metabolite Identification software is discussed. The generation of reports for the identified metabolites using Agilent MassHunter software is also covered.


Agilent 1290 Infinity LC 6530 Q-TOF Metabolite Identification Application Note - cover page
Brand
Agilent
Category
Other
Document type
Application Note
Language
English
Pages
8
File format
PDF
File size
361 KB
Published
02 July, 2012
Updated
28 September, 2023
MD5 checksum
0A255F292EA639A93BA0BEF917A55091

About this manual

This document details a workflow for analyzing the metabolism of pharmaceutical drug candidates. It utilizes the Agilent 1290 Infinity LC system for rapid separation and the Agilent 6530 Accurate-Mass Q-TOF LC/MS system for fast acquisition of mass spectra. The identified metabolites are then analyzed using Agilent MassHunter Metabolite Identification software to generate reports.

What's inside

  • Introduction
  • Equipment
  • Sample preparation
  • LC method
  • TOF MS method
  • Data analysis method
  • Results and discussion

Specifications

Flow rate0.8 mL/min
Column temperature60 °C
Mass range100-1000 m/z
Acquisition rate5 spectra/s

Frequently asked questions

What software is used for metabolite identification?

Agilent MassHunter Metabolite Identification software is used for fast, software-assisted identification of main metabolites.

What is the purpose of this application note?

This document describes a method for the rapid separation and identification of main metabolites generated from pharmaceutical drugs in in-vitro experiments.

What column dimensions are used for the separation?

The method uses a ZORBAX SB-C18 column with dimensions of 2.1 x 50 mm and a particle size of 1.8 ym.

What is the incubation temperature and duration for generating metabolites?

The incubation was carried out at 37 °C for 60 minutes.

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