Transfer and Optimization of Existing Methods for Analysis of Antibiotics in Meat to Agilent Poroshell 120 EC-C18 Column

This document describes a method for analyzing antibiotics in meat using an Agilent Poroshell 120 EC-C18 column. The method uses a gradient method and UV detection, and it can be quickly optimized.


Transfer and Optimization of Existing Methods for Analysis of Antibiotics in Meat to Agilent Poroshell 120 EC-C18 Column - cover page
Brand
Agilent
Document type
Application Note
Language
English
Pages
205
File format
PDF
File size
11.1 MB
Published
11 June, 2012
Updated
30 September, 2023
MD5 checksum
91029D4BE5336DD7D2C15176A0B4B227

About this manual

The document details the transfer of an existing analytical method originally designed for UV detection to a mass spectrometry (MS/MS) compatible protocol. The primary goal is to analyze antibiotics such as sulfamerazine and thiamphenicol in meat matrices more efficiently.

The study utilizes Agilent Poroshell 120 EC-C18 columns, which allow for rapid method optimization using short gradient times compared to traditional long columns. The optimized method was successfully demonstrated on an Agilent 6410 triple quadrupole LC/MS System coupled with an Agilent 1200 Series Rapid Resolution LC.

What's inside

  • Veterinary Drugs
  • Transfer and Optimization of Existing Methods
  • Analysis of Antibiotics in Meat
  • Agilent Poroshell 120 EC-C18 Columns
  • MS/MS Detection
  • Method Parameters for Various Column Dimensions

Specifications

Column Dimensions (Short)4.6 mm x 50 mm, 2.7 um
Column Dimensions (Medium)3.0 mm x 50 mm, 2.7 um
Column Dimensions (Long)2.1 mm x 100 mm, 2.7 um
Gradient Time (Optimized)12 min
Flow Rate (Short Column)2 mL/min

Frequently asked questions

Which Agilent system was used for the MS/MS analysis?

An Agilent 6410 triple quadrupole LC/MS System coupled with an Agilent 1200 Series Rapid Resolution LC.

What mobile phase was used for MS detection?

MS-compatible mobile phases consisting of volatile buffer components such as formic acid, ammonium formate buffer and ammonium acetate buffer.

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