• Home
  • Biopharmaceutical Research Services
  • Multi-Omics Services
  • Support
  • /assets/images/icon/icon-email-2.png

    Email:

    info@MtoZ-Biolabs.com

    What Key Considerations Exist for PMP Pre-column Derivatization of Monosaccharides and HPLC Analysis? Is Validation Needed?

      When performing pre-column derivatization of monosaccharides using PMP (1-Phenyl-3-methyl-5-pyrazolone) labeling and analyzing them via high-performance liquid chromatography (HPLC), the following key considerations should be addressed:

       

      Derivatization Conditions

      It is crucial to optimize the derivatization reaction conditions, including temperature, time, and pH, to ensure successful PMP derivatization of the monosaccharides.

       

      Sample Preparation

      Samples should be accurately prepared and free from contamination. Minimizing sample loss and contamination is critical for reliable results.

       

      Chromatographic Conditions

      Select an appropriate chromatography column and optimize the mobile phase to achieve effective separation. The retention time and peak shape of the monosaccharides may be influenced by the mobile phase components, such as the type and ratio of organic solvents and buffer salt concentration.

       

      Detector Setup

      HPLC analysis typically employs UV or fluorescence detectors. PMP-derivatized monosaccharides exhibit strong fluorescence at specific wavelengths, and selecting the appropriate detector can enhance both sensitivity and selectivity.

       

      Standard Curve

      Generate a standard curve for quantitative analysis, ensuring that the handling of standards is consistent with that of the sample preparation.

       

      Method validation is crucial to ensure the accuracy, reliability, and compliance of the analytical method with expected performance standards. Validation should encompass the following key areas:

       

      1. Precision and Accuracy

      Assess the method’s consistency and accuracy through repeated analyses.

       

      2. Linear Range and Detection Limit

      Confirm the method’s applicability to the expected sample concentration range and determine the minimum detectable monosaccharide concentration.

       

      3. Sample Stability

      Evaluate the stability of the sample under specific storage conditions and time.

       

      4. Recovery Rate

      Assess the loss of monosaccharides during analysis by spiking known amounts of standard into the sample.

       

      MtoZ Biolabs, an integrated chromatography and mass spectrometry (MS) services provider.

      Related Services

      HPLC Protein Analysis Service

    Submit Inquiry
    Name *
    Email Address *
    Phone Number
    Inquiry Project
    Project Description *

     

    How to order?


    /assets/images/icon/icon-message.png

    Submit Inquiry

    /assets/images/icon/icon-return.png