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Demonstrating Inertness for the Analysis of Nucleotides on the Agilent 1290 Infinity II Bio LC

Technical notes | 2022 | Agilent TechnologiesInstrumentation
HPLC
Industries
Pharma & Biopharma
Manufacturer
Agilent Technologies

Summary

Significance of the Topic


The analysis of metal-sensitive compounds such as nucleotides demands chromatographic systems with minimal surface interactions.
Unwanted adsorption to metal components can cause peak tailing, reduced recovery, and compromised data quality.
Demonstrating system inertness is essential for reliable quantification in biochromatography, ensuring high confidence in applications across pharmaceuticals, diagnostics, and research.

Objectives and Study Overview


This application note evaluates the inertness of the Agilent 1290 Infinity II Bio LC system using a test mixture of adenosine and a nonhydrolyzable nucleotide analog (AMPcP).
By comparing the chromatographic peak areas of equimolar amounts of these molecules over multiple injections, the study probes potential adsorption of phosphate groups to metal surfaces under biochromatographic conditions.
The primary goal is to determine the area ratio of AMPcP to adenosine and assess system performance in terms of reproducibility and low-adsorption behavior.

Methodology and Instrumentation


  • Agilent 1290 Infinity II Bio LC System modules: Flexible Pump (G7131A), Bio Multisampler with sample thermostat (G7137A), Multicolumn Thermostat (G7116B), Variable Wavelength Detector (G7114B) with biocompatible micro flow cell.
  • Column: Waters ACQUITY PREMIER HSS T3, 1.8 µm, 2.1 × 50 mm.

  • Mobile phase A: 10 mM ammonium acetate in water.
  • Mobile phase B: 90% acetonitrile, 10% water, 10 mM ammonium acetate, 0.1% TFA.
  • Gradient: 0 min at 5% B to 3 min at 95% B; stop time 3 min; post time 5 min.
  • Flow rate: 0.400 mL/min; column temperature: 35 °C; detection wavelength: 260 nm; injection volume: 1 µL; sample thermostat: 10 °C.

Results and Discussion


Five consecutive injections of the adenosine/AMPcP mixture yielded highly consistent retention times and peak areas.
The calculated area ratio of AMPcP to adenosine was 0.95 ± 0.01, indicating negligible adsorption of the phosphate-containing nucleotide to the flow path.
Relative standard deviations for retention time and peak area remained below 0.5%, demonstrating excellent reproducibility.
In contrast, stainless steel-based systems typically show area ratios well below unity due to strong interactions with phosphate groups.

Benefits and Practical Applications


The Agilent 1290 Infinity II Bio LC system offers a low-adsorption platform ideal for the analysis of metal-sensitive analytes such as nucleotides, phosphorylated peptides, and chelating biomolecules.
Its bioinert flow path and compatibility with high salt, urea, and extreme pH solvents support robust performance in biopharmaceutical QA/QC, metabolomics, and bioanalytical research.

Future Trends and Potential Applications


Continued development of bioinert materials will expand capabilities for intact protein and complex glycan analysis under challenging conditions.
Integration with mass spectrometry and high-throughput workflows will further enhance sensitivity and throughput.
Emerging column chemistries and surface treatments may offer tailored interactions for a wider range of metal-sensitive compounds.

Conclusion


The Agilent 1290 Infinity II Bio LC system, built with MP35N-based flow path materials, demonstrates outstanding inertness for nucleotide analysis.
Low adsorption, high reproducibility, and robust operation under biochromatographic conditions ensure confident quantification of phosphorylated analytes.
This platform is recommended for laboratories requiring reliable performance in the analysis of metal-sensitive compounds.

References


  1. Wakamatsu A et al. A Severe Peak Tailing of Phosphate Compounds Caused by Interaction with Stainless Steel Used for Liquid Chromatography and Electrospray Mass Spectrometry. Mass Spectrom. Appl. Sep. Sci. 2005;28(14):1823–1830.
  2. Fekete S. Defining Material Used in Biopharmaceutical Analysis. LCGC Europe. 2021;34(6):245–248.
  3. Schneider S. Comparability Studies for the Analysis of Nucleotides on Four Different LC Systems. Agilent Technologies Application Note 5994-4392EN; 2021.
  4. Patel A et al. PREMIER Standards to Investigate the Inertness of Chromatographic Surfaces. Waters Corporation Application Note 720007105EN; 2021.

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