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Impurity Detection with a New Light Emitting Diode Induced Fluorescence Detector Coupled to the Agilent 7100 Capillary Electrophoresis System

Applications | 2014 | Agilent TechnologiesInstrumentation
Capillary electrophoresis
Industries
Pharma & Biopharma, Proteomics
Manufacturer
Agilent Technologies

Summary

Significance of the Topic


Capillary gel electrophoresis (CGE) is widely used in biopharmaceutical development and quality control to assess protein purity and detect low-level impurities in monoclonal antibody preparations. High-sensitivity fluorescence detection is essential to ensure product safety and batch consistency. LED-induced fluorescence detection (LEDIF) offers potential advantages over laser-based systems including lower energy consumption, improved baseline stability, and longer light source lifetime.

Study Objectives and Overview


This study evaluates the performance of a Picometrics LEDIF detector coupled with the Agilent 7100 Capillary Electrophoresis system for detecting trace protein impurities in FQ-derivatized monoclonal antibody samples. Key goals include determining the limit of detection (LOD), limit of quantification (LOQ), accuracy and precision of impurity measurements, and comparison to established laser-based fluorescence detection methods.

Methodology


Sample preparation involved derivatization of monoclonal antibody (mAb) solutions with 3-(2-furoyl)-quinoline-2-carboxaldehyde (FQ) in the presence of SDS, N-ethylmaleimide, and potassium cyanide. The reaction was conducted at elevated temperature followed by cooling and direct injection into capillaries without additional purification. Both nonreducing and reducing conditions were applied to resolve intact antibody and its heavy and light chains. Spiked samples with standard proteins (12, 18, 29, 45 kDa) at 0.05–0.25% levels were prepared to assess quantification performance.

Instrumentation


  • Agilent 7100 Capillary Electrophoresis System
  • Picometrics Zetalif LEDIF detector with 480 nm excitation LED and 510 nm high-pass emission filter
  • 50 μm id fused silica capillaries (33 cm total, 21 cm effective length)
  • Photomultiplier tube voltage set at 610 V, rise time 0.5 s
  • Qubit protein assay for concentration measurement

Main Results and Discussion


  • The LEDIF detector achieved accurate quantification of protein impurities down to 0.05% with precision better than 10% RSD for concentrations ≥ 0.1%. At 0.05% spike level, an S/N of ~8 was observed, consistent with an extrapolated LOD of 0.02% (S/N>3).
  • Peak shapes and baseline noise were comparable to those reported for laser-based systems, confirming similar sensitivity.
  • Daily reproducibility was verified across two instruments and multiple runs, with maximum deviation from target impurity levels of 12% and average deviation of 7.1%.

Benefits and Practical Applications


LEDIF detection on a standard CE platform provides:
  • High sensitivity for impurity profiling in biotherapeutics without requirement for costly lasers
  • Stable baseline and reduced energy consumption
  • Extended operational lifetime of LED sources
  • Integration into existing workflows for QA/QC and process development

Future Trends and Potential Applications


  • Further development of LED sources with expanded wavelength options for multiplexed fluorescence detection
  • Miniaturization and integration with microfluidic CE platforms for high-throughput impurity screening
  • Advanced data analysis and chemometric methods to enhance detection of complex impurity profiles
  • Adoption in regulated environments for routine quality control of biopharmaceuticals

Conclusion


The combination of an Agilent 7100 CE system with a Picometrics LEDIF detector offers a robust, sensitive, and cost-effective alternative to laser-induced fluorescence detection for monitoring low-level protein impurities in monoclonal antibody preparations. The demonstrated performance aligns closely with laser-based methods while providing the practical benefits of LED technology.

References


  1. Ahuja S and Jimilar MI. Capillary electrophoresis methods for pharmaceutical analysis. Volume 9 Separation Sciences and Technology Series. Academic Press, 2008.
  2. Wenz C. Performance of commercially available gels for protein characterization by CGE with UV detection on the Agilent 7100 CE system. Agilent Technologies Application Note 5990-7976EN.
  3. Salas-Solano O et al. Optimization and validation of a quantitative CGE-SDS method for monoclonal antibodies. Anal Chem. 2006;78:6583–6594.
  4. Michels DA et al. Fluorescent derivatization method of proteins for characterization by CE-SDS with laser-induced fluorescence detection. Anal Chem. 2007;79:5963–5971.
  5. Michels DA, Parker M, Salas-Solano O. Quantitative impurity analysis of mAb size heterogeneity by CE-LIF. Electrophoresis. 2012;33:815–826.
  6. Rodat-Boutonnet A et al. Comparative study of LED-induced fluorescence and laser-induced fluorescence in SDS-CGE: application to antibodies. Electrophoresis. 2012;33:1709–1714.

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