Multiresidue Analysis of Veterinary Drugs in Bovine Liver by LC/MS/MS

Applications | 2015 | Agilent TechnologiesInstrumentation
Sample Preparation, Consumables, LC/MS, LC/MS/MS, LC/QQQ
Industries
Food & Agriculture
Manufacturer
Agilent Technologies

Significance of the Topic


The accurate detection of multiple veterinary drug residues in fatty food matrices such as bovine liver is critical for food safety and regulatory compliance. High lipid content interferes with chromatographic and mass spectrometric analysis, reducing sensitivity and precision. The use of a selective lipid‐removal sorbent simplifies sample preparation, minimizes matrix effects, and supports multiresidue monitoring programs.

Objectives and Study Overview


This study evaluated Agilent’s Bond Elut Enhanced Matrix Removal—Lipid (EMR—Lipid) dispersive solid‐phase extraction (dSPE) for cleanup of acidified acetonitrile liver extracts prior to LC/MS/MS analysis of 30 representative veterinary drugs. Key goals were to compare lipid‐removal efficiency and analyte recovery against traditional C18 and zirconia sorbents, optimize sample preparation conditions, and validate a robust multiresidue method.

Methodology and Instrumentation


Sample preparation comprised:
  • Weigh 2 g homogenized bovine liver, spike internal standard, and extract with 10 mL acetonitrile containing 5% formic acid.
  • Centrifuge and transfer 5 mL supernatant to EMR—Lipid dSPE tube with 5 mM ammonium acetate activation buffer; vortex and centrifuge.
  • Perform a polish step by adding MgSO₄/NaCl salt mix in an EMR—Lipid polish tube; vortex, centrifuge, then dilute with water for injection.
Instrumentation included an Agilent 1290 Infinity UHPLC coupled to a 6490 triple‐quadrupole mass spectrometer with Jet Stream electrospray. A Poroshell C18 column and a binary gradient of 0.1% formic acid in water/acetonitrile at 0.3 mL/min achieved separation of acidic, neutral, and basic analytes.

Main Results and Discussion


The EMR—Lipid cleanup removed 56% of coextractives by weight—significantly more than zirconia (50%) or C18 (35%). Postcolumn infusion experiments demonstrated dramatically reduced matrix suppression/enhancement. Optimization showed that 5% formic acid and 5 mM ammonium acetate buffer enhanced analyte recoveries and calibration linearity. A simplified non‐polish protocol improved tetracycline recoveries to >85%, though the polish step delivered acceptable precision. Compared to QuEChERS workflows with C18 or zirconia dSPE, EMR—Lipid delivered superior recoveries (>70% for 28/30 analytes) and RSDs below 10% for most compounds. Calibration curves were linear (R²>0.99) over 5–1,000 ng/g (Group 1) and 1–200 ng/g (Group 2). Method validation across four concentration levels achieved 70–120% accuracy for 93% of analytes with RSDs typically <8%.

Benefits and Practical Applications


  • Efficient, selective lipid removal improves data quality and instrument uptime.
  • Simplified workflow reduces sample handling time and risk of analyte loss.
  • Suitable for high‐throughput laboratories monitoring multiclass residues in fatty tissues.

Future Trends and Potential Applications


Further studies will explore EMR—Lipid’s performance in other complex matrices (milk, fish, egg) and extend to additional analyte classes, including emerging contaminants. Integration with automated sample preparation platforms and high‐resolution mass spectrometry may broaden scope and throughput.

Conclusion


The EMR—Lipid dSPE workflow combined with protein precipitation offers a fast, robust, and reproducible method for multiresidue veterinary drug analysis in bovine liver. Superior matrix cleanup and consistent recoveries facilitate reliable LC/MS/MS quantitation in high‐fat samples.

References


  • European Commission Decision 2002/657/EC on analytical method performance and interpretation.
  • Fagerquist et al., Anal. Chem. 2005, 77, 1473–1482.
  • Mastovska & Lightfield, J. Chromatogr. A 2008, 1202, 118–123.
  • Geis‐Asteggiante et al., J. Chromatogr. A 2012, 1258, 43–54.
  • Schneider et al., Anal. Bioanal. Chem. 2015, 407, 4423.
  • SANCO/12571/2013 Guidance on QC and validation procedures for pesticide residues analysis.

Content was automatically generated from an orignal PDF document using AI and may contain inaccuracies.

Downloadable PDF for viewing
 

Similar PDF

Complex Matrices: Minimizing Lipids, Maximizing Recovery - Food Testing Application Compendium: Volume 3
Multiclass Multiresidue Veterinary Drug Analysis in Beef Using Agilent Captiva EMR—Lipid Cartridge Cleanup and LC/MS/MS
Multiresidue Analysis of Pesticides in Avocado with Agilent Bond Elut EMR—Lipid by GC/MS/MS
Removal of Lipids for the Analysis of Toxicological Compounds in Plasma by LC/MS/MS