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Ultra-Sensitive Method for the Determination of 1,25 di-OH Vitamin D2 and 1,25 di-OH Vitamin D3 in Serum Using Supported Liquid Extraction Prior to LC-MS/MS

Applications | 2015 | BiotageInstrumentation
Sample Preparation, Consumables, LC/MS, LC/MS/MS, LC/QQQ
Industries
Clinical Research
Manufacturer
Shimadzu, SCIEX, Biotage

Summary

Importance of the topic


The active forms of vitamin D, 1,25 dihydroxyvitamin D2 and D3, are key regulators of calcium metabolism and cellular signaling. Accurate, ultra-sensitive measurement of these metabolites in serum is critical for clinical diagnostics, monitoring of metabolic bone diseases, and research into endocrine disorders.

Objectives and Study Overview


This application note describes a workflow to extract and quantify 1,25 di-OH vitamin D2 and D3 from human serum. The goal was to achieve a calibration range of 5–500 pg/mL, maximize sensitivity (LLOQ ~5 pg/mL), and ensure reproducible recoveries using supported liquid extraction followed by LC-MS/MS detection.

Methodology


Sample preparation combines serum with deuterated internal standard and 50% propan-2-ol to release protein-bound analytes. Supported liquid extraction is performed on ISOLUTE SLE+ 400 µL plates, loading by gravity and eluting with heptane. On-plate derivatization with PTAD in ethyl acetate/heptane and formation of methylamine complexes enhances MS response. Extracts are evaporated at ~40 °C and reconstituted in 70% methanol containing methylamine before analysis.

Instrumentation Used

  • Shimadzu Nexera UHPLC system
  • ACE Ultracore 2.5 Super C18 column (50 x 2.1 mm)
  • AB Sciex 5500 triple quadrupole mass spectrometer
  • Biotage Extrahera automation platform and TurboVap 96 evaporator

Main Results and Discussion

  • Recovery: 99–104% with %RSD ≤3.6 for both analytes
  • Linearity: 5–500 pg/mL (r² >0.994) with 1/x weighted regression
  • Sensitivity: LLOQ ~5 pg/mL demonstrated by spiked charcoal-stripped serum
  • Selectivity: No interference from 24,25 di-OH vitamin D3; baseline separation achieved

Benefits and Practical Applications


This method requires only 250 µL of serum and eliminates emulsions common in traditional liquid–liquid extraction. On-plate derivatization and methylamine complexation improve sensitivity with minimal additional cost. Automation on the Biotage Extrahera boosts sample throughput and consistency.

Future Trends and Opportunities

  • High-throughput integration with automated sample handlers for large-scale studies
  • Multiplexed assays including mono- and di-hydroxy vitamin D metabolites
  • Pharmacokinetic applications in vitamin D analog development
  • Comprehensive steroid profiling panels using similar workflows

Conclusion


The described SLE-LC-MS/MS protocol delivers robust, ultra-sensitive quantification of 1,25 di-OH vitamin D2 and D3 in serum. High recovery, reproducibility, and selectivity make it suitable for clinical research and quality control laboratories.

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

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