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Method Development for Enantiomers Using the Agilent 1200 Infinity Series Method Development Solution

Applications | 2014 | Agilent TechnologiesInstrumentation
HPLC
Industries
Pharma & Biopharma
Manufacturer
Agilent Technologies

Summary

Importance of the Topic


Chiral analysis of pharmaceuticals is essential to ensure drug safety and efficacy, as different enantiomers can exhibit distinct biological activities and side effects. Regulatory agencies mandate precise characterization and quantification of each stereoisomer during drug development, clinical studies, and manufacturing to guarantee product quality and patient safety.

Objectives and Study Overview


This work illustrates the use of the Agilent 1200 Infinity Series Method Development Solution combined with the Agilent Method Scouting Wizard to accelerate chiral method development. Two model analytes were selected: tofizopam, which possesses four stereoisomeric forms, and vanillyl-mandelic acid, featuring two enantiomers. The study evaluates multiple chiral stationary phases and mobile phase compositions to identify optimal separation conditions.

Methodology and Instrumentation


  • Instrumentation
    • Agilent 1200 Infinity Series Method Development Solution
    • Agilent 1290 Infinity Quaternary Pump
    • Agilent 1290 Infinity Autosampler
    • Agilent 1290 Infinity Thermostatted Column Compartments
    • Agilent 1200 Infinity Diode Array Detector
    • Agilent OpenLAB CDS ChemStation with Method Scouting Wizard
  • Chiral Phases
    • YMC CHIRAL Amylose-C
    • YMC CHIRAL Cellulose-C
    • YMC CHIRAL Cellulose-SB
  • Mobile Phases
    • Hexane
    • Ethanol with 1 % trifluoroacetic acid (TFA)
    • Ethanol with 1 % diethylamine (DEA)
  • Chromatographic Conditions
    • Flow rate: 1 mL/min
    • Injection volume: 5 µL
    • Column temperature: 25 °C
    • Sample temperature: 10 °C
    • Detection: 230 nm, reference 360 nm, 10 Hz, 10 mm cell
    • Isocratic runs with constant solvent composition throughout

Main Results and Discussion


Systematic column and solvent scouting revealed that:
  • Tofizopam’s four stereoisomers were baseline-resolved on the Cellulose-SB column using 80 % hexane/20 % ethanol. Adding 0.1 % DEA further improved summed resolution.
  • Vanillyl-mandelic acid enantiomers achieved optimal separation on Amylose-C with a ternary mixture of 80 % hexane, 10 % ethanol, and 10 % TFA.
The automated scouting sequences streamlined setup of isocratic runs, column switching, flushing, equilibration, and storage steps, reducing hands-on time.

Benefits and Practical Applications


  • Rapid method development with minimal manual intervention
  • Automated screening of columns and solvent conditions
  • Ability to analyze neutral, acidic, and basic chiral compounds in unified sequences
  • Support for up to six long columns without manual reconnection

Future Trends and Opportunities


Next-generation developments may include expanded chiral stationary phase libraries, integration with supercritical fluid chromatography and mass spectrometry, and application of machine-learning algorithms to predict optimal chromatographic conditions, further reducing experimental effort.

Conclusion


The Agilent 1200 Infinity Series Method Development Solution paired with the Method Scouting Wizard provides an efficient, automated platform for chiral method development. It delivers high-resolution separations of complex stereoisomeric mixtures while significantly reducing development time.

References


  1. US Food and Drug Administration. Development of New Stereoisomeric Drugs: Guidance for Industry; FDA, 1992.
  2. Zhang T. et al. Separation of Enantiomers and Conformers of Tofizopam Using Daicel Immobilized Polysaccharide-Derived Chiral Columns on an Agilent 1260 Infinity Analytical SFC System. Agilent Technologies Application Note 5990-9315EN, 2011.
  3. Gratzfeld-Hüsgen A. Agilent 1200 Series LC Method Development Solution for the Analysis of Degradation Products of Metoprolol Tablets. Agilent Technologies Application Note 5989-9339EN, 2010.

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