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Transfer of NIR calibrations for pharmaceutical formulations between different instruments
Eva-Lotta Bergman1, Henric Brage, Mats Josefson
1AstraZeneca R&D Mölndal, SE-431 83 Mölndal, Sweden. eva-lotta.bergman@astrazeneca.com
Journal of Pharmaceutical and Biomedical Analysis
|January 13, 2006
Summary
Calibration transfer for Near-Infrared (NIR) spectroscopy in pharmaceutical formulations is feasible across different instruments. Local centering is recommended for its simplicity and effectiveness, requiring fewer samples without content variation.
Area of Science:
- Analytical Chemistry
- Pharmaceutical Technology
- Spectroscopy
Background:
- Near-Infrared (NIR) spectroscopy is crucial for analyzing pharmaceutical formulations.
- Transferring analytical calibrations between different NIR instruments is challenging but essential for widespread application.
- Existing calibration transfer methods need evaluation for their efficacy with solid pharmaceutical products.
Purpose of the Study:
- To assess the performance of established calibration transfer techniques for Near-Infrared (NIR) spectroscopy.
- To evaluate the feasibility of transferring calibrations between diverse NIR instrument types and configurations for solid pharmaceutical assays.
- To compare the effectiveness of slope/bias correction, local centering, and piecewise direct standardization (PDS) methods.
Main Methods:
- Utilized two dispersive NIR instruments and one Fourier transform (FT) NIR instrument.
- Tested three calibration transfer methods: slope/bias correction, local centering, and PDS.
- Evaluated transferability across instruments with different configurations and types for four active ingredient assays.
Main Results:
- All tested calibration transfer methods demonstrated comparable performance.
- Successful calibration transfer was achieved between instruments of different types and configurations without loss of predictive ability.
- Slope/bias correction requires more samples with greater active ingredient variation compared to local centering.
- PDS requires optimization of sample selection and method-specific factors for successful transfer.
Conclusions:
- Calibration transfer using NIR spectroscopy is viable for solid pharmaceutical formulations across various instruments.
- Local centering is the preferred method due to its excellent performance, simplicity, minimal sample requirement, and independence from sample content variation.
- The study confirms the potential for robust calibration transfer, enhancing the flexibility and applicability of NIR spectroscopy in pharmaceutical analysis.