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Pharmaceutical development of solid-state formulations requires testing for uniformity and stability of active pharmaceutical ingredients and excipients. Solid-state properties such as component distribution and grain size are crucial factors of dissolution profile, which greatly affect drug efficacy and toxicity, and can only be analyzed spatially by chemical imaging (CI) techniques. Current CI techniques such as near infrared and confocal Raman spectroscopy do not offer high chemical and spatial resolution at speeds feasible for integration into the pharmaceutical quality control and quality assurance processes. We demonstrate fast chemical imaging by epi-detected sparse spectral sampling stimulated Raman scattering to quantify API and excipient degradation and distribution.
Yuxiao Wei,Isaac J Pence, andConor L Evans
"Quantitative analysis of drug tablet aging by sparse spectral sampling stimulated Raman scattering (S4RS)microscopy", Proc. SPIE PC12855, Advanced Chemical Microscopy for Life Science and Translational Medicine 2024, PC1285518 (13 March 2024); https://doi.org/10.1117/12.3001041
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Yuxiao Wei, Isaac J Pence, Conor L Evans, "Quantitative analysis of drug tablet aging by sparse spectral sampling stimulated Raman scattering microscopy," Proc. SPIE PC12855, Advanced Chemical Microscopy for Life Science and Translational Medicine 2024, PC1285518 (13 March 2024); https://doi.org/10.1117/12.3001041