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Raman spectroscopy solid dosage-form analysis

For formulated products an essential analysis is the assay for API content. This is usually performed by HPLC, but Raman spectroscopy can offer a quantitative analytical alternative. These applications have been extensively researched and reviewed by Strachan et al. [48] and provide over 30 literature references of where Raman spectroscopy has been used to determine the chemical content and physical form of API in solid dosage formulations. As no sample preparation is required the determination of multiple API forms (e.g. polymorphs, hydrates/solvates and amorphous content) provides a solid state analysis that is not possible by HPLC. However, as previously discussed sampling strategies must be employed to ensure the Raman measurement is representative of the whole sample. A potential solution is to sample the whole of a solid dosage form and not multiple regions of it. As presented in Chap. 3 the emerging technique of transmission Raman provides a method to do just this. With acquisition times in the order of seconds, this approach offers an alternative to HPLC and NIR analyses and is also applicable to tablet and capsule analysis in a PAT environment. [Pg.226]

Techniques that apply to in situ analysis of the dosage form, its precursor granulations, or powders are discussed. Applications of solid-state NMR, FTIR microspectroscopy, visual and scanning electron microscopy, Raman spectroscopy, NIR analysis, thermal techniques, mass spectrometry, and imaging techniques are presented. [Pg.263]


See other pages where Raman spectroscopy solid dosage-form analysis is mentioned: [Pg.226]    [Pg.14]    [Pg.236]    [Pg.241]    [Pg.226]    [Pg.595]    [Pg.600]    [Pg.268]    [Pg.442]    [Pg.598]    [Pg.378]    [Pg.421]    [Pg.451]    [Pg.242]   
See also in sourсe #XX -- [ Pg.252 ]




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