ResourceSpectroscopy

Quantification of Tablets Containing Multiple APIs Using Transmission Raman Spectroscopy

26 Feb 2019

The ability to predict multiple constituents of a final dosage form in one fast, nondestructive measurement can reduce analysis time and cost significantly. This is especially beneficial when quantification of multiple active pharmaceutical ingredients (APIs) is required for tests such as content uniformity, assay, and identity (ID). This example, based on a common cold and flu product, demonstrates the quantification of five components (three APIs and two excipients) with a nine‑second measurement. Nominal concentrations for the APIs ranged from 1 to 85 % w/w.

TRS100 Quantitative Pharmaceutical Analysis System

Agilent Technologies

The TRS100 enables fast, easy-to-use whole tablet or capsule content uniformity and polymorph screening for pharmaceutical finished-product testing and formulation development. Easier to implement than other spectroscopic methods, Agilent's transmission Raman spectroscopy (TRS) technology allows simple method development and deployment for quantitative analysis in quality control applications.

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Raman SpectroscopyRaman spectroscopy is used to discern the vibrational and rotational states of molecules and hence the chemical composition of a sample by measuring the inelastic scattering of monochromatic light. Explore a range of Raman spectrometers, including handheld/portable Raman spectrometers for QC/QA labs and in situ spectrometers for processes. Conduct Raman imaging for microanalysis of mixed samples using a Raman microscope. Raman spectrographs are also available. Find the best Raman spectroscopy products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.Active PharmaceuticalsThe Active Pharmaceutical Ingredient (API) of a drug is the component that causes the direct effect of the product. The remaining inactive components are known as excipients.Drug TestingIt is essential to test the efficacy and toxicity of drugs at every stage of their development to ensure that a pharmaceutical product is fit for purpose and safe for use before reaching the stage of mass production and distribution.
Quantification of Tablets Containing Multiple APIs Using Transmission Raman Spectroscopy