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Evaluation of impurities in simvastatin drug products with the use of FT-IR spectroscopy and selected chemometric techniques
2013
Open Chemistry
AbstractIn the present study a reversed phase high performance liquid chromatography (RP-HPLC) method with diode array detector (DAD) at room temperature was used for obtaining impurity profiles of 20 drug products containing simvastatin as an active substance. Fourier-transform infrared spectroscopy (FT-IR) was carried out to obtain absorption spectra of samples. The partial least squares (PLS) model was built to predict the relative content of lovastatin, the main impurity of simvastatin, and
doi:10.2478/s11532-013-0264-x
fatcat:drzag4nipfd5jgep7smwh6j3re