2021
DOI: 10.1016/j.saa.2020.119163
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Univariate and multivariate assisted spectrophotometric methods for determination of rosuvastatin calcium and fenofibrate in bulk powders and tablets along with their degradation products

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Cited by 8 publications
(5 citation statements)
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“…2021 -European Journal of Chemistry -CC BY NC -DOI: 10.5155/eurjchem.12.4.368-376.2144 For both PLS-2 and PCR, the concentration residuals were plotted against the actual concentrations of the prepared mixtures (Figures 7 and 8), and the residuals for all samples were found to be randomly distributed around zero [25][26][27][28][29][30][31][32][33]. The average recoveries of each drug using PLS-2 and PCR methods are summarized in Table 2.…”
Section: Multivariate Chemometric Methods: (Pls-2) and (Pcr)mentioning
confidence: 99%
See 1 more Smart Citation
“…2021 -European Journal of Chemistry -CC BY NC -DOI: 10.5155/eurjchem.12.4.368-376.2144 For both PLS-2 and PCR, the concentration residuals were plotted against the actual concentrations of the prepared mixtures (Figures 7 and 8), and the residuals for all samples were found to be randomly distributed around zero [25][26][27][28][29][30][31][32][33]. The average recoveries of each drug using PLS-2 and PCR methods are summarized in Table 2.…”
Section: Multivariate Chemometric Methods: (Pls-2) and (Pcr)mentioning
confidence: 99%
“…The validation set is composed of 5 laboratory-prepared mixtures containing different proportions of AMP, SQX, and DVD (Table 1). In addition, the concentrations of AMP, SQX, and DVD in the veterinary formulation extract were calculated using the optimized PLS-2 or PCR calibration model after being recorded in the same specified lambda range [25][26][27][28][29][30][31][32][33].…”
Section: Pls-2 and Pcrmentioning
confidence: 99%
“…This is due to the fact that some side components may greatly affect the safety and effectiveness of drugs. High-performance (HP) liquid chromatography (LC) with UV detection [ 1 , 2 ], reversed-phase HPLC with photodiode array [ 3 , 4 , 5 ], UV [ 6 , 7 ] or fluorescence [ 7 ] detectors, HP thin-layer chromatography with densitometry [ 1 , 2 , 4 ], capillary zone electrophoresis [ 8 , 9 , 10 ], and spectrophotometry combined with chemometrics [ 11 , 12 , 13 , 14 , 15 , 16 ] can be used to control the degradation and purity of drugs. At the same time, there are two main approaches to the analysis.…”
Section: Introductionmentioning
confidence: 99%
“…In the first case, active ingredients are determined in the presence of side components so that the content of the latter does not influence an analytical signal [ 1 , 2 , 3 , 8 , 11 , 12 ]. The second approach is the simultaneous determination of drug components, including related organic impurities and degradation products [ 4 , 5 , 6 , 7 , 9 , 10 , 13 , 14 , 15 , 16 ].…”
Section: Introductionmentioning
confidence: 99%
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