2014
DOI: 10.1016/j.saa.2014.02.140
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Two and three way spectrophotometric-assisted multivariate determination of linezolid in the presence of its alkaline and oxidative degradation products and application to pharmaceutical formulation

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Cited by 12 publications
(5 citation statements)
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“…The most frequently employed inverse least squares for building multivariate calibration models are PCR and PLS [ 23 25 ]. In the statistical study of spectra, PLS and PCR algorithms are frequently employed to extract detailed data from more general data [ 26 , 27 ]. The PLS and PCR algorithms simultaneously consider the data about replies and levels [ 28 , 29 ].…”
Section: Resultsmentioning
confidence: 99%
“…The most frequently employed inverse least squares for building multivariate calibration models are PCR and PLS [ 23 25 ]. In the statistical study of spectra, PLS and PCR algorithms are frequently employed to extract detailed data from more general data [ 26 , 27 ]. The PLS and PCR algorithms simultaneously consider the data about replies and levels [ 28 , 29 ].…”
Section: Resultsmentioning
confidence: 99%
“…Due to its chemical structure, LNZ is highly unstable under alkaline conditions and several degradation studies have been done to evaluate the compounds obtained under conditions of alkaline stress. Alkaline degradation and photodegradation products have been investigated by chromatography and spectrophotometry in LNZ commercial (tablets) and injectable samples (Bebawy, 2003;Lopes, Salgado, 2009;Lopes, Salgado, 2010;Kawy, Weshahy, Shokry, 2012;Hegazy et al, 2014). Chiral impurities from LNZ have been analyzed by MEKC in linezolid solution for infusion (Michalska, Pajchel, Tyski, 2008b).…”
Section: Introductionmentioning
confidence: 99%
“…The volume of distribution is between 40 and 50% and corresponds to total body water. The drug is eliminated via renal and nonrenal routes with a terminal plasma elimination half-life between 4.5 and 5.5 h. 3 Reviewing the analytical literature for LIN determination reveals several methods such as liquid chromatographic methods for quantitation of LIN in tablets and in biological uids; 2,[4][5][6][7][8][9][10][11][12] for example, a chiral liquid chromatography method has been reported 13 along with TLC densitometry, HPLC [14][15][16][17] and capillary zone electrophoresis. 18,19 Voltammetric methods have also been utilised for LIN determination 20,21 and such an approach has the potential to provide a portable, rapid, sensitive and cost-effective sensor.…”
Section: Introductionmentioning
confidence: 99%