2008
DOI: 10.1080/00032710801978566
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Development and Validation of Rapid Resolution RP-HPLC Method for Simultaneous Determination of Atorvastatin and Related Compounds by Use of Chemometrics

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Cited by 34 publications
(21 citation statements)
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“…The use of very low volumes of electrolyte (μL) and samples (nL) make the new MEKC procedures very interesting for determination of atorvastatin, purity evaluation and quantification of drug-related substances in a single analysis. The drawback of the proposed MEKC method is lower sensitivity compared to one obtained by RP-LC method for the same related substances [45]. The published UPLC method for simultaneous determination of atorvastatin and fenofibrate has better sensitivity and runtime of 3 min but the linearity, LOQ and LOD was established only for atorvastatin lactone [43].…”
Section: Capillary Electrophoresismentioning
confidence: 98%
See 1 more Smart Citation
“…The use of very low volumes of electrolyte (μL) and samples (nL) make the new MEKC procedures very interesting for determination of atorvastatin, purity evaluation and quantification of drug-related substances in a single analysis. The drawback of the proposed MEKC method is lower sensitivity compared to one obtained by RP-LC method for the same related substances [45]. The published UPLC method for simultaneous determination of atorvastatin and fenofibrate has better sensitivity and runtime of 3 min but the linearity, LOQ and LOD was established only for atorvastatin lactone [43].…”
Section: Capillary Electrophoresismentioning
confidence: 98%
“…Experimental design was used during method optimization and robustness testing [45]. Artificial Neural Networks were used for the modelling and prediction of chromatographic retention of atorvastatin and its impurities in micellar liquid chromatography [46].…”
Section: Atorvastatinmentioning
confidence: 99%
“…A rapid resolution HPLC method was used for separating and quantifying the related impurities of atorvastatin, including two epoxide impurities atorvastatin epoxy dihydroxy and atorvastatin epoxy diketone. The limit of detection (LOD) and limit of quantitation (LOQ) for atorvastatin epoxy dihydroxy and atorvastatin epoxy diketone were 0.025 and 0.075 g/ml, and 0.026 and 0.077 g/ml, respectively (Petkovska et al, 2008). Kong et al (2001) determined two epoxide terpenoid impurities (actein and 27-deoxyactein) in a traditional Chinese herbal preparation (Cimicifuga foetida L.).…”
Section: Hplc Methodsmentioning
confidence: 99%
“…On the other hand, some papers dealt with pharmaceutical analysis of atorvastatin with or without impurities [25][26][27]. Structure of atorvastatin and its impurities, which were investigated in present study is given in Fig.…”
Section: Introductionmentioning
confidence: 99%