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Journal ArticleDOI

Determination of pravastatin in tablets by capillary electrophoresis

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TLDR
The proposed capillary electrophoretic method was successfully applied for the analysis of PRA in the pharmaceutical tablet formulation and proved simple, precise and fast since the analysis can be performed in less than 5 min.
Abstract
Pravastatin (PRA) is an inhibitor of HMG-CoA reductase enzyme, which is clinically used as a hypolipidemic agent to reduce cholesterol level. A capillary electrophoretic method for the determination of PRA in pharmaceutical tablet formulations is described. PRA and lansoprazole as an internal standard (IS) were well migrated in the background electrolyte of 10 mM borate buffer (pH 8.5) and 10% acetonitrile using a fused silica capillary. The separation was achieved by applying 27.5 kV, detecting at 200 nm and injecting the sample for 0.5 s and with an average migration time (tm) for PRA and IS of 4.7 and 3.9 min, respectively, at ambient temperature. The results were precise and repeatable for areas of the peaks and peak normalization ratio (PNPRA/PNIS). Linearity was found in the concentration range of 1.56-7.78 x 10(-5) M. Intra-day and Inter-day assays were performed and reliable results were obtained. Limit of detection and limit of quantitation were 8 x 10(-6) and 2.4 x 10(-5) M, respectively. The proposed method was successfully applied for the analysis of PRA in the pharmaceutical tablet formulation. The method proved simple, precise and fast since the analysis can be performed in less than 5 min.

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Citations
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Journal ArticleDOI

Capillary electrophoresis for the analysis of small-molecule pharmaceuticals.

TL;DR: This paper reviews the application of CE to the analysis of small‐molecule pharmaceuticals and the different electrophoretic modes available and their advantages for pharmaceutical analysis are described.
Journal ArticleDOI

Development of a selective LC method for the determination of pravastatin sodium

TL;DR: In this article, a simple and rapid stability-indicating high-performance liquid chromatographic (HPLC) method for pravastatin sodium (PRA) was successfully developed and validated for the assay of in tablets.
Book ChapterDOI

Capillary electrophoresis for pharmaceutical analysis.

TL;DR: The areas of pharmaceutical analysis covered are enantiomer separation, analysis of small molecules such as amino acids or drug counter-ions, pharmaceutical assay, related substances determinations, and physiochemical measurements such as log P and pKa of compounds.
Journal ArticleDOI

A novel use of oxidative coupling reactions for determination of some statins (cholesterol-lowering drugs) in pharmaceutical formulations.

TL;DR: New, accurate and reliable spectrophotometric methods for the assay of three statin drugs, atorvastatin calcium (AVS, FVS and PVS), in pure form and pharmaceutical formulations have been described and Statistical treatment of the experimental results indicates that the methods are precise and accurate.
Journal ArticleDOI

Kinetic spectrophotometric determination of pravastatin in drug formulations via derivatization with 4-chloro-7-nitrobenzo-2-oxa-1,3-diazole (NBD-Cl)

TL;DR: In this paper, a simple and sensitive kinetic spectrophotometric method for the quantitative analysis of pravastatin sodium (PVS) in pure and pharmaceutical formulations has been described, which is based on the formation of colored product between PVS and 4-chloro-7-nitrobenzo-2-oxa-1,3-diazole (NBD-Cl) in acetone medium at 55°±2°C.
References
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Journal ArticleDOI

Pharmacodynamics and pharmacokinetics of the HMG-CoA reductase inhibitors. Similarities and differences.

TL;DR: The liver is the target organ for the statins, since it is the major site of cholesterol biosynthesis, lipoprotein production and LDLcatabolism, and the adverse effects of HMG-reductase inhibitors during long term treatment may depend in part upon the degree to which they act in extrahepatic tissues.
Journal ArticleDOI

Clinical pharmacokinetics of pravastatin: mechanisms of pharmacokinetic events.

TL;DR: The dual routes of pravastatin elimination reduce the need for dosage adjustment if the function of either the liver or kidney is impaired, and also reduce the possibility of drug interactions compared with other statins, which are largely eliminated by metabolism.
Journal ArticleDOI

Determination of the HMG–CoA reductase inhibitors simvastatin, lovastatin, and pravastatin in plasma by gas chromatography/chemical ionization mass spectrometry

TL;DR: A general method for the assay of the 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors lovastsatin, pravastatin, and simvastatin in plasma has been developed and validated and has sufficient sensitivity, precision, accuracy, and selectivity for the analysis of clinical samples containing the drugs administered at therapeutic doses.
Journal ArticleDOI

Pravastatin. A reappraisal of its pharmacological properties and clinical effectiveness in the management of coronary heart disease.

TL;DR: Pravastatin is an HMG-CoA reductase inhibitor which lowers plasma cholesterol levels by inhibiting de novo cholesterol synthesis and should be considered a first-line agent in patients with elevated cholesterol levels, multiple risk factors or coronary heart disease who are at high risk of cardiovascular morbidity.
Journal ArticleDOI

Analytical methods for the quantitative determination of 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors in biological samples

TL;DR: Most method may be used quantitative determination of statins in plasma and they are suitable for therapeutic drug monitoring purpose of these drugs.
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