Literature DB >> 21204112

Niacin and its metabolites: role of LC-MS/MS bioanalytical methods and update on clinical pharmacology. An overview.

Ramesh Mullangi1, Nuggehally R Srinivas.   

Abstract

Niacin (nicotinic acid), although an old drug, has seen a sudden surge in popularity for treatment of lipid disorders and other associated clinical conditions for the prevention of cardiovascular risk. Also, there has been considerable interest in clarifying the role of metabolic pathways of niacin in explaining the tolerability/adverse affect profile of the agent. Hence, it has become very important to quantify/monitor the levels of niacin and its metabolites in various clinical studies. This review describes the recent trends in the bioanalysis of niacin and its metabolites, where HPLC and LC-MS/MS assays have been successfully employed to measure the drug levels in various biological matrices arising from preclinical and clinical studies. In addition, this review encompass various considerations such as internal standard selection, extraction schemes, matrix effect, selectivity evaluation and optimization of mass spectral conditions to enable the development of sound bioanalytical methods for niacin alone or niacin along with its metabolites. Recent updates pertaining to the clinical pharmacology of niacin and ongoing debate for the clarification of adverse effects are also provided. Overall LC-MS/MS methods have proven to be choice of bioanalytical method for the quantification of niacin alone or with its metabolites in both preclinical and clinical studies. 2010 John Wiley & Sons, Ltd.

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Year:  2010        PMID: 21204112     DOI: 10.1002/bmc.1522

Source DB:  PubMed          Journal:  Biomed Chromatogr        ISSN: 0269-3879            Impact factor:   1.902


  6 in total

1.  Comparison of mouse urinary metabolic profiles after exposure to the inflammatory stressors γ radiation and lipopolysaccharide.

Authors:  Evagelia C Laiakis; Daniel R Hyduke; Albert J Fornace
Journal:  Radiat Res       Date:  2011-11-30       Impact factor: 2.841

2.  Gender differences in pharmacokinetics of a combination tablet of niacin extended-release/simvastatin in healthy Chinese volunteers.

Authors:  Xiao-lin Wang; Man Liu; Man Yang; Ya-nan Zhang; Dan Zhang; Li-na Zhang; Jing Han; Hui-chen Liu
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2013-12-18       Impact factor: 2.441

3.  Antiatherosclerotic Effects of 1-Methylnicotinamide in Apolipoprotein E/Low-Density Lipoprotein Receptor-Deficient Mice: A Comparison with Nicotinic Acid.

Authors:  Lukasz Mateuszuk; Agnieszka Jasztal; Edyta Maslak; Marlena Gasior-Glogowska; Malgorzata Baranska; Barbara Sitek; Renata Kostogrys; Agnieszka Zakrzewska; Agnieszka Kij; Maria Walczak; Stefan Chlopicki
Journal:  J Pharmacol Exp Ther       Date:  2015-12-02       Impact factor: 4.030

4.  Supplementing healthy rats with a high-niacin dose has no effect on muscle fiber distribution and muscle metabolic phenotype.

Authors:  Kristen Scholz; Anna Marie Kynast; Aline Couturier; Frank-Christoph Mooren; Karsten Krüger; Erika Most; Klaus Eder; Robert Ringseis
Journal:  Eur J Nutr       Date:  2013-11-24       Impact factor: 5.614

Review 5.  N-methyl-2-pyridone-5-carboxamide (2PY)-Major Metabolite of Nicotinamide: An Update on an Old Uremic Toxin.

Authors:  Aurélie Lenglet; Sophie Liabeuf; Sandra Bodeau; Loïc Louvet; Aurélien Mary; Agnès Boullier; Anne Sophie Lemaire-Hurtel; Alexia Jonet; Pascal Sonnet; Said Kamel; Ziad A Massy
Journal:  Toxins (Basel)       Date:  2016-11-15       Impact factor: 4.546

6.  Pharmacological doses of niacin stimulate the expression of genes involved in carnitine uptake and biosynthesis and improve the carnitine status of obese Zucker rats.

Authors:  Aline Couturier; Robert Ringseis; Erika Most; Klaus Eder
Journal:  BMC Pharmacol Toxicol       Date:  2014-07-09       Impact factor: 2.483

  6 in total

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