Chemical degradation kinetics of fibrates: bezafibrate, ciprofibrate and fenofibrate

ABSTRACT Fibrates are drugs used for the treatment of hypertriglyceridemia and for the prevention of atherosclerosis. Three drugs in the fibrate class, ciprofibrate, fenofibrate and bezafibrate, were chosen for this study because their raw materials are readily available and because scientific publications on these compounds is limited. To evaluate their intrinsic stability, the drugs were exposed to a test condition (temperature, oxidation, UV light exposure, hydrolysis at different pH values and metal ions in solution) and then were subjected to analysis by HPLC. The samples were run on a C18 column, with a flow rate of 1.0 mL min-1 in a mobile phase consisting of methanol: 0.01 % phosphoric acid v/v (80:20), with variable detection wavelengths in the UV spectra. The analysis methodology showed satisfactory performance parameters. The three drugs were very unstable, degrading in each of the conditions evaluated. The test conditions of acid and basic hydrolysis showed the most significant degradation. The results demonstrated that the drugs in this class are unstable. Based on these experimentally determined degradation kinetics, it is easy to understand and emphasize the importance of the lack of liquid dosage forms on the market for fibrates because of their instability.

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Main Authors: Oliveira,Marcelo Antonio de, Silva,Gerliane Damázio da, Campos,Michele Soares Tacchi
Format: Digital revista
Language:English
Published: Universidade de São Paulo, Faculdade de Ciências Farmacêuticas 2016
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502016000300545
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spelling oai:scielo:S1984-825020160003005452016-11-29Chemical degradation kinetics of fibrates: bezafibrate, ciprofibrate and fenofibrateOliveira,Marcelo Antonio deSilva,Gerliane Damázio daCampos,Michele Soares Tacchi Hypertriglyceridemia/fibrates Fibrates stability/study Fibrates degradation products/High Perfomance Liquid Chromatography (HPLC) Fibrates/Degradation kinetics. ABSTRACT Fibrates are drugs used for the treatment of hypertriglyceridemia and for the prevention of atherosclerosis. Three drugs in the fibrate class, ciprofibrate, fenofibrate and bezafibrate, were chosen for this study because their raw materials are readily available and because scientific publications on these compounds is limited. To evaluate their intrinsic stability, the drugs were exposed to a test condition (temperature, oxidation, UV light exposure, hydrolysis at different pH values and metal ions in solution) and then were subjected to analysis by HPLC. The samples were run on a C18 column, with a flow rate of 1.0 mL min-1 in a mobile phase consisting of methanol: 0.01 % phosphoric acid v/v (80:20), with variable detection wavelengths in the UV spectra. The analysis methodology showed satisfactory performance parameters. The three drugs were very unstable, degrading in each of the conditions evaluated. The test conditions of acid and basic hydrolysis showed the most significant degradation. The results demonstrated that the drugs in this class are unstable. Based on these experimentally determined degradation kinetics, it is easy to understand and emphasize the importance of the lack of liquid dosage forms on the market for fibrates because of their instability.info:eu-repo/semantics/openAccessUniversidade de São Paulo, Faculdade de Ciências FarmacêuticasBrazilian Journal of Pharmaceutical Sciences v.52 n.3 20162016-09-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502016000300545en10.1590/s1984-82502016000300019
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country Brasil
countrycode BR
component Revista
access En linea
databasecode rev-scielo-br
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region America del Sur
libraryname SciELO
language English
format Digital
author Oliveira,Marcelo Antonio de
Silva,Gerliane Damázio da
Campos,Michele Soares Tacchi
spellingShingle Oliveira,Marcelo Antonio de
Silva,Gerliane Damázio da
Campos,Michele Soares Tacchi
Chemical degradation kinetics of fibrates: bezafibrate, ciprofibrate and fenofibrate
author_facet Oliveira,Marcelo Antonio de
Silva,Gerliane Damázio da
Campos,Michele Soares Tacchi
author_sort Oliveira,Marcelo Antonio de
title Chemical degradation kinetics of fibrates: bezafibrate, ciprofibrate and fenofibrate
title_short Chemical degradation kinetics of fibrates: bezafibrate, ciprofibrate and fenofibrate
title_full Chemical degradation kinetics of fibrates: bezafibrate, ciprofibrate and fenofibrate
title_fullStr Chemical degradation kinetics of fibrates: bezafibrate, ciprofibrate and fenofibrate
title_full_unstemmed Chemical degradation kinetics of fibrates: bezafibrate, ciprofibrate and fenofibrate
title_sort chemical degradation kinetics of fibrates: bezafibrate, ciprofibrate and fenofibrate
description ABSTRACT Fibrates are drugs used for the treatment of hypertriglyceridemia and for the prevention of atherosclerosis. Three drugs in the fibrate class, ciprofibrate, fenofibrate and bezafibrate, were chosen for this study because their raw materials are readily available and because scientific publications on these compounds is limited. To evaluate their intrinsic stability, the drugs were exposed to a test condition (temperature, oxidation, UV light exposure, hydrolysis at different pH values and metal ions in solution) and then were subjected to analysis by HPLC. The samples were run on a C18 column, with a flow rate of 1.0 mL min-1 in a mobile phase consisting of methanol: 0.01 % phosphoric acid v/v (80:20), with variable detection wavelengths in the UV spectra. The analysis methodology showed satisfactory performance parameters. The three drugs were very unstable, degrading in each of the conditions evaluated. The test conditions of acid and basic hydrolysis showed the most significant degradation. The results demonstrated that the drugs in this class are unstable. Based on these experimentally determined degradation kinetics, it is easy to understand and emphasize the importance of the lack of liquid dosage forms on the market for fibrates because of their instability.
publisher Universidade de São Paulo, Faculdade de Ciências Farmacêuticas
publishDate 2016
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502016000300545
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