Isolation and structural elucidation of degradation products of alprazolam: Photostability studies of alprazolam tablets

Accelerated thermal, hydrolytic, and photochemical degradations of alprazolam were performed under several reaction conditions. The stress studies revealed the photolability of the drug as the most adverse stability factor; the main photodegradation products were isolated and properly characterized...

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Detalles Bibliográficos
Publicado: 2002
Materias:
pH
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00223549_v91_n5_p1274_Nudelman
http://hdl.handle.net/20.500.12110/paper_00223549_v91_n5_p1274_Nudelman
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spelling paper:paper_00223549_v91_n5_p1274_Nudelman2023-06-08T14:50:01Z Isolation and structural elucidation of degradation products of alprazolam: Photostability studies of alprazolam tablets Alprazolam Alprazolam photodegradation products Alprazolam stability Photochemical degradation Triazolobenzodiazepines alprazolam aminoquinoline derivative benzodiazepine derivative benzophenone derivative article chemical reaction kinetics drug degradation drug isolation drug stability drug storage hydrolysis pH photochemistry structure analysis tablet thermostability Accelerated thermal, hydrolytic, and photochemical degradations of alprazolam were performed under several reaction conditions. The stress studies revealed the photolability of the drug as the most adverse stability factor; the main photodegradation products were isolated and properly characterized as: triazolaminoquinoleine; 5-chloro-[5-methyl-4H-1,2,4-triazol-4-yl]benzophenone, and 1-methyl-6-phenyl-4h-s-triazo- [4,3-α][1,4]benzodiazepinone. Accelerated pH-dependent studies show that the photoinstability increases as the pH decreases; at pH 9.0, photodegradation does not occur, therefore, the photochemical degradation of alprazolam was performed in buffered solutions at pH 2.0 and 3.6. The higher rate of reaction was observed at pH = 2.0; consequently, acidic conditions should be avoided and appropriate light protection is recommended during the drug-development process, storage, and handling. The main degradation route for alprazolam tablets is also photochemical. © 2002 Wiley-Liss, Inc. 2002 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00223549_v91_n5_p1274_Nudelman http://hdl.handle.net/20.500.12110/paper_00223549_v91_n5_p1274_Nudelman
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Alprazolam
Alprazolam photodegradation products
Alprazolam stability
Photochemical degradation
Triazolobenzodiazepines
alprazolam
aminoquinoline derivative
benzodiazepine derivative
benzophenone derivative
article
chemical reaction kinetics
drug degradation
drug isolation
drug stability
drug storage
hydrolysis
pH
photochemistry
structure analysis
tablet
thermostability
spellingShingle Alprazolam
Alprazolam photodegradation products
Alprazolam stability
Photochemical degradation
Triazolobenzodiazepines
alprazolam
aminoquinoline derivative
benzodiazepine derivative
benzophenone derivative
article
chemical reaction kinetics
drug degradation
drug isolation
drug stability
drug storage
hydrolysis
pH
photochemistry
structure analysis
tablet
thermostability
Isolation and structural elucidation of degradation products of alprazolam: Photostability studies of alprazolam tablets
topic_facet Alprazolam
Alprazolam photodegradation products
Alprazolam stability
Photochemical degradation
Triazolobenzodiazepines
alprazolam
aminoquinoline derivative
benzodiazepine derivative
benzophenone derivative
article
chemical reaction kinetics
drug degradation
drug isolation
drug stability
drug storage
hydrolysis
pH
photochemistry
structure analysis
tablet
thermostability
description Accelerated thermal, hydrolytic, and photochemical degradations of alprazolam were performed under several reaction conditions. The stress studies revealed the photolability of the drug as the most adverse stability factor; the main photodegradation products were isolated and properly characterized as: triazolaminoquinoleine; 5-chloro-[5-methyl-4H-1,2,4-triazol-4-yl]benzophenone, and 1-methyl-6-phenyl-4h-s-triazo- [4,3-α][1,4]benzodiazepinone. Accelerated pH-dependent studies show that the photoinstability increases as the pH decreases; at pH 9.0, photodegradation does not occur, therefore, the photochemical degradation of alprazolam was performed in buffered solutions at pH 2.0 and 3.6. The higher rate of reaction was observed at pH = 2.0; consequently, acidic conditions should be avoided and appropriate light protection is recommended during the drug-development process, storage, and handling. The main degradation route for alprazolam tablets is also photochemical. © 2002 Wiley-Liss, Inc.
title Isolation and structural elucidation of degradation products of alprazolam: Photostability studies of alprazolam tablets
title_short Isolation and structural elucidation of degradation products of alprazolam: Photostability studies of alprazolam tablets
title_full Isolation and structural elucidation of degradation products of alprazolam: Photostability studies of alprazolam tablets
title_fullStr Isolation and structural elucidation of degradation products of alprazolam: Photostability studies of alprazolam tablets
title_full_unstemmed Isolation and structural elucidation of degradation products of alprazolam: Photostability studies of alprazolam tablets
title_sort isolation and structural elucidation of degradation products of alprazolam: photostability studies of alprazolam tablets
publishDate 2002
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00223549_v91_n5_p1274_Nudelman
http://hdl.handle.net/20.500.12110/paper_00223549_v91_n5_p1274_Nudelman
_version_ 1768544898757165056