Quality and stability of oral extemporaneous formulations developed from commercial tablets containing spironolactone

The purpose of this study was to develop extemporaneous liquid pharmaceutical formulations from commercial tablets containing spironolactone and to assess their stability for use in children or adults with difficulty in swallowing. The content and stability of spironolactone in the tablets, as...

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Main Authors: Aline Marques Rosa, Mirella Carla Galana Gerlin, Isabella Correa Alcântara, Rubia Adrieli Sversut, Teófilo Fernando Mazon Cardoso, Patrik Oening Rodrigues, Marcos Serrou do Amaral, Nájla Mohamad Kassab
Format: Article
Language:English
Published: São Paulo State University (UNESP) 2014-08-01
Series:Revista de Ciências Farmacêuticas Básica e Aplicada
Subjects:
Online Access:http://serv-bib.fcfar.unesp.br/seer/index.php/Cien_Farm/article/view/385/1603
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spelling doaj-31742799b78e40af941c614d9dcc05cb2021-04-02T13:49:13ZengSão Paulo State University (UNESP)Revista de Ciências Farmacêuticas Básica e Aplicada1808-45322014-08-01353385392Quality and stability of oral extemporaneous formulations developed from commercial tablets containing spironolactoneAline Marques Rosa0Mirella Carla Galana Gerlin1Isabella Correa Alcântara2Rubia Adrieli Sversut3Teófilo Fernando Mazon Cardoso4Patrik Oening Rodrigues5Marcos Serrou do Amaral6Nájla Mohamad Kassab7 Universidade Federal de Mato Grosso do Sul Universidade Federal de Mato Grosso do Sul Universidade Federal de Mato Grosso do Sul Universidade Federal de Mato Grosso do Sul Universidade Federal de Mato Grosso do Sul Universidade Federal de Mato Grosso do Sul Universidade Federal de Mato Grosso do Sul Universidade Federal de Mato Grosso do Sul The purpose of this study was to develop extemporaneous liquid pharmaceutical formulations from commercial tablets containing spironolactone and to assess their stability for use in children or adults with difficulty in swallowing. The content and stability of spironolactone in the tablets, as well as in water, 1.5% carboxymethylcellulose (CMC) or simple syrup dispersions were determined by high performance liquid chromatography (HPLC) analysis on a C18 silica column (250 mm  4.6 mm  5 µm), with a mobile phase of methanol:water (75:25 v/v), flowing at 1 mL/ min, and UV detection at 240 nm. The extemporaneous formulations were tested over a 35-day period at 8, 27, and 40 ºC. Drug content in the aqueous dispersion was far lower than expected, with significant fluctuations at all temperatures, owing to rapid sedimentation. The content proved adequate in aqueous 1.5% CMC dispersion at 27 ºC, with undesirable variations at the other temperatures. The syrup-based dispersion remained stable at all three temperatures, with suitable drug content and no significant variability. No degradation products were observed in any of the formulations. The syrup-based dispersion is easy to prepare, self-preserving, stable, palatable, offering satisfactory drug content per dose, and can therefore be recommended as an extemporaneous formulation for enhancing treatment adherence and effectiveness.http://serv-bib.fcfar.unesp.br/seer/index.php/Cien_Farm/article/view/385/1603PediatricsLiquid chromatographyExtemporaneous formulationsEdemaHypertension and Dispersion
collection DOAJ
language English
format Article
sources DOAJ
author Aline Marques Rosa
Mirella Carla Galana Gerlin
Isabella Correa Alcântara
Rubia Adrieli Sversut
Teófilo Fernando Mazon Cardoso
Patrik Oening Rodrigues
Marcos Serrou do Amaral
Nájla Mohamad Kassab
spellingShingle Aline Marques Rosa
Mirella Carla Galana Gerlin
Isabella Correa Alcântara
Rubia Adrieli Sversut
Teófilo Fernando Mazon Cardoso
Patrik Oening Rodrigues
Marcos Serrou do Amaral
Nájla Mohamad Kassab
Quality and stability of oral extemporaneous formulations developed from commercial tablets containing spironolactone
Revista de Ciências Farmacêuticas Básica e Aplicada
Pediatrics
Liquid chromatography
Extemporaneous formulations
Edema
Hypertension and Dispersion
author_facet Aline Marques Rosa
Mirella Carla Galana Gerlin
Isabella Correa Alcântara
Rubia Adrieli Sversut
Teófilo Fernando Mazon Cardoso
Patrik Oening Rodrigues
Marcos Serrou do Amaral
Nájla Mohamad Kassab
author_sort Aline Marques Rosa
title Quality and stability of oral extemporaneous formulations developed from commercial tablets containing spironolactone
title_short Quality and stability of oral extemporaneous formulations developed from commercial tablets containing spironolactone
title_full Quality and stability of oral extemporaneous formulations developed from commercial tablets containing spironolactone
title_fullStr Quality and stability of oral extemporaneous formulations developed from commercial tablets containing spironolactone
title_full_unstemmed Quality and stability of oral extemporaneous formulations developed from commercial tablets containing spironolactone
title_sort quality and stability of oral extemporaneous formulations developed from commercial tablets containing spironolactone
publisher São Paulo State University (UNESP)
series Revista de Ciências Farmacêuticas Básica e Aplicada
issn 1808-4532
publishDate 2014-08-01
description The purpose of this study was to develop extemporaneous liquid pharmaceutical formulations from commercial tablets containing spironolactone and to assess their stability for use in children or adults with difficulty in swallowing. The content and stability of spironolactone in the tablets, as well as in water, 1.5% carboxymethylcellulose (CMC) or simple syrup dispersions were determined by high performance liquid chromatography (HPLC) analysis on a C18 silica column (250 mm  4.6 mm  5 µm), with a mobile phase of methanol:water (75:25 v/v), flowing at 1 mL/ min, and UV detection at 240 nm. The extemporaneous formulations were tested over a 35-day period at 8, 27, and 40 ºC. Drug content in the aqueous dispersion was far lower than expected, with significant fluctuations at all temperatures, owing to rapid sedimentation. The content proved adequate in aqueous 1.5% CMC dispersion at 27 ºC, with undesirable variations at the other temperatures. The syrup-based dispersion remained stable at all three temperatures, with suitable drug content and no significant variability. No degradation products were observed in any of the formulations. The syrup-based dispersion is easy to prepare, self-preserving, stable, palatable, offering satisfactory drug content per dose, and can therefore be recommended as an extemporaneous formulation for enhancing treatment adherence and effectiveness.
topic Pediatrics
Liquid chromatography
Extemporaneous formulations
Edema
Hypertension and Dispersion
url http://serv-bib.fcfar.unesp.br/seer/index.php/Cien_Farm/article/view/385/1603
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