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...
Main Authors: | , , , , , , , |
---|---|
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 |
id |
doaj-31742799b78e40af941c614d9dcc05cb |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT alinemarquesrosa qualityandstabilityoforalextemporaneousformulationsdevelopedfromcommercialtabletscontainingspironolactone AT mirellacarlagalanagerlin qualityandstabilityoforalextemporaneousformulationsdevelopedfromcommercialtabletscontainingspironolactone AT isabellacorreaalcantara qualityandstabilityoforalextemporaneousformulationsdevelopedfromcommercialtabletscontainingspironolactone AT rubiaadrielisversut qualityandstabilityoforalextemporaneousformulationsdevelopedfromcommercialtabletscontainingspironolactone AT teofilofernandomazoncardoso qualityandstabilityoforalextemporaneousformulationsdevelopedfromcommercialtabletscontainingspironolactone AT patrikoeningrodrigues qualityandstabilityoforalextemporaneousformulationsdevelopedfromcommercialtabletscontainingspironolactone AT marcosserroudoamaral qualityandstabilityoforalextemporaneousformulationsdevelopedfromcommercialtabletscontainingspironolactone AT najlamohamadkassab qualityandstabilityoforalextemporaneousformulationsdevelopedfromcommercialtabletscontainingspironolactone |
_version_ |
1721563881588916224 |