Formulation and in-vitro evaluation of repaglinide microspheres prepared by spray drying technique

Repaglinide is a potent second generation oral hypoglycaemic agent widely used in treatment of non insulin dependent diabetic mellitus. The objective of the present study was to develop sustained release microspheres of repaglinide using ethyl cellulose and PEG 6000 as a matrix forming polymer. Mic...

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Autores principales: Kshirsagar, Sanjay J., Patel, Smit J., Madgulkar, Ashwini R., Bhalekar, Mangesh R.
Formato: Articulo Comunicacion
Lenguaje:Inglés
Publicado: 2011
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/8218
http://www.latamjpharm.org/resumenes/30/4/LAJOP_30_4_2_5.pdf
Aporte de:
id I19-R120-10915-8218
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Farmacia
Microesferas
ethyl cellulose; microsphere; PEG 6000; sustained release; spray drying
Sistemas de Liberación de Medicamentos
spellingShingle Farmacia
Microesferas
ethyl cellulose; microsphere; PEG 6000; sustained release; spray drying
Sistemas de Liberación de Medicamentos
Kshirsagar, Sanjay J.
Patel, Smit J.
Madgulkar, Ashwini R.
Bhalekar, Mangesh R.
Formulation and in-vitro evaluation of repaglinide microspheres prepared by spray drying technique
topic_facet Farmacia
Microesferas
ethyl cellulose; microsphere; PEG 6000; sustained release; spray drying
Sistemas de Liberación de Medicamentos
description Repaglinide is a potent second generation oral hypoglycaemic agent widely used in treatment of non insulin dependent diabetic mellitus. The objective of the present study was to develop sustained release microspheres of repaglinide using ethyl cellulose and PEG 6000 as a matrix forming polymer. Microspheres were prepared by taking various concentrations of ethyl cellulose and PEG 6000 by spray drying technique. Prepared microspheres were evaluated for process yield, drug entrapment, particle size, SEM, FTIR, DSC and in vitro drug release. Process yield and drug entrapment was 40-45 % and 90-95 %, respectively. Particle size ranged in 5-22 µm and SEM study showed spherical shape and rough surface of microspheres. FTIR study and DSC analysis revealed the stable nature and amorphous dispersion of drug in the polymer matrix. In vitro release studies indicate retardation of release upto 12 h which can control both fasting blood glucose level and postprandial blood glucose.
format Articulo
Comunicacion
author Kshirsagar, Sanjay J.
Patel, Smit J.
Madgulkar, Ashwini R.
Bhalekar, Mangesh R.
author_facet Kshirsagar, Sanjay J.
Patel, Smit J.
Madgulkar, Ashwini R.
Bhalekar, Mangesh R.
author_sort Kshirsagar, Sanjay J.
title Formulation and in-vitro evaluation of repaglinide microspheres prepared by spray drying technique
title_short Formulation and in-vitro evaluation of repaglinide microspheres prepared by spray drying technique
title_full Formulation and in-vitro evaluation of repaglinide microspheres prepared by spray drying technique
title_fullStr Formulation and in-vitro evaluation of repaglinide microspheres prepared by spray drying technique
title_full_unstemmed Formulation and in-vitro evaluation of repaglinide microspheres prepared by spray drying technique
title_sort formulation and in-vitro evaluation of repaglinide microspheres prepared by spray drying technique
publishDate 2011
url http://sedici.unlp.edu.ar/handle/10915/8218
http://www.latamjpharm.org/resumenes/30/4/LAJOP_30_4_2_5.pdf
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AT madgulkarashwinir formulationandinvitroevaluationofrepaglinidemicrospherespreparedbyspraydryingtechnique
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