Formulation and evaluation of chitosan/chondriotin sulphate complex microcapsules for controlled delivery of water soluble drug

Oral route of drug administration is the most preferred route of drug administration but this route has its own limitations like pH of gastric media and controlling release rate of water soluble drug. To overcome these limitations, formulations containing controlled release matrix need to be develop...

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Autores principales: Shivakumar, Hosakote G., Singh, Mangla N., Yadav, Hemant K.S., Ram, Yaduvanshi M.
Formato: Articulo
Lenguaje:Inglés
Publicado: 2011
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/8381
http://www.latamjpharm.org/resumenes/30/9/LAJOP_30_9_1_25.pdf
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id I19-R120-10915-8381
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Farmacia
Sistemas de Liberación de Medicamentos
Sulfatos de Condroitina
Propranolol
Quitosana
spellingShingle Farmacia
Sistemas de Liberación de Medicamentos
Sulfatos de Condroitina
Propranolol
Quitosana
Shivakumar, Hosakote G.
Singh, Mangla N.
Yadav, Hemant K.S.
Ram, Yaduvanshi M.
Formulation and evaluation of chitosan/chondriotin sulphate complex microcapsules for controlled delivery of water soluble drug
topic_facet Farmacia
Sistemas de Liberación de Medicamentos
Sulfatos de Condroitina
Propranolol
Quitosana
description Oral route of drug administration is the most preferred route of drug administration but this route has its own limitations like pH of gastric media and controlling release rate of water soluble drug. To overcome these limitations, formulations containing controlled release matrix need to be developed. Controlled release of drug can be achieved by incorporating the drug into a release rate controlling carriers. Chitosan (CH)/Chondroitin Sulphate (CS) complex microcapsules were prepared to encapsulate the cardio vascular drug Propranolol hydrochloride (PHCl) by emulsion-chemical crosslinking method using sodium tripolyphosphate (STPP) as cross-linking agent. The FT-IR and DSC spectra’s revealed that there is no chemical interaction between drug and polymers used. Encapsulation efficiency and in-vitro drug release was found to be 64-84 % and 55-85 % respectively. Among all the formulations the F4.1 showed controlled drug release. This study revealed that the cross linked microcapsules of chitosan and chondroitin sulphate can be used to control drug release rate of water soluble drug.
format Articulo
Articulo
author Shivakumar, Hosakote G.
Singh, Mangla N.
Yadav, Hemant K.S.
Ram, Yaduvanshi M.
author_facet Shivakumar, Hosakote G.
Singh, Mangla N.
Yadav, Hemant K.S.
Ram, Yaduvanshi M.
author_sort Shivakumar, Hosakote G.
title Formulation and evaluation of chitosan/chondriotin sulphate complex microcapsules for controlled delivery of water soluble drug
title_short Formulation and evaluation of chitosan/chondriotin sulphate complex microcapsules for controlled delivery of water soluble drug
title_full Formulation and evaluation of chitosan/chondriotin sulphate complex microcapsules for controlled delivery of water soluble drug
title_fullStr Formulation and evaluation of chitosan/chondriotin sulphate complex microcapsules for controlled delivery of water soluble drug
title_full_unstemmed Formulation and evaluation of chitosan/chondriotin sulphate complex microcapsules for controlled delivery of water soluble drug
title_sort formulation and evaluation of chitosan/chondriotin sulphate complex microcapsules for controlled delivery of water soluble drug
publishDate 2011
url http://sedici.unlp.edu.ar/handle/10915/8381
http://www.latamjpharm.org/resumenes/30/9/LAJOP_30_9_1_25.pdf
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AT yadavhemantks formulationandevaluationofchitosanchondriotinsulphatecomplexmicrocapsulesforcontrolleddeliveryofwatersolubledrug
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