Formulation and Evaluation of Thermosensitive Biogels for Nose to Brain Delivery of Doxepin

Thermoreversible biogels can serve as effective systems for delivery of drugs through nose with increased nasal residence time. The objective of this study was to use chitosan and glycerophosphate based thermoreversible systems for delivery of doxepin to brain through intranasal administration. Form...

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Main Authors: Anuja Naik, Hema Nair
Format: Article
Language:English
Published: Hindawi Limited 2014-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2014/847547
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spelling doaj-6d9b1f8ac7c64b9299cb78288a7807d72020-11-25T00:02:48ZengHindawi LimitedBioMed Research International2314-61332314-61412014-01-01201410.1155/2014/847547847547Formulation and Evaluation of Thermosensitive Biogels for Nose to Brain Delivery of DoxepinAnuja Naik0Hema Nair1Department of Pharmaceutics, Bombay College of Pharmacy, Kalina, Santacruz (E), Mumbai 400 098, IndiaDepartment of Pharmaceutics, Bombay College of Pharmacy, Kalina, Santacruz (E), Mumbai 400 098, IndiaThermoreversible biogels can serve as effective systems for delivery of drugs through nose with increased nasal residence time. The objective of this study was to use chitosan and glycerophosphate based thermoreversible systems for delivery of doxepin to brain through intranasal administration. Formulations were prepared by admixture of suitable dilutions of chitosan and glycerophosphate with or without polyethylene glycol, followed by addition of the antidepressant doxepin hydrochloride. Both systems were evaluated for gelling characteristics, rheology, mucoadhesion, in vitro release, and ex vivo permeation through sheep nasal mucosa. In vivo efficacy was evaluated in Swiss albino mice through the forced swim test. Nasal tissues of mice subjected to repeated exposure to formulation were evaluated histopathologically. Both formulations gelled rapidly at 37°C, returned to sol state on cooling, and exhibited thixotropy. Addition of polyethylene glycol decreased the glycerophosphate content required for gelation and rendered the formulation isotonic. Both gels showed good mucoadhesion, enhanced drug permeation, and provided prolonged in vitro release at 37°C. Efficacy of the formulation in treated groups was inferred from the measured pharmacodynamic parameter and histopathological reports of formulation treated groups showed no significant local toxicity. The biogels could be potential systems for effective drug delivery to brain via nose.http://dx.doi.org/10.1155/2014/847547
collection DOAJ
language English
format Article
sources DOAJ
author Anuja Naik
Hema Nair
spellingShingle Anuja Naik
Hema Nair
Formulation and Evaluation of Thermosensitive Biogels for Nose to Brain Delivery of Doxepin
BioMed Research International
author_facet Anuja Naik
Hema Nair
author_sort Anuja Naik
title Formulation and Evaluation of Thermosensitive Biogels for Nose to Brain Delivery of Doxepin
title_short Formulation and Evaluation of Thermosensitive Biogels for Nose to Brain Delivery of Doxepin
title_full Formulation and Evaluation of Thermosensitive Biogels for Nose to Brain Delivery of Doxepin
title_fullStr Formulation and Evaluation of Thermosensitive Biogels for Nose to Brain Delivery of Doxepin
title_full_unstemmed Formulation and Evaluation of Thermosensitive Biogels for Nose to Brain Delivery of Doxepin
title_sort formulation and evaluation of thermosensitive biogels for nose to brain delivery of doxepin
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2014-01-01
description Thermoreversible biogels can serve as effective systems for delivery of drugs through nose with increased nasal residence time. The objective of this study was to use chitosan and glycerophosphate based thermoreversible systems for delivery of doxepin to brain through intranasal administration. Formulations were prepared by admixture of suitable dilutions of chitosan and glycerophosphate with or without polyethylene glycol, followed by addition of the antidepressant doxepin hydrochloride. Both systems were evaluated for gelling characteristics, rheology, mucoadhesion, in vitro release, and ex vivo permeation through sheep nasal mucosa. In vivo efficacy was evaluated in Swiss albino mice through the forced swim test. Nasal tissues of mice subjected to repeated exposure to formulation were evaluated histopathologically. Both formulations gelled rapidly at 37°C, returned to sol state on cooling, and exhibited thixotropy. Addition of polyethylene glycol decreased the glycerophosphate content required for gelation and rendered the formulation isotonic. Both gels showed good mucoadhesion, enhanced drug permeation, and provided prolonged in vitro release at 37°C. Efficacy of the formulation in treated groups was inferred from the measured pharmacodynamic parameter and histopathological reports of formulation treated groups showed no significant local toxicity. The biogels could be potential systems for effective drug delivery to brain via nose.
url http://dx.doi.org/10.1155/2014/847547
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