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...
Main Authors: | , |
---|---|
Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2014-01-01
|
Series: | BioMed Research International |
Online Access: | http://dx.doi.org/10.1155/2014/847547 |
id |
doaj-6d9b1f8ac7c64b9299cb78288a7807d7 |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT anujanaik formulationandevaluationofthermosensitivebiogelsfornosetobraindeliveryofdoxepin AT hemanair formulationandevaluationofthermosensitivebiogelsfornosetobraindeliveryofdoxepin |
_version_ |
1725436470247817216 |