Bioadhesive Controlled Metronidazole Release Matrix Based on Chitosan and Xanthan Gum

Metronidazole, a common antibacterial drug, was incorporated into a hydrophilic polymer matrix composed of chitosan xanthan gum mixture. Hydrogel formation of this binary chitosan-xanthan gum combination was tested for its ability to control the release of metronidazole as a drug model. This prepara...

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Main Authors: Ala’a F. Eftaiha, Nidal Qinna, Iyad S. Rashid, Mayyas M. Al Remawi, Munther R. Al Shami, Tawfiq A. Arafat, Adnan A. Badwan
Format: Article
Language:English
Published: MDPI AG 2010-05-01
Series:Marine Drugs
Subjects:
Online Access:http://www.mdpi.com/1660-3397/8/5/1716/
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spelling doaj-aad86249e95c4028ae22864b311a6d512020-11-24T23:54:59ZengMDPI AGMarine Drugs1660-33972010-05-01851716173010.3390/md8051716Bioadhesive Controlled Metronidazole Release Matrix Based on Chitosan and Xanthan GumAla’a F. EftaihaNidal QinnaIyad S. RashidMayyas M. Al RemawiMunther R. Al ShamiTawfiq A. ArafatAdnan A. BadwanMetronidazole, a common antibacterial drug, was incorporated into a hydrophilic polymer matrix composed of chitosan xanthan gum mixture. Hydrogel formation of this binary chitosan-xanthan gum combination was tested for its ability to control the release of metronidazole as a drug model. This preparation (MZ-CR) was characterized by in vitro, ex vivo bioadhesion and in vivo bioavailability study. For comparison purposes a commercial extended release formulation of metronidazole (CMZ) was used as a reference. The in vitro drug-release profiles of metronidazole preparation and CMZ were similar in 0.1 M HCl and phosphate buffer pH 6.8. Moreover, metronidazole preparation and CMZ showed a similar detachment force to sheep stomach mucosa, while the bioadhesion of the metronidazole preparation was higher three times than CMZ to sheep duodenum. The results of in vivo study indicated that the absorption of metronidazole from the preparation was faster than that of CMZ. Also, MZ-CR leads to higher metronidazole Cmax and AUC relative to that of the CMZ. This increase in bioavailability might be explained by the bioadhesion of the preparation at the upper part of the small intestine that could result in an increase in the overall intestinal transit time. As a conclusion, formulating chitosan-xanthan gum mixture as a hydrophilic polymer matrix resulted in a superior pharmacokinetic parameters translated by better rate and extent of absorption of metronidazole. http://www.mdpi.com/1660-3397/8/5/1716/metronidazolechitosanxanthan gumbioadhesionbioavailability
collection DOAJ
language English
format Article
sources DOAJ
author Ala’a F. Eftaiha
Nidal Qinna
Iyad S. Rashid
Mayyas M. Al Remawi
Munther R. Al Shami
Tawfiq A. Arafat
Adnan A. Badwan
spellingShingle Ala’a F. Eftaiha
Nidal Qinna
Iyad S. Rashid
Mayyas M. Al Remawi
Munther R. Al Shami
Tawfiq A. Arafat
Adnan A. Badwan
Bioadhesive Controlled Metronidazole Release Matrix Based on Chitosan and Xanthan Gum
Marine Drugs
metronidazole
chitosan
xanthan gum
bioadhesion
bioavailability
author_facet Ala’a F. Eftaiha
Nidal Qinna
Iyad S. Rashid
Mayyas M. Al Remawi
Munther R. Al Shami
Tawfiq A. Arafat
Adnan A. Badwan
author_sort Ala’a F. Eftaiha
title Bioadhesive Controlled Metronidazole Release Matrix Based on Chitosan and Xanthan Gum
title_short Bioadhesive Controlled Metronidazole Release Matrix Based on Chitosan and Xanthan Gum
title_full Bioadhesive Controlled Metronidazole Release Matrix Based on Chitosan and Xanthan Gum
title_fullStr Bioadhesive Controlled Metronidazole Release Matrix Based on Chitosan and Xanthan Gum
title_full_unstemmed Bioadhesive Controlled Metronidazole Release Matrix Based on Chitosan and Xanthan Gum
title_sort bioadhesive controlled metronidazole release matrix based on chitosan and xanthan gum
publisher MDPI AG
series Marine Drugs
issn 1660-3397
publishDate 2010-05-01
description Metronidazole, a common antibacterial drug, was incorporated into a hydrophilic polymer matrix composed of chitosan xanthan gum mixture. Hydrogel formation of this binary chitosan-xanthan gum combination was tested for its ability to control the release of metronidazole as a drug model. This preparation (MZ-CR) was characterized by in vitro, ex vivo bioadhesion and in vivo bioavailability study. For comparison purposes a commercial extended release formulation of metronidazole (CMZ) was used as a reference. The in vitro drug-release profiles of metronidazole preparation and CMZ were similar in 0.1 M HCl and phosphate buffer pH 6.8. Moreover, metronidazole preparation and CMZ showed a similar detachment force to sheep stomach mucosa, while the bioadhesion of the metronidazole preparation was higher three times than CMZ to sheep duodenum. The results of in vivo study indicated that the absorption of metronidazole from the preparation was faster than that of CMZ. Also, MZ-CR leads to higher metronidazole Cmax and AUC relative to that of the CMZ. This increase in bioavailability might be explained by the bioadhesion of the preparation at the upper part of the small intestine that could result in an increase in the overall intestinal transit time. As a conclusion, formulating chitosan-xanthan gum mixture as a hydrophilic polymer matrix resulted in a superior pharmacokinetic parameters translated by better rate and extent of absorption of metronidazole.
topic metronidazole
chitosan
xanthan gum
bioadhesion
bioavailability
url http://www.mdpi.com/1660-3397/8/5/1716/
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