Evaluation of Carbomer, CMC and HPMC on Dissolution and Bioadhesion of buccoadhesive Cinnamaldehyde Tablets

Background and purpose: Transmucosal drug delivery unlike oral drug delivery has some advantages including deletion of first past effect and prevention of drug removal in gastro-intestinal tract and enzymatic flora. This study aimed at evaluating the effect of CMC, cerbomer and HPMC on Cinnamaldehyd...

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Main Authors: Majid Saeedi, Jafar Akbari, Katayoon Morteza-semnani, Sohrab Rostamkalaei, Fatemeh Fathalinejad, Elnaz Khoshvishkaie
Format: Article
Language:English
Published: Mazandaran University of Medical Sciences 2018-02-01
Series:Journal of Mazandaran University of Medical Sciences
Subjects:
Online Access:http://jmums.mazums.ac.ir/article-1-10475-en.html
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author Majid Saeedi
Jafar Akbari
Katayoon Morteza-semnani
Sohrab Rostamkalaei
Fatemeh Fathalinejad
Elnaz Khoshvishkaie
author_facet Majid Saeedi
Jafar Akbari
Katayoon Morteza-semnani
Sohrab Rostamkalaei
Fatemeh Fathalinejad
Elnaz Khoshvishkaie
author_sort Majid Saeedi
collection DOAJ
description Background and purpose: Transmucosal drug delivery unlike oral drug delivery has some advantages including deletion of first past effect and prevention of drug removal in gastro-intestinal tract and enzymatic flora. This study aimed at evaluating the effect of CMC, cerbomer and HPMC on Cinnamaldehyde release from formulation matrix and mucoadhesion of these formulations. Materials and methods: In this experimental research, nine formulations were selected and several tests including flowability, compressibility, hardness, assay, friability, swelling, and bioadhesive force were done. Results: According to the study, the angles of repose for all formulations were between 20.06±1.67 and 31.93±2.44. In addition, F5 and F6 had the most regular drug release patterns while F8 and F9 were found to have the fastest drug release. Maximum bioadhesive strength was observed in F8 and F9 but the minimum was observed in F3 and F4. Conclusion: Drug delivery studies are of great importance, particularly for the drugs that do not have therapeutic efficacy in other routs of administration. According to current findings, HPMC induces the best formulation for transmucosal drug delivery.
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spelling doaj.art-0b5ec28ca1c8447182e727a4509788f22023-01-25T07:42:25ZengMazandaran University of Medical SciencesJournal of Mazandaran University of Medical Sciences1735-92601735-92792018-02-01271577082Evaluation of Carbomer, CMC and HPMC on Dissolution and Bioadhesion of buccoadhesive Cinnamaldehyde TabletsMajid Saeedi0Jafar Akbari1Katayoon Morteza-semnani2Sohrab Rostamkalaei3Fatemeh Fathalinejad4Elnaz Khoshvishkaie5 Professor, Department of Pharmaceutics, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran Professor, Department of Pharmaceutics, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran Professor, Department of Medicinal Chemistry, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran Pharmaceutical Sciences Resident, Student Research Committee, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran Pharmacy Student, Student Research Committee, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran Pharmacy Student, Student Research Committee, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran Background and purpose: Transmucosal drug delivery unlike oral drug delivery has some advantages including deletion of first past effect and prevention of drug removal in gastro-intestinal tract and enzymatic flora. This study aimed at evaluating the effect of CMC, cerbomer and HPMC on Cinnamaldehyde release from formulation matrix and mucoadhesion of these formulations. Materials and methods: In this experimental research, nine formulations were selected and several tests including flowability, compressibility, hardness, assay, friability, swelling, and bioadhesive force were done. Results: According to the study, the angles of repose for all formulations were between 20.06±1.67 and 31.93±2.44. In addition, F5 and F6 had the most regular drug release patterns while F8 and F9 were found to have the fastest drug release. Maximum bioadhesive strength was observed in F8 and F9 but the minimum was observed in F3 and F4. Conclusion: Drug delivery studies are of great importance, particularly for the drugs that do not have therapeutic efficacy in other routs of administration. According to current findings, HPMC induces the best formulation for transmucosal drug delivery.http://jmums.mazums.ac.ir/article-1-10475-en.htmlcinnamaldehydemucoadhesivepolymerformulationtransmucosal drug delivery
spellingShingle Majid Saeedi
Jafar Akbari
Katayoon Morteza-semnani
Sohrab Rostamkalaei
Fatemeh Fathalinejad
Elnaz Khoshvishkaie
Evaluation of Carbomer, CMC and HPMC on Dissolution and Bioadhesion of buccoadhesive Cinnamaldehyde Tablets
Journal of Mazandaran University of Medical Sciences
cinnamaldehyde
mucoadhesive
polymer
formulation
transmucosal drug delivery
title Evaluation of Carbomer, CMC and HPMC on Dissolution and Bioadhesion of buccoadhesive Cinnamaldehyde Tablets
title_full Evaluation of Carbomer, CMC and HPMC on Dissolution and Bioadhesion of buccoadhesive Cinnamaldehyde Tablets
title_fullStr Evaluation of Carbomer, CMC and HPMC on Dissolution and Bioadhesion of buccoadhesive Cinnamaldehyde Tablets
title_full_unstemmed Evaluation of Carbomer, CMC and HPMC on Dissolution and Bioadhesion of buccoadhesive Cinnamaldehyde Tablets
title_short Evaluation of Carbomer, CMC and HPMC on Dissolution and Bioadhesion of buccoadhesive Cinnamaldehyde Tablets
title_sort evaluation of carbomer cmc and hpmc on dissolution and bioadhesion of buccoadhesive cinnamaldehyde tablets
topic cinnamaldehyde
mucoadhesive
polymer
formulation
transmucosal drug delivery
url http://jmums.mazums.ac.ir/article-1-10475-en.html
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