ROLE OF CHITOSAN, CARBOXY METHYL CELLULOS, POLYVINYL PYRROLIDONE, KYRON T134 AND PRIMOGEL TO DESIGN THE MOUTH DISINTEGRATING TELMISARTAN TABLET WITH EXTENDED RELEASE PROFILE

The Mouth Disintegrating Extended Release Telmisartan (MDERT) tablets are designed for adequate pharmacokinetic profile to avoid the unusual peaks and troughs. Although, there are extensive advance techniques used to deliver drugs. But oral route is still remains effective in most of the therapeutic...

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Main Authors: Muhammad Abdullah Akram, Taha Nazir, Saeed Ur Rasheed Nazir, Nida Taha
Format: Article
Language:English
Published: Universitas Gadjah Mada 2017-04-01
Series:Indonesian Journal of Pharmacy
Subjects:
CMC
PVP
Online Access:http://indonesianjpharm.farmasi.ugm.ac.id/index.php/3/article/view/823/814
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spelling doaj-283dc4237cb7403a827e496241f1ab022020-11-24T22:05:47ZengUniversitas Gadjah MadaIndonesian Journal of Pharmacy2338-94272338-94862017-04-012826573http://dx.doi.org/10.14499/indonesianjpharm28iss2pp65ROLE OF CHITOSAN, CARBOXY METHYL CELLULOS, POLYVINYL PYRROLIDONE, KYRON T134 AND PRIMOGEL TO DESIGN THE MOUTH DISINTEGRATING TELMISARTAN TABLET WITH EXTENDED RELEASE PROFILEMuhammad Abdullah Akram0Taha Nazir1Saeed Ur Rasheed Nazir2Nida Taha3Faculty of Pharmacy, University of Sargodha, Sargodha 40100 PakistanBiochemistry, Chemical Pathology, Molecular Biology Research Group, UMC&RC, University of Sargodha, Sargodha 40100 PakistanFaculty of Pharmacy, University of Sargodha, Sargodha 40100 PakistanICDTD Inc., 913 Northumberland Ave Saskatoon SK Canada.The Mouth Disintegrating Extended Release Telmisartan (MDERT) tablets are designed for adequate pharmacokinetic profile to avoid the unusual peaks and troughs. Although, there are extensive advance techniques used to deliver drugs. But oral route is still remains effective in most of the therapeutical situations. Thus we aimed this study to formulate a dosage form with dual character of orodispersion as well as extended effectiveness. MDERTS dosage form was prepared by direct compression method. The major components of this preparation were Telmisartan (TLM), Carboxy methyl cellulose polyvinyl Pyrrolidone, Chitosan, Talc, Mg-stearate, Lactose. The MDERTS dosage form was characterized with different determinants. While, the drug release curves of all 6 formulations upto 12h, DSC spectra of TLM, Kyron T134, Primogel, TLM+Kyron T134+Primogel, Chitosan, CMC and different excepients are presented as comprehensive scientific figures. DSC and FTIR spectroscopic studies indicate the compatibility of drugs with each other and with excipients. Moreover, the formulation F2 containing more than 10% of Kyron T had shown best results. Whereas, the overall results had shown that Kyron T containing tablets had best, in vitro dispersion time, wetting time and wetting volume, water absorption ratio. The order in which superdisintegrants and polymers had produced desirable effect is Kyron T134 > Kyron T134134 + primogel > primogel and for polymers chitosan> chitosan+CMC> chitosan +PVP> CMC> CMC+PVP> PVP. Thus, Kyron T is the best superdisintegrant of others which were used in present study and direct compression method is the best used to prepare extended release mouth disintegrating tablets.http://indonesianjpharm.farmasi.ugm.ac.id/index.php/3/article/view/823/814ChitosanCMCPVPKyron T134Primogel TLMMDERT’s
collection DOAJ
language English
format Article
sources DOAJ
author Muhammad Abdullah Akram
Taha Nazir
Saeed Ur Rasheed Nazir
Nida Taha
spellingShingle Muhammad Abdullah Akram
Taha Nazir
Saeed Ur Rasheed Nazir
Nida Taha
ROLE OF CHITOSAN, CARBOXY METHYL CELLULOS, POLYVINYL PYRROLIDONE, KYRON T134 AND PRIMOGEL TO DESIGN THE MOUTH DISINTEGRATING TELMISARTAN TABLET WITH EXTENDED RELEASE PROFILE
Indonesian Journal of Pharmacy
Chitosan
CMC
PVP
Kyron T134
Primogel TLM
MDERT’s
author_facet Muhammad Abdullah Akram
Taha Nazir
Saeed Ur Rasheed Nazir
Nida Taha
author_sort Muhammad Abdullah Akram
title ROLE OF CHITOSAN, CARBOXY METHYL CELLULOS, POLYVINYL PYRROLIDONE, KYRON T134 AND PRIMOGEL TO DESIGN THE MOUTH DISINTEGRATING TELMISARTAN TABLET WITH EXTENDED RELEASE PROFILE
title_short ROLE OF CHITOSAN, CARBOXY METHYL CELLULOS, POLYVINYL PYRROLIDONE, KYRON T134 AND PRIMOGEL TO DESIGN THE MOUTH DISINTEGRATING TELMISARTAN TABLET WITH EXTENDED RELEASE PROFILE
title_full ROLE OF CHITOSAN, CARBOXY METHYL CELLULOS, POLYVINYL PYRROLIDONE, KYRON T134 AND PRIMOGEL TO DESIGN THE MOUTH DISINTEGRATING TELMISARTAN TABLET WITH EXTENDED RELEASE PROFILE
title_fullStr ROLE OF CHITOSAN, CARBOXY METHYL CELLULOS, POLYVINYL PYRROLIDONE, KYRON T134 AND PRIMOGEL TO DESIGN THE MOUTH DISINTEGRATING TELMISARTAN TABLET WITH EXTENDED RELEASE PROFILE
title_full_unstemmed ROLE OF CHITOSAN, CARBOXY METHYL CELLULOS, POLYVINYL PYRROLIDONE, KYRON T134 AND PRIMOGEL TO DESIGN THE MOUTH DISINTEGRATING TELMISARTAN TABLET WITH EXTENDED RELEASE PROFILE
title_sort role of chitosan, carboxy methyl cellulos, polyvinyl pyrrolidone, kyron t134 and primogel to design the mouth disintegrating telmisartan tablet with extended release profile
publisher Universitas Gadjah Mada
series Indonesian Journal of Pharmacy
issn 2338-9427
2338-9486
publishDate 2017-04-01
description The Mouth Disintegrating Extended Release Telmisartan (MDERT) tablets are designed for adequate pharmacokinetic profile to avoid the unusual peaks and troughs. Although, there are extensive advance techniques used to deliver drugs. But oral route is still remains effective in most of the therapeutical situations. Thus we aimed this study to formulate a dosage form with dual character of orodispersion as well as extended effectiveness. MDERTS dosage form was prepared by direct compression method. The major components of this preparation were Telmisartan (TLM), Carboxy methyl cellulose polyvinyl Pyrrolidone, Chitosan, Talc, Mg-stearate, Lactose. The MDERTS dosage form was characterized with different determinants. While, the drug release curves of all 6 formulations upto 12h, DSC spectra of TLM, Kyron T134, Primogel, TLM+Kyron T134+Primogel, Chitosan, CMC and different excepients are presented as comprehensive scientific figures. DSC and FTIR spectroscopic studies indicate the compatibility of drugs with each other and with excipients. Moreover, the formulation F2 containing more than 10% of Kyron T had shown best results. Whereas, the overall results had shown that Kyron T containing tablets had best, in vitro dispersion time, wetting time and wetting volume, water absorption ratio. The order in which superdisintegrants and polymers had produced desirable effect is Kyron T134 > Kyron T134134 + primogel > primogel and for polymers chitosan> chitosan+CMC> chitosan +PVP> CMC> CMC+PVP> PVP. Thus, Kyron T is the best superdisintegrant of others which were used in present study and direct compression method is the best used to prepare extended release mouth disintegrating tablets.
topic Chitosan
CMC
PVP
Kyron T134
Primogel TLM
MDERT’s
url http://indonesianjpharm.farmasi.ugm.ac.id/index.php/3/article/view/823/814
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