Literature DB >> 20617405

Comparison between the effect of strongly and weakly cationic exchange resins on matrix physical properties and the controlled release of diphenhydramine hydrochloride from matrices.

Prasert Akkaramongkolporn1, Kaewnapa Wongsermsin, Praneet Opanasopit, Tanasait Ngawhirunpat.   

Abstract

This study focused on investigating and comparing between the effect of the strongly cationic exchange resin, Dowex 88 (Dow88), and the weakly cationic exchange resin, Amberlite IRP64 (Am64), on the physical properties of matrices and their drug release profiles. The matrices were prepared by direct compression of Methocel K4M (HPMC) or Ethocel 7FP (EC) polymeric matrix formers and contained diphenhydramine hydrochloride as a model drug. The addition of Dow88 to the matrices decreased matrix hardness and increased thickness, diameter, and friability. In contrast, the addition of Am64 increased matrix hardness and maintained the original thickness, diameter, and friability. In deionized water, both resins lowered drug release from HPMC-based matrices by virtue of the gelation property of matrix former and the drug exchange property of embedded resin, in other words in situ resinate formation. Dow88 strongly dissociated and lowered the drug release to a greater extent than Am64, which was weakly dissociated. However, Am64 could retard drug release under simulated gastrointestinal conditions. EC-based matrices containing either resin displayed a propensity for disintegration caused by swelling and wicking (water adsorption) actions by the resin. The results of this study provided useful information on the utilization of ion exchange resins as release modifiers in matrix systems.

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Year:  2010        PMID: 20617405      PMCID: PMC2974155          DOI: 10.1208/s12249-010-9472-2

Source DB:  PubMed          Journal:  AAPS PharmSciTech        ISSN: 1530-9932            Impact factor:   3.246


  12 in total

1.  Functionality comparison of 3 classes of superdisintegrants in promoting aspirin tablet disintegration and dissolution.

Authors:  Na Zhao; Larry L Augsburger
Journal:  AAPS PharmSciTech       Date:  2005-12-12       Impact factor: 3.246

2.  Release and diffusional modeling of metronidazole lipid matrices.

Authors:  Mine Ozyazici; Evren H Gökçe; Gökhan Ertan
Journal:  Eur J Pharm Biopharm       Date:  2006-02-28       Impact factor: 5.571

3.  The effect of compression force on surface structure, crushing strength, friability and disintegration time of erythromycin acistrate tablets.

Authors:  M Riippi; O Antikainen; T Niskanen; J Yliruusi
Journal:  Eur J Pharm Biopharm       Date:  1998-11       Impact factor: 5.571

4.  The effect of pore formers on the controlled release of cefadroxil from a polyurethane matrix.

Authors:  J E Kim; S R Kim; S H Lee; C H Lee; D D Kim
Journal:  Int J Pharm       Date:  2000-05-15       Impact factor: 5.875

5.  Development of sustained release matrix tablets of didanosine containing methacrylic and ethylcellulose polymers.

Authors:  Carla Sánchez-Lafuente; M Teresa Faucci; Mercedes Fernández-Arévalo; Josefa Alvarez-Fuentes; Antonio M Rabasco; Paola Mura
Journal:  Int J Pharm       Date:  2002-03-02       Impact factor: 5.875

6.  The influence of excipients on drug release from hydroxypropyl methylcellulose matrices.

Authors:  Marina Levina; Ali R Rajabi-Siahboomi
Journal:  J Pharm Sci       Date:  2004-11       Impact factor: 3.534

7.  Effect of a pharmaceutical cationic exchange resin on the properties of controlled release diphenhydramine hydrochloride matrices using Methocel K4M or Ethocel 7cP as matrix formers.

Authors:  Prasert Akkaramongkolporn; Tanasait Ngawhirunpat; Jurairat Nunthanid; Praneet Opanasopit
Journal:  AAPS PharmSciTech       Date:  2008-07-31       Impact factor: 3.246

8.  Effect of ion exchange resins on the drug release from matrix tablets.

Authors:  M Sriwongjanya; R Bodmeier
Journal:  Eur J Pharm Biopharm       Date:  1998-11       Impact factor: 5.571

9.  Swelling and erosion properties of hydroxypropylmethylcellulose (Hypromellose) matrices--influence of agitation rate and dissolution medium composition.

Authors:  Nicole Kavanagh; Owen I Corrigan
Journal:  Int J Pharm       Date:  2004-07-26       Impact factor: 5.875

10.  Physicochemical properties and mechanism of drug release from ethyl cellulose matrix tablets prepared by direct compression and hot-melt extrusion.

Authors:  Michael M Crowley; Britta Schroeder; Anke Fredersdorf; Sakae Obara; Mark Talarico; Shawn Kucera; James W McGinity
Journal:  Int J Pharm       Date:  2004-01-28       Impact factor: 5.875

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