Literature DB >> 1880728

Effect of formulation solubility and hygroscopicity on disintegrant efficiency in tablets prepared by wet granulation, in terms of dissolution.

J R Johnson1, L H Wang, M S Gordon, Z T Chowhan.   

Abstract

The effect of tablet formulation solubility and hygroscopicity on the dissolution efficiency of three "super disintegrants" (sodium starch glycolate, crospovidone, and croscarmellose sodium) in tablets prepared by wet granulation was investigated. Lactose, calcium phosphate dibasic, sorbitol, and naproxen sodium, alone or in combination, provided varying degrees of solubility and hygroscopicity in the formulations. To monitor in vitro dissolution, 1% p-aminobenzoic acid was added to the formulation as a tracer. The results indicate that highly soluble and/or hygroscopic ingredients decrease the effectiveness of super disintegrants in promoting in vitro dissolution. The greater the overall hygroscopicity and solubility of the tablet formulation, the larger the decrease in the efficiency of the super disintegrant.

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Year:  1991        PMID: 1880728     DOI: 10.1002/jps.2600800514

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  8 in total

1.  Correlation and prediction of moisture-mediated dissolution stability for benazepril hydrochloride tablets.

Authors:  Shoufeng Li; Bill Wei; Santo Fleres; Ann Comfort; Alan Royce
Journal:  Pharm Res       Date:  2004-04       Impact factor: 4.200

2.  Once daily, high-dose mesalazine controlled-release tablet for colonic delivery: optimization of formulation variables using Box-Behnken design.

Authors:  Ahmed Abd Elbary; Ahmed A Aboelwafa; Ibrahim M Al Sharabi
Journal:  AAPS PharmSciTech       Date:  2011-10-29       Impact factor: 3.246

3.  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

4.  Response surface methodology to optimize novel fast disintegrating tablets using β cyclodextrin as diluent.

Authors:  Sameer G Late; Ajay K Banga
Journal:  AAPS PharmSciTech       Date:  2010-11-18       Impact factor: 3.246

5.  Evaluation of strain-induced hydrophobicity of pharmaceutical blends and its effect on drug release rate under multiple compression conditions.

Authors:  Kalyana Pingali; Rafael Mendez; Daniel Lewis; Bozena Michniak-Kohn; Alberto Cuitiño; Fernando Muzzio
Journal:  Drug Dev Ind Pharm       Date:  2010-10-13       Impact factor: 3.225

6.  Calcium phosphates in pharmaceutical tableting. 2. Comparison of tableting properties.

Authors:  P C Schmidt; R Herzog
Journal:  Pharm World Sci       Date:  1993-06-18

7.  Fast disintegrating tablets: Opportunity in drug delivery system.

Authors:  Ved Parkash; Saurabh Maan; Shiv Kumar Yadav; Vikas Jogpal
Journal:  J Adv Pharm Technol Res       Date:  2011-10

8.  Immediate-Release Formulations Produced via Twin-Screw Melt Granulation: Systematic Evaluation of the Addition of Disintegrants.

Authors:  Kristina E Steffens; Karl G Wagner
Journal:  AAPS PharmSciTech       Date:  2021-06-16       Impact factor: 3.246

  8 in total

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