Literature DB >> 22899380

Functional assessment of four types of disintegrants and their effect on the spironolactone release properties.

John Rojas1, Santiago Guisao, Vanesa Ruge.   

Abstract

Spironolactone is a drug derived from sterols that exhibits an incomplete oral absorption due to its low water solubility and slow dissolution rate. In this study, formulations of spironolactone with four disintegrants named as croscarmellose sodium, crospovidone, sodium starch glycolate and microcrystalline cellulose II (MCCII) were conducted. The effect of those disintegrants on the tensile strength, disintegration time and dissolution rate of spironolactone-based compacts was evaluated using a factorial design with three categorical factors (filler, lubricant, and disintegrant). The swelling values, water uptake and water sorption studies of these disintegrants all suggested that MCCII compacts disintegrate by a wicking mechanism similar to that of crospovidone, whereas a swelling mechanism was dominant for sodium starch glycolate and croscarmellose sodium. The disintegration time of MCCII and sodium starch glycolate remained unchanged with magnesium stearate. However, this lubricant delayed the disintegration time of crospovidone and croscarmellose sodium. MCCII presented the fastest disintegration time independent of the medium and lubricant employed. The water sorption ratio and swelling values determined sodium starch glycolate followed by croscarmellose sodium as the largest swelling materials, whereas crospovidone and MCCII where the least swelling disintegrants. The swelling property of sodium starch glycolate and croscarmellose sodium was strongly affected by the medium pH. The disintegration time of spironolactone compacts was faster when starch was used as a filler due to the formation of soft compacts. In this case, the type of filler employed rather than the disintegrant had a major effect on the disintegration and dissolution times of spironolactone.

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Year:  2012        PMID: 22899380      PMCID: PMC3513459          DOI: 10.1208/s12249-012-9835-y

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


  12 in total

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2.  Preparation and assessment of novel coprocessed superdisintegrant consisting of crospovidone and sodium starch glycolate: a technical note.

Authors:  Mukesh C Gohel; Rajesh K Parikh; Bansari K Brahmbhatt; Aarohi R Shah
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Authors:  Y X Bi; H Sunada; Y Yonezawa; K Danjo
Journal:  Drug Dev Ind Pharm       Date:  1999-05       Impact factor: 3.225

7.  Powder compaction properties of sodium starch glycolate disintegrants.

Authors:  S Edge; D F Steele; J N Staniforth; A Chen; P M Woodcock
Journal:  Drug Dev Ind Pharm       Date:  2002-09       Impact factor: 3.225

8.  The influence of swelling capacity of superdisintegrants in different pH media on the dissolution of hydrochlorothiazide from directly compressed tablets.

Authors:  Na Zhao; Larry L Augsburger
Journal:  AAPS PharmSciTech       Date:  2005-09-20       Impact factor: 3.246

9.  Effect of maltodextrin and superdisintegrant in directly compressible powder mixtures prepared via co-spray drying.

Authors:  Y Gonnissen; J P Remon; C Vervaet
Journal:  Eur J Pharm Biopharm       Date:  2007-05-13       Impact factor: 5.571

10.  The influence of granulation on super disintegrant performance.

Authors:  Na Zhao; Larry L Augsburger
Journal:  Pharm Dev Technol       Date:  2006-02       Impact factor: 3.133

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7.  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

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9.  Biopharmaceutical Understanding of Excipient Variability on Drug Apparent Solubility Based on Drug Physicochemical Properties. Case Study: Superdisintegrants.

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