Literature DB >> 15198557

Physical properties and compact analysis of commonly used direct compression binders.

Yeli Zhang1, Yuet Law, Sibu Chakrabarti.   

Abstract

This study investigated the basic physico-chemical property and binding functionality of commonly used commercial direct compression binders/fillers. The compressibility of these materials was also analyzed using compression parameters derived from the Heckel, Kawakita, and Cooper-Eaton equations. Five classes of excipients were evaluated, including microcrystalline cellulose (MCC), starch, lactose, dicalcium phosphate (DCP), and sugar. In general, the starch category exhibited the highest moisture content followed by MCC, DCP, lactose, and finally sugar; DCP displayed the highest density, followed by sugar, lactose, starch, and MCC; the material particle size is highly processing dependent. The data also demonstrated that MCC had moderate flowability, excellent compressibility, and extremely good compact hardness; with some exceptions, starch, lactose, and sugar generally exhibited moderate flowability, compressibility, and hardness; DCP had excellent flowability, but poor compressibility and hardness. This research additionally confirmed the binding mechanism that had been well documented: MCC performs as binder because of its plastic deformation under pressure; fragmentation is the predominant mechanism in the case of lactose and DCP; starch and sugar perform by both mechanisms.

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Year:  2003        PMID: 15198557      PMCID: PMC2750655          DOI: 10.1208/pt040462

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


  9 in total

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Journal:  AAPS PharmSciTech       Date:  2000-07-21       Impact factor: 3.246

4.  Composite method to quantify powder flow as a screening method in early tablet or capsule formulation development.

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Journal:  AAPS PharmSciTech       Date:  2000-06-24       Impact factor: 3.246

5.  Relations between compaction data for some crystalline pharmaceutical materials.

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Journal:  Pharm Acta Helv       Date:  1975

6.  Dilution potential: a new perspective.

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Journal:  Pharm Dev Technol       Date:  1996-07       Impact factor: 3.133

7.  The tensile strength of lactose tablets.

Authors:  J T Fell; J M Newton
Journal:  J Pharm Pharmacol       Date:  1968-08       Impact factor: 3.765

8.  Modification of physical characteristics of microcrystalline cellulose by codrying with beta-cyclodextrins.

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Journal:  J Pharm Sci       Date:  1998-01       Impact factor: 3.534

9.  New methods characterizing avalanche behavior to determine powder flow.

Authors:  François Lavoie; Louis Cartilier; Roch Thibert
Journal:  Pharm Res       Date:  2002-06       Impact factor: 4.200

  9 in total
  12 in total

1.  Measuring surface roughness of pharmaceutical powders using vapor sorption methods.

Authors:  Daniel J Burnett; Jerry Y Y Heng; Frank Thielmann; Armando R Garcia; Majid Naderi; Manaswini Acharya
Journal:  AAPS PharmSciTech       Date:  2010-12-18       Impact factor: 3.246

2.  Effect of molecular weight of hydrolyzed gelatin on its binding properties in tablets: a technical note.

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5.  The influence of the compression force on zidovudine release from matrix tablets.

Authors:  Jucimary V Santos; Luís A E Batista de Carvalho; Maria Eugénia Tavares Pina
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9.  A Precise Prediction Method for the Properties of API-Containing Tablets Based on Data from Placebo Tablets.

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10.  Determination and estimation of pharmacokinetic profile of caffeine in form of extract of green tea leaves and its analogy with synthetic form.

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