Literature DB >> 7870671

The measurement of mixture homogeneity and dissolution to predict the degree of drug agglomerate breakdown achieved through powder mixing.

M M de Villiers1, J G Van der Watt.   

Abstract

Interactive mixing of agglomerates of small, cohesive particles with coarse carrier particles facilitate the deaggregation of agglomerates. In this study dispersion of agglomerates of microfine furosemide particles by such a mixing process was followed by measuring changes in the content uniformity and area under the dissolution curve. Interactive mixtures between agglomerates of different sized furosemide particles and coarse sodium chloride particles were prepared using different mixers, mixing times and mixer speeds. The dissolution rate of the drug from and content uniformity of the mixtures were measured, and degrees of dispersion were calculated. These degrees of dispersion were compared to the dispersion values obtained from the decrease in agglomerate size after mixing. An increase in mixing time led to an increase in dispersion. An initial fast deagglomeration, indicated by an increase in dissolution, increase in content uniformity and a decrease in particle size, was followed by substantially slower deaggregation of remaining agglomerates and smaller aggregates. For all mixtures studied the degree of dispersion estimated from dissolution measurements, when compared to equivalent content uniformity measurements, agreed closely with the degree of dispersion as indicated by the decrease in particle size. The use of the area under the dissolution curve to predict agglomerate breakdown proved useful and may find application in situations where it is impossible to follow directly deagglomeration through particle size measurements.

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Year:  1994        PMID: 7870671     DOI: 10.1023/a:1018997418322

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  4 in total

1.  Particle size distribution of the active ingredient for solid dosage forms of low dosage.

Authors:  M C Johnson
Journal:  Pharm Acta Helv       Date:  1972 Aug-Sep

Review 2.  British Pharmaceutical Conference Science Award lecture 1986. Order out of chaos.

Authors:  J N Staniforth
Journal:  J Pharm Pharmacol       Date:  1987-05       Impact factor: 3.765

3.  The use of ordered mixtures for improving the dissolution rate of low solubility compounds.

Authors:  C Nyström; M Westerberg
Journal:  J Pharm Pharmacol       Date:  1986-03       Impact factor: 3.765

4.  Extension of Johnson's equation of homogeneity of random mixtures.

Authors:  H Egermann
Journal:  J Pharm Pharmacol       Date:  1985-07       Impact factor: 3.765

  4 in total
  2 in total

1.  Preparation and characterization of highly porous direct compression carrier particles with improved drug loading during an interactive mixing process.

Authors:  Mingna Song; Ning Li; Louwrens R Tiedt; Michael D Degennaro; Melgardt M de Villiers
Journal:  AAPS PharmSciTech       Date:  2010-04-23       Impact factor: 3.246

2.  Development of an Aerosol Dose Collection Apparatus for In Vitro Dissolution Measurements of Orally Inhaled Drug Products.

Authors:  Robert Price; Jagdeep Shur; William Ganley; Gonçalo Farias; Nikoletta Fotaki; Denise S Conti; Renishkumar Delvadia; Mohammad Absar; Bhawana Saluja; Sau Lee
Journal:  AAPS J       Date:  2020-02-13       Impact factor: 4.009

  2 in total

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