Literature DB >> 39988

Effect of drug content and drug particle size on the change in particle size during tablet compression.

N Kitamori, T Makino.   

Abstract

Three size fractions for each of three poorly soluble drugs were compressed into 10 mm diameter tablets of four different dilution ratios. The compression was carried out on a physical testing instrument at four compression levels of 49.0, 98.1, 196.2 and 294.3 MN m-2. The effect of drug content and drug particle size on the change in particle size during tableting was examined by the determination of the dissolution rate for disintegrated tablets. A linear relation was obtained when plotting 1n(T80%) versus drug content. There was a critical particle size where the phenomena of cleavage and bonding during tableting balanced each other, but this varied with drug content.

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Year:  1979        PMID: 39988     DOI: 10.1111/j.2042-7158.1979.tb13572.x

Source DB:  PubMed          Journal:  J Pharm Pharmacol        ISSN: 0022-3573            Impact factor:   3.765


  3 in total

1.  In situ determination of delavirdine mesylate particle size in solid oral dosage forms.

Authors:  J G White
Journal:  Pharm Res       Date:  1999-04       Impact factor: 4.200

2.  Studies on tableting properties of lactose. Part III. The consolidation behaviour of sieve fractions of crystalline alpha-lactose monohydrate.

Authors:  A H De Boer; H Vromans; C F Lerk; G K Bolhuis; K D Kussendrager; H Bosch
Journal:  Pharm Weekbl Sci       Date:  1986-04-25

3.  Modeling of Disintegration and Dissolution Behavior of Mefenamic Acid Formulation Using Numeric Solution of Noyes-Whitney Equation with Cellular Automata on Microtomographic and Algorithmically Generated Surfaces.

Authors:  Reiji Yokoyama; Go Kimura; Christian M Schlepütz; Jörg Huwyler; Maxim Puchkov
Journal:  Pharmaceutics       Date:  2018-12-03       Impact factor: 6.321

  3 in total

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