Literature DB >> 16749898

Compression physics in the formulation development of tablets.

Sarsvatkumar Patel1, Aditya Mohan Kaushal, Arvind Kumar Bansal.   

Abstract

The advantages of high-precision dosing, manufacturing efficiency, and patient compliance make tablets the most popular dosage forms. Compaction, an essential manufacturing step in the manufacture of tablets, includes compression (i.e., volume reduction and particle rearrangement), and consolidation (i.e., interparticulate bond formation). The success of the compaction process depends not only on the physico-technical properties of drugs and excipients, especially their deformation behavior, but also on the choice of instrument settings with respect to rate and magnitude of force transfer. This review discusses various properties of drugs and excipients, such as moisture content, particle size and distribution, polymorphism, amorphism, crystal habit, hydration state, and lubricant and binder level of the blend that have an influence on compaction. Tableting speed and pre/main compression force profile, also have a bearing on the quality of the final tablet. Mechanistic aspects of tableting can be studied using, instrumented punches/dies, instrumented tableting machines, and compaction simulators. These have potential application in pharmaceutical research and development, such as studying basic compaction mechanism, process variables, scale-up parameters, trouble shooting problem batches, creating compaction data bank, and fingerprinting of new active pharmaceutical ingredients (APIs) or excipients. Also, the mathematical equations used to describe compaction events have been covered. These equations describe density-pressure relationships that predict the pressures required for achieving an optimum density. This understanding has found active application in solving the analytical problems related to tableting such as capping, lamination, picking, sticking, etc. Mathematical models, force-time, force-distance, and die-wall force parameters of tableting are used to describe work of compaction, elasticity' plasticity, and time dependent deformation behavior of pharmaceuticals. Various indices of tableting performance such as the bonding index, brittle fracture index, and strain index can be used to predict compaction related problems. Compaction related physico-technical properties of commonly used tableting excipients have been reviewed with emphasis on selecting suitable combination to minimize tableting problems. Specialized tools such as co-processing of API and excipients can be used to improve their functionality.

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Year:  2006        PMID: 16749898     DOI: 10.1615/critrevtherdrugcarriersyst.v23.i1.10

Source DB:  PubMed          Journal:  Crit Rev Ther Drug Carrier Syst        ISSN: 0743-4863            Impact factor:   4.889


  15 in total

1.  Image analysis quantification of sticking and picking events of pharmaceutical powders compressed on a rotary tablet press simulator.

Authors:  Germinal Mollereau; Vincent Mazel; Virginie Busignies; Pierre Tchoreloff; Fabrice Mouveaux; Philippe Rivière
Journal:  Pharm Res       Date:  2013-09       Impact factor: 4.200

2.  A new twist in the old story-can compression induce mixing of phase separated solid dispersions? A case study of spray-dried miconazole-PVP VA64 solid dispersions.

Authors:  Abhishek Singh; Jan Van Humbeeck; Guy Van den Mooter
Journal:  Pharm Res       Date:  2014-05-22       Impact factor: 4.200

3.  Understanding the Tabletability Differences between Indomethacin Polymorphs Using Powder Brillouin Light Scattering.

Authors:  Beth A Young; Dherya Bahl; Lewis L Stevens
Journal:  Pharm Res       Date:  2019-08-19       Impact factor: 4.200

4.  Compression Modulus and Apparent Density of Polymeric Excipients during Compression-Impact on Tabletability.

Authors:  Barbara V Schönfeld; Ulrich Westedt; Karl G Wagner
Journal:  Pharmaceutics       Date:  2022-04-22       Impact factor: 6.525

Review 5.  An overview of famotidine polymorphs: solid-state characteristics, thermodynamics, polymorphic transformation and quality control.

Authors:  Shan-Yang Lin
Journal:  Pharm Res       Date:  2014-03-01       Impact factor: 4.200

6.  Multiple-unit tablet of probiotic bacteria for improved storage stability, acid tolerability, and in vivo intestinal protective effect.

Authors:  Hee Jun Park; Ga Hyeon Lee; Joonho Jun; Miwon Son; Myung Joo Kang
Journal:  Drug Des Devel Ther       Date:  2016-04-07       Impact factor: 4.162

7.  The Disintegration Process in Microcrystalline Cellulose Based Tablets, Part 1: Influence of Temperature, Porosity and Superdisintegrants.

Authors:  Samy Yassin; Daniel J Goodwin; Andrew Anderson; Juraj Sibik; D Ian Wilson; Lynn F Gladden; J Axel Zeitler
Journal:  J Pharm Sci       Date:  2015-06-12       Impact factor: 3.534

8.  Visualization and quantification of deformation behavior of clopidogrel bisulfate polymorphs during tableting.

Authors:  Xian-Zhen Yin; Li Wu; Ying Li; Tao Guo; Hai-Yan Li; Ti-Qiao Xiao; Peter York; Ashwini Nangia; Shuang-Ying Gui; Ji-Wen Zhang
Journal:  Sci Rep       Date:  2016-02-25       Impact factor: 4.379

9.  Tableting properties of microcrystalline cellulose obtained from wheat straw measured with a single punch bench top tablet press.

Authors:  Jovana Krivokapić; Jasna Ivanović; Jelena Djuriš; Djordje Medarević; Zorica Potpara; Zoran Maksimović; Svetlana Ibrić
Journal:  Saudi Pharm J       Date:  2020-05-04       Impact factor: 4.330

10.  Understanding the Role of Water in 1,10-Phenanthroline Monohydrate.

Authors:  Doris E Braun; Anna Schneeberger; Ulrich J Griesser
Journal:  CrystEngComm       Date:  2017-11-07       Impact factor: 3.545

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