Literature DB >> 31493266

Benefits of Fractal Approaches in Solid Dosage Form Development.

Renata Abreu-Villela1, Martin Kuentz2, Isidoro Caraballo3.   

Abstract

Pharmaceutical formulations are complex systems consisting of active pharmaceutical ingredient(s) and a number of excipients selected to provide the intended performance of the product. The understanding of materials' properties and technological processes is a requirement for building quality into pharmaceutical products. Such understanding is gained mostly from empirical correlations of material and process factors with quality attributes of the final product. However, it seems also important to gain knowledge based on mechanistic considerations. Promising is here to study morphological and/or topological characteristics of particles and their aggregates. These geometric aspects must be taken into account to better understand how product attributes emerge from raw materials, which includes, for example, mechanical tablet properties, disintegration or dissolution behavior. Regulatory agencies worldwide are promoting the use of physical models in pharmaceutics to design quality into a final product. This review deals with pharmaceutical applications of theoretical models, focusing on percolation theory, fractal, and multifractal geometry. The use of these so-called fractal approaches improves the understanding of different aspects in the development of solid dosage forms, for example by identifying critical drug and excipient concentrations, as well as to study effects of heterogeneity on dosage form performance. The aim is to link micro- and macrostructure to the emerging quality attributes of the pharmaceutical solid dosage forms as a strategy to enhance mechanistic understanding and to advance pharmaceutical development and manufacturing processes.

Keywords:  fractal geometry; fractal-like kinetics; geometric distribution; percolation theory; solid dosage forms

Mesh:

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Year:  2019        PMID: 31493266     DOI: 10.1007/s11095-019-2685-5

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


  69 in total

1.  A new theoretical approach to tablet strength of a binary mixture consisting of a well and a poorly compactable substance.

Authors:  M Kuentz; H Leuenberger
Journal:  Eur J Pharm Biopharm       Date:  2000-03       Impact factor: 5.571

Review 2.  On the heterogeneity of drug dissolution and release.

Authors:  P Macheras; A Dokoumetzidis
Journal:  Pharm Res       Date:  2000-02       Impact factor: 4.200

Review 3.  Modelling during drug development.

Authors:  L P Balant; M Gex-Fabry
Journal:  Eur J Pharm Biopharm       Date:  2000-07       Impact factor: 5.571

4.  Multifractal properties of resistor diode percolation.

Authors:  Olaf Stenull; Hans-Karl Janssen
Journal:  Phys Rev E Stat Nonlin Soft Matter Phys       Date:  2002-02-27

5.  Fracture in disordered media and tensile strength of microcrystalline cellulose tablets at low relative densities.

Authors:  M Kuentz; H Leuenberger; M Kolb
Journal:  Int J Pharm       Date:  1999-05-25       Impact factor: 5.875

6.  Comparison of different mathematical models for the tensile strength-relative density profiles of binary tablets.

Authors:  Ninfa Ramírez; Luz María Melgoza; Martin Kuentz; Horacio Sandoval; Isidoro Caraballo
Journal:  Eur J Pharm Sci       Date:  2004-05       Impact factor: 4.384

7.  On the use of the Weibull function for the discernment of drug release mechanisms.

Authors:  Vasiliki Papadopoulou; Kosmas Kosmidis; Marilena Vlachou; Panos Macheras
Journal:  Int J Pharm       Date:  2005-12-20       Impact factor: 5.875

8.  Use of fractal geometry to determine effects of surface morphology on drug dissolution.

Authors:  D Farin; D Avnir
Journal:  J Pharm Sci       Date:  1992-01       Impact factor: 3.534

9.  Nitrogen Sorption Studies of Silica Particles Obtained in Emulsion and Microemulsion Media.

Authors:  Jordi Esquena; Conxita Solans; Joan Llorens
Journal:  J Colloid Interface Sci       Date:  2000-05-15       Impact factor: 8.128

10.  Evaluation of tablet formation of different lactoses by 3D modeling and fractal analysis.

Authors:  Z Jelcic; K Hauschild; M Ogiermann; K M Picker-Freyer
Journal:  Drug Dev Ind Pharm       Date:  2007-04       Impact factor: 3.225

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  1 in total

1.  Assessment of the Extrusion Process and Printability of Suspension-Type Drug-Loaded AffinisolTM Filaments for 3D Printing.

Authors:  Gloria Mora-Castaño; Mónica Millán-Jiménez; Vicente Linares; Isidoro Caraballo
Journal:  Pharmaceutics       Date:  2022-04-15       Impact factor: 6.525

  1 in total

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