Literature DB >> 16184321

Viscoelastic characterization of compacted pharmaceutical excipient materials by analysis of frequency-dependent mechanical relaxation processes.

K Welch1, S Mousavi, B Lundberg, M Strømme.   

Abstract

A newly developed method for determining the frequency-dependent complex Young's modulus was employed to analyze the mechanical response of compacted microcrystalline cellulose, sorbitol, ethyl cellulose and starch for frequencies up to 20 kHz. A Debye-like relaxation was observed in all the studied pharmaceutical excipient materials and a comparison with corresponding dielectric spectroscopy data was made. The location in frequency of the relaxation peak was shown to correlate to the measured tensile strength of the tablets, and the relaxation was interpreted as the vibrational response of the interparticle hydrogen and van der Waals bindings in the tablets. Further, the measured relaxation strength, holding information about the energy loss involved in the relaxation processes, showed that the weakest material in terms of tensile strength, starch, is the material among the four tested ones that is able to absorb the most energy within its structure when exposed to external perturbations inducing vibrations in the studied frequency range. The results indicate that mechanical relaxation analysis performed over relatively broad frequency ranges should be useful for predicting material properties of importance for the functionality of a material in applications such as, e.g., drug delivery, drug storage and handling, and also for clarifying the origin of hitherto unexplained molecular processes.

Entities:  

Year:  2005        PMID: 16184321     DOI: 10.1140/epje/i2005-10032-8

Source DB:  PubMed          Journal:  Eur Phys J E Soft Matter        ISSN: 1292-8941            Impact factor:   1.890


  7 in total

1.  Micro-scale measurement of the mechanical properties of compressed pharmaceutical powders. 2: The dynamic moduli of microcrystalline cellulose.

Authors:  B C Hancock; C R Dalton; S Clas
Journal:  Int J Pharm       Date:  2001-10-09       Impact factor: 5.875

2.  Assessing tablet bond types from structural features that affect tablet tensile strength.

Authors:  H Olsson; C Nyström
Journal:  Pharm Res       Date:  2001-02       Impact factor: 4.200

3.  Development of a dual approach to assess powder flow from avalanching behavior.

Authors:  Y S Lee; R Poynter; F Podczeck; J M Newton
Journal:  AAPS PharmSciTech       Date:  2000-07-21       Impact factor: 3.246

4.  The strength of compressed tablets. III. The relation of parcticle size, bonding and capping in tablets of sodium chloride, aspirin and hexamine.

Authors:  E SHOTTON; D GANDERTON
Journal:  J Pharm Pharmacol       Date:  1961-12       Impact factor: 3.765

5.  Nondestructive viscoelastic analysis of anisotropy in compressed tablets.

Authors:  D V Moe; E G Rippie
Journal:  J Pharm Sci       Date:  1997-01       Impact factor: 3.534

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

Authors:  T Tsai; J S Wu; H O Ho; M T Sheu
Journal:  J Pharm Sci       Date:  1998-01       Impact factor: 3.534

7.  Evaluation of strength-enhancing factors of a ductile binder in direct compression of sodium bicarbonate and calcium carbonate powders.

Authors:  S Mattsson; C Nyström
Journal:  Eur J Pharm Sci       Date:  2000-03       Impact factor: 4.384

  7 in total
  1 in total

1.  Understanding the effect of environmental history on bilayer tablet interfacial shear strength.

Authors:  Gerard Klinzing; Antonios Zavaliangos
Journal:  Pharm Res       Date:  2013-01-19       Impact factor: 4.200

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.