Literature DB >> 16463008

Depth profiling of compression-induced disorders and polymorphic transition on tablet surfaces with grazing incidence X-ray diffraction.

Mikko Koivisto1, Paula Heinänen, Veli Pekka Tanninen, Vesa-Pekka Lehto.   

Abstract

PURPOSE: The importance of induced crystal disorders like crystallite size, crystal defects, and amorphicity with respect to the dissolution rate of the drug has been discussed in many cases. Thus, the characterization of these properties is of great importance in the pharmaceutical formulation development, although the exact correlation between disorders and dissolution rate is still unclear. The aim of this study was to analyze pharmaceutical tablets with grazing incidence X-ray diffraction, which enables the depth profiling of the crystallographic properties of the tablets. To study and clarify the potential of grazing incidence diffraction in the analysis of pharmaceutical materials, the effect of the compaction process on the surface of tablets was examined.
METHODS: Carbamazepine, tolbutamide, and chlorpropamide tablets, compacted using different compression pressures, were studied using grazing incidence angle X-ray diffraction. The effects of compression on the crystallographic properties were investigated as a function of the distance from the tablet surface.
RESULTS: The surfaces of the tolbutamide and chlorpropamide tablets were disordered due to the compression. The manifestation of the disorder was deduced to be due to amorphicity, small crystallite size, and amount of crystal defects. The changes were mainly on the surface and diminished strongly as a function of the distance from the surface of the tablet. Moreover, the changes were dependent on the compression pressure used. The changes on the surface of the carbamazepine tablets were also due to the compression but these changes were not clearly dependent on the depth nor the compression pressure. The partial phase transition took place in the chlorpropamide tablets due to the compression. The magnitude of the transition was not highest on the surface because amorphization and texturization also took place on the tablet surface during the compression.
CONCLUSIONS: The present study proved that grazing incidence X-ray diffraction is a potential novel research tool to reveal crystallographic transformations taking place on the surfaces of the tablets induced, for example, by compression pressure.

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Year:  2006        PMID: 16463008     DOI: 10.1007/s11095-006-9785-8

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


  11 in total

Review 1.  Theoretical approaches to physical transformations of active pharmaceutical ingredients during manufacturing processes.

Authors:  K R Morris; U J Griesser; C J Eckhardt; J G Stowell
Journal:  Adv Drug Deliv Rev       Date:  2001-05-16       Impact factor: 15.470

2.  What is the true solubility advantage for amorphous pharmaceuticals?

Authors:  B C Hancock; M Parks
Journal:  Pharm Res       Date:  2000-04       Impact factor: 4.200

3.  The Cambridge Structural Database: a quarter of a million crystal structures and rising.

Authors:  Frank H Allen
Journal:  Acta Crystallogr B       Date:  2002-05-29

4.  Effects of temperature and pressure during compression on polymorphic transformation and crushing strength of chlorpropamide tablets.

Authors:  T Matsumoto; N Kaneniwa; S Higuchi; M Otsuka
Journal:  J Pharm Pharmacol       Date:  1991-02       Impact factor: 3.765

5.  Program for evaluating drug dissolution kinetics in preformulation.

Authors:  M Nicklasson; A B Magnusson
Journal:  Pharm Res       Date:  1985-11       Impact factor: 4.200

Review 6.  Characteristics and significance of the amorphous state in pharmaceutical systems.

Authors:  B C Hancock; G Zografi
Journal:  J Pharm Sci       Date:  1997-01       Impact factor: 3.534

7.  X-ray structural studies and physicochemical properties of cimetidine polymorphism.

Authors:  M Shibata; H Kokubo; K Morimoto; K Morisaka; T Ishida; M Inoue
Journal:  J Pharm Sci       Date:  1983-12       Impact factor: 3.534

8.  Characterization of tolbutamide polymorphs (Burger's forms II and IV) and polymorphic transition behavior.

Authors:  K Kimura; F Hirayama; K Uekama
Journal:  J Pharm Sci       Date:  1999-04       Impact factor: 3.534

9.  Quantitative determination of polymorphic composition in intact compacts by parallel-beam X-ray powder diffractometry II. Data correction for analysis of phase transformations as a function of pressure.

Authors:  Peter L D Wildfong; Nicole A Morley; Michael D Moore; Kenneth R Morris
Journal:  J Pharm Biomed Anal       Date:  2005-09-01       Impact factor: 3.935

10.  Use of glancing angle X-ray powder diffractometry to depth-profile phase transformations during dissolution of indomethacin and theophylline tablets.

Authors:  Smita Debnath; Paul Predecki; Raj Suryanarayanan
Journal:  Pharm Res       Date:  2004-01       Impact factor: 4.200

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  1 in total

1.  Investigation of solid phase composition on tablet surfaces by grazing incidence X-ray diffraction.

Authors:  Vishal Koradia; Mikko Tenho; Heidi Lopez de Diego; Michiel Ringkjøbing-Elema; Jørn Møller-Sonnergaard; Jarno Salonen; Vesa-Pekka Lehto; Jukka Rantanen
Journal:  Pharm Res       Date:  2011-07-09       Impact factor: 4.200

  1 in total

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