Literature DB >> 12403060

Neotame anhydrate polymorphs. II: Quantitation and relative physical stability.

Zedong Dong1, Eric J Munson, Steve A Schroeder, Indra Prakash, David J W Grant.   

Abstract

PURPOSE: To study the relative thermodynamic and kinetic stabilities of neotame anhydrate polymorphs A, D, F, and G, and to develop a quantitative method for analyzing polymorphic mixtures of A and G by powder X-ray diffractometry (PXRD).
METHODS: Based on the melting points, heats of fusion, and densities of the four polymorphs, thermodynamic rules were applied to study their thermodynamic relationships. The phase transition temperature of Forms A and G was estimated from their heats of solution and intrinsic dissolution rates (J) in 2-propanol. Using PXRD, a method for the quantitative analysis of polymorphic mixtures of Forms A and G was developed. Binary polymorphic mixtures of Forms A, D, F, or G were stored under zero relative humidity at 23 or 70 degrees C, and their compositions were monitored by PXRD.
RESULTS: The endothermic enthalpy of solution of A, D, F, and G follows the rank order: G (29.71 +/- 0.82 kJ/mol, n = 4) > A (28.48 +/- 0.51 kJ/mol, n = 4) > D (20.43 +/- 0.45 kJ/mol, n = 4) > F (18.77 +/- 0.31 kJ/mol, n = 4). The van't Hoff plots of ln(J) against 1/T for A and G show good linearity between 25 degrees C and 32 degrees C. At 23 degrees C polymorphic mixtures remain unchanged for 4 months. However, at 70 degrees C the phase transition is fast and the relative stability of the four polymorphs follows the rank order: G > D > F and G > A.
CONCLUSIONS: PXRD provides a reliable and accurate technique for the quantitative analysis of polymorphic mixtures of Forms A and G. Among the four polymorphs, A-G and A-D are enantiotropic pairs, whereas D-F, D-G, F-G are monotropic pairs. The phase transition temperature between A and G lies within the range 35-70 degrees C.

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Year:  2002        PMID: 12403060     DOI: 10.1023/a:1020334305038

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


  6 in total

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Authors:  C H Gu; D J Grant
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Journal:  J Pharm Sci       Date:  1992-08       Impact factor: 3.534

3.  Inferring thermodynamic stability relationship of polymorphs from melting data.

Authors:  L Yu
Journal:  J Pharm Sci       Date:  1995-08       Impact factor: 3.534

4.  Some parameters describing the dissolution rate of salicylic acid at controlled pH.

Authors:  J H Collett; J A Rees; N A Dickinson
Journal:  J Pharm Pharmacol       Date:  1972-09       Impact factor: 3.765

5.  Neotame anhydrate polymorphs I: preparation and characterization.

Authors:  Zedong Doug; Brian E Padden; Jonathon S Salsbury; Eric J Munson; Steve A Schroeder; Indra Prakash; David J W Grant
Journal:  Pharm Res       Date:  2002-03       Impact factor: 4.200

6.  Characterization of polymorphism of gepirone hydrochloride.

Authors:  R J Behme; D Brooke; R F Farney; T T Kensler
Journal:  J Pharm Sci       Date:  1985-10       Impact factor: 3.534

  6 in total
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1.  An improved thermoanalytical approach to quantifying trace levels of polymorphic impurity in drug powders.

Authors:  Henry H Y Tong; Boris Y Shekunov; John P Chan; Cedric K F Mok; Henry C M Hung; Albert H L Chow
Journal:  Int J Pharm       Date:  2005-05-13       Impact factor: 5.875

  1 in total

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