Literature DB >> 17372699

Isothermal crystallization of Imwitor 742 from supercooled liquid state.

Kohsaku Kawakami1.   

Abstract

PURPOSE: Crystallization behavior of Imwitor 742 was investigated for use as a liquid-filled capsule carrier.
MATERIALS AND METHODS: The crystallization behavior of Imwitor 742 was assessed using DSC, X-ray diffraction, and microscopy. The physical stability of Imwitor 742 under refrigerated and ambient conditions was estimated by isothermal crystallization studies using DSC. The effect of hard capsule shells and additives on crystallization kinetics was also examined.
RESULTS: When Imwitor 742 was cooled in the DSC measurement, the form alpha appeared at -20 degrees C. When this form was heated from -40 degrees C, melt-crystallization into the form beta + beta' was initiated at -30 degrees C, followed by successive melting. Isothermal crystallization studies at temperatures higher than -14 degrees C yielded the form beta + beta'. The crystallization behavior was explained in terms of the Avrami model fitting by assuming 2-dimensional crystal growth. Kinetic analysis suggested that the liquid state of Imwitor 742 was maintained for 46 h and 40 months at 5 and 25 degrees C, respectively, although the deviation in induction time was expected to be large at these temperatures. Addition of hard capsule shells promoted the crystallization behavior, while addition of drug or water prolonged the induction time.
CONCLUSION: The supercooled liquid state of Imwitor 742 was quite stable. However, additives to retard crystallization should be used, because the deviation in the induction time was very large. Hard capsule shells enhanced the crystallization of Imwitor 742, possibly by acting as nuclei for crystal growth.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17372699     DOI: 10.1007/s11095-006-9193-0

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


  17 in total

Review 1.  Solid dispersion of poorly water-soluble drugs: early promises, subsequent problems, and recent breakthroughs.

Authors:  A T Serajuddin
Journal:  J Pharm Sci       Date:  1999-10       Impact factor: 3.534

Review 2.  Amorphous pharmaceutical solids: preparation, characterization and stabilization.

Authors:  L Yu
Journal:  Adv Drug Deliv Rev       Date:  2001-05-16       Impact factor: 15.470

Review 3.  Microemulsion-based media as novel drug delivery systems.

Authors:  M J Lawrence; G D Rees
Journal:  Adv Drug Deliv Rev       Date:  2000-12-06       Impact factor: 15.470

Review 4.  Reversibility of enantiotropically related polymorphic transformations from a practical viewpoint: thermal analysis of kinetically reversible/irreversible polymorphic transformations.

Authors:  Kohsaku Kawakami
Journal:  J Pharm Sci       Date:  2007-05       Impact factor: 3.534

Review 5.  Chemical reactivity in solid-state pharmaceuticals: formulation implications.

Authors:  S R Byrn; W Xu; A W Newman
Journal:  Adv Drug Deliv Rev       Date:  2001-05-16       Impact factor: 15.470

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

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

Review 7.  Pharmaceutical solids: a strategic approach to regulatory considerations.

Authors:  S Byrn; R Pfeiffer; M Ganey; C Hoiberg; G Poochikian
Journal:  Pharm Res       Date:  1995-07       Impact factor: 4.200

8.  Microemulsion formulation for enhanced absorption of poorly soluble drugs. I. Prescription design.

Authors:  Kohsaku Kawakami; Takayoshi Yoshikawa; Yasushi Moroto; Eri Kanaoka; Koji Takahashi; Yoshitaka Nishihara; Kazuyoshi Masuda
Journal:  J Control Release       Date:  2002-05-17       Impact factor: 9.776

9.  Microemulsion formulation for enhanced absorption of poorly soluble drugs. II. In vivo study.

Authors:  Kohsaku Kawakami; Takayoshi Yoshikawa; Takashi Hayashi; Yoshitaka Nishihara; Kazuyoshi Masuda
Journal:  J Control Release       Date:  2002-05-17       Impact factor: 9.776

10.  Physical characteristics and chemical degradation of amorphous quinapril hydrochloride.

Authors:  Y Guo; S R Byrn; G Zografi
Journal:  J Pharm Sci       Date:  2000-01       Impact factor: 3.534

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.