4.7 Article

Acceleration of Crystal Growth of Amorphous Griseofulvin by Low-Concentration Poly(ethylene oxide): Aspects of Crystallization Kinetics and Molecular Mobility

期刊

MOLECULAR PHARMACEUTICS
卷 14, 期 7, 页码 2262-2272

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.molpharmaceut.7b00097

关键词

crystal growth; molecular mobility; dielectric spectroscopy; griseofulvin; poly(ethylene oxide)

资金

  1. National Science Foundation of China [81402877, 21474049]
  2. Program of State Key Laboratory of Natural Medicines-China Pharmaceutical University [SKLNMZZYQ201604]
  3. Graduate Innovative Research Project of Jiangsu Province [KYLX16_1180]
  4. Program for Jiangsu Province Innovative Research Team

向作者/读者索取更多资源

This study aims to investigate the crystallization behavior and molecular dynamics of amorphous griseofulvin (GSF) in the presence of low-concentration poly(ethylene oxide) (PEO). We observe that the addition of 3% w/w PEO remarkably increases the crystal growth rate of GSF by two orders of magnitude in both the supercooled liquid and glassy states. The liquid dynamics of amorphous GSF in the presence and absence of PEO are characterized by dielectric spectroscopy. With an increase of the PEO content, the alpha-relaxation times of the systems decrease, indicating the increase of global molecular mobility. The couplings-between molecular mobility and crystallization kinetics of GSF systems show strong time-dependences below T-g. The overlapping of a-relaxation times of GSF in presence and absence of PEO as a function of T-g/T suggest the plasticization effect of PEO additives. However, the crystallization kinetics of amorphous GSF containing low-concentration PEO do not overlap with those of pure GSF on a T-g/T scale. The remarkable accelerating effect of crystal growth of amorphous GSV by low-concentration PEO can be partially attributed to the increase of global mobility. The high segmental mobility of PEO is expected to strongly affect the crystal growth rates of GSF. These findings are relevant for understanding and predicting the physical stability of amorphous pharmaceutical solid dispersions.

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