Investigation of griseofulvin and hydroxypropylmethyl cellulose acetate succinate miscibility in ball milled solid dispersions

被引:31
作者
Al-Obaidi, Hisham [1 ]
Lawrence, M. Jayne [1 ]
Al-Saden, Noor [1 ]
Ke, Peng [2 ]
机构
[1] Kings Coll London, Inst Pharmaceut Sci, London SE1 9NH, England
[2] Univ London, Sch Pharm, Dept Pharmaceut, London WC1N 1AX, England
关键词
Amorphous solid dispersions; Glass transition; Crystallinity; Hydrogen bonds; Flory-Huggins interaction parameter; AMORPHOUS MOLECULAR DISPERSIONS; DRUG; CRYSTALLINE; SOLUBILITY; STABILITY; PHASE; PVP;
D O I
10.1016/j.ijpharm.2012.12.045
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Solid dispersions of varying weight ratios compositions of the nonionic drug, griseofulvin and the hydrophilic, anionic polymer, hydroxylpropylmethyl cellulose acetate succinate, have been prepared by ball milling and the resulting samples characterized using a combination of Fourier transform infra-red spectroscopy, X-ray powder diffraction and differential scanning calorimetry. The results suggest that griseofulvin forms hydrogen bonds with the hydroxylpropylmethyl cellulose acetate succinate polymer when prepared in the form of a solid dispersion but not when prepared in a physical mixture of the same composition. As anticipated, the actual measured glass transition temperature of the solid dispersions displayed a linear relationship between that predicted using the Gordon-Taylor and Fox equations assuming ideal mixing, but interestingly only at griseofulvin contents less than 50 wt%. At griseofulvin concentrations greater than this, the measured glass transition temperature of the solid dispersions was almost constant. Furthermore, the crystalline content of the solid dispersions, as determined by differential scanning calorimetry and X-ray powder diffraction followed a similar trend in that the crystalline content significantly decreased at ratios less than 50 wt% of griseofulvin. When the physical mixtures of griseofulvin and the hydroxylpropylmethyl cellulose acetate succinate polymer were analyzed using the Flory-Huggins model, a negative free energy of mixing with an interaction parameter of -0.23 were obtained. Taken together these results suggest that anionic hydrophilic hydroxylpropylmethyl cellulose acetate succinate polymer is a good solvent for crystalline nonionic griseofulvin with the solubility of griseofulvin in the solid dispersion being was estimated to be within the range 40-50 wt%. Below this solubility limit, the amorphous drug exists as amorphous glassy solution while above these values the system is supersaturated and glassy suspension and solution may coexist. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:95 / 102
页数:8
相关论文
共 17 条
[1]  
Al-Obaidi H., INT J PHARM UNPUB
[2]   Characterization and stability of ternary solid dispersions with PVP and PHPMA [J].
Al-Obaidi, Hisham ;
Ke, Peng ;
Brocchini, Steve ;
Buckton, Graham .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2011, 419 (1-2) :20-27
[3]   Evaluation of Griseofulvin Binary and Ternary Solid Dispersions with HPMCAS [J].
Al-Obaidi, Hisham ;
Buckton, Graham .
AAPS PHARMSCITECH, 2009, 10 (04) :1172-1177
[4]   Anomalous Properties of Spray Dried Solid Dispersions [J].
Al-Obaidi, Hisham ;
Brocchini, Steve ;
Buckton, Graham .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 98 (12) :4724-4737
[5]   LASER RAMAN INVESTIGATION OF PHARMACEUTICAL SOLIDS - GRISEOFULVIN AND ITS SOLVATES [J].
BOLTON, BA ;
PRASAD, PN .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1981, 70 (07) :789-793
[6]   Drug-polymer interaction and its significance on the physical stability of nifedipine amorphous dispersion in microparticles of an ammonio methacrylate copolymer and ethylcellulose binary blend [J].
Huang, Jingjun ;
Wigent, Rodney J. ;
Schwartz, Joseph B. .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2008, 97 (01) :251-262
[7]   Theoretical and Experimental Investigation on the Solid Solubility and Miscibility of Naproxen in Poly(vinylpyrrolidone) [J].
Paudel, Amrit ;
Van Humbeeck, Jan ;
Van den Mooter, Guy .
MOLECULAR PHARMACEUTICS, 2010, 7 (04) :1133-1148
[8]   Evaluation of Drug-Polymer Miscibility in Amorphous Solid Dispersion Systems [J].
Rumondor, Alfred C. F. ;
Ivanisevic, Igor ;
Bates, Simon ;
Alonzo, David E. ;
Taylor, Lynne S. .
PHARMACEUTICAL RESEARCH, 2009, 26 (11) :2523-2534
[9]   Phase Behavior of Poly(vinylpyrrolidone) Containing Amorphous Solid Dispersions in the Presence of Moisture [J].
Rumondor, Alfred C. F. ;
Marsac, Patrick J. ;
Stanford, Lindsay A. ;
Taylor, Lynne S. .
MOLECULAR PHARMACEUTICS, 2009, 6 (05) :1492-1505
[10]   Amorphous Drug-PVP Dispersions: Application of Theoretical, Thermal and Spectroscopic Analytical Techniques to the Study of a Molecule With Intermolecular Bonds in Both the Crystalline and Pure Amorphous State [J].
Tobyn, Michael ;
Brown, Jonathan ;
Dennis, Andrew B. ;
Fakes, Michael ;
Gao, Qi ;
Gamble, John ;
Khimyak, Yaroslav Z. ;
Mcgeorge, Gary ;
Patel, Chhaya ;
Sinclair, Wayne ;
Timmins, Peter ;
Yin, Shawn .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 98 (09) :3456-3468