Similarities in the release rates of different drugs from polyethylene glycol 6000 solid dispersions
暂无分享,去创建一个
J. Dubois | J. Ford | J L Ford | J L Dubois
[1] W I Higuchi,et al. Dissolution rates of polyphase mixtures. , 1965, Journal of pharmaceutical sciences.
[2] S. Riegelman,et al. Preparation and dissolution characteristics of several fast-release solid dispersions of griseofulvin. , 1969, Journal of pharmaceutical sciences.
[3] W. Higuchi,et al. Dissolution rates of high energy polyvinylpyrrolidone (PVP)-sulfathiazole coprecipitates. , 1969, Journal of pharmaceutical sciences.
[4] M. H. Rubinstein,et al. The effect of composition and ageing on the dissolution rates of chlorpropamide‐urea solid dispersions , 1977, The Journal of pharmacy and pharmacology.
[5] Ford Jl,et al. Phase equilibria and dissolution rates of indomethacin-polyethylene glycol 6000 solid dispersions. , 1978 .
[6] O. Corrigan,et al. Mechanism of drug dissolution rate enhancement from β‐cyclodextrin‐drug systems , 1982 .
[7] Ford Jl. The influence of polyethylene glycol molecular weight variation on the properties of glutethimide-polyethylene glycol solid dispersions. , 1984 .