Preformulation study of etoposide: II. Increased solubility and dissolution rate by solid-solid dispersions
暂无分享,去创建一个
[1] S. Riegelman,et al. Preparation and dissolution characteristics of several fast-release solid dispersions of griseofulvin. , 1969, Journal of pharmaceutical sciences.
[2] W. Higuchi,et al. Dissolution rates of high energy polyvinylpyrrolidone (PVP)-sulfathiazole coprecipitates. , 1969, Journal of pharmaceutical sciences.
[3] S. Riegelman,et al. Pharmaceutical applications of solid dispersion systems. , 1971, Journal of pharmaceutical sciences.
[4] D. Baumann. [New drugs. 8]. , 1972, Pharmazeutische Praxis.
[5] Stanley A. Kaplan,et al. Biopharmaceutical Considerations in Drug Formulation Design and Evaluation , 1972 .
[6] B. Issell,et al. Etoposide (VP-16-213). , 1979, Cancer treatment reviews.
[7] C. Anastasiadou,et al. Solid Dispersions: Comparison of Prepared Melts and Coprecipitates of Diazepam and Polyoxyethylene Glycol 4000 , 1983 .
[8] J. Ford,et al. The Effect of Particle Size on Some In-Vitro and In-Vivo Properties of Indomethacin-Polyethylene Glycol 6000 Solid Dispersions , 1985 .
[9] M. Alonso,et al. Biopharmaceutical Study of Glybornuride-Polyethylene Glycol Systems , 1986 .
[10] M. Slevin,et al. The Clinical Pharmacology of Etoposide and Teniposide , 1987, Clinical pharmacokinetics.
[11] D. Chow,et al. Stability-indicating high-performance liquid chromatography of etoposide at various pH conditions using a reversed-phase octyl column. , 1987, Journal of chromatography.
[12] A. Florence,et al. Effects of hydrotropic agents on the solubility, precipitation, and protein binding of etoposide. , 1989, Journal of pharmaceutical sciences.