共 100 条
[1]
Keck C.M., Muller R.H., Drug nanocrystals of poorly soluble drugs produced by high pressure homogenization, Eur J Pharm Biopharm, 62, pp. 3-16, (2006)
[2]
Merisko-Liversidge E., Liversidge G.G., Cooper E.R., Nanosizing: A formulation approach for poorly-water-soluble compounds, Eur J Pharm Sci, 18, pp. 113-120, (2003)
[3]
Muller R.H., Bohm B., Grau M.J., Handbook of Pharmaceutical Controlled Release, pp. 345-357, (2000)
[4]
Muller R.H., Jacobs C., Kayser O., Modified-Release Drug Delivery Systems, pp. 135-149, (2003)
[5]
Muller R.H., Akkar A, Encyclopedia of Nanoscience and Nanotechnology, pp. 627-638, (2004)
[6]
Martin A., Swarbrick J., Physical Pharmacy: Physical Chemical Principles in the Pharmaceutical Sciences, (1993)
[7]
Duchene D., Ponchel G., Bioadhesion of solid oral dosage forms, why and how?, Eur J Pharm Biopharm, 44, pp. 15-23, (1997)
[8]
Rao G.C., Kumar M.S., Mathivanan N., Rao M.E., Nanosuspension as the most promising approach in nanoparticulate drug delivery system, Pharmazie, 59, pp. 5-9, (2004)
[9]
Langguth P., Hanafy A., Frezel D., Nanosuspension formulation for low soluble drugs: Pharmacokinetic evaluation using spironolactone as model compound, Drug Dev Ind Pharm, 31, pp. 319-329, (2005)
[10]
Kreuter J., Colloidal Drug Delivery Systems, pp. 219-242, (1994)