-
1
-
-
1642460578
-
Nanosuspensions as the most promising approach in nanoparticulate drug delivery systems
-
Rao G.C., Kumar M.S., Mathivanan N., and Rao M.E. Nanosuspensions as the most promising approach in nanoparticulate drug delivery systems. Pharmazie 59 (2004) 5-9
-
(2004)
Pharmazie
, vol.59
, pp. 5-9
-
-
Rao, G.C.1
Kumar, M.S.2
Mathivanan, N.3
Rao, M.E.4
-
2
-
-
34547875583
-
-
G.G. Liversidge, K.C. Cundy, J. Bishop, D. Czekai, Surface modified drug nanoparticles United States Patent No. 5145684 (1991).
-
-
-
-
3
-
-
0029080002
-
Particle size reduction for improvement of oral bioavailability of hydrophobic drugs: I. Absolute oral bioavailabilty of nanocrystalline danazol in beagel dogs
-
Liversidge G.G., and Cundy K.C. Particle size reduction for improvement of oral bioavailability of hydrophobic drugs: I. Absolute oral bioavailabilty of nanocrystalline danazol in beagel dogs. Int. J. Pharm. 125 (1995) 91-97
-
(1995)
Int. J. Pharm.
, vol.125
, pp. 91-97
-
-
Liversidge, G.G.1
Cundy, K.C.2
-
4
-
-
33344478634
-
Effect of particle size reduction on dissolution and oral absorption of a poorly water-soluble drug, cilostazol, in beagle dogs
-
Jinno J., Kamada N., Miyake M., Yamada K., Mukai T., Odomi M., Toguchi H., Liversidge G.G., Higaki K., and Kimura T. Effect of particle size reduction on dissolution and oral absorption of a poorly water-soluble drug, cilostazol, in beagle dogs. J. Control. Release 111 (2006) 56-64
-
(2006)
J. Control. Release
, vol.111
, pp. 56-64
-
-
Jinno, J.1
Kamada, N.2
Miyake, M.3
Yamada, K.4
Mukai, T.5
Odomi, M.6
Toguchi, H.7
Liversidge, G.G.8
Higaki, K.9
Kimura, T.10
-
5
-
-
34547869440
-
-
R.H. Müller, R. Becker, B. Kruss, K. Peters, Pharmaceutical nanosuspensions for medicament administration as systems with increased saturation solubility and rate of solution United States Patent No. 5858410 (1998).
-
-
-
-
6
-
-
16244398708
-
Nanosuspension formulations for low-soluble drugs: pharmacokinetic evaluation using spironolactone as model compound
-
Langguth P., Hanafy A., Frenzel D., Grenier P., Nhamias A., Ohlig T., Vergnault G., and Spahn-Langguth H. Nanosuspension formulations for low-soluble drugs: pharmacokinetic evaluation using spironolactone as model compound. Drug Dev. Ind. Pharm. 31 (2005) 319-329
-
(2005)
Drug Dev. Ind. Pharm.
, vol.31
, pp. 319-329
-
-
Langguth, P.1
Hanafy, A.2
Frenzel, D.3
Grenier, P.4
Nhamias, A.5
Ohlig, T.6
Vergnault, G.7
Spahn-Langguth, H.8
-
8
-
-
0023900514
-
The metabolism and disposition of fenofibrate in rat, guinea pig, and dog
-
Weil A., Caldwell J., and Strolin-Benedetti M. The metabolism and disposition of fenofibrate in rat, guinea pig, and dog. Drug Metab. Dispos. 16 (1988) 302-309
-
(1988)
Drug Metab. Dispos.
, vol.16
, pp. 302-309
-
-
Weil, A.1
Caldwell, J.2
Strolin-Benedetti, M.3
-
9
-
-
0028110096
-
The fibrates in clinical practice: focus on micronised fenofibrate
-
(Suppl)
-
Shepherd J. The fibrates in clinical practice: focus on micronised fenofibrate. Atherosclerosis 110 (1994) S55-S63 (Suppl)
-
(1994)
Atherosclerosis
, vol.110
-
-
Shepherd, J.1
-
10
-
-
0024852955
-
Stability of extemporaneously compounded spironolactone suspensions
-
Mathur L.K., and Wickman A. Stability of extemporaneously compounded spironolactone suspensions. Am. J. Hosp. Pharm. 46 (1989) 2040-2042
-
(1989)
Am. J. Hosp. Pharm.
, vol.46
, pp. 2040-2042
-
-
Mathur, L.K.1
Wickman, A.2
-
11
-
-
0027376647
-
Stability of spironolactone in an extemporaneously prepared suspension at two temperatures
-
Nahata M.C., Morosco R.S., and Hipple T.F. Stability of spironolactone in an extemporaneously prepared suspension at two temperatures. Ann. Pharmacother. 27 (1993) 1198-1199
-
(1993)
Ann. Pharmacother.
, vol.27
, pp. 1198-1199
-
-
Nahata, M.C.1
Morosco, R.S.2
Hipple, T.F.3
-
13
-
-
34547880580
-
-
Kommentar zum Europäischen Arzneibuch. Vol. 5; D-H. 2006, Stuttgart, Eschborn: Wissenschaftliche Verlagsgesellschaft mgH, Govi Verlag. 4.00/1322.
-
-
-
-
14
-
-
27544498867
-
Dissolution and solubility behavior of fenofibrate in sodium lauryl sulfate solutions
-
Granero G.E., Ramachandran C., and Amidon G.L. Dissolution and solubility behavior of fenofibrate in sodium lauryl sulfate solutions. Drug Dev. Ind. Pharm. 31 (2005) 917-922
-
(2005)
Drug Dev. Ind. Pharm.
, vol.31
, pp. 917-922
-
-
Granero, G.E.1
Ramachandran, C.2
Amidon, G.L.3
-
15
-
-
0033805179
-
In vitro-in vivo correlations for lipophilic, poorly water-soluble drugs
-
Dressman J.B., and Reppas C. In vitro-in vivo correlations for lipophilic, poorly water-soluble drugs. Eur. J. Pharm. Sci. 11 Suppl 2 (2000) S73-S80
-
(2000)
Eur. J. Pharm. Sci.
, vol.11
, Issue.SUPPL. 2
-
-
Dressman, J.B.1
Reppas, C.2
-
16
-
-
33947487639
-
The rate of solution of solid substances in their own solutions
-
Noyes A.A., and Whitney W.R. The rate of solution of solid substances in their own solutions. J. Am. Chem. Soc. 19 (1897) 930-934
-
(1897)
J. Am. Chem. Soc.
, vol.19
, pp. 930-934
-
-
Noyes, A.A.1
Whitney, W.R.2
-
17
-
-
0032714228
-
Inhibition of P-glycoprotein by d-alpha-tocopheryl polyethylene glycol 1000 succinate (TPGS)
-
Dintaman J.M., and Silverman J.A. Inhibition of P-glycoprotein by d-alpha-tocopheryl polyethylene glycol 1000 succinate (TPGS). Pharm. Res. 16 (1999) 1550-1556
-
(1999)
Pharm. Res.
, vol.16
, pp. 1550-1556
-
-
Dintaman, J.M.1
Silverman, J.A.2
-
18
-
-
17644380257
-
Predicting drug disposition via application of BCS: transport/absorption/elimination interplay and development of a biopharmaceutics drug disposition classification system
-
Wu C.Y., and Benet L.Z. Predicting drug disposition via application of BCS: transport/absorption/elimination interplay and development of a biopharmaceutics drug disposition classification system. Pharm. Res. 22 (2005) 11-23
-
(2005)
Pharm. Res.
, vol.22
, pp. 11-23
-
-
Wu, C.Y.1
Benet, L.Z.2
|