-
2
-
-
0028948839
-
Theoretical basis for a biopharmaceutical drug classification: The correlation of in vivo drug product dissolution and in vivo bioavailability
-
Amidon, G.L., Leenernäs, H., Shah, V.P., and Crison, J.R. 1995. Theoretical basis for a biopharmaceutical drug classification: the correlation of in vivo drug product dissolution and in vivo bioavailability. Pharm. Res. 12 (3):413-420.
-
(1995)
Pharm. Res
, vol.12
, Issue.3
, pp. 413-420
-
-
Amidon, G.L.1
Leenernäs, H.2
Shah, V.P.3
Crison, J.R.4
-
3
-
-
0037723978
-
Coadsorption of sodium dodecyl sulfate with hydrophobically modified nonionic cellulose polymers. 1. Role of polymer hydrophobic modification
-
Berglund, K.D., Przybycien, T.M., and Tilton, R.D. 2003a. Coadsorption of sodium dodecyl sulfate with hydrophobically modified nonionic cellulose polymers. 1. Role of polymer hydrophobic modification. Langmuir 19:2705-2713.
-
(2003)
Langmuir
, vol.19
, pp. 2705-2713
-
-
Berglund, K.D.1
Przybycien, T.M.2
Tilton, R.D.3
-
4
-
-
0038399883
-
Coadsorption of sodium dodecyl sulfate with hydrophobically modified nonionic cellulose polymers. 2. Role of surface selectivity in adsorption hysteresis
-
Berglund, K.D., Przybycien, T.M., and Tilton, R.D. 2003b. Coadsorption of sodium dodecyl sulfate with hydrophobically modified nonionic cellulose polymers. 2. Role of surface selectivity in adsorption hysteresis. Langmuir 19:2714-2721.
-
(2003)
Langmuir
, vol.19
, pp. 2714-2721
-
-
Berglund, K.D.1
Przybycien, T.M.2
Tilton, R.D.3
-
5
-
-
19144364655
-
Role of polymeric stabilizers for drug nanocrystal dispersions
-
Choi, J.-Y., Yoo, J.Y., Kwak, H.-S., Nam, B.U., and Lee, J. 2005. Role of polymeric stabilizers for drug nanocrystal dispersions. Curr. Appl. Physics 5:472-474.
-
(2005)
Curr. Appl. Physics
, vol.5
, pp. 472-474
-
-
Choi, J.-Y.1
Yoo, J.Y.2
Kwak, H.-S.3
Nam, B.U.4
Lee, J.5
-
6
-
-
0037074108
-
The mechanisms of drug release from solid dispersions in water-soluble polymers
-
Craig, D.Q.M. 2002. The mechanisms of drug release from solid dispersions in water-soluble polymers. Int. J. Pharm. 231:131-144.
-
(2002)
Int. J. Pharm
, vol.231
, pp. 131-144
-
-
Craig, D.Q.M.1
-
7
-
-
0031121843
-
Microviscosity in clusters of ethyl hydroxyethyl cellulose and sodium dodecyl sulfate formed in dilute aqueous solutions as determined with fluorescence probe techniques
-
Evertsson, H., and Nilsson, S. 1997. Microviscosity in clusters of ethyl hydroxyethyl cellulose and sodium dodecyl sulfate formed in dilute aqueous solutions as determined with fluorescence probe techniques. Macromolecules 30:2377-2385.
-
(1997)
Macromolecules
, vol.30
, pp. 2377-2385
-
-
Evertsson, H.1
Nilsson, S.2
-
8
-
-
0033964139
-
Nanosuspensions of poorly soluble drugs - reproducibility of small scale production
-
Grau, M.J., Kayser, O., and Müller, R.H. 2000. Nanosuspensions of poorly soluble drugs - reproducibility of small scale production. Int. J. Pharm. 196:155-157.
-
(2000)
Int. J. Pharm
, vol.196
, pp. 155-157
-
-
Grau, M.J.1
Kayser, O.2
Müller, R.H.3
-
9
-
-
0006706873
-
A different approach to nanothermodynamics
-
Hill, T.L. 2001. A different approach to nanothermodynamics. Nano Lett. 1:273-275.
-
(2001)
Nano Lett
, vol.1
, pp. 273-275
-
-
Hill, T.L.1
-
10
-
-
50849095728
-
-
Kumar, C.S.S.R. (ed.) 2006. Preparation methods of drug nanoparticles. In Biological and Pharmaceutical Nanomaterials (Nanotechnologies for the Lifesciences, 2). Weinheim: Wiley Science, 225.
-
Kumar, C.S.S.R. (ed.) 2006. Preparation methods of drug nanoparticles. In Biological and Pharmaceutical Nanomaterials (Nanotechnologies for the Lifesciences, vol. 2). Weinheim: Wiley Science, 225.
-
-
-
-
11
-
-
0141507950
-
Drug nano- and microparticles processed into solid dosage forms: Physical properties
-
Lee, J. 2003. Drug nano- and microparticles processed into solid dosage forms: physical properties. J. Pharm. Sci. 92 (10):2057-2068.
-
(2003)
J. Pharm. Sci
, vol.92
, Issue.10
, pp. 2057-2068
-
-
Lee, J.1
-
12
-
-
4344569319
-
Intrinsic adhesion forces of lubricants to steel surface
-
Lee, J. 2004. Intrinsic adhesion forces of lubricants to steel surface. J. Pharm. Sci. 93(9):2310-2318.
-
(2004)
J. Pharm. Sci
, vol.93
, Issue.9
, pp. 2310-2318
-
-
Lee, J.1
-
13
-
-
15244348244
-
Amphiphilic amino acid copolymers as stabilizers for the preparation of nanocrystal dispersion
-
Lee, J., Lee, S.-J., Choi, J.-Y., Yoo, J.Y., and Ahn, C.-H. 2005. Amphiphilic amino acid copolymers as stabilizers for the preparation of nanocrystal dispersion. Eur. J. Pharm. Sci. 24:441-449.
-
(2005)
Eur. J. Pharm. Sci
, vol.24
, pp. 441-449
-
-
Lee, J.1
Lee, S.-J.2
Choi, J.-Y.3
Yoo, J.Y.4
Ahn, C.-H.5
-
14
-
-
0034601240
-
Improving drug solubility for oral delivery using solid dispersions
-
Leuner, C., and Dressman, J. 2000. Improving drug solubility for oral delivery using solid dispersions. Eur. J. Pharm. Biopharm. 50:47-60.
-
(2000)
Eur. J. Pharm. Biopharm
, vol.50
, pp. 47-60
-
-
Leuner, C.1
Dressman, J.2
-
15
-
-
50849086369
-
Particle size reduction, in water-insoluble drug formation
-
Liu, R, ed, Interpharm Press
-
Liu, R. (ed). 2000. Particle size reduction, in water-insoluble drug formation. IL: Buffalo Grove, Interpharm Press, 455-492.
-
(2000)
IL: Buffalo Grove
, pp. 455-492
-
-
-
16
-
-
0028824401
-
Drug particle size reduction for decreasing gastic irritancy and enhancing absorption of naproxen in rats
-
Liversidge, G.G., and Conzentino, P. 1995. Drug particle size reduction for decreasing gastic irritancy and enhancing absorption of naproxen in rats. Int. J. Pharm. 125:309-313.
-
(1995)
Int. J. Pharm
, vol.125
, pp. 309-313
-
-
Liversidge, G.G.1
Conzentino, P.2
-
17
-
-
0029080002
-
Particle size reduction for improvement of oral bioavailability of hydrophobic drugs: I. Absolute oral bioavailability of nanocrystalline danazol in beagle dogs
-
Liversidge, G.G., and Cundy, K. 1995. Particle size reduction for improvement of oral bioavailability of hydrophobic drugs: I. Absolute oral bioavailability of nanocrystalline danazol in beagle dogs. Int. J. Pharm. 125:91-97.
-
(1995)
Int. J. Pharm
, vol.125
, pp. 91-97
-
-
Liversidge, G.G.1
Cundy, K.2
-
18
-
-
9044235775
-
Formulation and antitumor activity evaluation of nanocrystalline suspensions of poorly soluble anticancer drugs
-
Merisko-Liversidge, E., Sarpotdar, P., Bruno, J., Hajj, S., Wei, L., Peltier, N., Rake, J., Shaw, J.M., Pugh, S., Pollin, L., Jones, J., Corbett, T., Cooper, E., and Liversidge, G.G. 1996. Formulation and antitumor activity evaluation of nanocrystalline suspensions of poorly soluble anticancer drugs. Pharm. Res. 13:272-278.
-
(1996)
Pharm. Res
, vol.13
, pp. 272-278
-
-
Merisko-Liversidge, E.1
Sarpotdar, P.2
Bruno, J.3
Hajj, S.4
Wei, L.5
Peltier, N.6
Rake, J.7
Shaw, J.M.8
Pugh, S.9
Pollin, L.10
Jones, J.11
Corbett, T.12
Cooper, E.13
Liversidge, G.G.14
-
20
-
-
0000783540
-
Interactions between colloidal particles and soluble polymers
-
Ploehn, H.J., and Russel, W.B. 1990. Interactions between colloidal particles and soluble polymers. Adv. Chemi Eng 15:137-228.
-
(1990)
Adv. Chemi Eng
, vol.15
, pp. 137-228
-
-
Ploehn, H.J.1
Russel, W.B.2
-
21
-
-
0036913259
-
Dissolution rate enhancement by in situ micronization of poorly water-soluble drugs
-
Rasenack, N., and Muller, B.W. 2002. Dissolution rate enhancement by in situ micronization of poorly water-soluble drugs. Pharm. Res. 19(12):1894-1900.
-
(2002)
Pharm. Res
, vol.19
, Issue.12
, pp. 1894-1900
-
-
Rasenack, N.1
Muller, B.W.2
-
23
-
-
0032885450
-
Solid dispersion of poorly water-soluble drugs: Early promises, subsequent problems, and recent breakthroughs
-
Serajuddin, A.T.M. 1999. Solid dispersion of poorly water-soluble drugs: early promises, subsequent problems, and recent breakthroughs. J. Pharm. Sci. 88 (10):1058-1066.
-
(1999)
J. Pharm. Sci
, vol.88
, Issue.10
, pp. 1058-1066
-
-
Serajuddin, A.T.M.1
-
24
-
-
0036501741
-
Molecular weight dependence of shear-induced structures in nematic semiflexible polymer solutions
-
Siddiquee, S.K., and Egmond, J.W. 2002. Molecular weight dependence of shear-induced structures in nematic semiflexible polymer solutions. J. Rheol. 46 (2):367-381.
-
(2002)
J. Rheol
, vol.46
, Issue.2
, pp. 367-381
-
-
Siddiquee, S.K.1
Egmond, J.W.2
-
25
-
-
0346494421
-
Increased physical stability and improved dissolution properties of itraconazole, a class II drug, by solid dispersions that combine fast- and slow-dissolving polymers
-
Six, K., Verreck, G., Peeters, J., Brewster, M., and van den Mooter, G. 2004. Increased physical stability and improved dissolution properties of itraconazole, a class II drug, by solid dispersions that combine fast- and slow-dissolving polymers. J. Pharm. Sci. 93 (1):124-131.
-
(2004)
J. Pharm. Sci
, vol.93
, Issue.1
, pp. 124-131
-
-
Six, K.1
Verreck, G.2
Peeters, J.3
Brewster, M.4
van den Mooter, G.5
-
26
-
-
33745416604
-
Oral absorption of poorly water-soluble drugs: Computer simulation of fraction absorbed in humans from a miniscale dissolution test
-
Takano, R., Sugano, K., Higashida, A., Hayashi, Y., Machida, M., Aso, Y., and Yamashita, S. 2006. Oral absorption of poorly water-soluble drugs: computer simulation of fraction absorbed in humans from a miniscale dissolution test. Pharm. Res. 23 (6):1144-1156.
-
(2006)
Pharm. Res
, vol.23
, Issue.6
, pp. 1144-1156
-
-
Takano, R.1
Sugano, K.2
Higashida, A.3
Hayashi, Y.4
Machida, M.5
Aso, Y.6
Yamashita, S.7
-
27
-
-
0033800221
-
Drug targeting
-
Torchilin, V. 2000. Drug targeting. Eur. J. Pharm. Sci. 11(suppl 2):S81.
-
(2000)
Eur. J. Pharm. Sci
, vol.11
, Issue.SUPPL. 2
-
-
Torchilin, V.1
-
28
-
-
0032842991
-
Effect of grinding with hydroxypropyl cellulose on the dissolution and particle size of a poorly water-soluble drug
-
Yamada, T., Saito, N., and Imai, T. 1999. Effect of grinding with hydroxypropyl cellulose on the dissolution and particle size of a poorly water-soluble drug. Chem. Pharm. Bull. 47 (9):1311-1313.
-
(1999)
Chem. Pharm. Bull
, vol.47
, Issue.9
, pp. 1311-1313
-
-
Yamada, T.1
Saito, N.2
Imai, T.3
-
29
-
-
0030695406
-
Sterile filtration of nanocrystal drug formulation
-
Zheng, J.Y., and Bosch, H.W. 1997. Sterile filtration of nanocrystal drug formulation. Drug Devel Ind Pharm 23(11):1087-1093.
-
(1997)
Drug Devel Ind Pharm
, vol.23
, Issue.11
, pp. 1087-1093
-
-
Zheng, J.Y.1
Bosch, H.W.2
|