-
1
-
-
0033427120
-
An integrated absorption model for determining causes of poor oral drug absorption
-
Yu, L. X., An integrated absorption model for determining causes of poor oral drug absorption, Pharm. Res., 16, 1883, 1999.
-
(1999)
Pharm. Res
, vol.16
, pp. 1883
-
-
Yu, L.X.1
-
2
-
-
0034461768
-
Drug-like properties and the causes of poor solubility and poor permeability
-
Lipinski, C. A., Drug-like properties and the causes of poor solubility and poor permeability, J. Pharmacol. Toxicol. Methods, 44, 235, 2000.
-
(2000)
J. Pharmacol. Toxicol. Methods
, vol.44
, pp. 235
-
-
Lipinski, C.A.1
-
3
-
-
0036096613
-
Formulation approaches for orally administered poorly soluble drugs
-
Pinnamaneni, S., Das, N. G., and Das, S. K., Formulation approaches for orally administered poorly soluble drugs, Pharmazie, 57, 291, 2002.
-
(2002)
Pharmazie
, vol.57
, pp. 291
-
-
Pinnamaneni, S.1
Das, N.G.2
Das, S.K.3
-
4
-
-
33751014029
-
Formulation of poorly water-soluble drugs for oral administration: Physicochemical and physiological issues and the lipid formulation classification system
-
Pouton, C. W., Formulation of poorly water-soluble drugs for oral administration: physicochemical and physiological issues and the lipid formulation classification system, Eur. J. Pharm. Sci., 29, 278, 2006.
-
(2006)
Eur. J. Pharm. Sci
, vol.29
, pp. 278
-
-
Pouton, C.W.1
-
7
-
-
7944225198
-
Dissolution testing for solid oral drug products: Theoretical consideration
-
September
-
Zhang, H. and Yu, L. X., Dissolution testing for solid oral drug products: theoretical consideration, Am. Pharm. Rev., 5, 26-31, September 2004.
-
(2004)
Am. Pharm. Rev
, vol.5
, pp. 26-31
-
-
Zhang, H.1
Yu, L.X.2
-
8
-
-
10344257263
-
Acceptable analytical practices for dissolution testing of poorly soluble compounds
-
December
-
Brown, C. K. et al., Acceptable analytical practices for dissolution testing of poorly soluble compounds, Pharm. Technol., 28, 56-65, December 2004.
-
(2004)
Pharm. Technol
, vol.28
, pp. 56-65
-
-
Brown, C.K.1
-
9
-
-
0028948839
-
A theoretical basis for a biopharmaceutic drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability
-
Amidon, G. L. et al., A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability, Pharm. Res., 12, 413, 1995.
-
(1995)
Pharm. Res
, vol.12
, pp. 413
-
-
Amidon, G.L.1
-
10
-
-
0035997323
-
Biopharmaceutics classification system: The scientific basis for biowaiver extension
-
Yu, L. X. et al., Biopharmaceutics classification system: the scientific basis for biowaiver extension, Pharm. Res., 19, 921, 2002.
-
(2002)
Pharm. Res
, vol.19
, pp. 921
-
-
Yu, L.X.1
-
11
-
-
1242337282
-
The high solubility definition of the current FDA Guidance on Biopharmaceutics Classification System may be too strict for acidic drugs
-
Yazdanian, M. et al., The high solubility definition of the current FDA Guidance on Biopharmaceutics Classification System may be too strict for acidic drugs, Pharm. Res., 21, 293, 2004.
-
(2004)
Pharm. Res
, vol.21
, pp. 293
-
-
Yazdanian, M.1
-
12
-
-
33745416604
-
Oral absorption of poorly water-soluble drugs: Computer simulation of fraction absorbed in humans from a miniscale dissolution test
-
Takano, R. et al., Oral absorption of poorly water-soluble drugs: computer simulation of fraction absorbed in humans from a miniscale dissolution test, Pharm. Res., 23, 1144, 2006.
-
(2006)
Pharm. Res
, vol.23
, pp. 1144
-
-
Takano, R.1
-
13
-
-
0037312695
-
Nanosizing: A formulation approach for poorly water-soluble compounds
-
Merisko-Liversige, E. et al., Nanosizing: a formulation approach for poorly water-soluble compounds, Eur. J. Pharm. Sci., 18, 113, 2003.
-
(2003)
Eur. J. Pharm. Sci
, vol.18
, pp. 113
-
-
Merisko-Liversige, E.1
-
14
-
-
0034874245
-
Ritonavir: An extraordinary example of conformational polymorphism
-
Bauer, J. et al., Ritonavir: an extraordinary example of conformational polymorphism, Pharm. Res., 18, 859, 2001.
-
(2001)
Pharm. Res
, vol.18
, pp. 859
-
-
Bauer, J.1
-
15
-
-
53849097772
-
-
Advisory Committee for Pharmaceutical Science October 5, Accessed December 1, 2006
-
Yu, L., Implementing Quality by Design: OGD initiatives. Advisory Committee for Pharmaceutical Science October 5, 2006. http://www.fda.gov/ohrms/dockets/ac/06/slides/2006-4241s1-index.htm. Accessed December 1, 2006.
-
(2006)
Implementing Quality by Design: OGD initiatives
-
-
Yu, L.1
-
16
-
-
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, S73, 2000.
-
(2000)
Eur. J. Pharm. Sci
, vol.11
, pp. S73
-
-
Dressman, J.B.1
Reppas, C.2
-
17
-
-
78649703437
-
Steps for development of a dissolution test for sparingly water-soluble drug products
-
February
-
Noory, C. et al., Steps for development of a dissolution test for sparingly water-soluble drug products, Dissol. Technol., 7, 3, February 2000.
-
(2000)
Dissol. Technol
, vol.7
, pp. 3
-
-
Noory, C.1
-
18
-
-
32244434196
-
Characterization of the human upper gastrointestinal contents under conditions simulating bioavailability/bioequivalence studies
-
Kalantzi, L. et al., Characterization of the human upper gastrointestinal contents under conditions simulating bioavailability/bioequivalence studies, Pharm. Res., 23, 165, 2006.
-
(2006)
Pharm. Res
, vol.23
, pp. 165
-
-
Kalantzi, L.1
-
19
-
-
21544447265
-
Simulation of fasting gastric conditions and its importance for the in vivo dissolution of lipophilic compounds
-
Vertzoni, M. et al., Simulation of fasting gastric conditions and its importance for the in vivo dissolution of lipophilic compounds, Eur. J. Pharm. Biopharm., 60, 413, 2005.
-
(2005)
Eur. J. Pharm. Biopharm
, vol.60
, pp. 413
-
-
Vertzoni, M.1
-
20
-
-
0033452575
-
Forecasting the in vivo performance of four low solubility drugs from their in vitro dissolution data
-
Nicolaides, E. et al., Forecasting the in vivo performance of four low solubility drugs from their in vitro dissolution data, Pharm. Res., 16, 1876, 1999.
-
(1999)
Pharm. Res
, vol.16
, pp. 1876
-
-
Nicolaides, E.1
-
22
-
-
84974601997
-
Evaluation of dissolution hydrodynamics in the USP, peak and flat-bottom vessels using different solubility drugs
-
February
-
Mirza. T. et al., Evaluation of dissolution hydrodynamics in the USP, peak and flat-bottom vessels using different solubility drugs, Dissol. Technol., 12, 11-16, February 2005.
-
(2005)
Dissol. Technol
, vol.12
, pp. 11-16
-
-
Mirza, T.1
-
23
-
-
85046914095
-
Evaluation of USP apparatus 3 for dissolution testing of immediate-release products
-
Yu, L. X., Wang, J. T. and Hussain, A. S., Evaluation of USP apparatus 3 for dissolution testing of immediate-release products, AAPS Pharm. Sci., 4, E1, 2002.
-
(2002)
AAPS Pharm. Sci
, vol.4
, pp. E1
-
-
Yu, L.X.1
Wang, J.T.2
Hussain, A.S.3
-
25
-
-
0037723973
-
Quality evaluation of generic drugs by dissolution test: Changing the USP dissolution medium to distinguish between active and non-active mebendazole polymorphs
-
Swanepoel, E., Liebenberg, W. and de Villiers, M. M., Quality evaluation of generic drugs by dissolution test: changing the USP dissolution medium to distinguish between active and non-active mebendazole polymorphs, Eur. J. Pharm. Biopharm., 55, 345, 2003.
-
(2003)
Eur. J. Pharm. Biopharm
, vol.55
, pp. 345
-
-
Swanepoel, E.1
Liebenberg, W.2
de Villiers, M.M.3
|