-
1
-
-
0346613495
-
Crystal engineering: strategies and architectures
-
Aakeröy CB (1997) Crystal engineering: strategies and architectures. Acta Cryst 53:569-586.
-
(1997)
Acta Cryst
, vol.53
, pp. 569-586
-
-
Aakeröy, C.B.1
-
2
-
-
33747355497
-
Crystal modification of dipyridamole using different solvents and crystallisation conditions
-
1-2
-
Adhiyaman R and Basu SK (2006) Crystal modification of dipyridamole using different solvents and crystallisation conditions. Int J Pharm 321(1-2):27-34.
-
(2006)
Int J Pharm
, vol.321
, pp. 27-34
-
-
Adhiyaman, R.1
Basu, S.K.2
-
3
-
-
0028948839
-
A theoretical basis for a biopharmaceutics drug classification: the correlation of in vivo drug product dissolution and in vivo bioavailability
-
Amidon GL, Lennernas H, Shah VP, and Crison JR (1995) A theoretical basis for a biopharmaceutics drug classification: the correlation of in vivo drug product dissolution and in vivo bioavailability. Pharm Res 12:413-420.
-
(1995)
Pharm Res
, vol.12
, pp. 413-420
-
-
Amidon, G.L.1
Lennernas, H.2
Shah, V.P.3
Crison, J.R.4
-
5
-
-
34547651036
-
Current perspectives in dissolution testing of conventional and novel dosage forms
-
Azarmi S, Roac W, and Lobenberg R (2007) Current perspectives in dissolution testing of conventional and novel dosage forms. Int J Pharm 328:12-21.
-
(2007)
Int J Pharm
, vol.328
, pp. 12-21
-
-
Azarmi, S.1
Roac, W.2
Lobenberg, R.3
-
6
-
-
3242754188
-
Shear distribution and variability in the USP apparatus 2 under turbulent conditions
-
Baxter JL, Muzzio FJ, and Kukura J (2004) Shear distribution and variability in the USP apparatus 2 under turbulent conditions. Int J Pharm 279:9-17.
-
(2004)
Int J Pharm
, vol.279
, pp. 9-17
-
-
Baxter, J.L.1
Muzzio, F.J.2
Kukura, J.3
-
7
-
-
13844276813
-
Hydrodynamicsinduced variability in the USP apparatus II dissolution test
-
Baxter JL, Muzzio FJ, and Kukura J (2005) Hydrodynamicsinduced variability in the USP apparatus II dissolution test. Int J Pharm 292:17-28.
-
(2005)
Int J Pharm
, vol.292
, pp. 17-28
-
-
Baxter, J.L.1
Muzzio, F.J.2
Kukura, J.3
-
8
-
-
34548023425
-
Crystal engineering of active pharmaceutical ingredients to improve solubility and dissolution rates
-
Blagden N, de Matas M, Gavan PT, and York P (2007) Crystal engineering of active pharmaceutical ingredients to improve solubility and dissolution rates. Adv Drug Deliv Rev 59:617-630.
-
(2007)
Adv Drug Deliv Rev
, vol.59
, pp. 617-630
-
-
Blagden, N.1
de Matas, M.2
Gavan, P.T.3
York, P.4
-
10
-
-
0002642747
-
Reaktionsgeschwindigkeit in heterogenen Systemen
-
Brunner E (1904) Reaktionsgeschwindigkeit in heterogenen Systemen. Z Phys Chem 43:56-102.
-
(1904)
Z Phys Chem
, vol.43
, pp. 56-102
-
-
Brunner, E.1
-
11
-
-
35248822616
-
The utility of cyclodextrins for enhancing oral bioavailability
-
Carrier RL, Miller LA, and Ahmed I (2007) The utility of cyclodextrins for enhancing oral bioavailability. J Control Release 123:78-99.
-
(2007)
J Control Release
, vol.123
, pp. 78-99
-
-
Carrier, R.L.1
Miller, L.A.2
Ahmed, I.3
-
13
-
-
23844434967
-
Preparation and evaluation of glibenclamidepolyglycolized glycerides solid dispersions with silicon dioxide by spray drying technique
-
Chauhan B, Shimpi S, and Paradkar A (2005) Preparation and evaluation of glibenclamidepolyglycolized glycerides solid dispersions with silicon dioxide by spray drying technique. Eur J Pharm Sci 26:219-230.
-
(2005)
Eur J Pharm Sci
, vol.26
, pp. 219-230
-
-
Chauhan, B.1
Shimpi, S.2
Paradkar, A.3
-
14
-
-
10444279209
-
Cyclodextrin-based pharmaceutics: past, present and future
-
Davis ME and Brewster ME (2004) Cyclodextrin-based pharmaceutics: past, present and future. Nat Rev Drug Discov 3:1023-1035.
-
(2004)
Nat Rev Drug Discov
, vol.3
, pp. 1023-1035
-
-
Davis, M.E.1
Brewster, M.E.2
-
15
-
-
0035988096
-
Cooperative effect of the artificial chaperones and guanidinium chloride on lysozyme renaturation at high concentrations
-
Dong XY, Shi JH, and Sun Y (2002) Cooperative effect of the artificial chaperones and guanidinium chloride on lysozyme renaturation at high concentrations. Biotechnol Prog 18:663-665.
-
(2002)
Biotechnol Prog
, vol.18
, pp. 663-665
-
-
Dong, X.Y.1
Shi, J.H.2
Sun, Y.3
-
17
-
-
33845409810
-
Use of surfactants as plasticizers in preparing solid dispersions of poorly soluble API: selection of polymer-surfactant combinations using solubility parameters and testing the processability
-
Ghebremeskel AN, Vemavarapu C, and Lodaya M. (2007) Use of surfactants as plasticizers in preparing solid dispersions of poorly soluble API: selection of polymer-surfactant combinations using solubility parameters and testing the processability. Int J Pharm 328:119-129.
-
(2007)
Int J Pharm
, vol.328
, pp. 119-129
-
-
Ghebremeskel, A.N.1
Vemavarapu, C.2
Lodaya, M.3
-
19
-
-
0033795023
-
Functional changes in ß-Lactoglobulin upon conjugation with carboxymethyl cyclodextrin
-
Hattori M, Okada Y, and Takahashi K (2000) Functional changes in ß-Lactoglobulin upon conjugation with carboxymethyl cyclodextrin. J Agric Food Chem 48:3789-3794.
-
(2000)
J Agric Food Chem
, vol.48
, pp. 3789-3794
-
-
Hattori, M.1
Okada, Y.2
Takahashi, K.3
-
21
-
-
33746868980
-
The effects of milling on the surface properties of form I paracetamol crystals
-
Heng JYY, Thielmann F, and Williams DR (2006) The effects of milling on the surface properties of form I paracetamol crystals. Pharm Res 23(8):1918-1927.
-
(2006)
Pharm Res
, vol.23
, Issue.8
, pp. 1918-1927
-
-
Heng, J.Y.Y.1
Thielmann, F.2
Williams, D.R.3
-
22
-
-
84887725686
-
Dependence of reaction velocity upon surface and agitation
-
Hixson AW and Crowell JH (1931) Dependence of reaction velocity upon surface and agitation. Ind Eng Chem 23:923-931.
-
(1931)
Ind Eng Chem
, vol.23
, pp. 923-931
-
-
Hixson, A.W.1
Crowell, J.H.2
-
23
-
-
33846256269
-
Influence of different polymers on the crystallization tendency of molecularly dispersed amorphous felodipine
-
Konno H and Taylor LS (2006) Influence of different polymers on the crystallization tendency of molecularly dispersed amorphous felodipine. J Pharm Sci 95:2692-2705.
-
(2006)
J Pharm Sci
, vol.95
, pp. 2692-2705
-
-
Konno, H.1
Taylor, L.S.2
-
24
-
-
0029058924
-
Regiospecific intestinal-absorption of the HIV protease inhibitor L-735,524 in Beagle dogs
-
Kwei GY, Novak LB, Hettrick LA, Reiss ER, Ostovic D, Loper AE, Lui CY, Higgins RJ, Chen IW, and Lin JH (1995) Regiospecific intestinal-absorption of the HIV protease inhibitor L-735,524 in Beagle dogs. Pharm Res 12:884-888.
-
(1995)
Pharm Res
, vol.12
, pp. 884-888
-
-
Kwei, G.Y.1
Novak, L.B.2
Hettrick, L.A.3
Reiss, E.R.4
Ostovic, D.5
Loper, A.E.6
Lui, C.Y.7
Higgins, R.J.8
Chen, I.W.9
Lin, J.H.10
-
25
-
-
33846250003
-
Evaluation of the USP dissolution test method A for enteric-coated particles by planar laser-induced fluorescence
-
Miller DA, Gamba M, Sauer D, Purvis TP, Clemens NT, and Williams RO (2007) Evaluation of the USP dissolution test method A for enteric-coated particles by planar laser-induced fluorescence. Int J Pharm 330:61-72.
-
(2007)
Int J Pharm
, vol.330
, pp. 61-72
-
-
Miller, D.A.1
Gamba, M.2
Sauer, D.3
Purvis, T.P.4
Clemens, N.T.5
Williams, R.O.6
-
26
-
-
0002642747
-
Theorie der Reaktionsgeschwindigkeit in heterogenen systemen
-
Nernst W (1904) Theorie der Reaktionsgeschwindigkeit in heterogenen systemen. Z Phys Chem 47:52-55.
-
(1904)
Z Phys Chem
, vol.47
, pp. 52-55
-
-
Nernst, W.1
-
27
-
-
0037413404
-
Crystal modification of phenytoin using different solvents and crystallisation conditions
-
Nokhodchi A, Bolourtchian N, and Dinarvand R (2003) Crystal modification of phenytoin using different solvents and crystallisation conditions. Int J Pharm 250(1):85-97.
-
(2003)
Int J Pharm
, vol.250
, Issue.1
, pp. 85-97
-
-
Nokhodchi, A.1
Bolourtchian, N.2
Dinarvand, R.3
-
28
-
-
33947487639
-
The rate of solution of solid substances in their own solutions
-
Noyes AA and Whitney WR (1897) The rate of solution of solid substances in their own solutions. J Am Chem Soc 19:930-934.
-
(1897)
J Am Chem Soc
, vol.19
, pp. 930-934
-
-
Noyes, A.A.1
Whitney, W.R.2
-
29
-
-
0036084634
-
Structural basis for cyclodextrins' suppression of human growth hormone aggregation
-
Otzen DE, Knudsen BR, Aachmann F, Larsen KL, and Wimmer R (1999) Structural basis for cyclodextrins' suppression of human growth hormone aggregation. Protein Sci 11:1779-1787.
-
(1999)
Protein Sci
, vol.11
, pp. 1779-1787
-
-
Otzen, D.E.1
Knudsen, B.R.2
Aachmann, F.3
Larsen, K.L.4
Wimmer, R.5
-
30
-
-
0038713880
-
Crystal engineering of novel co-crystals of a triazole drug with 1,4-dicarboxylic acids
-
Remenar JF, Morisette SL, Peterson ML, Moulton B, MacPhee MJ, Guzman HR, and Almarsson O (2003) Crystal engineering of novel co-crystals of a triazole drug with 1,4-dicarboxylic acids. J Am Chem Soc 125:8456-8457.
-
(2003)
J Am Chem Soc
, vol.125
, pp. 8456-8457
-
-
Remenar, J.F.1
Morisette, S.L.2
Peterson, M.L.3
Moulton, B.4
MacPhee, M.J.5
Guzman, H.R.6
Almarsson, O.7
-
31
-
-
23844556556
-
A three step supercritical process to improve the dissolution rate of Eflucimibe
-
Rodier E, Lochard H, Sauceau M, Letourneau J-J, Freiss B, and Fages J (2005) A three step supercritical process to improve the dissolution rate of Eflucimibe. Eur J Pharm Sci 26:184-193.
-
(2005)
Eur J Pharm Sci
, vol.26
, pp. 184-193
-
-
Rodier, E.1
Lochard, H.2
Sauceau, M.3
Letourneau, J.-J.4
Freiss, B.5
Fages, J.6
-
32
-
-
0345465964
-
Influence of cyclodextrins on the stability of the peptide salmon calcitonin in aqueous solution
-
Sigurjonsdottir JF, Loftsson T, and Masson M (1999) Influence of cyclodextrins on the stability of the peptide salmon calcitonin in aqueous solution. Int J Pharm 186:205-213.
-
(1999)
Int J Pharm
, vol.186
, pp. 205-213
-
-
Sigurjonsdottir, J.F.1
Loftsson, T.2
Masson, M.3
-
33
-
-
0042452386
-
-
Pharmaceutical Dosage Forms: Tablets, (Lieberman HA, Lachman L, and Schwartz JB, eds.), Marcel Dekker Inc., New York
-
Stavchansky R and McGinity J. Bioavailability and tablet technology, in: Pharmaceutical Dosage Forms: Tablets, Volume 2, (Lieberman HA, Lachman L, and Schwartz JB, eds.), Marcel Dekker Inc., New York, 1998, pp. 349-353.
-
(1998)
Bioavailability and tablet technology
, vol.2
, pp. 349-353
-
-
Stavchansky, R.1
McGinity, J.2
-
34
-
-
0031042310
-
Cyclodextrins-enabling excipients: their present and future use in pharmaceuticals
-
Thompson DO (1997) Cyclodextrins-enabling excipients: their present and future use in pharmaceuticals. Crit Rev Ther Drug Carr Syst 14(1):1-104.
-
(1997)
Crit Rev Ther Drug Carr Syst
, vol.14
, Issue.1
, pp. 1-104
-
-
Thompson, D.O.1
-
36
-
-
0003701605
-
-
U.S. Food and Drug Administration, Center for Drug Evaluation and Research, Office of Training and Communications, Division of Communications Management, Drug Information Branch, HFD-210, Rockville, MD
-
U.S. Food and Drug Administration, Center for Drug Evaluation and Research (1997a) Guidance for Industry: Extended-Release Oral Dosage Forms: Development, Evaluation, and Application of In Vitro/In Vivo Correlations, Office of Training and Communications, Division of Communications Management, Drug Information Branch, HFD-210, Rockville, MD.
-
(1997)
Guidance for Industry: Extended-Release Oral Dosage Forms: Development, Evaluation, and Application of In Vitro/In Vivo Correlations
-
-
-
37
-
-
0003428585
-
-
U.S. Food and Drug Administration, Center for Drug Evaluation and Research, Office of Training and Communications, Division of Communications Management, Drug Information Branch, HFD-210, Rockville, MD
-
U.S. Food and Drug Administration, Center for Drug Evaluation and Research (1997b) Guidance for Industry: Dissolution Testing of Immediate-Release Solid Oral Dosage Forms, Office of Training and Communications, Division of Communications Management, Drug Information Branch, HFD-210, Rockville, MD.
-
(1997)
Guidance for Industry: Dissolution Testing of Immediate-Release Solid Oral Dosage Forms
-
-
-
38
-
-
0003455057
-
-
U.S. Food and Drug Administration, Center for Drug Evaluation and Research, Office of Training and Communications, Division of Communications Management, Drug Information Branch, HFD-210, Rockville, MD
-
U.S. Food and Drug Administration, Center for Drug Evaluation and Research (2000) Guidance for Industry: Waiver of In Vivo Bioavailability and Bioequivalence Studies for Immediate-Release Solid Oral Dosage Forms Based on a Biopharmaceutics Classification System, Office of Training and Communications, Division of Communications Management, Drug Information Branch, HFD-210, Rockville, MD.
-
(2000)
Guidance for Industry: Waiver of In Vivo Bioavailability and Bioequivalence Studies for Immediate-Release Solid Oral Dosage Forms Based on a Biopharmaceutics Classification System
-
-
-
39
-
-
0003455042
-
-
U.S. Food and Drug Administration, Center for Drug Evaluation and Research, Office of Training and Communications, Division of Communications Management, Drug Information Branch, HFD-210, Rockville, MD
-
U.S. Food and Drug Administration, Center for Drug Evaluation and Research (2003) Guidance for Industry: Bioavailability and Bioequivalence Studies for Orally Administered Drug Products-General Considerations, Office of Training and Communications, Division of Communications Management, Drug Information Branch, HFD-210, Rockville, MD.
-
(2003)
Guidance for Industry: Bioavailability and Bioequivalence Studies for Orally Administered Drug Products-General Considerations
-
-
-
40
-
-
84885771574
-
-
USP 31, United States Pharmacopoeia
-
USP 31 (2008) General Monograph on Dissolution , United States Pharmacopoeia, Volume 31.
-
(2008)
General Monograph on Dissolution
, vol.31
-
-
-
41
-
-
36549042006
-
Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs
-
Vasconcelos T, Sarmento B, and Costa P (2007) Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs. Drug Disc Today 12(23/24):1068-1075.
-
(2007)
Drug Disc Today
, vol.12
, Issue.23-24
, pp. 1068-1075
-
-
Vasconcelos, T.1
Sarmento, B.2
Costa, P.3
-
42
-
-
84962123941
-
Rate of dissolution in vivo and in vitro, Part II
-
Wagner JG (1970) Rate of dissolution in vivo and in vitro, Part II. Drug Intell. Clin Pharm 4:32.
-
(1970)
Drug Intell. Clin Pharm
, vol.4
, pp. 32
-
-
Wagner, J.G.1
-
43
-
-
37349028271
-
Biorelevant dissolution testing of colon-specific delivery systems activated by colonic microflora
-
Yang L (2008) Biorelevant dissolution testing of colon-specific delivery systems activated by colonic microflora. J Control Release 125:77-86.
-
(2008)
J Control Release
, vol.125
, pp. 77-86
-
-
Yang, L.1
-
44
-
-
85016967291
-
-
Transport Processes in Pharmaceutical Systems, Amidon GL, Lee PI, and Topp EM, eds., Marcel Dekker Inc., New York
-
Yu LX and Amidon GL. (1999) Analytical solutions to mass transfer, in: Transport Processes in Pharmaceutical Systems, Volume 102 (Amidon GL, Lee PI, and Topp EM, eds.), Marcel Dekker Inc., New York, pp. 23-54.
-
(1999)
Analytical solutions to mass transfer
, vol.102
, pp. 23-54
-
-
Yu, L.X.1
Amidon, G.L.2
-
45
-
-
52449111401
-
Evaluation of USP apparatus 3 for dissolution testing of immediate-release products
-
Article 1
-
Yu LX, Wang JT, and Hussain AS (2002) Evaluation of USP apparatus 3 for dissolution testing of immediate-release products. AAPS PharmSci 4(1): Article 1.
-
(2002)
AAPS PharmSci
, vol.4
, Issue.1
-
-
Yu, L.X.1
Wang, J.T.2
Hussain, A.S.3
|