-
1
-
-
0141477785
-
Beyond bioavailability testing
-
Banakar UV, Block LH,. Beyond bioavailability testing. Pharm Technol 1983; 7: 107-117.
-
(1983)
Pharm Technol
, vol.7
, pp. 107-117
-
-
Banakar, U.V.1
Block, L.H.2
-
2
-
-
0034080127
-
Dissolution testing as a prognostic tool for oral drug absorption: Dissolution behavior of glibenclamide
-
Löbenberg R, et al,. Dissolution testing as a prognostic tool for oral drug absorption: dissolution behavior of glibenclamide. Pharm Res 2000; 17: 439-444.
-
(2000)
Pharm Res
, vol.17
, pp. 439-444
-
-
Löbenberg, R.1
-
3
-
-
57449102059
-
Dissolution and dissolution testing
-
Swarbrick J. ed. 3rd edn. New York: Informa Healthcare USA, Inc
-
Dyas AM, Shah UU,. Dissolution and dissolution testing. In:, Swarbrick J, ed. Encyclopedia of Pharmaceutical Technology, Vol. 1, 3rd edn. New York: Informa Healthcare USA, Inc., 2007: 908-928.
-
(2007)
Encyclopedia of Pharmaceutical Technology
, vol.1
, pp. 908-928
-
-
Dyas, A.M.1
Shah, U.U.2
-
4
-
-
0031913402
-
Dissolution testing as a prognostic tool for oral drug absorption: Immediate release dosage forms
-
Dressman JB, et al,. Dissolution testing as a prognostic tool for oral drug absorption: immediate release dosage forms. Pharm Res 1998; 15: 11-22.
-
(1998)
Pharm Res
, vol.15
, pp. 11-22
-
-
Dressman, J.B.1
-
5
-
-
84867576296
-
Roles of dissolution testing: Regulatory, industry and academic perspectives: Role of dissolution testing in regulating pharmaceuticals
-
Shah VP, Williams RL,. Roles of dissolution testing: regulatory, industry and academic perspectives: role of dissolution testing in regulating pharmaceuticals. Dissolution Technol 1999; 8: 7-10.
-
(1999)
Dissolution Technol
, vol.8
, pp. 7-10
-
-
Shah, V.P.1
Williams, R.L.2
-
6
-
-
0032819165
-
Unconventional dissolution methodologies
-
Pillay V, Fassihi R,. Unconventional dissolution methodologies. J Pharm Sci 1999; 88: 843-851.
-
(1999)
J Pharm Sci
, vol.88
, pp. 843-851
-
-
Pillay, V.1
Fassihi, R.2
-
7
-
-
33947487639
-
The rate of solution of solid substances in their own solutions
-
Noyes AW, Whitney WR,. The rate of solution of solid substances in their own solutions. J Am Chem Soc 1897; 19: 930-934.
-
(1897)
J Am Chem Soc
, vol.19
, pp. 930-934
-
-
Noyes, A.W.1
Whitney, W.R.2
-
8
-
-
33747348812
-
Über die Auflösungsgeschwindigkeit Fester Körper
-
Brunner L, Tolloczko S,. Über die Auflösungsgeschwindigkeit Fester Körper. Z Phys Chem 1900; 35: 282-290.
-
(1900)
Z Phys Chem
, vol.35
, pp. 282-290
-
-
Brunner, L.1
Tolloczko, S.2
-
9
-
-
33747373878
-
A century of dissolution research: From Noyes and Whitney to the biopharmaceutics classification system
-
Dokoumetzidis A, Macheras P,. A century of dissolution research: from Noyes and Whitney to the biopharmaceutics classification system. Int J Pharm 2006; 321: 1-11.
-
(2006)
Int J Pharm
, vol.321
, pp. 1-11
-
-
Dokoumetzidis, A.1
MacHeras, P.2
-
10
-
-
84867582280
-
The dissolution procedure
-
Rockville, MD: The United States Pharmacopeial Convention, Inc
-
The dissolution procedure. United States Pharmacopeia and National Formulary USP32-NF27. Rockville, MD: The United States Pharmacopeial Convention, Inc., 2009: 601.
-
(2009)
United States Pharmacopeia and National Formulary USP32 - NF27
, pp. 601
-
-
-
11
-
-
10344257263
-
Acceptable analytical practices for dissolution testing of poorly soluble compounds
-
Brown CK, et al,. Acceptable analytical practices for dissolution testing of poorly soluble compounds. Pharm Technol 2004; 28: 56-65.
-
(2004)
Pharm Technol
, vol.28
, pp. 56-65
-
-
Brown, C.K.1
-
12
-
-
78649710378
-
Dissolution testing for poorly soluble drugs: A continuing perspective
-
Gowthamarajan K, Singh SK,. Dissolution testing for poorly soluble drugs: a continuing perspective. Dissolution Technol 2010; 17: 24-33.
-
(2010)
Dissolution Technol
, vol.17
, pp. 24-33
-
-
Gowthamarajan, K.1
Singh, S.K.2
-
13
-
-
0028948839
-
A theoretical basis for a biopharmaceutic drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability
-
Amidon GL, et al,. A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm Res 1995; 12: 413-420.
-
(1995)
Pharm Res
, vol.12
, pp. 413-420
-
-
Amidon, G.L.1
-
14
-
-
0035997323
-
Biopharmaceutics classification system: The scientific basis for biowaver extensions
-
Yu LX, et al,. Biopharmaceutics classification system: the scientific basis for biowaver extensions. Pharm Res 2002; 19: 921-925.
-
(2002)
Pharm Res
, vol.19
, pp. 921-925
-
-
Yu, L.X.1
-
15
-
-
51249095402
-
Use of the biopharmaceutical classification system in early drug development
-
Ku MS,. Use of the biopharmaceutical classification system in early drug development. AAPS J 2008; 10: 208-212.
-
(2008)
AAPS J
, vol.10
, pp. 208-212
-
-
Ku, M.S.1
-
16
-
-
33144454819
-
Comparison of statistical analysis and bayesian networks in the evaluation of dissolution performance of BCS class II model drugs
-
Wilson WI, et al,. Comparison of statistical analysis and bayesian networks in the evaluation of dissolution performance of BCS class II model drugs. J Pharm Sci 2005; 94: 2764-2776.
-
(2005)
J Pharm Sci
, vol.94
, pp. 2764-2776
-
-
Wilson, W.I.1
-
17
-
-
33746101876
-
Role of surfactant and pH on dissolution properties of fenofibrate and glipizide - A technical note
-
Jamzad S, Fassihi R,. Role of surfactant and pH on dissolution properties of fenofibrate and glipizide-a technical note. AAPS PharmSciTech 2006; 7: E33.
-
(2006)
AAPS PharmSciTech
, vol.7
-
-
Jamzad, S.1
Fassihi, R.2
-
18
-
-
20344383278
-
Surfactant effects upon dissolution patterns of carbamazepine immediate release tablets
-
Lee J, et al,. Surfactant effects upon dissolution patterns of carbamazepine immediate release tablets. Arch Pharm Res 2005; 28: 120-126.
-
(2005)
Arch Pharm Res
, vol.28
, pp. 120-126
-
-
Lee, J.1
-
19
-
-
0029045705
-
In vitro dissolution of sparingly water-soluble drug dosage forms
-
Shah VP, et al,. In vitro dissolution of sparingly water-soluble drug dosage forms. Int J Pharm 1995; 125: 99-106.
-
(1995)
Int J Pharm
, vol.125
, pp. 99-106
-
-
Shah, V.P.1
-
20
-
-
0013239454
-
Surfactants in pharmaceutical products and systems
-
Swarbrick J. ed. 3rd edn. New York: Informa Healthcare USA, Inc
-
Corrigan OI, Healy AM,. Surfactants in pharmaceutical products and systems. In:, Swarbrick J, ed. Encyclopedia of Pharmaceutical Technology, Vol. 5, 3rd edn. New York: Informa Healthcare USA, Inc., 2007: 3583-3596.
-
(2007)
Encyclopedia of Pharmaceutical Technology
, vol.5
, pp. 3583-3596
-
-
Corrigan, O.I.1
Healy, A.M.2
-
21
-
-
27344441229
-
Micellar solubilization of drugs
-
Rangel-Yagui CO, et al,. Micellar solubilization of drugs. J Pharm Pharm Sci 2005; 8: 147-163.
-
(2005)
J Pharm Pharm Sci
, vol.8
, pp. 147-163
-
-
Rangel-Yagui, C.O.1
-
22
-
-
0037452442
-
The usefulness of sugar surfactants as solubilizing agents in parenteral formulations
-
Söderlind E, et al,. The usefulness of sugar surfactants as solubilizing agents in parenteral formulations. Int J Pharm 2003; 252: 61-71.
-
(2003)
Int J Pharm
, vol.252
, pp. 61-71
-
-
Söderlind, E.1
-
23
-
-
0026373840
-
Theory of surfactant self-assembly: A predictive molecular thermodynamic approach
-
Nagarajan R, Ruckenstein E,. Theory of surfactant self-assembly: a predictive molecular thermodynamic approach. Langmuir 1991; 7: 2934-2969.
-
(1991)
Langmuir
, vol.7
, pp. 2934-2969
-
-
Nagarajan, R.1
Ruckenstein, E.2
-
24
-
-
0025239160
-
Role of surfactant on drug release from tablets
-
Heng PWS, et al,. Role of surfactant on drug release from tablets. Drug Dev Ind Pharm 1990; 16: 951-962.
-
(1990)
Drug Dev Ind Pharm
, vol.16
, pp. 951-962
-
-
Heng, P.W.S.1
-
25
-
-
8444233994
-
The role of various surfactants on the release of salbutamol from suppositories
-
Hanaee J, et al,. The role of various surfactants on the release of salbutamol from suppositories. Farmaco 2004; 59: 903-906.
-
(2004)
Farmaco
, vol.59
, pp. 903-906
-
-
Hanaee, J.1
-
26
-
-
33845956662
-
Effect of surfactant on dissolution of spherical particles in micellar systems
-
Allaboun H, et al,. Effect of surfactant on dissolution of spherical particles in micellar systems. Eur J Pharm Biopharm 2007; 65: 188-197.
-
(2007)
Eur J Pharm Biopharm
, vol.65
, pp. 188-197
-
-
Allaboun, H.1
-
27
-
-
0033000119
-
Design and characterization of a surfactant-enriched tablet formulation for oral delivery of a poorly water-soluble immunosuppressive agent
-
Ruddy SB, et al,. Design and characterization of a surfactant-enriched tablet formulation for oral delivery of a poorly water-soluble immunosuppressive agent. Int J Pharm 1999; 182: 173-186.
-
(1999)
Int J Pharm
, vol.182
, pp. 173-186
-
-
Ruddy, S.B.1
-
28
-
-
0037406422
-
Dissolution behavior of a poorly water soluble compound in the presence of tween 80
-
Chen LR, et al,. Dissolution behavior of a poorly water soluble compound in the presence of tween 80. Pharm Res 2003; 20: 797-801.
-
(2003)
Pharm Res
, vol.20
, pp. 797-801
-
-
Chen, L.R.1
-
29
-
-
0037452425
-
Evaluating dissolution profiles of an anti-HIV agent using ANOVA and non-linear regression models in JMP software
-
Qazi S, et al,. Evaluating dissolution profiles of an anti-HIV agent using ANOVA and non-linear regression models in JMP software. Int J Pharm 2003; 252: 27-39.
-
(2003)
Int J Pharm
, vol.252
, pp. 27-39
-
-
Qazi, S.1
-
30
-
-
0000274955
-
Interactions between water-soluble cellulose derivatives and surfactants. 1. The HPMC/SDS/Water System
-
Nilsson S,. Interactions between water-soluble cellulose derivatives and surfactants. 1. The HPMC/SDS/Water System. Macromolecules 1995; 28: 7837-7844.
-
(1995)
Macromolecules
, vol.28
, pp. 7837-7844
-
-
Nilsson, S.1
-
31
-
-
0006282320
-
Binding of surfactants by polymers
-
Saito S,. Binding of surfactants by polymers. J Colloid Sci 1960; 15: 282-286.
-
(1960)
J Colloid Sci
, vol.15
, pp. 282-286
-
-
Saito, S.1
-
32
-
-
0021346134
-
The effect of anionic surfactants on the release of chlorpheniramine from a polymer matrix
-
Daly PB, et al,. The effect of anionic surfactants on the release of chlorpheniramine from a polymer matrix. Int J Pharm 1984; 18: 201-205.
-
(1984)
Int J Pharm
, vol.18
, pp. 201-205
-
-
Daly, P.B.1
-
33
-
-
0026114547
-
Hydroxypropylmethylcellulose-anionic surfactant interactions in aqueous systems
-
Alli D, et al,. Hydroxypropylmethylcellulose-anionic surfactant interactions in aqueous systems. J Appl Polym Sci 2003; 42: 947-956.
-
(2003)
J Appl Polym Sci
, vol.42
, pp. 947-956
-
-
Alli, D.1
-
34
-
-
0014126586
-
Correlation of dissolution rate and griseofulvin absorption in man
-
Katchen B, Symchowicz S,. Correlation of dissolution rate and griseofulvin absorption in man. J Pharm Sci 1967; 56: 1108-1111.
-
(1967)
J Pharm Sci
, vol.56
, pp. 1108-1111
-
-
Katchen, B.1
Symchowicz, S.2
-
35
-
-
0014316388
-
Griseofulvin absorption in man after single and repeated treatment and its correlation with dissolution rates
-
Symchowicz S, Katchen B,. Griseofulvin absorption in man after single and repeated treatment and its correlation with dissolution rates. J Pharm Sci 1968; 57: 1383-1386.
-
(1968)
J Pharm Sci
, vol.57
, pp. 1383-1386
-
-
Symchowicz, S.1
Katchen, B.2
-
36
-
-
0014815890
-
Oral absorption of griseofulvin in dogs: Increased absorption via solid dispersion in polyethylene glycol 6000
-
Chiou WL, Riegleman S,. Oral absorption of griseofulvin in dogs: increased absorption via solid dispersion in polyethylene glycol 6000. J Pharm Sci 1970; 59: 937-942.
-
(1970)
J Pharm Sci
, vol.59
, pp. 937-942
-
-
Chiou, W.L.1
Riegleman, S.2
-
37
-
-
0019959476
-
Analytical methodology applicable in dissolution testing of norethindrone-mestranol tablets
-
Goehl TJ, et al,. Analytical methodology applicable in dissolution testing of norethindrone-mestranol tablets. Int J Pharm 1982; 11: 181-186.
-
(1982)
Int J Pharm
, vol.11
, pp. 181-186
-
-
Goehl, T.J.1
-
38
-
-
1242337285
-
Solubilizing excipients in oral and injectable formulations
-
Strickley RG,. Solubilizing excipients in oral and injectable formulations. Pharm Res 2004; 21: 201-230.
-
(2004)
Pharm Res
, vol.21
, pp. 201-230
-
-
Strickley, R.G.1
-
39
-
-
0025907961
-
Co-solvent systems in dissolution testing: Theoretical considerations
-
Corrigan OI,. Co-solvent systems in dissolution testing: theoretical considerations. Drug Dev Ind Pharm 1991; 17: 695-708.
-
(1991)
Drug Dev Ind Pharm
, vol.17
, pp. 695-708
-
-
Corrigan, O.I.1
-
40
-
-
28544434033
-
Solubility of rofecoxib in the presence of aqueous solutions of glycerol, propylene glycol, ethanol, span 20, tween 80 and sodium lauryl sulfate at (298.15, 303.15 and 308.15) K
-
Liu C, et al,. Solubility of rofecoxib in the presence of aqueous solutions of glycerol, propylene glycol, ethanol, span 20, tween 80 and sodium lauryl sulfate at (298.15, 303.15 and 308.15) K. J Chem Eng Data 2005; 50: 2061-2064.
-
(2005)
J Chem Eng Data
, vol.50
, pp. 2061-2064
-
-
Liu, C.1
-
41
-
-
0032103706
-
Formulation design and bioavailability assessment of lipidic self-emulsifying formulations of halofantrine
-
Khoo S-M, et al,. Formulation design and bioavailability assessment of lipidic self-emulsifying formulations of halofantrine. Int J Pharm 1998; 167: 155-164.
-
(1998)
Int J Pharm
, vol.167
, pp. 155-164
-
-
Khoo, S.-M.1
-
42
-
-
0018411626
-
A partially organic dissolution medium for griseofulvin dosage forms
-
Walkling WD, et al,. A partially organic dissolution medium for griseofulvin dosage forms. Drug Dev Ind Pharm 1979; 5: 17-27.
-
(1979)
Drug Dev Ind Pharm
, vol.5
, pp. 17-27
-
-
Walkling, W.D.1
-
43
-
-
0029845241
-
Development of a dissolution medium for glibenclamide
-
El-Massik MA, et al,. Development of a dissolution medium for glibenclamide. Int J Pharm 1996; 140: 69-76.
-
(1996)
Int J Pharm
, vol.140
, pp. 69-76
-
-
El-Massik, M.A.1
-
44
-
-
84856570378
-
Flow-through cell appartus (USP apparatus 4): Operation and features
-
Fotaki N,. Flow-through cell appartus (USP apparatus 4): operation and features. Dissolution Technol 2011; 18: 46-49.
-
(2011)
Dissolution Technol
, vol.18
, pp. 46-49
-
-
Fotaki, N.1
-
45
-
-
0032432763
-
A flow-through dissolution method for a two-component drug formulation where the actives have markedly differing solubility properties
-
Butler WCG, Bateman SR,. A flow-through dissolution method for a two-component drug formulation where the actives have markedly differing solubility properties. Int J Pharm 1998; 173: 211-219.
-
(1998)
Int J Pharm
, vol.173
, pp. 211-219
-
-
Butler, W.C.G.1
Bateman, S.R.2
-
46
-
-
84862237821
-
Dissolution testing of oral modified-release dosage forms
-
doi: 10.1111/j.2042-7158.2012.01477.x
-
Garbacz G, Klein S,. Dissolution testing of oral modified-release dosage forms. J Pharm Pharmacol 2012. doi: 10.1111/j.2042-7158.2012.01477.x.
-
(2012)
J Pharm Pharmacol
-
-
Garbacz, G.1
Klein, S.2
-
47
-
-
0025963891
-
A collaborative study of the in vitro dissolution of phenacetin crystals comparing the flow through method with the USP paddle method
-
Nicklasson M, et al,. A collaborative study of the in vitro dissolution of phenacetin crystals comparing the flow through method with the USP paddle method. Int J Pharm 1991; 69: 255-264.
-
(1991)
Int J Pharm
, vol.69
, pp. 255-264
-
-
Nicklasson, M.1
-
48
-
-
84962059563
-
Apparatus 4 flow through cell: Some thoughts on operational characteristics
-
Brown W,. Apparatus 4 flow through cell: some thoughts on operational characteristics. Dissolution Technol 2005; 12: 28-32.
-
(2005)
Dissolution Technol
, vol.12
, pp. 28-32
-
-
Brown, W.1
-
49
-
-
0345281617
-
Sink conditions in the flow-through cell during dissolution
-
Posti J, Speiser PP,. Sink conditions in the flow-through cell during dissolution. Int J Pharm 1980; 5: 101-107.
-
(1980)
Int J Pharm
, vol.5
, pp. 101-107
-
-
Posti, J.1
Speiser, P.P.2
-
50
-
-
0028359787
-
Application of flow-through dissolution method for the evaluation of oral formulations of nifedipine
-
Quershi SA, et al,. Application of flow-through dissolution method for the evaluation of oral formulations of nifedipine. Drug Dev Ind Pharm 1994; 20: 1869-1882.
-
(1994)
Drug Dev Ind Pharm
, vol.20
, pp. 1869-1882
-
-
Quershi, S.A.1
-
51
-
-
67349213891
-
Classification of the flow regimes in the flow-through cell
-
Kakhi M,. Classification of the flow regimes in the flow-through cell. Eur J Pharm Sci 2009; 37: 531-544.
-
(2009)
Eur J Pharm Sci
, vol.37
, pp. 531-544
-
-
Kakhi, M.1
-
52
-
-
0030737622
-
Studies on dissolution testing of the nifedipine gastrointestinal therapeutic system. I. Description of a two-phase in vitro dissolution test
-
Grundy JS, et al,. Studies on dissolution testing of the nifedipine gastrointestinal therapeutic system. I. Description of a two-phase in vitro dissolution test. J Control Release 1997; 48: 1-8.
-
(1997)
J Control Release
, vol.48
, pp. 1-8
-
-
Grundy, J.S.1
-
54
-
-
0014138173
-
Establishment of sink conditions in dissolution rate determinations
-
Gibaldi M, Feldman S,. Establishment of sink conditions in dissolution rate determinations. J Pharm Sci 1967; 56: 1238-1242.
-
(1967)
J Pharm Sci
, vol.56
, pp. 1238-1242
-
-
Gibaldi, M.1
Feldman, S.2
-
55
-
-
0343924508
-
Design and evaluation of two-phase partition-dissolution method and its use in evaluating artemisinin tablets
-
Hoa NT, Kinget R,. Design and evaluation of two-phase partition-dissolution method and its use in evaluating artemisinin tablets. J Pharm Sci 1996; 85: 1060-1063.
-
(1996)
J Pharm Sci
, vol.85
, pp. 1060-1063
-
-
Hoa, N.T.1
Kinget, R.2
-
56
-
-
0029785621
-
Dissolution testing of artemisinin solid oral dosage forms
-
Ngo TH, et al,. Dissolution testing of artemisinin solid oral dosage forms. Int J Pharm 1996; 138: 185-190.
-
(1996)
Int J Pharm
, vol.138
, pp. 185-190
-
-
Ngo, T.H.1
-
57
-
-
0030964577
-
In vitro absorption studies and their relevance to absorption from the GI tract
-
Ungell A-L,. In vitro absorption studies and their relevance to absorption from the GI tract. Drug Dev Ind Pharm 1997; 23: 879-892.
-
(1997)
Drug Dev Ind Pharm
, vol.23
, pp. 879-892
-
-
Ungell, A.-L.1
-
58
-
-
20744444385
-
Experimental determination of octanol-water partition coefficients of quercetin and related flavonoids
-
Rothwell JA, et al,. Experimental determination of octanol-water partition coefficients of quercetin and related flavonoids. J Agric Food Chem 2005; 53: 4355-4360.
-
(2005)
J Agric Food Chem
, vol.53
, pp. 4355-4360
-
-
Rothwell, J.A.1
-
59
-
-
0035866672
-
High-throughput permeability pH profile and high-throughput alkane/water log P with artificial membranes
-
Wohnsland F, Faller B,. High-throughput permeability pH profile and high-throughput alkane/water log P with artificial membranes. J Med Chem 2001; 44: 923-930.
-
(2001)
J Med Chem
, vol.44
, pp. 923-930
-
-
Wohnsland, F.1
Faller, B.2
-
60
-
-
72449210513
-
Dissolution of poorly water-soluble drugs in biphasic media using USP 4 and fiber optic system
-
Vangani S, et al,. Dissolution of poorly water-soluble drugs in biphasic media using USP 4 and fiber optic system. Clin Res Regul Aff 2009; 26: 8-19.
-
(2009)
Clin Res Regul Aff
, vol.26
, pp. 8-19
-
-
Vangani, S.1
-
61
-
-
0030017609
-
Novel approach to the analysis of in vitro-in vivo relationships
-
Polli JE, et al,. Novel approach to the analysis of in vitro-in vivo relationships. J Pharm Sci 1996; 85: 753-760.
-
(1996)
J Pharm Sci
, vol.85
, pp. 753-760
-
-
Polli, J.E.1
-
62
-
-
0030810301
-
In vitro -in vivo relationships for oral extended-release drug products
-
Mauger DT, Chinchilli VM,. In vitro -in vivo relationships for oral extended-release drug products. J Biopharm Stat 1997; 7: 565-578.
-
(1997)
J Biopharm Stat
, vol.7
, pp. 565-578
-
-
Mauger, D.T.1
Chinchilli, V.M.2
-
63
-
-
77955654004
-
Prediciting in vivo absorption behavior of oral modified release dosage forms containing pH-dependent poorly soluble drugs using a novel pH-adjusted biphasic in vitro dissolution test
-
Heigoldt U, et al,. Prediciting in vivo absorption behavior of oral modified release dosage forms containing pH-dependent poorly soluble drugs using a novel pH-adjusted biphasic in vitro dissolution test. Eur J Pharm Biopharm 2010; 76: 105-111.
-
(2010)
Eur J Pharm Biopharm
, vol.76
, pp. 105-111
-
-
Heigoldt, U.1
-
64
-
-
0028197699
-
Dissolution system for nifedipine sustained release formulations
-
Chaudhary RS, et al,. Dissolution system for nifedipine sustained release formulations. Drug Dev Ind Pharm 1994; 20: 1267-1274.
-
(1994)
Drug Dev Ind Pharm
, vol.20
, pp. 1267-1274
-
-
Chaudhary, R.S.1
-
65
-
-
3843097202
-
Classification of orally administered drugs on the world health organization model list of essential medicines according to the biopharmaceutics classification system
-
Lindenberg M, et al,. Classification of orally administered drugs on the world health organization model list of essential medicines according to the biopharmaceutics classification system. Eur J Pharm Biopharm 2004; 58: 265-278.
-
(2004)
Eur J Pharm Biopharm
, vol.58
, pp. 265-278
-
-
Lindenberg, M.1
-
66
-
-
0000167929
-
Nifedipine
-
Florey K. ed. New York: Academic Press
-
Ali SL,. Nifedipine. In:, Florey K, ed. Analytical Profiles of Drug Substances, Vol. 18. New York: Academic Press, 1989: 221-288.
-
(1989)
Analytical Profiles of Drug Substances
, vol.18
, pp. 221-288
-
-
Ali, S.L.1
-
67
-
-
0023698052
-
Complexation of nifedipine with substituted phenolic ligands
-
Boje KM, et al,. Complexation of nifedipine with substituted phenolic ligands. Pharm Res 1988; 5: 655-659.
-
(1988)
Pharm Res
, vol.5
, pp. 655-659
-
-
Boje, K.M.1
-
68
-
-
0021814061
-
Interactions of organic calcium channel antagonists with calcium channels in single frog atrial cells
-
Uehara A, Hume JR,. Interactions of organic calcium channel antagonists with calcium channels in single frog atrial cells. J Gen Physiol 1985; 85: 621-647.
-
(1985)
J Gen Physiol
, vol.85
, pp. 621-647
-
-
Uehara, A.1
Hume, J.R.2
-
70
-
-
0001334658
-
Design principles for orally bioavailable drugs
-
Navia MA, Chaturvedi PR,. Design principles for orally bioavailable drugs. Drug Discov Today 1996; 1: 179-189.
-
(1996)
Drug Discov Today
, vol.1
, pp. 179-189
-
-
Navia, M.A.1
Chaturvedi, P.R.2
-
71
-
-
0030874214
-
Studies on dissolution testing of the nifedipine gastrointestinal therapeutic system. II. Improved in vitro-in vivo correlation using a two-phase dissolution test
-
Grundy JS, et al,. Studies on dissolution testing of the nifedipine gastrointestinal therapeutic system. II. Improved in vitro-in vivo correlation using a two-phase dissolution test. J Control Release 1997; 48: 9-17.
-
(1997)
J Control Release
, vol.48
, pp. 9-17
-
-
Grundy, J.S.1
-
72
-
-
84857934469
-
Towards biorelevant dissolution: An application of a biphasic dissolution model as a discrimination tool for HPMC matrices containing a model BCS class II drug
-
Phillips DJ, et al,. Towards biorelevant dissolution: an application of a biphasic dissolution model as a discrimination tool for HPMC matrices containing a model BCS class II drug. Dissolution Technol 2012; 19: 25-34.
-
(2012)
Dissolution Technol
, vol.19
, pp. 25-34
-
-
Phillips, D.J.1
-
73
-
-
35649003947
-
The influence of hydro-alcoholic media on hypromellose matrix systems
-
Levina M, et al,. The influence of hydro-alcoholic media on hypromellose matrix systems. Drug Dev Ind Pharm 2007; 33: 1125-1134.
-
(2007)
Drug Dev Ind Pharm
, vol.33
, pp. 1125-1134
-
-
Levina, M.1
-
74
-
-
0031750861
-
Evaluation of various dissolution media for predicting in vivo performance of class i and II drugs
-
Galia E, et al,. Evaluation of various dissolution media for predicting in vivo performance of class I and II drugs. Pharm Res 1998; 15: 698-705.
-
(1998)
Pharm Res
, vol.15
, pp. 698-705
-
-
Galia, E.1
-
75
-
-
33751014029
-
Formulation of poorly water-soluble drugs for oral administration: Physicochemical and physiological issues and the lipid formulation classification system
-
Pouton CW,. Formulation of poorly water-soluble drugs for oral administration: physicochemical and physiological issues and the lipid formulation classification system. Eur J Pharm Sci 2006; 29: 278-287.
-
(2006)
Eur J Pharm Sci
, vol.29
, pp. 278-287
-
-
Pouton, C.W.1
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