-
1
-
-
0031131811
-
Vitro evaluation of flutamide-carrier systems: Part 1: Preparation and evaluation of flutamide systems with polyvinyl pyrrolidone and polyethylene glycol 4000 and 6000
-
Adel MS, Geneidi AS, Ali Shoukri R, Saad I. (1997). In vitro evaluation of flutamide-carrier systems. Part 1: Preparation and evaluation of flutamide systems with polyvinyl pyrrolidone and polyethylene glycol 4000 and 6000. Pharmazie 52:373-375 (Pubitemid 127489679)
-
(1997)
Pharmazie
, vol.52
, Issue.5
, pp. 373-375
-
-
Adel, M.S.1
Geneidi, A.S.2
Shoukri, R.A.3
Saad, I.4
-
2
-
-
34248535178
-
Studies on dissolution enhancement and mathematical modeling of drug release of a poorly water-soluble drug using water-soluble carriers
-
DOI 10.1016/j.ejpb.2006.07.007, PII S0939641106001901
-
Ahuja N, Katare OP, Singh B. (2007). Studies on dissolution enhancement and mathematical modeling of drug release of a poorly water-soluble drug using water-soluble carriers. Eur J Pharm Biopharm 65:26-38 (Pubitemid 44827692)
-
(2007)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.65
, Issue.1
, pp. 26-38
-
-
Ahuja, N.1
Katare, O.P.2
Singh, B.3
-
3
-
-
6944243071
-
Enhancing the bioavailability of ABT-963 using solid dispersion containing Pluronic F-68
-
DOI 10.1016/j.ijpharm.2004.08.009, PII S0378517304004776
-
Chen Y, Zhang GG, Neilly J, Marsh K, Mawhinney D, Sanzgiri YD. (2004). Enhancing the bioavailability of ABT-963 using solid dispersion containing Pluronic F-68. Int J Pharm 286:69-80 (Pubitemid 39410474)
-
(2004)
International Journal of Pharmaceutics
, vol.286
, Issue.1-2
, pp. 69-80
-
-
Chen, Y.1
Zhang, G.G.Z.2
Neilly, J.3
Marsh, K.4
Mawhinney, D.5
Sanzgiri, Y.D.6
-
4
-
-
1242321019
-
Characterization of Ibuproxam Binary and Ternary Dispersions with Hydrophilic Carriers
-
DOI 10.1081/DDC-120027513
-
Cirri M, Mura P, Rabasco AM, Ginés JM, Moyano JR, Gnzalez- Rodrguez ML. (2004). Characterization of ibuproxam binary and ternary dispersions with hydrophilic carriers. Drug Dev Ind Pharm 30:65-74 (Pubitemid 38240477)
-
(2004)
Drug Development and Industrial Pharmacy
, vol.30
, Issue.1
, pp. 65-74
-
-
Cirri, M.1
Mura, P.2
Rabasco, A.M.3
Gines, J.M.4
Moyano, J.R.5
Gonzalez-Rodriguez, M.L.6
-
5
-
-
75449102533
-
Lyophilization monophase solution technique for improvement of the physicochemical properties of an anticancer drug, flutamide
-
Elgindy N, Elkhodairy K, Molokhia A, Elzoghby A. (2010). Lyophilization monophase solution technique for improvement of the physicochemical properties of an anticancer drug, flutamide. Eur J Pharm Biopharm 74:397-405
-
(2010)
Eur J Pharm Biopharm
, vol.74
, pp. 397-405
-
-
Elgindy, N.1
Elkhodairy, K.2
Molokhia, A.3
Elzoghby, A.4
-
6
-
-
48849096338
-
Free flowing solid dispersions of the anti-HIV drug UC 781 with Poloxamer 407 and a maximum amount of TPGS 1000: Investigating the relationship between physicochemical characteristics and dissolution behaviour
-
Goddeeris C, Van den Mooter G. (2008). Free flowing solid dispersions of the anti-HIV drug UC 781 with Poloxamer 407 and a maximum amount of TPGS 1000: investigating the relationship between physicochemical characteristics and dissolution behaviour. Eur J Pharm Sci 35:104-113
-
(2008)
Eur J Pharm Sci
, vol.35
, pp. 104-113
-
-
Goddeeris, C.1
Van Den Mooter, G.2
-
7
-
-
0013795160
-
Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures. I. Theoretical considerations and discussion of the literature
-
Goldberg AH, Gibaldi M, Kanig JL. (1965). Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures. I. Theoretical considerations and discussion of the literature. J Pharm Sci 54:1145-1148
-
(1965)
J Pharm Sci
, vol.54
, pp. 1145-1148
-
-
Goldberg, A.H.1
Gibaldi, M.2
Kanig, J.L.3
-
8
-
-
0030638567
-
Characteristics and significance of the amorphous state in pharmaceutical systems
-
Hancock BC, Zografi G. (1997). Characteristics and significance of the amorphous state in pharmaceutical systems. J Pharm Sci 86:1-12
-
(1997)
J Pharm Sci
, vol.86
, pp. 1-12
-
-
Hancock, B.C.1
Zografi, G.2
-
10
-
-
0037151313
-
Pluronic block copolymers as novel polymer therapeutics for drug and gene delivery
-
DOI 10.1016/S0168-3659(02)00009-3, PII S0168365902000093
-
Kabanov AV, Batrakova EV, Alakhov VY. (2002). Pluronic block copolymers as novel polymer therapeutics for drug and gene delivery. J Control Release 82:189-212 (Pubitemid 34880178)
-
(2002)
Journal of Controlled Release
, vol.82
, Issue.2-3
, pp. 189-212
-
-
Kabanov, A.V.1
Batrakova, E.V.2
Alakhov, V.Y.3
-
11
-
-
34249092945
-
Investigation of the release mechanism of a sparingly water-soluble drug from solid dispersions in hydrophilic carriers based on physical state of drug, particle size distribution and drug-polymer interactions
-
DOI 10.1016/j.ejpb.2006.11.020, PII S0939641106003390
-
Karavas E, Georgarakis E, Sigalas MP, Avgoustakis K, Bikiaris D. (2007). Investigation of the release mechanism of a sparingly water-soluble drug from solid dispersions in hydrophilic carriers based on physical state of drug, particle size distribution and drug-polymer interactions. Eur J Pharm Biopharm 66:334-347 (Pubitemid 46778978)
-
(2007)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.66
, Issue.3
, pp. 334-347
-
-
Karavas, E.1
Georgarakis, E.2
Sigalas, M.P.3
Avgoustakis, K.4
Bikiaris, D.5
-
12
-
-
34248533288
-
Novel ultra-rapid freezing particle engineering process for enhancement of dissolution rates of poorly water-soluble drugs
-
Kirk AO, Josh DE, Bo C, Brian DS, Thomas EM, Keith PJ, Robert OW. (2007). Novel ultra-rapid freezing particle engineering process for enhancement of dissolution rates of poorly water-soluble drugs. Eur J Pharm Biopharm 65:57-67
-
(2007)
Eur J Pharm Biopharm
, vol.65
, pp. 57-67
-
-
Kirk, A.O.1
Josh, D.E.2
Bo, C.3
Brian, D.S.4
Thomas, E.M.5
Keith, P.J.6
Robert, O.W.7
-
13
-
-
0036141742
-
Improvement of dissolution and oral absorption of ER-34122, a poorly water-soluble dual 5-lipoxygenase/cyclooxygenase inhibitor with anti-inflammatory activity by preparing solid dispersion
-
DOI 10.1002/jps.10020
-
Kushida I, Ichikawa M, Asakawa N. (2002). Improvement of dissolution and oral absorption of ER-34122, a poorly water-soluble dual 5-lipoxygenase/ cyclooxygenase inhibitor with anti-inflammatory activity by preparing solid dispersion. J Pharm Sci 91:258-266 (Pubitemid 34074484)
-
(2002)
Journal of Pharmaceutical Sciences
, vol.91
, Issue.1
, pp. 258-266
-
-
Kushida, I.1
Ichikawa, M.2
Asakawa, N.3
-
14
-
-
0034601240
-
Improving drug solubility for oral delivery using solid dispersions
-
DOI 10.1016/S0939-6411(00)00076-X, PII S093964110000076X
-
Leuner C, Dressman J. (2000). Improving drug solubility for oral delivery using solid dispersions. Eur J Pharm Biopharm 50:47-60 (Pubitemid 30326688)
-
(2000)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.50
, Issue.1
, pp. 47-60
-
-
Leuner, C.1
Dressman, J.2
-
15
-
-
18744420378
-
Influence of polyethylene glycol 4000 on the polymorphic forms of diflunisal
-
DOI 10.1016/S0928-0987(99)00006-8, PII S0928098799000068
-
Martãnez-Ohárriz MC, Martãn C, Goñi MM, Rodrãguez-Espinosa C, Tros-Ilarduya MC, Zornoza A. (1999). Influence of polyethylene glycol 4000 on the polymorphic forms of diflunisal. Eur J Pharm Sci 8:127-132 (Pubitemid 29189158)
-
(1999)
European Journal of Pharmaceutical Sciences
, vol.8
, Issue.2
, pp. 127-132
-
-
Martinez-Oharriz, M.C.1
Martin, C.2
Goni, M.M.3
Rodriguez-Espinosa, C.4
Tros-Ilarduya, M.C.5
Zornoza, A.6
-
16
-
-
1142297630
-
Characterization of curcumin-PVP solid dispersion obtained by spray drying
-
DOI 10.1016/j.ijpharm.2003.11.014
-
Paradkar A, Ambike AA, Jadhav BK, Mahadik KR. (2004). Characterization of curcumin-PVP solid dispersion obtained by spray drying. Int J Pharm 271:281-286 (Pubitemid 38210105)
-
(2004)
International Journal of Pharmaceutics
, vol.271
, Issue.1-2
, pp. 281-286
-
-
Paradkar, A.1
Ambike, A.A.2
Jadhav, B.K.3
Mahadik, K.R.4
-
18
-
-
0033974586
-
Comparison of surface modification and solid dispersion techniques for drug dissolution
-
DOI 10.1016/S0378-5173(99)00350-6, PII S0378517399003506
-
Rouchotas C, Cassidy OE, Rowley G. (2000). Comparison of surface modification and solid dispersion techniques for drug dissolution. Int J Pharm 195:1-6 (Pubitemid 30089481)
-
(2000)
International Journal of Pharmaceutics
, vol.195
, Issue.1-2
, pp. 1-6
-
-
Rouchotas, C.1
Cassidy, O.E.2
Rowley, G.3
-
19
-
-
85008071016
-
Studies on absorption of eutectic mixture. I. A comparison of the behavior of eutectic mixture of sulfathiazole and that of ordinary sulfathiazole in man
-
Sekiguchi K, Obi N. (1961). Studies on absorption of eutectic mixture. I. A comparison of the behavior of eutectic mixture of sulfathiazole and that of ordinary sulfathiazole in man. Chem Pharm Bull 9:866-872
-
(1961)
Chem Pharm Bull
, vol.9
, pp. 866-872
-
-
Sekiguchi, K.1
Obi, N.2
-
20
-
-
38649102798
-
Enhanced dissolution of silymarin/polyvinylpyrrolidone solid dispersion pellets prepared by a one-step fluid-bed coating technique
-
DOI 10.1016/j.powtec.2007.05.029, PII S0032591007002884
-
Sun N, Wei X, Wu B, Chen J, Lu Y, Wu W. (2008). Enhanced dissolution of silymarin/polyvinylpyrrolidone solid dispersion pellets prepared by a one-step fluid-bed coating technique. Powder Technol 182:72-80 (Pubitemid 351173199)
-
(2008)
Powder Technology
, vol.182
, Issue.1
, pp. 72-80
-
-
Sun, N.1
Wei, X.2
Wu, B.3
Chen, J.4
Lu, Y.5
Wu, W.6
-
21
-
-
0036181889
-
Practical aspects of lyophilization using non-aqueous co-solvent systems
-
DOI 10.1016/S0928-0987(01)00221-4, PII S0928098701002214
-
Teagarden DL, Baker DS. (2002). Practical aspects of lyophilization using non-aqueous co-solvent systems. Eur J Pharm Sci 15:115-133 (Pubitemid 34155373)
-
(2002)
European Journal of Pharmaceutical Sciences
, vol.15
, Issue.2
, pp. 115-133
-
-
Teagarden, D.L.1
Baker, D.S.2
-
22
-
-
24644459343
-
Un nuevo método de cromatografía de líquidos de alto rendimiento y de fase inversa para la determinación de flutamida en liposomas, plasma de sangre de rata y formas de dosificación en comprimidos
-
Umrethia ML, Ghosh PK, Majithiya RJ, Murthy RSR. (2005). A new reverse phase high performance liquid chromatographic method for determination of flutamide in liposomes, rat blood plasma and tablet dosage forms. Ars Pharm, 46:109-124 (Pubitemid 41285634)
-
(2005)
Ars Pharmaceutica
, vol.46
, Issue.2
, pp. 109-124
-
-
Umrethia, M.L.1
Ghosh, P.K.2
Majithiya, R.J.3
Murthy, R.S.R.4
-
23
-
-
0032513499
-
Physico-chemical characterization of solid dispersions of temazepam with polyethylene glycol 6000 and PVP K30
-
DOI 10.1016/S0378-5173(97)00401-8, PII S0378517397004018
-
Van den Mooter G, Augustijns P, Blaton N, Kinget R. (1998). Physicochemical characterization of solid dispersions of temazepam with polyethylene glycol 6000 and PVP K30. Int J Pharm 164:67-80 (Pubitemid 28160099)
-
(1998)
International Journal of Pharmaceutics
, vol.164
, Issue.1-2
, pp. 67-80
-
-
Van Den Mooter, G.1
Augustijns, P.2
Blaton, N.3
Kinget, R.4
-
24
-
-
1442334238
-
Incorporation of Lipophilic Drugs in Sugar Glasses by Lyophilization using a Mixture of Water and Tertiary Butyl Alcohol as Solvent
-
DOI 10.1002/jps.10590
-
Van Drooge DJ, Hinrichs WL, Frijlink HW. (2004). Incorporation of lipophilic drugs in sugar glasses by lyophilization using a mixture of water and tertiary butyl alcohol as solvent. J Pharm Sci 93:713-725 (Pubitemid 38332303)
-
(2004)
Journal of Pharmaceutical Sciences
, vol.93
, Issue.3
, pp. 713-725
-
-
Van Drooge, D.J.1
Hinrichs, W.L.J.2
Frijlink, H.W.3
-
25
-
-
32344452100
-
Preparation of hydrophobic drugs cyclodextrin complex by lyophilization monophase solution
-
DOI 10.1080/03639040500388359, PII P81173Q16G824008
-
Wang Z, Deng Y, Sun S, Zhang X. (2006). Preparation of hydrophobic drugs cyclodextrin complex by lyophilization monophase solution. Drug Dev Ind Pharm 32:73-83 (Pubitemid 43220916)
-
(2006)
Drug Development and Industrial Pharmacy
, vol.32
, Issue.1
, pp. 73-83
-
-
Wang, Z.1
Deng, Y.2
Sun, S.3
Zhang, X.4
-
26
-
-
0242334090
-
Spray freezing into liquid (SFL) particle engineering technology to enhance dissolution of poorly water soluble drugs: Organic solvent versus organic/aqueous co-solvent systems
-
DOI 10.1016/S0928-0987(03)00203-3
-
Williams III RO, Johnson KP, Hu J. (2003). Spray freezing into liquid (SFL) particle engineering technology to enhance dissolution of poorly water soluble drugs: organic solvent versus organic/ aqueous cosolvent systems. Eur J Pharm Sci 20:295-303 (Pubitemid 37338535)
-
(2003)
European Journal of Pharmaceutical Sciences
, vol.20
, Issue.3
, pp. 295-303
-
-
Hu, J.1
Johnston, K.P.2
Williams III, R.O.3
-
27
-
-
0242266530
-
Establishment of new preparation method for solid dispersion formulation of tacrolimus
-
DOI 10.1016/j.ijpharm.2003.07.010
-
Yamashita K, Nakate T, Okimoto K, Ohike A, Tokunaga Y, Ibuki R, Higaki K, Kimura T. (2003). Establishment of new preparation method for solid dispersion formulation of tacrolimus. Int J Pharm 267:79-91 (Pubitemid 37352952)
-
(2003)
International Journal of Pharmaceutics
, vol.267
, Issue.1-2
, pp. 79-91
-
-
Yamashita, K.1
Nakate, T.2
Okimoto, K.3
Ohike, A.4
Tokunaga, Y.5
Ibuki, R.6
Higaki, K.7
Kimura, T.8
-
28
-
-
0035897584
-
Amorphous pharmaceutical solids: Preparation, characterization and stabilization
-
DOI 10.1016/S0169-409X(01)00098-9, PII S0169409X01000989
-
Yu L. (2001). Amorphous pharmaceutical solids: preparation, characterization and stabilization. Adv Drug Deliv Rev 48:27-42 (Pubitemid 32454482)
-
(2001)
Advanced Drug Delivery Reviews
, vol.48
, Issue.1
, pp. 27-42
-
-
Yu, L.1
-
29
-
-
0346094166
-
Comparison of the effect of chitosan and polyvinylpyrrolidone on dissolution properties and analgesic effect of naproxen
-
DOI 10.1016/S0939-6411(03)00112-7
-
Zerrouk N, Mennini N, Maestrelli F, Chemtob C, Mura P. (2004). Comparison of the effect of chitosan and polyvinylpyrrolidone on dissolution properties and analgesic effect of naproxen. Eur J Pharm Biopharm 57:93-99 (Pubitemid 38058807)
-
(2004)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.57
, Issue.1
, pp. 93-99
-
-
Zerrouk, N.1
Mennini, N.2
Maestrelli, F.3
Chemtob, C.4
Mura, P.5
-
30
-
-
85060773562
-
Hydroxypropyl- β-cyclodextrin-flutamide inclusion complex. I. Formulation, physical characterization and absorption studies using the Caco-2 in vitro model
-
Zhong Z, Bruce S, Glen k, James D, Leonard IW. (2000). Hydroxypropyl- β-cyclodextrin-flutamide inclusion complex. I. Formulation, physical characterization and absorption studies using the Caco-2 in vitro model. J Pharm Pharmaceut Sci 3:220-227
-
(2000)
J Pharm Pharmaceut Sci
, vol.3
, pp. 220-227
-
-
Zhong, Z.1
Bruce, S.2
Glen, K.3
James, D.4
Leonard, I.W.5
|