-
1
-
-
23844542459
-
Effect of solubilizing and microemulsifying excipients in polyethylene glycol 6000 solid dispersion on enhanced dissolution and bioavailability of ketoconazole
-
Heo M.-Y., Piao Z.-Z., Kim T.-W., Cao Q.-R., Kim A., and Lee B.-J. Effect of solubilizing and microemulsifying excipients in polyethylene glycol 6000 solid dispersion on enhanced dissolution and bioavailability of ketoconazole. Arch. Pharm. Res. 28 (2005) 604-611
-
(2005)
Arch. Pharm. Res.
, vol.28
, pp. 604-611
-
-
Heo, M.-Y.1
Piao, Z.-Z.2
Kim, T.-W.3
Cao, Q.-R.4
Kim, A.5
Lee, B.-J.6
-
2
-
-
0032885450
-
Solid dispersion of poorly water-soluble drugs: early promises, subsequents problems, and recent breakthroughs
-
Serajuddin A.T.M. Solid dispersion of poorly water-soluble drugs: early promises, subsequents problems, and recent breakthroughs. J. Pharm. Sci. 88 (1999) 1058-1066
-
(1999)
J. Pharm. Sci.
, vol.88
, pp. 1058-1066
-
-
Serajuddin, A.T.M.1
-
3
-
-
0346157322
-
Bioavailability enhancement of a poorly water-soluble drug by solid dispersion in polyethylene glycol-polysorbate 80 mixture
-
Joshi H.N., Tejwani R.W., Davidovich M., Sahasrabudhe V.P., Jemal M., Bathala M.S., Varia S.A., and Serajuddin A.T.M. Bioavailability enhancement of a poorly water-soluble drug by solid dispersion in polyethylene glycol-polysorbate 80 mixture. Int. J. Pharm. 269 (2004) 251-258
-
(2004)
Int. J. Pharm.
, vol.269
, pp. 251-258
-
-
Joshi, H.N.1
Tejwani, R.W.2
Davidovich, M.3
Sahasrabudhe, V.P.4
Jemal, M.5
Bathala, M.S.6
Varia, S.A.7
Serajuddin, A.T.M.8
-
4
-
-
0242320527
-
Enhanced bioavailability of piroxicam using Gelucire 44/14 and Labrasol: in vitro and in vivo evaluation
-
Yüksel N., Karataş A., Özkan Y., Savaşer A., Özkan S.A., and Baykara T. Enhanced bioavailability of piroxicam using Gelucire 44/14 and Labrasol: in vitro and in vivo evaluation. Eur. J. Pharm. Biopharm. 56 (2003) 453-459
-
(2003)
Eur. J. Pharm. Biopharm.
, vol.56
, pp. 453-459
-
-
Yüksel, N.1
Karataş, A.2
Özkan, Y.3
Savaşer, A.4
Özkan, S.A.5
Baykara, T.6
-
5
-
-
0034032146
-
Physicochemical characterization of solid dispersions of the antiviral agent UC-781 with polyethylene glycol 6000 and Gelucire 44/14
-
Damian F., Blaton N., Naesens L., Balzarini J., Kinget R., Augustijnsa P., and Mooter G.V.d. Physicochemical characterization of solid dispersions of the antiviral agent UC-781 with polyethylene glycol 6000 and Gelucire 44/14. Eur. J. Pharm. Sci. 10 (2000) 311-322
-
(2000)
Eur. J. Pharm. Sci.
, vol.10
, pp. 311-322
-
-
Damian, F.1
Blaton, N.2
Naesens, L.3
Balzarini, J.4
Kinget, R.5
Augustijnsa, P.6
Mooter, G.V.d.7
-
6
-
-
33845619564
-
Effect of the melt granulation technique on the dissolution characteristics of griseofulvin
-
Yang D., Kulkarni R., Behmeb R.J., and Kotiyanl P.N. Effect of the melt granulation technique on the dissolution characteristics of griseofulvin. Int. J. Pharm. 329 (2007) 72-80
-
(2007)
Int. J. Pharm.
, vol.329
, pp. 72-80
-
-
Yang, D.1
Kulkarni, R.2
Behmeb, R.J.3
Kotiyanl, P.N.4
-
7
-
-
0024536377
-
Microenvironmental pH control of drug dissolution
-
Doherty C., and York P. Microenvironmental pH control of drug dissolution. Int. J. Pharm. 50 (1989) 223-232
-
(1989)
Int. J. Pharm.
, vol.50
, pp. 223-232
-
-
Doherty, C.1
York, P.2
-
8
-
-
33747179333
-
Strategies for the design of hydrophilic matrix tablets with controlled microenvironmental pH
-
Siepe S., Lueckel B., Kramer A., Ries A., and Gurny R. Strategies for the design of hydrophilic matrix tablets with controlled microenvironmental pH. Int. J. Pharm. 316 (2006) 14-20
-
(2006)
Int. J. Pharm.
, vol.316
, pp. 14-20
-
-
Siepe, S.1
Lueckel, B.2
Kramer, A.3
Ries, A.4
Gurny, R.5
-
9
-
-
0034713306
-
Influence of admixed citric acid on the release profile of pelanserin hydrochloride from HPMC matrix tablets
-
Espinoza R., Hong E., and Villafuerte L. Influence of admixed citric acid on the release profile of pelanserin hydrochloride from HPMC matrix tablets. Int. J. Pharm. 201 (2000) 165-173
-
(2000)
Int. J. Pharm.
, vol.201
, pp. 165-173
-
-
Espinoza, R.1
Hong, E.2
Villafuerte, L.3
-
10
-
-
0034660109
-
pH-independent release of a weakly basic drug from water-insoluble and -soluble matrix tablets
-
Streubel A., Siepmann J., Dashevsky A., and Bodmeier R. pH-independent release of a weakly basic drug from water-insoluble and -soluble matrix tablets. J. Control. Release 67 (2000) 101-110
-
(2000)
J. Control. Release
, vol.67
, pp. 101-110
-
-
Streubel, A.1
Siepmann, J.2
Dashevsky, A.3
Bodmeier, R.4
-
11
-
-
23244448580
-
Development of a single unit extended release formulation for ZK 811 752, a weakly basic drug
-
Kranz H., Guthmannb C., Wagner T., Lipp R., and Reinhard J. Development of a single unit extended release formulation for ZK 811 752, a weakly basic drug. Eur. J. Pharm. Sci. 26 (2005) 47-53
-
(2005)
Eur. J. Pharm. Sci.
, vol.26
, pp. 47-53
-
-
Kranz, H.1
Guthmannb, C.2
Wagner, T.3
Lipp, R.4
Reinhard, J.5
-
12
-
-
14844320556
-
Influence of micro-environmental pH on the gel layer behavior and release of a basic drug from various hydrophilic matrices
-
Varma M.V.S., Kaushal A.M., and Garg S. Influence of micro-environmental pH on the gel layer behavior and release of a basic drug from various hydrophilic matrices. J. Control. Release 103 (2005) 499-510
-
(2005)
J. Control. Release
, vol.103
, pp. 499-510
-
-
Varma, M.V.S.1
Kaushal, A.M.2
Garg, S.3
-
13
-
-
37849189719
-
pH-independent drug release of an extremely poorly soluble weakly acidic drug from multiparticulate extended release formulations
-
Riis T., Bauer-Brandl A., Wagner T., and Kranz H. pH-independent drug release of an extremely poorly soluble weakly acidic drug from multiparticulate extended release formulations. Eur. J. Pharm. Biopharm. 65 (2007) 78-84
-
(2007)
Eur. J. Pharm. Biopharm.
, vol.65
, pp. 78-84
-
-
Riis, T.1
Bauer-Brandl, A.2
Wagner, T.3
Kranz, H.4
-
14
-
-
52249114680
-
Modulation of microenvironmental pH and crystallinity of ionizable telmisartan using alkalizers in solid dispersions for controlled release
-
Tran P.H.L., Tran H.T.T., and Lee B.-J. Modulation of microenvironmental pH and crystallinity of ionizable telmisartan using alkalizers in solid dispersions for controlled release. J. Control. Release 129 (2008) 59-65
-
(2008)
J. Control. Release
, vol.129
, pp. 59-65
-
-
Tran, P.H.L.1
Tran, H.T.T.2
Lee, B.-J.3
-
15
-
-
0009221314
-
Crystal structure and spectroscopy study of 2-[(2,6-dichlorophenyl)amino]phenylacetoxyacetic acid (aceclofenac)
-
Alvarez-Laurena A., Piniella J.F., Carrasco E., Ginebreda A., Yulia S., and Germain G. Crystal structure and spectroscopy study of 2-[(2,6-dichlorophenyl)amino]phenylacetoxyacetic acid (aceclofenac). J. Crystallogr. Spectrosc. Res. 22 (1992) 323-328
-
(1992)
J. Crystallogr. Spectrosc. Res.
, vol.22
, pp. 323-328
-
-
Alvarez-Laurena, A.1
Piniella, J.F.2
Carrasco, E.3
Ginebreda, A.4
Yulia, S.5
Germain, G.6
-
16
-
-
62949129366
-
Enhanced bioavailability of poorly water-soluble aceclofenac using PEG-based solid dispersion in rats, beagle dogs and human subjects
-
New Orleans, LA, USA
-
B.-J. Lee, H. Jung, Enhanced bioavailability of poorly water-soluble aceclofenac using PEG-based solid dispersion in rats, beagle dogs and human subjects, AAPS Annual Meeting, New Orleans, LA, USA, 1999, pp. 14-18.
-
(1999)
AAPS Annual Meeting
, pp. 14-18
-
-
Lee, B.-J.1
Jung, H.2
-
17
-
-
38349100118
-
Enhancement of dissolution rate and bioavailability of aceclofenac: a chitosan-based solvent change approach
-
Mutalik S., Anju P., Manoj K., and Usha A.N. Enhancement of dissolution rate and bioavailability of aceclofenac: a chitosan-based solvent change approach. Int. J. Pharm. 350 (2008) 279-290
-
(2008)
Int. J. Pharm.
, vol.350
, pp. 279-290
-
-
Mutalik, S.1
Anju, P.2
Manoj, K.3
Usha, A.N.4
-
19
-
-
36549042006
-
Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs
-
Vasconcelos T., Sarmento B., and Costa P. Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs. Drug Discov. Today 12 (2007) 1068-1075
-
(2007)
Drug Discov. Today
, vol.12
, pp. 1068-1075
-
-
Vasconcelos, T.1
Sarmento, B.2
Costa, P.3
-
20
-
-
33845351355
-
A review of poloxamer 407 pharmaceutical and pharmacological characteristics
-
Dumortier G., Grossiord J.L., Agnely F., and Chaumeil J.C. A review of poloxamer 407 pharmaceutical and pharmacological characteristics. Pharm. Res. 23 (2006) 2709-2728
-
(2006)
Pharm. Res.
, vol.23
, pp. 2709-2728
-
-
Dumortier, G.1
Grossiord, J.L.2
Agnely, F.3
Chaumeil, J.C.4
-
21
-
-
33646813333
-
Bioavailability of seocalcitol. II: Development and characterisation of self-microemulsifying drug delivery systems (SMEDDS) for oral administration containing medium and long chain triglycerides
-
Grove M., Müllertz A., Nielsen J.L., and Pedersen G.P. Bioavailability of seocalcitol. II: Development and characterisation of self-microemulsifying drug delivery systems (SMEDDS) for oral administration containing medium and long chain triglycerides. Eur. J. Pharm. Sci. 28 (2006) 233-242
-
(2006)
Eur. J. Pharm. Sci.
, vol.28
, pp. 233-242
-
-
Grove, M.1
Müllertz, A.2
Nielsen, J.L.3
Pedersen, G.P.4
-
22
-
-
17444370493
-
Diclofenac salts. II: Solid dispersions in PEG 6000 and Gelucire 50/13
-
Fini A., Moyano J.R., Ginés J.M., Perez-Martinez J.I., and Rabasco A.M. Diclofenac salts. II: Solid dispersions in PEG 6000 and Gelucire 50/13. Eur. J. Pharm. Biopharm. 60 (2005) 99-111
-
(2005)
Eur. J. Pharm. Biopharm.
, vol.60
, pp. 99-111
-
-
Fini, A.1
Moyano, J.R.2
Ginés, J.M.3
Perez-Martinez, J.I.4
Rabasco, A.M.5
-
23
-
-
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
-
Hu J., Johnston K.P., and Williams III R.O. Spray freezing into liquid (SFL) particle engineering technology to enhance dissolution of poorly water soluble drugs: organic solvent versus organic/aqueous co-solvent systems. Eur. J. Pharm. Sci. 20 (2003) 295-303
-
(2003)
Eur. J. Pharm. Sci.
, vol.20
, pp. 295-303
-
-
Hu, J.1
Johnston, K.P.2
Williams III, R.O.3
-
24
-
-
0034601240
-
Improving drug solubility for oral delivery using solid dispersions
-
Leuner C., and Dressman J. Improving drug solubility for oral delivery using solid dispersions. Eur. J. Pharm. Biopharm. 50 (2000) 47-60
-
(2000)
Eur. J. Pharm. Biopharm.
, vol.50
, pp. 47-60
-
-
Leuner, C.1
Dressman, J.2
-
25
-
-
0042201862
-
Synthesis, characterization, and multilayer assemblies of acid and base polyimides
-
Song N., and Wang Z.Y. Synthesis, characterization, and multilayer assemblies of acid and base polyimides. Macromolecules 36 (2003) 5885-5890
-
(2003)
Macromolecules
, vol.36
, pp. 5885-5890
-
-
Song, N.1
Wang, Z.Y.2
-
27
-
-
34247609989
-
Development and bioavailability assessment of ramipril nanoemulsion formulation
-
Shafiq S., Shakeel F., Talegaonkar S., Ahmad F.J., Khar R.K., and Ali M. Development and bioavailability assessment of ramipril nanoemulsion formulation. Eur. J. Pharm. Biopharm. 66 (2007) 227-243
-
(2007)
Eur. J. Pharm. Biopharm.
, vol.66
, pp. 227-243
-
-
Shafiq, S.1
Shakeel, F.2
Talegaonkar, S.3
Ahmad, F.J.4
Khar, R.K.5
Ali, M.6
-
28
-
-
38349165563
-
Effect of pharmaceutical excipients on aqueous stability of rabeprazole sodium
-
Ren S., Park M.-J., Sah H., and Lee B.-J. Effect of pharmaceutical excipients on aqueous stability of rabeprazole sodium. Int. J. Pharm. 350 (2008) 197-204
-
(2008)
Int. J. Pharm.
, vol.350
, pp. 197-204
-
-
Ren, S.1
Park, M.-J.2
Sah, H.3
Lee, B.-J.4
-
29
-
-
8844282676
-
Studies of formation of W/O nano-emulsions
-
Porras M., Solans C., González C., Martínez A., Guinart A., and Gutiérrez J.M. Studies of formation of W/O nano-emulsions. Colloids Surf. A 249 (2004) 115-118
-
(2004)
Colloids Surf. A
, vol.249
, pp. 115-118
-
-
Porras, M.1
Solans, C.2
González, C.3
Martínez, A.4
Guinart, A.5
Gutiérrez, J.M.6
|