-
1
-
-
0028194817
-
Self-emulsifying drug delivery systems (SEDDS) with polyglycolzed glycerides for improving in vitro dissolution and oral absorption of lipophilic drugs
-
Shah NH, Carvajal MT, Patel CI et al. Self-emulsifying drug delivery systems (SEDDS) with polyglycolzed glycerides for improving in vitro dissolution and oral absorption of lipophilic drugs. Int J Pharm, 1994, 106(1):15
-
(1994)
Int J Pharm
, vol.106
, Issue.1
, pp. 15
-
-
Shah, N.H.1
Carvajal, M.T.2
Patel, C.I.3
-
2
-
-
0029562489
-
Lipid microemulsions for improving drug dissolution and oral absorption: Physical and biopharaceutical aspects
-
Constantinides, PP. Lipid microemulsions for improving drug dissolution and oral absorption: physical and biopharaceutical aspects. Pharm Res, 1995, 12(11):1561
-
(1995)
Pharm Res
, vol.12
, Issue.11
, pp. 1561
-
-
Constantinides, P.P.1
-
3
-
-
0028335905
-
Reudced inter- and intraindividual variability in cyclosporin pharmacokinetics from a micrioemulsion formulation
-
Kovarik JM, Mueller EA, Van B, et al. Reudced inter- and intraindividual variability in cyclosporin pharmacokinetics from a micrioemulsion formulation. J Pharm Sci, 1994, 83(3):444
-
(1994)
J Pharm Sci
, vol.83
, Issue.3
, pp. 444
-
-
Kovarik, J.M.1
Mueller, E.A.2
Van, B.3
-
4
-
-
0033805858
-
Lipid formulation for oral administration of drugs: Nonemulsifying, self-emulsifying and 'self-microemulsifying' drug delivery systems
-
Pouton CW. Lipid formulation for oral administration of drugs: nonemulsifying, self-emulsifying and 'self-microemulsifying' drug delivery systems. Eur J Pharmac Sci, 2000, 11(Suppl):S93
-
(2000)
Eur J Pharmac Sci
, vol.11
, Issue.SUPPL.
-
-
Pouton, C.W.1
-
5
-
-
0028000096
-
Rationale for the development of Sandimmune Neoral
-
Vonderscher J, Meinzer A. Rationale for the development of Sandimmune Neoral. Transplant Proc, 1994, 26(5):2925
-
(1994)
Transplant Proc
, vol.26
, Issue.5
, pp. 2925
-
-
Vonderscher, J.1
Meinzer, A.2
-
6
-
-
0034601204
-
Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs
-
Gershanik T, Benita S. Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs. Eur J Pharma Biopharmac, 2000, 50 (1):179
-
(2000)
Eur J Pharma Biopharmac
, vol.50
, Issue.1
, pp. 179
-
-
Gershanik, T.1
Benita, S.2
-
7
-
-
0027301116
-
An investigation into the physico-chemical properties of self-emulsifying measurements and particle size analysis
-
Craing DQM, Lievens HSR, Pitt KG, et al. An investigation into the physico-chemical properties of self-emulsifying measurements and particle size analysis. Int J Pharm, 1993, 96 (1-2):147
-
(1993)
Int J Pharm
, vol.96
, Issue.1-2
, pp. 147
-
-
Craing, D.Q.M.1
Lievens, H.S.R.2
Pitt, K.G.3
-
8
-
-
0028033391
-
Intestinal permeability enhancement: Efficacy, acute local toxicity and reversibility
-
Swenson ES, Milisen WB, Curatolo W. Intestinal permeability enhancement: efficacy, acute local toxicity and reversibility. Pharm Res, 1994, 11(8):1132
-
(1994)
Pharm Res
, vol.11
, Issue.8
, pp. 1132
-
-
Swenson, E.S.1
Milisen, W.B.2
Curatolo, W.3
-
9
-
-
0028949717
-
An investigation into the mechanisms of self-emulsification using particle seze analysis and low frequency dielectric spectroscopy
-
Craig DQM, Barker SA, Banning D, et al. An investigation into the mechanisms of self-emulsification using particle seze analysis and low frequency dielectric spectroscopy. Int J Pharm, 1995, 114(1): 103
-
(1995)
Int J Pharm
, vol.114
, Issue.1
, pp. 103
-
-
Craig, D.Q.M.1
Barker, S.A.2
Banning, D.3
-
10
-
-
0026586447
-
Self-emulsifying drug delivery systems: Formulation and biopharmaceutic evaluation of an investigational lipophilic compound
-
Charman SA, Charman WN, Rogge MC, et al. Self-emulsifying drug delivery systems: formulation and biopharmaceutic evaluation of an investigational lipophilic compound. Pharm Res, 1992, 9(1): 87
-
(1992)
Pharm Res
, vol.9
, Issue.1
, pp. 87
-
-
Charman, S.A.1
Charman, W.N.2
Rogge, M.C.3
-
11
-
-
0035895309
-
Self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10: Formulation, development and bioavailability assessment
-
Kommuru TR, Gurley B, Khan MA, et al. Self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10: formulation, development and bioavailability assessment. Int J Pharmac, 2001, 212(1): 233
-
(2001)
Int J Pharmac
, vol.212
, Issue.1
, pp. 233
-
-
Kommuru, T.R.1
Gurley, B.2
Khan, M.A.3
-
12
-
-
0038682404
-
Self-microemulsifying drug delivery systems for improving dissolution of drugs: In vitro/in vivo evaluation
-
Farah N, Laforet JP, Denis J. Self-microemulsifying drug delivery systems for improving dissolution of drugs: in vitro/in vivo evaluation. Pharm Res, 1994, 11(Suppl):S202
-
(1994)
Pharm Res
, vol.11
, Issue.SUPPL.
-
-
Farah, N.1
Laforet, J.P.2
Denis, J.3
-
13
-
-
0343487750
-
Formulation of self-meulsifying drug delivery systems
-
Pouton CW. Formulation of self-meulsifying drug delivery systems. Adv Drug Delivery Rev, 1997, 25(1):47
-
(1997)
Adv Drug Delivery Rev
, vol.25
, Issue.1
, pp. 47
-
-
Pouton, C.W.1
-
14
-
-
0028329964
-
Improved dose linearity of cyclosporin pharmacokinetics from a microemulsion formulation
-
Mueller EA, Kovarik JM, Van B, et al. Improved dose linearity of cyclosporin pharmacokinetics from a microemulsion formulation. Pharm Res, 1999, 11(3):301
-
(1999)
Pharm Res
, vol.11
, Issue.3
, pp. 301
-
-
Mueller, E.A.1
Kovarik, J.M.2
Van, B.3
-
15
-
-
0343907176
-
Structure and activity of gastrointestinal lipases
-
Embleton JK, Pouton CW. Structure and activity of gastrointestinal lipases. Adv Drug Delivery Res, 1997, 25(1):15
-
(1997)
Adv Drug Delivery Res
, vol.25
, Issue.1
, pp. 15
-
-
Embleton, J.K.1
Pouton, C.W.2
-
16
-
-
0343051926
-
Lipolysis of oily formulations in the gastrointestinal tract
-
Macregor KJ, Embleton JK, Perry EA, et al. Lipolysis of oily formulations in the gastrointestinal tract. Adv Drug Delivery Rev, 1997, 25(1):33
-
(1997)
Adv Drug Delivery Rev
, vol.25
, Issue.1
, pp. 33
-
-
Macregor, K.J.1
Embleton, J.K.2
Perry, E.A.3
-
17
-
-
0030298897
-
Positively charged self-emulsifying oil formulation for improving oral bioavailability of progesteroin
-
Positively charged self-emulsifying oil formulation for improving oral bioavailability of progesteroin. Pharm Dev Technol, 1996, 1 (1):147
-
(1996)
Pharm Dev Technol
, vol.1
, Issue.1
, pp. 147
-
-
-
18
-
-
0031780652
-
Interaction of the self-emulsifying lipid drug delivery system with mucosa of everted rat intestime as a function of surface charge and droplet size
-
Gershanik T, Benzeno S, Benita S. Interaction of the self-emulsifying lipid drug delivery system with mucosa of everted rat intestime as a function of surface charge and droplet size. Pharm Res, 1998, 15:863
-
(1998)
Pharm Res
, vol.15
, pp. 863
-
-
Gershanik, T.1
Benzeno, S.2
Benita, S.3
-
19
-
-
0034671698
-
Charge-dependent interaction of self-emulsifying oil formulation (SEOF) with Caco-2 cells monolayers: Binding, effects on barrier function and cytotoxicity
-
Gershanik T, Haltner E, Lehr CM, et al. Charge-dependent interaction of self-emulsifying oil formulation (SEOF) with Caco-2 cells monolayers: binding, effects on barrier function and cytotoxicity. Int J Pharmac, 2000, 211(1-2):29
-
(2000)
Int J Pharmac
, vol.211
, Issue.1-2
, pp. 29
-
-
Gershanik, T.1
Haltner, E.2
Lehr, C.M.3
-
20
-
-
0026586447
-
Self-emulsifying systems; formulation and biological evaluation of an investigative lipophilic compound
-
Charman SA, Charman WN, ROgge MC, et al. Self-emulsifying systems; formulation and biological evaluation of an investigative lipophilic compound. Pharm Res, 1992, 9(1):87
-
(1992)
Pharm Res
, vol.9
, Issue.1
, pp. 87
-
-
Charman, S.A.1
Charman, W.N.2
Rogge, M.C.3
|