-
1
-
-
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 Pharm Biopharm 2000; 50:179-188.
-
(2000)
Eur J Pharm Biopharm
, vol.50
, pp. 179-188
-
-
Gershanik, T.1
Benita, S.2
-
2
-
-
0035895309
-
Self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10:formulation development and bioavailability assessment
-
Kommuru TR, Gurley B, Khan MA, Reddy ID. Self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10:formulation development and bioavailability assessment. Int J Pharm 2001; 212:233-246.
-
(2001)
Int J Pharm
, vol.212
, pp. 233-246
-
-
Kommuru, T.R.1
Gurley, B.2
Khan, M.A.3
Reddy, I.D.4
-
3
-
-
0032103706
-
Formulation design and bioavailability assessment of lipidic self-emulsifying formulations of halofantrine
-
Khoo SM, Humberstone AJ, Porter CJH, Edwards GA, Charman WN. 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
Humberstone, A.J.2
Porter, C.J.H.3
Edwards, G.A.4
Charman, W.N.5
-
4
-
-
0033992180
-
Enhanced absorption of indomethacin after oral or rectal administration of self-emulsifying system containing indomethacin to rats
-
Kim JY, Ku YS. Enhanced absorption of indomethacin after oral or rectal administration of self-emulsifying system containing indomethacin to rats. Int J Pharm 2000; 194:81-89.
-
(2000)
Int J Pharm
, vol.194
, pp. 81-89
-
-
Kim, J.Y.1
Ku, Y.S.2
-
5
-
-
0342617694
-
Lipid-based vehicles for oral delivery of poorly water soluble drugs
-
Humberstone AJ, Charman WN. Lipid-based vehicles for oral delivery of poorly water soluble drugs. Adv Drug Delivery Rev 1997; 25:103-128.
-
(1997)
Adv Drug Delivery Rev
, vol.25
, pp. 103-128
-
-
Humberstone, A.J.1
Charman, W.N.2
-
6
-
-
0033805858
-
Lipid formulations for oral administration of drugs: Non-emulsifying, self-emulsifying and self-microemulsifying drug delivery systems
-
Pouton CW. Lipid formulations for oral administration of drugs: non-emulsifying, self-emulsifying and self-microemulsifying drug delivery systems. Eur J Pharm Sci 2000; 11 (suppl. 2):S93-S98.
-
(2000)
Eur J Pharm Sci
, vol.11
, Issue.SUPPL. 2
-
-
Pouton, C.W.1
-
7
-
-
0029562489
-
Lipid microemulsions for improving drug dissolution and oral absorption: Physical and biopharmaceutical aspects
-
Constantinides PP. Lipid microemulsions for improving drug dissolution and oral absorption: physical and biopharmaceutical aspects. Pharm Res 1995; 12(11):1561-1572.
-
(1995)
Pharm Res
, vol.12
, Issue.11
, pp. 1561-1572
-
-
Constantinides, P.P.1
-
8
-
-
0343487750
-
Formulation of self-emulsifying drug delivery systems
-
Pouton CW. Formulation of self-emulsifying drug delivery systems. Adv Drug Delivery Rev 1997; 25:47-58.
-
(1997)
Adv Drug Delivery Rev
, vol.25
, pp. 47-58
-
-
Pouton, C.W.1
-
9
-
-
0034614208
-
Microemulsion-based media as novel drug delivery systems
-
Lawrence MJ, Rees CD. Microemulsion-based media as novel drug delivery systems. Adv Drug Delivery Rev 2000; 45:89-121.
-
(2000)
Adv Drug Delivery Rev
, vol.45
, pp. 89-121
-
-
Lawrence, M.J.1
Rees, C.D.2
-
10
-
-
0034952580
-
Physicochemical characterisation of drug-containing phospholipid- stabilised o/w emulsion for intravenous administration
-
Norden TP, Siekmann B, Lundquist S, Malmsten M. Physicochemical characterisation of drug-containing phospholipid-stabilised o/w emulsion for intravenous administration. Eur J Pharm Sci 2001; 13:393-401.
-
(2001)
Eur J Pharm Sci
, vol.13
, pp. 393-401
-
-
Norden, T.P.1
Siekmann, B.2
Lundquist, S.3
Malmsten, M.4
-
11
-
-
0034889914
-
The influence of formulation variables on the properties of pellets contaning a self-emulsifying mixture
-
Newton N, Peterson J, Podczeck F, Clarke A, Booth S. The influence of formulation variables on the properties of pellets contaning a self-emulsifying mixture. J Pharm Sci 2001; 90:987-995.
-
(2001)
J Pharm Sci
, vol.90
, pp. 987-995
-
-
Newton, N.1
Peterson, J.2
Podczeck, F.3
Clarke, A.4
Booth, S.5
-
12
-
-
0037093744
-
Improvement of physicochemical properties of N-4472, part I formulation design by using self-microemulsifying system
-
Itoh K, Tozuka Y, Oguchi T, Yamamoto K. Improvement of physicochemical properties of N-4472, part I formulation design by using self-microemulsifying system. Int J Pharm 2002; 238:153-160.
-
(2002)
Int J Pharm
, vol.238
, pp. 153-160
-
-
Itoh, K.1
Tozuka, Y.2
Oguchi, T.3
Yamamoto, K.4
-
13
-
-
0037139412
-
Preparation and in vitro characterization of a eutectic based semisolid self-nanoemulsified drug delivery system (SNEDDS) of ubiquinone: Mechanism and progress of emulsion formation
-
Nazzal S, Smalyukh II, Lavrentovich OD, Khan MA. Preparation and in vitro characterization of a eutectic based semisolid self-nanoemulsified drug delivery system (SNEDDS) of ubiquinone: mechanism and progress of emulsion formation. Int J Pharm 2002; 235:247-265.
-
(2002)
Int J Pharm
, vol.235
, pp. 247-265
-
-
Nazzal, S.1
Smalyukh, I.I.2
Lavrentovich, O.D.3
Khan, M.A.4
-
14
-
-
0028948839
-
A theoretical basis for a biopharmaceutic drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability
-
Amidon CL, Lennernas H, Shah VP, Crison JR. A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm Res 1995; 12(3):413-420.
-
(1995)
Pharm Res
, vol.12
, Issue.3
, pp. 413-420
-
-
Amidon, C.L.1
Lennernas, H.2
Shah, V.P.3
Crison, J.R.4
-
15
-
-
1842684453
-
Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs
-
Gursoy RN, Benita S. Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs. Biomedicine & Pharmacotherapy 2004; 58:173-182.
-
(2004)
Biomedicine & Pharmacotherapy
, vol.58
, pp. 173-182
-
-
Gursoy, R.N.1
Benita, S.2
-
16
-
-
0033051406
-
A new method for dissolution studies of lipid-filled capsules employing nifedipine as a model drug
-
Pillay V, Fassihi R. A new method for dissolution studies of lipid-filled capsules employing nifedipine as a model drug. Pharm Res 1999; 16:333-337.
-
(1999)
Pharm Res
, vol.16
, pp. 333-337
-
-
Pillay, V.1
Fassihi, R.2
-
17
-
-
0342804284
-
Melt extrusion - An alternative method for enhancing the dissolution rate of 17 β-estradiol hemihydrate
-
Hülsmann S, Backensfeld T, Keitel S, Bodmeier R. Melt extrusion - an alternative method for enhancing the dissolution rate of 17 β-estradiol hemihydrate. Eur J Pharm Biopharm 2000; 49:237-242.
-
(2000)
Eur J Pharm Biopharm
, vol.49
, pp. 237-242
-
-
Hülsmann, S.1
Backensfeld, T.2
Keitel, S.3
Bodmeier, R.4
-
18
-
-
0042156881
-
An investigation into the structure and bioavailability of α-tocopherol dispersions in Gélucire 44/14
-
Barker SA, Yap SP, Yuen KH, McCoy CP, Murphy JR, Craig DQM. An investigation into the structure and bioavailability of α-tocopherol dispersions in Gélucire 44/14. J Control Release 2003; 91:477-488.
-
(2003)
J Control Release
, vol.91
, pp. 477-488
-
-
Barker, S.A.1
Yap, S.P.2
Yuen, K.H.3
McCoy, C.P.4
Murphy, J.R.5
Craig, D.Q.M.6
-
19
-
-
33645269763
-
-
Gattefossé Holding, editor. Composition à usage pharmaceutique ou cosmétique apte à former une microémulsion. FR patent FR2710535 B1. 1995 Nov 1995
-
Farah N, Denis J. Gattefossé Holding, editor. Composition à usage pharmaceutique ou cosmétique apte à former une microémulsion. FR patent FR2710535 B1. 1995 Nov 1995.
-
-
-
Farah, N.1
Denis, J.2
-
20
-
-
0242320527
-
Enhanced bioavailability of piroxicam using Gélucire 44/14 and Labrasol: In vitro and in vivo evaluation
-
Yüksel N, Karatas A, Özkan Y, Savaser A, Özkan SA, Baykara T. Enhanced bioavailability of piroxicam using Gélucire 44/14 and Labrasol: in vitro and in vivo evaluation. Eur J Pharm Biopharm 2003; 56:453-459.
-
(2003)
Eur J Pharm Biopharm
, vol.56
, pp. 453-459
-
-
Yüksel, N.1
Karatas, A.2
Özkan, Y.3
Savaser, A.4
Özkan, S.A.5
Baykara, T.6
-
21
-
-
33645258762
-
-
Gattefossé Holding, editor. Composition pharmaceutique à usage oral comprenant un principe actif susceptible de subir un important effet de premier passage intestinal. FR patent FR2827770 A1. 2003 Jan 2003
-
Benameur H, Jannin V, Marchaud D. Gattefossé Holding, editor. Composition pharmaceutique à usage oral comprenant un principe actif susceptible de subir un important effet de premier passage intestinal. FR patent FR2827770 A1. 2003 Jan 2003.
-
-
-
Benameur, H.1
Jannin, V.2
Marchaud, D.3
-
22
-
-
1842609789
-
Development of self-microemulsifying drug delivery systems (SMEDDS) for oral bioavailability enhancement of simvastatin in beagle dogs
-
Kang BK, Lee JS, Chon SK et al. Development of self-microemulsifying drug delivery systems (SMEDDS) for oral bioavailability enhancement of simvastatin in beagle dogs. Int J Pharm 2004; 274:65-73.
-
(2004)
Int J Pharm
, vol.274
, pp. 65-73
-
-
Kang, B.K.1
Lee, J.S.2
Chon, S.K.3
-
23
-
-
0344413661
-
Evaluation of oral formulations of gentamicin containing labrasol in beagle dogs
-
Rama Prasad YV, Eaimtrakarn S, Ishida M et al. Evaluation of oral formulations of gentamicin containing labrasol in beagle dogs. Int J Pharm 2003; 268:13-21.
-
(2003)
Int J Pharm
, vol.268
, pp. 13-21
-
-
Rama Prasad, Y.V.1
Eaimtrakarn, S.2
Ishida, M.3
-
24
-
-
2442429537
-
Effect of a lipoidic excipient on the absorption profile of compound UK 81252 in dogs after oral administration
-
Chang RK, Shojaei AH. Effect of a lipoidic excipient on the absorption profile of compound UK 81252 in dogs after oral administration. J Pharm Pharmaceut Sci 2004; 7:8-12.
-
(2004)
J Pharm Pharmaceut Sci
, vol.7
, pp. 8-12
-
-
Chang, R.K.1
Shojaei, A.H.2
-
25
-
-
1142309794
-
In situ intestinal absorption studies on low molecular weight heparin in rats using Labrasol as absorption enhancer
-
Rama Prasad YV, Minamimoto T, Yoshikawa Y et al. In situ intestinal absorption studies on low molecular weight heparin in rats using Labrasol as absorption enhancer. Int J Pharm 2004; 271:225-232.
-
(2004)
Int J Pharm
, vol.271
, pp. 225-232
-
-
Rama Prasad, Y.V.1
Minamimoto, T.2
Yoshikawa, Y.3
-
26
-
-
2442671307
-
Impact of excipients on the absorption of P-glycoprotein substrates in vitro and in vivo
-
Cornaire G, Woodley J, Hermann P, Cloarec A, Arellano C Houin G. Impact of excipients on the absorption of P-glycoprotein substrates in vitro and in vivo. Int J Pharm 2004; 278:119-131.
-
(2004)
Int J Pharm
, vol.278
, pp. 119-131
-
-
Cornaire, G.1
Woodley, J.2
Hermann, P.3
Cloarec, A.4
Arellano, C.5
Houin, G.6
-
27
-
-
0141680636
-
Effect of lipid excipients on in vitro pancreatic lipase activity
-
Subramanian R, Wasan KM. Effect of lipid excipients on in vitro pancreatic lipase activity. Drug Dev Ind Pharm 2003; 29:885-890.
-
(2003)
Drug Dev Ind Pharm
, vol.29
, pp. 885-890
-
-
Subramanian, R.1
Wasan, K.M.2
-
28
-
-
0034854134
-
Comparison of the lymphatic transport of Halofantrine administred in disperse systems containing three different unsaturated fatty acid
-
Holm P, Mullertz A, Pedersen GP, Kristensen HC. Comparison of the lymphatic transport of Halofantrine administred in disperse systems containing three different unsaturated fatty acid. Pharm Res 2001; 18(9):1299-1304.
-
(2001)
Pharm Res
, vol.18
, Issue.9
, pp. 1299-1304
-
-
Holm, P.1
Mullertz, A.2
Pedersen, G.P.3
Kristensen, H.C.4
-
29
-
-
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
-
30
-
-
2442698649
-
Influence of cryogenic grinding on properties of a self-emulsifying formulation
-
Chambin O, Jannin V, Champion D, Chevalier C, Rochat-Gonthier MH, Pourcelot Y. Influence of cryogenic grinding on properties of a self-emulsifying formulation. Int J Pharm 2004; 278:79-89.
-
(2004)
Int J Pharm
, vol.278
, pp. 79-89
-
-
Chambin, O.1
Jannin, V.2
Champion, D.3
Chevalier, C.4
Rochat-Gonthier, M.H.5
Pourcelot, Y.6
-
31
-
-
0035667509
-
Enhanced drug dissolution and bulk properties of solid dispersions granulated with a surface adsorbent
-
Gupta MK, Goldman D, Bogner RH, Tseng YC. Enhanced drug dissolution and bulk properties of solid dispersions granulated with a surface adsorbent. Pharm Dev Technol 2001; 6(4):563-572.
-
(2001)
Pharm Dev Technol
, vol.6
, Issue.4
, pp. 563-572
-
-
Gupta, M.K.1
Goldman, D.2
Bogner, R.H.3
Tseng, Y.C.4
-
32
-
-
0037685267
-
The preparation of agglomerates containing solid dispersions of diazepam by melt granulation in a high shear mixer
-
Seo A, Holm P, Kristensen HG, Schaefer T. The preparation of agglomerates containing solid dispersions of diazepam by melt granulation in a high shear mixer. Int J Pharm 2003; 259:161-171.
-
(2003)
Int J Pharm
, vol.259
, pp. 161-171
-
-
Seo, A.1
Holm, P.2
Kristensen, H.G.3
Schaefer, T.4
-
33
-
-
0034032146
-
Physicochemical characterization of solid dispersions of the antiviral agent UC-781 with polyethylene glycol 6000 and Gélucire 44/14
-
Damian F, Blaton N, Naesens L et al. Physicochemical characterization of solid dispersions of the antiviral agent UC-781 with polyethylene glycol 6000 and Gélucire 44/14. Eur J Pharm Sci 2000; 10:311-322.
-
(2000)
Eur J Pharm Sci
, vol.10
, pp. 311-322
-
-
Damian, F.1
Blaton, N.2
Naesens, L.3
-
34
-
-
0025864425
-
Preformulation studies on solid dispersions containing triamterene or temazepam in polyethylene glycols or Gélucire 44/14 for liquid filing of hard gelatin capsules
-
Dordunoo SK, Ford JL, Rubinstein MH. Preformulation studies on solid dispersions containing triamterene or temazepam in polyethylene glycols or Gélucire 44/14 for liquid filing of hard gelatin capsules. Drug Dev Ind Pharm 1991; 17:1685-1713.
-
(1991)
Drug Dev Ind Pharm
, vol.17
, pp. 1685-1713
-
-
Dordunoo, S.K.1
Ford, J.L.2
Rubinstein, M.H.3
-
35
-
-
33645255140
-
-
Nouveaux procédés de préparation à partir d'émulsions sèches de formes orales solides à libération modifée et retardée de leurs principes actifs. French Patent 86 02694. 1986 24 Fév
-
Farah N, Rollet M. Nouveaux procédés de préparation à partir d'émulsions sèches de formes orales solides à libération modifée et retardée de leurs principes actifs. French Patent 86 02694. 1986 24 Fév.
-
-
-
Farah, N.1
Rollet, M.2
-
36
-
-
0023750062
-
Dry adsorbed emulsions: An oral sustained drug delivery system
-
Berthod A, Rollet M, Farah N. Dry adsorbed emulsions: an oral sustained drug delivery system. J Pharm Sci 1988; 77:216-221.
-
(1988)
J Pharm Sci
, vol.77
, pp. 216-221
-
-
Berthod, A.1
Rollet, M.2
Farah, N.3
-
37
-
-
0033822219
-
Dry adsorbed emulsion: 1. Characterization of an intricate physicochemical structure
-
Chambin O, Bellone C, Champion D, Rochat-Gonthier MH, Pourcelot Y. Dry adsorbed emulsion: 1. Characterization of an intricate physicochemical structure. J Pharm Sci 2000; 89:991-999.
-
(2000)
J Pharm Sci
, vol.89
, pp. 991-999
-
-
Chambin, O.1
Bellone, C.2
Champion, D.3
Rochat-Gonthier, M.H.4
Pourcelot, Y.5
-
38
-
-
0037139409
-
Dry adsorbed emulsions. Dissolution behaviour of an intricate formulation
-
Chambin O, Bérard V, Rochat-Gonthier MH, Pourcelot Y. Dry adsorbed emulsions. Dissolution behaviour of an intricate formulation. Int J Pharm 2002; 235:169-178.
-
(2002)
Int J Pharm
, vol.235
, pp. 169-178
-
-
Chambin, O.1
Bérard, V.2
Rochat-Gonthier, M.H.3
Pourcelot, Y.4
-
39
-
-
0032507707
-
Formulation of a lyophilized dry emulsion tablet for the delivery of poorly soluble drugs
-
Corveleyn S, Remon JP. Formulation of a lyophilized dry emulsion tablet for the delivery of poorly soluble drugs. Int J Pharm 1998; 166:6574.
-
(1998)
Int J Pharm
, vol.166
, pp. 6574
-
-
Corveleyn, S.1
Remon, J.P.2
-
40
-
-
0032531364
-
Solid state characterisation of a dry emulsion: A potential drug delivery system
-
Pedersen GP, Fäldt P, Bergenstahl B, Kristensen HG. Solid state characterisation of a dry emulsion: a potential drug delivery system. Int J Pharm 1998; 171:257-270.
-
(1998)
Int J Pharm
, vol.171
, pp. 257-270
-
-
Pedersen, G.P.1
Fäldt, P.2
Bergenstahl, B.3
Kristensen, H.G.4
-
41
-
-
0041667788
-
Spray-dried redispersible oil-in-water emulsion to improve oral bioavail ability of poorly soluble drugs
-
Dollo G, Le Corre P, Guérin A, Chevanne F, Burgot JL, Leverge R. Spray-dried redispersible oil-in-water emulsion to improve oral bioavail ability of poorly soluble drugs. Eur J Pharm Sci 2003; 19:273-280.
-
(2003)
Eur J Pharm Sci
, vol.19
, pp. 273-280
-
-
Dollo, G.1
Le Corre, P.2
Guérin, A.3
Chevanne, F.4
Burgot, J.L.5
Leverge, R.6
-
43
-
-
8444221211
-
Process characteristics and compaction of spray-dried emulsions containing a drug dissolved in lipid
-
Hansen T, Holm P, Schultz K. Process characteristics and compaction of spray-dried emulsions containing a drug dissolved in lipid. Int J Pharm 2004; 287:55-66.
-
(2004)
Int J Pharm
, vol.287
, pp. 55-66
-
-
Hansen, T.1
Holm, P.2
Schultz, K.3
|