-
1
-
-
0026692103
-
Stealth liposomes: An improved sustained release system for 1-beta-D-arabinofuranosylcytosine
-
Allen T.M., Mehra T., Hansen C., Chin Y.C. Stealth liposomes: an improved sustained release system for 1-beta-D-arabinofuranosylcytosine. Cancer Res. 52:1992;2431-2439.
-
(1992)
Cancer Res.
, vol.52
, pp. 2431-2439
-
-
Allen, T.M.1
Mehra, T.2
Hansen, C.3
Chin, Y.C.4
-
3
-
-
0027141071
-
Submicron emulsions as colloidal drug carriers for intravenous administration: Comprehensive physicochemical characterization
-
Benita S., Levy M.Y. Submicron emulsions as colloidal drug carriers for intravenous administration: comprehensive physicochemical characterization. J. Pharm. Sci. 82:1993;1069-1079.
-
(1993)
J. Pharm. Sci.
, vol.82
, pp. 1069-1079
-
-
Benita, S.1
Levy, M.Y.2
-
4
-
-
0027931758
-
The release of drugs from monoglyceride-water liquid crystalline phases
-
Burrows R., Collett J.H., Attwood D. The release of drugs from monoglyceride-water liquid crystalline phases. Int. J. Pharm. 111:1994;283-293.
-
(1994)
Int. J. Pharm.
, vol.111
, pp. 283-293
-
-
Burrows, R.1
Collett, J.H.2
Attwood, D.3
-
5
-
-
0030944466
-
Effect of dissolution media and additives on the drug release from cubic phase delivery systems
-
Chang C.-M., Bodmeier R. Effect of dissolution media and additives on the drug release from cubic phase delivery systems. J. Controlled Release. 46:1997;215-222.
-
(1997)
J. Controlled Release
, vol.46
, pp. 215-222
-
-
Chang, C.-M.1
Bodmeier, R.2
-
6
-
-
0032445939
-
Low viscosity monoglyceride-based drug delivery systems transforming into a highly viscous cubic phase
-
Chang C.-M., Bodmeier R. Low viscosity monoglyceride-based drug delivery systems transforming into a highly viscous cubic phase. Int. J. Pharm. 173:1998;51-60.
-
(1998)
Int. J. Pharm.
, vol.173
, pp. 51-60
-
-
Chang, C.-M.1
Bodmeier, R.2
-
7
-
-
0036211404
-
Self-assembled "nanocubicle" as a carrier for peroral insulin delivery
-
Chung H., Kim J., Um J.Y., Kwon I.C., Jeong S.Y. Self-assembled "nanocubicle" as a carrier for peroral insulin delivery. Diabetologia. 45:2002;448-451.
-
(2002)
Diabetologia
, vol.45
, pp. 448-451
-
-
Chung, H.1
Kim, J.2
Um, J.Y.3
Kwon, I.C.4
Jeong, S.Y.5
-
8
-
-
0025476418
-
Cubic phases as drug delivery systems
-
Engstrom S. Cubic phases as drug delivery systems. Polym. Preprint. 31:1990;157-158.
-
(1990)
Polym. Preprint.
, vol.31
, pp. 157-158
-
-
Engstrom, S.1
-
11
-
-
0000464488
-
Cubic phases as delivery systems for peptide drugs
-
Dunn, R.L., Ottenbrite, R.M. (Eds.). American Chemical Society, Washington
-
Ericsson, B., Eriksson, P.O., Löfroth, J.E., Engström, S., 1991. Cubic phases as delivery systems for peptide drugs. In: Dunn, R.L., Ottenbrite, R.M. (Eds.), Polymeric Drugs and Drug Delivery. American Chemical Society, Washington, pp. 251-265.
-
(1991)
Polymeric Drugs and Drug Delivery
, pp. 251-265
-
-
Ericsson, B.1
Eriksson, P.O.2
Löfroth, J.E.3
Engström, S.4
-
13
-
-
0031372220
-
Submicron particles of reversed lipid phases in water stabilized by a nonionic amphiphilic polymer
-
Gustafsson J., Ljusberg-Wahren H., Almgren M., Larsson K. Submicron particles of reversed lipid phases in water stabilized by a nonionic amphiphilic polymer. Langmuir. 13:1997;6964-6971.
-
(1997)
Langmuir
, vol.13
, pp. 6964-6971
-
-
Gustafsson, J.1
Ljusberg-Wahren, H.2
Almgren, M.3
Larsson, K.4
-
15
-
-
0035683882
-
Release kinetics of acyclovir from a suspension of acyclovir incorporated in a cubic phase delivery system
-
Helledi L.S., Schubert L. Release kinetics of acyclovir from a suspension of acyclovir incorporated in a cubic phase delivery system. Drug Dev. Ind. Pharm. 27:2001;1073-1081.
-
(2001)
Drug Dev. Ind. Pharm.
, vol.27
, pp. 1073-1081
-
-
Helledi, L.S.1
Schubert, L.2
-
16
-
-
84984085038
-
Diffusional models useful in biopharmaceutics
-
Higuchi W.I. Diffusional models useful in biopharmaceutics. J. Pharm. Sci. 56:1967;315-324.
-
(1967)
J. Pharm. Sci.
, vol.56
, pp. 315-324
-
-
Higuchi, W.I.1
-
17
-
-
0012606765
-
Drug formulations that form a dispersed cubic phase when mixed with water
-
Kim J.S., Kim H.K., Chung H., Sohn Y.T., Kwon I.C., Jeong S.Y. Drug formulations that form a dispersed cubic phase when mixed with water. Proc. Int. Symp. Control. Rel. Bioact. Mater. 27:2000;1118-1119.
-
(2000)
Proc. Int. Symp. Control. Rel. Bioact. Mater.
, vol.27
, pp. 1118-1119
-
-
Kim, J.S.1
Kim, H.K.2
Chung, H.3
Sohn, Y.T.4
Kwon, I.C.5
Jeong, S.Y.6
-
18
-
-
33751157778
-
Phase behaviour in the system pine oil monoglycerides-poloxamer 407-water at 20°C
-
Landh T. Phase behaviour in the system pine oil monoglycerides-poloxamer 407-water at 20°C. J. Phys. Chem. 98:1994;8453-8467.
-
(1994)
J. Phys. Chem.
, vol.98
, pp. 8453-8467
-
-
Landh, T.1
-
19
-
-
0037900084
-
-
Particles, method of preparing said particles and uses thereof. U.S. Patent 5,531,925, July 2
-
Landh, T., Larsson, K., 1996. Particles, method of preparing said particles and uses thereof. U.S. Patent 5,531,925, July 2.
-
(1996)
-
-
Landh, T.1
Larsson, K.2
-
21
-
-
0032675259
-
Colloidal dispersions of ordered lipid-water phases
-
Larsson K. Colloidal dispersions of ordered lipid-water phases. Disp. Sci. Tech. 20:1999;27-34.
-
(1999)
Disp. Sci. Tech.
, vol.20
, pp. 27-34
-
-
Larsson, K.1
-
22
-
-
8644243613
-
Partition coefficients and their uses
-
Leo A., Hansch C., Elkins D. Partition coefficients and their uses. Chemical Reviews. 71:1971;525-616.
-
(1971)
Chemical Reviews
, vol.71
, pp. 525-616
-
-
Leo, A.1
Hansch, C.2
Elkins, D.3
-
24
-
-
0025612149
-
Drug release from submicronized o/w emulsion: A new in vitro kinetic evaluation model
-
Levy M.Y., Benita S. Drug release from submicronized o/w emulsion: a new in vitro kinetic evaluation model. Int. J. Pharm. 66:1990;29-37.
-
(1990)
Int. J. Pharm.
, vol.66
, pp. 29-37
-
-
Levy, M.Y.1
Benita, S.2
-
25
-
-
85031148693
-
-
Functionalized cubic liquid crystalline phase materials and methods for their preparation and use. U.S. Patent Application 20020158226, October 31
-
Lynch, M.L., Spicer, P.T., 2002. Functionalized cubic liquid crystalline phase materials and methods for their preparation and use. U.S. Patent Application 20020158226, October 31.
-
(2002)
-
-
Lynch, M.L.1
Spicer, P.T.2
-
26
-
-
0027319288
-
A new in vitro technique for the evaluation of drug release profile from colloidal carriers - Ultrafiltration technique at low pressure
-
Magenheim B., Levy M.Y., Benita S. A new in vitro technique for the evaluation of drug release profile from colloidal carriers - ultrafiltration technique at low pressure. Int. J. Pharm. 94:1993;115-123.
-
(1993)
Int. J. Pharm.
, vol.94
, pp. 115-123
-
-
Magenheim, B.1
Levy, M.Y.2
Benita, S.3
-
27
-
-
0037562012
-
-
Merck & Co., Rahway, NJ, USA
-
Merck Index, 1989. Eleventh edition. Merck & Co., Rahway, NJ, USA.
-
(1989)
Eleventh Edition
-
-
-
30
-
-
0000481232
-
Imaging soft matter with the atomic force microscope: Cubosomes and hexosomes
-
Neto C., Aloisi G., Baglioni P., Larsson K. Imaging soft matter with the atomic force microscope: cubosomes and hexosomes. J. Phys. Chem. B. 103:1999;3896-3899.
-
(1999)
J. Phys. Chem. B
, vol.103
, pp. 3896-3899
-
-
Neto, C.1
Aloisi, G.2
Baglioni, P.3
Larsson, K.4
-
32
-
-
85031157840
-
An X-ray study on colloidal monoglyceride-water dispersions
-
Müller, R.H., Benita, S., Böhm B. (Eds.). Medpharm, Stuttgart
-
Siekmann, B., Bunjes, H., Koch, M.H.J., Westesen, K., 1998. An X-ray study on colloidal monoglyceride-water dispersions. In: Müller, R.H., Benita, S., Böhm B. (Eds.), Emulsions and Nanosuspensions for the Formulation of Poorly Soluble Drugs. Medpharm, Stuttgart, pp. 318-319.
-
(1998)
Emulsions and Nanosuspensions for the Formulation of Poorly Soluble Drugs
, pp. 318-319
-
-
Siekmann, B.1
Bunjes, H.2
Koch, M.H.J.3
Westesen, K.4
-
33
-
-
0037026284
-
Preparation and structural investigations of colloidal dispersions prepared from cubic monoglyceride-water phases
-
Siekmann B., Bunjes H., Koch M.H.J., Westesen K. Preparation and structural investigations of colloidal dispersions prepared from cubic monoglyceride-water phases. Int. J. Pharm. 244:2002;33-43.
-
(2002)
Int. J. Pharm.
, vol.244
, pp. 33-43
-
-
Siekmann, B.1
Bunjes, H.2
Koch, M.H.J.3
Westesen, K.4
-
34
-
-
0035909186
-
Novel process for producing cubic liquid crystalline nanoparticles (cubosomes)
-
Spicer P.T., Hayden K.L., Lynch M.L., Ofori-Boateng A., Burns J.L. Novel process for producing cubic liquid crystalline nanoparticles (cubosomes). Langmuir. 17:2001;5748-5756.
-
(2001)
Langmuir
, vol.17
, pp. 5748-5756
-
-
Spicer, P.T.1
Hayden, K.L.2
Lynch, M.L.3
Ofori-Boateng, A.4
Burns, J.L.5
-
35
-
-
0036294084
-
Effect of molecular size and charge on IAM retention in comparison to partitioning in liposomes and n-octanol
-
Taillardat-Bertschinger A., Marca Martinet C.A., Carrupt P.-A., Reist M., Caron G., Fruttero R., Testa B. Effect of molecular size and charge on IAM retention in comparison to partitioning in liposomes and n-octanol. Pharm. Res. 19:2002;729-737.
-
(2002)
Pharm. Res.
, vol.19
, pp. 729-737
-
-
Taillardat-Bertschinger, A.1
Marca Martinet, C.A.2
Carrupt, P.-A.3
Reist, M.4
Caron, G.5
Fruttero, R.6
Testa, B.7
-
36
-
-
0024317312
-
Evaluation of non-sink dialysis method for the measurement of drug release from colloids: Effect of drug partition
-
Washington C. Evaluation of non-sink dialysis method for the measurement of drug release from colloids: effect of drug partition. Int. J. Pharm. 56:1989;71-74.
-
(1989)
Int. J. Pharm.
, vol.56
, pp. 71-74
-
-
Washington, C.1
-
37
-
-
0000941783
-
A cubic-phase delivery system composed of glyceryl monooleate and water for sustained release of water-soluble drugs
-
Wyatt, D.M., Dorschel, D., 1992. A cubic-phase delivery system composed of glyceryl monooleate and water for sustained release of water-soluble drugs. Pharm. Tech., 117-130.
-
(1992)
Pharm. Tech.
, pp. 117-130
-
-
Wyatt, D.M.1
Dorschel, D.2
|