-
1
-
-
34447536520
-
When poor solubility becomes an issue: From early stage to proof of concept
-
Stegemann S, Leveiller F, Franchi D, et al. When poor solubility becomes an issue: from early stage to proof of concept. Eur J Pharm Sci 2007;31:249-61
-
(2007)
Eur J Pharm Sci
, vol.31
, pp. 249-61
-
-
Stegemann, S.1
Leveiller, F.2
Franchi, D.3
-
2
-
-
68349160715
-
Lipid-An emerging platform for oral delivery of drugs with poor bioavailability
-
Chakraborty S, Shukla D, Mishra B, Singh S. Lipid-An emerging platform for oral delivery of drugs with poor bioavailability. Eur J Pharm Biopharm 2009;73:1-15
-
(2009)
Eur J Pharm Biopharm
, vol.73
, pp. 1-15
-
-
Chakraborty, S.1
Shukla, D.2
Mishra, B.3
Singh, S.4
-
3
-
-
0026695458
-
Enhancement of the oral absorption of cyclosporin in man
-
Drewe J, Meier R, Vonderscher J, et al. Enhancement of the oral absorption of cyclosporin in man. Br J Clin Pharmacol 1992;34:60-4
-
(1992)
Br J Clin Pharmacol
, vol.34
, pp. 60-4
-
-
Drewe, J.1
Meier, R.2
Vonderscher, J.3
-
4
-
-
0028335905
-
Reduced inter-and intraindividual variability in cyclosporine pharmacokinetics from a microemulsion formulation
-
Kovarik JM, Mueller EA, van Bree JB, et al. Reduced inter-and intraindividual variability in cyclosporine pharmacokinetics from a microemulsion formulation. J Pharm Sci 1994;83:444-6
-
(1994)
J Pharm Sci
, vol.83
, pp. 444-6
-
-
Kovarik, J.M.1
Mueller, E.A.2
Van Bree, J.B.3
-
5
-
-
0344514705
-
Lipid drug delivery and rational formulation design for lipophilic drugs with low oral bioavailability, applied to cyclosporine
-
Odeberg JM, Kaufmann P, Kroon KG, et al. Lipid drug delivery and rational formulation design for lipophilic drugs with low oral bioavailability, applied to cyclosporine. Eur J Pharm Sci 2003;20:375-8
-
(2003)
Eur J Pharm Sci
, vol.20
, pp. 375-8
-
-
Odeberg, J.M.1
Kaufmann, P.2
Kroon, K.G.3
-
6
-
-
0035940057
-
Intestinal lymphatic drug transport: An update
-
Porter CJH, Charman WN. Intestinal lymphatic drug transport: an update. Adv Drug Deliv Rev 2001;50:61-80
-
(2001)
Adv Drug Deliv Rev
, vol.50
, pp. 61-80
-
-
Cjh, P.1
Charman, W.N.2
-
7
-
-
1842452082
-
Panchagnula R Multiunit matrix based particulate systems (MUMPS) for controlled delivery of nifedipine. Formulation development using extrusion-spheronization and in vitro evaluation
-
Sood A, Ashokraj Y, Panchagnula R Multiunit matrix based particulate systems (MUMPS) for controlled delivery of nifedipine. Formulation development using extrusion-spheronization and in vitro evaluation. Pharm Tech 2004;28:62-71
-
(2004)
Pharm Tech
, vol.28
, pp. 62-71
-
-
Sood, A.1
Ashokraj, Y.2
-
8
-
-
84892537488
-
Controlled release multiple units and single unit doses
-
Bechgaard H, Nielsen G. Controlled release multiple units and single unit doses. Drug Dev Ind Pharm 1978;4:53-7
-
(1978)
Drug Dev Ind Pharm
, vol.4
, pp. 53-7
-
-
Bechgaard, H.1
Nielsen, G.2
-
10
-
-
1842484974
-
Wet spheronization by rotary processing-a multistage single-pot process for producing spheroids
-
Gu L, Liew CV, Heng PWS. Wet spheronization by rotary processing-a multistage single-pot process for producing spheroids. Drug Dev Ind Pharm 2004;30:111-19
-
(2004)
Drug Dev Ind Pharm
, vol.30
, pp. 111-19
-
-
Gu, L.1
Liew, C.V.2
Heng, P.W.S.3
-
11
-
-
0002776175
-
A new technique for the production of spherical particles
-
Reynolds AD. A new technique for the production of spherical particles. Manuf Chem Aeros News 1970;41:40-3
-
(1970)
Manuf Chem Aeros News
, vol.41
, pp. 40-3
-
-
Reynolds, A.D.1
-
12
-
-
0003455042
-
-
U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), March Available from [Last accessed 10 September 2010]
-
Guidance for Industry: bioavailability and bioequivalence studies for orally administered drug products-general considerations. U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), March 2003. Available from: http://www.fda.gov/ downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidaances/ucm070124. pdf [Last accessed 10 September 2010]
-
(2003)
Guidance for Industry: Bioavailability and Bioequivalence Studies for Orally Administered Drug Products-general Considerations
-
-
-
13
-
-
84892537488
-
Controlled-release multiple-units and single-unit doses-A literature review
-
Bechgaard H, Nielsen GH. Controlled-release multiple-units and single-unit doses-A literature review. Drug Dev Ind Pharm 1978;4:53-67
-
(1978)
Drug Dev Ind Pharm
, vol.4
, pp. 53-67
-
-
Bechgaard, H.1
Nielsen, G.H.2
-
14
-
-
11844283277
-
Effect of adsorbents on the absorption of lansoprazole with surfactant
-
Ito Y, Arai H, Uchino K, et al. Effect of adsorbents on the absorption of lansoprazole with surfactant. Int J Pharm 2005;289:69-77
-
(2005)
Int J Pharm
, vol.289
, pp. 69-77
-
-
Ito, Y.1
Arai, H.2
Uchino, K.3
-
15
-
-
0033034920
-
Chaumeila JC Gastrointestinal transit of pellets in rats: Effect of size and density
-
Tuleua C, Andrieuxb C, Boyc P, Chaumeila JC Gastrointestinal transit of pellets in rats: effect of size and density. Int J Pharm 1999;180:123-13
-
(1999)
Int J Pharm
, vol.180
, pp. 123-13
-
-
Tuleua, C.1
Andrieuxb, C.2
Boyc, P.3
-
16
-
-
0028830177
-
Extrusion-spheronization: A literature review
-
Vervaet C, Baert L, Remon JP. Extrusion-spheronization: a literature review. Int J Pharm 1995;116:131-46
-
(1995)
Int J Pharm
, vol.116
, pp. 131-46
-
-
Vervaet, C.1
Baert, L.2
Remon, J.P.3
-
18
-
-
0034889151
-
Controlled release of tramadol hydrochloride from matrices prepared using glyceryl behenate
-
Obaidet AA, Obaidet RM. Controlled release of tramadol hydrochloride from matrices prepared using glyceryl behenate. Eur J Pharm Biopharm 2001;52:231-5
-
(2001)
Eur J Pharm Biopharm
, vol.52
, pp. 231-5
-
-
Obaidet, A.A.1
Obaidet, R.M.2
-
19
-
-
70349983345
-
Studies on the lipase induced degradation of lipid based drug delivery systems
-
Schwab M, Sax G, Schulze S, Winter G. Studies on the lipase induced degradation of lipid based drug delivery systems. J Control Release 2009;140:27-33
-
(2009)
J Control Release
, vol.140
, pp. 27-33
-
-
Schwab, M.1
Sax, G.2
Schulze, S.3
Winter, G.4
-
20
-
-
0032473563
-
Cullis PR Recent advances in liposome technologies and their applications for systemic gene delivery
-
Chonna A, Cullis PR Recent advances in liposome technologies and their applications for systemic gene delivery. Adv Drug Deliv Rev 1998;30:73-83
-
(1998)
Adv Drug Deliv Rev
, vol.30
, pp. 73-83
-
-
Chonna, A.1
-
22
-
-
79251512177
-
-
Available from [Last accessed 10 September 2010]
-
Rxlist. Available from: www.rxlist.com [Last accessed 10 September 2010]
-
Rxlist
-
-
-
23
-
-
0035667509
-
Enhanced drug dissolution and bulk properties of solid dispersions granulated with a surface adsorbent
-
Gupta MK, Goldman D, Bogner RH, et al. Enhanced drug dissolution and bulk properties of solid dispersions granulated with a surface adsorbent. Pharm Dev Technol 2001;6:563-72
-
(2001)
Pharm Dev Technol
, vol.6
, pp. 563-72
-
-
Gupta, M.K.1
Goldman, D.2
Bogner, R.H.3
-
24
-
-
79251496305
-
-
Elsevier, Academic Press, CA, USA
-
Duzgunes N. Methods in enzymology, liposomes. Volume 391. Elsevier Academic Press, CA, USA; 2005. p. 71-96
-
(2005)
Methods in Enzymology, Liposomes.
, vol.391
, pp. 71-96
-
-
Duzgunes, N.1
-
26
-
-
23444461908
-
Successful treatment of resistant visceral leishmaniasis with liposomal amphotericin B
-
Gokhale PC, Kshirsagar NA, Khan MU, et al. Successful treatment of resistant visceral leishmaniasis with liposomal amphotericin B. Trans Roy Soc Trop Med Hyg 1994;88:228
-
(1994)
Trans Roy Soc Trop Med Hyg
, vol.88
, pp. 228
-
-
Gokhale, P.C.1
Kshirsagar, N.A.2
Khan, M.U.3
-
27
-
-
0028941401
-
Successful treatment of antimony-resistant visceral leishmaniasis with liposomal amphotericin B (L-amp-LRC) in child
-
Karande SC, John Boby KF, Kshirsagar NA. Successful treatment of antimony-resistant visceral leishmaniasis with liposomal amphotericin B (L-amp-LRC) in child. Trop Doc 1995;25:80-1
-
(1995)
Trop Doc
, vol.25
, pp. 80-1
-
-
Karande, S.C.1
John Boby, K.F.2
Kshirsagar, N.A.3
-
28
-
-
0030179394
-
Drug delivery system: Targeting of pentamidines to specific sites using sugar grafted liposomes
-
Banerjee G, Nandi G, Mahato SB, et al. Drug delivery system: targeting of pentamidines to specific sites using sugar grafted liposomes. J Antimicrob Chemother 1996;38:145-50
-
(1996)
J Antimicrob Chemother
, vol.38
, pp. 145-50
-
-
Banerjee, G.1
Nandi, G.2
Mahato, S.B.3
-
30
-
-
0028866688
-
Circumvention of multidrug resistance in neoplastic cells through scavenger receptor mediated drug delivery
-
Mukhopadhyay A, Mukhopadhyay B, Basu K. Circumvention of multidrug resistance in neoplastic cells through scavenger receptor mediated drug delivery. FEBS Lett 1995;276:95-8
-
(1995)
FEBS Lett
, vol.276
, pp. 95-8
-
-
Mukhopadhyay, A.1
Mukhopadhyay, B.2
Basu, K.3
-
31
-
-
0031810270
-
Ralhan R Thermosensitive liposomal taxol formulation: Heat-mediated targeted drug delivery in murine melanoma
-
Sharma D, Chelvi TP, Kaur J, Ralhan R Thermosensitive liposomal taxol formulation: heat-mediated targeted drug delivery in murine melanoma. Melan Res 1998;8:240-4
-
(1998)
Melan Res
, vol.8
, pp. 240-4
-
-
Sharma, D.1
Chelvi, T.P.2
Kaur, J.3
-
32
-
-
0029658463
-
Novel taxol formulation: Polyvinylpyrrolidone nanoparticle-encapsulated taxol for drug delivery in cancer therapy
-
Sharma D, Chelvi TP, Kaur J, et al. Novel taxol formulation: polyvinylpyrrolidone nanoparticle-encapsulated taxol for drug delivery in cancer therapy. Oncol Res 1996;8:281-6
-
(1996)
Oncol Res
, vol.8
, pp. 281-6
-
-
Sharma, D.1
Chelvi, T.P.2
Kaur, J.3
-
33
-
-
0031862352
-
Brain drug delivery system bearing dopamine hydrochloride for effective management of parkinsonism
-
Jain NK, Rana AC, Jain SK. Brain drug delivery system bearing dopamine hydrochloride for effective management of parkinsonism. Drug Dev Ind Pharm 1998;24:671-5
-
(1998)
Drug Dev Ind Pharm
, vol.24
, pp. 671-5
-
-
Jain, N.K.1
Rana, A.C.2
Jain, S.K.3
-
34
-
-
0030890637
-
Lung specific stealth liposomes: Stability, biodistribution and toxicity of liposomal antitubercular drugs in mice
-
Deol P, Khuller GK. Lung specific stealth liposomes: stability, biodistribution and toxicity of liposomal antitubercular drugs in mice. Biochim Biophys Acta 1997;1334:161-72
-
(1997)
Biochim Biophys Acta
, vol.1334
, pp. 161-72
-
-
Deol, P.1
Khuller, G.K.2
-
35
-
-
0028963739
-
In vitro evaluation of polymerized liposomes as an oral drug delivery system
-
Okada J, Cohen S, Langer R In vitro evaluation of polymerized liposomes as an oral drug delivery system. Pharm Res 1995;12:576-82
-
(1995)
Pharm Res
, vol.12
, pp. 576-82
-
-
Okada, J.1
Cohen, S.2
Langer, R.3
-
36
-
-
0029905843
-
Lectin-bearing polymerized liposomes as potential oral vaccine carriers
-
Chen H, Torchilin V, Langer R Lectin-bearing polymerized liposomes as potential oral vaccine carriers. Pharm Res 1996;13:1378-83
-
(1996)
Pharm Res
, vol.13
, pp. 1378-83
-
-
Chen, H.1
Torchilin, V.2
Langer, R.3
-
37
-
-
0031800381
-
Novel applications of liposomes
-
Lasic DD. Novel applications of liposomes. Trends Biotechnol 1998;16:307-21
-
(1998)
Trends Biotechnol
, vol.16
, pp. 307-21
-
-
Lasic, D.D.1
-
38
-
-
0031746121
-
Bioadhesive liposomes bearing levonorgestrel as controlled drug delivery system
-
Uppadhyay AK, Dixit VK. Bioadhesive liposomes bearing levonorgestrel as controlled drug delivery system. Pharmazie 1998;53:421-2
-
(1998)
Pharmazie
, vol.53
, pp. 421-2
-
-
Uppadhyay, A.K.1
Dixit, V.K.2
-
39
-
-
70350344325
-
N-Trimethyl chitosan-coated multivesicular liposomes for oxymatrine oral delivery
-
Cao J, Sun J, Wang X, et al. N-Trimethyl chitosan-coated multivesicular liposomes for oxymatrine oral delivery. Drug Dev Ind Pharm 2009;35:1339-47
-
(2009)
Drug Dev Ind Pharm
, vol.35
, pp. 1339-47
-
-
Cao, J.1
Sun, J.2
Wang, X.3
-
40
-
-
77951270392
-
Alginate-loaded liposomes can protect encapsulated alkaline phosphatase functionality when exposed to gastric pH
-
Smith AM, Jaime-Fonseca MR, Grover LM, et al. Alginate-loaded liposomes can protect encapsulated alkaline phosphatase functionality when exposed to gastric pH. J Agric Food Chem 2010;58:4719-24
-
(2010)
J Agric Food Chem
, vol.58
, pp. 4719-24
-
-
Smith, A.M.1
Jaime-Fonseca, M.R.2
Grover, L.M.3
-
41
-
-
77649242982
-
Carbopol-lectin conjugate coated liposomes for oral peptide delivery
-
Werle M, Makhlof A, Takeuchi H. Carbopol-lectin conjugate coated liposomes for oral peptide delivery. Chem Pharm Bull 2010;58:432-4
-
(2010)
Chem Pharm Bull
, vol.58
, pp. 432-4
-
-
Werle, M.1
Makhlof, A.2
Takeuchi, H.3
-
42
-
-
0034949616
-
Formulation and evaluation of a folic acid receptor-targeted oral vancomycin liposomal dosage form
-
Anderson KE, Eliot LA, Stevenson BR, Rogers JA. Formulation and evaluation of a folic acid receptor-targeted oral vancomycin liposomal dosage form. Pharm Res 2001;18:316-22
-
(2001)
Pharm Res
, vol.18
, pp. 316-22
-
-
Anderson, K.E.1
Eliot, L.A.2
Stevenson, B.R.3
Rogers, J.A.4
-
43
-
-
0032526501
-
Oral administration of liposomes containing cyclosporine: A pharmacokinetic study
-
Al-Meshal MA, Khidr SH, Bayomi MA, Al-Angary AA. Oral administration of liposomes containing cyclosporine: a pharmacokinetic study. Int J Pharm 1998;168:163-8
-
(1998)
Int J Pharm
, vol.168
, pp. 163-8
-
-
Al-Meshal, M.A.1
Khidr, S.H.2
Bayomi, M.A.3
Al-Angary, A.A.4
-
44
-
-
5344233384
-
The effect of various liposome formulations on insulin penetration across Caco-2 cell monolayer
-
Degim Z, Unal N, Essiz D, Abbasoglu U. The effect of various liposome formulations on insulin penetration across Caco-2 cell monolayer. Life Sci 2004;75:2819-27
-
(2004)
Life Sci
, vol.75
, pp. 2819-27
-
-
Degim, Z.1
Unal, N.2
Essiz, D.3
Abbasoglu, U.4
-
45
-
-
0011479137
-
Preservation of dry liposomes does not require retention of residual water
-
Crowe JH, Spargo BJ, Crowe LM. Preservation of dry liposomes does not require retention of residual water. Proc Natl Acad Sci USA 1987;84:1537-40
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 1537-40
-
-
Crowe, J.H.1
Spargo, B.J.2
Crowe, L.M.3
-
46
-
-
0027979363
-
Formulation and in vitro performance of liposome powder aerosol
-
Schreier H, Mobley WC, Concessio N, et al. Formulation and In vitro performance of liposome powder aerosol. STP Pharm Sci 1994;4:38-44
-
(1994)
STP Pharm Sci
, vol.4
, pp. 38-44
-
-
Schreier, H.1
Mobley, W.C.2
Concessio, N.3
-
49
-
-
79251496869
-
Liposomes: Preparation and application
-
Maierhofer G. Liposomes: preparation and application. Am Clin Prod Rev 1985;4:33-44
-
(1985)
Am Clin Prod Rev
, vol.4
, pp. 33-44
-
-
Maierhofer, G.1
-
50
-
-
0036040083
-
Development of non-toxic liposomal formulations for gene and drug delivery to the lung
-
Mozafari MR, Reed CJ, Rostron C. Development of non-toxic liposomal formulations for gene and drug delivery to the lung. Technol Health Care 2002;10:342-4
-
(2002)
Technol Health Care
, vol.10
, pp. 342-4
-
-
Mozafari, M.R.1
Reed, C.J.2
Rostron, C.3
-
51
-
-
0036427088
-
Construction of stable anionic liposome-plasmid particles using the heating method: A preliminary investigation
-
Mozafari MR, Reed CJ, Rostron C, et al. Construction of stable anionic liposome-plasmid particles using the heating method: a preliminary investigation. Cell Mol Biol Lett 2002;7:923-7
-
(2002)
Cell Mol Biol Lett
, vol.7
, pp. 923-7
-
-
Mozafari, M.R.1
Reed, C.J.2
Rostron, C.3
-
52
-
-
31544461008
-
Transfection of human airway epithelial cells using a lipid-based vector prepared by the heating method
-
Mozafari MR, Reed CJ, Rostron C, Martin DS. Transfection of human airway epithelial cells using a lipid-based vector prepared by the heating method. J Aerosol Med 2004;17:100
-
(2004)
J Aerosol Med
, vol.17
, pp. 100
-
-
Mozafari, M.R.1
Reed, C.J.2
Rostron, C.3
Martin, D.S.4
-
53
-
-
0030949023
-
Cytotoxicity of solid lipid nanoparticles as a function of the lipid matrix and the surfactant
-
Muller RH, Ruhl D, Runge S, et al. Cytotoxicity of solid lipid nanoparticles as a function of the lipid matrix and the surfactant. Pharm Res 1997;14:458-62
-
(1997)
Pharm Res
, vol.14
, pp. 458-62
-
-
Muller, R.H.1
Ruhl, D.2
Runge, S.3
-
54
-
-
58249120619
-
Formulation and pharmacokinetics of lipid nanoparticles of a chemically sensitive nitrogen mustard derivative: Chlorambucil
-
Sharma P, Ganta S, Denny WA, Garg S. Formulation and pharmacokinetics of lipid nanoparticles of a chemically sensitive nitrogen mustard derivative: chlorambucil. Int J Pharm 2009;367:187-94
-
(2009)
Int J Pharm
, vol.367
, pp. 187-94
-
-
Sharma, P.1
Ganta, S.2
Denny, W.A.3
Garg, S.4
-
55
-
-
53949108970
-
Investigation of the carbopol gel of solid lipid nanoparticles for the transdermal iontophoretic delivery of triamcinolone acetonide acetate
-
Liu W, Hu M, Liu W, et al. Investigation of the carbopol gel of solid lipid nanoparticles for the transdermal iontophoretic delivery of triamcinolone acetonide acetate. Int J Pharm 2008;364:135-41
-
(2008)
Int J Pharm
, vol.364
, pp. 135-41
-
-
Liu, W.1
Hu, M.2
Liu, W.3
-
56
-
-
52949112251
-
Lipid nanoparticles as vehicles for topical psoralen delivery: Solid lipid nanoparticles (SLN) versus nanostructured lipid carriers (NLC)
-
Fang JY, Fang CL, Liu CH, Su YH. Lipid nanoparticles as vehicles for topical psoralen delivery: solid lipid nanoparticles (SLN) versus nanostructured lipid carriers (NLC). Eur J Pharm Biopharm 2008;70:633-40
-
(2008)
Eur J Pharm Biopharm
, vol.70
, pp. 633-40
-
-
Fang, J.Y.1
Fang, C.L.2
Liu, C.H.3
Su, Y.H.4
-
57
-
-
0035946615
-
Solid lipid nanoparticles\production, characterization and applications
-
Mehnert W, Mader K. Solid lipid nanoparticles\production, characterization and applications. Adv Drug Deliv Rev 2001;47:165-96
-
(2001)
Adv Drug Deliv Rev
, vol.47
, pp. 165-96
-
-
Mehnert, W.1
Mader, K.2
-
58
-
-
0028917883
-
Do nanoparticles prepared from lipids solid at room temperature always possess a solid lipid matrix?
-
Westesen K, Bunjes H. Do nanoparticles prepared from lipids solid at room temperature always possess a solid lipid matrix? Int J Pharm 1995;115:129-31
-
(1995)
Int J Pharm
, vol.115
, pp. 129-31
-
-
Westesen, K.1
Bunjes, H.2
-
59
-
-
44749090963
-
Studies on PEG-modified SLNs loading vinorelbine bitartrate (I): Preparation and evaluation in vitro
-
Wan F, You J, Sun Y, et al. Studies on PEG-modified SLNs loading vinorelbine bitartrate (I): preparation and evaluation in vitro. Int J Pharm 2008;359:104-10
-
(2008)
Int J Pharm
, vol.359
, pp. 104-10
-
-
Wan, F.1
You, J.2
Sun, Y.3
-
60
-
-
40949106038
-
Preparation and stabilization of nifedipine lipid nanoparticles
-
Kamiya S, Yamada M, Kurita T, et al. Preparation and stabilization of nifedipine lipid nanoparticles. Int J Pharm 2008;354:242-7
-
(2008)
Int J Pharm
, vol.354
, pp. 242-7
-
-
Kamiya, S.1
Yamada, M.2
Kurita, T.3
-
61
-
-
57149108667
-
A proline-rich peptide improves cell transfection of solid lipid nanoparticle-based non-viral vectors
-
Pozo-Rodriguez AD, Pujals S, Delgado D, et al. A proline-rich peptide improves cell transfection of solid lipid nanoparticle-based non-viral vectors. J Control Release 2009;133:52-9
-
(2009)
J Control Release
, vol.133
, pp. 52-9
-
-
Pozo-Rodriguez, A.D.1
Pujals, S.2
Delgado, D.3
-
62
-
-
58549089321
-
Enhancement of gastrointestinal absorption of quercetin by solid lipid nanoparticles
-
Li HL, Zhao XB, Ma YK, et al. Enhancement of gastrointestinal absorption of quercetin by solid lipid nanoparticles. J Control Release 2009;133:238-44
-
(2009)
J Control Release
, vol.133
, pp. 238-44
-
-
Li, H.L.1
Zhao, X.B.2
Ma, Y.K.3
-
63
-
-
62949184949
-
Development of new lipid-based paclitaxel nanoparticles using sequential simplex optimization
-
Dong X, Mattingly CA, Tseng M, et al. Development of new lipid-based paclitaxel nanoparticles using sequential simplex optimization. Eur J Pharm Biopharm 2009;72:9-17
-
(2009)
Eur J Pharm Biopharm
, vol.72
, pp. 9-17
-
-
Dong, X.1
Mattingly, C.A.2
Tseng, M.3
-
64
-
-
34547905415
-
Production of solid lipid nanoparticle suspensions using supercritical fluid extraction of emulsions (SFEE) for pulmonary delivery using the AERx system
-
Chattopadhyaya P, Shekunova BY, Yimb D, et al. Production of solid lipid nanoparticle suspensions using supercritical fluid extraction of emulsions (SFEE) for pulmonary delivery using the AERx system. Adv Drug Deliv Rev 2007;59:444-5
-
(2007)
Adv Drug Deliv Rev
, vol.59
, pp. 444-5
-
-
Chattopadhyaya, P.1
Shekunova, B.Y.2
Yimb, D.3
-
65
-
-
0037130209
-
Residual polyvinyl alcohol associated with poly (D,L-lactide-co- glycolide) nanoparticles affects their physical properties and cellular uptake
-
Sahoo SK, Panyam J, Prabha S, Labhasetwar V. Residual polyvinyl alcohol associated with poly (D,L-lactide-co-glycolide) nanoparticles affects their physical properties and cellular uptake. J Control Release 2002;82:105-14
-
(2002)
J Control Release
, vol.82
, pp. 105-14
-
-
Sahoo, S.K.1
Panyam, J.2
Prabha, S.3
Labhasetwar, V.4
-
66
-
-
0028285718
-
Solid lipid nanoparticles (SLN) for controlled drug delivery. I. Production, characterization and sterilization
-
Schwarz C, Mehnert W, Lucks JS, Muller RH. Solid lipid nanoparticles (SLN) for controlled drug delivery. I. Production, characterization and sterilization. J Control Release 1994;30:83-96
-
(1994)
J Control Release
, vol.30
, pp. 83-96
-
-
Schwarz, C.1
Mehnert, W.2
Lucks, J.S.3
Muller, R.H.4
-
67
-
-
0038032150
-
Solid lipid nanoparticles (SLN) for controlled drug delivery - A review of the state of the art
-
Muller RH, Mader K, Gohla S. Solid lipid nanoparticles (SLN) for controlled drug delivery-a review of the state of the art. Eur J Pharm Biopharm 2000;50:161-77
-
(2000)
Eur J Pharm Biopharm
, vol.50
, pp. 161-77
-
-
Muller, R.H.1
Mader, K.2
Gohla, S.3
-
68
-
-
39849097998
-
Cyclosporine-loaded solid lipid nanoparticles (SLN): Drug-lipid physicochemical interactions and characterization of drug incorporation
-
Muller RH, Runge SA, Ravelli V, et al. Cyclosporine-loaded solid lipid nanoparticles (SLN): drug-lipid physicochemical interactions and characterization of drug incorporation. Eur J Pharm Biopharm 2008;68:535-44
-
(2008)
Eur J Pharm Biopharm
, vol.68
, pp. 535-44
-
-
Muller, R.H.1
Runge, S.A.2
Ravelli, V.3
-
69
-
-
84981669961
-
Biological implications of the use of surfactants in medicines: And the biphasic effects of surfactants in biological systems
-
Florence AT, Gillan JMN. Biological implications of the use of surfactants in medicines: and the biphasic effects of surfactants in biological systems. Pest Sci 1975;6:429-39
-
(1975)
Pest Sci
, vol.6
, pp. 429-39
-
-
Florence, A.T.1
Gillan, J.M.N.2
-
71
-
-
13544268427
-
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;9:87-93
-
(1995)
Pharm Res
, vol.9
, pp. 87-93
-
-
Constantinides, P.P.1
-
72
-
-
0342617694
-
Lipid-based vehicles for the oral delivery for poorly water soluble drugs
-
Humberstone AJ, Charman WN. Lipid-based vehicles for the oral delivery for poorly water soluble drugs. Adv Drug Deliv Rev 1997;25:47-58
-
(1997)
Adv Drug Deliv Rev
, vol.25
, pp. 47-58
-
-
Humberstone, A.J.1
Charman, W.N.2
-
73
-
-
0022366625
-
Self-emulsifying drug delivery systems: Assessment of the efficiency of emulsification
-
Pouton CW. Self-emulsifying drug delivery systems: assessment of the efficiency of emulsification. Int J Pharm 2000;17:335-48
-
(2000)
Int J Pharm
, vol.17
, pp. 335-48
-
-
Pouton, C.W.1
-
74
-
-
0035984949
-
Lipid-based formulations for intestinal lymphatic delivery
-
O'Driscoll CM. Lipid-based formulations for intestinal lymphatic delivery. Eur J Pharm Sci 2002;15:405-15
-
(2002)
Eur J Pharm Sci
, vol.15
, pp. 405-15
-
-
O'Driscoll, C.M.1
-
75
-
-
0026586447
-
Self-emulsifying drug delivery systems: Formulation and biopharmaceutical evaluation of an investigational lipophilic compound
-
Charman SA, Charman WN, Rogge MC, et al. Self-emulsifying drug delivery systems: formulation and biopharmaceutical evaluation of an investigational lipophilic compound. Pharm Res 1992;9:87-93
-
(1992)
Pharm Res
, vol.9
, pp. 87-93
-
-
Charman, S.A.1
Charman, W.N.2
Rogge, M.C.3
-
76
-
-
0028194817
-
Self-emulsifying drug delivery systems (SEDDS) with polyglycolized 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 polyglycolized glycerides for improving in vitro dissolution and oral absorption of lipophilic drugs. Int J Pharm 1994;106:15-23
-
(1994)
Int J Pharm
, vol.106
, pp. 15-23
-
-
Shah, N.H.1
Carvajal, M.T.2
Patel, C.I.3
-
77
-
-
0032103706
-
Formulation design and bioavailability assessment of lipidic self-emulsifying formulations of halofantrine
-
Khoo SM, Humberstone AJ, Porter CJH, et al. Formulation design and bioavailability assessment of lipidic self-emulsifying formulations of halofantrine. Int J Pharm 1998;167:155-64
-
(1998)
Int J Pharm
, vol.167
, pp. 155-64
-
-
Khoo, S.M.1
Humberstone, A.J.2
Cjh, P.3
-
78
-
-
0034889914
-
The influence of formulation variables on the properties of pellets containing a self-emulsifying mixture
-
Newton M, Petersson J, Podczeck F, et al. The influence of formulation variables on the properties of pellets containing a self-emulsifying mixture. J Pharm Sci 2001;90:987-95
-
(2001)
J Pharm Sci
, vol.90
, pp. 987-95
-
-
Newton, M.1
Petersson, J.2
Podczeck, F.3
-
79
-
-
0347481432
-
Solid double microemulsions for improved absorption of scarcely bioavailable drugs
-
Chiellini EE, Bellich B, Macchiavelli S, et al. Solid double microemulsions for improved absorption of scarcely bioavailable drugs. Pharm J Slovenia 2003;54:469-70
-
(2003)
Pharm J Slovenia
, vol.54
, pp. 469-70
-
-
Chiellini, E.E.1
Bellich, B.2
MacChiavelli, S.3
-
80
-
-
52949125231
-
A new solid self-microemulsifying formulation prepared by spray-drying to improve the oral bioavailability of poorly water soluble drugs
-
Yi T, Wan J, Xu H, et al. A new solid self-microemulsifying formulation prepared by spray-drying to improve the oral bioavailability of poorly water soluble drugs. Eur J Pharm Biopharm 2008;70:439-44
-
(2008)
Eur J Pharm Biopharm
, vol.70
, pp. 439-44
-
-
Yi, T.1
Wan, J.2
Xu, H.3
-
81
-
-
67449116319
-
Enhanced oral bioavailability of dexibuprofen by a novel solid Self-emulsifying drug delivery system (SEDDS)
-
Balakrishnan P, Lee BJ, Oh DH, et al. Enhanced oral bioavailability of dexibuprofen by a novel solid Self-emulsifying drug delivery system (SEDDS). Eur J Pharm Biopharm 2009;72:539-45
-
(2009)
Eur J Pharm Biopharm
, vol.72
, pp. 539-45
-
-
Balakrishnan, P.1
Lee, B.J.2
Oh, D.H.3
-
82
-
-
13544270954
-
Self-emulsifying pellets prepared by wet granulation in high-shear mixer: Influence of formulation variables and preliminary study on the in vitro absorption
-
Franceschinis E, Voinovich D, Grassi M, et al. Self-emulsifying pellets prepared by wet granulation in high-shear mixer: influence of formulation variables and preliminary study on the in vitro absorption. Int J Pharm 2005;291:87-97
-
(2005)
Int J Pharm
, vol.291
, pp. 87-97
-
-
Franceschinis, E.1
Voinovich, D.2
Grassi, M.3
-
83
-
-
34247536269
-
Preparation and characterization of a self-emulsifying pellet formulation
-
Abdalla A, Mader K. Preparation and characterization of a self-emulsifying pellet formulation. Eur J Pharm Biopharm 2007;66:220-6
-
(2007)
Eur J Pharm Biopharm
, vol.66
, pp. 220-6
-
-
Abdalla, A.1
Mader, K.2
-
84
-
-
43249131737
-
Bi-layered self-emulsifying pellets prepared by co-extrusion and spheronization: Influence of formulation variables and preliminary study on the in vivo absorption
-
Iosio T, Voinovich D, Grassi M, et al. Bi-layered self-emulsifying pellets prepared by co-extrusion and spheronization: influence of formulation variables and preliminary study on the in vivo absorption. Eur J Pharm Biopharm 2008;69:686-97
-
(2008)
Eur J Pharm Biopharm
, vol.69
, pp. 686-97
-
-
Iosio, T.1
Voinovich, D.2
Grassi, M.3
-
86
-
-
0023421375
-
Twin screw extruders: Development of technology analysis of flow
-
White JL, Szdlowski W, Min K, Kim MH. Twin screw extruders: development of technology analysis of flow. Adv Polym Technol 1987;7:295-332
-
(1987)
Adv Polym Technol
, vol.7
, pp. 295-332
-
-
White, J.L.1
Szdlowski, W.2
Min, K.3
Kim, M.H.4
-
87
-
-
0037433817
-
Prediction of degree of deformation and crystallization time of molten droplets in pastilation process
-
Kim JW, Ulrich J. Prediction of degree of deformation and crystallization time of molten droplets in pastilation process. Int J Pharm 2003;257:205-15
-
(2003)
Int J Pharm
, vol.257
, pp. 205-15
-
-
Kim, J.W.1
Ulrich, J.2
-
88
-
-
0026012568
-
And evaluation of sustained release ibuprofen-wax microspheres. I. Effect of formulation variables on physical characteristics
-
Adeyeye CM, Price JC Development and evaluation of sustained release ibuprofen-wax microspheres. I. Effect of formulation variables on physical characteristics. Pharm Res 1991;8:1377-83
-
(1991)
Pharm Res
, vol.8
, pp. 1377-83
-
-
Adeyeye, C.M.1
Price, J.C.2
-
89
-
-
0037436996
-
Preparation and evaluation of ibuprofen beads by melt solidification technique
-
Paradkar AR, Maheshwari M, Ketkar AR, Chauhan B. Preparation and evaluation of ibuprofen beads by melt solidification technique. Int J Pharm 2003;255:33-42
-
(2003)
Int J Pharm
, vol.255
, pp. 33-42
-
-
Paradkar, A.R.1
Maheshwari, M.2
Ketkar, A.R.3
Chauhan, B.4
-
90
-
-
34548011965
-
Pelletisation with meltable binders in sustained release formulations with lipid based excipient
-
Schaeffer T. Pelletisation with meltable binders in sustained release formulations with lipid based excipient. Bull Tech Gattefosse 2004;97:113-24
-
(2004)
Bull Tech Gattefosse
, vol.97
, pp. 113-24
-
-
Schaeffer, T.1
-
91
-
-
0034757135
-
Melt pelletization in high shear mixer using a hydrophobic melt binder: Influence of some apparatus and process variables
-
Voinovich D, Moneghini M, Perissutti B, Franceschinis E. Melt pelletization in high shear mixer using a hydrophobic melt binder: influence of some apparatus and process variables. Eur J Pharm BioPharm 2001;52:305-13
-
(2001)
Eur J Pharm BioPharm
, vol.52
, pp. 305-13
-
-
Voinovich, D.1
Moneghini, M.2
Perissutti, B.3
Franceschinis, E.4
-
92
-
-
0027733608
-
Melt pelletization in a high shear mixer. IV. Effects of process variables in a laboratory scale mixer
-
Schaefer T, Taagegaard B, Thomsen LJ, Kristensen HG. Melt pelletization in a high shear mixer. IV. Effects of process variables in a laboratory scale mixer. Eur J Pharm Sci 1993;1:125-31
-
(1993)
Eur J Pharm Sci
, vol.1
, pp. 125-31
-
-
Schaefer, T.1
Taagegaard, B.2
Thomsen, L.J.3
Kristensen, H.G.4
-
93
-
-
0021330354
-
The evaluation of formulation and processing conditions of a melt granulation process
-
McTaggart CM, Ganley JA, Sickmneller A, Walker SE. The evaluation of formulation and processing conditions of a melt granulation process. Int J Pharm 1984;19:139-48
-
(1984)
Int J Pharm
, vol.19
, pp. 139-48
-
-
McTaggart, C.M.1
Ganley, J.A.2
Sickmneller, A.3
Walker, S.E.4
-
94
-
-
0037685267
-
The preparation of agglomerates containing solid dispersions of diazepam by melt agglomeration in a high shear mixer
-
Seo A, Holm P, Kristensen HG, Schaefer T. The preparation of agglomerates containing solid dispersions of diazepam by melt agglomeration in a high shear mixer. Int J Pharm 2003;259:161-71
-
(2003)
Int J Pharm
, vol.259
, pp. 161-71
-
-
Seo, A.1
Holm, P.2
Kristensen, H.G.3
Schaefer, T.4
-
95
-
-
0025864425
-
Preformulation studies on solid dispersions containing triamterene or temazepam in polyethylene glycols or Gelucire 44/14 for liquid filling of hard gelatin capsules
-
Dordunoo SK, Ford JL, Rubinstein A. Preformulation studies on solid dispersions containing triamterene or temazepam in polyethylene glycols or Gelucire 44/14 for liquid filling of hard gelatin capsules. Drug Dev Ind Pharm 1991;17:1685-713
-
(1991)
Drug Dev Ind Pharm
, vol.17
, pp. 1685-713
-
-
Dordunoo, S.K.1
Ford, J.L.2
Rubinstein, A.3
-
96
-
-
0034032146
-
Physicochemical characterization of solid dispersions of the antiviral agent UC-781 with polyethylene glycol 6000 and Gelucire 44/14
-
Damian F, Balton N, Naesens L, et al. Physicochemical characterization of solid dispersions of the antiviral agent UC-781 with polyethylene glycol 6000 and Gelucire 44/14. Eur J Pharm Sci 2003;10:311-22
-
(2003)
Eur J Pharm Sci
, vol.10
, pp. 311-22
-
-
Damian, F.1
Balton, N.2
Naesens, L.3
-
97
-
-
79251517944
-
Thermoplastic pelletizing with a high-shear granulator
-
Jannin V. Thermoplastic pelletizing with a high-shear granulator. Glatt Int Times 2004;18:12-14
-
(2004)
Glatt Int Times
, vol.18
, pp. 12-14
-
-
Jannin, V.1
-
98
-
-
0030896881
-
Preparation ofspherical beads without any use of solvents by a novel tumbling melt granulation (TMG) method
-
Maejima T, Osawa T, Nakajima K, Kobayashi M. Preparation ofspherical beads without any use of solvents by a novel tumbling melt granulation (TMG) method. Chem Pharm Bull 1997;45(3):518-24
-
(1997)
Chem Pharm Bull
, vol.45
, Issue.3
, pp. 518-24
-
-
Maejima, T.1
Osawa, T.2
Nakajima, K.3
Kobayashi, M.4
-
99
-
-
0032826026
-
Melt pelletisation of a hygroscopic drug in a high shear mixer. Part 1. Influence of process variables
-
Thies R, Kleinebudde P. Melt pelletisation of a hygroscopic drug in a high shear mixer. Part 1. Influence of process variables. Int J Pharm 1999;188:131-43
-
(1999)
Int J Pharm
, vol.188
, pp. 131-43
-
-
Thies, R.1
Kleinebudde, P.2
-
100
-
-
0034255003
-
Preparation in high-shear mixer of sustained-release pellets by melt pelletization
-
Voinovich D, Moneghini M, Perissutti B, et al. Preparation in high-shear mixer of sustained-release pellets by melt pelletization. Int J Pharm 2000;203:235-44
-
(2000)
Int J Pharm
, vol.203
, pp. 235-44
-
-
Voinovich, D.1
Moneghini, M.2
Perissutti, B.3
-
101
-
-
0030576621
-
Melt pelletization in a high shear mixer. VIII. Effects of binder viscosity
-
Schaefer T, Mathiesen C. Melt pelletization in a high shear mixer. VIII. Effects of binder viscosity. Int J Pharm 1996;139:125-38
-
(1996)
Int J Pharm
, vol.139
, pp. 125-38
-
-
Schaefer, T.1
Mathiesen, C.2
-
102
-
-
0022650603
-
The current status of solid dispersions
-
Ford JL. The current status of solid dispersions. Pharm Acta Helv 1986;61:69-88
-
(1986)
Pharm Acta Helv
, vol.61
, pp. 69-88
-
-
Ford, J.L.1
-
103
-
-
20444508016
-
Oral olid gentamicin preparation using emulsifier and adsorbent
-
Ito Y, Kusawake T, Ishida M, et al. Oral olid gentamicin preparation using emulsifier and adsorbent. J Control Release 2005;105:23-31
-
(2005)
J Control Release
, vol.105
, pp. 23-31
-
-
Ito, Y.1
Kusawake, T.2
Ishida, M.3
-
104
-
-
11844283277
-
Effect of adsorbents on the absorption of lansoprazole with surfactant
-
Ito Y, Araik H, Uchino K, et al. Effect of adsorbents on the absorption of lansoprazole with surfactant. Int J Pharm 2005;289:69-77
-
(2005)
Int J Pharm
, vol.289
, pp. 69-77
-
-
Ito, Y.1
Araik, H.2
Uchino, K.3
-
105
-
-
0032996555
-
Description and preliminary evaluation of a new ultrasonic atomizer for spray-congealing process
-
Rodriguez L, Passerini N, Cavallari C, et al. Description and preliminary evaluation of a new ultrasonic atomizer for spray-congealing process. Int J Pharm 1999;183:133-43
-
(1999)
Int J Pharm
, vol.183
, pp. 133-43
-
-
Rodriguez, L.1
Passerini, N.2
Cavallari, C.3
-
106
-
-
33745481304
-
Evaluation of melt granulation and ultrasonic spray congealing as techniques to enhance the dissolution of praziquantel
-
Passerini N, Albertini B, Perissuti B, et al. Evaluation of melt granulation and ultrasonic spray congealing as techniques to enhance the dissolution of praziquantel. Int J Pharm 2006;318:92-102
-
(2006)
Int J Pharm
, vol.318
, pp. 92-102
-
-
Passerini, N.1
Albertini, B.2
Perissuti, B.3
-
107
-
-
20344387251
-
Thermal and fractal analysis of diclofenac/Gelucire 50/13 microparticles obtained by ultrasound-assisted atomization
-
Cavallari C, Rodriguez B, Albertini N, et al. Thermal and fractal analysis of diclofenac/Gelucire 50/13 microparticles obtained by ultrasound-assisted atomization. J Pharm Sci 2005;94:1124-34
-
(2005)
J Pharm Sci
, vol.94
, pp. 1124-34
-
-
Cavallari, C.1
Rodriguez, B.2
Albertini, N.3
-
108
-
-
34648812679
-
Pharmaceutical applications of hot-melt extrusion: Part i
-
Crowley MM, Zhang F, Repka MA, et al. Pharmaceutical applications of hot-melt extrusion: part I. Drug Dev Ind Pharm 2007;33:909-26
-
(2007)
Drug Dev Ind Pharm
, vol.33
, pp. 909-26
-
-
Crowley, M.M.1
Zhang, F.2
Repka, M.A.3
-
109
-
-
0034601240
-
Improving drug solubility for oral delivery using solid solutions
-
Leuner C, Dressman J. Improving drug solubility for oral delivery using solid solutions. Eur J Pharm Biopharm 2000;50:47-60
-
(2000)
Eur J Pharm Biopharm
, vol.50
, pp. 47-60
-
-
Leuner, C.1
Dressman, J.2
-
110
-
-
0037173515
-
The role of kneading paddle and the effects of screw revolution speed and water content on the preparation of solid dispersions using a twin-screw extruder
-
Nakamichi K, Nakano T, Yasuura H, et al. The role of kneading paddle and the effects of screw revolution speed and water content on the preparation of solid dispersions using a twin-screw extruder. Int J Pharm 2002;241:203-11
-
(2002)
Int J Pharm
, vol.241
, pp. 203-11
-
-
Nakamichi, K.1
Nakano, T.2
Yasuura, H.3
-
111
-
-
24644475058
-
Melt extrusion-based dosage forms: Excipients and processing conditions for pharmaceutical formulations
-
Verreck G, Brewster ME. Melt extrusion-based dosage forms: excipients and processing conditions for pharmaceutical formulations. Bull Tech Gattefosse 2004;97:85-95
-
(2004)
Bull Tech Gattefosse
, vol.97
, pp. 85-95
-
-
Verreck, G.1
Brewster, M.E.2
-
112
-
-
1842865536
-
Melt extrusion: From process to drug delivery technology
-
Breitenbach J. Melt extrusion: from process to drug delivery technology. Eur J Pharm Biopharm 2002;54:107-17
-
(2002)
Eur J Pharm Biopharm
, vol.54
, pp. 107-17
-
-
Breitenbach, J.1
-
113
-
-
0036221349
-
The influence of pellet shape and film coating on the filling of pellets into hard shell capsules
-
Chopra R, Podczeck F, Newton JM, Alderborn G. The influence of pellet shape and film coating on the filling of pellets into hard shell capsules. Eur J Pharm Biopharm 2002;53:327-33
-
(2002)
Eur J Pharm Biopharm
, vol.53
, pp. 327-33
-
-
Chopra, R.1
Podczeck, F.2
Newton, J.M.3
Alderborn, G.4
-
116
-
-
8844224097
-
The preparation of spherical granules by extrusion/spheronization without microcrystalline cellulose
-
Chatchawalsaisin J, Podczeck F, Newton JM, Boutel S. The preparation of spherical granules by extrusion/spheronization without microcrystalline cellulose. Pharm Technol 2004;16:21-7
-
(2004)
Pharm Technol
, vol.16
, pp. 21-7
-
-
Chatchawalsaisin, J.1
Podczeck, F.2
Newton, J.M.3
Boutel, S.4
-
117
-
-
0027467113
-
Capacity of lipophilic auxiliary substances to give spheres by extrusion-spheronization
-
Edimo A, Leterme P, Denis J, et al. Capacity of lipophilic auxiliary substances to give spheres by extrusion-spheronization. Drug Dev Ind Pharm 1993;19:827-42
-
(1993)
Drug Dev Ind Pharm
, vol.19
, pp. 827-42
-
-
Edimo, A.1
Leterme, P.2
Denis, J.3
-
118
-
-
58349106438
-
Spheronization of solid lipid extrudates
-
Reitz C, Kleinebudde P. Spheronization of solid lipid extrudates. Powder Technol 2009;189:238-44
-
(2009)
Powder Technol
, vol.189
, pp. 238-44
-
-
Reitz, C.1
Kleinebudde, P.2
-
119
-
-
0342804284
-
Melt extrusion-an alternative method for enhancing the dissolution rate of 17-bestradiol hemihydrate
-
Hulsmann S, Backensfeld T, Keitel S, Bodmeier R. Melt extrusion-an alternative method for enhancing the dissolution rate of 17-bestradiol hemihydrate. Eur J Pharm Biopharm 2000;49:237-42
-
(2000)
Eur J Pharm Biopharm
, vol.49
, pp. 237-42
-
-
Hulsmann, S.1
Backensfeld, T.2
Keitel, S.3
Bodmeier, R.4
-
120
-
-
33751518550
-
Controlled drug release from pellets containing water-insoluble drugs dissolved in a selfemulsifying system
-
Serratoni M, Newton M, Booth S, Clarke A. Controlled drug release from pellets containing water-insoluble drugs dissolved in a selfemulsifying system. Eur J Pharm Biopharm 2007;65:94-8
-
(2007)
Eur J Pharm Biopharm
, vol.65
, pp. 94-8
-
-
Serratoni, M.1
Newton, M.2
Booth, S.3
Clarke, A.4
-
121
-
-
1842689132
-
In vitro and in vivo evaluation of a matrix-in-cylinder system for sustained drug delivery
-
Mehuys E, Vervaet C, Gielen I, et al. In vitro and in vivo evaluation of a matrix-in-cylinder system for sustained drug delivery. J Control Release 2004;96:261-71
-
(2004)
J Control Release
, vol.96
, pp. 261-71
-
-
Mehuys, E.1
Vervaet, C.2
Gielen, I.3
-
122
-
-
1642441894
-
Hot-melt extruded ethylcellulose cylinders containing a HPMC-Gelucire® core for sustained drug delivery
-
Mehuys E, Vervaet C, Remon JP. Hot-melt extruded ethylcellulose cylinders containing a HPMC-Gelucire® core for sustained drug delivery. J Control Release 2004;94:273-80
-
(2004)
J Control Release
, vol.94
, pp. 273-80
-
-
Mehuys, E.1
Vervaet, C.2
Remon, J.P.3
-
123
-
-
25844440815
-
Human bioavailability of propranolol from a matrix-incylinder systemwith aHPMC-Gelucire® core
-
Mehuys E, Remon JP, Korst A, et al. Human bioavailability of propranolol from a matrix-incylinder systemwith aHPMC-Gelucire® core. J Control Release 2005;107:523-36
-
(2005)
J Control Release
, vol.107
, pp. 523-36
-
-
Mehuys, E.1
Remon, J.P.2
Korst, A.3
-
124
-
-
33645235365
-
Mathematical model to predict the size of the pellets formed in freeze pelletization techniques: Parameters affecting pellet size
-
Cheboyina S, O'Haver J, Wyandt CM. Mathematical model to predict the size of the pellets formed in freeze pelletization techniques: parameters affecting pellet size. J Pharm Sci 2006;95:167-80
-
(2006)
J Pharm Sci
, vol.95
, pp. 167-80
-
-
Cheboyina, S.1
O'Haver, J.2
Wyandt, C.M.3
-
125
-
-
52049116688
-
Wax-based sustained release matrix pellets prepared by a novel freeze pelletization technique I. Formulation and process variables affecting pellet characteristics
-
Cheboyina S, Wyandt CM. Wax-based sustained release matrix pellets prepared by a novel freeze pelletization technique I. Formulation and process variables affecting pellet characteristics. Int J Pharm 2008;359:158-66
-
(2008)
Int J Pharm
, vol.359
, pp. 158-66
-
-
Cheboyina, S.1
Wyandt, C.M.2
-
126
-
-
5644249232
-
A novel freeze pelletization technique for preparing matrix pellets
-
Cheboyina S, Chambliss WG, Wyandt CM. A novel freeze pelletization technique for preparing matrix pellets. Pharm Tech 2004;28:98-110
-
(2004)
Pharm Tech
, vol.28
, pp. 98-110
-
-
Cheboyina, S.1
Chambliss, W.G.2
Wyandt, C.M.3
-
127
-
-
84893020470
-
-
Available from [Last accessed on 10 September 2010]
-
Sandvik Materials Technology. Available from: http://www.processsystems. sandvik. com/[Last accessed on 10 September 2010]
-
Sandvik Materials Technology
-
-
-
128
-
-
79251490564
-
Pastillation-A novel technology for development of oral lipid based multiparticulate controlled release dosage form
-
9-11 December 2009; Program and Abstracts, Hobart
-
Shukla D, Chakraborty S, Singh S, Mishra B. Pastillation-A novel technology for development of oral lipid based multiparticulate controlled release dosage form. Australasian Pharmaceutical Sciences Association Annual Conference, 9-11 December 2009; Program and Abstracts, Hobart; 2009. p. 106
-
(2009)
Australasian Pharmaceutical Sciences Association Annual Conference
, pp. 106
-
-
Shukla, D.1
Chakraborty, S.2
Singh, S.3
Mishra, B.4
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