-
1
-
-
57849103430
-
Dissolution and powder flow characterization of solid self-emulsified drug delivery system (SEDDS)
-
V. Agarwal, A. Siddiqui, H. Ali, and S. Nazzal Dissolution and powder flow characterization of solid self-emulsified drug delivery system (SEDDS) Int. J. Pharm. 366 2009 44 52
-
(2009)
Int. J. Pharm.
, vol.366
, pp. 44-52
-
-
Agarwal, V.1
Siddiqui, A.2
Ali, H.3
Nazzal, S.4
-
2
-
-
0028948839
-
A theoretical basis for a biopharmaceutic drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability
-
G.L. Amidon, H. Lennernas, V.P. Shah, and J.R. Crison A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability Pharm. Res. 12 1995 413
-
(1995)
Pharm. Res.
, vol.12
, pp. 413
-
-
Amidon, G.L.1
Lennernas, H.2
Shah, V.P.3
Crison, J.R.4
-
3
-
-
0028040373
-
Calcitonin-loaded liposomes: Stability under acidic conditions and bile salts-induced disruption resulting in calcitonin-phospholipid complex formation
-
DOI 10.1016/0005-2736(94)90337-9
-
A. Arien, N. Henry-Toulme, and B. Dupuy Calcitonin loaded liposomes: stability under acidic conditions and bile salts-induced disruption resulting in calcitonin-phospholipid complex formation Biochim. Biophys. Acta 1193 1994 93 100 (Pubitemid 24234183)
-
(1994)
Biochimica et Biophysica Acta - Biomembranes
, vol.1193
, Issue.1
, pp. 93-100
-
-
Arien, A.1
Henry-Toulme, N.2
Dupuy, B.3
-
4
-
-
84907352341
-
-
CFR, 2011. Code of Federal Regulations Subpart B - Listing of specific substances Affirmed as GRAS, Section 184.1400, 21CFR184.1400
-
CFR, 2011. Code of Federal Regulations. Part 184 - Direct Food substances affirmed as Generally Recognized as Safe. Subpart B - Listing of specific substances Affirmed as GRAS, Section 184.1400, 21CFR184.1400, p. 3.
-
Part 184 - Direct Food Substances Affirmed As Generally Recognized As Safe
, pp. 3
-
-
-
5
-
-
68349160715
-
Lipid - An emerging platform for oral delivery of drugs with poor bioavailability review article
-
S. Chakraborty, D. Shukla, B. Mishra, and S. Singh Lipid - an emerging platform for oral delivery of drugs with poor bioavailability review article Eur. J. Pharm. Biopharm. 73 2009 1 15
-
(2009)
Eur. J. Pharm. Biopharm.
, vol.73
, pp. 1-15
-
-
Chakraborty, S.1
Shukla, D.2
Mishra, B.3
Singh, S.4
-
6
-
-
84862284061
-
-
6th ed., European Department for the Quality of Medicines, Strasburg (Supplement 2008)
-
European Pharmacopeia, 2008. 6th ed., European Department for the Quality of Medicines, Strasburg, pp. 1411-1412 (Supplement 2008).
-
(2008)
European Pharmacopeia
, pp. 1411-1412
-
-
-
7
-
-
84923690893
-
Guidance for Industry: Immediate Release Solid Oral Dosage Forms - Scale-up and Postapproval Changes: Chemistry, Manufacturing, and Controls
-
FDA Center for Drug Evaluation and Research, Rockville, MD
-
FDA, 1995. Guidance for Industry: Immediate Release Solid Oral Dosage Forms - Scale-up and Postapproval Changes: Chemistry, Manufacturing, and Controls; In Vitro Dissolution Testing, and In Vivo Bioequivalance Documentation. Center for Drug Evaluation and Research, Rockville, MD.
-
(1995)
Vitro Dissolution Testing, and in Vivo Bioequivalance Documentation
-
-
-
9
-
-
84923690893
-
Guidance for Industry: SUPAC-MR: Modified Release Solid Oral Dosage Forms - Scale-up and Postapproval Changes, Chemistry, Manufacturing, and Controls
-
FDA Center for Drug Evaluation and Research, Rockville, MD
-
FDA, 1997b. Guidance for Industry: SUPAC-MR: Modified Release Solid Oral Dosage Forms - Scale-up and Postapproval Changes: Chemistry, Manufacturing, and Controls; In Vitro Dissolution Testing, and In Vivo Bioequivalance Documentation. Center for Drug Evaluation and Research, Rockville, MD.
-
(1997)
Vitro Dissolution Testing, and in Vivo Bioequivalance Documentation
-
-
-
12
-
-
58849131429
-
The glass menagerie: Diatoms for novel applications in nanotechnology
-
R. Gordon, D. Losic, M.A. Tiffany, S.S. Nagy, and F.A.S. Sterrenburg The glass menagerie: diatoms for novel applications in nanotechnology Trends Biotechnol. 27 2009 116 127
-
(2009)
Trends Biotechnol.
, vol.27
, pp. 116-127
-
-
Gordon, R.1
Losic, D.2
Tiffany, M.A.3
Nagy, S.S.4
Sterrenburg, F.A.S.5
-
13
-
-
0242322069
-
Comparison of the Four Anhydrous Polymorphs of Carbamazepine and the Crystal Structure of Form I
-
DOI 10.1002/jps.10455
-
A.L. Grzesiak, M. Lang, K. Kim, and A.J. Matzeger Comparison of the four anhydrous polymorphs of carbamazepine and the crystal structure of form I J. Pharm. Sci. 92 2003 2260 2271 (Pubitemid 37356699)
-
(2003)
Journal of Pharmaceutical Sciences
, vol.92
, Issue.11
, pp. 2260-2271
-
-
Grzesiak, A.L.1
Lang, M.2
Kim, K.3
Matzger, A.J.4
-
14
-
-
4444316612
-
Grouping solvents by statistical analysis of solvent property parameters: Implication to polymorph screening
-
C. Gua, H. Lib, R. Gandhia, and K. Raghavana Grouping solvents by statistical analysis of solvent property parameters: implication to polymorph screening Int. J. Pharm. 283 2004 117 125
-
(2004)
Int. J. Pharm.
, vol.283
, pp. 117-125
-
-
Gua, C.1
Lib, H.2
Gandhia, R.3
Raghavana, K.4
-
16
-
-
38949117575
-
Approaches for the development of solid and semi-solid lipid-based formulations
-
DOI 10.1016/j.addr.2007.09.006, PII S0169409X0700316X
-
V. Jannin, J. Musakhanian, and D. Marchaud Approaches for the development of solid and semi-solid lipid-based formulations Adv. Drug Deliver. Rev. 60 2008 734 746 (Pubitemid 351215578)
-
(2008)
Advanced Drug Delivery Reviews
, vol.60
, Issue.6
, pp. 734-746
-
-
Jannin, V.1
Musakhanian, J.2
Marchaud, D.3
-
17
-
-
72449174745
-
Solvent effects on the crystallization and preferential nucleation of carbamazepine anhydrous polymorphs: A molecular recognition perspective
-
C.R. Kelly, and N. RodrIguez-Hornedo Solvent effects on the crystallization and preferential nucleation of carbamazepine anhydrous polymorphs: a molecular recognition perspective Organic Process Res. Develop. 13 2009 1291 1300
-
(2009)
Organic Process Res. Develop.
, vol.13
, pp. 1291-1300
-
-
Kelly, C.R.1
Rodriguez-Hornedo, N.2
-
18
-
-
33746541075
-
Enhancing mechanism of Labrasol on intestinal membrane permeability of the hydrophilic drug gentamicin sulfate
-
DOI 10.1016/j.ejpb.2006.03.011, PII S0939641106000816
-
K. Koga, Y. Kusawake, Y. Ito, N. Sugioka, N. Shibata, and K. Takada Enhancing mechanism of Labrasol on intestinal membrane permeability of the hydrophilic drug gentamicin sulfate Eur. J. Pharm. Biopharm. 64 2006 82 91 (Pubitemid 44142241)
-
(2006)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.64
, Issue.1
, pp. 82-91
-
-
Koga, K.1
Kusawake, Y.2
Ito, Y.3
Sugioka, N.4
Shibata, N.5
Takada, K.6
-
19
-
-
84887047562
-
Graphene oxide decorated diatom silica particles as a new nano-hybrid: Towards smart natural drug microcarriers
-
T. Kumeria, M. Bariana, T. Altalhi, M. Kurkuri, C.T. Gibson, W. Yang, and D. Losic Graphene oxide decorated diatom silica particles as a new nano-hybrid: towards smart natural drug microcarriers J. Mater. Chem. 1 2013 6302 6311
-
(2013)
J. Mater. Chem.
, vol.1
, pp. 6302-6311
-
-
Kumeria, T.1
Bariana, M.2
Altalhi, T.3
Kurkuri, M.4
Gibson, C.T.5
Yang, W.6
Losic, D.7
-
20
-
-
0034601240
-
Improving drug solubility for oral delivery using solid dispersions
-
DOI 10.1016/S0939-6411(00)00076-X, PII S093964110000076X
-
C. Leuner, and J. Dressman Improving drug solubility for oral delivery using solid dispersions Eur. J. Pharm. Biopharm. 50 2000 47 60 (Pubitemid 30326688)
-
(2000)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.50
, Issue.1
, pp. 47-60
-
-
Leuner, C.1
Dressman, J.2
-
21
-
-
0003060719
-
Carbamazepine, valproic acid, phenobarbital, and ethosuximide
-
W.E. Evans, J.J. Schentag, J.W. Jusko, 3rd ed. Vancouver
-
R. Levy, A.J. Wilensky, and G.D. Anderson Carbamazepine, valproic acid, phenobarbital, and ethosuximide W.E. Evans, J.J. Schentag, J.W. Jusko, Applied Pharmacokinetics. Principles of Therapeutic Drug Monitoring. Applied Therapeutics 3rd ed. 1992 Vancouver 1 29
-
(1992)
Applied Pharmacokinetics. Principles of Therapeutic Drug Monitoring. Applied Therapeutics
, pp. 1-29
-
-
Levy, R.1
Wilensky, A.J.2
Anderson, G.D.3
-
22
-
-
0034112024
-
In situ dehydration of carbamazepine dihydrate: A novel technique to prepare amorphous anhydrous carbamazepine
-
DOI 10.1081/PDT-100100540
-
Y. Li, J. Han, G. Zhang, D. Grant, and R. Saryanarajanan In situ dehydration of CBZ dihydrate: a novel technique to prepare amorphous anhydrous carbamazepine Pharm. Dev. Tech. 5 2 2000 257 266 (Pubitemid 30247106)
-
(2000)
Pharmaceutical Development and Technology
, vol.5
, Issue.2
, pp. 257-266
-
-
Li, Y.1
Han, J.2
Zhang, G.G.Z.3
Grant, D.J.W.4
Suryanarayanan, R.5
-
23
-
-
68249108871
-
Diatomaceous lessons in nanotechnology and advanced materials
-
D. Losic, J.G. Mitchell, and N.H. Voelcker Diatomaceous lessons in nanotechnology and advanced materials Adv. Mater. 21 2009 2947 2958
-
(2009)
Adv. Mater.
, vol.21
, pp. 2947-2958
-
-
Losic, D.1
Mitchell, J.G.2
Voelcker, N.H.3
-
24
-
-
77955780510
-
Surface functionalization of diatoms with dopamine modified iron oxide nanoparticles: Toward magnetically guided drug microcarriers with biologically derived morphologies
-
D. Losic, Y. Yu, M. Sin Aw, S. Simovic, B. Tierry, and J. Addai-Mensah Surface functionalization of diatoms with dopamine modified iron oxide nanoparticles: toward magnetically guided drug microcarriers with biologically derived morphologies Chem. Commun. 46 2010 6323 6325
-
(2010)
Chem. Commun.
, vol.46
, pp. 6323-6325
-
-
Losic, D.1
Yu, Y.2
Sin Aw, M.3
Simovic, S.4
Tierry, B.5
Addai-Mensah, J.6
-
25
-
-
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
-
DOI 10.1016/S0378-5173(02)00003-0, PII S0378517302000030
-
S. Nazzal, I.I. Smalyukh, O.D. Lavrentovich, and M.A. Khan 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. 235 2002 247 265 (Pubitemid 34185455)
-
(2002)
International Journal of Pharmaceutics
, vol.235
, Issue.1-2
, pp. 247-265
-
-
Nazzal, S.1
Smalyukh, I.I.2
Lavrentovich, O.D.3
Khan, M.A.4
-
26
-
-
0042383291
-
Improvement of cefpodoxime proxetil oral absorption in rats by an oil-in-water submicron emulsion
-
DOI 10.1016/S0378-5173(03)00365-X
-
G. Nicolaos, S. Crauste-Manciet, R. Farinotti, and D. Brossard Improvement of cefpodoxime proxetil oral absorption in rats by an oil-in water submicron emulsion Int. J. Pharm. 263 2003 165 171 (Pubitemid 37087943)
-
(2003)
International Journal of Pharmaceutics
, vol.263
, Issue.1-2
, pp. 165-171
-
-
Nicolaos, G.1
Crauste-Manciet, S.2
Farinotti, R.3
Brossard, D.4
-
27
-
-
33645306276
-
Mixed-micellar proliposomal systems for enhanced oral delivery of progesterone
-
P. Potluri, and G.V. Betageri Mixed-micellar proliposomal systems for enhanced oral delivery of progesterone Drug Deliver. 13 2006 227 232
-
(2006)
Drug Deliver.
, vol.13
, pp. 227-232
-
-
Potluri, P.1
Betageri, G.V.2
-
28
-
-
33751014029
-
Formulation of poorly water-soluble drugs for oral administration: Physicochemical and physiological issues and the lipid formulation classification system
-
DOI 10.1016/j.ejps.2006.04.016, PII S0928098706001151
-
C.W. Pouton Formulation of poorly water-soluble drugs for oral administration: physicochemical and physiological issues and the lipid formulation classification system Eur. J. Pharm. Sci. 29 2006 278 287 (Pubitemid 44740131)
-
(2006)
European Journal of Pharmaceutical Sciences
, vol.29
, Issue.34 SPEC. ISSUE.
, pp. 278-287
-
-
Pouton, C.W.1
-
29
-
-
39149113817
-
Formulation of lipid-based delivery systems for oral administration: Materials, methods and strategies
-
C.W. Pouton, and C.J.H. Porter Formulation of lipid-based delivery systems for oral administration: materials, methods and strategies Adv. Drug Deliver. Rev. 60 2008 625 637
-
(2008)
Adv. Drug Deliver. Rev.
, vol.60
, pp. 625-637
-
-
Pouton, C.W.1
Porter, C.J.H.2
-
30
-
-
45849150105
-
Conventional and alternative methods to improve oral bioavailability of lipophilic drugs
-
B.G. Prajapati, and M. Pate Conventional and alternative methods to improve oral bioavailability of lipophilic drugs Asian J. Pharm. 1 2007 1 8
-
(2007)
Asian J. Pharm.
, vol.1
, pp. 1-8
-
-
Prajapati, B.G.1
Pate, M.2
-
31
-
-
79957521117
-
Enhanced bioavailability and retinal accumulation of lutein from self-emulsifying phospholipid suspension (SEPS)
-
S. Shanmugam, J.H. Park, K.S. Kim, Z.Z. Piao, C.S. Yong, H.G. Choi, and J.S. Woo Enhanced bioavailability and retinal accumulation of lutein from self-emulsifying phospholipid suspension (SEPS) Int. J. Pharm. 412 2011 99 105
-
(2011)
Int. J. Pharm.
, vol.412
, pp. 99-105
-
-
Shanmugam, S.1
Park, J.H.2
Kim, K.S.3
Piao, Z.Z.4
Yong, C.S.5
Choi, H.G.6
Woo, J.S.7
-
32
-
-
80052020031
-
Silica materials in drug delivery applications
-
S. Simovic, N.G. Eskandar, M. Sinn Aw, D. Losic, and C. Prestige Silica materials in drug delivery applications Curr. Drug Discov. Technol. 8 3 2011 250 268
-
(2011)
Curr. Drug Discov. Technol.
, vol.8
, Issue.3
, pp. 250-268
-
-
Simovic, S.1
Eskandar, N.G.2
Sinn Aw, M.3
Losic, D.4
Prestige, C.5
-
33
-
-
80053128421
-
Silica microcapsules from diatoms as a new carrier for delivery of therapeutics
-
M. Sinn Aw, S. Simovic, Y. Yu, J. Addai-Mensah, and D. Losic Silica microcapsules from diatoms as a new carrier for delivery of therapeutics Nanomedicine 6 7 2011 1159 1173
-
(2011)
Nanomedicine
, vol.6
, Issue.7
, pp. 1159-1173
-
-
Sinn Aw, M.1
Simovic, S.2
Yu, Y.3
Addai-Mensah, J.4
Losic, D.5
-
34
-
-
84855275050
-
Porous silica microshells from diatoms as biocarrier for drug delivery applications
-
M. Sinn Aw, S. Simovic, Y. Yu, J. Addai-Mensah, and D. Losic Porous silica microshells from diatoms as biocarrier for drug delivery applications Powder Technol. 223 2012 52 58
-
(2012)
Powder Technol.
, vol.223
, pp. 52-58
-
-
Sinn Aw, M.1
Simovic, S.2
Yu, Y.3
Addai-Mensah, J.4
Losic, D.5
-
35
-
-
0003205569
-
Size reduction and size enlargement
-
R. Perry, D. Green, seventh ed. McGraw-Hill New York Section 20
-
R. Snow, T. Allen, B. Ennis, and J. Litster Size reduction and size enlargement R. Perry, D. Green, Perry's Chemical Engineers' Handbook seventh ed. 1997 McGraw-Hill New York 8 Section 20
-
(1997)
Perry's Chemical Engineers' Handbook
, pp. 8
-
-
Snow, R.1
Allen, T.2
Ennis, B.3
Litster, J.4
-
36
-
-
68249102027
-
Ordered mesoporous silica material SBA-15: A broad-spectrum formulation platform for poorly soluble drugs
-
M.V. Speybroeck, V. Barillaro, T. Do Thi, R. Mellaerts, J. Martens, J.V. Humbeeck, J. Vermant, P. Annaert, and G.P. Van den Mooter Ordered mesoporous silica material SBA-15: a broad-spectrum formulation platform for poorly soluble drugs J. Pharm. Sci. 98 2009 2648 2658
-
(2009)
J. Pharm. Sci.
, vol.98
, pp. 2648-2658
-
-
Speybroeck, M.V.1
Barillaro, V.2
Do Thi, T.3
Mellaerts, R.4
Martens, J.5
Humbeeck, J.V.6
Vermant, J.7
Annaert, P.8
Van Den Mooter, G.P.9
-
38
-
-
55749096749
-
Ordered mesoporous materials for drug delivery
-
S. Wang Ordered mesoporous materials for drug delivery Micropor. Mesopor. Mat. 117 2009 1 9
-
(2009)
Micropor. Mesopor. Mat.
, vol.117
, pp. 1-9
-
-
Wang, S.1
-
39
-
-
57449109685
-
Design and optimization of a new self-nanoemulsifying drug delivery system
-
L. Wang, J. Dong, J. Eastoe, and X. Li Design and optimization of a new self-nanoemulsifying drug delivery system J. Colloid Interface Sci. 330 2009 443 448
-
(2009)
J. Colloid Interface Sci.
, vol.330
, pp. 443-448
-
-
Wang, L.1
Dong, J.2
Eastoe, J.3
Li, X.4
-
40
-
-
70349826289
-
Optimized preparation of vinpocetine proliposomes by a novel method and in vivo evaluation of its pharmacokinetics in New Zealand rabbits
-
H. Xu, L. He, S. Nie, J. Guan, X. Zhang, and X. Yang Optimized preparation of vinpocetine proliposomes by a novel method and in vivo evaluation of its pharmacokinetics in New Zealand rabbits J. Control. Rel. 140 2009 61 68
-
(2009)
J. Control. Rel.
, vol.140
, pp. 61-68
-
-
Xu, H.1
He, L.2
Nie, S.3
Guan, J.4
Zhang, X.5
Yang, X.6
-
41
-
-
0036394710
-
Estimation of initial dissolution rate of drug substance by thermal analysis: Application for carbamazepine hydrate
-
DOI 10.1081/PDT-120002234
-
Y. Yoshihashi, E. Yonemochi, and K. Terada Estimation of initial dissolution rate of drug substance by thermal analysis: application for carbamazepine Pharm. Dev. Technol. 7 1 2002 89 95 (Pubitemid 35154418)
-
(2002)
Pharmaceutical Development and Technology
, vol.7
, Issue.1
, pp. 89-95
-
-
Yoshihashi, Y.1
Yonemochi, E.2
Terada, K.3
-
42
-
-
77957958699
-
Synthesis of self-supporting gold microstructures with 3-d morphologies by direct replication of diatom templates
-
Y. Yu, J. Addai-Mensah, and D. Losic Synthesis of self-supporting gold microstructures with 3-d morphologies by direct replication of diatom templates Langmuir 26 2010 14068 14072
-
(2010)
Langmuir
, vol.26
, pp. 14068-14072
-
-
Yu, Y.1
Addai-Mensah, J.2
Losic, D.3
|