-
1
-
-
27744515510
-
Excipient selection can significantly affect solid-state phase transformation in formulation during wet granulation
-
Airaksinen S, Karkalainen M, Kivikero N, et al. Excipient selection can significantly affect solid-state phase transformation in formulation during wet granulation. AAPS PharmSciTech 2005;6:E311-22
-
(2005)
AAPS PharmSciTech.
, vol.6
-
-
Airaksinen, S.1
Karkalainen, M.2
Kivikero, N.3
-
2
-
-
0033047536
-
The safety of pharmaceutical excipients
-
De Jong HJ. The safety of pharmaceutical excipients. Therapie 1999;54:11-14 (Pubitemid 29145965)
-
(1999)
Therapie
, vol.54
, Issue.1
, pp. 11-14
-
-
De Jong, H.J.1
-
3
-
-
0033732478
-
Pharmaceutical excipient development: The need for preclinical guidance
-
Baldrick P. Pharmaceutical Excipient development: the need for preclinical guidance. Regul Toxicol Pharmacol 2000;9:210-18
-
(2000)
Regul. Toxicol. Pharmacol.
, vol.9
, pp. 210-218
-
-
Baldrick, P.1
-
5
-
-
76549134059
-
Novel multifunctional pharmaceutical excipients derived from microcrystalline cellulose-starch microparticulate composites prepared by compatibilized reactive polymer blending
-
Builders PF, Bonaventure AM, Tisalade A, et al. Novel multifunctional pharmaceutical excipients derived from microcrystalline cellulose-starch microparticulate composites prepared by compatibilized reactive polymer blending. Int J Pharm 2010;388:159-67
-
(2010)
Int. J. Pharm.
, vol.388
, pp. 159-167
-
-
Builders, P.F.1
Bonaventure, A.M.2
Tisalade, A.3
-
6
-
-
84856103802
-
Reliable binders made new again by clever modification
-
February/March: 1-2
-
Shaffer C. Reliable binders made new again by clever modification. Pharm Formulation Qual 2010;February/March:1-2
-
(2010)
Pharm. Formulation. Qual.
-
-
Shaffer, C.1
-
7
-
-
0033527272
-
Regulatory issues with excipients
-
Robertson MI. Regulatory issues with excipients. Int J Pharm 1999;187:273-6
-
(1999)
Int. J. Pharm.
, vol.187
, pp. 273-276
-
-
Robertson, M.I.1
-
8
-
-
84856112972
-
Functionality and performance of excipients
-
October: 1-8
-
Moreton RC. Functionality and performance of excipients. Pharm Technol 2006;October:1-8
-
(2006)
Pharm. Technol.
-
-
Moreton, R.C.1
-
9
-
-
0042320719
-
A review and classification of: Emerging excipients in parenteral medications
-
Apte SP, Ugwu SO. A review and classification of emerging excipients in parenteral medications. Pharm Technol 2003;27:46-60 (Pubitemid 37101917)
-
(2003)
Pharmaceutical Technology
, vol.27
, Issue.3
, pp. 46-60
-
-
Apte, S.P.1
Ugwu, S.O.2
-
10
-
-
76149135185
-
High functionality excipients: A review
-
Deorkar N, Baker M. High functionality excipients: a review. Tablets Capsules 2008;6:22-7
-
(2008)
Tablets Capsules
, vol.6
, pp. 22-27
-
-
Deorkar, N.1
Baker, M.2
-
11
-
-
84887939959
-
Emerging role of excipients in the pharmaceutical industry
-
August:
-
Sonal SM, Jiny VK, Aneesh TP, et al. Emerging role of excipients in the pharmaceutical industry. Pharm Biol World 2008;August:63-6
-
(2008)
Pharm. Biol. World
, pp. 63-66
-
-
Sonal, S.M.1
Jiny, V.K.2
Aneesh, T.P.3
-
12
-
-
0033816196
-
Intestinal permeation enhancers
-
Aungst BJ. Intestinal permeation enhancers. J Pharm Sci 2000;89:429-42
-
(2000)
J. Pharm. Sci.
, vol.89
, pp. 429-442
-
-
Aungst, B.J.1
-
13
-
-
46749122375
-
Safe and effective permeation enhancers for oral drug delivery
-
Whitehead K, Karr N, Mitragotri S. Safe and effective permeation enhancers for oral drug delivery. Pharm Res 2008;25:1782-8
-
(2008)
Pharm. Res.
, vol.25
, pp. 1782-1788
-
-
Whitehead, K.1
Karr, N.2
Mitragotri, S.3
-
14
-
-
77953359223
-
The effects of excipients on transporter mediated absorption
-
Goole J, Lindley DJ, Roth W, et al. The effects of excipients on transporter mediated absorption. Int J Pharm 2010;393:17-31
-
(2010)
Int. J. Pharm.
, vol.393
, pp. 17-31
-
-
Goole, J.1
Lindley, D.J.2
Roth, W.3
-
15
-
-
39749137361
-
Difficulties in the production of identical drug products from a pharmaceutical technology viewpoint
-
DOI 10.2165/00126839-200809020-00001
-
Genazzani AA, Pattarino F. Difficulties in the production of identical drug products from pharmaceutical technology viewpoint. Drugs R D 2008;9:65-72 (Pubitemid 351311220)
-
(2008)
Drugs in R and D
, vol.9
, Issue.2
, pp. 65-72
-
-
Genazzani, A.A.1
Pattarino, F.2
-
17
-
-
71849101103
-
Alternative routes of administration for systemic delivery of protein pharmaceuticals
-
Moeller EH, Jorgensen L. Alternative routes of administration for systemic delivery of protein pharmaceuticals. Drug Discov Today Technol 2008;5:e90-4
-
(2008)
Drug. Discov. Today Technol.
, vol.5
-
-
Moeller, E.H.1
Jorgensen, L.2
-
18
-
-
2942612987
-
Membrane transporter/receptor-targeted prodrug design: Strategies for human and veterinary drug development
-
DOI 10.1016/j.addr.2004.02.006, PII S0169409X04000699, Veterinary Drug Delivery: Part VI
-
Majumdar S, Duvvuri S, Mitra AK. Membrane transporter/receptor-targeted prodrug design: strategies for human and veterinary drug development. Adv Drug Deliv Rev 2004;56:1437-52 (Pubitemid 38748825)
-
(2004)
Advanced Drug Delivery Reviews
, vol.56
, Issue.10
, pp. 1437-1452
-
-
Majumdar, S.1
Duvvuri, S.2
Mitra, A.K.3
-
19
-
-
40649116006
-
Discovery of tight junction modulators: Significance for drug development and delivery
-
Johnson PH, Frank D, Constantino HR. Discovery of tight junction modulators: significance for drug development and delivery. Drug Discov Today 2008;13:261-7
-
(2008)
Drug. Discov. Today
, vol.13
, pp. 261-267
-
-
Johnson, P.H.1
Frank, D.2
Constantino, H.R.3
-
20
-
-
0033120873
-
Transcellular uptake mechanisms of the intestinal epithelial barrier - Part one
-
DOI 10.1016/S1461-5347(99)00142-X, PII S146153479900142X
-
Daugherty AL, Mrsny R. Transcellular uptake mechanisms of the intestinal epithelial barrier: part one. Pharm Sci Technol Today 1999;4:144-51 (Pubitemid 29195747)
-
(1999)
Pharmaceutical Science and Technology Today
, vol.2
, Issue.4
, pp. 144-151
-
-
Daugherty, A.L.1
Mrsny, R.J.2
-
21
-
-
67749115965
-
Enhanced intracellular delivery using arginine-rich peptides by the addition penetration accelerating sequences Pas
-
Takayama K, Nakase I, Michiue H. Enhanced intracellular delivery using arginine-rich peptides by the addition penetration accelerating sequences (Pas). J Control Release 2009;138:128-33
-
(2009)
J. Control. Release.
, vol.138
, pp. 128-133
-
-
Takayama, K.1
Nakase, I.2
Michiue, H.3
-
22
-
-
0042167430
-
P-glycoprotein inhibitors and their screening: A perspective from bioavailability enhancement
-
DOI 10.1016/S1043-6618(03)00158-0
-
Varma MVS, Ashokraj Y, Dey CS, Panchagnula R. P-glycoprotein inhibitors: and their screening: a perspective from bioavailability enhancement. Pharmacol Res 2003;48:347-59 (Pubitemid 36945333)
-
(2003)
Pharmacological Research
, vol.48
, Issue.4
, pp. 347-359
-
-
Varma, M.V.S.1
Ashokraj, Y.2
Dey, C.S.3
Panchagnula, R.4
-
23
-
-
0032917517
-
Effect of chitosan on epithelial permeability and structure
-
DOI 10.1016/S0378-5173(99)00030-7, PII S0378517399000307
-
Dodane V, Khan MA, Merwin JR. Effect of chitosan on epithelial permeability and structure. Int J Pharm 1999;182:21-32 (Pubitemid 29229791)
-
(1999)
International Journal of Pharmaceutics
, vol.182
, Issue.1
, pp. 21-32
-
-
Dodane, V.1
Amin Khan, M.2
Merwin, J.R.3
-
24
-
-
0028124642
-
Chitosan as a novel nasal delivery system for peptide drugs
-
DOI 10.1023/A:1018901302450
-
Illum L, Farraj NF, Davis SS. Chitosan as a novel nasal delivery system for peptide drugs. Pharm Res 1994;11:1186-9 (Pubitemid 24259861)
-
(1994)
Pharmaceutical Research
, vol.11
, Issue.8
, pp. 1186-1189
-
-
Illum, L.1
Farraj, N.F.2
Davis, S.S.3
-
25
-
-
19344364333
-
Buccal penetration enhancement properties of N-trimethyl chitosan: Influence of quaternization degree on absorption of a high molecular weight molecule
-
DOI 10.1016/j.ijpharm.2005.03.017, PII S0378517305002000
-
Sandri G, Rossi S, Bonferoni MC. Buccal penetration enhancement properties of N-trimethyl chitosan: influence of quaternisation degree on absorption of high molecular weight molecule. Int J Pharm 2005;297:146-55 (Pubitemid 40720274)
-
(2005)
International Journal of Pharmaceutics
, vol.297
, Issue.1-2
, pp. 146-155
-
-
Sandri, G.1
Rossi, S.2
Bonferoni, M.C.3
Ferrari, F.4
Zambito, Y.5
Di Colo, G.6
Caramella, C.7
-
26
-
-
29244456136
-
Enhancement of bronchial octreotide absorption by chitosan and N-trimethyl chitosan shows linear in vitro/in vivo correlation
-
DOI 10.1016/j.jconrel.2005.10.001, PII S0168365905005262
-
Florea BI, Thanou M, Junginger HE, Borchard G. Enhancement of bronchial octreotide absorption by chitosan and N-trimethyl chitosan shows linear in vitro/in vivo correlation. J Control Release 2006;110:353-61 (Pubitemid 41827489)
-
(2006)
Journal of Controlled Release
, vol.110
, Issue.2
, pp. 353-361
-
-
Florea, B.I.1
Thanou, M.2
Junginger, H.E.3
Borchard, G.4
-
27
-
-
42649106817
-
Transdermal permeation enhancement of N-trimethyl chitosan for testosterone
-
He W, Guo X, Zhang M. Transdermal permeation enhancement of N-trimethyl chitosan for testosterone. Int J Pharm 2008;356:82-7
-
(2008)
Int. J. Pharm.
, vol.356
, pp. 82-87
-
-
He, W.1
Guo, X.2
Zhang, M.3
-
28
-
-
0034601240
-
Improving drug solubility for oral delivery using solid dispersions
-
DOI 10.1016/S0939-6411(00)00076-X, PII S093964110000076X
-
Leuner C, Dressman J. Improving drug solubility for oral delivery using solid dispersions. Eur J Pharm Biopharm 2000;50:47-60 (Pubitemid 30326688)
-
(2000)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.50
, Issue.1
, pp. 47-60
-
-
Leuner, C.1
Dressman, J.2
-
30
-
-
34447536520
-
When poor solubility becomes an issue: From early stage to proof of concept
-
DOI 10.1016/j.ejps.2007.05.110, PII S0928098707002345
-
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 (Pubitemid 47079001)
-
(2007)
European Journal of Pharmaceutical Sciences
, vol.31
, Issue.5
, pp. 249-261
-
-
Stegemann, S.1
Leveiller, F.2
Franchi, D.3
-
31
-
-
0037406422
-
Dissolution behavior of a poorly water soluble compound in the presence of Tween 80
-
DOI 10.1023/A:1023493821302
-
Chen LR, Wesley JA, Bhattachar S, et al. Dissolution behavior of a poorly water soluble compound in the presence of Tween 80. Pharm Res 2003;20:797-801 (Pubitemid 36515313)
-
(2003)
Pharmaceutical Research
, vol.20
, Issue.5
, pp. 797-801
-
-
Chen, L.R.1
Wesley, J.A.2
Bhattachar, S.3
Ruiz, B.4
Bahash, K.5
Babu, S.R.6
-
32
-
-
33947487639
-
The rate of solution of solids in their own solutions
-
Noyes AA, Whitney WR. The rate of solution of solids in their own solutions. J Am Chem Soc 1897;19:930-4
-
(1897)
J. Am. Chem. Soc.
, vol.19
, pp. 930-934
-
-
Noyes, A.A.1
Whitney, W.R.2
-
33
-
-
0343527392
-
Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standards
-
DOI 10.1016/S0939-6411(00)00091-6, PII S0939641100000916
-
Lobenberg R, Amidon GL. Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standards. Eur J Pharm Biopharm 2000;50:3-12 (Pubitemid 30326685)
-
(2000)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.50
, Issue.1
, pp. 3-12
-
-
Lobenberg, R.1
Amidon, G.L.2
-
34
-
-
1242337285
-
Solubilizing Excipients in Oral and Injectable Formulations
-
DOI 10.1023/B:PHAM.0000016235.32639.23
-
Strickley RG. Solubilizing excipients in oral and injectable formulations. Pharm Res 2004;21:201-30 (Pubitemid 38221966)
-
(2004)
Pharmaceutical Research
, vol.21
, Issue.2
, pp. 201-230
-
-
Strickley, R.G.1
-
37
-
-
80052695630
-
Strategies for solubility enhancement of poorly soluble drugs
-
Patil SK, Wagh KS, Parik VB, et al. Strategies for solubility enhancement of poorly soluble drugs. IJPSRR 2011;8:74-80
-
(2011)
IJPSRR
, vol.8
, pp. 74-80
-
-
Patil, S.K.1
Wagh, K.S.2
Parik, V.B.3
-
39
-
-
33644892211
-
Solubilization behavior of a poorly soluble drug under combined use of surfactants and cosolvents
-
Kawakami K, Oda N, Myoshi K, et al. Solubilization behavior of a poorly soluble drug under combined use of surfactants and cosolvents. Eur J Pharm Sci 2006;28:7-14
-
(2006)
Eur. J. Pharm. Sci.
, vol.28
, pp. 7-14
-
-
Kawakami, K.1
Oda, N.2
Myoshi, K.3
-
40
-
-
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
-
Pouton CW. Formulation of poorly water-soluble drugs for oral administration: physicochemical and physiological issues and the lipid formulation classification system. Eur J Pharm Sci 2006;29:278-87 (Pubitemid 44740131)
-
(2006)
European Journal of Pharmaceutical Sciences
, vol.29
, Issue.3-4 SPEC. ISSUE
, pp. 278-287
-
-
Pouton, C.W.1
-
41
-
-
39149113817
-
Formulation of lipid-based delivery systems for oral administration: Materials methods and strategies
-
Pouton CW, Porter CJH. Formulation of lipid-based delivery systems for oral administration: materials, methods and strategies. Adv Drug Deliv Rev 2008;60:625-37
-
(2008)
Adv. Drug. Deliv. Rev.
, vol.60
, pp. 625-637
-
-
Pouton, C.W.1
Porter, C.J.H.2
-
42
-
-
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:S93-8
-
(2000)
Eur. J. Pharm. Sci.
, vol.11
-
-
Pouton, C.W.1
-
43
-
-
1842684453
-
Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs
-
DOI 10.1016/j.biopha.2004.02.001, PII S0753332204000319
-
Gursoy RN, Benita S. Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs. Biomed Pharmacother 2004;58:173-82 (Pubitemid 38479922)
-
(2004)
Biomedicine and Pharmacotherapy
, vol.58
, Issue.3
, pp. 173-182
-
-
Gursoy, R.N.1
Benita, S.2
-
44
-
-
79952026399
-
Novel strategies for poorly water soluble drugs
-
Bindu MB, Kusum B, Banji D. Novel strategies for poorly water soluble drugs. IJPSRR 2010;4:76-84
-
(2010)
IJPSRR
, vol.4
, pp. 76-84
-
-
Bindu, M.B.1
Kusum, B.2
Banji, D.3
-
45
-
-
34548134519
-
Cyclodextrins as pharmaceutical solubilizers
-
DOI 10.1016/j.addr.2007.05.012, PII S0169409X07000841
-
Brewster ME, Loftsson T. Cyclodextrins as pharmaceutical solubilizers. Adv Drug Deliv Rev 2007;59:645-66 (Pubitemid 47299263)
-
(2007)
Advanced Drug Delivery Reviews
, vol.59
, Issue.7
, pp. 645-666
-
-
Brewster, M.E.1
Loftsson, T.2
-
48
-
-
0033151655
-
Excipients as stabilizers
-
DOI 10.1016/S1461-5347(99)00158-3, PII S1461534799001583
-
Crowley PJ. Excipients as stabilizers. Pharm Sci Technol Today 1999;2:237-43 (Pubitemid 29272083)
-
(1999)
Pharmaceutical Science and Technology Today
, vol.2
, Issue.6
, pp. 237-243
-
-
Crowley, P.J.1
-
49
-
-
0037376928
-
Pharmaceutical profiling in drug discovery
-
DOI 10.1016/S1359-6446(03)02649-7, PII S1359644603026497
-
Kerns EH, Di L. Pharmaceutical profiling in drug discovery. Drug Discov Today 2003;8:316-23 (Pubitemid 36332223)
-
(2003)
Drug Discovery Today
, vol.8
, Issue.7
, pp. 316-323
-
-
Kerns, E.H.1
Di, L.2
-
51
-
-
0032940406
-
Quality and functionality of excipients
-
DOI 10.1016/S0014-827X(98)00101-3, PII S0014827X98001013
-
Pifferi G, Santoro P, Pedrani M. Quality and functionality of excipients. Il Farmaco 1999;54:1-14 (Pubitemid 29187013)
-
(1999)
Farmaco
, vol.54
, Issue.1-2
, pp. 1-14
-
-
Pifferi, G.1
Santoro, P.2
Pedrani, M.3
-
52
-
-
42749083249
-
PH control of nucleophilic/ electrophilic oxidation
-
Freed AL, Strohmeyer HE, Mahjour M, et al. pH control of nucleophilic/ electrophilic oxidation. Int J Pharm 2008;357:180-8
-
(2008)
Int. J. Pharm.
, vol.357
, pp. 180-188
-
-
Freed, A.L.1
Strohmeyer, H.E.2
Mahjour, M.3
-
54
-
-
0029819323
-
Pharmaceutical applications of cyclodextrins. 1. Drug solubilization and stabilization
-
DOI 10.1021/js950534b
-
Loftsson T, Brewster ME. Pharmaceutical applications of cyclodextrins. 1. Drug solubilisation and stabilization. J Pharm Sci 1996;85:1017-25 (Pubitemid 26338912)
-
(1996)
Journal of Pharmaceutical Sciences
, vol.85
, Issue.10
, pp. 1017-1025
-
-
Loftsson, T.1
Brewster, M.E.2
-
56
-
-
77955050125
-
Approaches to improve the stability of the antiviral agent UC781 in aqueous solutions
-
Damian F, Fabian J, Friend DR, Kiser PF. Approaches to improve the stability of the antiviral agent UC781 in aqueous solutions. Int J Pharm 2010;396:1-10
-
(2010)
Int. J. Pharm.
, vol.396
, pp. 1-10
-
-
Damian, F.1
Fabian, J.2
Friend, D.R.3
Kiser, P.F.4
-
57
-
-
0030006768
-
The effect of pH, buffer type and drug concentration on the photodegradation of ciprofloxacin
-
DOI 10.1016/0378-5173(95)04332-2
-
Torniainen K, Tammiletho S, Ulvi V. The effect of pH, buffer type and drug concentration on the photodegradation of ciprofloxacin. Int J Pharm 1996;132:53-61 (Pubitemid 26158711)
-
(1996)
International Journal of Pharmaceutics
, vol.132
, Issue.1-2
, pp. 53-61
-
-
Torniainen, K.1
Tammilehto, S.2
Ulvi, V.3
-
58
-
-
0346373763
-
Coprocessed Excipients for Solid Dosage Forms
-
Nachaegari SK, Bansal AK. Coprocessed excipients for solid dosage forms. Pharm Tech 2004;January:52-64 (Pubitemid 38095734)
-
(2004)
Pharmaceutical Technology
, vol.28
, Issue.1
, pp. 52-64
-
-
Nachaegari, S.K.1
Bansal, A.K.2
-
60
-
-
0033766050
-
Starch acetates - Multifunctional direct compression excipients
-
Korhonen O, Raatikainen P, Harjunen P, et al. Starch acetates - multifunctional direct compression excipients. Pharm Res 2000;17:1138-43
-
(2000)
Pharm. Res.
, vol.17
, pp. 1138-1143
-
-
Korhonen, O.1
Raatikainen, P.2
Harjunen, P.3
-
61
-
-
68649091305
-
Polymeric plant-derived excipients in drug delivery
-
Beneke CE, Viljoen AM, Hamman JH. Polymeric plant-derived excipients in drug delivery. Molecules 2009;14:2602-20
-
(2009)
Molecules
, vol.14
, pp. 2602-2620
-
-
Beneke, C.E.1
Viljoen, A.M.2
Hamman, J.H.3
-
62
-
-
84255166182
-
Coprocessing of excipients: A review on excipient development for improved tabletting performance
-
Marwaha M, Sandhu D, Marwaha RK. Coprocessing of excipients: A review on excipient development for improved tabletting performance. Int J Appl Pharm 2010;2:41-7
-
(2010)
Int. J. Appl. Pharm.
, vol.2
, pp. 41-47
-
-
Marwaha, M.1
Sandhu, D.2
Marwaha, R.K.3
-
65
-
-
78649742248
-
Development and evaluation of a directly compressible co-processed multifunction sustained release agent for tablets
-
Ayyappan J, Umapathi P, Darlin Q. Development and evaluation of a directly compressible co-processed multifunction sustained release agent for tablets. Int J Pharm Pharm Sci 2010;2:201-5
-
(2010)
Int. J. Pharm. Pharm. Sci.
, vol.2
, pp. 201-205
-
-
Ayyappan, J.1
Umapathi, P.2
Darlin, Q.3
-
66
-
-
80053939620
-
Co-processed MCC-Eudragit E excipients for extrusion-spheronization
-
published online 13 July 2011;:10.1016/j.ejpb.2011.07.013
-
Goyanes A, Souto C, Martinez-Pacheco R. Co-processed MCC-Eudragit E excipients for extrusion-spheronization. Eur J Pharm Biopharm 2011;published online 13 July 2011; doi:10.1016/j.ejpb.2011.07.013
-
(2011)
Eur. J. Pharm. Biopharm.
-
-
Goyanes, A.1
Souto, C.2
Martinez-Pacheco, R.3
-
67
-
-
79955974328
-
A novel multifunctional pharmaceutical excipient: Modification of the permeability of starch by processing with magnesium silicate
-
Rashid I, Al-Remawi M, Leharne SA, et al. A novel multifunctional pharmaceutical excipient: Modification of the permeability of starch by processing with magnesium silicate. Int J Pharm 2011;411:18-26
-
(2011)
Int. J. Pharm.
, vol.411
, pp. 18-26
-
-
Rashid, I.1
Al-Remawi, M.2
Leharne, S.A.3
-
68
-
-
37849189719
-
PH-independent drug release of an extremely poorly soluble weakly acidic drug from multiparticulate extended release formulations
-
DOI 10.1016/j.ejpb.2006.07.001, PII S0939641106001615
-
Riis T, Bauer-Brandl A, Wagner T, Kranz H. pH-independent drug release of an extremely poorly soluble weakly acidic drug from multiparticulate extended release formulations. Eur J Pharm Biopharm 2007;65:78-84 (Pubitemid 44827687)
-
(2007)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.65
, Issue.1
, pp. 78-84
-
-
Riis, T.1
Bauer-Brandl, A.2
Wagner, T.3
Kranz, H.4
-
70
-
-
38549148812
-
Design and evaluation of matrix based controlled release tablets of diclofenac sodium and chondroitin sulphate
-
Avachat A, Kotwal V. Design and evaluation of matrix based controlled release tablets of diclofenac sodium and chondroitin sulphate. AAPS PharmSciTech 2007;8:E1-6
-
(2007)
AAPS PharmSciTech.
, vol.8
-
-
Avachat, A.1
Kotwal, V.2
-
71
-
-
0029032750
-
Swelling and drug release behavior of xanthan gum matrix tablets
-
Talukdar MM, Kinget R. Swelling and drug release behavior of xanthan gum matrix tablets. Int J Pharm 1995;120:63-72
-
(1995)
Int. J. Pharm.
, vol.120
, pp. 63-72
-
-
Talukdar, M.M.1
Kinget, R.2
-
73
-
-
0037161324
-
Guar-based monolithic matrix systems: Effect of ionizable and non-ionizable substances and excipients on gel dynamics and release kinetics
-
DOI 10.1016/S0168-3659(01)00546-6, PII S0168365901005466
-
Durig T, Fassihi R. Guar-based monolithic systems: effect of ionizable and non-ionizable substances and excipients on gel dynamics and release kinetics. J Control Release 2002;80:45-56 (Pubitemid 34273747)
-
(2002)
Journal of Controlled Release
, vol.80
, Issue.1-3
, pp. 45-56
-
-
Durig, T.1
Fassihi, R.2
-
74
-
-
33847268238
-
High-amylose carboxymethyl starch matrices for oral sustained drug-release: In vitro and in vivo evaluation
-
Nabais T, Brouillet F, Kyriacos S, et al. High-amylose carboxymethyl starch matrices for oral sustained drug-release: in vitro and in vivo evaluation. Eur J Pharm Biopharm 2007;65:371-8
-
(2007)
Eur. J. Pharm. Biopharm.
, vol.65
, pp. 371-378
-
-
Nabais, T.1
Brouillet, F.2
Kyriacos, S.3
-
75
-
-
2142770192
-
Drug release from carbomer:carbomer sodium salt matrices with potential use as mucoadhesive drug delivery system
-
DOI 10.1016/j.ijpharm.2004.02.006, PII S0378517304001097
-
Llabot JM, Manzo RH, Allemandi DA. Drug release from carbomer:carbomer sodium salt matrices with potential use as mucoadhesive drug delivery system. Int J Pharm 2004;276:59-66 (Pubitemid 38542988)
-
(2004)
International Journal of Pharmaceutics
, vol.276
, Issue.1-2
, pp. 59-66
-
-
Llabot, J.M.1
Manzo, R.H.2
Allemandi, D.A.3
-
76
-
-
34250802136
-
Swelling and erosion of pectin matrix tablets and their impact on drug release behavior
-
DOI 10.1016/j.ejpb.2006.12.014, PII S0939641106003808
-
Sriamornsak P, Thirawong N, Weerapol Y, et al. Swelling and erosion of pectin matrix tablets and their impact on drug release behavior. Eur J Pharm Biopharm 2007;67:211-19 (Pubitemid 46991322)
-
(2007)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.67
, Issue.1
, pp. 211-219
-
-
Sriamornsak, P.1
Thirawong, N.2
Weerapol, Y.3
Nunthanid, J.4
Sungthongjeen, S.5
-
77
-
-
34347213452
-
Effect of oppositely charged polymer and dissolution medium on swelling, erosion, and drug release from chitosan matrices
-
DOI 10.1208/pt0802027, 44
-
Bhise KS, Dhumal RS, Chauhan B, et al. Effect of oppositely charged polymer and dissolution medium on swelling erosion and drug release from chitosan matrices. AAPS PharmSciTech 2007;8:E1-9 (Pubitemid 47007411)
-
(2007)
AAPS PharmSciTech
, vol.8
, Issue.2
-
-
Bhise, K.S.1
Dhumal, R.S.2
Chauhan, B.3
Paradkar, A.4
Kadam, S.S.5
-
78
-
-
36549061102
-
Preparation of an extended-release matrix tablet using chitosan/Carbopol interpolymer complex
-
DOI 10.1016/j.ijpharm.2007.06.024, PII S0378517307005194
-
Park S-H, Chun M-K, Choi H-K. Preparation of an extended release matrix tablet using chitosan/Carbopol interpolymer complex. Int J Pharm 2008;347:39-44 (Pubitemid 350180315)
-
(2008)
International Journal of Pharmaceutics
, vol.347
, Issue.1-2
, pp. 39-44
-
-
Park, S.-H.1
Chun, M.-K.2
Choi, H.-K.3
-
79
-
-
71049155416
-
Interpolyelectrolyte complexes of Eudragit EPO with sodium alginate as potential carriers for colonic drug delivery: Monitoring of structural transformation and composition changes during swellability and release evaluating
-
Moustafine RI, Salachova AR, Frolova ES, et al. Interpolyelectrolyte complexes of Eudragit EPO with sodium alginate as potential carriers for colonic drug delivery: monitoring of structural transformation and composition changes during swellability and release evaluating. Drug Dev Ind Pharm 2009;35:1439-51
-
(2009)
Drug. Dev. Ind. Pharm.
, vol.35
, pp. 1439-1451
-
-
Moustafine, R.I.1
Salachova, A.R.2
Frolova, E.S.3
-
81
-
-
55849090299
-
Responsive polymers in controlled drug delivery
-
Bajpai AK, Shukla SK, Bhanu S, et al. Responsive polymers in controlled drug delivery. Prog Polym Sci 2008;33:1088-118
-
(2008)
Prog. Polym. Sci.
, vol.33
, pp. 1088-1118
-
-
Bajpai, A.K.1
Shukla, S.K.2
Bhanu, S.3
-
83
-
-
71749113420
-
Architecture and composition influence on he properties of some smart polymeric materials designed as matrices in drug delivery systems
-
Vasile C, Dumitriu RP, Cheaburu CN, Oprea AM. Architecture and composition influence on he properties of some smart polymeric materials designed as matrices in drug delivery systems. Appl Surface Sci 2009;256S:S65-71
-
(2009)
Appl. Surface. Sci.
, vol.256 S
-
-
Vasile, C.1
Dumitriu, R.P.2
Cheaburu, C.N.3
Oprea, A.M.4
-
85
-
-
0037413385
-
Enhanced transport of a novel anti-HIV agent - Cosalane and its congeners across human intestinal epithelial (Caco-2) cell monolayers
-
DOI 10.1016/S0378-5173(02)00523-9, PII S0378517302005239
-
Udata C, Patel J, Pal D, et al. Enhanced transport of a novel anti-HIV agent - cosalane and its congeners across human intestinal epithelial (Caco-2) cell monolayers. Int J Pharm 2003;250:157-68 (Pubitemid 35447946)
-
(2003)
International Journal of Pharmaceutics
, vol.250
, Issue.1
, pp. 157-168
-
-
Udata, C.1
Patel, J.2
Pal, D.3
Hejchman, E.4
Cushman, M.5
Mitra, A.K.6
-
86
-
-
0034027744
-
3-antagonist in a human intestinal cell line (Caco-2)
-
DOI 10.1016/S0928-0987(99)00092-5, PII S0928098799000925
-
Kamm W, Jonczyk A, Jung T, et al. Evaluation of absorption enhancement for a potent cyclopeptidic alphanubeta3-antagonist in a human intestinal cell line (Caco-2). Eur J Pharm Sci 2000;10:205-14 (Pubitemid 30190096)
-
(2000)
European Journal of Pharmaceutical Sciences
, vol.10
, Issue.3
, pp. 205-214
-
-
Kamm, W.1
Jonczyk, A.2
Jung, T.3
Luckenbach, G.4
Raddatz, P.5
Kissel, T.6
-
87
-
-
27744448891
-
Absorption enhancement, mechanistic and toxicity studies of medium chain fatty acids, cyclodextrins and bile salts as peroral absorption enhancers
-
DOI 10.1016/j.farmac.2005.08.008, PII S0014827X05001874
-
Sharma P, Varma MVS, Chawla HPS, et al. Absorption enhancement, mechanistic and toxicity studies of medium chain fatty acids, cyclodextrins and bile salts as peroral absorption enhancers. Il Farmaco 2005;60:884-93 (Pubitemid 41586262)
-
(2005)
Farmaco
, vol.60
, Issue.11-12
, pp. 884-893
-
-
Sharma, P.1
Varma, M.V.S.2
Chawla, H.P.S.3
Panchagnula, R.4
-
88
-
-
34248673162
-
Absorption enhancement of poorly absorbed hydrophilic compounds from various mucosal sites by combination of mucolytic agent and non-ionic surfactant
-
DOI 10.1016/j.ijpharm.2007.01.027, PII S0378517307000609
-
Takatsuka S, Morita T, Horikiri Y, et al. Absorption enhancement of poorly absorbed hydrophilic compounds from various mucosal sites by combination of mucolytic agent and non-ionic surfactant. Int J Pharm 2007;338:87-93 (Pubitemid 46777222)
-
(2007)
International Journal of Pharmaceutics
, vol.338
, Issue.1-2
, pp. 87-93
-
-
Takatsuka, S.1
Morita, T.2
Horikiri, Y.3
Yamahara, H.4
Saji, H.5
-
89
-
-
38049183272
-
Mechanistic understanding of oral drug absorption enhancement of chromolyn sodium by an amino acid derivative
-
Alani AWG, Robinson JR. Mechanistic understanding of oral drug absorption enhancement of chromolyn sodium by an amino acid derivative. Pharm Res 2007;25:48-54
-
(2007)
Pharm. Res.
, vol.25
, pp. 48-54
-
-
Alani, A.W.G.1
Robinson, J.R.2
-
90
-
-
11844272009
-
The impact of deltag on the oral bioavailability of low bioavailable therapeutic agents
-
Salama NN, Fasano A, Thakar M, Eddington ND. The impact of DeltaG on the oral bioavailability of low bioavailable therapeutic agents. J Pharmacol Exp Ther 2004;312:199-205
-
(2004)
J. Pharmacol. Exp. Ther.
, vol.312
, pp. 199-205
-
-
Salama, N.N.1
Fasano, A.2
Thakar, M.3
Eddington, N.D.4
-
91
-
-
14344266887
-
Evaluation of dodecylmaltoside as a permeability enhancer for insulin using human carcinoma cells
-
DOI 10.1002/jps.20234
-
Tirumalasetty PP, Eley JG. Evaluation of dodecylmaltoside as a permeability enhancer of insulin using human carcinoma cells. J Pharm Sci 2005;94:246-55 (Pubitemid 40293322)
-
(2005)
Journal of Pharmaceutical Sciences
, vol.94
, Issue.2
, pp. 246-255
-
-
Tirumalasetty, P.P.1
Eley, J.G.2
-
92
-
-
35348961566
-
Modulation of Ganciclovir intestinal absorption in presence of absorption enhancers
-
DOI 10.1002/jps.20888
-
Shah P, Jogani V, Mishra P, et al. Modulation of ganciclovir intestinal absorption in presence of absorption enhancers. J Pharm Sci 2007;96:2710-22 (Pubitemid 47597820)
-
(2007)
Journal of Pharmaceutical Sciences
, vol.96
, Issue.10
, pp. 2710-2722
-
-
Shah, P.1
Jogani, V.2
Mishra, P.3
Mishra, A.K.4
Bagchi, T.5
Misra, A.6
-
93
-
-
52449102429
-
Complexation hydrogels for oral insulin delivery: Effects of polymer dosing on in vivo efficacy
-
Tuesca A, Nakamura K, Morishita M, et al. Complexation hydrogels for oral insulin delivery: effects of polymer dosing on in vivo efficacy. J Pharm Sci 2008;97:2607-18
-
(2008)
J. Pharm. Sci.
, vol.97
, pp. 2607-2618
-
-
Tuesca, A.1
Nakamura, K.2
Morishita, M.3
-
94
-
-
70349843043
-
Evaluation of intestinal absorption enhancement and localmucosal toxicity of two promoters I studies in isolated rat and human colonic mucosae
-
Maher S, Kennelly R, Bzik VA, et al. Evaluation of intestinal absorption enhancement and localmucosal toxicity of two promoters. I. Studies in isolated rat and human colonic mucosae. Eur J Pharm Sci 2009;38:291-300
-
(2009)
Eur. J. Pharm. Sci.
, Issue.38
, pp. 291-230
-
-
Maher, S.1
Kennelly, R.2
Bzik, V.A.3
-
96
-
-
75849130569
-
Effect of sinomenine on the in vitro intestinal epithelial transport of selected compounds
-
Lu Z, Chen W, Viljoen A, Hamman J. Effect of sinomenine on the in vitro intestinal epithelial transport of selected compounds. Phytother Res 2010;24:211-18
-
(2010)
Phytother. Res.
, vol.24
, pp. 211-218
-
-
Lu, Z.1
Chen, W.2
Viljoen, A.3
Hamman, J.4
-
97
-
-
0033843181
-
Oral absorption of peptides through the cobalamin (vitamin B12) pathway in the rat intestine
-
DOI 10.1023/A:1007556108673
-
Alsenz J, Russell-Jones GJ, Westwood S, et al. Oral absorption of peptides through the cobalamin (vitamin B12) pathway in the rat intestine. Pharm Res 2000;17:825-32 (Pubitemid 30666963)
-
(2000)
Pharmaceutical Research
, vol.17
, Issue.7
, pp. 825-832
-
-
Alsenz, J.1
Russell-Jones, G.J.2
Westwood, S.3
Levet-Trafit, B.4
De Smidt, P.C.5
-
98
-
-
0034938085
-
Model prodrugs designed for the intestinal peptide transporter. A synthetic approach for coupling of hydroxy-containing compounds to dipeptides
-
DOI 10.1016/S0928-0987(01)00137-3, PII S0928098701001373
-
Friedrichsen GM, Nielsen CU, Steffansen B, Begtrup M. Model prodrugs designed for the intestinal peptide transporter. A synthetic approach for coupling of hydroxyl-containing compounds to dipeptides. Eur J Pharm Sci 2001;14:13-19 (Pubitemid 32655410)
-
(2001)
European Journal of Pharmaceutical Sciences
, vol.14
, Issue.1
, pp. 13-19
-
-
Friedrichsen, G.M.1
Nielsen, C.U.2
Steffansen, B.3
Begtrup, M.4
-
99
-
-
1942487690
-
A novel per-oral insulin formulation: Proof of concept study in non-diabetic subjects
-
DOI 10.1111/j.1464-5491.2004.01160.x
-
Kidron M, Dinh S, Menachem A, et al. A novel peroral insulin formulation: proof of concept study in non-diabetic subjects. Diabet Med 2003;21:354-7 (Pubitemid 38519671)
-
(2004)
Diabetic Medicine
, vol.21
, Issue.4
, pp. 354-357
-
-
Kidron, M.1
Dinh, S.2
Menachem, Y.3
Abbast, R.4
Variano, B.5
Goldberg, M.6
Arbit, E.7
Bar-On, H.8
-
100
-
-
70349198899
-
Efficiency of cell-penetrating peptides on the nasal and intestinal absorption of therapeutic peptides and proteins
-
Khafagy ES, Morishita M, Kamei N, et al. Efficiency of cell-penetrating peptides on the nasal and intestinal absorption of therapeutic peptides and proteins. Int J Pharm 2009;381:49-55
-
(2009)
Int. J. Pharm.
, vol.381
, pp. 49-55
-
-
Khafagy, E.S.1
Morishita, M.2
Kamei, N.3
-
101
-
-
77955269563
-
Molecular imaging analysis of intestinal insulin absorption boosted by cell-penetrating peptides by using positron emission tomography
-
Kamei N, Morishita M, Kanayama Y, et al. Molecular imaging analysis of intestinal insulin absorption boosted by cell-penetrating peptides by using positron emission tomography. J Control Release 2010;146:16-22
-
(2010)
J. Control. Release.
, vol.146
, pp. 16-22
-
-
Kamei, N.1
Morishita, M.2
Kanayama, Y.3
-
102
-
-
0030790290
-
Mechanistic roles of neutral surfactants on concurrent polarized and passive membrane transport of a model peptide in Caco-2 cells
-
DOI 10.1021/js960483y
-
Nerurkar MM, Ho NFH, Burton PS, et al. Mechanistic roles of neutral surfactants on concurrent polarized and passive membrane transport of a model peptide in Caco-2 cells. J Pharm Sci 1997;86:813-21 (Pubitemid 27297493)
-
(1997)
Journal of Pharmaceutical Sciences
, vol.86
, Issue.7
, pp. 813-821
-
-
Nerurkar, M.M.1
Ho, N.F.H.2
Burton, P.S.3
Vidmar, T.J.4
Borchardt, R.T.5
-
104
-
-
0028948839
-
A theoretical basis for a biopharmaceutic drug classification: The correlation of the in vitro drug productdissolution and in vivo bioavailability
-
Amidon GL, Lennernas H, Shah V, et al. A theoretical basis for a biopharmaceutic drug classification: the correlation of the in vitro drug productdissolution and in vivo bioavailability. Pharm Res 1995;12:413-20
-
(1995)
Pharm. Res.
, vol.12
, pp. 413-420
-
-
Amidon, G.L.1
Lennernas, H.2
Shah, V.3
|