-
1
-
-
2642572791
-
Glibenclamide transdermal patches: Physicochemical, pharmacodynamic, and pharmacokinetic evaluations
-
DOI 10.1002/jps.20058
-
S. Mutalik, and N. Udupa Glibenclamide transdermal patches: physicochemical, pharmacodynamic, and pharmacokinetic evaluations J. Pharm. Sci. 93 6 2004 1577 1594 (Pubitemid 38725029)
-
(2004)
Journal of Pharmaceutical Sciences
, vol.93
, Issue.6
, pp. 1577-1594
-
-
Mutalik, S.1
Udupa, N.2
-
2
-
-
0020967084
-
Pharmacokinetics and effects of glibenclamide in two formulations, HB 419 and HB 420, in type 2 diabetes
-
H.J. Arnqvist, B.E. Karlberg, and A. Melander Pharmacokinetics and effects of glibenclamide in two formulations, HB 419 and HB 420, in type 2 diabetes Ann. Clin. Res. 37 1983 21 25 (Pubitemid 14124718)
-
(1983)
Annals of Clinical Research
, vol.15
, Issue.SUPPL. 37
, pp. 21-25
-
-
Arnqvist, H.J.1
Karlberg, B.E.2
Melander, A.3
-
3
-
-
0022909293
-
Correlations between in vitro dissolution, in vivo bioavailability and hypoglycaemic effect of oral glibenclamide
-
DOI 10.1007/BF00606655
-
J.B. Chalk, M. Patterson, M.T. Smith, and M.J. Eadie Correlation between in vitro dissolution, in vivo bioavailability and hypoglycaemic effect of oral glibenclamide Eur. J. Clin. Pharmacol. 31 1986 177 182 (Pubitemid 17014586)
-
(1986)
European Journal of Clinical Pharmacology
, vol.31
, Issue.2
, pp. 177-182
-
-
Chalk, J.B.1
Patterson, M.2
Smith, M.T.3
Eadie, M.J.4
-
4
-
-
10644275105
-
Enhancement of dissolution rate of poorly-soluble active ingredients by supercritical fluid processes: Part I: Micronization of neat particles
-
DOI 10.1016/j.ijpharm.2004.09.007, PII S0378517304005411
-
M. Perrut, J. Jung, and F. Leboeuf Enhancement of dissolution rate of poorly-soluble active ingredients by supercritical fluid processes. Part I: micronization of neat particles Int. J. Pharm. 288 2005 3 10 (Pubitemid 39656449)
-
(2005)
International Journal of Pharmaceutics
, vol.288
, Issue.1
, pp. 3-10
-
-
Perrut, M.1
Jung, J.2
Leboeuf, F.3
-
5
-
-
0343515548
-
Bioavailability and in vitro liberation of glibenclamide from a new dosage form
-
W. Rupp, M. Badian, W. Heptner, and V. Malerczyk Bioavailability and in vitro liberation of glibenclamide from a new dosage form Biopharm. Pharmacokinet., Eur. Congr. 2nd. 1 1984 413 420
-
(1984)
Biopharm. Pharmacokinet., Eur. Congr. 2nd.
, vol.1
, pp. 413-420
-
-
Rupp, W.1
Badian, M.2
Heptner, W.3
Malerczyk, V.4
-
7
-
-
0022608689
-
Effect of sodium lauryl sulphate and tween(R)80 on the therapeutic efficacy of glibenclamide tablet formulations in terms of BSL lowering in rabbits and diabetic human volunteers
-
J. Singh Effect of sodium lauryl sulfate and Tween 80 on the therapeutic efficacy of glibenclamide tablet formulations in terms of BSL lowering in rabbits and diabetic human volunteers Drug Dev. Ind. Pharm. 12 1986 851 866 (Pubitemid 16120824)
-
(1986)
Drug Development and Industrial Pharmacy
, vol.12
, Issue.6
, pp. 851-866
-
-
Singh, J.1
-
8
-
-
0021218129
-
The effect of in-vivo dispersion and gastric emptying on glibenclamide absorption from a novel, rapidly dissolving capsule formulation
-
J.A. Ganley, J. McEven, R.T. Calvert, and C.J. Barker The effect of in vivo dispension and gastric emptying on glibenclamide absorption from a novel, rapidly dissolving capsule formulation J. Pharm. Pharmacol. 36 1984 734 739 (Pubitemid 14021953)
-
(1984)
Journal of Pharmacy and Pharmacology
, vol.36
, Issue.11
, pp. 734-739
-
-
Ganley, J.A.1
Mcewen, J.2
Calvert, R.T.3
Barker, M.C.J.4
-
9
-
-
0029802558
-
Effect of grinding of cyclodextrin and glibenclamide on tablet properties. Part I. In vitro
-
A. Mitrevej, N. Sinchaipanid, V. Junyaprasert, and L. Warintornuwat Effect of grinding of cyclodextrin and glibenclamide on tablet properties Drug Dev. Ind. Pharm. 22 1996 1237 1241 (Pubitemid 26413041)
-
(1996)
Drug Development and Industrial Pharmacy
, vol.22
, Issue.12
, pp. 1237-1241
-
-
Mitrevej, A.1
Sinchaipanid, N.2
Junyaprasert, V.3
Warintornuwat, L.4
-
10
-
-
47249130261
-
Formulation of fast disintegrating tablets of ternary solid dispersions consisting of TPGS 1000 and HPMC 2910 or PVPVA 64 to improve the dissolution of the anti-HIV drug UC 871
-
C. Goddeeris, T. Willems, and G.V.D. Mooter Formulation of fast disintegrating tablets of ternary solid dispersions consisting of TPGS 1000 and HPMC 2910 or PVPVA 64 to improve the dissolution of the anti-HIV drug UC 871 Eur. J. Pharm. Sci. 34 2008 293 302
-
(2008)
Eur. J. Pharm. Sci.
, vol.34
, pp. 293-302
-
-
Goddeeris, C.1
Willems, T.2
Mooter, G.V.D.3
-
11
-
-
1142303337
-
What is the true solubility advantage for amorphous pharmaceuticals?
-
DOI 10.1023/A:1007516718048
-
B.C. Hancock, and M. Parks What is the true solubility advantage for amorphous pharmaceuticals? Pharm. Res. 17 2000 397 404 (Pubitemid 30395293)
-
(2000)
Pharmaceutical Research
, vol.17
, Issue.4
, pp. 397-404
-
-
Hancock, B.C.1
Parks, M.2
-
12
-
-
0030638567
-
Characteristics and significance of the amorphous state in pharmaceutical systems
-
B.C. Hancock, and G. Zografi Characteristics and significance of the amorphous state in pharmaceutical systems J. Pharm. Sci. 86 1997 1 12
-
(1997)
J. Pharm. Sci.
, vol.86
, pp. 1-12
-
-
Hancock, B.C.1
Zografi, G.2
-
14
-
-
77956431273
-
Study of the amorphous glibenclamide drug: Analysis of the molecular dynamics of quenched and cryomilled material
-
Z. Wojnarowska, K. Grzybowska, K. Adrjanowicz, and K. Kaminski Study of the amorphous glibenclamide drug: analysis of the molecular dynamics of quenched and cryomilled material Mol. Pharm. 7 2010 1692 1707
-
(2010)
Mol. Pharm.
, vol.7
, pp. 1692-1707
-
-
Wojnarowska, Z.1
Grzybowska, K.2
Adrjanowicz, K.3
Kaminski, K.4
-
15
-
-
4143055826
-
Preparation of microcrystals by in situ micronization
-
DOI 10.1016/j.powtec.2004.04.021, PII S0032591004001792
-
N. Rasenack, H. Steckel, and B.W. Müller Preparation of microcrystals by in situ micronization Powder Technol. 143-144 2004 291 296 (Pubitemid 39091949)
-
(2004)
Powder Technology
, vol.143-144
, pp. 291-296
-
-
Rasenack, N.1
Steckel, H.2
Muller, B.W.3
-
16
-
-
33750089277
-
Preparation and in vitro/in vivo evaluation of nano-sized crystals for dissolution rate enhancement of ucb-35440-3, a highly dosed poorly water-soluble weak base
-
DOI 10.1016/j.ejpb.2006.05.008, PII S0939641106001408
-
J. Hecq, M. Deleers, D. Franara, H. Vranckx, P. Boulanger, S.L. Lamer, and K. Amighi Preparation and in vitro/in vivo evaluation of nano-sized crystals for dissolution rate enchancement of ucb-35440-3, a highly dosed poorly water-soluble weak base Eur. J. Pharm. Biopharm. 64 2006 360 368 (Pubitemid 44585201)
-
(2006)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.64
, Issue.3
, pp. 360-368
-
-
Hecq, J.1
Deleers, M.2
Fanara, D.3
Vranckx, H.4
Boulanger, P.5
Le Lamer, S.6
Amighi, K.7
-
17
-
-
0036375657
-
Mixing and characterization of nanosized powders: An assessment of different techniques
-
DOI 10.1023/A:1020184524538
-
D. Wei, H.R. Dave, and R. Pfeffer Mixing and characterization of nanosized powders: an assessment of different techniques J. Nanopart. Res. 42 2002 21 41 (Pubitemid 135713399)
-
(2002)
Journal of Nanoparticle Research
, vol.4
, Issue.1-2
, pp. 21-41
-
-
Wei, D.1
Dave, R.2
Pfeffer, R.3
-
18
-
-
0034110573
-
Synthesis of nanoparticles with novel technology: High-gravity reactive precipitation
-
J.F. Chen, Y.H. Wang, F. Guo, X.M. Wang, and C. Zheng Synthesis of nanoparticles with novel technology: highgravity reactive precipitation Ind. Eng. Chem. Res. 39 2000 948 954 (Pubitemid 30210636)
-
(2000)
Industrial and Engineering Chemistry Research
, vol.39
, Issue.4
, pp. 948-954
-
-
Chen, J.-F.1
Wang, Y.-H.2
Guo, F.3
Wang, X.-M.4
Zheng, C.5
-
19
-
-
0348048800
-
Feasibility of preparing nanodrugs by high-gravity reactive precipitation
-
DOI 10.1016/j.ijpharm.2003.09.044
-
J.F. Chen, M.Y. Zhou, L. Shao, Y.H. Wang, J. Yun, N.Y.K. Chew, and H.K. Chan Feasibility of preparing nanodrugs by high gravity reactive precipitation Int. J. Pharm. 269 2004 267 274 (Pubitemid 38032839)
-
(2004)
International Journal of Pharmaceutics
, vol.269
, Issue.1
, pp. 267-274
-
-
Chen, J.-F.1
Zhou, M.-Y.2
Shao, L.3
Wang, Y.-Y.4
Yun, J.5
Chew, N.Y.K.6
Chan, H.-K.7
-
20
-
-
33748701219
-
Preparation of amorphous cefuroxime axetil nanoparticles by controlled nanoprecipitation method without surfactants
-
DOI 10.1016/j.ijpharm.2006.05.048, PII S0378517306004315
-
J.Y. Zhang, Z.G. Shen, J. Zhong, T.T. Hu, J.F. Chen, Z.Q. Ma, and J. Yun Preparation of amorphous cefuroxime axetil nanoparticles by controlled nanoprecipitation method without surfactants Int. J. Pharm. 323 2006 153 160 (Pubitemid 44397363)
-
(2006)
International Journal of Pharmaceutics
, vol.323
, Issue.1-2
, pp. 153-160
-
-
Zhang, J.-Y.1
Shen, Z.-G.2
Zhong, J.3
Hu, T.-T.4
Chen, J.-F.5
Ma, Z.-Q.6
Yun, J.7
-
21
-
-
0034042048
-
Rapid expansion from supercritical to aqueous solution to produce submicron suspensions of water-insoluble drugs
-
DOI 10.1021/bp000032q
-
T.J. Young, S.M. Mawson, K.P. Johnston, I.B. Henriksen, G.W. Pace, and A.K. Mishra Rapid expansion from supercritical to aqueous solution to produce submicron suspensions of water-insoluble drugs Biotechnol. Prog. 16 2000 402 407 (Pubitemid 30369011)
-
(2000)
Biotechnology Progress
, vol.16
, Issue.3
, pp. 402-407
-
-
Young, T.J.1
Mawson, S.2
Johnston, K.P.3
Henriksen, I.B.4
Pace, G.W.5
Mishra, A.K.6
-
22
-
-
0037189994
-
Enhanced drug dissolution using evaporative precipitation into aqueous solution
-
M. Sarkari, J. Brown Chen, X.S. Swinnea, R.O. Williams III, and K.P. Johnston Enhanced drug dissolution using evaporative precipitation into aqueous solution Int. J. Pharm. 243 1-2 2002 17 31
-
(2002)
Int. J. Pharm.
, vol.243
, Issue.12
, pp. 17-31
-
-
Sarkari, M.1
Brown Chen, J.2
Swinnea, X.S.3
Williams Iii, R.O.4
Johnston, K.P.5
-
23
-
-
21644446038
-
Development and characterization of a scalable controlled precipitation process to enhance the dissolution of poorly water-soluble drugs
-
DOI 10.1023/B:PHAM.0000048196.61887.e5
-
T.L. Rogers, I.B. Gillespie, J.E. Hitt, K.L. Fransen, C.A. Crowl, C.J. Tucker, G.B. Kupperblatt, J.N. Becker, D.L. Wilson, and C. Todd Development and characterization of a scalable controlled precipitation process to enhance the dissolution of poorly water-soluble drugs Pharm. Res. 21 2004 2048 2057 (Pubitemid 40941225)
-
(2004)
Pharmaceutical Research
, vol.21
, Issue.11
, pp. 2048-2057
-
-
Rogers, T.L.1
Gillespie, I.B.2
Hitt, J.E.3
Fransen, K.L.4
Crowl, C.A.5
Tucker, C.J.6
Kupperblatt, G.B.7
Becker, J.N.8
Wilson, D.L.9
Todd, C.10
Broomall, C.F.11
Evans, J.C.12
Elder, E.J.13
-
24
-
-
33750325780
-
Drug nanoparticles by antisolvent precipitation: Mixing energy versus surfactant stabilization
-
DOI 10.1021/la061122t
-
M.E. Matteucci, M.A. Hotze, K.P. Johnston, and R.O. Williams III Drug nanoparticles by antisolvent precipitation: mixing energy versus surfactant stabilization Langmuir 22 2006 8951 8959 (Pubitemid 44626160)
-
(2006)
Langmuir
, vol.22
, Issue.21
, pp. 8951-8959
-
-
Matteucci, M.E.1
Hotze, M.A.2
Johnston, K.P.3
Williams III, R.O.4
-
25
-
-
67349131897
-
Combination chemotherapeutic dry powder aerosols via controlled nanoparticle agglomeration
-
N. EI-Gendy, and C. Berkland Combination chemotherapeutic dry powder aerosols via controlled nanoparticle agglomeration Pharm. Res. 26 2009 1752 1763
-
(2009)
Pharm. Res.
, vol.26
, pp. 1752-1763
-
-
Ei-Gendy, N.1
Berkland, C.2
-
27
-
-
67349118498
-
Micronization of atorvastatin calcium by antisolvent precipitation process
-
H.X. Zhang, J.X. Wanga, Z.B. Zhang, Y. Le, Z.G. Shen, and J.F. Chen Micronization of atorvastatin calcium by antisolvent precipitation process Int. J. Pharm. 374 2009 106 113
-
(2009)
Int. J. Pharm.
, vol.374
, pp. 106-113
-
-
Zhang, H.X.1
Wanga, J.X.2
Zhang, Z.B.3
Le, Y.4
Shen, Z.G.5
Chen, J.F.6
-
28
-
-
0031750464
-
Crystalline properties of carbamazepine in sustained release hydrophilic matrix tablets based on hydroxypropyl methylcellulose
-
I. Katzhendlera, R. Azouryb, and M. Friedmana Crystalline properties of carbamazepine in sustained release hydrophilic matrix tablets based on hydroxypropyl methylcellulose J. Controll. Release 54 1998 69 85
-
(1998)
J. Controll. Release
, vol.54
, pp. 69-85
-
-
Katzhendlera, I.1
Azouryb, R.2
Friedmana, M.3
-
29
-
-
64649088132
-
Amorphous compositions using concentration enhancing polymers for improved bioavailability of itraconazole
-
J.C. Dinunzio, D.A. Miller, W. Yang, G.W. Mcginity, and R.O. Williams Amorphous compositions using concentration enhancing polymers for improved bioavailability of itraconazole Mol. Pharm. 5 2008 968 980
-
(2008)
Mol. Pharm.
, vol.5
, pp. 968-980
-
-
Dinunzio, J.C.1
Miller, D.A.2
Yang, W.3
McGinity, G.W.4
Williams, R.O.5
-
31
-
-
4344604026
-
Physicochemical parameters associated with nanoparticle formation in the salting-out, emulsification-diffusion, and nanoprecipitation methods
-
DOI 10.1023/B:PHAM.0000036917.75634.be
-
S. Galindo-Rodriguez, S.E. Allemann, H. Fessi, and E. Doelker Physicochemical parameters associated with nanoparticle formation in the tsaltingout, emulsification-diffusion, and nanoprecipitation methods Pharm. Res. 21 2004 1428 1439 (Pubitemid 39149658)
-
(2004)
Pharmaceutical Research
, vol.21
, Issue.8
, pp. 1428-1439
-
-
Galindo-Rodriguez, S.1
Allemann, E.2
Fessi, H.3
Doelker, E.4
-
32
-
-
34548023425
-
Crystal engineering of active pharmaceutical ingredients to improve solubility and dissolution rates
-
DOI 10.1016/j.addr.2007.05.011, PII S0169409X07000828
-
N. Blagden, M. de Matas, P.T. Gavan, and P. York Crystal engineering of active pharmaceutical ingredients to improve solubility and dissolution rates Adv. Drug Deliv. Rev. 59 2007 617 630 (Pubitemid 47285407)
-
(2007)
Advanced Drug Delivery Reviews
, vol.59
, Issue.7
, pp. 617-630
-
-
Blagden, N.1
De Matas, M.2
Gavan, P.T.3
York, P.4
|