-
2
-
-
84859998651
-
A biopharmaceutical classification-based rightfirst-Time formulation approach to reduce human pharmacokinetic variability and project cycle time from first-in-human to clinical proof-of-concept
-
Ku MS, Dulin W. A biopharmaceutical classification-based rightfirst-Time formulation approach to reduce human pharmacokinetic variability and project cycle time from first-in-human to clinical proof-of-concept. Pharm Dev Technol. 2012; 17:285-302.
-
(2012)
Pharm Dev Technol
, vol.17
, pp. 285-283
-
-
Ku, M.S.1
Dulin, W.2
-
4
-
-
34548049483
-
Nanosizing-oral formulation development and biopharmaceutical evaluation
-
Kesisoglou F, Panmai S, Wu Y. Nanosizing-oral formulation development and biopharmaceutical evaluation. Adv Drug Deliv Rev. 2007;59:631-44.
-
(2007)
Adv Drug Deliv Rev
, vol.59
, pp. 631-634
-
-
Kesisoglou, F.1
Panmai, S.2
Wu, Y.3
-
5
-
-
79957861493
-
Nanosizing for oral and parenteral drug delivery: A perspective on formulating poorlywater soluble compounds using wet media milling technology
-
Merisko-Liversidge E, Liversidge GG. Nanosizing for oral and parenteral drug delivery: a perspective on formulating poorlywater soluble compounds using wet media milling technology. Adv Drug Deliv Rev. 2011;63:427-40.
-
(2011)
Adv Drug Deliv Rev
, vol.63
, pp. 427-424
-
-
Merisko-Liversidge, E.1
Liversidge, G.G.2
-
6
-
-
41949100244
-
Drug nanoparticles: Formulating poorly water-soluble compounds
-
Merisko-Liversidge EM, Liversidge GG. Drug nanoparticles: formulating poorly water-soluble compounds. Toxicol Pathol. 2008;36:43-8.
-
(2008)
Toxicol Pathol
, vol.36
, pp. 43-48
-
-
Merisko-Liversidge, E.M.1
Liversidge, G.G.2
-
7
-
-
77956882799
-
Nanocrystals: Industrially feasible multifunctional formulation technology for poorly soluble actives
-
Shegokar R, Müller RH. Nanocrystals: industrially feasible multifunctional formulation technology for poorly soluble actives. Int J Pharm. 2010;399:129-39.
-
(2010)
Int J Pharm
, vol.399
, pp. 129-123
-
-
Shegokar, R.1
Müller, R.H.2
-
8
-
-
53949092998
-
Topdown production of drug nanocrystals: Nanosuspension stabilization, miniaturization and transformation into solid products
-
Van Eerdenbrugh B, Van den Mooter G, Augustijns P. Topdown production of drug nanocrystals: nanosuspension stabilization, miniaturization and transformation into solid products. Int J Pharm. 2008;364:64-75.
-
(2008)
Int J Pharm
, vol.364
, pp. 64-67
-
-
Van Eerdenbrugh, B.1
Van Den Mooter, G.2
Augustijns, P.3
-
9
-
-
0035292910
-
Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract
-
Horter D, Dressman JB. Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract. Adv Drug Deliv Rev. 2001;46:75-87.
-
(2001)
Adv Drug Deliv Rev
, vol.46
, pp. 75-78
-
-
Horter, D.1
Dressman, J.B.2
-
10
-
-
0031913402
-
Dissolution testing as a prognostic tool for oral drug adsorption: Immediate release dosage forms
-
Dressman JB, Amidon GL, Reppas C, Shah VP. Dissolution testing as a prognostic tool for oral drug adsorption: immediate release dosage forms. Pharm Res. 1998;15:11-22.
-
(1998)
Pharm Res
, vol.15
, pp. 11-12
-
-
Dressman, J.B.1
Amidon, G.L.2
Reppas, C.3
Shah, V.P.4
-
11
-
-
0029023516
-
The effect of particle size and shape on the surface specific dissolution rate of micronized practically insoluble drugs
-
Mosharraf M, Nystrom C. The effect of particle size and shape on the surface specific dissolution rate of micronized practically insoluble drugs. Int J Pharm. 1995;122:35-47.
-
(1995)
Int J Pharm
, vol.122
, pp. 35-34
-
-
Mosharraf, M.1
Nystrom, C.2
-
12
-
-
84857502649
-
A formulation strategy for gamma secretase inhibitor elnd006, a bcs class ii compound: Development of a nanosuspension formulation with improved oral bioavailability and reduced food effects in dogs
-
Quinn K, Gullapalli RP, Merisko-Liversidge E, Goldbach E, Wong A, Liversidge GG, et al. A formulation strategy for gamma secretase inhibitor ELND006, a BCS class II compound: development of a nanosuspension formulation with improved oral bioavailability and reduced food effects in dogs. J Pharm Sci. 2012;101:1462-74.
-
(2012)
J Pharm Sci
, vol.101
, pp. 1462-1467
-
-
Quinn, K.1
Gullapalli, R.P.2
Merisko-Liversidge, E.3
Goldbach, E.4
Wong, A.5
Liversidge, G.G.6
-
13
-
-
20844446627
-
The role of biopharmaceutics in the development of a clinical nanoparticle formulation of mk-0869: A beagle dog model predicts improved bioavailability and diminished food effect on absorption in human
-
Wu Y, Loper A, Landis E, Hettrick L, Novak L, Lynn K, et al. The role of biopharmaceutics in the development of a clinical nanoparticle formulation of MK-0869: a beagle dog model predicts improved bioavailability and diminished food effect on absorption in human. Int J Pharm. 2004;285:135-46.
-
(2004)
Int J Pharm
, vol.285
, pp. 135-134
-
-
Wu, Y.1
Loper, A.2
Landis, E.3
Hettrick, L.4
Novak, L.5
Lynn, K.6
-
14
-
-
79959317121
-
Investigation of nanosized crystalline form to improve the oral bioavailability of poorly water soluble cilostazol
-
Miao X, Sun C, Jiang T, Zheng L, Wang T, Wang S. Investigation of nanosized crystalline form to improve the oral bioavailability of poorly water soluble cilostazol. J Pharm Pharm Sci. 2011;14 (2):196-214.
-
(2011)
J Pharm Pharm Sci
, vol.14
, Issue.2
, pp. 196-192
-
-
Miao, X.1
Sun, C.2
Jiang, T.3
Zheng, L.4
Wang, T.5
Wang, S.6
-
15
-
-
0023709168
-
Physiochemical aspects of drug release. Viii. The relation between particle size and surface specific dissolution rate in agitated suspensions
-
Nystrom C, Bisrat M. Physiochemical aspects of drug release. VIII. The relation between particle size and surface specific dissolution rate in agitated suspensions. Int J Pharm. 1998;47:223-31.
-
(1998)
Int J Pharm
, vol.47
, pp. 223-223
-
-
Nystrom, C.1
Bisrat, M.2
-
16
-
-
0342897023
-
Nanosuspensions for the formulation of poorly soluble drugs i. Preparation by a size-reduction technique
-
Muller RH, Peters K. Nanosuspensions for the formulation of poorly soluble drugs I. Preparation by a size-reduction technique. Int J Pharm. 1998;160:229-37.
-
(1998)
Int J Pharm
, vol.160
, pp. 229-223
-
-
Muller, R.H.1
Peters, K.2
-
17
-
-
77649191330
-
Possible reduction of effective thickness of intestinal unstirred water layer by particle drifting effect
-
Sugano K. Possible reduction of effective thickness of intestinal unstirred water layer by particle drifting effect. Int J Pharm. 2010;387:103-9.
-
(2010)
Int J Pharm
, vol.387
, pp. 103-109
-
-
Sugano, K.1
-
18
-
-
67349159812
-
Theoretical investigation of passive intestinal membrane permeability using monte carlo method to generate druglike molecule population
-
Sugano K. Theoretical investigation of passive intestinal membrane permeability using Monte Carlo method to generate druglike molecule population. Int J Pharm. 2009;373:55-61.
-
(2009)
Int J Pharm
, vol.373
, pp. 55-56
-
-
Sugano, K.1
-
19
-
-
51649091116
-
Conversion of nanosuspensions into dry powders by spray drying: A case study
-
Chaubal MV, Popescu C. Conversion of nanosuspensions into dry powders by spray drying: a case study. Pharm Res. 2008;25 (10):2302-8.
-
(2008)
Pharm Res
, vol.25
, Issue.10
, pp. 2302-2308
-
-
Chaubal, M.V.1
Popescu, C.2
-
20
-
-
83955162904
-
Fabrication of quercetin nanocrystals: Comparison of different methods
-
Kakran M, Shegokar R, Sahoo NG, Shaal LA, Li L, Müller RH. Fabrication of quercetin nanocrystals: comparison of different methods. Eur J Pharm Biopharm. 2012;80:113-21.
-
(2012)
Eur J Pharm Biopharm
, vol.80
, pp. 113-112
-
-
Kakran, M.1
Shegokar, R.2
Sahoo, N.G.3
Shaal, L.A.4
Li, L.5
Müller, R.H.6
-
21
-
-
33344478634
-
Effect of particle size reduction on dissolution and oral absorption of a poorly water-soluble drug, cilostazol, in beagle dogs
-
Jinno J, Kamada N, Miyake M, Yamada K, Mukai T, Odomi M, et al. Effect of particle size reduction on dissolution and oral absorption of a poorly water-soluble drug, cilostazol, in beagle dogs. J Control Release. 2006;111:56-64.
-
(2006)
J Control Release
, vol.111
, pp. 56-56
-
-
Jinno, J.1
Kamada, N.2
Miyake, M.3
Yamada, K.4
Mukai, T.5
Odomi, M.6
-
22
-
-
77955656443
-
Forecasting in vivo oral absorption and food effect of micronized and nanosized aprepitant formulations in humans
-
Shono Y, Jantratid E, Kesisoglou F, Reppas C, Dressmam JB. Forecasting in vivo oral absorption and food effect of micronized and nanosized aprepitant formulations in humans. Eur J Pharm Biopharm. 2010;76:95-104.
-
(2010)
Eur J Pharm Biopharm
, vol.76
, pp. 95-91
-
-
Shono, Y.1
Jantratid, E.2
Kesisoglou, F.3
Reppas, C.4
Dressmam, J.B.5
-
23
-
-
0037227770
-
Carbendazim: Disposition, cellular permeability, metabolite identification, and pharmacokinetic comparison with its nanoparticle
-
Jia L, Wong H, Wang Y, Garza M, Weitman SD. Carbendazim: disposition, cellular permeability, metabolite identification, and pharmacokinetic comparison with its nanoparticle. J Pharm Sci. 2003;92:161-72.
-
(2003)
J Pharm Sci
, vol.92
, pp. 161-167
-
-
Jia, L.1
Wong, H.2
Wang, Y.3
Garza, M.4
Weitman, S.D.5
-
24
-
-
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
-
Hecq J, Deleers M, Fanara D, Vranckx H, Boulanger P, Le Lamer S, et al. 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. Eur J Pharm Biopharm. 2006;64:360-8.
-
(2006)
Eur J Pharm Biopharm
, vol.64
, pp. 360-368
-
-
Hecq, J.1
Deleers, M.2
Fanara, D.3
Vranckx, H.4
Boulanger, P.5
Le Lamer, S.6
-
25
-
-
71049183092
-
Particle size reduction for improvement of oral absorption of the poorly soluble drug ug558 in rats during early development
-
Sigfridsson K, Lundqvist AJ, Strimfors M. Particle size reduction for improvement of oral absorption of the poorly soluble drug UG558 in rats during early development. Drug Dev Ind Pharm. 2009;35:1479-86.
-
(2009)
Drug Dev Ind Pharm
, vol.35
, pp. 1479-1478
-
-
Sigfridsson, K.1
Lundqvist, A.J.2
Strimfors, M.3
-
26
-
-
11144354093
-
Influence of physicochemical properties and intestinal region on the absorption of 3-fluoro-2-pyrimidylmethyl 3-(2,2-difluoro-2-(2-pyridyl) ethylamino)-6-chloropyrazin-2-one-1-Acetamide, a water insoluble thrombin inhibitor, in dog
-
Euler D, Frech P, Karki S, Cowden C, Pearce G, Mehta P, et al. Influence of physicochemical properties and intestinal region on the absorption of 3-fluoro-2-pyrimidylmethyl 3-(2,2-difluoro-2-(2-pyridyl) ethylamino)-6- chloropyrazin-2-one-1-Acetamide, a water insoluble thrombin inhibitor, in dog. Int J Pharm. 2004;275:19-27.
-
(2004)
Int J Pharm
, vol.275
, pp. 19-12
-
-
Euler, D.1
Frech, P.2
Karki, S.3
Cowden, C.4
Pearce, G.5
Mehta, P.6
-
27
-
-
0036689390
-
Effect of nanonization on absorption of 301029: Ex vivo and in vivo pharmacokinetic correlations determined by liquid chromatography/mass spectrometry
-
Jia L, Wong H, Cerna C, Weitman SD. Effect of nanonization on absorption of 301029: ex vivo and in vivo pharmacokinetic correlations determined by liquid chromatography/mass spectrometry. Pharm Res. 2002;19:1091-6.
-
(2002)
Pharm Res
, vol.19
, pp. 1091-1096
-
-
Jia, L.1
Wong, H.2
Cerna, C.3
Weitman, S.D.4
-
28
-
-
0027243792
-
Improved oral absorption of a poorly watersoluble drug, ho-221, by wet-bead milling producing particles in submicron region
-
Kondo N, Iwao T, Masuda H, Yamanouchi K, Ishihara Y, Yamada N, et al. Improved oral absorption of a poorly watersoluble drug, HO-221, by wet-bead milling producing particles in submicron region. Chem Pharm Bull (Tokyo). 1993;41:737-40.
-
(1993)
Chem Pharm Bull (Tokyo
, vol.41
, pp. 737-734
-
-
Kondo, N.1
Iwao, T.2
Masuda, H.3
Yamanouchi, K.4
Ishihara, Y.5
Yamada, N.6
-
29
-
-
0029080002
-
Particle size reduction for improvement of oral bioavailability of hydrophobic drugs: I. Absolute oral bioavailability of nanocrystalline danazol in beagle dogs
-
LiversidgeGG, CundyKC. Particle size reduction for improvement of oral bioavailability of hydrophobic drugs: I. Absolute oral bioavailability of nanocrystalline danazol in beagle dogs. Int J Pharm. 1995;125:91-7.
-
(1995)
Int J Pharm
, Issue.125
, pp. 91-97
-
-
Liversidge, G.G.1
Cundy, K.C.2
-
30
-
-
61349191553
-
Enhancement of oral bioavailability of an hivattachment inhibitor by nanosizing and amorphous formulation approaches
-
Fakes MG, Vakkalagadda BJ, Qian F, Desikan S, Gandhi RB, Lai C, et al. Enhancement of oral bioavailability of an HIVattachment inhibitor by nanosizing and amorphous formulation approaches. Int J Pharm. 2009;370:167-74.
-
(2009)
Int J Pharm
, vol.370
, pp. 167-167
-
-
Fakes, M.G.1
Vakkalagadda, B.J.2
Qian, F.3
Desikan, S.4
Gandhi, R.B.5
Lai, C.6
-
31
-
-
3943083748
-
-
Wyeth Pharmaceuticals Inc. Philadelphia: Wyeth Pharmaceuticals
-
Wyeth Pharmaceuticals, Inc.Rapamune(R) prescribing information. Philadelphia: Wyeth Pharmaceuticals; 2006.
-
(2006)
Rapamune(R) Prescribing Information
-
-
-
32
-
-
32944458444
-
Pharmacokinetics of aprepitant after single and multiple oral doses in healthy volunteers
-
Majumdar AK, Howard L, Goldberg MR, Hickey L, Constanzer M, Rothenberg PL, et al. Pharmacokinetics of aprepitant after single and multiple oral doses in healthy volunteers. J Clin Pharmacol. 2006;46:291-300.
-
(2006)
J Clin Pharmacol
, vol.46
, pp. 291-293
-
-
Majumdar, A.K.1
Howard, L.2
Goldberg, M.R.3
Hickey, L.4
Constanzer, M.5
Rothenberg, P.L.6
-
33
-
-
33847094347
-
-
Par Pharmaceutical Companies Inc. Woodcliff: Par Pharmaceutical Companies
-
Par Pharmaceutical Companies, Inc. Megace(R) ES prescribing information. Woodcliff: Par Pharmaceutical Companies; 2005.
-
(2005)
Megace(R) ES Prescribing Information
-
-
-
35
-
-
34548027773
-
-
Abbott Laboratories. Abbott Park: Abbott Laboratories
-
Abbott Laboratories. TriCor(R) prescribing information. Abbott Park: Abbott Laboratories; 2004.
-
(2004)
TriCor(R) Prescribing Information
-
-
-
36
-
-
84869123618
-
-
First Horizon Pharmaceutical Corporation. Roswell: First Horizon Pharmaceutical Corporation
-
First Horizon Pharmaceutical Corporation. TriglideTM prescribing information. Roswell: First Horizon Pharmaceutical Corporation; 2005.
-
(2005)
TriglideTM Prescribing Information
-
-
|