-
1
-
-
0034117515
-
Preparation and in vivo ocular absorption studies of disulfiram solid dispersion
-
Nabekura T, Ito Y, Cai H, et al. Preparation and in-vivo ocular absorption studies of disulfiram solid dispersion. Biol Pharm Bull 2000;23:616-20 (Pubitemid 30321283)
-
(2000)
Biological and Pharmaceutical Bulletin
, vol.23
, Issue.5
, pp. 616-620
-
-
Nabekura, T.1
Ito, Y.2
Cai, H.3
Terao, M.4
Hori, R.5
-
2
-
-
61849145863
-
Improvement in chemical and physical stability of fluvastatin drug through hydrogen bonding interactions with different polymer matrices
-
Papageorgiou GZ, Papadimitriou S, Karavas E, et al. Improvement in chemical and physical stability of fluvastatin drug through hydrogen bonding interactions with different polymer matrices. Curr Drug Deliv 2009;6:101-12
-
(2009)
Curr Drug Deliv
, vol.6
, pp. 101-112
-
-
Papageorgiou, G.Z.1
Papadimitriou, S.2
Karavas, E.3
-
3
-
-
67549083692
-
Manik Formulation of sustained-release dosage form of verapamil hydrochloride by solid dispersion technique using Eudragit RLPO or Kollidon-SR
-
Sahoo J, Murthy PN, Biswal S, Manik Formulation of sustained-release dosage form of verapamil hydrochloride by solid dispersion technique using Eudragit RLPO or Kollidon-SR. AAPS PharmSciTech 2009;10:27-33
-
(2009)
AAPS PharmSciTech
, vol.10
, pp. 27-33
-
-
Sahoo, J.1
Murthy, P.N.2
Biswal, S.3
-
4
-
-
57149132106
-
Studies on formulation development of mucoadhesive sustained release itraconazole tablet using response surface methodology
-
Madgulkar A, Kadam S, Pokharkar V. Studies on formulation development of mucoadhesive sustained release itraconazole tablet using response surface methodology. AAPS Pharm Sci Tech 2008;9:998-1005
-
(2008)
AAPS Pharm Sci Tech
, vol.9
, pp. 998-1005
-
-
Madgulkar, A.1
Kadam, S.2
Pokharkar, V.3
-
5
-
-
19644361858
-
Tabletting of solid dispersion particles consisting of indomethacin and porous silica particles
-
DOI 10.1248/cpb.53.487
-
Takeuchi H, Nagira S, Tanimura S, et al. Tabletting of solid dispersion particles consisting of indomethacin and porous silica particles. Chem Pharm Bull 2005;53:487-91 (Pubitemid 40740614)
-
(2005)
Chemical and Pharmaceutical Bulletin
, vol.53
, Issue.5
, pp. 487-491
-
-
Takeuchi, H.1
Nagira, S.2
Tanimura, S.3
Yamamoto, H.4
Kawashima, Y.5
-
6
-
-
70449524333
-
A Novel itraconazole bioadhesive film for vaginal delivery: Design, optimization, and physicodynamic characterization
-
Dobaria NB, Badhan AC, Mashru RC. A Novel itraconazole bioadhesive film for vaginal delivery: design, optimization, and physicodynamic characterization. AAPS Pharm Sci Tech 2009;10:951-9
-
(2009)
AAPS Pharm Sci Tech
, vol.10
, pp. 951-959
-
-
Dobaria, N.B.1
Badhan, A.C.2
Mashru, R.C.3
-
7
-
-
34347231328
-
Characterization of a cyclosporine solid dispersion for inhalation
-
DOI 10.1208/aapsj0902021, 21
-
Zijlstra GS, Rijkeboer M, Jan van Drooge D, et al. Characterization of a cyclosporine solid dispersion for inhalation. AAPS J 2007;9:E190-9 (Pubitemid 47007410)
-
(2007)
AAPS Journal
, vol.9
, Issue.2
-
-
Zijlstra, G.S.1
Rijkeboer, M.2
Van Drooge, D.J.3
Sutter, M.4
Jiskoot, W.5
Van De Weert, M.6
Hinrichs, W.L.J.7
Frijlink, H.W.8
-
8
-
-
50149101509
-
Effect of formulation parameters on 2-methoxyestradiol release from injectable cylindrical poly(DLlactide-co-glycolide) implants
-
Desai KG, Mallery SR, Schwendeman SP. Effect of formulation parameters on 2-methoxyestradiol release from injectable cylindrical poly(DLlactide-co- glycolide) implants. Eur J Pharm Biopharm 2008;70:187-98
-
(2008)
Eur J Pharm Biopharm
, vol.70
, pp. 187-198
-
-
Desai, K.G.1
Mallery, S.R.2
Schwendeman, S.P.3
-
9
-
-
67650450177
-
In vitro and in vivo characterization on amorphous solid dispersion of cyclosporine A for inhalation therapy
-
Onoue S, Sato H, Kawabata Y, et al. In vitro and in vivo characterization on amorphous solid dispersion of cyclosporine A for inhalation therapy. J Control Release 2009;138(1):16-23
-
(2009)
J Control Release
, vol.138
, Issue.1
, pp. 16-23
-
-
Onoue, S.1
Sato, H.2
Kawabata, Y.3
-
10
-
-
70349170163
-
Study on mechanism for amorphous drug stabilization using Gelucire 50/13
-
Shimpi SL, Mahadik KR, Paradkar AR. Study on mechanism for amorphous drug stabilization using Gelucire 50/13. Chem Pharm Bull 2009;57:937-42
-
(2009)
Chem Pharm Bull
, vol.57
, pp. 937-942
-
-
Shimpi, S.L.1
Mahadik, K.R.2
Paradkar, A.R.3
-
11
-
-
79551492832
-
Effect of particle size of drug on conversion of crystals to an amorphous state in a solid dispersion with crospovidone
-
Sugamura Y, Fujii M, Nakanishi S, et al. Effect of particle size of drug on conversion of crystals to an amorphous state in a solid dispersion with crospovidone. Chem Pharm Bull 2011;59:235-8
-
(2011)
Chem Pharm Bull
, vol.59
, pp. 235-238
-
-
Sugamura, Y.1
Fujii, M.2
Nakanishi, S.3
-
12
-
-
77649280447
-
An investigation into the mechanisms of rapid release of standard extract from Ginkgo biloba leaf in polyethylene glycol 6000 solid dispersions
-
Yuebin GE. An investigation into the mechanisms of rapid release of standard extract from Ginkgo biloba leaf in polyethylene glycol 6000 solid dispersions. Yakugaku Zasshi 2010;130:425-30
-
(2010)
Yakugaku Zasshi
, vol.130
, pp. 425-430
-
-
Yuebin, G.E.1
-
13
-
-
79953645317
-
Solid dispersions of carvedilol with porous silica
-
Kovacic B, Vrecer F, Planinsek O. Solid dispersions of carvedilol with porous silica. Chem Pharm Bull 2011;59:427-33
-
(2011)
Chem Pharm Bull
, vol.59
, pp. 427-4433
-
-
Kovacic, B.1
Vrecer, F.2
Planinsek, O.3
-
14
-
-
52949135898
-
Surface composition and contact angle relationship for differently prepared solid dispersions
-
Dahlberg C, Millgyist-Fureby A, Schuleit M. Surface composition and contact angle relationship for differently prepared solid dispersions. Eur J Pharm Biopharm 2008;70:478-85
-
(2008)
Eur J Pharm Biopharm
, vol.70
, pp. 478-485
-
-
Dahlberg, C.1
Millgyist-Fureby, A.2
Schuleit, M.3
-
15
-
-
37549059974
-
Development of Prednisone: Polyethylene Glycol 6000 fast-release tablets from solid dispersions: Solid-state characterization, dissolution behavior, and formulation parameters
-
Leonardi D, Barrera MG, Lamas MC, Salomo'n CJ. Development of Prednisone:polyethylene Glycol 6000 fast-release tablets from solid dispersions: solid-state characterization, dissolution behavior, and formulation parameters. AAPS Pharm Sci Tech 2007;8:E1-8
-
(2007)
AAPS Pharm Sci Tech
, vol.8
-
-
Leonardi, D.1
Barrera, M.G.2
Lamas, M.C.3
Salomo'n, C.J.4
-
16
-
-
77955368629
-
Development and in vitro evaluation of ibuprofen mouth dissolving tablets using solid dispersion technique
-
Jain SK, Shukla M, Shrivastava V. Development and in vitro evaluation of ibuprofen mouth dissolving tablets using solid dispersion technique. Chem Pharm Bull 2010;58:1037-42
-
(2010)
Chem Pharm Bull
, Issue.58
, pp. 1037-1042
-
-
Jain, S.K.1
Shukla, M.2
Shrivastava, V.3
-
17
-
-
1842611878
-
Physicochemical Characterization of Solid Dispersions of Indomethacin with PEG 6000, Myrj 52, Lactose, Sorbitol, Dextrin, and Eudragit E100
-
DOI 10.1081/DDC-120030426
-
Valizadeh H, Nokhodchi A, Qarakhani N, et al. Physicochemical characterization of solid dispersions of indomethacin with PEG 6000, Myrj 52, lactose, sorbitol, dextrin, and Eudragit E100. Drug Dev Ind Pharm 2004;30:303-17 (Pubitemid 38451755)
-
(2004)
Drug Development and Industrial Pharmacy
, vol.30
, Issue.3
, pp. 303-317
-
-
Valizadeh, H.1
Nokhodchi, A.2
Qarakhani, N.3
Zakeri-Milani, P.4
Azarmi, S.5
Hassanzadeh, D.6
Lobenberg, R.7
-
18
-
-
79953663043
-
Solubility, dissolution rate and bioavailability enhancement of irbesartan by solid dispersion technique
-
Boghra RJ, Kothawade PC, Belgamwar VS, et al. Solubility, dissolution rate and bioavailability enhancement of irbesartan by solid dispersion technique. Chem Pharm Bull 2011;59:438-41
-
(2011)
Chem Pharm Bull
, vol.59
, pp. 438-441
-
-
Boghra, R.J.1
Kothawade, P.C.2
Belgamwar, V.S.3
-
19
-
-
16644366133
-
Improved dissolution of an insoluble drug using a 4-fluid nozzle spray-drying technique
-
DOI 10.1248/cpb.52.1066
-
Chen R, Tagawa M, Hoshi N, et al. Improved dissolution of an insoluble drug using a 4-fluid nozzle spray-drying technique. Chem Pharm Bull 2004;52:1066-70 (Pubitemid 41679544)
-
(2004)
Chemical and Pharmaceutical Bulletin
, vol.52
, Issue.9
, pp. 1066-1070
-
-
Chen, R.1
Tagawa, M.2
Hoshi, N.3
Ogura, T.4
Okamoto, H.5
Danjo, K.6
-
20
-
-
75549090079
-
Kneading technique for preparation of binary solid dispersion of meloxicam with Poloxamer 188
-
Ghareeb MM, Abdulrasool AA, Hussein AA, Noordin MI. Kneading technique for preparation of binary solid dispersion of meloxicam with Poloxamer 188. AAPS Pharm Sci Tech 2009;10:1206-15
-
(2009)
AAPS Pharm Sci Tech
, vol.10
, pp. 1206-1215
-
-
Ghareeb, M.M.1
Abdulrasool, A.A.2
Hussein, A.A.3
Noordin, M.I.4
-
21
-
-
79959305480
-
Physicochemical characterization and dissolution properties of Meloxicam-Gelucire 50/13 Binary Systems
-
EL-Badry M. Physicochemical characterization and dissolution properties of Meloxicam-Gelucire 50/13 Binary Systems. Sci Pharm 2011;79:375-86
-
(2011)
Sci Pharm
, Issue.79
, pp. 375-386
-
-
El-Badry, M.1
-
22
-
-
80955135462
-
The use of spray-drying to enhance celecoxib solubility
-
Fouad EA, EL-Badry M, Mahrous GM, et al. The use of spray-drying to enhance celecoxib solubility. Drug Dev Ind Pharm 2011;37:1463-72
-
(2011)
Drug Dev Ind Pharm
, Issue.37
, pp. 1463-1472
-
-
Fouad, E.A.1
El-Badry, M.2
Mahrous, G.M.3
-
23
-
-
74149089070
-
To enhance dissolution rate of poorly water-soluble drugs: Glucosamine hydrochloride as a potential carrier in solid dispersion formulations
-
Al-Hamidi H, Edwards AA, Mohammad MA, Nokhodchi A. To enhance dissolution rate of poorly water-soluble drugs: glucosamine hydrochloride as a potential carrier in solid dispersion formulations. Colloids Surf B Biointerfaces 2010;76:170-8
-
(2010)
Colloids Surf B Biointerfaces
, vol.76
, pp. 170-178
-
-
Al-Hamidi, H.1
Edwards, A.A.2
Mohammad, M.A.3
Nokhodchi, A.4
-
24
-
-
34247191205
-
Effect of hydrophilic swellable polymers on dissolution enhancement of carbamazepine solid dispersions studied using response surface methodology
-
DOI 10.1208/pt0802027, 27
-
Rane Y, Mashru R, Sankalia M, Sankalia J. Effect of hydrophilic swellable polymers on dissolution enhancement of carbamazepine solid dispersions studied using response surface methodology. AAPS Pharm Sci Tech 2007;27:E1-E11 (Pubitemid 46620643)
-
(2007)
AAPS PharmSciTech
, vol.8
, Issue.2
-
-
Rane, Y.1
Mashru, R.2
Sankalia, M.3
Sankalia, J.4
-
25
-
-
80053573435
-
Comparison of HPMC based polymers performance as carriers for manufacture of solid dispersions using the melt extruder
-
Ghosh I, Snyder J, Vippagunta R, et al. Comparison of HPMC based polymers performance as carriers for manufacture of solid dispersions using the melt extruder. Int J Pharm 2011;419:12-19
-
(2011)
Int J Pharm
, vol.419
, pp. 12-19
-
-
Ghosh, I.1
Snyder, J.2
Vippagunta, R.3
-
26
-
-
84860385670
-
Evaluation of polymer carriers with regard to the bioavailability enhancement of bifendate solid dispersions prepared by hot-melt extrusion
-
Feng J, Xu L, Gao R, et al. Evaluation of polymer carriers with regard to the bioavailability enhancement of bifendate solid dispersions prepared by hot-melt extrusion. Drug Dev Ind Pharm 2012;38(6):735-43
-
(2012)
Drug Dev Ind Pharm
, vol.38
, Issue.6
, pp. 735-743
-
-
Feng, J.1
Xu, L.2
Gao, R.3
-
27
-
-
34547143790
-
Part II: Bioavailability in beagle dogs of nimodipine solid dispersions prepared by hot-melt extrusion
-
DOI 10.1080/03639040601050205, PII 780838140
-
Zheng X, Yang R, Zhang Y, et al. Part II: bioavailability in beagle dogs of nimodipine solid dispersions prepared by hot-melt extrusion. Drug Dev Ind Pharm 2007;33:783-9 (Pubitemid 47123804)
-
(2007)
Drug Development and Industrial Pharmacy
, vol.33
, Issue.7
, pp. 783-789
-
-
Zheng, X.1
Yang, R.2
Zhang, Y.3
Wang, Z.4
Tang, X.5
Zheng, L.6
-
28
-
-
79955636907
-
Physical state and dissolution of ibuprofen formulated by co-spray drying with mesoporous silica: Effect of pore and particle size
-
Shen SC, Ng WK, Chia L, et al. Physical state and dissolution of ibuprofen formulated by co-spray drying with mesoporous silica: effect of pore and particle size. Int J Pharm 2011;410:188-95
-
(2011)
Int J Pharm
, Issue.410
, pp. 188-195
-
-
Shen, S.C.1
Ng, W.K.2
Chia, L.3
-
29
-
-
0035800245
-
A comparison of alternative polymer excipients and processing methods for making solid dispersions of a poorly water soluble drug
-
DOI 10.1016/S0378-5173(01)00709-8, PII S0378517301007098
-
Broman E, Khoo C, Taylor LS. A comparison of alternative polymer excipients and processing methods for making solid dispersions of poorly water soluble drugs. Int J Pharm 2001;222:139-51 (Pubitemid 32525795)
-
(2001)
International Journal of Pharmaceutics
, vol.222
, Issue.1
, pp. 139-151
-
-
Broman, E.1
Khoo, C.2
Taylor, L.S.3
-
30
-
-
34249092945
-
Investigation of the release mechanism of a sparingly water-soluble drug from solid dispersions in hydrophilic carriers based on physical state of drug, particle size distribution and drug-polymer interactions
-
DOI 10.1016/j.ejpb.2006.11.020, PII S0939641106003390
-
Karavas S, Georgarakis E, Sigalas MP, et al. Investigation of the release mechanism of a sparingly water-soluble drug from solid dispersions in hydrophilic carriers based on physical state of drug, particle size distribution and drug-polymer interactions. Eur J Pharm Biopharm 2007;66:334-47 (Pubitemid 46778978)
-
(2007)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.66
, Issue.3
, pp. 334-347
-
-
Karavas, E.1
Georgarakis, E.2
Sigalas, M.P.3
Avgoustakis, K.4
Bikiaris, D.5
-
31
-
-
33745080296
-
Dissolution improvement of high drug-loaded solid dispersion
-
52
-
Okonogi S, Puttipipatkhachorn S. Dissolution improvement of high drug-loaded solid dispersion. AAPS PharmSciTech 2006;7:E1-6 (Pubitemid 43884216)
-
(2006)
AAPS PharmSciTech
, vol.7
, Issue.2
-
-
Okonogi, S.1
Puttipipatkhachorn, S.2
-
32
-
-
77955688263
-
Dissolution enhancement of a drug exhibiting thermal and acidic decomposition characteristics by fusion processing: A comparative study of hot melt extrusion and KinetiSol dispersing
-
Hughey JR, DiNunzio JC, Bennett RC, et al. Dissolution enhancement of a drug exhibiting thermal and acidic decomposition characteristics by fusion processing: A comparative study of hot melt extrusion and KinetiSol dispersing. AAPS Pharm Sci Tech 2010;11(2):760-74
-
(2010)
AAPS Pharm Sci Tech
, vol.11
, Issue.2
, pp. 760-774
-
-
Hughey, J.R.1
DiNunzio, J.C.2
Bennett, R.C.3
-
33
-
-
63649143585
-
Solubility enhancement of lovastatin by modified locust bean gum using solid dispersion techniques
-
Patel M, Tekade A, Gattani S, Surana S. Solubility enhancement of lovastatin by modified locust bean gum using solid dispersion techniques. AAPS Pharm Sci Tech 2008;9:1262-9
-
(2008)
AAPS Pharm Sci Tech
, vol.9
, pp. 1262-1269
-
-
Patel, M.1
Tekade, A.2
Gattani, S.3
Surana, S.4
-
34
-
-
4444233011
-
Application of nilvadipine solid dispersion to tablet formulation and manufacturing using crospovidone and methylcellulose as dispersion carriers
-
DOI 10.1248/cpb.52.244
-
Hirasawa N, Ishise S, Miyata H, Danjo K. Application of nilvadipine solid dispersion to tablet formulation and manufacturing using crospovidone and methylcellulose as dispersion carriers. Chem Pharm Bull 2004;52:244-7 (Pubitemid 41656758)
-
(2004)
Chemical and Pharmaceutical Bulletin
, vol.52
, Issue.2
, pp. 244-247
-
-
Hirasawa, N.1
Ishise, S.2
Miyata, H.3
Danjo, K.4
-
35
-
-
41549099985
-
Preparation of functional composite particles of salbutamol sulfate using a 4-fluid nozzle spray-drying technique
-
DOI 10.1248/cpb.56.254
-
Chen R, Okamoto H, Danjo K. Preparation of functional composite particles of salbutamol sulfate using a 4-Fluid Nozzle Spray-Drying Technique. Chem Pharm Bull 2008;56:254-9 (Pubitemid 351463233)
-
(2008)
Chemical and Pharmaceutical Bulletin
, vol.56
, Issue.3
, pp. 254-259
-
-
Chen, R.1
Okamoto, H.2
Danjo, K.3
-
36
-
-
0036593674
-
Preparation of solid dispersion for ethenzamide-carbopol and theophylline-carbopol systems using a twin screw extruder
-
DOI 10.1248/cpb.50.802
-
Ozawa M, Hasegawa K, Yonezawa Y, Sunada H. Preparation of solid dispersion for ethenzamide-carbopol and theophylline-carbopol systems using a twin screw extruder. Chem Pharm Bull 2002;50:802-7 (Pubitemid 41694898)
-
(2002)
Chemical and Pharmaceutical Bulletin
, vol.50
, Issue.6
, pp. 802-807
-
-
Ozawa, M.1
Hasegawa, K.2
Yonezawa, Y.3
Sunada, H.4
-
37
-
-
36248933027
-
Preparation and evaluation of ibuprofen solid dispersion systems with Kollidon particles using a pulse combustion dryer system
-
DOI 10.1248/cpb.55.1545
-
Xu L, Li SM, Sunada H. Preparation and evaluation of ibuprofen solid dispersion systems with kollidon particles using a pulse combustion dryer system. Chem Pharm Bull 2007;55:1545-50 (Pubitemid 350126158)
-
(2007)
Chemical and Pharmaceutical Bulletin
, vol.55
, Issue.11
, pp. 1545-1550
-
-
Xu, L.1
Li, S.M.2
Sunada, H.3
-
38
-
-
77953418699
-
Characterization of solid dispersions of itraconazole and vitamin E TPGS prepared by microwave technology
-
Moneghini M, De Zordi N, Solinas D, et al. Characterization of solid dispersions of itraconazole and vitamin E TPGS prepared by microwave technology. Future Med Chem 2010;2:237-46
-
(2010)
Future Med Chem
, Issue.2
, pp. 237-246
-
-
Moneghini, M.1
De Zordi, N.2
Solinas, D.3
-
39
-
-
78649684484
-
Microwave induced solubility enhancement of poorly water soluble atorvastatin calcium
-
Maurya D, Belgamwar V, Tekade A. Microwave induced solubility enhancement of poorly water soluble atorvastatin calcium. J Pharm Pharmacol 2010;62:1599-606
-
(2010)
J Pharm Pharmacol
, vol.62
, pp. 1599-1606
-
-
Maurya, D.1
Belgamwar, V.2
Tekade, A.3
-
40
-
-
79952725911
-
Preparation and evaluation of cremophor-free paclitaxel solid dispersion by a supercritical antisolvent process
-
Park JH, Yan YD, Chi SC, et al. Preparation and evaluation of cremophor-free paclitaxel solid dispersion by a supercritical antisolvent process. J Pharm Pharmacol 2011;63:491-9
-
(2011)
J Pharm Pharmacol
, Issue.63
, pp. 491-499
-
-
Park, J.H.1
Yan, Y.D.2
Chi, S.C.3
-
41
-
-
78650678715
-
Spray freeze drying with polyvinylpyrrolidone and sodium caprate for improved dissolution and oral bioavailability of oleanolic acid, a BCS class IV compound
-
Tong HH, Du Z, Wang GN, et al. Spray freeze drying with polyvinylpyrrolidone and sodium caprate for improved dissolution and oral bioavailability of oleanolic acid, a BCS class IV compound. Int J Pharm 2011;404:148-58
-
(2011)
Int J Pharm
, Issue.404
, pp. 148-158
-
-
Tong, H.H.1
Du, Z.2
Wang, G.N.3
-
43
-
-
77955302991
-
Study of the physicochemical properties and oral bioavailability of the solid dispersion of cantharidin with polyethylene glycol 4000
-
Dang YJ, Hu CH, An LN, Zhu CY. Study of the physicochemical properties and oral bioavailability of the solid dispersion of cantharidin with polyethylene glycol 4000. Methods Find Exp Clin Pharmacol 2010;32:157-62
-
(2010)
Methods Find Exp Clin Pharmacol
, vol.32
, pp. 157-162
-
-
Dang, Y.J.1
Hu, C.H.2
An, L.N.3
Zhu, C.Y.4
-
44
-
-
77953028658
-
Applications of KinetiSol dispersing for the production of plasticizer free amorphous solid dispersions
-
DiNunzio JC, Brough C, Miller DA, et al. Applications of KinetiSol dispersing for the production of plasticizer free amorphous solid dispersions. Eur J Pharm Sci 2010;40:179-87
-
(2010)
Eur J Pharm Sci
, vol.40
, pp. 179-187
-
-
DiNunzio, J.C.1
Brough, C.2
Miller, D.A.3
-
45
-
-
77954203501
-
Preparation and evaluation of solid dispersions of piroxicam and Eudragit S100 by spherical crystallization technique
-
Maghsoodi M, Sadeghpoor F. Preparation and evaluation of solid dispersions of piroxicam and Eudragit S100 by spherical crystallization technique. Drug Dev Ind Pharm 2010;36:917-25
-
(2010)
Drug Dev Ind Pharm
, Issue.36
, pp. 917-925
-
-
Maghsoodi, M.1
Sadeghpoor, F.2
-
46
-
-
46949110167
-
Preparation of a solid dispersion by a dropping method to improve the rate of dissolution of meloxicam
-
DOI 10.1080/03639040801925735, PII 794853082
-
Bashiri-Shahroodi A, Nassab PR, Szabó-Re've'sz P, Rajkó R. Preparation of a solid dispersion by a dropping method to improve the rate of dissolution of meloxicam. Drug Dev Ind Pharm 2008;34:781-8 (Pubitemid 351962351)
-
(2008)
Drug Development and Industrial Pharmacy
, vol.34
, Issue.7
, pp. 781-788
-
-
Bashiri-Shahroodi, A.1
Nassab, P.R.2
Szabo-Revesz, P.3
Rajko, R.4
-
47
-
-
33847103562
-
2 on crystalline to amorphous conversion of carbamazepine
-
DOI 10.1016/j.ijpharm.2006.12.010, PII S0378517306010684
-
Ugaonkar S, Nunes AC, Needham TE. Effect of n-scCO(2) on crystalline to amorphous conversion of carbamazepine. Int J Pharm 2007;333:152-61 (Pubitemid 46283281)
-
(2007)
International Journal of Pharmaceutics
, vol.333
, Issue.1-2
, pp. 152-161
-
-
Ugaonkar, S.1
Nunes, A.C.2
Needham, T.E.3
-
48
-
-
34047250983
-
Solid dispersions of itraconazole and enteric polymers made by ultra-rapid freezing
-
DOI 10.1016/j.ijpharm.2006.11.043, PII S0378517306010003
-
Overhoff KA, Moreno A, Miller DA, et al. Solid dispersions of itraconazole and enteric polymers made by ultra-rapid freezing. Int J Pharm 2007;336(1):122-32 (Pubitemid 46551563)
-
(2007)
International Journal of Pharmaceutics
, vol.336
, Issue.1
, pp. 122-132
-
-
Overhoff, K.A.1
Moreno, A.2
Miller, D.A.3
Johnston, K.P.4
Williams III, R.O.5
-
49
-
-
33747609302
-
Etodolac-liquid-filled dispersion into hard gelatin capsules: An approach to improve dissolution and stability of etodolac formulation
-
DOI 10.1080/03639040500534192, PII J71M7U4170912431
-
Barakat NS. Etodolac-liquid-filled dispersion into hard gelatin capsules: An approach to improve dissolution and stability of etodolac formulation. Drug Dev Ind Pharm 2006;32:865-76 (Pubitemid 44266771)
-
(2006)
Drug Development and Industrial Pharmacy
, vol.32
, Issue.7
, pp. 865-876
-
-
Barakat, N.S.1
-
50
-
-
71649105279
-
Anomalous properties of spray dried solid dispersions
-
Al-Obaidi H, Brocchini S, Buckton G. Anomalous properties of spray dried solid dispersions. J Pharm Sci 2009;98:4724-37
-
(2009)
J Pharm Sci
, vol.98
, pp. 4724-4737
-
-
Al-Obaidi, H.1
Brocchini, S.2
Buckton, G.3
-
51
-
-
80054690161
-
Interplay of formulation and process methodology on the extent of nifedipine molecular dispersion in polymers
-
Huang J, Li Y, Wigent RJ, et al. Interplay of formulation and process methodology on the extent of nifedipine molecular dispersion in polymers. Int J Pharm 2011;420:59-67
-
(2011)
Int J Pharm
, Issue.420
, pp. 59-67
-
-
Huang, J.1
Li, Y.2
Wigent, R.J.3
-
52
-
-
78650527889
-
Silymarin solid dispersions: Characterization and influence of preparation methods on dissolution
-
Sonali D, Tejal S, Vaishali T, Tejal G. Silymarin solid dispersions: characterization and influence of preparation methods on dissolution. Acta Pharm 2010;60:427-43
-
(2010)
Acta Pharm
, vol.60
, pp. 427-43
-
-
Sonali, D.1
Tejal, S.2
Vaishali, T.3
Tejal, G.4
-
53
-
-
67650178803
-
Formation and characterization of solid dispersions of piroxicam and polyvinylpyrrolidone using spray drying and precipitation with compressed antisolvent
-
Wu K, Li J, Wang W, Winstead DA. Formation and characterization of solid dispersions of piroxicam and polyvinylpyrrolidone using spray drying and precipitation with compressed antisolvent. J Pharm Sci 2009;98:2422-31
-
(2009)
J Pharm Sci
, vol.98
, pp. 2422-2431
-
-
Wu, K.1
Li, J.2
Wang, W.3
Winstead, D.A.4
-
54
-
-
1442309058
-
9-tetrahydrocannabinol
-
DOI 10.1016/j.ejps.2003.11.014, PII S0928098703003348
-
van Drooge DJ, Hinrichs WL, Wegman KA, et al. Solid dispersions based on inulin for the stabilisation and formulation of delta 9-tetrahydrocannabinol. Eur J Pharm Sci 2004;21(4):511-18 (Pubitemid 38283925)
-
(2004)
European Journal of Pharmaceutical Sciences
, vol.21
, Issue.4
, pp. 511-518
-
-
Van Drooge, D.J.1
Hinrichs, W.L.J.2
Wegman, K.A.M.3
Visser, M.R.4
Eissens, A.C.5
Frijlink, H.W.6
-
55
-
-
0021127054
-
Crystallinity and dissolution rate of tolbutamide solid dispersions prepared by the melt method
-
McGinity JW, Maincent P, Steinfink H. Crystallinity and dissolution rate of tolbutamide solid dispersions prepared by the melt method. J Pharm Sci 1984;73:1441-4 (Pubitemid 14021903)
-
(1984)
Journal of Pharmaceutical Sciences
, vol.73
, Issue.10
, pp. 1441-1444
-
-
McGinity, J.W.1
Maincent, P.2
Steinfink, H.3
-
56
-
-
0017283119
-
Some factors influencing dissolution rate from salicylic acid-urea solid dispersions
-
Collett JH, Flood BL, Sale FR. Some factors influencing dissolution rate from salicylic acid-urea solid dispersions. J Pharm Pharmcol 1976;28:305-8
-
(1976)
J Pharm Pharmcol
, vol.28
, pp. 305-308
-
-
Collett, J.H.1
Flood, B.L.2
Sale, F.R.3
-
57
-
-
75549090079
-
Kneading technique for preparation of binary solid dispersion of meloxicam with poloxamer 188
-
Ghareeb MM, Abdulrasool AA, Hussein AA, Noordin MI. Kneading technique for preparation of binary solid dispersion of meloxicam with poloxamer 188. AAPS Pharm Sci Tech 2009;10(4):1206-15
-
(2009)
AAPS Pharm Sci Tech
, vol.10
, Issue.4
, pp. 1206-1215
-
-
Ghareeb, M.M.1
Abdulrasool, A.A.2
Hussein, A.A.3
Noordin, M.I.4
-
58
-
-
70349244686
-
A model-based methodology for spray-drying process development
-
Dobry DE, Settell DM, Baumann JM, et al. A model-based methodology for spray-drying process development. J Pharm Innov 2009;4(3):133-42
-
(2009)
J Pharm Innov
, vol.4
, Issue.3
, pp. 133-142
-
-
Dobry, D.E.1
Settell, D.M.2
Baumann, J.M.3
-
59
-
-
33747888621
-
Preparation of a solid dispersion of felodipine using a solvent wetting method
-
Kim EJ, Chun MK, Jang JS, et al. Preparation of a solid dispersion of felodipine using a solvent wetting method. Eur J Pharm Biopharm 2006;64(2):200-5
-
(2006)
Eur J Pharm Biopharm
, vol.64
, Issue.2
, pp. 200-205
-
-
Kim, E.J.1
Chun, M.K.2
Jang, J.S.3
-
60
-
-
82155175653
-
Influence of solvent evaporation rate and formulation factors on solid dispersion physical stability
-
Wu JX, Yang M, Berg Fv, et al. Influence of solvent evaporation rate and formulation factors on solid dispersion physical stability. Eur J Pharm Sci 2011;44(5):610-20
-
(2011)
Eur J Pharm Sci
, vol.44
, Issue.5
, pp. 610-620
-
-
Wu, J.X.1
Yang, M.2
Berg, F.V.3
-
61
-
-
84859455331
-
Preparation, characterization and in vivo evaluation of antihyperglycemic activity of microwave generated repaglinide solid dispersion
-
Zawar LR, Bari SB. Preparation, characterization and in vivo evaluation of antihyperglycemic activity of microwave generated repaglinide solid dispersion. Chem Pharm Bull 2012;60(4):482-7
-
(2012)
Chem Pharm Bull
, vol.60
, Issue.4
, pp. 482-487
-
-
Zawar, L.R.1
Bari, S.B.2
-
62
-
-
0037173515
-
The role of the kneading paddle and the effects of screw revolution speed and water content on the preparation of solid dispersions using a twin-screw extruder
-
DOI 10.1016/S0378-5173(02)00134-5, PII S0378517302001345
-
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(2):203-11 (Pubitemid 34718022)
-
(2002)
International Journal of Pharmaceutics
, vol.241
, Issue.2
, pp. 203-211
-
-
Nakamichi, K.1
Nakano, T.2
Yasuura, H.3
Izumi, S.4
Kawashima, Y.5
-
63
-
-
67651147937
-
Influence of the microwave technology on the physical-chemical properties of solid dispersion with nimesulide
-
Moneghini M, Zingone G, De Zordi N. Influence of the microwave technology on the physical-chemical properties of solid dispersion with nimesulide. Powder Technol 2009;195:259-63
-
(2009)
Powder Technol
, vol.195
, pp. 259-263
-
-
Moneghini, M.1
Zingone, G.2
De Zordi, N.3
-
64
-
-
47949102126
-
Microwave generated solid dispersions containing ibuprofen
-
Moneghini M, Bellich B, Baxa P, Princivalle F. Microwave generated solid dispersions containing ibuprofen. Int J Pharm 2008;361(1-2):125-30
-
(2008)
Int J Pharm
, vol.361
, Issue.1-2
, pp. 125-130
-
-
Moneghini, M.1
Bellich, B.2
Baxa, P.3
Princivalle, F.4
-
65
-
-
84856251917
-
Enhancement of dissolution rate of atorvastatin calcium using solid dispersions by dropping method
-
Kanakam VB. Enhancement of dissolution rate of atorvastatin calcium using solid dispersions by dropping method. Int J Pharm Tech Res 2011;3(2):652-9
-
(2011)
Int J Pharm Tech Res
, vol.3
, Issue.2
, pp. 652-659
-
-
Kanakam, V.B.1
-
66
-
-
0036746811
-
Improvement of dissolution rates of poorly water soluble APIs using novel spray freezing into liquid technology
-
Hu J, Rogers TL, Brown J, et al. Improvement of dissolution rates of poorly water soluble APIs using novel spray freezing into liquid technology. Pharm Res 2002;19(9):1278-84
-
(2002)
Pharm Res
, vol.19
, Issue.9
, pp. 1278-1284
-
-
Hu, J.1
Rogers, T.L.2
Brown, J.3
-
67
-
-
0037333353
-
Enhanced aqueous dissolution of a poorly water soluble drug by novel particle engineering technology: Spray-freezing into liquid with atmospheric freeze-drying
-
DOI 10.1023/A:1022628826404
-
Rogers TL, Nelsen AC, Sarkari M, et al. Enhanced aqueous dissolution of a poorly water soluble drug by novel particle engineering technology: spray-freezing into liquid with atmospheric freeze-drying. Pharm Res 2003;20(3):485-93 (Pubitemid 36292193)
-
(2003)
Pharmaceutical Research
, vol.20
, Issue.3
, pp. 485-493
-
-
Rogers, T.L.1
Nelsen, A.C.2
Sarkari, M.3
Young, T.J.4
Johnston, K.P.5
Williams III, R.O.6
-
68
-
-
79954421015
-
Comparison of spray freeze drying and the solvent evaporation method for preparing solid dispersions of baicalein with Pluronic F68 to improve dissolution and oral bioavailability
-
He X, Pei L, Tong HH, Zheng Y. Comparison of spray freeze drying and the solvent evaporation method for preparing solid dispersions of baicalein with Pluronic F68 to improve dissolution and oral bioavailability. AAPS Pharm Sci Tech 2011;12(1):104-13
-
(2011)
AAPS Pharm Sci Tech
, vol.12
, Issue.1
, pp. 104-113
-
-
He, X.1
Pei, L.2
Tong, H.H.3
Zheng, Y.4
-
69
-
-
0029586490
-
Enhancement of dissolution of glyburide by solid dispersion and lyophilization techniques
-
DOI 10.1016/0378-5173(95)04114-1
-
Betageri GV, Makarla KR. Enhancement of dissolution of glyburide by solid dispersion and lyophilization techniques. Int J Pharm 1995;126(1-2):155-60 (Pubitemid 26015632)
-
(1995)
International Journal of Pharmaceutics
, vol.126
, Issue.1-2
, pp. 155-160
-
-
Betageri, G.V.1
Makarla, K.R.2
-
70
-
-
80054697562
-
Pharmaceutical development and preliminary clinical testing of an oral solid dispersion formulation of docetaxel (ModraDoc001)
-
Moes JJ, Koolen SL, Huitema AD, et al. Pharmaceutical development and preliminary clinical testing of an oral solid dispersion formulation of docetaxel (ModraDoc001). Int J Pharm 2011;420(2):244-50
-
Int J Pharm 2011
, vol.420
, Issue.2
, pp. 244-250
-
-
Moes, J.J.1
Koolen, S.L.2
Huitema, A.D.3
-
71
-
-
67649810756
-
Comparison of solid dispersions produced by supercritical antisolvent and spray-freezing technologies
-
Badens E, Majerik V, Horvath G, et al. Comparison of solid dispersions produced by supercritical antisolvent and spray-freezing technologies. Int J Pharm 2009;377(1-2):25-34
-
(2009)
Int J Pharm
, vol.377
, Issue.1-2
, pp. 25-34
-
-
Badens, E.1
Majerik, V.2
Horvath, G.3
-
72
-
-
84861092432
-
Applications of supercritical fluids to enhance the dissolution behaviors of Furosemide by generation of microparticles and solid dispersions
-
De Zordi N, Moneghini M, Kikic I, et al. Applications of supercritical fluids to enhance the dissolution behaviors of Furosemide by generation of microparticles and solid dispersions. Eur J Pharm Biopharm 2012;81(1):131-41
-
(2012)
Eur J Pharm Biopharm
, vol.81
, Issue.1
, pp. 131-141
-
-
De Zordi, N.1
Moneghini, M.2
Kikic, I.3
-
73
-
-
0035800251
-
Processing of carbamazepine - PEG 4000 solid dispersions with supercritical carbon dioxide: Preparation, characterisation, and in vitro dissolution
-
DOI 10.1016/S0378-5173(01)00711-6, PII S0378517301007116
-
Moneghini M, Kikic I, Voinovich D, et al. Processing of carbamazepine-PEG 4000 solid dispersions with supercritical carbon dioxide: Preparation, characterisation, and in vitro dissolution. Int J Pharm 2001;222(1):129-38 (Pubitemid 32525794)
-
(2001)
International Journal of Pharmaceutics
, vol.222
, Issue.1
, pp. 129-138
-
-
Moneghini, M.1
Kikic, I.2
Voinovich, D.3
Perissutti, B.4
Filipovic-Grcic, J.5
-
74
-
-
34547196307
-
Rapidly dissolving repaglinide powders produced by the ultra-rapid freezing process
-
Purvis T, Mattucci ME, Crisp MT, et al. Rapidly dissolving repaglinide powders produced by the ultra-rapid freezing process. AAPS Pharm Sci Tech 2007;8(3):E58
-
(2007)
AAPS Pharm Sci Tech
, vol.8
, Issue.3
-
-
Purvis, T.1
Mattucci, M.E.2
Crisp, M.T.3
-
75
-
-
38049112810
-
Effect of stabilizer on the maximum degree and extent of supersaturation and oral absorption of tacrolimus made by ultra-rapid freezing
-
Overhoff KA, McConville JT, Yang W, et al. Effect of stabilizer on the maximum degree and extent of supersaturation and oral absorption of tacrolimus made by ultra-rapid freezing. Pharm Res 2008;25(1):167-75
-
(2008)
Pharm Res
, vol.25
, Issue.1
, pp. 167-175
-
-
Overhoff, K.A.1
McConville, J.T.2
Yang, W.3
-
76
-
-
34548306554
-
Improvement of the dissolution rate of nitrendipine using a new pulse combustion drying method
-
DOI 10.1248/cpb.55.1119
-
Wang L, Cui FD, Sunada H. Improvement of the dissolution rate of nitrendipine using a new pulse combustion drying method. Chem Pharm Bull (Tokyo)2007;55(8):1119-25 (Pubitemid 47344960)
-
(2007)
Chemical and Pharmaceutical Bulletin
, vol.55
, Issue.8
, pp. 1119-1125
-
-
Wang, L.1
Cui, F.-D.2
Sunada, H.3
-
77
-
-
37249030951
-
-
Available from: http://www.pulsedry. com/tech.php
-
Available from
-
-
-
78
-
-
33748480366
-
The effect of poloxamer viscosity on liquid-filling of solid dispersions in hard gelatin capsules
-
DOI 10.1080/03639040600559081, PII UR6243420P5P3R22
-
Kattige A, Rowley G. The effect of poloxamer viscosity on liquid-filling of solid dispersions in hard gelatin capsules. Drug Dev Ind Pharm 2006;32(8):981-90 (Pubitemid 44359760)
-
(2006)
Drug Development and Industrial Pharmacy
, vol.32
, Issue.8
, pp. 981-990
-
-
Kattige, A.1
Rowley, G.2
-
79
-
-
33745137414
-
Fast dissolving valdecoxib tablets containing solid dispersion of valdecoxib
-
Patel MM, Patel DM. Fast dissolving valdecoxib tablets containing solid dispersion of valdecoxib. Indian J Pharm Sci 2006;68(2):222-5
-
(2006)
Indian J Pharm Sci
, vol.68
, Issue.2
, pp. 222-225
-
-
Patel, M.M.1
Patel, D.M.2
-
80
-
-
80054796578
-
Solid dispersions, part I: Recent evolutions and future opportunities in manufacturing methods for dissolution rate enhancement of poorly water-soluble drugs
-
Bikiaris DN. Solid dispersions, part I: recent evolutions and future opportunities in manufacturing methods for dissolution rate enhancement of poorly water-soluble drugs. Expert Opin Drug Deliv 2011;8(11):1501-19
-
(2011)
Expert Opin Drug Deliv
, vol.8
, Issue.11
, pp. 1501-1519
-
-
Bikiaris, D.N.1
-
81
-
-
80054829203
-
Solid Dispersions, Part II: New strategies in manufacturing methods for dissolution rate enhancement of poorly water-soluble drugs
-
Bikiaris DN. Solid Dispersions, Part II: new strategies in manufacturing methods for dissolution rate enhancement of poorly water-soluble drugs. Expert Opin Drug Deliv 2011;8(12):1663-80
-
(2011)
Expert Opin Drug Deliv
, vol.8
, Issue.12
, pp. 1663-1680
-
-
Bikiaris, D.N.1
-
82
-
-
51449086188
-
Evaluation of SLS: APG mixed surfactant systems as carrier for solid dispersion
-
Patel AR, Joshi VY. Evaluation of SLS: APG mixed surfactant systems as carrier for solid dispersion. AAPS PharmSciTech 2008;9:583-90
-
(2008)
AAPS PharmSciTech
, vol.9
, pp. 583-590
-
-
Patel, A.R.1
Joshi, V.Y.2
-
83
-
-
77951498256
-
Characterization and stability of solid dispersions based on PEG/polymer blends
-
Bley H, Fussnegger B, Bodmeier R. Characterization and stability of solid dispersions based on PEG/polymer blends. Int J Pharm 2010;390:165-73
-
(2010)
Int J Pharm
, Issue.390
, pp. 165-173
-
-
Bley, H.1
Fussnegger, B.2
Bodmeier, R.3
-
84
-
-
77955257620
-
Evaluation of the microstructure of semicrystalline solid dispersions
-
Zhu Q, Taylor LS, Harris MT. Evaluation of the microstructure of semicrystalline solid dispersions. Mol Pharm 2010;7(4):1291-300
-
(2010)
Mol Pharm
, vol.7
, Issue.4
, pp. 1291-1300
-
-
Zhu, Q.1
Taylor, L.S.2
Harris, M.T.3
-
85
-
-
84856537046
-
Crystallinity evaluation of tacrolimus solid dispersions by chemometric analysis
-
Zidan AS, Rahman Z, Sayeed V, et al. Crystallinity evaluation of tacrolimus solid dispersions by chemometric analysis. Int J Pharm 2012;423(2):341-50
-
(2012)
Int J Pharm
, vol.423
, Issue.2
, pp. 341-350
-
-
Zidan, A.S.1
Rahman, Z.2
Sayeed, V.3
-
86
-
-
80054765250
-
CLSM as quantitative method to determine the size of drug crystals in a solid dispersion
-
de Waard H, Hessels MJ, Boon M, et al. CLSM as quantitative method to determine the size of drug crystals in a solid dispersion. Pharm Res 2011;28:2567-74
-
(2011)
Pharm Res
, vol.28
, pp. 2567-2574
-
-
De Waard, H.1
Hessels, M.J.2
Boon, M.3
-
87
-
-
34548297155
-
1H-NMR spin-lattice relaxation
-
DOI 10.1248/cpb.55.1227
-
Aso Y, Yoshioka S, Miyazaki T, et al. Miscibility of nifedipine and hydrophilic polymers as measured by 1H-NMR Spin-Lattice Relaxation. Chem Pharm Bull 2007;55:1227-31 (Pubitemid 47344979)
-
(2007)
Chemical and Pharmaceutical Bulletin
, vol.55
, Issue.8
, pp. 1227-1231
-
-
Aso, Y.1
Yoshioka, S.2
Miyazaki, T.3
Kawanishi, T.4
Tanaka, K.5
Kitamura, S.6
Takakura, A.7
Hayashi, T.8
Muranushi, N.9
-
88
-
-
69549116454
-
Nanoscale thermal analysis of pharmaceutical solid dispersions
-
Zhang J, Bunker M, Chen X, et al. Nanoscale thermal analysis of pharmaceutical solid dispersions. Int J Pharm 2009;380:170-3
-
(2009)
Int J Pharm
, vol.380
, pp. 170-173
-
-
Zhang, J.1
Bunker, M.2
Chen, X.3
-
89
-
-
33748514818
-
Characterization of poly(ethylene oxide) as a drug carrier in hot-melt extrusion
-
DOI 10.1080/03639040600559057, PII JTN8255753U59W9X
-
Li L, AbuBaker O, Shao ZJ. Characterization of poly(ethylene oxide) as a drug carrier in hot-melt extrusion. Drug Dev Ind Pharm 2006;32:991-1002 (Pubitemid 44359761)
-
(2006)
Drug Development and Industrial Pharmacy
, vol.32
, Issue.8
, pp. 991-1002
-
-
Li, L.1
AbuBaker, O.2
Shao, Z.3
-
90
-
-
79851514146
-
Atomic Force Microscopy-based screening of drug-excipient miscibility and stability of solid dispersions
-
Lauer ME, Grassmann O, Siam M, et al. Atomic Force Microscopy-based screening of drug-excipient miscibility and stability of solid dispersions. Pharm Res 2011;28:572-84
-
(2011)
Pharm Res
, vol.28
, pp. 572-584
-
-
Lauer, M.E.1
Grassmann, O.2
Siam, M.3
-
91
-
-
70350220585
-
Evaluation of drug-polymer miscibility in amorphous solid dispersion systems
-
Rumondor AC, Ivanisevic I, Bates S, et al. Evaluation of drug-polymer miscibility in amorphous solid dispersion systems. Pharm Res 2009;26:2523-34
-
(2009)
Pharm Res
, vol.26
, pp. 2523-2534
-
-
Rumondor, A.C.1
Ivanisevic, I.2
Bates, S.3
-
92
-
-
68949119479
-
Amorphous drug-PVP dispersions: Application of theoretical, thermal and spectroscopic analytical techniques to the study of a molecule with intermolecular bonds in both the crystalline and pure amorphous state
-
Tobyn M, Brown J, Dennis AB, et al. Amorphous drug-PVP dispersions: Application of theoretical, thermal and spectroscopic analytical techniques to the study of a molecule with intermolecular bonds in both the crystalline and pure amorphous state. J Pharm Sci 2009;98:3456-68
-
(2009)
J Pharm Sci
, vol.98
, pp. 3456-3468
-
-
Tobyn, M.1
Brown, J.2
Dennis, A.B.3
-
93
-
-
84858797264
-
Evaluation of amorphous solid dispersion properties using thermal analysis techniques
-
Baird JA, Taylor LS. Evaluation of amorphous solid dispersion properties using thermal analysis techniques. Adv Drug Deliv Rev 2012;64(5):396-421
-
(2012)
Adv Drug Deliv Rev
, vol.64
, Issue.5
, pp. 396-421
-
-
Baird, J.A.1
Taylor, L.S.2
-
94
-
-
79959744350
-
Investigation of physicochemical factors affecting the stability of a pH-modulated solid dispersion and a tablet during storage
-
Tran PH, Tran TT, Park JB, et al. Investigation of physicochemical factors affecting the stability of a pH-modulated solid dispersion and a tablet during storage. Int J Pharm 2011;414:48-55
-
(2011)
Int J Pharm
, vol.414
, pp. 48-55
-
-
Tran, P.H.1
Tran, T.T.2
Park, J.B.3
-
95
-
-
79955592721
-
Nanoparticle formation and growth during in vitro dissolution of ketoconazole solid dispersion
-
Kanaujia P, Lau G, Ng WK, et al. Nanoparticle formation and growth during in vitro dissolution of ketoconazole solid dispersion. J Pharm Sci 2011;100:2876-85
-
(2011)
J Pharm Sci
, Issue.100
, pp. 2876-2885
-
-
Kanaujia, P.1
Lau, G.2
Ng, W.K.3
-
96
-
-
83555168268
-
Understanding the tendency of amorphous solid dispersions to undergo amorphous-amorphous phase separation in the presence of absorbed moisture
-
Rumondor AC, Wikstrom H, Van Eerdenbrugh B, Taylor LS. Understanding the tendency of amorphous solid dispersions to undergo amorphous-amorphous phase separation in the presence of absorbed moisture. AAPS PharmSciTech 2011;12(4):1209-19
-
(2011)
AAPS PharmSciTech
, vol.12
, Issue.4
, pp. 1209-1219
-
-
Rumondor, A.C.1
Wikstrom, H.2
Van Eerdenbrugh, B.3
Taylor, L.S.4
-
97
-
-
0346494421
-
Increased Physical Stability and Improved Dissolution Properties of Itraconazole, a Class II Drug, by Solid Dispersions that Combine Fast- and Slow-Dissolving Polymers
-
DOI 10.1002/jps.10522
-
Six K, Verreck G, Peeters J, et al. Increased physical stability and improved dissolution properties of itraconazole, a class II drug, by solid dispersions that combine fast- and slow-dissolving polymers. J Pharm Sci 2004;93:124-31 (Pubitemid 38081820)
-
(2004)
Journal of Pharmaceutical Sciences
, vol.93
, Issue.1
, pp. 124-131
-
-
Six, K.1
Verreck, G.2
Peeters, J.3
Brewster, M.4
Van Den Mooter, G.5
-
98
-
-
12244283119
-
Characterization of solid dispersions of itraconazole and hydroxypropylmethylcellulose prepared by melt extrusion - Part I
-
DOI 10.1016/S0378-5173(02)00591-4, PII S0378517302005914
-
Verreck G, Six K, Van den Mooter G, et al. Characterization of solid dispersions of itraconazole and hydroxypropylmethylcellulose prepared by melt extrusion-Part 1. Int J Pharm 2003;251:165-74 (Pubitemid 36071471)
-
(2003)
International Journal of Pharmaceutics
, vol.251
, Issue.1-2
, pp. 165-174
-
-
Verreck, G.1
Six, K.2
Van Den Mooter, G.3
Baert, L.4
Peeters, J.5
Brewster, M.E.6
-
99
-
-
0242353023
-
An attempt to stabilize nilvadipine solid dispersion by the use of ternary systems
-
DOI 10.1081/DDC-120025456
-
Hirasawa N, Ishise S, Miyata H, Danio K. An attempt to stabilize nilvadipine solid dispersion by the use of ternary systems. Drug Dev Ind Pharm 2003;29(9):997-1004 (Pubitemid 37346101)
-
(2003)
Drug Development and Industrial Pharmacy
, vol.29
, Issue.9
, pp. 997-1004
-
-
Hirasawa, N.1
Ishise, S.2
Miyata, H.3
Danjo, K.4
-
100
-
-
77953236977
-
Predicting the formation and stability of amorphous small molecule binary mixtures from computationally determined flory-huggins interaction parameter and phase diagram
-
Pajula K, Taskinen M, Lehto VP, et al. Predicting the formation and stability of amorphous small molecule binary mixtures from computationally determined Flory-Huggins interaction parameter and phase diagram. Mol Pharm 2010;7(3):795-804
-
(2010)
Mol Pharm
, vol.7
, Issue.3
, pp. 795-804
-
-
Pajula, K.1
Taskinen, M.2
Lehto, V.P.3
-
101
-
-
75749094421
-
Review: Physical chemistry of solid dispersions
-
Janssens S, Van den Mooter G. Review: Physical chemistry of solid dispersions. J Pharm Pharmacol 2009;61(12):1571-86
-
(2009)
J Pharm Pharmacol
, vol.61
, Issue.12
, pp. 1571-1586
-
-
Janssens, S.1
Van Den Mooter, G.2
-
102
-
-
27744590957
-
Controlled release of drug via methylcellulose-carboxyvinylpolymer interpolymer complex solid dispersion
-
Ozeki T, Yuasa H, Okada H. Controlled release of drug via methylcellulose-carboxyvinylpolymer interpolymer complex solid dispersion. AAPS Pharm Sci Tech 2005;6(2):E231-6
-
(2005)
AAPS Pharm Sci Tech
, vol.6
, Issue.2
-
-
Ozeki, T.1
Yuasa, H.2
Okada, H.3
-
103
-
-
0033991012
-
Controlled release from solid dispersion composed of poly(ethylene oxide)-carbopol interpolymer complex with various cross-linking degrees of carbopol
-
Ozeki T, Yuasa H, Kanaya Y. Controlled release from solid dispersion composed of poly(ethylene oxide)-carbopol interpolymer complex with various cross-linking degrees of carbopol. J Control Release 2000;63(3):287-95
-
(2000)
J Control Release
, vol.63
, Issue.3
, pp. 287-295
-
-
Ozeki, T.1
Yuasa, H.2
Kanaya, Y.3
-
104
-
-
79960200912
-
Preparation and characterization of pH-independent sustained release tablets containing solid dispersion granules of a poorly water-soluble drug
-
Tran HT, Park JB, Hong KH, et al. Preparation and characterization of pH-independent sustained release tablets containing solid dispersion granules of a poorly water-soluble drug. Int J Pharm 2011;415(1-2):83-8
-
(2011)
Int J Pharm
, vol.415
, Issue.1-2
, pp. 83-88
-
-
Tran, H.T.1
Park, J.B.2
Hong, K.H.3
-
105
-
-
79952048160
-
Colon delivery of budesonide using solid dispersion in dextran foe the treatment and secondary prevention of ulcerative colitis in rat
-
Varshosaz J, Ahmadi F, Emami J, et al. Colon delivery of budesonide using solid dispersion in dextran foe the treatment and secondary prevention of ulcerative colitis in rat. Int J Prev Med 2010;1(2):115-23
-
(2010)
Int J Prev Med
, vol.1
, Issue.2
, pp. 115-123
-
-
Varshosaz, J.1
Ahmadi, F.2
Emami, J.3
-
106
-
-
77951485229
-
Dissolution-modulating mechanism of pH modifiers in solid dispersion containing weakly acidic or basic drugs with poor water solubility
-
Tran PH, Tran TT, Lee KH, et al. Dissolution-modulating mechanism of pH modifiers in solid dispersion containing weakly acidic or basic drugs with poor water solubility. Expert Opin Drug Deliv 2010;7:647-61
-
(2010)
Expert Opin Drug Deliv
, vol.7
, pp. 647-661
-
-
Tran, P.H.1
Tran, T.T.2
Lee, K.H.3
-
107
-
-
70649111297
-
The role of acidifiers in solid dispersions and physical mixtures
-
Tran TT, Tran PH, Choi HG, et al. The role of acidifiers in solid dispersions and physical mixtures. Int J Pharm 2010;384:60-6
-
(2010)
Int J Pharm
, vol.384
, pp. 60-6
-
-
Tran, T.T.1
Tran, P.H.2
Choi, H.G.3
-
108
-
-
33645758286
-
Development of novel sustained-release system, disintegration-controlled matrix tablet (DCMT) with solid dispersion granules of nivadipine (II): in vivo evaluation
-
Tanaka N, Imai K, Okimoto K, et al. Development of novel sustained-release system, disintegration-controlled matrix tablet (DCMT) with solid dispersion granules of nivadipine (II): in vivo evaluation. J Control Release 2006;112(1):51-6
-
(2006)
J Control Release
, vol.112
, Issue.1
, pp. 51-56
-
-
Tanaka, N.1
Imai, K.2
Okimoto, K.3
-
109
-
-
0031703807
-
Development of diclofenac sodium controlled release solid dispersion powders and capsules by freeze drying technique using ethylcellulose and chitosan as carriers
-
Dangprasirt P, Pongwai S. Development of diclofenac sodium controlled release solid dispersion powders and capsules by freeze drying technique using ethylcellulose and chitosan as carriers. Drug Dev Ind Pharm 1998;24:947-53 (Pubitemid 28470971)
-
(1998)
Drug Development and Industrial Pharmacy
, vol.24
, Issue.10
, pp. 947-953
-
-
Dangprasirt, P.1
Pongwai, S.2
-
110
-
-
79952939074
-
Development and evaluation of injection-molded sustained-release tablets containing ethylcellulose and polyethylene oxide
-
Quinten T, De Beer T, Almeida A, et al. Development and evaluation of injection-molded sustained-release tablets containing ethylcellulose and polyethylene oxide. Drug Dev Ind Pharm 2011;37:149-59
-
(2011)
Drug Dev Ind Pharm
, Issue.37
, pp. 149-159
-
-
Quinten, T.1
De Beer, T.2
Almeida, A.3
-
111
-
-
60749129536
-
Monolithic osmotic tablet containing solid dispersion of 10-hydroxycamptothecin
-
Chen H, Jiang G, Ding F. Monolithic osmotic tablet containing solid dispersion of 10-hydroxycamptothecin. Drug Dev Ind Pharm 2009;35:131-7
-
(2009)
Drug Dev Ind Pharm
, vol.35
, pp. 131-137
-
-
Chen, H.1
Jiang, G.2
Ding, F.3
-
112
-
-
42049097210
-
Development of extended release coevaporates and coprecipitates of promethazine HCl with acrylic polymers: Formulation considerations
-
DOI 10.1248/cpb.56.504
-
Dahiya S, Pathak K, Sharma R. Development of extended release coevaporates and coprecipitates of promethazine HCl with acrylic polymers: formulation considerations. Chem Pharm Bull (Tokyo) 2008;56:504-8 (Pubitemid 351520134)
-
(2008)
Chemical and Pharmaceutical Bulletin
, vol.56
, Issue.4
, pp. 504-508
-
-
Dahiya, S.1
Pathak, K.2
Sharma, R.3
-
113
-
-
0043158947
-
Design of sustained-release nitrendipine microspheres having solid dispersion structure by quasi-emulsion solvent diffusion method
-
DOI 10.1016/S0168-3659(03)00275-X
-
Cui F, Yang M, Jiang Y, et al. Design of sustained-release nitrendipine microspheres having solid dispersion structure by quasi-emulsion solvent diffusion method. J Control Release 2003;91(3):375-84 (Pubitemid 36976768)
-
(2003)
Journal of Controlled Release
, vol.91
, Issue.3
, pp. 375-384
-
-
Cui, F.1
Yang, M.2
Jiang, Y.3
Cun, D.4
Lin, W.5
Fan, Y.6
Kawashima, Y.7
-
114
-
-
0034255252
-
Stabilization and sustained-release effect of Misoprostol with Methacrylate copolymer
-
DOI 10.1016/S0378-5173(00)00451-8, PII S0378517300004518
-
Chen D, Tsay RJ, Lin HI, et al. Stabilization and sustained-release effect of misoprostol with methacrylate copolymer. Int J Pharm 2000;203:141-8 (Pubitemid 30627634)
-
(2000)
International Journal of Pharmaceutics
, vol.203
, Issue.1-2
, pp. 141-148
-
-
Chen, D.1
Tsay, R.-J.2
Lin, H.-I.3
Chen, H.4
Chao, S.-C.5
Ku, H.6
-
117
-
-
37249030951
-
-
Available from: http://www.fujichemical. co.jp/images/whatsnew/uploads/ 2010/10/Fuji-Email-Blast-CSD-SEP09-2008.pdf\
-
Available from
-
-
-
118
-
-
37249030951
-
-
Available from: http://xspray.com/technology.
-
Available from
-
-
-
119
-
-
37249030951
-
-
Available from: http://www. karolinskadevelopment.com/portfolio/ pharmaceutical-formulation/xspraymicroparticles-ab/
-
Available from
-
-
-
120
-
-
84877584533
-
-
Available from: http://www.ondrugdelivery.com/publications/Oral%202010/ Mayne.pdf\
-
Available from: http://www.smblab.be/index.php/formulation/lidose/121. Available from: http://www. ondrugdelivery.com/publications/Oral%202010/Mayne. pdf \
-
-
-
-
121
-
-
84877577022
-
-
Available from: http://chemistry-today. teknoscienze.com/pdf/hardung- CaseStudy-EXCIPENTS2010. pdf
-
-
-
-
122
-
-
84855764431
-
Soluplus- as an effective absorption enhancer of poorly soluble drugs in vitro and in vivo
-
Linn M, Collnot EM, Djuric D, et al. Soluplus- as an effective absorption enhancer of poorly soluble drugs in vitro and in vivo. Eur J Pharm Sci 2012;45(3):336-43
-
(2012)
Eur J Pharm Sci
, vol.45
, Issue.3
, pp. 336-343
-
-
Linn, M.1
Collnot, E.M.2
Djuric, D.3
-
123
-
-
84877581116
-
-
Available from: http://scidok.sulb.unisaarland. de/volltexte/2012/4551/ pdf/Linn-dissertation.pdf
-
-
-
-
124
-
-
67549096885
-
Preparation and characterization of co-grinded mixtures of aceclofenac and Neusilin US2 for dissolution enhancement of aceclofenac
-
Vadher AH, Parikh JR, Parikh RH, Solanki AB. Preparation and characterization of co-grinded mixtures of aceclofenac and Neusilin US2 for dissolution enhancement of aceclofenac. AAPS PharmSciTech 2009;10(2):606-14
-
(2009)
AAPS PharmSciTech
, vol.10
, Issue.2
, pp. 606-614
-
-
Vadher, A.H.1
Parikh, J.R.2
Parikh, R.H.3
Solanki, A.B.4
-
125
-
-
79958831448
-
Manufacture and performance evaluation of a stable amorphous complex of an acidic drug molecule and Neusilin
-
Maclean J, Medina C, Daurio D, et al. Manufacture and performance evaluation of a stable amorphous complex of an acidic drug molecule and Neusilin. J Pharm Sci 2011;100(8):3332-44
-
J Pharm Sci 2011
, vol.100
, Issue.8
, pp. 3332-3344
-
-
Maclean, J.1
Medina, C.2
Daurio, D.3
-
126
-
-
68949084952
-
Effect of the pH grade of silicates on chemical stability of coground amorphous quinapril hydrochloride and its stabilization using pH-modifiers
-
Hailu SA, Bonger RH. Effect of the pH grade of silicates on chemical stability of coground amorphous quinapril hydrochloride and its stabilization using pH-modifiers. J Pharm Sci 2009;98(9):3358-72
-
(2009)
J Pharm Sci
, vol.98
, Issue.9
, pp. 3358-3372
-
-
Hailu, S.A.1
Bonger, R.H.2
-
127
-
-
84877575617
-
-
Available from: http://www.neusilin.com/multicms/neusilin/pdf/articles/ 26/fuji-emailblast-neusilin-sep09-v2.pdf
-
-
-
-
128
-
-
33749431861
-
Amorphization of indomethacin by co-grinding with Neusilin US2: Amorphization kinetics, physical stability and mechanism
-
DOI 10.1007/s11095-006-9062-x
-
Bahl D, Bogner RH. Amorphization of indomethacin by co-grinding with Neusilin US2: Amorphization kinetics, physical stability and mechanism. Pharm Res 2006;23(10):2317-25 (Pubitemid 44511512)
-
(2006)
Pharmaceutical Research
, vol.23
, Issue.10
, pp. 2317-2325
-
-
Bahl, D.1
Bogner, R.H.2
-
129
-
-
0037369754
-
Formation of physically stable amorphous drugs by milling with neusilin
-
DOI 10.1002/jps.10308
-
Gupta MK, Vanwert A, Bogner RH. Formation of physically stable amorphous drugs by milling with Neusilin. J Pharm Sci 2003;92(3):536-51 (Pubitemid 36258968)
-
(2003)
Journal of Pharmaceutical Sciences
, vol.92
, Issue.3
, pp. 536-551
-
-
Gupta, M.K.1
Vanwert, A.2
Bogner, R.H.3
-
130
-
-
84877576211
-
-
Available from: http://www. ondrugdelivery.com/publications/ Oral%20May%202011/Oral%20Drug%20Delivery%20May%202011%20lo%20res.pdf
-
-
-
-
131
-
-
84877577666
-
-
133. Fujisawa Pharmaceutical Co., Ltd. Fast release solid preparation of dihydropyridine a compound. US4654206
-
Available from: http://www. ondrugdelivery.com/publications/Oral%202010/ Oral-Drug-Delivery-2010-ONdrugDelivery.pdf 133. Fujisawa Pharmaceutical Co., Ltd. Fast release solid preparation of dihydropyridine a compound. US4654206; 1987
-
(1987)
-
-
-
156
-
-
84880172047
-
-
Pentech Pharmaceuticals Inc. US6503927
-
Pentech Pharmaceuticals, Inc. Amorphous paroxetine composition. US6503927; 2003
-
(2003)
Amorphous paroxetine composition
-
-
-
168
-
-
84867779567
-
-
Sanofi-aventis U.S. LLC. US7713548
-
Sanofi-aventis U.S. LLC. Amorphous solid dispersions. US7713548; 2010
-
(2010)
Amorphous solid dispersions
-
-
|