-
3
-
-
0034601240
-
Improving drug solubility for oral delivery using solid dispersions
-
Leuner C and Dressman J. Improving drug solubility for oral delivery using solid dispersions. Eur. J. Pharm. Biopharm. (2000) 50: 47-60.
-
(2000)
Eur. J. Pharm.
, vol.50
, pp. 47-60
-
-
Leuner, C.1
Dressman, J.2
-
4
-
-
84858797264
-
Evaluation of amorphous solid dispersion properties using thermal analysis techniques
-
Baird JA and Taylor LS. Evaluation of amorphous solid dispersion properties using thermal analysis techniques. Adv. Drug Deliv. Rev. (2012) 64: 396-421.
-
(2012)
Adv. Drug Deliv. Rev
, vol.64
, pp. 396-421
-
-
Baird, J.A.1
Taylor, L.S.2
-
5
-
-
36549042006
-
Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs
-
Vasconcelos Tf, Sarmento B and Costa P. Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs. Drug Discov. Today(2007) 12: 1068-1075.
-
(2007)
Drug Discov. Today
, vol.12
, pp. 1068-1075
-
-
Tf, V.1
Sarmento, B.2
Costa, P.3
-
6
-
-
84862142131
-
Preparation, characterization and stability studies of glassy solid dispersions of indomethacin using PVP and isomalt as carriers
-
Khodaverdi E, Khalili N, Zangiabadi F and Homayouni A. Preparation, characterization and stability studies of glassy solid dispersions of indomethacin using PVP and isomalt as carriers. Iran. J. Basic. Med. Sci. (2012) 15: 820-832.
-
(2012)
Iran. J. Basic. Med. Sci
, vol.15
, pp. 820-832
-
-
Khodaverdi, E.1
Khalili, N.2
Zangiabadi, F.3
Homayouni, A.4
-
7
-
-
34447641982
-
Liquisolid technique for dissolution rate enhancement of a high dose water-insoluble drug (carbamazepine)
-
Javadzadeh Y, Jafari-Navimipour B and Nokhodchi A. Liquisolid technique for dissolution rate enhancement of a high dose water-insoluble drug (carbamazepine). Int. J. Pharm. (2007) 341: 26-34.
-
(2007)
Int. J. Pharm
, vol.341
, pp. 26-34
-
-
Javadzadeh, Y.1
Jafari-Navimipour, B.2
Nokhodchi, A.3
-
8
-
-
27444438012
-
The effect of type and concentration of vehicles on the dissolution rate of a poorly soluble drug (indomethacin) from liquisolid compacts
-
Nokhodchi A, Javadzadeh Y, Siahi-Shadbad MR and Barzegar-Jalali M. The effect of type and concentration of vehicles on the dissolution rate of a poorly soluble drug (indomethacin) from liquisolid compacts. J. Pharm. Pharm. Sci. (2005) 8: 18-25.
-
(2005)
J. Pharm. Pharm. Sci
, vol.8
, pp. 18-25
-
-
Nokhodchi, A.1
Javadzadeh, Y.2
Siahi-Shadbad, M.R.3
Barzegar-Jalali, M.4
-
9
-
-
34548032742
-
Salt formation to improve drug solubility
-
Serajuddin ATM. Salt formation to improve drug solubility.Adv. Drug Deliv. Rev. (2007) 59: 603-616.
-
(2007)
Adv. Drug Deliv. Rev
, vol.59
, pp. 603-616
-
-
Serajuddin, A.1
-
10
-
-
84867825837
-
Solid dispersions: A strategy for poorly aqueous soluble drugs and technology updates
-
Alam MA, Ali R, Al-Jenoobi FI and Al-Mohizea AM. Solid dispersions: a strategy for poorly aqueous soluble drugs and technology updates. Expert. Opin. Drug Deliv. (2012) 9: 1419-1440.
-
(2012)
Expert. Opin. Drug Deliv
, vol.9
, pp. 1419-1440
-
-
Alam, M.A.1
Ali, R.2
Al-Jenoobi, F.I.3
Al-Mohizea, A.M.4
-
11
-
-
77951538902
-
Combining HME & solubilization: Soluplus - The solid solution
-
Hardung H, Djuric D and Ali S. Combining HME & solubilization: Soluplus - The solid solution. Drug Deliv. Tech. (2010) 10: 20-27.
-
(2010)
Drug Deliv. Tech
, vol.10
, pp. 20-27
-
-
Hardung, H.1
Djuric, D.2
Ali, S.3
-
12
-
-
82255179553
-
Comparison of electrospun and extruded Soluplus -based solid dosage forms of improved dissolution
-
Nagy ZK, Balogh A, Vajna B, Farkas A, Patyi G, Kramarics A and Marosi G. Comparison of electrospun and extruded Soluplus -based solid dosage forms of improved dissolution. J. Pharm. Sci. (2012) 101: 322-332.
-
(2012)
J. Pharm. Sci
, vol.101
, pp. 322-332
-
-
Nagy, Z.K.1
Balogh, A.2
Vajna, B.3
Farkas, A.4
Patyi, G.5
Kramarics, A.6
Marosi, G.7
-
13
-
-
84855764431
-
Soluplus as an effective absorption enhancer of poorly soluble drugs in-vitro and in-vivo
-
Linn M, Collnot E-M, Djuric D, Hempel K, Fabian E, Kolter K and Lehr CM. Soluplus as an effective absorption enhancer of poorly soluble drugs in-vitro and in-vivo. Eur. J. Pharm. Sci. (2012) 45: 336-343.
-
(2012)
Eur. J. Pharm. Sci
, vol.45
, pp. 336-343
-
-
Linn, M.1
Collnot, E.-M.2
Djuric, D.3
Hempel, K.4
Fabian, E.5
Kolter, K.6
Lehr, C.M.7
-
14
-
-
84867401371
-
Dissolution enhancement of poorly water-soluble APIs processed by hot-melt extrusion using hydrophilic polymers
-
Maniruzzaman M, Rana MM, Boateng JS, Mitchell JC and Douroumis D. Dissolution enhancement of poorly water-soluble APIs processed by hot-melt extrusion using hydrophilic polymers. Drug Dev. Ind. Pharm. (2013) 39: 218-227.
-
(2013)
Drug Dev. Ind. Pharm
, vol.39
, pp. 218-227
-
-
Maniruzzaman, M.1
Rana, M.M.2
Boateng, J.S.3
Mitchell, J.C.4
Douroumis, D.5
-
15
-
-
84891645389
-
Bicalutamide nanocrystals with improved oral bioavailability: In vitro and in vivo evaluation
-
Pokharkar VB, Malhi T and Mandpe L. Bicalutamide nanocrystals with improved oral bioavailability: in vitro and in vivo evaluation. Pharm. Dev. Tech. (2013) 18: 660-666.
-
(2013)
Pharm. Dev. Tech
, vol.18
, pp. 660-666
-
-
Pokharkar, V.B.1
Malhi, T.2
Mandpe, L.3
-
16
-
-
0037093678
-
Determination of celecoxib in pharmaceutical formulations using UV spectrophotometry and liquid chromatography
-
Saha RN, Sajeev C, Jadhav PR, Patil SP and Srinivasan N. Determination of celecoxib in pharmaceutical formulations using UV spectrophotometry and liquid chromatography. J. Pharm. Biomed. Anal. (2002) 28: 741-751.
-
(2002)
J. Pharm. Biomed. Anal
, vol.28
, pp. 741-751
-
-
Saha, R.N.1
Sajeev, C.2
Jadhav, P.R.3
Patil, S.P.4
Srinivasan, N.5
-
17
-
-
78650366422
-
Mechanism of dissolution enhancement and bioavailability of poorly water soluble celecoxib by preparing stable amorphous nanoparticles
-
Wang S, Liu Y, Sun C, Hao Y, Jiang T and Zheng L. Mechanism of dissolution enhancement and bioavailability of poorly water soluble celecoxib by preparing stable amorphous nanoparticles. J. Pharm. Pharm. Sci. (2010) 13: 589-606.
-
(2010)
J. Pharm. Pharm. Sci
, vol.13
, pp. 589-606
-
-
Wang, S.1
Liu, Y.2
Sun, C.3
Hao, Y.4
Jiang, T.5
Zheng, L.6
-
18
-
-
3843097202
-
Classifcation of orally administered drugs on the World Health Organization Model list of Essential Medicines according to the biopharmaceutics classifcation system
-
Lindenberg M, Kopp S and Dressman JB. Classifcation of orally administered drugs on the World Health Organization Model list of Essential Medicines according to the biopharmaceutics classifcation system. Eur. J. Pharm. Biopharm. (2004) 58: 265-278.
-
(2004)
Eur. J. Pharm. Biopharm
, vol.58
, pp. 265-278
-
-
Lindenberg, M.1
Kopp, S.2
Dressman, J.B.3
-
19
-
-
67349199134
-
Advantages of celecoxib nanosuspension formulation and transformation into tablets
-
Dolenc A, Kristl J, Baumgartner S and Planinsek O. Advantages of celecoxib nanosuspension formulation and transformation into tablets. Int. J. Pharm. (2009) 376: 204-212.
-
(2009)
Int. J. Pharm
, vol.376
, pp. 204-212
-
-
Dolenc, A.1
Kristl, J.2
Baumgartner, S.3
Planinsek, O.4
-
20
-
-
68349150895
-
Prediction of food effects on the absorption of celecoxib based on biorelevant dissolution testing coupled with physiologically based pharmacokinetic modeling
-
Shono Y, Jantratid E, Janssen N, Kesisoglou F, Mao Y, Vertzoni M, Reppas C and Dressman J. Prediction of food effects on the absorption of celecoxib based on biorelevant dissolution testing coupled with physiologically based pharmacokinetic modeling. Europ. J. Pharm. Biopharm. (2009) 73: 107-114.
-
(2009)
Europ. J. Pharm. Biopharm
, vol.73
, pp. 107-114
-
-
Shono, Y.1
Jantratid, E.2
Janssen, N.3
Kesisoglou, F.4
Mao, Y.5
Vertzoni, M.6
Reppas, C.7
Dressman, J.8
-
21
-
-
80955135462
-
The use of spray-drying to enhance celecoxib solubility
-
Fouad EA, El-Badry M, Mahrous GM, Alanazi FK, Neau SH and Alsarra IA. The use of spray-drying to enhance celecoxib solubility. Drug Dev. Ind. Pharm. (2011) 37: 1463-1472.
-
(2011)
Drug Dev. Ind. Pharm
, vol.37
, pp. 1463-1472
-
-
Fouad, E.A.1
El-Badry, M.2
Mahrous, G.M.3
Alanazi, F.K.4
Neau, S.H.5
Alsarra, I.A.6
-
22
-
-
78649653372
-
Physicochemical characterization and drug-release properties of celecoxib hot-melt extruded glass solutions
-
Andrews GP, Abu-Diak O, Kusmanto F, Hornsby P, Hui Z and Jones DS. Physicochemical characterization and drug-release properties of celecoxib hot-melt extruded glass solutions. J. Pharm. Pharmacol. (2010) 62: 1580-1590.
-
(2010)
J. Pharm. Pharmacol
, vol.62
, pp. 1580-1590
-
-
Andrews, G.P.1
Abu-Diak, O.2
Kusmanto, F.3
Hornsby, P.4
Hui, Z.5
Jones, D.S.6
-
23
-
-
6344247455
-
Stability and solubility of celecoxib-PVP amorphous dispersions: A molecular perspective
-
Gupta P, Kakumanu VK and Bansal AK. Stability and solubility of celecoxib-PVP amorphous dispersions: a molecular perspective. Pharm. Res. (2004) 21: 1762-1769.
-
(2004)
Pharm. Res
, vol.21
, pp. 1762-1769
-
-
Gupta, P.1
Kakumanu, V.K.2
Bansal, A.K.3
-
24
-
-
1442310829
-
Solubility enhancement of celecoxib using beta-cyclodextrin inclusion complexes
-
Rawat S and Jain SK. Solubility enhancement of celecoxib using beta-cyclodextrin inclusion complexes. Eur. J. Pharm. Biopharm. (2004) 57: 263-267.
-
(2004)
Eur. J. Pharm. Biopharm
, vol.57
, pp. 263-267
-
-
Rawat, S.1
Jain, S.K.2
-
25
-
-
33745399852
-
Design and evaluation of celecoxib porous particles using melt sonocrystallization
-
Paradkar A, Maheshwari M, Kamble R, Grimsey I and York P. Design and evaluation of celecoxib porous particles using melt sonocrystallization. Pharm. Res. (2006) 23: 1395-1400.
-
(2006)
Pharm. Res
, vol.23
, pp. 1395-1400
-
-
Paradkar, A.1
Maheshwari, M.2
Kamble, R.3
Grimsey, I.4
York, P.5
-
26
-
-
34548322706
-
Infuence of polymers on the bioavailability of microencapsulated celecoxib
-
Homar M, Ubrich N, Ghazouani FE, Kristl J, Kerč J and Maincent P. Infuence of polymers on the bioavailability of microencapsulated celecoxib. J. Microencapsul. (2007) 24: 621-633.
-
(2007)
J.
, vol.24
, pp. 621-633
-
-
Homar, M.1
Ubrich, N.2
Ghazouani, F.E.3
Kristl, J.4
Kerč, J.5
Maincent, P.6
-
27
-
-
33646822128
-
Improved solubilization of Celecoxib in U-type nonionic microemulsions and their structural transitions with progressive aqueous dilution
-
Garti N, Avrahami M and Aserin A. Improved solubilization of Celecoxib in U-type nonionic microemulsions and their structural transitions with progressive aqueous dilution. J. Collod Interf. Sci. (2006) 299: 352-365.
-
(2006)
J. Collod Interf. Sci
, vol.299
, pp. 352-365
-
-
Garti, N.1
Avrahami, M.2
Aserin, A.3
-
28
-
-
0035073301
-
Modeling and comparison of dissolution profles
-
Costa P and Sousa Lobo JM. Modeling and comparison of dissolution profles. Eur. J. Pharm. Sci. (2001) 13: 123-133.
-
(2001)
Eur. J. Pharm. Sci
, vol.13
, pp. 123-133
-
-
Costa, P.1
Sousa Lobo, J.M.2
-
29
-
-
23144465464
-
Solubility enhancement of Cox-2 inhibitors using various solvent systems
-
Seedher N and Bhatia S. Solubility enhancement of Cox-2 inhibitors using various solvent systems. AAPS Pharm. Sci. Tech. (2003) 4: 1-9.
-
(2003)
AAPS Pharm. Sci. Tech
, vol.4
, pp. 1-9
-
-
Seedher, N.1
Bhatia, S.2
-
30
-
-
75749094421
-
Review: Physical chemistry of solid dispersions
-
Janssens S and Van Den Mooter G. Review: Physical chemistry of solid dispersions. J. Pharm. Pharmacol. (2009) 61: 1571-1586.
-
(2009)
J. Pharm. Pharmacol
, vol.61
, pp. 1571-1586
-
-
Janssens, S.1
Van Den Mooter, G.2
-
31
-
-
84877921505
-
Manufacturing of solid dispersions of poorly
-
Paudel A, Worku ZA, Meeus J, Guns S and Vanden Mooter G. Manufacturing of solid dispersions of poorly water soluble drugs by spray drying: Formulation and process considerations. Int. J. Pharm. (2013) 453: 253-84.
-
(2013)
Int. J. Pharm
, vol.453
, pp. 84
-
-
Paudel, A.1
Worku, Z.A.2
Meeus, J.3
Guns, S.4
Vanden Mooter, G.5
-
32
-
-
0242334087
-
Characterization of solid-state forms of celecoxib
-
Chawla G, Gupta P, Thilagavathi R, Chakraborti AK and Bansal AK. Characterization of solid-state forms of celecoxib. Eur. J. Pharm. Sci. (2003) 20: 305-317.
-
(2003)
Eur. J. Pharm. Sci
, vol.20
, pp. 305-317
-
-
Chawla, G.1
Gupta, P.2
Thilagavathi, R.3
Chakraborti, A.K.4
Bansal, A.K.5
-
33
-
-
84863719303
-
Hot melt mixing and foaming of soluplus and indomethacin
-
Terife G, Wang P, Faridi N and Gogos CG. Hot melt mixing and foaming of soluplus and indomethacin. J. Polym. Eng. Sci. (2012) 52: 1629-1639.
-
(2012)
J. Polym. Eng. Sci
, vol.52
, pp. 1629-1639
-
-
Terife, G.1
Wang, P.2
Faridi, N.3
Gogos, C.G.4
-
34
-
-
27144512688
-
Role of molecular interaction in stability of celecoxib-PVP amorphous systems
-
Gupta P, Thilagavathi R, Chakraborti AK and Bansal AK. Role of molecular interaction in stability of celecoxib-PVP amorphous systems. Mol. Pharm. (2005) 2: 384-391.
-
(2005)
Mol. Pharm
, vol.2
, pp. 384-391
-
-
Gupta, P.1
Thilagavathi, R.2
Chakraborti, A.K.3
Bansal, A.K.4
-
35
-
-
77952196842
-
Wettability and surface chemistry of crystalline and amorphous forms of a poorly water soluble drug
-
Puri V, Dantuluri AK, Kumar M, Karar N and Bansal AK. Wettability and surface chemistry of crystalline and amorphous forms of a poorly water soluble drug. Eur. J. pharm. Sci. (2010) 40: 84-93.
-
(2010)
Eur. J. Pharm. Sci
, vol.40
, pp. 84-93
-
-
Puri, V.1
Dantuluri, A.K.2
Kumar, M.3
Karar, N.4
Bansal, A.K.5
-
37
-
-
84862897078
-
Mechanistic insights into the dissolution of spray-dried amorphous solid dispersions
-
Langham ZA, Booth J, Hughes LP, Reynolds GK and Wren SAC. Mechanistic insights into the dissolution of spray-dried amorphous solid dispersions. J. Pharm. Sci. (2012) 101: 2798-2810.
-
(2012)
J. Pharm. Sci
, vol.101
, pp. 2798-2810
-
-
Langham, Z.A.1
Booth, J.2
Hughes, L.P.3
Reynolds, G.K.4
Wren, S.5
-
38
-
-
3042549390
-
Anomalous dissolution behaviour of tablets prepared from sugar glass-based solid dispersions
-
van Drooge DJ, Hinrichs WL and Frijlink HW. Anomalous dissolution behaviour of tablets prepared from sugar glass-based solid dispersions. J. Control. Release(2004) 97: 441-452.
-
(2004)
J. Control. Release
, vol.97
, pp. 441-452
-
-
Van Drooge, D.J.1
Hinrichs, W.L.2
Frijlink, H.W.3
-
39
-
-
84875134614
-
The effect of PEG molecular weights on dissolution behavior of simvastatin in solid dispersions
-
Bolourchian N, Mahboobian MM and Dadashzadeh S. The effect of PEG molecular weights on dissolution behavior of simvastatin in solid dispersions. Iran. J. Pharm. Res. (2013) 12: 11-20.
-
(2013)
Iran. J. Pharm. Res
, vol.12
, pp. 11-20
-
-
Bolourchian, N.1
Mahboobian, M.M.2
Dadashzadeh, S.3
-
40
-
-
1842865536
-
Melt extrusion: From process to drug delivery technology
-
Breitenbach J. Melt extrusion: from process to drug delivery technology. Eur. J. Pharm. Biopharm. (2002) 54: 107-117.
-
(2002)
Eur. J. Pharm. Biopharm
, vol.54
, pp. 107-117
-
-
Breitenbach, J.1
-
41
-
-
84878626156
-
Enhanced dissolution rate of celecoxib using PVP and/or HPMC-based solid dispersions prepared by spray drying method
-
Lee J, Kim M, Yoon H, Shim C, Ko H, Cho S, Lee D and Khang G. Enhanced dissolution rate of celecoxib using PVP and/or HPMC-based solid dispersions prepared by spray drying method. J. Pharm. Invest. (2013) 43: 205-213.
-
(2013)
J. Pharm. Invest
, vol.43
, pp. 205-213
-
-
Lee, J.1
Kim, M.2
Yoon, H.3
Shim, C.4
Ko, H.5
Cho, S.6
Lee, D.7
Khang, G.8
-
42
-
-
0037074108
-
The mechanisms of drug release from solid dispersions in water-soluble polymers
-
Craig DQM. The mechanisms of drug release from solid dispersions in water-soluble polymers. Int. J. Pharm. (2002) 231: 131-144.
-
(2002)
Int. J. Pharm
, vol.231
, pp. 131-144
-
-
Craig, D.1
|