-
2
-
-
0034601240
-
Improving drug solubility for oral delivery using solid dispersions
-
Dressman J, Leuner C. Improving drug solubility for oral delivery using solid dispersions. Eur J Pharm Biopharm. 2000; 50: 47-60.
-
(2000)
Eur J Pharm Biopharm.
, vol.50
, pp. 47-60
-
-
Dressman, J.1
Leuner, C.2
-
3
-
-
0034665061
-
The formulation of Halofantrine as either non-solubilizing PEG-6000 or solubilizing lipid based solid dispersions: Physical stability and absolute bioavailability assessment
-
Khoo S, Christopher JH, Charman WN. The formulation of Halofantrine as either non-solubilizing PEG-6000 or solubilizing lipid based solid dispersions: physical stability and absolute bioavailability assessment. Int J Pharm. 2000; 205(1-2): 65-78.
-
(2000)
Int J Pharm.
, vol.205
, Issue.1-2
, pp. 65-78
-
-
Khoo, S.1
Christopher, J.H.2
Charman, W.N.3
-
4
-
-
77953450589
-
Preparation and evaluation of ternary mixing itraconazole solid dispersions by spray drying method
-
Rajarajan S, Baby B, Ramesh K, Singh D. Preparation and evaluation of ternary mixing itraconazole solid dispersions by spray drying method. J Pharm Sci Res. 2009; 11(1): 22-25
-
(2009)
J Pharm Sci Res.
, vol.11
, Issue.1
, pp. 22-25
-
-
Rajarajan, S.1
Baby, B.2
Ramesh, K.3
Singh, D.4
-
5
-
-
84886041009
-
In: The Merck Index
-
14th ed., Merck, Whitehouse Station, NJ, USA
-
Oneil M, Heckelman PE, Koch CB. In: The Merck Index. An Encyclopedia of Chemicals: Drugs and Biologicals, 14th ed., Merck, Whitehouse Station, NJ, USA, 2006; p. 503.
-
(2006)
An Encyclopedia of Chemicals: Drugs and Biologicals
, pp. 503
-
-
Oneil, M.1
Heckelman, P.E.2
Koch, C.B.3
-
6
-
-
33947210775
-
Selection of reliable reference genes for q PCR studies on chondroprotective action
-
Toegel S, Huang W, Piana C, Unger FM, Wirth M, Goldring MB, Gabor F. Selection of reliable reference genes for q PCR studies on chondroprotective action. BMC Mol Biol. 2007; 8:13.
-
(2007)
BMC Mol Biol.
, vol.8
, pp. 13
-
-
Toegel, S.1
Huang, W.2
Piana, C.3
Unger, F.M.4
Wirth, M.5
Goldring, M.B.6
Gabor, F.7
-
7
-
-
0037067363
-
Pharmacological studies of diacerein in animal models of inflammation arthritis and bone resorption
-
Tamura T, Shirai T, Kosaka N, Ohmori K, Takafumi N. Pharmacological studies of diacerein in animal models of inflammation arthritis and bone resorption. Eur J Pharmacol. 2002; 448: 81-87.
-
(2002)
Eur J Pharmacol.
, vol.448
, pp. 81-87
-
-
Tamura, T.1
Shirai, T.2
Kosaka, N.3
Ohmori, K.4
Takafumi, N.5
-
8
-
-
0035134180
-
An active metabolite of diacerein, suppresses the interleukin-1β-inducedproteoglycan degradation in cultured rabbit articular chondrocytes
-
Tamura T, Ohmori K. Rhehin. An active metabolite of diacerein, suppresses the interleukin-1β-inducedproteoglycan degradation in cultured rabbit articular chondrocytes. Jpn J Pharmacol. 2001; 85: 101-104.
-
(2001)
Jpn J Pharmacol.
, vol.85
, pp. 101-104
-
-
Tamura, T.1
Rhehin, O.K.2
-
9
-
-
84886060424
-
-
Diacerein Product Description, Ltd. (accessed on August 10,). Available at
-
Diacerein Product Description. Xian Guanyu Bio-Tech Co. Ltd. (accessed on August 10, 2009). Available at http://www.bikudo.com/product_search/d etails/44285/diacerein.html
-
(2009)
Xian Guanyu Bio-Tech Co
-
-
-
10
-
-
84885962568
-
Diacerein Capsules
-
(accessed on August 10,). Available at
-
Diacerein Capsules. Ostomod. (accessed on August 10, 2009). Available at http://www.cipladoc.com/therapeutic/pdf _cipla/ostomod.pdf
-
(2009)
Ostomod
-
-
-
12
-
-
23144440785
-
Triamterene β-cyclodextrin systems: Preparation, characterization and in-vivo evaluation
-
Mukne AP, Nagarsenker MS. Triamterene β-cyclodextrin systems: preparation, characterization and in-vivo evaluation. AAPS PharmSciTech. 2004; 5: 19-24.
-
(2004)
AAPS PharmSciTech.
, vol.5
, pp. 19-24
-
-
Mukne, A.P.1
Nagarsenker, M.S.2
-
13
-
-
0035073301
-
Modeling and comparison of dissolution profiles
-
Costa P, Sousa L. Modeling and comparison of dissolution profiles. Eur J Pharm Sci. 2001; 13(2): 123-133.
-
(2001)
Eur J Pharm Sci.
, vol.13
, Issue.2
, pp. 123-133
-
-
Costa, P.1
Sousa, L.2
-
14
-
-
0344673395
-
Methods to enhance the complexation efficiency of cyclodextrin
-
Loftsson T, Masson M, Sigurjonsdottir JF. Methods to enhance the complexation efficiency of cyclodextrin. STP Pharma Sci. 1999; 9: 237-242.
-
(1999)
STP Pharma Sci.
, vol.9
, pp. 237-242
-
-
Loftsson, T.1
Masson, M.2
Sigurjonsdottir, J.F.3
-
15
-
-
13544273358
-
Physical properties and dissolution behaviour of nifedipine/mannitol solid dispersions prepared by hot melt method
-
Zajc N, Obreza A, Bele M, Srcic S. Physical properties and dissolution behaviour of nifedipine/mannitol solid dispersions prepared by hot melt method. Int J Pharm. 2005; 291: 51-58
-
(2005)
Int J Pharm.
, vol.291
, pp. 51-58
-
-
Zajc, N.1
Obreza, A.2
Bele, M.3
Srcic, S.4
-
16
-
-
80054856792
-
Enhancement of celecoxib solubility by solid disperson using mannitol
-
Punitha S, Vedha Hari BN, Karthikeyan D. Enhancement of celecoxib solubility by solid disperson using mannitol. Int J Pharm Pharm Sci. 2010; 2(4): 109-111.
-
(2010)
Int J Pharm Pharm Sci.
, vol.2
, Issue.4
, pp. 109-111
-
-
Punitha, S.1
Vedha Hari, B.N.2
Karthikeyan, D.3
-
17
-
-
2342652446
-
Mathematical comparison of dissolution profiles
-
Moore JW, Flanner H. Mathematical comparison of dissolution profiles. Pharm Technol. 1996; 20: 64-74.
-
(1996)
Pharm Technol.
, vol.20
, pp. 64-74
-
-
Moore, J.W.1
Flanner, H.2
-
18
-
-
34248535178
-
Studies on dissolution enhancement and mathematical modeling of drug release of a poorly water-soluble drug using water soluble carriers
-
Ahuja N, Katare OP, Singh B. Studies on dissolution enhancement and mathematical modeling of drug release of a poorly water-soluble drug using water soluble carriers. Eur J Pharm Biopharm. 2007; 65 (1): 26-38.
-
(2007)
Eur J Pharm Biopharm.
, vol.65
, Issue.1
, pp. 26-38
-
-
Ahuja, N.1
Katare, O.P.2
Singh, B.3
-
19
-
-
0031864961
-
A review of methods used to compare dissolution profile data
-
O'Hara T, Dunne A, Butler J, Devane J. A review of methods used to compare dissolution profile data. Pharm Sci Technol To. 1998; 1(5): 214-223.
-
(1998)
Pharm Sci Technol To.
, vol.1
, Issue.5
, pp. 214-223
-
-
O'Hara, T.1
Dunne, A.2
Butler, J.3
Devane, J.4
-
22
-
-
0029847154
-
Properties of solid dispersions of naproxen in various polyethylene glycols
-
Mura P, Manderioli A, Bramanti G, Ceccarelli L. Properties of solid dispersions of naproxen in various polyethylene glycols. Drug Dev Ind Pharm. 1996; 22(9-10): 909-916.
-
(1996)
Drug Dev Ind Pharm.
, vol.22
, Issue.9-10
, pp. 909-916
-
-
Mura, P.1
Manderioli, A.2
Bramanti, G.3
Ceccarelli, L.4
-
23
-
-
0025269652
-
Improved dissolution of poorly water soluble drug from solid dispersions in poly ethylene:Polysorbste 80 mixtures
-
Serajudin ATM, Sheen PC, Augustine M A. Improved dissolution of poorly water soluble drug from solid dispersions in poly ethylene:polysorbste 80 mixtures. J Pharm Sci 1990; 79: 463-464.
-
(1990)
J Pharm Sci
, vol.79
, pp. 463-464
-
-
Serajudin, A.T.M.1
Sheen, P.C.2
Augustine, M.A.3
-
24
-
-
0024218073
-
Effect of vehicle amphiphilicity on the dissolution and bioavailability of a poorly watersoluble drug from solid dispersions
-
Serajuddin ATM, Sheen PC, Mufson D, Bernstein DF, Augustine MA. Effect of vehicle amphiphilicity on the dissolution and bioavailability of a poorly watersoluble drug from solid dispersions. J Pharm Sci. 1988; 77: 414-417.
-
(1988)
J Pharm Sci.
, vol.77
, pp. 414-417
-
-
Serajuddin, A.T.M.1
Sheen, P.C.2
Mufson, D.3
Bernstein, D.F.4
Augustine, M.A.5
-
25
-
-
51449104992
-
Enhancement of dissolution rate of gliclazide using solid dispersions with polyethylene glycol 6000
-
Biswal S, Sahoo J, Murthy PN, Giradkar RP. Enhancement of dissolution rate of gliclazide using solid dispersions with polyethylene glycol 6000. AAPS PharmSciTech. 2008; 9(2): 563-570
-
(2008)
AAPS PharmSciTech.
, vol.9
, Issue.2
, pp. 563-570
-
-
Biswal, S.1
Sahoo, J.2
Murthy, P.N.3
Giradkar, R.P.4
-
26
-
-
1242321019
-
Characterization of ibuproxam binary and ternary dispersions with hydrophilic carriers
-
Cirri M, Mura P, Rabasco AM, Gines JM, Moyano JR. Characterization of ibuproxam binary and ternary dispersions with hydrophilic carriers. Drug Dev Ind Pharm. 2004; 30(1): 65-74.
-
(2004)
Drug Dev Ind Pharm.
, vol.30
, Issue.1
, pp. 65-74
-
-
Cirri, M.1
Mura, P.2
Rabasco, A.M.3
Gines, J.M.4
Moyano, J.R.5
-
27
-
-
0035964465
-
In-vitro and in-vivo evaluation of carbamazepine-PEG 6000 solid dispersions
-
Zerrouk N, Chemtob C, Arnaud P, Toscani S. In-vitro and in-vivo evaluation of carbamazepine-PEG 6000 solid dispersions. Int J Pharm. 2001; 225(1-2): 49-62.
-
(2001)
Int J Pharm.
, vol.225
, Issue.1-2
, pp. 49-62
-
-
Zerrouk, N.1
Chemtob, C.2
Arnaud, P.3
Toscani, S.4
-
28
-
-
0034601240
-
Improving drug solubility for oral delivery using solid dispersions
-
Leuner C, Dressman J. Improving drug solubility for oral delivery using solid dispersions. Eur J Pharm Biopharm. 2000; 50: 47-60.
-
(2000)
Eur J Pharm Biopharm.
, vol.50
, pp. 47-60
-
-
Leuner, C.1
Dressman, J.2
-
29
-
-
1842609789
-
Development of selfmicroemulsifying drug delivery systems (SMEDDS) for oral bioavailability enhancement of simvastatin in beagle dogs
-
Kang BK, Lee JS, Chon SK, Jeong SY, Yuk SH. Development of selfmicroemulsifying drug delivery systems (SMEDDS) for oral bioavailability enhancement of simvastatin in beagle dogs. Int J Pharm. 2004; 274: 65-73.
-
(2004)
Int J Pharm.
, vol.274
, pp. 65-73
-
-
Kang, B.K.1
Lee, J.S.2
Chon, S.K.3
Jeong, S.Y.4
Yuk, S.H.5
-
30
-
-
33646850912
-
Effect of hydrogen bonding interactions on the release mechanism of felodipine from nanodispersions with polyvinylpyrrolidone
-
Karavas E, Ktistis G, Xenakis A, Georgarakis E. Effect of hydrogen bonding interactions on the release mechanism of felodipine from nanodispersions with polyvinylpyrrolidone. Eur J Pharm Biopharm. 2006; 63: 103-114.
-
(2006)
Eur J Pharm Biopharm.
, vol.63
, pp. 103-114
-
-
Karavas, E.1
Ktistis, G.2
Xenakis, A.3
Georgarakis, E.4
-
31
-
-
33751014029
-
Formulation of poorly water-soluble drugs for oral administration: Physicochemical and physiological issues and the lipid formulation classification system
-
Pouton CW. Formulation of poorly water-soluble drugs for oral administration: physicochemical and physiological issues and the lipid formulation classification system. Eur J Pharm Sci. 2006; 29: 278-287.
-
(2006)
Eur J Pharm Sci.
, vol.29
, pp. 278-287
-
-
Pouton, C.W.1
-
33
-
-
0032965054
-
Preparation of biodegradable microparticles using solution enhanced dispersion by supercritical fluids (SEDS)
-
Ghaderi R, Artursson P, Carifors J. Preparation of biodegradable microparticles using solution enhanced dispersion by supercritical fluids (SEDS). Pharm Res. 1999;16: 676-681.
-
(1999)
Pharm Res.
, vol.16
, pp. 676-681
-
-
Ghaderi, R.1
Artursson, P.2
Carifors, J.3
-
34
-
-
33747033371
-
Development, characterization and stabilization of amorphous form of a low Tg drug
-
Pokharkar VB, Mandpe LP, Padamwar MN, Ambike AA, Mahadik KR. Development, characterization and stabilization of amorphous form of a low Tg drug. Powder Technol. 2006; 167: 20-25.
-
(2006)
Powder Technol.
, vol.167
, pp. 20-25
-
-
Pokharkar, V.B.1
Mandpe, L.P.2
Padamwar, M.N.3
Ambike, A.A.4
Mahadik, K.R.5
-
35
-
-
0032989612
-
A calorimetric investigation into the interaction between paracetamol and polyethylene glycol 4000 in physical mixes and solid dispersions
-
Lioyd GR, Craig DQ, Smith A. A calorimetric investigation into the interaction between paracetamol and polyethylene glycol 4000 in physical mixes and solid dispersions. Eur J Pharm Biopharm.1999; 48: 59-65.
-
(1999)
Eur J Pharm Biopharm.
, vol.48
, pp. 59-65
-
-
Lioyd, G.R.1
Craig, D.Q.2
Smith, A.3
-
36
-
-
0031423468
-
Spectroscopic characterization of interactions between PVP and indomethacin in amorphous molecular dispersions
-
Taylor LS, Zografi G. Spectroscopic characterization of interactions between PVP and indomethacin in amorphous molecular dispersions. Pharm Res. 1997; 14: 1691-1698
-
(1997)
Pharm Res.
, vol.14
, pp. 1691-1698
-
-
Taylor, L.S.1
Zografi, G.2
-
38
-
-
0034601240
-
Improving drug solubility for oral delivery using solid dispersions
-
Leuner C, Dressman J. Improving drug solubility for oral delivery using solid dispersions. Eur J Pharm Biopharm. 2000; 50: 47-60.
-
(2000)
Eur J Pharm Biopharm.
, vol.50
, pp. 47-60
-
-
Leuner, C.1
Dressman, J.2
-
39
-
-
0032513499
-
Physicochemical characterization of solid dispersions of temazepam with polyethylene glycol 6000 and PVP K-30
-
Mooter GV, Augustijns P, Blaton N and Kinget R. Physicochemical characterization of solid dispersions of temazepam with polyethylene glycol 6000 and PVP K-30. 1998. Int J Pharm; 164: 67-80.
-
(1998)
Int J Pharm
, vol.164
, pp. 67-80
-
-
Mooter, G.V.1
Augustijns, P.2
Blaton, N.3
Kinget, R.4
-
40
-
-
67149144842
-
Synergistic enhancement of itraconazole dissolution by ternary system formation with Pluronic F-68 and hydroxypropylmethylcellulose
-
El-Maghraby GM, Alomrani AH. Synergistic enhancement of itraconazole dissolution by ternary system formation with Pluronic F-68 and hydroxypropylmethylcellulose. 2009. Sci Pharm; 77: 401-417.
-
(2009)
Sci Pharm
, vol.77
, pp. 401-417
-
-
El-Maghraby, G.M.1
Alomrani, A.H.2
-
41
-
-
0032768725
-
Solid state studies of drug cyclodextrin inclusion complexes in PEG 6000 prepared by a new method
-
Wulff M, Aldén M. Solid state studies of drug cyclodextrin inclusion complexes in PEG 6000 prepared by a new method. Eur J Pharm Sci. 1999; 8: 269-281.
-
(1999)
Eur J Pharm Sci.
, vol.8
, pp. 269-281
-
-
Wulff, M.1
Aldén, M.2
-
42
-
-
3042550643
-
Development and evaluation of glyburide fast dissolving tablets using solid dispersion technique
-
Valleri M, Mura P, Maestrelli F, Cirri M, Ballerini R. Development and evaluation of glyburide fast dissolving tablets using solid dispersion technique. Drug Dev Ind Pharm. 2004; 30: 525-534.
-
(2004)
Drug Dev Ind Pharm.
, vol.30
, pp. 525-534
-
-
Valleri, M.1
Mura, P.2
Maestrelli, F.3
Cirri, M.4
Ballerini, R.5
-
43
-
-
19544378015
-
Improving the solubility of ampelopsin by solid dispersions and inclusion complexes
-
Ruan LP, Yu BY, Fu GM, Zhu DN. Improving the solubility of ampelopsin by solid dispersions and inclusion complexes. J Pharm Biomed Anal. 2005; 38: 457-464.
-
(2005)
J Pharm Biomed Anal.
, vol.38
, pp. 457-464
-
-
Ruan, L.P.1
Yu, B.Y.2
Fu, G.M.3
Zhu, D.N.4
-
44
-
-
23144461484
-
Preparation of solid dispersions of non steroidal anti-inflammatory drugs with acrylic polymers and studies on mechanisms of drug polymer interactions
-
Pignatello R, Ferro M, Puglisi G. Preparation of solid dispersions of non steroidal anti-inflammatory drugs with acrylic polymers and studies on mechanisms of drug polymer interactions. AAPS PharmSciTech. 2002; 3: E10.
-
(2002)
AAPS PharmSciTech.
, vol.3
-
-
Pignatello, R.1
Ferro, M.2
Puglisi, G.3
-
45
-
-
17644421075
-
Preparation and in-vitro characterization of a semi solid dispersion of flurbiprofen with Gelucire 44/14 and Labrasol
-
Soliman MS, Khan MA. Preparation and in-vitro characterization of a semi solid dispersion of flurbiprofen with Gelucire 44/14 and Labrasol. Pharmazie. 2005; 60: 288-293.
-
(2005)
Pharmazie.
, vol.60
, pp. 288-293
-
-
Soliman, M.S.1
Khan, M.A.2
-
46
-
-
0003520774
-
-
5th ed., John Wiley and Sons Inc., NY, USA
-
Silverstein RM, Bassler GC, Morrill TC. Spectroscopic Identification of organic compounds. 5th ed., John Wiley and Sons Inc., NY, USA, 1991.
-
(1991)
Spectroscopic Identification of organic compounds
-
-
Silverstein, R.M.1
Bassler, G.C.2
Morrill, T.C.3
|