-
1
-
-
53549113334
-
Improved dissolution of a poorly water soluble drug in solid dispersions with polymeric and non-polymeric hydrophilic additives
-
Chawla G, Bansal AK. Improved dissolution of a poorly water soluble drug in solid dispersions with polymeric and non-polymeric hydrophilic additives. Acta Pharm. 2008,58: 257-274.
-
(2008)
Acta Pharm.
, vol.58
, pp. 257-274
-
-
Chawla, G.1
Bansal, A.K.2
-
2
-
-
0015124656
-
Pharmaceutical applications of solid dispersion systems
-
Chiou WL, Riegelman S. Pharmaceutical applications of solid dispersion systems. J Pharm Sci. 1971, 60: 1281-302.
-
(1971)
J Pharm Sci.
, vol.60
, pp. 1281-1302
-
-
Chiou, W.L.1
Riegelman, S.2
-
4
-
-
0037074108
-
The mechanisms of drug release from solid dispersions in water-soluble polymers
-
Craig DQ. 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.Q.1
-
5
-
-
0032513499
-
Physicochemical characterization of solid dispersions of temazepam with polyethylene glycol 6000 and PVP K30
-
Van den Mooter G, Augustijns P, Blaton N, et al. Physicochemical characterization of solid dispersions of temazepam with polyethylene glycol 6000 and PVP K30. Int J Pharm. 1998, 164: 67-80.
-
(1998)
Int J Pharm.
, vol.164
, pp. 67-80
-
-
Mooter, V.N.G.1
Augustijns, P.2
Blaton, N.3
-
6
-
-
6944243071
-
Enhancing the bioavailability of ABT-963 using solid dispersion containing PluronicF-68
-
Chen Y, Zhang GG. Neilly J, et al. Enhancing the bioavailability of ABT-963 using solid dispersion containing PluronicF-68. Int J Pharm. 2004, 286: 69-80.
-
(2004)
Int J Pharm.
, vol.286
, pp. 69-80
-
-
Chen, Y.1
Zhang, G.G.2
Neilly, J.3
-
7
-
-
77949446521
-
Physicochemical characterization of solid dispersion systems of tadalafil with poloxamer 407
-
Vyas V, Sancheti P, Karekar P, et al. Physicochemical characterization of solid dispersion systems of tadalafil with poloxamer 407. Acta Pharm. 2009, 59: 453-461.
-
(2009)
Acta Pharm.
, vol.59
, pp. 453-461
-
-
Vyas, V.1
Sancheti, P.2
Karekar, P.3
-
8
-
-
0033674037
-
Direct estimation of the in vivo dissolution of spironolactone, in two particle size ranges, using the single-pass perfusion technique (Loc-I-Gut) in humans
-
Bonlokke L, Hovgaard L, Kristensen HG, et al. Direct estimation of the in vivo dissolution of spironolactone, in two particle size ranges, using the single-pass perfusion technique (Loc-I-Gut) in humans. Eur J Pharm Sci. 2001,12: 239-250.
-
(2001)
Eur J Pharm Sci.
, vol.12
, pp. 239-250
-
-
Bonlokke, L.1
Hovgaard, L.2
Kristensen, H.G.3
-
9
-
-
0017670012
-
Factors influencing comparative bioavailability of spironolactone tablets
-
Clarke JM, Ramsay LE, Shelton JR, et al. Factors influencing comparative bioavailability of spironolactone tablets. J Pharm Sci. 1977, 66: 1429-1432.
-
(1977)
J Pharm Sci.
, vol.66
, pp. 1429-1432
-
-
Clarke, J.M.1
Ramsay, L.E.2
Shelton, J.R.3
-
10
-
-
0019946573
-
Effect of micronization on the bioavailability and pharmacologic activity ofspironolactone
-
McInnes GT, Asbury MJ, Ramsay LE, et al. Effect of micronization on the bioavailability and pharmacologic activity ofspironolactone. J Clin Pharmacol. 1982, 22:410-417.
-
(1982)
J Clin Pharmacol.
, vol.22
, pp. 410-417
-
-
Mcinnes, G.T.1
Asbury, M.J.2
Ramsay, L.E.3
-
11
-
-
0344073961
-
Water-soluble β-cyclodextrins in paediatric oral solutions of spironolactone:solubilization and stability of spironolactone in solutions of β-cyclodextrin derivatives
-
Kaukonen A, Kilpelainen I, Mannermaa J. Water-soluble β-cyclodextrins in paediatric oral solutions of spironolactone:solubilization and stability of spironolactone in solutions of β-cyclodextrin derivatives. Int J Pharm. 1997, 159:.
-
(1997)
Int J Pharm.
, vol.159
, pp. 159-170
-
-
Kaukonen, A.1
Kilpelainen, I.2
Mannermaa, J.3
-
12
-
-
34548240849
-
Solid dispersion of spironolactone with porous silica prepared by the solvent method
-
Uchino T, Yasuno N, Yanagihara Y, et al. Solid dispersion of spironolactone with porous silica prepared by the solvent method. Pharmazie. 2007, 62: 599-603.
-
(2007)
Pharmazie.
, vol.62
, pp. 599-603
-
-
Uchino, T.1
Yasuno, N.2
Yanagihara, Y.3
-
13
-
-
61649125836
-
"Preparation and characterization of spironolactone-loaded gelucire microparticles using spray-drying technique
-
Yassin A, Alanazi F, El-Badry M, et al. "Preparation and characterization of spironolactone-loaded gelucire microparticles using spray-drying technique. Drug Dev Ind Pharm.2009, 35: 297-304.
-
(2009)
Drug Dev Ind Pharm.
, vol.35
, pp. 297-304
-
-
Yassin, A.1
Alanazi, F.2
El-Badry, M.3
-
14
-
-
0038361622
-
Enhancement of dissolution rates of spironolactone and diazepam via polyols and PEG solid dispersion system
-
Geneidi AS, Hamacher H. Enhancement of dissolution rates of spironolactone and diazepam via polyols and PEG solid dispersion system. Farm Ind. 1980, 42: 401-404.
-
(1980)
Farm Ind.
, vol.42
, pp. 401-404
-
-
Geneidi, A.S.1
Hamacher, H.2
-
16
-
-
0016422844
-
The concept of dissolution efficiency
-
Khan KA. The concept of dissolution efficiency. J Pharm Pharmacol. 1975, 27: 48-49.
-
(1975)
J Pharm Pharmacol.
, vol.27
, pp. 48-49
-
-
Khan, K.A.1
-
17
-
-
0037139418
-
Preparation and in vitro evaluation of solid dispersions of halofantrine
-
Abdul-Fattah AM, Bhargava HN. Preparation and in vitro evaluation of solid dispersions of halofantrine. Int J Pharm. 2002, 235: 17-33.
-
(2002)
Int J Pharm.
, vol.235
, pp. 17-33
-
-
Abdul-Fattah, A.M.1
Bhargava, H.N.2
-
18
-
-
77953398631
-
Enhancement of water solubility of felodipine by preparing solid dispersion using polyethylene glycol 6000 and poly-vinyl alcohol
-
Bhole P, Patil V. Enhancement of water solubility of felodipine by preparing solid dispersion using polyethylene glycol 6000 and poly-vinyl alcohol. Asian J Pharm Sci. 2009, 3: 240-244.
-
(2009)
Asian J Pharm Sci.
, vol.3
, pp. 240-244
-
-
Bhole, P.1
Patil, V.2
-
20
-
-
0025610778
-
Polyethylene glycols and drug release
-
Craig DQ. Polyethylene glycols and drug release. Drug Dev Ind Pharm. 1990, 16: 2501-2526.
-
(1990)
Drug Dev Ind Pharm.
, vol.16
, pp. 2501-2526
-
-
Craig, D.Q.1
-
21
-
-
44349129780
-
Preparation and evaluation of immediate release ibuprofen solid dispersions using polyethylene glycol 4000
-
Newa M, Bhandari KH, Xun Li D, et al. Preparation and evaluation of immediate release ibuprofen solid dispersions using polyethylene glycol 4000. Biol Pharm Bull. 2008, 31:939-945.
-
(2008)
Biol Pharm Bull.
, vol.31
, pp. 939-945
-
-
Newa, M.1
Bhandari, K.H.2
Li, D.X.3
-
22
-
-
0028067367
-
Dissolution rate study of fresh and aging triamterene-urea solid dispersions
-
Gines, JM, Arias MJ, Holgado MA, et al. Dissolution rate study of fresh and aging triamterene-urea solid dispersions. Drug Dev Ind Pharm. 1994, 20: 2729-2740.
-
(1994)
Drug Dev Ind Pharm.
, vol.20
, pp. 2729-2740
-
-
Gines, J.M.1
Arias, M.J.2
Holgado, M.A.3
-
23
-
-
77952884792
-
Increasing solubility and dissolution rate of drugs via eutectic mixtures: itraconazole-poloxamer 188 system
-
Liu D, Fei X, Wang S, et al. Increasing solubility and dissolution rate of drugs via eutectic mixtures: itraconazole-poloxamer 188 system. Asian J Pharm Sci. 2006, 1:213-221.
-
(2006)
Asian J Pharm Sci.
, vol.1
, pp. 213-221
-
-
Liu, D.1
Fei, X.2
Wang, S.3
-
24
-
-
34548270616
-
Preparation, characterization and in vivo evaluation of ibuprofen binary solid dispersions with poloxamer 188
-
Newa M, Bhandari KH, Xun LD, et al. Preparation, characterization and in vivo evaluation of ibuprofen binary solid dispersions with poloxamer 188. Int J Pharm. 2007,343: 228-237.
-
(2007)
Int J Pharm.
, vol.343
, pp. 228-237
-
-
Newa, M.1
Bhandari, K.H.2
Xun, L.D.3
-
25
-
-
34247637282
-
Process optimization and characterization of poloxamer solid dispersions of a poorlywater-soluble drug
-
Shah T, Amin A, Parikh J, et al. Process optimization and characterization of poloxamer solid dispersions of a poorlywater-soluble drug, AAPS Pharm Sci Tech 2007, 8: E1-E5.
-
(2007)
AAPS Pharm Sci Tech
, vol.8
-
-
Shah, T.1
Amin, A.2
Parikh, J.3
-
26
-
-
62849088828
-
Formulation and evaluation of solid dispersions of an anti-diabetic drug
-
Mehta A. Formulation and evaluation of solid dispersions of an anti-diabetic drug. Cur Trends Biotech Pharm. 2009,3: 76-84.
-
(2009)
Cur Trends Biotech Pharm.
, vol.3
, pp. 76-84
-
-
Mehta, A.1
-
27
-
-
69749103682
-
Nanocrystal technology, drug delivery and clinical applications
-
Junghanns JU, Muller RH. Nanocrystal technology, drug delivery and clinical applications. Int J Nanomed. 2008, 3:295-309.
-
(2008)
Int J Nanomed.
, vol.3
, pp. 295-309
-
-
Junghanns, J.U.1
Muller, R.H.2
-
28
-
-
6344237328
-
A novel formulation for poorly soluble and poorly bioavailable drugs
-
Rathbone M, Hadgraft J, Roberts M, editors. New York: Marcel Dekker
-
Muller RH, Jacobs C, Kayser OD. A novel formulation for poorly soluble and poorly bioavailable drugs. In: Rathbone M, Hadgraft J, Roberts M, editors. Modified-release drug delivery technology. New York: Marcel Dekker, 2003. p.135-150.
-
(2003)
Modified-release drug delivery technology
, pp. 135-150
-
-
Muller, R.H.1
Jacobs, C.2
Kayser, O.D.3
-
29
-
-
62849088828
-
Formulation and evaluation of solid dispersions of an anti-diabetic drug
-
Mehta A. Formulation and evaluation of solid dispersions of an anti-diabetic drug. Cur Trends Biotech Pharmacy. 2009,3: 76-84.
-
(2009)
Cur Trends Biotech Pharmacy
, vol.3
, pp. 76-84
-
-
Mehta, A.1
-
30
-
-
67349203808
-
Preparation and characterization of spironolactone nanoparticles by antisolvent precipitation
-
Dong Y, Ng WK, Shen S, et al. Preparation and characterization of spironolactone nanoparticles by antisolvent precipitation. Int J Pharm. 2009, 375: 84-88.
-
(2009)
Int J Pharm.
, vol.375
, pp. 84-88
-
-
Dong, Y.1
Ng, W.K.2
Shen, S.3
-
31
-
-
0034032146
-
Physicochemical characterization of solid dispersions of the antiviral agent UC-781 with polyethylene glycol 6000 and gelucire 44/14
-
Damian F, Blaton N, Naesens L, et al. Physicochemical characterization of solid dispersions of the antiviral agent UC-781 with polyethylene glycol 6000 and gelucire 44/14. Eur J Pharm Sci. 2000, 311-322.
-
(2000)
Eur J Pharm Sci.
, pp. 311-322
-
-
Damian, F.1
Blaton, N.2
Naesens, L.3
-
32
-
-
0030273103
-
Dissolution properties and in vivo behaviour of triamterene in solid dispersions with polyethylene glycols
-
Arias MJ, Gines JM, Moyano JR, et al. Dissolution properties and in vivo behaviour of triamterene in solid dispersions with polyethylene glycols. Pharm Acta Helv. 1996, 71: 229-235.
-
(1996)
Pharm Acta Helv.
, vol.71
, pp. 229-235
-
-
Arias, M.J.1
Gines, J.M.2
Moyano, J.R.3
-
33
-
-
1642378056
-
Fundamentals of solid dispersions
-
Habib M, editor. Lancaster: Technomic Publishing Company
-
Habib M, Venkatram S, Hussain M. Fundamentals of solid dispersions. In: Habib M, editor. Pharmaceutical solid dispersion technology. Lancaster: Technomic Publishing Company, 2001. p. 7-36.
-
(2001)
Pharmaceutical solid dispersion technology
, pp. 7-36
-
-
Habib, M.1
Venkatram, S.2
Hussain, M.3
-
34
-
-
33846151408
-
Studies on mechanism of enhanced dissolution of albendazole solid dispersions with crystalline carriers
-
Kalaiselvan R, Mohanta G, Manna P, et al. Studies on mechanism of enhanced dissolution of albendazole solid dispersions with crystalline carriers. Indian J Pharm Sci. 2006, 68: 599-607.
-
(2006)
Indian J Pharm Sci.
, vol.68
, pp. 599-607
-
-
Kalaiselvan, R.1
Mohanta, G.2
Manna, P.3
-
35
-
-
64649094850
-
Enhanced bioavailability of a poorly soluble VR1 antagonist using an amorphous solid dispersion approach: a case study
-
Kennedy M, Hu J, Gao P, et al. Enhanced bioavailability of a poorly soluble VR1 antagonist using an amorphous solid dispersion approach: a case study. Mol Pharm. 2008, 5:981-993.
-
(2008)
Mol Pharm.
, vol.5
, pp. 981-993
-
-
Kennedy, M.1
Hu, J.2
Gao, P.3
|