-
1
-
-
3242736468
-
β-cyclodextrin as a suitable solubilizing agent for in-situ absorption study of poorly water soluble drugs
-
Saitoh, H.; Oda, M.; Kobayashi, M.; Aungst, B. J. β-cyclodextrin as a suitable solubilizing agent for in-situ absorption study of poorly water soluble drugs. Int. J. Pharm. 2000, 280, 95-102.
-
(2000)
Int. J. Pharm
, vol.280
, pp. 95-102
-
-
Saitoh, H.1
Oda, M.2
Kobayashi, M.3
Aungst, B.J.4
-
2
-
-
32644443823
-
Phase solubility and inclusion complex of itraconazole with β-cyclodextrin using supercritical carbon dioxide
-
Al-Marzouqi, A. H.; Shehatta, I.; Jobe, B.; Towanda, A. Phase solubility and inclusion complex of itraconazole with β-cyclodextrin using supercritical carbon dioxide. J. Pharm. Sci. 2006, 95, 292-304.
-
(2006)
J. Pharm. Sci
, vol.95
, pp. 292-304
-
-
Al-Marzouqi, A.H.1
Shehatta, I.2
Jobe, B.3
Towanda, A.4
-
3
-
-
0348025526
-
-
Publication Division of The Royal Pharmaceutical Society of Great Britain: London
-
Rowe, R. C.; Sheskey, P. J.; Owen, S. C. Handbook of Pharmaceutical Excipients; Publication Division of The Royal Pharmaceutical Society of Great Britain: London, 2006; pp 217-220.
-
(2006)
Handbook of Pharmaceutical Excipients
, pp. 217-220
-
-
Rowe, R.C.1
Sheskey, P.J.2
Owen, S.C.3
-
4
-
-
27744575591
-
Cyclodextrin in drug delivery: An updated review
-
Ahuja, A.; Challa, R.; Ali, J.; Khar, R. K. Cyclodextrin in drug delivery: An updated review. AAPS PharmSciTech 2005, 6 (2), E329-E357.
-
(2005)
AAPS PharmSciTech
, vol.6
, Issue.2
-
-
Ahuja, A.1
Challa, R.2
Ali, J.3
Khar, R.K.4
-
5
-
-
24344508654
-
Evaluation of cyclodextrin solubilization of drugs
-
Loftsson, T.; Hreinsdottir, D.; Masson, M. Evaluation of cyclodextrin solubilization of drugs. Int. J. Pharm. 2005, 302, 18-28.
-
(2005)
Int. J. Pharm
, vol.302
, pp. 18-28
-
-
Loftsson, T.1
Hreinsdottir, D.2
Masson, M.3
-
7
-
-
40549101273
-
-
Online. Available at
-
Drug Information Online. Available at http://www.drugs.com.
-
Drug Information
-
-
-
9
-
-
0004170639
-
-
Controller of Publications: Delhi, India
-
Indian Pharmacopoeia; Controller of Publications: Delhi, India, 1996.
-
(1996)
Indian Pharmacopoeia
-
-
-
12
-
-
0032966667
-
Improvement of in vitro dissolution of praziquantel by complexation with α, β- and γ- cyclodextrins
-
Becket, G.; Schep, L. J.; Tan, M. Y. Improvement of in vitro dissolution of praziquantel by complexation with α, β- and γ- cyclodextrins. Int. J. Pharm. 1999, 179, 65-71.
-
(1999)
Int. J. Pharm
, vol.179
, pp. 65-71
-
-
Becket, G.1
Schep, L.J.2
Tan, M.Y.3
-
13
-
-
13544258798
-
Preformulation study of the inclusion complex warfarin-β-cyclodextrin
-
Zingone, G.; Rubessa, F. Preformulation study of the inclusion complex warfarin-β-cyclodextrin. Int. J. Pharm. 2005, 291, 3-10.
-
(2005)
Int. J. Pharm
, vol.291
, pp. 3-10
-
-
Zingone, G.1
Rubessa, F.2
-
14
-
-
3042602325
-
Influence of preparation methodology on solid-state properties of an acidic drug-cyclodextrin system
-
Govindarajan, R.; Nagarsenkar, M. S. Influence of preparation methodology on solid-state properties of an acidic drug-cyclodextrin system. J. Pharm. Pharmacol. 2004, 56, 725-733.
-
(2004)
J. Pharm. Pharmacol
, vol.56
, pp. 725-733
-
-
Govindarajan, R.1
Nagarsenkar, M.S.2
-
15
-
-
84882928614
-
Intrinsic drug dissolution testing using the stationary disk system
-
Viegas, T. X.; Curatella, R. U.; Vanuinkle, L. L.; Brinker, G. Intrinsic drug dissolution testing using the stationary disk system. Dissolution Technologies 2001,8,1-4.
-
(2001)
Dissolution Technologies
, vol.8
, pp. 1-4
-
-
Viegas, T.X.1
Curatella, R.U.2
Vanuinkle, L.L.3
Brinker, G.4
-
17
-
-
0034006672
-
pH-metric solubility. 2. Correlation between the acid-base titration and the saturation shake-flask solubility-pH methods
-
Avdeef, A.; Berger, C. M.; Brownell, C. pH-metric solubility. 2. Correlation between the acid-base titration and the saturation shake-flask solubility-pH methods. Pharm. Res. 2000, 17, 85-89.
-
(2000)
Pharm. Res
, vol.17
, pp. 85-89
-
-
Avdeef, A.1
Berger, C.M.2
Brownell, C.3
-
18
-
-
56849097780
-
-
Ancel, H. C.; Allen, L. V.; Popovich, N. G. Pharmaceutical Dosage Forms and Drug Delivery Systems, 7th ed,; B. I. Publications. Pvt. Ltd.: 2000; p 75.
-
Ancel, H. C.; Allen, L. V.; Popovich, N. G. Pharmaceutical Dosage Forms and Drug Delivery Systems, 7th ed,; B. I. Publications. Pvt. Ltd.: 2000; p 75.
-
-
-
-
19
-
-
56849097510
-
-
3rd ed, Marcel Dekker Inc, New York
-
Bolton, S. Pharmaceutical Statistics. Practical and Clinical Applications, 3rd ed.; Marcel Dekker Inc., New York, 1997; Vol. 80, pp 591-623.
-
(1997)
Pharmaceutical Statistics. Practical and Clinical Applications
, vol.80
, pp. 591-623
-
-
Bolton, S.1
-
20
-
-
7644236294
-
Past, present and future of cyclodextrin research
-
Szejtli, J. Past, present and future of cyclodextrin research. Pure. Appl. Chem. 2004, 76, 1825-1845.
-
(2004)
Pure. Appl. Chem
, vol.76
, pp. 1825-1845
-
-
Szejtli, J.1
-
21
-
-
0034957345
-
Controlled and complete release of a model poorly water soluble drug, prednisolone, from hydroxypropyl methyl cellulose matrix tablets using (SBE) 7m-β-cyclodextrin as a solubilizing agent
-
Rao, V. M.; Haslam, J. L.; Stella, V. J. Controlled and complete release of a model poorly water soluble drug, prednisolone, from hydroxypropyl methyl cellulose matrix tablets using (SBE) 7m-β-cyclodextrin as a solubilizing agent. J. Pharm. Sci. 2001, 90, 807-816.
-
(2001)
J. Pharm. Sci
, vol.90
, pp. 807-816
-
-
Rao, V.M.1
Haslam, J.L.2
Stella, V.J.3
-
22
-
-
0034874915
-
Influence of the preparation method on the physicochemical properties of tolbutamide/cyclodextrin binary system
-
Veiga, F.; Fernandes, C.; Maincent, P. Influence of the preparation method on the physicochemical properties of tolbutamide/cyclodextrin binary system. Drug Dev. Ind. Pharm. 2001, 27, 523-532.
-
(2001)
Drug Dev. Ind. Pharm
, vol.27
, pp. 523-532
-
-
Veiga, F.1
Fernandes, C.2
Maincent, P.3
-
23
-
-
34248661543
-
β-cyclodextrin complexes of celecoxib: Molecular modeling, characterization and -dissolution studies
-
Article
-
Reddy, M. N.; Rehana, T.; Ramakrishna, S.; Chowdary, K. P. R.; Diwan, P. V. β-cyclodextrin complexes of celecoxib: Molecular modeling, characterization and -dissolution studies. AAPS PharmSci. 2004, 6 (1), Article 7.
-
(2004)
AAPS PharmSci
, vol.6
, Issue.1
, pp. 7
-
-
Reddy, M.N.1
Rehana, T.2
Ramakrishna, S.3
Chowdary, K.P.R.4
Diwan, P.V.5
-
24
-
-
0034028738
-
Study of omeprazole-γ-cyclodextrin complexation in the solid state
-
Arias, M. J.; Moyano, J. R.; Munoz, P.; Gines, J. M.; Justo, A.; Giordano, F. Study of omeprazole-γ-cyclodextrin complexation in the solid state. Drug Dev. Ind. Pharm. 2000, 26, 253-259.
-
(2000)
Drug Dev. Ind. Pharm
, vol.26
, pp. 253-259
-
-
Arias, M.J.1
Moyano, J.R.2
Munoz, P.3
Gines, J.M.4
Justo, A.5
Giordano, F.6
-
25
-
-
0345491940
-
Improvement of dissolution and bioavailability of nitrendipine by inclusion in hydroxypropyl β- -cyclodextrins
-
Yong, C. S.; Choi, H. G.; Kim, D. D.; Jun, H. W.; Yoo, B. K. Improvement of dissolution and bioavailability of nitrendipine by inclusion in hydroxypropyl β- -cyclodextrins. Drug Dev. Ind. Pharm. 2003, 29, 1085-1094.
-
(2003)
Drug Dev. Ind. Pharm
, vol.29
, pp. 1085-1094
-
-
Yong, C.S.1
Choi, H.G.2
Kim, D.D.3
Jun, H.W.4
Yoo, B.K.5
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