-
1
-
-
40549089922
-
Indomethacin-saccharin cocrystal: Design, synthesis and preliminary pharmaceutical characterization
-
S. Basavoju, D. Boström, and S.P. Velaga Indomethacin-saccharin cocrystal: design, synthesis and preliminary pharmaceutical characterization Pharm. Res. 25 2008 530 541
-
(2008)
Pharm. Res.
, vol.25
, pp. 530-541
-
-
Basavoju, S.1
Boström, D.2
Velaga, S.P.3
-
2
-
-
84872470263
-
Characterization, quantification and stability of differently prepared amorphous forms of some oral hypoglycaemic agents
-
R. Chadha, S. Bhandari, P. Arora, and R. Chhikara Characterization, quantification and stability of differently prepared amorphous forms of some oral hypoglycaemic agents Pharm. Dev. Technol. 18 2013 504 514
-
(2013)
Pharm. Dev. Technol.
, vol.18
, pp. 504-514
-
-
Chadha, R.1
Bhandari, S.2
Arora, P.3
Chhikara, R.4
-
4
-
-
79954476664
-
Coformer selection in pharmaceutical cocrystal development: A case study of a meloxicam aspirin cocrystal that exhibits enhanced solubility and pharmacokinetics
-
M.L. Cheney, D.R. Weyna, N. Shan, M. Hanna, L. Wojias, and M.J. Zaworotko Coformer selection in pharmaceutical cocrystal development: a case study of a meloxicam aspirin cocrystal that exhibits enhanced solubility and pharmacokinetics J. Pharm. Sci. 100 2011 2172 2181
-
(2011)
J. Pharm. Sci.
, vol.100
, pp. 2172-2181
-
-
Cheney, M.L.1
Weyna, D.R.2
Shan, N.3
Hanna, M.4
Wojias, L.5
Zaworotko, M.J.6
-
5
-
-
0034808093
-
Repaglinide: A review of its therapeutic use in type 2 diabetes mellitus
-
C.R. Culy, and B. Jarvis Repaglinide: a review of its therapeutic use in type 2 diabetes mellitus Drugs 61 2001 1625 1660
-
(2001)
Drugs
, vol.61
, pp. 1625-1660
-
-
Culy, C.R.1
Jarvis, B.2
-
6
-
-
79956030072
-
Repaglinide-cyclodextrin complexes: Preparation, characterization and in vivo evaluation of antihyperglycemic activity
-
N.S. Desai, D.M. Bramhane, and M.S. Nagarsenker Repaglinide-cyclodextrin complexes: preparation, characterization and in vivo evaluation of antihyperglycemic activity J. Incl. Phenom. Macrocycl. Chem. 70 2011 217 225
-
(2011)
J. Incl. Phenom. Macrocycl. Chem.
, vol.70
, pp. 217-225
-
-
Desai, N.S.1
Bramhane, D.M.2
Nagarsenker, M.S.3
-
7
-
-
0033781630
-
Nateglinide
-
C.J. Dunn, and D. Faulds Nateglinide Drugs 60 2000 607 615
-
(2000)
Drugs
, vol.60
, pp. 607-615
-
-
Dunn, C.J.1
Faulds, D.2
-
8
-
-
84867401728
-
Coformer selection based on degradation pathway of drugs: A case study of adefovir dipivoxil-saccharin and adefovir dipivoxil-nicotinamide cocrystals
-
Y. Gao, J. Gao, Z. Liu, H. Kan, H. Zu, W. Sun, J. Zhang, and S. Qian Coformer selection based on degradation pathway of drugs: a case study of adefovir dipivoxil-saccharin and adefovir dipivoxil-nicotinamide cocrystals Int. J. Pharm. 438 2012 327 335
-
(2012)
Int. J. Pharm.
, vol.438
, pp. 327-335
-
-
Gao, Y.1
Gao, J.2
Liu, Z.3
Kan, H.4
Zu, H.5
Sun, W.6
Zhang, J.7
Qian, S.8
-
9
-
-
79952732175
-
Enhanced dissolution and stability of adefovir dipivoxil by cocrystal formation
-
Y. Gao, H. Zu, and J. Zhang Enhanced dissolution and stability of adefovir dipivoxil by cocrystal formation J. Pharm. Pharmacol. 63 2011 483 490
-
(2011)
J. Pharm. Pharmacol.
, vol.63
, pp. 483-490
-
-
Gao, Y.1
Zu, H.2
Zhang, J.3
-
10
-
-
0031593457
-
Bioavailability of repaglinide, a novel antidiabetic agent, administered orally in tablet or solution form or intravenously in healthy male volunteers
-
V. Hatorp, S. Oliver, and C.A. Su Bioavailability of repaglinide, a novel antidiabetic agent, administered orally in tablet or solution form or intravenously in healthy male volunteers Int. J. Clin. Pharmacol. Ther. 36 1998 636 641
-
(1998)
Int. J. Clin. Pharmacol. Ther.
, vol.36
, pp. 636-641
-
-
Hatorp, V.1
Oliver, S.2
Su, C.A.3
-
11
-
-
78649678462
-
Bioavailability of indomethacin-saccharin cocrystals
-
M.S. Jung, J.S. Kim, M.S. Kim, A. Alhalaweh, W. Cho, S.J. Hwang, and S.P. Velaga Bioavailability of indomethacin-saccharin cocrystals J. Pharm. Pharmacol. 62 2010 1560 1568
-
(2010)
J. Pharm. Pharmacol.
, vol.62
, pp. 1560-1568
-
-
Jung, M.S.1
Kim, J.S.2
Kim, M.S.3
Alhalaweh, A.4
Cho, W.5
Hwang, S.J.6
Velaga, S.P.7
-
12
-
-
84862504521
-
Enhancement of solubility of repaglinide by solid dispersion technique
-
R. Kavitha, and A.A.H. Sathali Enhancement of solubility of repaglinide by solid dispersion technique Int. J. Chem. Sci. 10 2012 377 390
-
(2012)
Int. J. Chem. Sci.
, vol.10
, pp. 377-390
-
-
Kavitha, R.1
Sathali, A.A.H.2
-
13
-
-
44749087764
-
Physicochemical properties and oral bioavailability of amorphous atorvastatin hemi-calcium using spray-drying and SAS process
-
J.S. Kim, M.S. Kim, S.J. Jin, S. Lee, and S.J. Hwanq Physicochemical properties and oral bioavailability of amorphous atorvastatin hemi-calcium using spray-drying and SAS process Int. J. Pharm. 359 2008 211 219
-
(2008)
Int. J. Pharm.
, vol.359
, pp. 211-219
-
-
Kim, J.S.1
Kim, M.S.2
Jin, S.J.3
Lee, S.4
Hwanq, S.J.5
-
14
-
-
80053505508
-
Coamorphous drug systems: Enhanced physical stability and dissolution rate of indomethacin and naproxen
-
K. Löbmann, R. Laitinen, H. Grohqanz, K.C. Gordon, and T. Rades Coamorphous drug systems: enhanced physical stability and dissolution rate of indomethacin and naproxen Mol. Pharm. 8 2011 1919 1928
-
(2011)
Mol. Pharm.
, vol.8
, pp. 1919-1928
-
-
Löbmann, K.1
Laitinen, R.2
Grohqanz, H.3
Gordon, K.C.4
Rades, T.5
-
15
-
-
84884158112
-
A theoretical and spectroscopic study of co-amorphous naproxen and indomethacin
-
doi:10.1016/j.ijpharm.2012.05.016 in press
-
Löbmann, K.; Laitinen, R.; Grohqanz, H.; Strachan, C.; Randes, T.; Gordon, K.C.; in press. A theoretical and spectroscopic study of co-amorphous naproxen and indomethacin. Int. J. Pharm, http://dx.doi.org/10.1016/j.ijpharm. 2012.05.016.
-
Int. J. Pharm.
-
-
Löbmann, K.1
Laitinen, R.2
Grohqanz, H.3
Strachan, C.4
Randes, T.5
Gordon K., .C.6
-
16
-
-
84861092839
-
Co-amorphous simvastatin and glipizide combinations show improved physical stability without evidence of intermolecular interactions
-
K. Löbmann, C. Strachan, H. Grohqanz, T. Rades, O. Korhonen, and R. Laitinen Co-amorphous simvastatin and glipizide combinations show improved physical stability without evidence of intermolecular interactions Eur. J. Pharm. Biopharm. 81 2012 159 169
-
(2012)
Eur. J. Pharm. Biopharm.
, vol.81
, pp. 159-169
-
-
Löbmann, K.1
Strachan, C.2
Grohqanz, H.3
Rades, T.4
Korhonen, O.5
Laitinen, R.6
-
17
-
-
33646403422
-
Ionization, lipophilicity and solubility properties of repaglinide
-
Z. Mandić, and V. Gabelica Ionization, lipophilicity and solubility properties of repaglinide J. Pharm. Biomed. Anal. 41 2006 866 871
-
(2006)
J. Pharm. Biomed. Anal.
, vol.41
, pp. 866-871
-
-
Mandić, Z.1
Gabelica, V.2
-
18
-
-
0033737460
-
Crystallization behavior of taltirelin polymorphs in a mixture of water and methanol
-
S. Maruyama, and H. Ooshima Crystallization behavior of taltirelin polymorphs in a mixture of water and methanol J. Cryst. Growth 212 2000 239 245
-
(2000)
J. Cryst. Growth
, vol.212
, pp. 239-245
-
-
Maruyama, S.1
Ooshima, H.2
-
19
-
-
33746899402
-
Use of a glutaric acid cocrystal to improve oral bioavailability of a low solubility API
-
D.P. McNamara, S.L. Childs, J. Giordano, A. Iarriccio, J. Cassidy, M.S. Shet, R. Mannion, E. O'Donnell, and A. Park Use of a glutaric acid cocrystal to improve oral bioavailability of a low solubility API Pharm. Res. 23 2006 1888 1897
-
(2006)
Pharm. Res.
, vol.23
, pp. 1888-1897
-
-
McNamara, D.P.1
Childs, S.L.2
Giordano, J.3
Iarriccio, A.4
Cassidy, J.5
Shet, M.S.6
Mannion, R.7
O'Donnell, E.8
Park, A.9
-
20
-
-
77958579211
-
Phase solubility studies of the inclusion complexes of repaglinide with β-cyclodextrin and β-cyclodextrin derivatives
-
C. Nicolescu, C. Arama, A. Nedelcu, and C.M. Monciu Phase solubility studies of the inclusion complexes of repaglinide with β-cyclodextrin and β-cyclodextrin derivatives Farmacia 58 2010 620 628
-
(2010)
Farmacia
, vol.58
, pp. 620-628
-
-
Nicolescu, C.1
Arama, C.2
Nedelcu, A.3
Monciu, C.M.4
-
21
-
-
84863266312
-
Milling induces disorder in crystalline griseofulvin and order in its amorphous counterpart
-
A. Otte, Y. Zhang, M.T. Carvajal, and R. Pinal Milling induces disorder in crystalline griseofulvin and order in its amorphous counterpart CrystEngComm 14 2012 2560 2570
-
(2012)
CrystEngComm
, vol.14
, pp. 2560-2570
-
-
Otte, A.1
Zhang, Y.2
Carvajal, M.T.3
Pinal, R.4
-
22
-
-
34547196307
-
Rapidly dissolving REPAGLINIDE powders produced by the ultra-rapid freezing process
-
T. Purvis, M.E. Mattucci, M.T. Mrisp, K.P. Johnston, and R.O. Williams 3rd. Rapidly dissolving REPAGLINIDE powders produced by the ultra-rapid freezing process AAPS PharmSciTech 8 2007 E52 E60
-
(2007)
AAPS PharmSciTech
, vol.8
-
-
Purvis, T.1
Mattucci, M.E.2
Mrisp, M.T.3
Johnston, K.P.4
Williams III, R.O.5
-
23
-
-
84856104937
-
Repaglinide: A review of its use in type 2 diabetes mellitus
-
L.J. Scott Repaglinide: a review of its use in type 2 diabetes mellitus Drugs 72 2012 249 272
-
(2012)
Drugs
, vol.72
, pp. 249-272
-
-
Scott, L.J.1
-
24
-
-
0003042011
-
Free energy barrier to nucleation of amorphous-to-crystalline transformation selects the scale of microstructure of crystallized materials
-
F.G. Shi, H.Y. Tong, and J.D. Ayers Free energy barrier to nucleation of amorphous-to-crystalline transformation selects the scale of microstructure of crystallized materials Appl. Phys. Lett. 67 1995 350 352
-
(1995)
Appl. Phys. Lett.
, vol.67
, pp. 350-352
-
-
Shi, F.G.1
Tong, H.Y.2
Ayers, J.D.3
-
26
-
-
45849111476
-
Dissolution rates and supersaturation behavior of amorphous REPAGLINIDE particles produced by controlled precipitation
-
P. Sinswat, M.E. Matteucci, K.P. Johnston, and R.O. Williams 3rd. Dissolution rates and supersaturation behavior of amorphous REPAGLINIDE particles produced by controlled precipitation J. Biomed. Nanotechnol. 3 2007 18 27
-
(2007)
J. Biomed. Nanotechnol.
, vol.3
, pp. 18-27
-
-
Sinswat, P.1
Matteucci, M.E.2
Johnston, K.P.3
Williams III, R.O.4
-
27
-
-
47749112075
-
Solid state structural studies of saccharin salts with some heterocyclic bases
-
P. Sudhakar, S.V. Kumar, P. Vishweshwar, J.M. Babu, and K. Vyas Solid state structural studies of saccharin salts with some heterocyclic bases CrystEngComm 10 2008 996 1002
-
(2008)
CrystEngComm
, vol.10
, pp. 996-1002
-
-
Sudhakar, P.1
Kumar, S.V.2
Vishweshwar, P.3
Babu, J.M.4
Vyas, K.5
-
28
-
-
0031423468
-
Spectroscopic characterization of interactions between PVP and indomethacin in amorphous molecular dispersions
-
L.S. Taylor, and G. Zografi Spectroscopic characterization of interactions between PVP and indomethacin in amorphous molecular dispersions Pharm. Res. 14 1997 1691 1698
-
(1997)
Pharm. Res.
, vol.14
, pp. 1691-1698
-
-
Taylor, L.S.1
Zografi, G.2
-
30
-
-
0032692543
-
Repaglinide - A new compound for the treatment of patients with type 2 diabetes
-
B.H. Wolffenbuttel Repaglinide - a new compound for the treatment of patients with type 2 diabetes Neth. J. Med. 55 1999 229 234
-
(1999)
Neth. J. Med.
, vol.55
, pp. 229-234
-
-
Wolffenbuttel, B.H.1
-
31
-
-
84872166445
-
Molecular dynamics simulation of amorphous indomethacin
-
T.X. Xiang, and B.D. Anderson Molecular dynamics simulation of amorphous indomethacin Mol. Pharm. 10 2013 102 114
-
(2013)
Mol. Pharm.
, vol.10
, pp. 102-114
-
-
Xiang, T.X.1
Anderson, B.D.2
-
32
-
-
0034595299
-
Physicochemical properties of amorphous precipitates of cimetidine-indomethacin binary system
-
S. Yamamura, H. Gotoh, Y. Sakamoto, and Y. Momose Physicochemical properties of amorphous precipitates of cimetidine-indomethacin binary system Eur. J. Pharm. Biopharm. 49 2000 259 265
-
(2000)
Eur. J. Pharm. Biopharm.
, vol.49
, pp. 259-265
-
-
Yamamura, S.1
Gotoh, H.2
Sakamoto, Y.3
Momose, Y.4
-
33
-
-
77951652999
-
Comparison of bioavailability of amorphous versus crystalline itraconazole nanoparticles via pulmonary administration in rats
-
W. Yang, K.P. Johnston, and R.O. Williams 3rd. Comparison of bioavailability of amorphous versus crystalline itraconazole nanoparticles via pulmonary administration in rats Eur. J. Pharm. Biopharm. 75 2010 33 41
-
(2010)
Eur. J. Pharm. Biopharm.
, vol.75
, pp. 33-41
-
-
Yang, W.1
Johnston, K.P.2
Williams III, R.O.3
|