-
2
-
-
0023696056
-
Distribution of water in pharmaceutical systems
-
Kontny, M.J. Distribution of water in pharmaceutical systems. Drug Dev. Ind. Pharm. 1988, 14 (14), 1991-2027.
-
(1988)
Drug Dev. Ind. Pharm.
, vol.14
, Issue.14
, pp. 1991-2027
-
-
Kontny, M.J.1
-
4
-
-
0035668586
-
Effect of carrier excipient and processing on stability of indorenate hydrochloride/excipients mixtures
-
Villalobos-Henández, J.R.; Villafuerte-Robles, L. Effect of carrier excipient and processing on stability of indorenate hydrochloride/ excipients mixtures. Pharm. Dev. Technol. 2001, 6 (4), 551-561.
-
(2001)
Pharm. Dev. Technol.
, vol.6
, Issue.4
, pp. 551-561
-
-
Villalobos-Henández, J.R.1
Villafuerte-Robles, L.2
-
7
-
-
0016741619
-
A factorial design for compatibility studies in preformulation work
-
Leuenberger, H. A factorial design for compatibility studies in preformulation work. Pharm. Acta Helv. 1975, 50 (4), 88-91.
-
(1975)
Pharm. Acta Helv.
, vol.50
, Issue.4
, pp. 88-91
-
-
Leuenberger, H.1
-
9
-
-
0027234850
-
Identification of stabilizing and destabilizing effects of excipient-drug interactions in solid dosage form design
-
Dürig, T.; Fassihi, A.R. Identification of stabilizing and destabilizing effects of excipient-drug interactions in solid dosage form design. Int. J. Pharm. 1993, 97, 161-170.
-
(1993)
Int. J. Pharm.
, vol.97
, pp. 161-170
-
-
Dürig, T.1
Fassihi, A.R.2
-
10
-
-
0032809138
-
Selection of solid dosage form composition through drug-excipient compatibility testing
-
Serajuddin, A.T.M.; Thakur, A.B.; Ghoshal, R.N.; Fakes, M.G.; Ranadive, S.A.; Morris, K.R.; Sailesh, A.V. Selection of solid dosage form composition through drug-excipient compatibility testing. J. Pharm. Sci. 1999, 88 (7), 696-704.
-
(1999)
J. Pharm. Sci.
, vol.88
, Issue.7
, pp. 696-704
-
-
Serajuddin, A.T.M.1
Thakur, A.B.2
Ghoshal, R.N.3
Fakes, M.G.4
Ranadive, S.A.5
Morris, K.R.6
Sailesh, A.V.7
-
11
-
-
0038669070
-
A new approach to accelerated drug-excipient compatibility testing
-
Sims, J.L.; Carreira, J.A.; Carrier, D.J.; Crabtree, S.R.; Eason, L.; Hancock, St.A.; Simcox, C.E. A new approach to accelerated drug-excipient compatibility testing. Pharm. Dev. Technol. 2003, 8 (2), 119-126.
-
(2003)
Pharm. Dev. Technol.
, vol.8
, Issue.2
, pp. 119-126
-
-
Sims, J.L.1
Carreira, J.A.2
Carrier, D.J.3
Crabtree, S.R.4
Eason, L.5
Hancock, St.A.6
Simcox, C.E.7
-
12
-
-
0343049107
-
Characterization and compatibility studies between policosanol, a new hypocholesterolemic drug, and tablet excipients using differential scanning calorimetry
-
Martinez, L.; Uribarri, E.; Laguna, A. Characterization and compatibility studies between policosanol, a new hypocholesterolemic drug, and tablet excipients using differential scanning calorimetry. Arch. Pharm. Pharm. Med. Chem. 1999, 332, 439-441.
-
(1999)
Arch. Pharm. Pharm. Med. Chem.
, vol.332
, pp. 439-441
-
-
Martinez, L.1
Uribarri, E.2
Laguna, A.3
-
13
-
-
28844508552
-
Compatibility studies between oflaxacin and tablet excipients through differential scanning calorimetry (DSC)
-
Logonathan, V.; Senthilkumar, S.; Reddy, M.; Sivaparasadha, V.; Sreekant, N.; Ubaidulla, U.; Manimaran, S. Compatibility studies between oflaxacin and tablet excipients through differential scanning calorimetry (DSC). Int. J. Pharm. Excip. 2003, 90-94.
-
(2003)
Int. J. Pharm. Excip.
, pp. 90-94
-
-
Logonathan, V.1
Senthilkumar, S.2
Reddy, M.3
Sivaparasadha, V.4
Sreekant, N.5
Ubaidulla, U.6
Manimaran, S.7
-
14
-
-
0042123924
-
Degradation of components in drug formulations: A comparison between HPLC and DSC methods
-
Ceschel, G.G.; Badiello, R.; Ronchi, C.; Maffei, P. Degradation of components in drug formulations: a comparison between HPLC and DSC methods. J. Pharm. Biomed. Anal. 2003, 32, 1067-1072.
-
(2003)
J. Pharm. Biomed. Anal.
, vol.32
, pp. 1067-1072
-
-
Ceschel, G.G.1
Badiello, R.2
Ronchi, C.3
Maffei, P.4
-
15
-
-
0037452403
-
Further investigations into the use of high sensitivity differential scanning calorimetry as a means of predicting drug-excipient interactions
-
McDaid, F.M.; Barker, S.A.; Fitzpatrick, S.; Petts, C.R.; Craig, D.Q.M. Further investigations into the use of high sensitivity differential scanning calorimetry as a means of predicting drug-excipient interactions. Int. J. Pharm. 2003, 252, 235-240.
-
(2003)
Int. J. Pharm.
, vol.252
, pp. 235-240
-
-
McDaid, F.M.1
Barker, S.A.2
Fitzpatrick, S.3
Petts, C.R.4
Craig, D.Q.M.5
-
16
-
-
0032531356
-
Use of isothermal heat conduction microcalorimetry to evaluate stability and excipient compatibility of a solid drug
-
Selzer, T.; Radau, M.; Kreuter, J. Use of isothermal heat conduction microcalorimetry to evaluate stability and excipient compatibility of a solid drug. Int. J. Pharm. 1998, 171, 227-241.
-
(1998)
Int. J. Pharm.
, vol.171
, pp. 227-241
-
-
Selzer, T.1
Radau, M.2
Kreuter, J.3
-
17
-
-
0035861404
-
Rapid, practical and predictive excipient compatibility screening using isothermal microcalorimetry
-
Schmitt, E.A.; Peck, K.; Sun, Y.; Geoffroy, J.M. Rapid, practical and predictive excipient compatibility screening using isothermal microcalorimetry. Thermochim. Acta 2001, 380 (2), 175-184.
-
(2001)
Thermochim. Acta
, vol.380
, Issue.2
, pp. 175-184
-
-
Schmitt, E.A.1
Peck, K.2
Sun, Y.3
Geoffroy, J.M.4
-
18
-
-
0025910790
-
A comparison of diffuse reflectance FT-IR spectroscopy and DSC in the characterization of drug-excipient interaction
-
Hartauer, K.J.; Guillory, J.K. A comparison of diffuse reflectance FT-IR spectroscopy and DSC in the characterization of drug-excipient interaction. Drug Dev. Ind. Pharm. 1991, 77, 617-630.
-
(1991)
Drug Dev. Ind. Pharm.
, vol.77
, pp. 617-630
-
-
Hartauer, K.J.1
Guillory, J.K.2
-
19
-
-
0019966739
-
Solid-state stability of aspirin in the presence of excipients: Kinetic interpretation, modeling and prediction
-
Mroso, P.V.; Wan Po, A.L.; Irwin, W.J. Solid-state stability of aspirin in the presence of excipients: kinetic interpretation, modeling and prediction. J. Pharm. Sci. 1982, 71 (10), 1096-1101.
-
(1982)
J. Pharm. Sci.
, vol.71
, Issue.10
, pp. 1096-1101
-
-
Mroso, P.V.1
Wan Po, A.L.2
Irwin, W.J.3
-
20
-
-
0035897596
-
Chemical reactivity in solid-state pharmaceuticals: Formulation implications
-
Byrn, S.R.; Xu, W.; Newman, A.W. Chemical reactivity in solid-state pharmaceuticals: formulation implications. Adv. Drug Deliv. Rev. 2001, 48, 115-136.
-
(2001)
Adv. Drug Deliv. Rev.
, vol.48
, pp. 115-136
-
-
Byrn, S.R.1
Xu, W.2
Newman, A.W.3
-
21
-
-
0031936142
-
Maillard reaction of lactose and fluoxetine hydrochloride, a secondary amine
-
Wirth, D.D.; Baertschi, St.W.; Johnson, R.A.; Maple, St.R.; Miller, M.S.; Hallenbeck, D.K.; Gregg, St.M. Maillard reaction of lactose and fluoxetine hydrochloride, a secondary amine. J. Pharm. Sci. 1998, 87 (1), 31-39.
-
(1998)
J. Pharm. Sci.
, vol.87
, Issue.1
, pp. 31-39
-
-
Wirth, D.D.1
Baertschi, St.W.2
Johnson, R.A.3
Maple, St.R.4
Miller, M.S.5
Hallenbeck, D.K.6
Gregg, St.M.7
-
22
-
-
0020673325
-
A design for drug-excipient interaction studies
-
Van Doren, A. A design for drug-excipient interaction studies. Drug Dev. Ind. Pharm. 1983, 9, 43-55.
-
(1983)
Drug Dev. Ind. Pharm.
, vol.9
, pp. 43-55
-
-
Van Doren, A.1
-
23
-
-
11144357547
-
Application of high throughput technologies to drug substance and drug product development
-
Gardner, C.R.; Almarsson, O.; Chen, H.; Morissette, S.; Peterson, M.; Zhang, Z.; Wang, S.; Lemmo, A.; Gonzales-Zugasti, J.; Monagle, J.; Marchionna, J.; Ellis, St.; McNutley, Ch.; Johnson, A.; Levinson, D.; Cima, M. Application of high throughput technologies to drug substance and drug product development. Comput. Chem. Eng. 2004, 28, 943-953.
-
(2004)
Comput. Chem. Eng.
, vol.28
, pp. 943-953
-
-
Gardner, C.R.1
Almarsson, O.2
Chen, H.3
Morissette, S.4
Peterson, M.5
Zhang, Z.6
Wang, S.7
Lemmo, A.8
Gonzales-Zugasti, J.9
Monagle, J.10
Marchionna, J.11
Ellis, St.12
McNutley, Ch.13
Johnson, A.14
Levinson, D.15
Cima, M.16
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