Chemistry Reference
In-Depth Information
59. Brettman, B.K., Cheng, K., Myerson, A.S., and Trout, B.L. (2013) Electrospun formulations
containing crystalline active pharmaceutical ingredients.
Pharm. Res.
, 30:238-246.
60. Nagy, Z.K., Balogh, A., Dravavolgyi, G., Ferguson, J., Pataki, J., Vajna, B., and Marosi, G.
(2013) Solvent-free melt electrospinning for preparation of fast dissolving drug delivery
system and comparison with solvent-based electrospun and melt extruded systems.
J. Pharm.
Sci.
, 102(2):508-517.
61. Moser, J.D., Broyles, J., Liu, L., Miller, E., and Wang, M. (2008) Enhancing bioavailability of
poorly soluble drugs using spray dried solid dispersions. Part I.
Am. Pharm. Rev.
, (September
-
October):68-73.
62. Moser, J.D., Broyles, J., Liu, L., Miller, E., and Wang, M. (2008) Enhancing bioavailability
of poorly soluble drugs using spray dried solid dispersions. Part II.
Am. Pharm. Rev.
,
(November-December):94-99.
63. Schwegman, J.J., Hardwick, L.M., and Akers, M. (2005) Practical formulation and process
development of freeze-dried products.
Pharm. Dev. Technol.
, 10:151-173.
64. Janssens, S., De Zeure, A., Paudel, A., Van Humbeeck, Rombaut, P., and Van den Mooter, G.
(2010) Influence of preparation methods on solid state supersaturation of amorphous solid
dispersions: a case study with itraconazole and Eudragit E100.
Pharm. Res.
, 27(5):775-785.
65. Ng, Y.C., Yan, Z., McAuley, W.J., and Qi, S. (2013) Stabilisation of amorphous drugs under
high humidity using pharmaceutical thin films.
Eur. J. Pharm. Biopharm.
, 84:555-565.
66. Lee, T. and Lee, J. (2003) Drug-carrier screening on a chip.
Pharm. Technol.
, (January):40-48.
67. Baumann, J., Dobry, D., and Ray, R. (2013) Amorphous dispersion formulation development:
phase-appropriate integrated approaches to optimizing performance, manufacturability,
stability and dosage form.
Drug Dev. Deliv.
, 13(6):30-37.
68. Alsenz, J. and Kansy, M. (2007) High throughput solubility measurement in drug discovery
and development.
Adv. Drug Deliv. Rev.
, 59:546-567.
69. Alsenz, J., Meister, E., and Haenel, E. (2007) Development of a partially automated solubility
screening (PASS) assay for early drug development.
J. Pharm. Sci.
, 96(7):1748-1762.
70. Hsieh, S., Yue, H., Nicholson, S., Roberts, D., Schild, R., Gamble, J., and Lindrud, M. (2013)
Modeling of the secondary drying and the fate of organic solvents for spray dried dispersion
(SDD) product. AIChE Annual Meeting. Abstract available at
http://www3.aiche.org/
319900
(accessed January 25, 2014).
71. Zhang, G.G.Z., Law, D., Schmitt, E.A., and Qiu, Y. (2004) Phase transformation considera-
tions during process development and manufacture of solid oral dosage forms.
Adv. Drug
Deliv. Rev.
, 56:371-390.
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