D. Alli, S. Bolton, and N.G. Gaylord Hydroxypropylmethylcellulose-anionic surfactant interactions in aqueous systems J. Appl. Polym. Sci. 42 1991 947 956
I. Alsarra, F. Alanazi, S. Ahmed, A. Bosela, S. Alhamed, H. Mowafy, and S. Neau Comparative study of itraconazole-cyclodextrin inclusion complex and its commercial product Arch. Pharm. Res. 33 2010 1009 1017
G.L. Amidon, H. Lennernas, V.P. Shah, and J.R. Crison A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability Pharm. Res. 12 1995 413 420
R.A. Bellantone Fundamentals of Amorphous Systems: Thermodynamic Aspects N. Shah, H. Sandhu, D.S. Choi, H. Chokshi, A.W. Malick, Amorphous Solid Dispersions 2014 Springer New York 3 34
L.D. Bruce, N.H. Shah, A. Waseem Malick, M.H. Infeld, and J.W. McGinity Properties of hot-melt extruded tablet formulations for the colonic delivery of 5-aminosalicylic acid Eur. J. Pharm. Biopharm. 59 2005 85 97
W.C.G. Butler, and S.R. Bateman A flow-through dissolution method for a two component drug formulation where the actives have markedly differing solubility properties Int. J. Pharm. 173 1998 211 219
R.S. Chaudhary, S.S. Gangwal, V.K. Gupta, Y.N. Shah, K.C. Jindal, and S. Khanna Dissolution system for nifedipine sustained release formulations Drug Dev. Ind. Pharm. 20 1994 1267 1274
L.R. Chen, J.A. Wesley, S. Bhattachar, B. Ruiz, K. Bahash, and S.R. Babu Dissolution behavior of a poorly water soluble compound in the presence of Tween 80 Pharm. Res. 20 2003 797 801
W.L. Chiou, and S. Riegelman Oral absorption of griseofulvin in dogs: increased absorption via solid dispersion in polyethylene glycol 6000 J. Pharm. Sci. 59 1970 937 942
Convention, U.S. Dissolution The United States Pharmacopoeia 29 2011 United book Press Baltimore, MD
P.B. Daly, S.S. Davis, and J.W. Keimerley The effect of anionic surfactants on the release of chlorpheniramine from a polymer matrix tablet Int. J. Pharm. 18 1984 201 205
J.B. Dressman, and C. Reppas In vitro-in vivo correlations for lipophilic, poorly water-soluble drugs Eur. J. Pharm. Sci. 11 Supplement 2 2000 S73 S80
H.S. Ghazal, A.M. Dyas, J.L. Ford, and G.A. Hutcheon In vitro evaluation of the dissolution behaviour of itraconazole in bio-relevant media Int. J. Pharm. 366 2009 117 123
M. Gibaldi, and S. Feldman Establishment of sink conditions in dissolution rate determinations. Theoretical considerations and application to nondisintegrating dosage forms J. Pharm. Sci. 56 1967 1238 1242
Gilis, P.A., De Conde, V., Vandecruys, R., 1995. Beads having a core coated with an antifungal and a polymer. US Patent 5633015, in: Patent, U. (Ed.).
E.D. Goddard Polymer - surfactant interaction part I. uncharged water-soluble polymers and charged surfactants Colloids Surf. 19 1986 255 300
J.S. Grundy, K.E. Anderson, J.A. Rogers, and R.T. Foster Studies on dissolution testing of the nifedipine gastrointestinal therapeutic system. I. Description of a two-phase in vitro dissolution test J. Control. Release 48 1997 1 8
J.S. Grundy, K.E. Anderson, J.A. Rogers, and R.T. Foster Studies on dissolution testing of the nifedipine gastrointestinal therapeutic system. II. Improved in vitro-in vivo correlation using a two-phase dissolution test J. Control. Release 48 1997 9 17
H. Hardung, D. Djuric, and S. Ali Combining HME & solubilization: soluplus® - the solid solution Drug Deliv. Technol. 10 2010 20 27
P.M. Henrichs, J. Tribone, D.J. Massa, and J.M. Hewitt Blend miscibility of bisphenol A polycarbonate and poly(ethylene terephthalate) as studied by solid-state high-resolution carbon-13 NMR spectroscopy Macromolecules 21 1988 1282 1291
T.L. Hwang, and A.J. Shaka Water suppression that works. excitation sculpting using arbitrary wave-forms and pulsed-field gradients J. Magn. Reson. Ser. A 112 1995 275 279
S. Janssens, S. Nagels, H.N.d. Armas, W. D'Autry, A. Van Schepdael, and G. Van den Mooter Formulation and characterization of ternary solid dispersions made up of Itraconazole and two excipients, TPGS 1000 and PVPVA 64, that were selected based on a supersaturation screening study Eur. J. Pharm. Biopharm. 69 2008 158 166
M.N. Jones The interaction of sodium dodecyl sulfate with polyethylene oxide J. Colloid Interface Sci. 23 1967 36 42
B. Katchen, and S. Symchowicz Correlation of dissolution rate and griseofulvin absorption in man J. Pharm. Sci. 56 1967 1108 1111
K. Kogermann, A. Penkina, K. Predbannikova, K. Jeeger, P. Veski, J. Rantanen, and K. Naelapää Dissolution testing of amorphous solid dispersions Int. J. Pharm. 444 2013 40 46
G. Levy Papers presented before the industrial pharmacy section American Pharmaceutical Association: Dallas Meeting, Dallas, USA 1966 233 252
K.E. Lewis, and C.P. Robinson The interaction of sodium dodecyl sulfate with methyl cellulose and polyvinyl alcohol J. Colloid Interface Sci. 32 1970 539 546
M. Linn, E.M. Collnot, D. Djuric, K. Hempel, E. Fabian, K. Kolter, and C.M. Lehr Soluplus® as an effective absorption enhancer of poorly soluble drugs in vitro and in vivo Eur. J. Pharm. Sci. 45 2012 336 343
T. Loftsson, and M.E. Brewster Pharmaceutical applications of cyclodextrins: basic science and product development J. Pharm. Pharmacol. 62 2010 1607 1621
R. Mahajan, J. Chawla, and M. Bakshi Depression in the cloud point of Tween in the presence of glycol additives and triblock polymers Colloid Polym. Sci. 282 2004 1165 1168
M.E. Matteucci, J.C. Paguio, M.A. Miller, R.O. Williams III, and K.P. Johnston Highly supersaturated solutions from dissolution of amorphous itraconazole microparticles at pH 6.8. Mol. Pharm. 6 2009 375 385
D.A. Miller, J.T. McConville, W. Yang, R.O. Williams III, and J.W. McGinity Hot-melt extrusion for enhanced delivery of drug particles J. Pharm. Sci. 96 2007 361 376
A.-M. Misselyn-Bauduin, A. Thibaut, J. Grandjean, G. Broze, and R. Jérôme Investigation of the interactions of polyvinylpyrrolidone with mixtures of anionic and nonionic surfactants or anionic and zwitterionic surfactants by pulsed field gradient NMR J. Colloid Interface Sci. 238 2001 1 7
S. Nilsson Interactions between Water-soluble cellulose derivatives and surfactants. 1. The HPMC/SDS/water system Macromolecules 28 1995 7837 7844
A. Paudel, M. Geppi, and G. Van den Mooter Structural and dynamic properties of amorphous solid dispersions: the role of solid-state nuclear magnetic resonance spectroscopy and relaxometry J. Pharm. Sci. 103 2014 2635 2662
A. Pestieau, F. Krier, P. Lebrun, A. Brouwers, B. Streel, and B. Evrard Optimization of a PGSS (particles from gas saturated solutions) process for a fenofibrate lipid-based solid dispersion formulation Int. J. Pharm. 485 2015 295 305
T.N. Pham, S.A. Watson, A.J. Edwards, M. Chavda, J.S. Clawson, M. Strohmeier, and F.G. Vogt Analysis of amorphous solid dispersions using 2D solid-state NMR and (1)H T(1) relaxation measurements Mol. Pharm. 7 2010 1667 1691
E. Pharmacopoeia Recommendations on Methods for Dosage Forms Testing, European Pharmacopoeia 2010 Druckerei C. H. Beck Nördlingen, Germany 665 667
E. Pharmacopoeia E. Pharmacopoeia, Monograph 2.9.1. Desintegration of Tablets And Capsules 2014 Druckerei C. H. Beck Nördlingen, Germany
D.J. Phillips, S.R. Pygall, V. Brett Cooper, and J.C. Mann Toward biorelevant dissolution: application of a biphasic dissolution model as a discriminating tool for HPMC matrices containing a model BCS class II drug Dissolut. Technol. 19 2012 25 34
D.J. Phillips, S.R. Pygall, V.B. Cooper, and J.C. Mann Overcoming sink limitations in dissolution testing: a review of traditional methods and the potential utility of biphasic systems J. Pharm. Pharmacol. 64 2012 1549 1559
O. Policianova, J. Brus, M. Hruby, M. Urbanova, A. Zhigunov, J. Kredatusova, and L. Kobera Structural diversity of solid dispersions of acetylsalicylic acid as seen by solid-state NMR Mol. Pharm. 11 2014 516 530
J. Posti, and P.P. Speiser Sink conditions in the flow-through cell during dissolution Int. J. Pharm. 5 1980 101 107
C. Potter, Y. Tian, G. Walker, C. McCoy, P. Hornsby, C. Donnelly, D.S. Jones, and G.P. Andrews Novel supercritical carbon dioxide impregnation technique for the production of amorphous solid drug dispersions: a comparison to hot melt extrusion Mol. Pharm. 12 2015 1377 1390
S. Saito Binding of surfactants by polymers J. Colloid Sci. 15 1960 283 286
S. Saito, T. Taniguchi, and K. Kitamura Interactions of anionic surfactants with nonionic polymers. Comparison of guanidinium, tetraalkylammonium, and alkali metal ions as counterions J. Colloid Interface Sci. 37 1971 154 164
A.L. Sarode, H. Sandhu, N. Shah, W. Malick, and H. Zia Hot melt extrusion (HME) for amorphous solid dispersions: predictive tools for processing and impact of drug-polymer interactions on supersaturation Eur. J. Pharm. Sci. 48 2012 371 384
S. Shah, S. Maddineni, J. Lu, and M.A. Repka Melt extrusion with poorly soluble drugs Int. J. Pharm. 453 2013 233 252
Y. Shi, P. Gao, Y. Gong, and H. Ping Application of a biphasic test for characterization of in vitro drug release of immediate release formulations of celecoxib and its relevance to in vivo absorption Mol. Pharm. 7 2010 1458 1465
Y. Sun Dong, L. Sang-Heon, K. Eunhee, J. Hun, J. Jae-Young, P. Jong Woo, and L. Kyu-Hyun Bioavailability of itraconazole in rats and rabbits after administration of tablets containing solid dispersion particles Drug Dev. Ind. Pharm. 26 2000 27 34
S. Symchowicz, and B. Katchen Griseofulvin absorption in man after single and repeated treatments and its correlation with dissolution rates J. Pharm. Sci. 57 1968 1383 1386
A.S. Tatton, T.N. Pham, F.G. Vogt, D. Iuga, A.J. Edwards, and S.P. Brown Probing hydrogen bonding in cocrystals and amorphous dispersions using (14)N-(1)H HMQC solid-state NMR Mol. Pharm. 10 2013 999 1007
J. Thiry, F. Krier, and B. Evrard A review of pharmaceutical extrusion: critical process parameters and scaling-up Int. J. Pharm. 479 2015 227 240
N. Thu Hoa, and R. Kinget Design and evaluation of two-phase partition-dissolution method and its use in evaluating artemisinin tablets J. Pharm. Sci. 85 1996 1060 1063
Y. Tian, J. Booth, E. Meehan, D.S. Jones, S. Li, G.P. Andrews, Y. Tian, J. Booth, E. Meehan, D.S. Jones, S. Li, and G.P. Andrews Construction of drug-polymer thermodynamic phase diagrams using Flory-Huggins interaction theory: identifying the relevance of temperature and drug weight fraction to phase separation within solid dispersions Mol. Pharm. 10 2013 236 248
M. Vogtherr, A. Marx, A.C. Mieden, and C. Saal Investigation of solubilising effects of bile salts on an active pharmaceutical ingredient with unusual pH dependent solubility by NMR spectroscopy Eur. J. Pharm. Biopharm. 92 2015 32 41
T. Watanabe, S. Hasegawa, N. Wakiyama, A. Kusai, and M. Senna Comparison between polyvinylpyrrolidone and silica nanoparticles as carriers for indomethacin in a solid state dispersion Int. J. Pharm. 250 2003 283 286
D.H. Wu, A.D. Chen, and C.S. Johnson An improved diffusion-ordered spectroscopy experiment incorporating bipolar-gradient pulses J. Magn. Reson. Ser. A 115 1995 260 264
X. Yuan, D. Sperger, and E.J. Munson Investigating miscibility and molecular mobility of nifedipine-PVP amorphous solid dispersions using solid-state NMR spectroscopy Mol. Pharm. 11 2014 329 337
K. Zhang, H. Yu, Q. Luo, S. Yang, X. Lin, Y. Zhang, B. Tian, and X. Tang Increased dissolution and oral absorption of itraconazole/Soluplus extrudate compared with itraconazole nanosuspension Eur. J. Pharm. Biopharm. 85 2013 1285 1292
