Evaluation of solid dispersions on a molecular level by the Raman mapping technique.

[1]  S. Riegelman,et al.  Pharmaceutical applications of solid dispersion systems. , 1971, Journal of pharmaceutical sciences.

[2]  G. Alderborn,et al.  The effect of pre-compaction processing and storage conditions on powder and compaction properties of some crystalline materials , 1994 .

[3]  J. Henck,et al.  Polymorphism in binary mixtures, as exemplified by nimodipine , 1995 .

[4]  Bruno C. Hancock,et al.  Characteristics and Significance of the Amorphous State in Pharmaceutical Systems , 1997 .

[5]  J. Newton,et al.  Interaction between water and poly(vinylpyrrolidone) containing polyethylene glycol. , 1999, Journal of pharmaceutical sciences.

[6]  R. Skwierczynski Interaction between water and poly(vinylpyrrolidone) containing polyethylene glycol , 1999 .

[7]  R. Skwierczynski Disorder, molecular mobility, and solid-state kinetics: the two-environment model. , 1999, Journal of pharmaceutical sciences.

[8]  J Dressman,et al.  Improving drug solubility for oral delivery using solid dispersions. , 2000, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[9]  L. S. Taylor,et al.  Evaluation of solid-state forms present in tablets by Raman spectroscopy. , 2000, Journal of pharmaceutical sciences.

[10]  L. S. Taylor,et al.  A comparison of alternative polymer excipients and processing methods for making solid dispersions of a poorly water soluble drug. , 2001, International journal of pharmaceutics.

[11]  Nobuyuki Suzuki,et al.  Physical property of troglitazone, an equal mixture of four stereoisomers. , 2002, International journal of pharmaceutics.

[12]  Steven W Booth,et al.  Quantitative analysis of mannitol polymorphs. FT-Raman spectroscopy. , 2002, Journal of pharmaceutical and biomedical analysis.

[13]  C. R. Petts,et al.  Effect of moisture on polyvinylpyrrolidone in accelerated stability testing. , 2002, International journal of pharmaceutics.

[14]  M. Gohel,et al.  Processing of Nimesulide-PEG 400-PG-PVP Solid Dispersions: Preparation, Characterization, and In Vitro Dissolution , 2003, Drug development and industrial pharmacy.

[15]  A. Juppo,et al.  Evaluation of polar lipid-hydrophilic polymer microparticles. , 2003, International journal of pharmaceutics.

[16]  Yoshiaki Watanabe,et al.  Solid-State Variation of Troglitazone Drug Substance by Using a Different Recrystallization Method , 2003, Drug development and industrial pharmacy.

[17]  Ulrich J. Griesser,et al.  Qualitative and quantitative study of polymorphic forms in drug formulations by near infrared FT-Raman spectroscopy , 2003 .

[18]  Lynne S. Taylor,et al.  Spectroscopic Characterization of Interactions Between PVP and Indomethacin in Amorphous Molecular Dispersions , 1997, Pharmaceutical Research.

[19]  Susumu Hasegawa,et al.  Uniformity and physical states of troglitazone in solid dispersions determined by electron probe microanalysis and microthermal analysis. , 2004, International journal of pharmaceutics.

[20]  Ian Larson,et al.  Measurement of lactose crystallinity using Raman spectroscopy. , 2005, Journal of pharmaceutical and biomedical analysis.

[21]  H. Wikström,et al.  In-line monitoring of hydrate formation during wet granulation using Raman spectroscopy. , 2005, Journal of pharmaceutical sciences.

[22]  Nikin Patel,et al.  Identifying and Mapping Surface Amorphous Domains , 2005, Pharmaceutical Research.

[23]  Chengsheng Liu,et al.  Characteristics of Rofecoxib-Polyethylene Glycol 4000 Solid Dispersions and Tablets Based on Solid Dispersions , 2005, Pharmaceutical development and technology.

[24]  G. Slegers,et al.  Determination of the relative amounts of three crystal forms of a benzimidazole drug in complex finished formulations by FT-Raman spectroscopy. , 2005, Journal of pharmaceutical and biomedical analysis.

[25]  E. Yonemochi,et al.  Effects of water content in physical mixture and heating temperature on crystallinity of troglitazone-PVP K30 solid dispersions prepared by closed melting method. , 2005, International journal of pharmaceutics.

[26]  M. Sheikhzadeh,et al.  Solid-State Characterization of Buspirone Hydrochloride Polymorphs , 2006, Pharmaceutical Research.

[27]  Lynne S Taylor,et al.  Hyphenation of Raman spectroscopy with gravimetric analysis to interrogate water-solid interactions in pharmaceutical systems. , 2007, Journal of pharmaceutical and biomedical analysis.

[28]  L. Hovgaard,et al.  Characterization and Physical Stability of Tolfenamic Acid-PVP K30 Solid Dispersions , 2007, Pharmaceutical development and technology.