Physicochemical properties of direct compression tablets with spray dried and ball milled solid dispersions of tadalafil in PVP-VA.
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W. Sawicki | K. Wlodarski | L. Tajber | K Wlodarski | W Sawicki | L Tajber
[1] Ping I. Lee,et al. Evolution of supersaturation of amorphous pharmaceuticals: nonlinear rate of supersaturation generation regulated by matrix diffusion. , 2015, Molecular pharmaceutics.
[2] A. Paradkar,et al. Development of spray-dried co-precipitate of amorphous celecoxib containing storage and compression stabilizers , 2007, Acta pharmaceutica.
[3] M Paluch,et al. Physicochemical properties of tadalafil solid dispersions - Impact of polymer on the apparent solubility and dissolution rate of tadalafil. , 2015, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[4] Wouter L J Hinrichs,et al. Improved dissolution behavior of lipophilic drugs by solid dispersions: the production process as starting point for formulation considerations , 2011, Expert opinion on drug delivery.
[5] M. Paluch,et al. Effect of amorphization method on telmisartan solubility and the tableting process. , 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[6] G. Marosi,et al. Downstream processing of polymer-based amorphous solid dispersions to generate tablet formulations. , 2015, International journal of pharmaceutics.
[7] J. Mcginity,et al. Use of highly compressible Ceolus™ microcrystalline cellulose for improved dosage form properties containing a hydrophilic solid dispersion , 2012, Drug development and industrial pharmacy.
[8] Feng Qian,et al. Is a distinctive single Tg a reliable indicator for the homogeneity of amorphous solid dispersion? , 2010, International journal of pharmaceutics.
[9] Amrit Paudel,et al. Manufacturing of solid dispersions of poorly water soluble drugs by spray drying: formulation and process considerations. , 2013, International journal of pharmaceutics.
[10] K. Kamiński,et al. Dielectric relaxation and crystallization kinetics of ibuprofen at ambient and elevated pressure. , 2010, The journal of physical chemistry. B.
[11] Li Di,et al. Drug-like property concepts in pharmaceutical design. , 2009, Current pharmaceutical design.
[12] W. Sawicki,et al. Physical stability of solid dispersions with respect to thermodynamic solubility of tadalafil in PVP-VA. , 2015, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[13] S. M. Badr-Eldin,et al. Inclusion complexes of tadalafil with natural and chemically modified beta-cyclodextrins. I: preparation and in-vitro evaluation. , 2008, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[14] M. Samaha,et al. Tadalafil inclusion in microporous silica as effective dissolution enhancer: optimization of loading procedure and molecular state characterization. , 2011, Journal of pharmaceutical sciences.
[15] K. Grzybowska,et al. The influence of amorphization methods on the apparent solubility and dissolution rate of tadalafil. , 2014, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[16] A. Sallam,et al. Evaluation of Tadalafil Nanosuspensions and Their PEG Solid Dispersion Matrices for Enhancing Its Dissolution Properties , 2014, AAPS PharmSciTech.
[17] Feng Qian,et al. Formulation and process design for a solid dosage form containing a spray-dried amorphous dispersion of ibipinabant , 2013, Pharmaceutical development and technology.
[18] M. Descamps,et al. A new protocol to determine the solubility of drugs into polymer matrixes. , 2013, Molecular pharmaceutics.
[19] Patrick J. Marsac,et al. Theoretical and Practical Approaches for Prediction of Drug–Polymer Miscibility and Solubility , 2006, Pharmaceutical Research.
[20] Y. Kalia,et al. Stabilization of supersaturated solutions of a lipophilic drug for dermal delivery. , 2001, International journal of pharmaceutics.
[21] G. Fetih,et al. Solubility and dissolution enhancement of tadalafil using self-nanoemulsifying drug delivery system. , 2014, Journal of oleo science.
[22] J. Breitenbach. Melt extrusion can bring new benefits to HIV therapy , 2006 .
[23] Beom-Jin Lee,et al. Current trends and future perspectives of solid dispersions containing poorly water-soluble drugs. , 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[24] W. Xiaoli,et al. Nimodipine (NM) tablets with high dissolution containing NM solid dispersions prepared by hot-melt extrusion , 2011, Drug development and industrial pharmacy.
[25] Dave A. Miller,et al. The use of inorganic salts to improve the dissolution characteristics of tablets containing Soluplus®-based solid dispersions. , 2013, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[26] A. Bansal,et al. Investigation of atypical dissolution behavior of an encapsulated amorphous solid dispersion. , 2011, Journal of pharmaceutical sciences.
[27] 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.
[28] Hywel D Williams,et al. Strategies to Address Low Drug Solubility in Discovery and Development , 2013, Pharmacological Reviews.
[29] Jeong-Sook Park,et al. Improved physicochemical characteristics of felodipine solid dispersion particles by supercritical anti-solvent precipitation process. , 2005, International journal of pharmaceutics.
[30] K. Grzybowska,et al. Physical stability of the amorphous anticholesterol agent (ezetimibe): the role of molecular mobility. , 2014, Molecular pharmaceutics.