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Spring and parachute: How cocrystals enhance solubility. Definition of the hydrogen bond (IUPAC Recommendations 2011). Available from: Īrunan E, Desiraju GR, Klein RA, Sadlej J, Scheiner S, Alkorta I, et al. Advanced methodologies for cocrystal synthesis. Available from: ĭouroumis D, Ross SA, Nokhodchi A. Pharmaceutical aspects of salt and cocrystal forms of APIs and characterization challenges. Properties of solid dispersion of piroxicam in Pluronic F-98. Supercritical fluid technologies and tissue engineering scaffolds. Quirk RA, France RM, Shakesheff KM, Howdle SM. Solid Dispersions: an Approach to Enhance Solubility of poorly Water Soluble Drug. Sridhar I, Doshi A, Joshi B, Wankhede V, Doshi J. Pharmaceutical cocrystals: from serendipity to design to application. Kavanagh ON, Croker DM, Walker GM, Zaworotko MJ. Pharmacokinetic profiles of two tablet formulations of piroxicam. Solid state transformations in consequence of electrospraying - A novel polymorphic form of piroxicam.
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Characterization of piroxicam crystal modifications. Insight into the solubility and dissolution behavior of piroxicam anhydrate and monohydrate forms. Paaver U, Lust A, Mirza S, Rantanen J, Veski P, Heinämäki J, et al. Enhanced bioavailability of piroxicam via salt formation with ethanolamines. Investigation of the piroxicam/hydroxypropyl-β-cyclodextrin inclusion complexation by means of a supercritical solvent in the presence of auxiliary agents. Biowaiver monographs for immediate release solid oral dosage forms: Piroxicam. Shohin IE, Kulinich JI, Ramenskaya G V., Abrahamsson B, Kopp S, Langguth P, et al.
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