Keywords: Celecoxib; Solid Dispersion; Dissolution rate; Solubility; polyvinylpyrrolidine; superdisintegrants. Served as the expert reviewer of the PhD thesis of one student.
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Edu/ theses- dissertations/ 216. Abstract: Solid dispersion formulation is a promising method to maintain in vivo drug solubility and to improve drug efficacy.
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Pharmaceutical strategies to overcome poor solubility in solid dosage forms. Thesis title: Examination of the relationship between.Formulation of solid dispersion of the drug has attracted considerable interest as a means of improving dissolution process of a range of. Hargreaves, 1982.
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In pharmaceuticals, an active pharmaceutical ingredient ( API) may be medicinally favourable, but have undesirable physical properties, such as poor solubility, that potentially limit. Infrared Study of Solid Dispersions ofβ- Cyclodextrin with.
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Dissertation Health Social Care. Congratulations to Katerina Puncochova for successfully defending her thesis titled “ Investigation of dissolution mechanisms and release kinetics of poorly soluble drugs from amorphous solid dispersions” and obtaining the PhD degree.
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Structural characterisation in the solid state is an important step in understanding the physical and chemical properties of a material. Article Page ScienceDirect IOPscience SLN CP formulations show the highest UV protection abilities because of owing to the high crystallinity of the solid lipid than the other solid lipids.
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Stability to dispersion at neutral pH only whereas non- ionic surfactants can provide stability to dispersion at different pH.