“…Various technological approaches are used to improve the solubility and oral bioavailability of silymarin components. [54][55][56][57][58][59][60][61][62] For example, using a nanostructured lipid carriers silymarin form, signicantly higher (12.46 fold) brain silybin concentration was achieved. 62 A linear relationship between oral silymarin dose and maximum silybin plasma concentration (C max ) was found in human volunteers, but not in animal models (rat, rabbit, and dog).…”
Recent developments in chemistry, biosynthesis, analytical methods, and transformations of flavonolignans from silymarin are presented. Their pharmacology, biological activities, SAR and safety with special attention to the chirality are discussed.
“…Various technological approaches are used to improve the solubility and oral bioavailability of silymarin components. [54][55][56][57][58][59][60][61][62] For example, using a nanostructured lipid carriers silymarin form, signicantly higher (12.46 fold) brain silybin concentration was achieved. 62 A linear relationship between oral silymarin dose and maximum silybin plasma concentration (C max ) was found in human volunteers, but not in animal models (rat, rabbit, and dog).…”
Recent developments in chemistry, biosynthesis, analytical methods, and transformations of flavonolignans from silymarin are presented. Their pharmacology, biological activities, SAR and safety with special attention to the chirality are discussed.
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