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US 2015/0030671 A1Published application
Methods and formulations for enhancing the absorption and decreasing the absorption variability of orally administered drugs, vitamins and nutrients
AssigneeZomanex, LLC
InventorCurtis A. Spilburg
Life of this patent
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Abstract
A method of preparing and composition of bioavailable hydrophobic, poorly water soluble drugs. It uses for example, lecithin, sterol, a calcium salt, and solvent; mixing to form liposomes and then the solvent driven off; the ratios used and physical form differ from others, and maximize performance.
Claims34
A solid powdered dried liposomal form drug composition for water insoluble hydrophobic oil or crystalline drug actives, comprising:
- an emulsifier;
- a plant derived sterol or ester derived from said sterol, a calcium salt, and
- a drug active effective amount of hydrophobic drug.
The method of preparing a dried powdered liposomal form of drug delivery system for water insoluble hydrophobic oil or crystalline drug actives, comprising:
- mixing simultaneously an emulsifier(s) or mixtures thereof with a plant derived sterol or esters derived from said plant sterol in which the fatty acid ester moiety is derived from a vegetable oil, and a drug active, with a non-polar solvent;
- removing the solvent to leave a solid residue of the mixed components;
- adding water to the solid residue of the mixed components at a temperature less than the decomposition temperature of any one of the mixed components;
- homogenizing the aqueous mixture;
- drying the homogenized mixture;
- adding a calcium salt to the dried, homogenized mixture;
- and
- providing the dried solid residue of the mixed components in a solid pharmaceutical carrier format.
5 more elements
Dependencies are inferred from the claim text.