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Drug-lipid complexes are chemically and physically defined nonvesicular associations of drugs with certain lipids.
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Drug solubility and
bioavailability. It has been well explained that solubility, dissolution and gastrointestinal permeability are fundamental parameters that control rate and extent of
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Bioavailability: The percent of dose entering the systemic circulation after administration of a given dosage form.
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Pharmacokinetics (from Ancient Greek pharmakon "
drug" and kinetikos "moving, putting in motion"; see chemical kinetics), sometimes abbreviated as PK, is a branch of pharmacology dedicated to determining the fate of substances administered to a living organism. The substances of interest include any chemical xenobiotic such as: pharmaceutical drugs, pesticides, food additives, cosmetics, etc.
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