Process of agglomeration that converts fine powders or granules of bulk drugs and excipients into small, free-flowing, spherical, or semi-spherical…
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Artificial spherical lipid bilayer droplet formed mainly from phospholipids having a core of water phase, small enough to form a relatively stable dispersion in aqueous media and with potential use in drug delivery.
liposome
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Transition of a solid crystalline phase to another phase having the same chemical composition but a dif- ferent crystal structure.
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Insertion or grafting of a biological, living, inert, or radioactive material into the body.
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Concentration of a drug that must be achieved in the plasma before any desired therapeutic or pharmacological effect can be…
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Number that expresses the reduction in the numbers of a microorganism, brought about by a sterilizaion process.
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Specific case of drug embedding in insoluble excipients (typically in a polymer) in order to achieve extended release.
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Tablet, which does not contain a disintegrant and which is sucked to dissolve in the mouth to produce either a…
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Initial, typically larger than the maintenance dose of a drug given to a patient at the start of pharmacotherapy.
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