Transition of a solid crystalline phase to another phase having the same chemical composition but a dif- ferent crystal structure.
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Formation of microparticles encapsulating a drug.
microencapsulation
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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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A Biologically active substance, which when biodistributed in the body is expected to modify one or more of its functions.
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Emulsions in which the dispersed droplets are in the micron-size range.
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Time required to achieve the minimum effective plasma concentration following administration of the dosage form.
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Lowest concentration of an antibacterial drug necessary to inhibit the growth of a microorganism.
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A Solid spherical particles of micron-size range, used as matrix dosage forms.
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Exploratory activity that begins early in pharmaceutics, involving studies designed to determine the compatibility of excipients with the active substance…
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