Formation of microparticles encapsulating a drug.
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The process of separating the lighter particles of a powder from the heavier ones by means of an up- ward-directed stream of fluid (gas or liquid).
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Summary of operations carried out to convert a pharmacologically active compound into a dosage form suitable for administration.
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Powder particles, which have been aggregated to form larger irregular particles, usually of 0.5–2 mm diameter.
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Used on tablets, granules, pellets, and capsules to make them resistant to gastric fluids but designed to disintegrate, disrupt, or…
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Use of products containing genetic material (e.g., pDNA, antisense DNA, si RNA) to treat a disease or condition, or to…
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Non-fluid colloidal network or polymer network that is expanded throughout its whole volume by a fluid.
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The Process of contact and adhesion whereby particles in dispersion form larger-size clusters.
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Time required to achieve the minimum effective plasma concentration following administration of the dosage form.
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