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Description
[5] In 1950, Neal E
This has been studied primarily in cultured cells and animal models
Solid dosage forms for oral administration may be prepared, e.g., by mixing the active ingredient(s) with one or more pharmaceutically-acceptable carriers or diluents and, optionally, one or more fillers, extenders, binders, humectants, disintegrating agents, solution retarding agents, absorption accelerators, wetting agents, absorbents, lubricants, and/or coloring agents
However, several organs were relatively larger, e.g., liver, brain, kidney, and heart (307, 308)
