| 摘要 |
A bead of a drug such as aspirin or acetaminophen formed from a small spheriodal seed particle of the drug or of an inert material coated with an adhesive and layers of drug particles likewise adhered by said adhesive, is provided. The beads may be rendered suitable for time release by coating a plurality of said beads. An 8-12% polyvinylpyrrolidone (PVP) solution may be used as the adhesive, the PVP complexing with aspirin and acetaminophen to reduce irritation of the user. Additionally, a method for manufacturing a drug in small beads having time releasae properties is also provided.
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