U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Pulsatile particles drug delivery system

Patent 5260069 Issued on November 9, 1993. Estimated Expiration Date: Icon_subject November 27, 2012. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

Sustained release tablets and method of making same
Patent #: 4684516
Issued on: 08/04/1987
Inventor: Bhutani

Intestine drug delivery
Patent #: 4863744
Issued on: 09/05/1989
Inventor: Urquhart ,   et al.

Time-controlled explosion systems and processes for preparing the same
Patent #: 4871549
Issued on: 10/03/1989
Inventor: Ueda ,   et al.

Multi-unit delivery system Patent #: 5110597
Issued on: 05/05/1992
Inventor: Wong, et al.

Inventor

Assignee

Application

No. 982761 filed on 11/27/1992

US Classes:

424/451, Capsules (e.g., of gelatin, of chocolate, etc.)424/438, Specially adapted for ruminant animal424/493Containing polysaccharides (e.g., sugars)

Examiners

Primary: Page, Thurman K.
Assistant: Benston, W.

Attorney, Agent or Firm

International Class

A61K 009/48

Abstract

Unit dosage form for delivering drugs into the body in a series of sequential, pulsatle releasing events employs conventional pharmaceutical equipment and processes for optimum economy, reliability, and bioavailability. The system can be used with drugs which cannot be released by diffusion through a porous coating, such as water insoluble drugs. A plurality of populations of pellets is provided within a unit dosage form such as a capsule or tablet. The pellets are composed of a core containing the drug and a swelling agent which expands in volume when exposed to water. The core is enclosed within a membrane or coating which is permeable to water. The membrane is composed of a water insoluble and permeable film forming polymer, a water soluble film forming polymer and a permeability reducing agent. When the unit dose releases the pellets into the digestive tract, water diffuses through the coating and into the core. As water is taken up by the swelling agent, the core expands, exerting force on the coating until it bursts, releasing the drug. The permeability reducing agent reduces the rate at which water reaches the swelling agent, thereby delaying release time. The water soluble polymer dissolves, weakening the coating so that it bursts sooner. By varying the proportions of the three coating ingredients and/or coating thickness from one pellet population to another, the release timing of the pellets can be very effectively controlled.

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