Pulsatile drug delivery device using stimuli sensitive hydrogel

• US 5,226,902 A
• Filed: 07/30/1991
• Issued: 07/13/1993
• Est. Priority Date: 07/30/1991
• Status: Expired due to Term

• Current Assignee: Jacques Ph. D. Gonella, Leonard Jacob, Samyang Corporation (Samyang Holdings Corporation), Samyang Genex Corporation (Samyang Holdings Corporation), University of Utah (State of Utah), ThermoLase Corp. (Thermo Fisher Scientific Incorporated), University of Utah A Nonprofit Corporation of UT
• Original Assignee: University of Utah (State of Utah)
• Inventors: Valuev, Lev I., Kim, Sung W., Bae, You H.
• Primary Examiner(s): NOT, DEFINED
• Assistant Examiner(s): NOT, DEFINED
• Application Number:
  US07/737,675
• Time in Patent Office: 714 Days
• Field of Search: 604/890.1-892.1, 424/451, 424/456, 424/457, 424/422, 424/423, 424/486, 514/944, 514/953, 514/962, 514/965
• US Class Current: 604/892.1
• CPC Class Codes: A61K 9/0004 Osmotic delivery systems; Sustained release driven by osmosis, thermal energy or gas
• CPC Class Codes: Y02A 50/30 Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Abstract

A device for the dispensing of a biologically active material into the surrounding environment is disclosed which consists of at least one wall enclosing a compartment which contains a swollen stimuli sensitive hydrogel in which the biologically active material is entrained in solution. The hydrogel deswells or shrinks in response to contact by external physical or chemical stimuli releasing the biologically active material into the portion of the compartment previously occupied by the swollen hydrogel. The wall enclosing the compartment is rigid and contains means allowing the passage of the biologically active material from the compartment to the surrounding environment and also for transmitting the external stimuli to the swollen hydrogel in said compartment. The wall may contain orifices or be permeable to the active material and external stimuli depending upon the drug and the stimuli to be used. The hydrogel reversibly deswells, shrinks or contracts in response to stimuli, such as temperature, pH, ionic strength, glucose concentration or metabolites in the body and then reswells and reentrains active material not diffused from the compartment when the stimuli is removed. The wall may consist of one or more layers which, in combination, provide for the expeditious delivery of the active substance either through permeation through the wall or through orifices in the wall and also for the conducting of the external stimuli through the wall into the compartment to trigger the deswelling of the hydrogel.

Claims

1. A device for the dispensing of a biologically active material into a surrounding environment by bulk diffusion comprising a wall defining an interior compartment;

said compartment containing a swollen stimuli sensitive hydrogel in which the biologically active material is entrained in solution which hydrogel deswells in response to contact by external stimuli thereby releasing said biologically active material into said compartment of outward diffusion;

said wall being rigid and containing means allowing the passage of said biologically active material released from said deswollen hydrogel from said compartment by outward diffusion to said surrounding environment and also containing means for transmitting said external stimuli from said outside environment to said swollen hydrogel in said compartment.

2. The device of claim 1 wherein the biologically active material is squeezed from the hydrogel as said hydrogel deswells causing said biologically active material to enter into the portion of the compartment previously occupied by the deswollen hydrogel thereby allowing said biologically active substance to be released through said wall and into the environment surrounding said device.

3. The device of claim 1 wherein said wall contains orifices and wherein the means for allowing the passage of said biologically active material from said compartment to said surrounding environment is through said orifices.

4. The device of claim 3 wherein said orifices are sized to prevent the passage of deswollen hydrogel from said compartment into the surrounding environment.

5. The device of claim 4 wherein said wall is made from a material which is impermeable to the passage of said biologically active substance and chemical stimuli.

6. The device of claim 5 wherein said material is selected from the group consisting of natural polymers, synthetic polymers, ceramics and metallic materials.

7. The device of claim 4 wherein said wall made from a material which is impermeable to the passage of said biologically active substance but is permeable to the passage of chemical stimuli.

8. The device of claim 7 wherein the chemical stimuli is change in pH and said wall is made from a material which is permeable to chemical agents affecting hydrogen ion concentration.

9. The device of claim 8 wherein said wall is made from a material selected from the group consisting of cellulose esters, cellulose ethers, cellulose ester-ethers, cellulose acrylate, cellulose diacrylate, cellulose triacrylate, cellulose acetate, cellulose diacetate, cellulose triacetate, hydroxypropyl methylcellulose, and mixtures thereof.

10. The device of claim 2 wherein said wall is permeable to both diffusion of the biologically active material and physical and chemical stimuli thereby allowing outward diffusion of the biologically active material from said compartment into the surrounding environment and inward diffusion of chemical stimuli through said wall into said compartment.

11. The device of claim 10 wherein said wall is constructed of a material selected from the group consisting of dialysis membrane materials.

12. The device of claim 11 wherein said dialysis membrane materials are selected from the group consisting of cellulose acetate, regenerated cellulose, polysulfone, and polymethylmethacrylate.

13. The device of claim 12 wherein the chemical stimuli is glucose concentration and said wall is permeable to the passage of glucose and insulin or an insulin substitute.

14. The device of claim 10 wherein said wall is constructed of materials that allow diffusion of signal molecules and basal diffusion of beneficial drugs selected from the group consisting of ultra filtration porous polymer membranes;

hydrogel membranes having appropriate water content for diffusion of signal molecules and drugs; and

copolymers of water soluble monomer and water insoluble monomers.

15. The device of claim 14 wherein said material is an ultra filtration porous polymer membrane.

16. The device of claim 15 wherein the, porous polymer membrane is a member selected from the group consisting of ethylene vinylacetate, polypropylene, polyvinylidene difluoride, and polycarbonate.

17. The device of claim 14 wherein said material is a hydrogel membrane having appropriate Water content for diffusion of signal molecules and drugs.

18. The device of claim 17 wherein said hydrogel membrane is a hydrophilic polymer selected from the group consisting of polyhydroxyethyl methacrylate, polyvinylpyrrolidone, polyacrylamide and alkyl derivatives thereof.

19. The device of claim 14 wherein said material is a copolymer of a water soluble monomer and a water insoluble monomer.

20. The device of claim 19 wherein said water soluble monomer is a member selected from the group consisting of vinylpyrrolidone, hydroxyethylmethacrylate, acrylamide, alkyl derivatives of acrylamide (N-ethylacrylamide, N,N-dimethylacrylamide, N-methylacylamide, N,N-diethylacrylamide and the like), acrylic acid, methacrylic acid, and the like, and said water insoluble monomer is a member selected from the group consisting of styrene, alkylmethacrylates, and alkylacrylates.

21. The device of claim 10 wherein said wall is at least partially surrounded by a second outer wall wherein said outer wall contains at least one opening exposing said wall to the surrounding environment providing a passageway for the diffusion of said biologically active substance and said chemical stimuli.

22. The device of claim 21 wherein said outer wall is a flexible membrane permeable to chemical stimuli but impermeable to the biologically active substance.

23. The device of claim 21 wherein said outer wall is a flexible membrane impermeable to both chemical stimuli and the biologically active substance.

24. The device of claim 21 wherein said outer wall is a flexible membrane permeable to both chemical stimuli and the biologically active substance.

25. The device of claim 2 wherein said wall is a structured porous support said wall being surrounded by a second flexible membrane outer wall said wall and outer wall both containing communicating apertures which provide a channel for the delivery of said biologically active substance from said compartment to said surrounding environment.

26. The device of claim 25 wherein said outer wall is a flexible membrane permeable to chemical stimuli but impermeable to the biologically active substance.