Minimally Invasive Medical Implant Devices for Controlled Drug Delivery

• US 20070275035A1
• Filed: 05/24/2007
• Published: 11/29/2007
• Est. Priority Date: 05/24/2006
• Status: Abandoned Application

• Current Assignee: MicroCHIPS Inc.
• Original Assignee: MicroCHIPS Inc.
• Inventors: Herman, Stephen J., Staples, Mark A., Santini, John T.
• Application Number:
  US11/753,330
• Publication Number:
  US 20070275035A1
• Time in Patent Office: Days
• US Class Current: 424/426
• CPC Class Codes: A61K 9/0024 Solid, semi-solid or solidifying implants, which are implanted or injected in body tissue compositions for intravenous administration, normal injectable solutions or dispersions for, e.g. subcutaneous administration A61K9/0019; brain implants A61K9/0085; (coated) prostheses, catheters or stents A61L
• CPC Class Codes: A61K 9/0097 Micromachined devices; Microelectromechanical systems [MEMS]; Devices obtained by lithographic treatment of silicon; Devices comprising chips intradermal microneedle arrays A61K9/0021; MEMS in general B81B7/02
• CPC Class Codes: A61M 31/002 Devices for releasing a drug at a continuous and controlled rate for a prolonged period of time artificial gland structures or devices A61F2/022; intra-uterine contraceptive devices A61F6/14; tampons for introducing into the vagina A61F13/20, A61L15/00; suppositories or bougies for intra-vaginal or intra-uterine application A61K9/02; physical forms of medicinal preparations for sustained or differential drug release A61K9/20, A61K9/50

Abstract

Implantable medical devices and methods of use are provided for controlled drug delivery. The devices may include an elongated body dimensioned to facilitate minimally invasive and complete implantation into a patient, wherein the elongated body portion comprises a first, closed end portion, a second closed end portion and an intermediate portion disposed between and connected to the first closed end portion and the second closed end portion; two or more discrete reservoirs disposed in the elongated body portion, each reservoir having one or more openings; a drug formulation, which comprises at least one drug, disposed in the two more discrete reservoirs; and reservoir caps closing off the one or more openings of each reservoir, wherein release of the drug in vivo is controlled at least in part by the in vivo disintegration or permeabilization of the discrete reservoir caps.

Claims

1. An implantable medical device for controlled drug delivery comprising:

an elongated body dimensioned to facilitate minimally invasive and complete implantation into a patient, wherein the elongated body portion comprises a first, closed end portion, a second, closed end portion and an intermediate portion disposed between and connected to the first closed end portion and the second closed end portion;

two or more discrete reservoirs disposed in the elongated body portion, each reservoir having one or more openings;

a drug formulation, which comprises at least one drug, disposed in the two more discrete reservoirs; and

reservoir caps closing off the one or more openings of each reservoir,

wherein release of the drug in vivo is controlled at least in part by the in vivo disintegration or permeabilization of the discrete reservoir caps.

2. The device of claim 1, wherein the intermediate portion is substantially tubular in shape, and the first closed end portion comprises a rounded end.

3. The device of claim 2, wherein the device is suitable for passing through a trochar, hollow needle, or catheter.

4. The device of claim 1, wherein the elongated body is formed of a polymer.

5. The device of claim 1, wherein the elongated body is formed of a metal.

6. The device of claim 1, wherein the reservoir caps comprises a polymer which disintegrates in vivo.

7. The device of claim 1, wherein the drug formulation is in a solid form.

8. The device of claim 7, wherein the drug formulation comprises microparticles or nanoparticles of a drug.

9. The device of claim 7, wherein the drug formulation in each reservoir is in a monolithic structure form.

10. The device of claim 1, wherein the drug comprises a protein, a peptide, or a nucleic acid.

11. The device of claim 1, wherein the discrete reservoirs are microreservoirs.

12. The device of claim 1, wherein the drug is a vaccine.

13. The device of claim 1, wherein the drug is a chemotherapeutic agent or a hormone.

14. The device of claim 1, wherein the device comprises a linear array of three or more reservoirs, each containing a drug formulation and having a discrete reservoir cap closing off at least one opening of each reservoir.

15. The device of claim 1, wherein at least two of the reservoir caps differ from one another in composition or thickness or both.

16. The device of claim 1, wherein at least one of the reservoirs extends into the elongated body in a substantially traverse direction to a depth which is more than 50% of the maximum traverse width of the intermediate body portion.

17. The device of claim 1, wherein at least one of the reservoirs has a first opening and an opposing second opening located distal to one another in the traverse direction in the intermediate portion of the elongated device body.

18. The device of claim 1, wherein the elongated body defines a plurality of reservoirs about the circumference of the device and wherein the reservoirs extend the substantial length of the elongated body.

27. A method of the administration of a drug to a patient comprising:

injecting the implantable medical device of claim 1 into a tissue site in a patient; and

releasing the drug from the medical device to the tissue site.

28. The method of claim 27, wherein the step of injecting is subcutaneous or intramuscular.

29. The method of claim 27, wherein the tissue site is a tumor mass.

30. The method of claim 27, wherein the tissue site is in the brain, the peritoneal cavity, an intracranial cavity, or the pleural space.

31. The method of claim 27, wherein the step of injecting comprises passing the implantable medical device through the hollow bore of a needle, cannula, catheter, or trocar.

19. An implantable medical device for controlled drug delivery comprising,

a first solid unit of a drug formulation which comprises at least one drug, the first solid unit have a proximal end, a distal end, and one or more longitudinal exterior surfaces therebetween;

a second solid unit of the drug formulation which comprises the at least one drug, the second solid unit have a proximal end, a distal end, and one or more longitudinal exterior surfaces therebetween;

a layer of a first membrane material coating the longitudinal exterior surfaces of the first solid unit;

a layer of a second membrane material coating the longitudinal exterior surfaces of the second solid unit; and

a substantially impermeable seal member sandwiched between the proximal end of the first solid unit and the distal end of the second solid unit, such that the first solid unit, seal member, and second solid unit are connected together aligned in an elongated rod shaped form, which is dimensioned to facilitate minimally invasive and complete implantation into a patient,

wherein release of the drug in vivo is controlled at least in part by the in viva disintegration or permeabilization of the first and second membrane materials.

20. The implantable medical device of claim 19, wherein release of the drug from the first solid unit occurs at a different time or rate than release of the drug from the second solid unit.

21. The implantable medical device of claim 19, wherein the first and second units each have a cylindrically shaped exterior surface, and the seal member is disk shaped.

22. The implantable medical device of claim 19, wherein the seal member comprises a non-degradable polymer.

23. The implantable medical device of claim 19, wherein the first membrane material, the second membrane material, or both membrane materials comprise a biodegradable polymer.

24. The implantable medical device of claim 19, wherein drug formulation further comprises one or more pharmaceutically acceptable excipient materials.

25. The implantable medical device of claim 19, which comprises three or more of the membrane coated solid units of drug formulation and two or more of the seal members.

26. The implantable medical device of claim 19, further comprising a plurality of rods connecting the seal members.