Transdermal Electrotransport Delivery Device Including An Antimicrobial Compatible Reservoir Composition

• US 20070100274A1
• Filed: 11/03/2006
• Published: 05/03/2007
• Est. Priority Date: 04/04/2001
• Status: Active Grant

• Current Assignee: ALZA Corporation (Johnson & Johnson)
• Original Assignee: ALZA Corporation (Johnson & Johnson)
• Inventors: Cormier, Michel, Young, Wendy
• Granted Patent: US 7,801,599 B2
• Time in Patent Office: Days
• US Class Current: 604/20
• CPC Class Codes: A61N 1/30 Apparatus for iontophoresis, i.e. transfer of media in ionic state by an electromotoric force into the body, or cataphoresis
• CPC Class Codes: A61P 25/04 Centrally acting analgesics, e.g. opioids

Abstract

A transdermal electrotransport drug delivery device having an anode, a cathode and a source of electrical power electrically connected to the anode and the cathode. At least one of the anode and the cathode includes an electrode and a reservoir comprised of a housing composed of a polymeric material and an aqueous medium in contact with the housing. The aqueous medium includes (i) a drug or an electrolyte salt or a mixture thereof, (ii) propylene glycol, and (iii) an antimicrobial agent in an amount sufficient to inhibit microbial growth in the aqueous medium. The propylene glycol prevents the antimicrobial agent from being adsorbed by other materials used in the construction of the delivery device. A process for preparing a transdermal electrotransport drug delivery device is also provided.

Claims

1. A transdermal electrotransport drug delivery or body analyte sampling device comprised of an anode, a cathode and a source of electrical power electrically connected to the anode and the cathode, at least one of the anode and the cathode including an electrode and a reservoir comprised of a housing, said housing comprised of a polymeric material and an aqueous medium in contact with the housing, said aqueous medium comprised of (i) a drug or an electrolyte salt or a mixture thereof;

(ii) propylene glycol; and

(iii) an antimicrobial agent in an amount sufficient to inhibit microbial growth in the aqueous medium wherein the propylene glycol is present in an amount which renders the antimicrobial agent compatible with the device.

2. The transdermal electrotransport drug delivery or body analyte sampling device according to claim 1, wherein said aqueous medium has a pH in the range of about 4.0 to about 9.0.

3. The transdermal electrotransport drug delivery or body analyte sampling device according to claim 2, wherein said aqueous medium has a pH in the range of about 5.0 to about 8.0.

4. The transdermal electrotransport drug delivery or body analyte sampling device according to claim 1, wherein said aqueous medium comprises a buffer, a drug or an electrolyte salt or a mixture thereof, propylene glycol and an antimicrobial agent in an amount sufficient to inhibit microbial growth in the aqueous medium.

5. The transdermal electrotransport drug delivery or body analyte sampling device according to claim 1, wherein the polymeric housing material is selected from the group consisting of polyethylene terephthalate, polyethylene terephthalate modified with cyclohexane dimethylol, polypropylene, polyethylene, polyethylene copolymers, and mixtures thereof.

6. The transdermal electrotransport drug delivery or body analyte sampling device according to claim 1, wherein said reservoir is substantially drug free.

7. The transdermal electrotransport drug delivery or body analyte sampling device according to claim 1, wherein said anode includes an anodic electrode and an anodic reservoir, said anodic reservoir comprised of a polymeric housing, said anodic reservoir containing a drug.

8. The transdermal electrotransport drug delivery or body analyte sampling device according to claim 7, wherein said anodic reservoir contains a fentanyl-based active agent.

9. The transdermal electrotransport drug delivery or body analyte sampling device according to claim 1, wherein said antimicrobial agent is selected from the group consisting of methylparaben, ethylparaben and propylparaben, propyl gallate, butylated hydroxyanisole (BHA), burylated hydroxytoluene, t-butyl-hydroquinone, chloroxylenol, chlorohexidine, dichlorobenzyl alcohol, dehydroacetic acid, hexetidine and triclosan.

10. The transdermal electrotransport drug delivery or body analyte sampling device according to claim 1, wherein said antimicrobial agent is a paraben.

11. The transdermal electrotransport drug delivery or body analyte sampling device according to claim 1, wherein said antimicrobial agent is present in a concentration at least about 0.005% by weight.

12. The transdermal electrotransport drug delivery or body analyte sampling device according to claim 11, wherein said aqueous medium contains from about 0.005% by weight to about 2% by weight of said antimicrobial agent.

13. The transdermal electrotransport drug delivery or body analyte sampling device according to claim 12, wherein said aqueous medium contains from about 0.01% by weight to about 1% by weight of said antimicrobial agent.

16. The transdermal electrotransport drug delivery or body analyte sampling device according to claim 1, wherein the antimicrobial agent is one of substantially neutral in charge in the aqueous medium and has a charge that is not driven transdermally by the charge of the electrode in contact with the aqueous medium when in operation.

17. The transdermal electrotransport drug delivery or body analyte sampling device according to claim 16, wherein the antimicrobial agent in the aqueous medium is of a charge that is not driven transdermally by the charge of the electrode in contact with the aqueous medium when in operation.

18. The transdermal electrotransport drug delivery or body analyte sampling device according to claim 16, wherein the antimicrobial agent in the aqueous medium is of a charge that is not driven transdermally by the charge of the electrode in contact with the aqueous medium which is at pH from 5 to 8 when in operation, said propylene glycol is present in a range of 5% by weight to 30% by weight to render soluble said antimicrobial agent in a concentration of 0.005% to 2% by weight in the aqueous medium.

19. The transdermal electrotransport drug delivery or body analyte sampling device according to claim 16, wherein the antimicrobial agent in the aqueous medium is of a charge that is not driven transdermally by the charge of the electrode in contact with the aqueous medium which is at pH from 5 to 8 when in operation, said propylene glycol being present in a range of 5% by weight to 30% by weight to render soluble said antimicrobial agent in a concentration of 1% to 2% by weight in the aqueous medium.

14. The transdermal electrotransport drug delivery or body analyte sampling device wherein said propylene glycol is present in a range of about 5% by weight to about 50% by weight.

15. The transdermal electrotransport drug delivery or body analyte sampling device according to claim 14, wherein said propylene glycol is present in a range of about 5% by weight to about 30% by weight.

20. A transdermal electrotransport drug delivery or body analyte sampling device, comprising:

an anode;

a cathode, at least one of said anode and cathode including an electrode and a reservoir comprised of a housing, said housing comprised of a polymeric material;

a source of electrical power electrically connected to said anode and cathode; and

an aqueous medium in contact with said housing, said aqueous medium comprised of a drug or an electrolyte salt or a mixture thereof, propylene glycol and an antimicrobial agent in an amount sufficient to inhibit microbial growth in the aqueous medium, wherein the propylene glycol is present in an amount which renders the antimicrobial agent compatible with the device and said antimicrobial agent is present in a concentration at least about 0.005% by weight.

21. A transdermal electrotransport drug delivery or body analyte sampling device, comprising:

an anode;

a cathode, at least one of said anode and cathode including an electrode and a reservoir comprised of a housing, said housing comprised of a polymeric material;

a source of electrical power electrically connected to said anode and cathode; and

an aqueous medium in contact with said housing, said aqueous medium comprised of a drug or an electrolyte salt or a mixture thereof, propylene glycol and an antimicrobial agent in an amount sufficient to inhibit microbial growth in the aqueous medium said antimicrobial agent being dissolved but is substantially neutral in charge in the presence of propylene glycol in the aqueous medium which is at pH from 5 to 8 when in operation.