Iontophoretic delivery method

• US 5,167,616 A
• Filed: 12/14/1989
• Issued: 12/01/1992
• Est. Priority Date: 12/14/1989
• Status: Expired due to Term

• Current Assignee: ALZA Corporation (Johnson & Johnson)
• Original Assignee: ALZA Corporation (Johnson & Johnson)
• Inventors: Gyory, J. Richard, Haak, Ronald P., Yieh, Jane
• Primary Examiner(s): Howell, Kyle L.
• Assistant Examiner(s): NASSER, ROBERT L
• Application Number:
  US07/452,136
• Time in Patent Office: 1,083 Days
• Field of Search: 604/20, 128/804, 128/422, 128/419 R, 128/632, 128/647, 128/604, 128/128, 128/734
• US Class Current: 604/20
• CPC Class Codes: A61K 9/0009 involving or responsive to electricity, magnetism or acoustic waves; Galenical aspects of sonophoresis, iontophoresis, electroporation or electroosmosis microelectromechanical systems A61K9/0097
• CPC Class Codes: A61N 1/0428 Specially adapted for iontophoresis, e.g. AC, DC or including drug reservoirs

Abstract

An improved method for delivering a drug or beneficial agent transdermally to humans by iontophoresis is provided. The method includes selecting and iontophoretically delivering the drug through a skin site which optimizes the transdermal delivery rate of the drug while minimizing inter-patient variability in skin resistance.

Claims

1. A method of optimizing the transdermal flux of a beneficial agent from an iontophoretic agent delivery device through intact human skin and decreasing inter-patient skin resistance variability, comprising:

selecting a skin site on intact back skin of the human;

placing the iontophoretic delivery device in agent transmitting relation with the intact back skin site, the delivery device contacting the back skin site over an area of about 1 to 200 cm² ; and

iontophoretically delivering the agent through the back skin at a pharmaceutically effective rate, at an optimized transdermal flux compared to human skin sites other than back skin and at a transdermal flux which exhibits decreased inter-patient skin resistance variability compared to human skin sites other than back skin.

2. The method of claim 1, wherein the device includes a donor electrode assembly containing the beneficial agent and a return electrode assembly containing an electrolyte, and the method of placing the delivery device in agent transmitting relation with the back skin site includes (i) placing the donor electrode assembly in agent transmitting relation with the intact back skin site and (ii) placing the return electrode assembly in electrolyte transmitting relation with a skin site spaced apart from the selected intact back skin site.

3. The method of claim 2, wherein the method of placing the delivery device includes adhering the donor electrode assembly to the back skin site using an ion-conducting adhesive.

4. The method of claim 1, wherein the method of placing the delivery device in agent transmitting relation with the back skin site includes placing a donor electrode assembly containing the beneficial agent on the intact back skin site, placing a return electrode assembly on a skin site spaced apart from the intact back skin site and electrically connecting an electrical power source to the donor and return electrode assemblies.

5. The method of claim 4, including placing the donor electrode assembly in agent transmitting relation with a first intact back skin site and placing the return electrode assembly in electrolyte transmitting relation with a second intact back skin site, he second back skin site being spaced apart from the first back skin site.

6. The method of claim 4, including fixing the voltage of the power source.

7. The method of claim 6, wherein the voltage is fixed in the range of about 1 to 10 volts.

8. The method of claim 1, wherein the beneficial agent is a drug.

9. The method of claim 1, wherein the beneficial agent is selected from the group consisting of peptides, polypeptides, proteins and macromolecules having a molecular weight of a least about 300 daltons.

10. The method of claim 1, wherein the beneficial agent is selected from the group consisting of insulin, growth hormones, buserelin, leuprolide, LHRH, metoclopramide, fentanyl, lidocaine, ketoprofen, sufentanil, terbutaline, droperidol, heparin, interferon, scopolamine, testosterone, gonadorelin, ciclopirox olamine, buspirone, calcitonin, cromolyn sodium, and midazolam.

12. The method of claim 1 or 11, including co-delivering the beneficial agent with a skin permeation enhancer through the intact back skin.

17. The method of claim 12, wherein the skin permeation enhancer comprises a surfactant.

11. A method of optimizing transdermal flux of a beneficial agent from an iontophoretic delivery device to a human patient, comprising:

(a) selecting a skin site on intact back skin of the human patient,

(b) placing a donor electrode assembly, which assembly contains a beneficial agent, in agent transmitting relation with the selected intact back skin site, the donor electrode assembly contacting the back skin site over an area of about 0.5 to 100 cm²,

(c) placing a counter electrode assembly, which assembly contains an electrolyte, in electrolyte transmitting relation with a skin site spaced apart from the selected intact back skin site,

(d) connecting an electric power source to the donor and counter electrode assemblies, and

(e) iontophoretically delivering the agent through the back skin at a harmaceutically effective rate, at an optimized transdermal flux compared to human skin sites other than back skin, and at a transdermal flux which exhibits decreased inter-patient skin resistance compared to human skin sites other than back skin.

13. The method of claim 11, wherein the power source comprises a battery having a voltage in the range of about 1 to 10 volts.

14. The method of claim 11, wherein the beneficial agent is a drug.

15. The method of claim 11, wherein the beneficial agent is selected from the group consisting of peptides, polypeptides, proteins and macromolecules having a molecular weight of at least about 300 daltons.

16. The method of claim 11, wherein the beneficial agent is selected from the group consisting of insulin, growth hormones, buserelin, leuprolide, LHRH, metoclopramide, fentanyl, lidocaine, ketoprofen, sufentanil, terbutaline, droperidol, heparin, interferon, scopolamine, testosterone, gonadorelin, ciclopirox olamine, buspirone, calcitonin, cromolyn sodium, and midazolam.