Electrolytic transdermal delivery of polypeptides

• US 4,878,892 A
• Filed: 02/10/1987
• Issued: 11/07/1989
• Est. Priority Date: 02/10/1987
• Status: Expired due to Term

• Current Assignee: Drug Delivery Systems Incorporated
• Original Assignee: Drug Delivery Systems Incorporated
• Inventors: Sibalis, Dan, Rosen, Sanford
• Primary Examiner(s): NOT, DEFINED
• Assistant Examiner(s): Polutta, Mark O.
• Application Number:
  US07/012,889
• Time in Patent Office: 1,001 Days
• Field of Search: 604/20
• 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

The invention comprises in combination:

(a) a polypeptide having from about three to about 20 peptide units in aqueous solution or suspension, and

(b) an electrolytic device for transdermal transport of the polypeptide to the bloodstrem of the patient.

It may be useful to enhance the transdermal delivery of the polypeptide by adding an aqueous cosolute/cosolvent with negative Setschenow constants.

The electrolytic device preferably comprises a hydrophilic reservoir containing a supply of the aqueous polypeptide solution or suspension, an electric battery, two extended contacts, and optionally a semipermeable membrane between the reservoir and the patient'"'"'s skin.

Representative polypeptides include oxytocin, angiotensin I, II, and III, substance P, vasopressin, lypressin, desmopressin, leuprolide acetate, antripeptin, and the like.

Claims

1. A transdermal patch for delivering at least one drug directly to the bloodstream of the patient comprising in combination:

(a) an active ingredient comprising at least one polypeptide having from three to 20 peptide units selected from the group consisting of vasopressin, lypressin, atriopeptin, oxytocin, desmopressin, a dynorphin, leuprolide, an angiotensin, and mixtures thereof contained in a drug reservoir, and

(b) electrolytic means for transdermal transport of the polypeptide characterized by a current density from about 0.5 microampere/cm² to about 1 milliampere/cm²,

whereby the skin of the patient is neither irritated nor erythematized.

2. A transdermal patch as in claim 1, wherein the polypeptide comprises vasopressin.

3. A transdermal patch as in claim 1, wherein the polypeptide comprises lypressin.

4. A transdermal patch as in claim 1, wherein the polypeptide comprises atriopeptin.

5. A transdermal patch as in claim 1, wherein the electrolytic means comprises a battery, an anode, a cathode, said drug reservoir, and barrier means between the electrodes.

6. A transdermal patch as in claim 1, further comprising an aqueous solvent for the polypeptide.

7. A transdermal patch as in claim 6, further comprising a dissociating cosolvent.

8. A transdermal patch as in claim 7, wherein the dissociating cosolvent is selected from the group consisting of urea, alkylderivatives of urea, guanidine salt, butanol, 2-butanol, water-soluble amides with more than three carbon atoms, sodium and potassium iodide, sodium perchlorate, sodium butyrate, and any other salt with negative Setschenow constants.

9. A transdermal patch as in claim 1, further comprising at least one compound selected from the group consisting of buffering agents, chelating agents, antioxidants, preservatives, and biocides.

10. A transdermal patch as in claim 6, further comprising a semipermeable membrane on the skin side of the drug reservoir.

11. A transdermal patch as in claim 1, wherein at least one polypeptide is LH-RH analog further comprising testosterone.

12. A transdermal patch as in claim 1, wherein at least one polypeptide is LH-RH analog further comprising Flutamide.

13. A transdermal patch as in claim 5, further comprising current controlling means whereby the current density of the patch is from 0.5 microamperes/cm² to about 10 microamperes/cm².

14. A transdermal patch for delivering at least one drug directly to the bloodstream of the patient comprising in combination:

(a) an active ingredient comprising at least one nonionic polypeptide having from three to 20 peptide units contained in a drug reservoir, and

(b) electrolytic means for transdermal transport of the nonionic polypeptide characterized by a current density from about 0.5 microampere/cm² to about 1 milliampere/cm², whereby the skin of the patient is neither irritated nor erythematized.

15. A transdermal patch as in claim 14, wherein the nonionic polypeptide is selected from the group consisting of vasopressin, lypressin, atriopeptin, oxytocin, desmopression, leuprolide a dynorphin, an angiotensin, and mixtures thereof.

16. A transdermal patch as in claim 14, wherein the electrolytic means comprises a battery, an anode, a cathode, a drug reservoir, and a barrier means between the electrodes.

17. A transdermal patch as in claim 14, comprising an aqueous solvent for the nonionic polypeptide.

18. A transdermal patch as in claim 14, further comprising at least one compound from the group consisting of buffering agents, chelating agents, antioxidants, preservatives, biocides, and dissociating cosolvents with a negative Setschenow constant.

19. A transdermal patch as in claim 16, further comprising current controlling means whereby the current density of the patch is from about 0.5 microampere/cm² to about 10 microamperes/cm².