Method for transdermal iontophoretic delivery of chelated agents
Embodiments provide devices, systems and methods for the transdermal delivery of chelated compounds. One embodiment provides a method for the iontophoretic transdermal delivery of a chelated iron complex for the treatment of anemia. A first patch comprising an active electrode and a chelated iron complex is applied to the skin; a second patch containing an electrode is also applied. An electrical current is then delivered to the skin from the active electrode. The chelated complex is transported across the skin via electromotive force from the current, with the iron being substantially chromogenically unreactive with the skin during transport so that there is little or no tattooing of the skin due to the formation of insoluble oxidative products. The complex is then dissociated by phagocytosis or related process to release the iron where it may be bound by transferrin or ferritin and carried to other sites for storage or metabolic use.
1. A method for the iontophoretic transdermal delivery of a chelated iron complex, the method comprising:
applying a patch to the skin of a subject, the patch comprising an electrode and iron comprising a chelated iron complex comprising ferric pyrophosphate;
delivering an electrical current to the skin using the electrode;
thus transporting the chelated iron complex across the skin, wherein the iron is sufficiently electrostatically bound by the chelating agent so that the iron is not available to form insoluble salts within the skin during transport, thereby reducing chromogenic reactions with the skin relative to the transport of non-chelated iron; and
dissociating the chelated iron complex in tissue to release the iron.
2. A method for treating iron deficiency in a patient, the method comprising:
applying a patch to the skin of the patient, the patch comprising an electrode and iron comprising a chelated iron complex comprising ferric pyrophosphate;
delivering an electrical current to the skin using the electrode;
thus transporting a therapeutically effective amount of the chelated iron complex across the skin, wherein the complex is transported across the skin without precipitation of iron in the skin, thereby reducing chromogenic reactions with the skin relative to the transport of non-chelated iron; and
dissociating the complex in tissue to release the iron, thus treating said iron deficiency.
3. The method of claim 2 , wherein the complex is transported without an increase in the electrical impedance in the skin from precipitation of iron in the skin.
4. The method of claim 2 , wherein the complex is transported without a temperature increase in the skin from ohmic heating from precipitation of iron in the skin.
5. A method for treating iron deficiency in a patient, the method comprising:
applying a patch to the skin of the patient, the patch comprising an electrode and iron comprising a chelated iron complex comprising ferric pyrophosphate;
delivering an electrical current to the skin using the electrode;
thus transporting a therapeutically effective amount of the chelated iron complex across the skin, wherein the iron is sufficiently electrostatically bound by the chelating agent so that the iron is not available to form insoluble salts within the skin during transport, thereby reducing chromogenic reactions with the skin relative to the transport of non-chelated iron; and
dissociating the complex in tissue to release the iron, thus treating said iron deficiency.
6. The method of claim 5 , wherein the dissociation of the complex releases iron available for heme synthesis.
7. The method of claim 5 , further comprising: enhancing one of an amount of heme synthesis or blood hemoglobin with the released iron.
8. The method of claim 5 , wherein up to about 10 mg of elemental iron is transported across the skin.
9. The method of claim 5 , wherein up to about 20 mg of elemental iron is transported across the skin.
10. The method of claim 5 , wherein up to about 30 mg of elemental iron is transported across the skin.
11. The method of claim 5 , further comprising: titrating the transport of the chelated iron complex in response to a biomarker of iron status.
12. The method of claim 11 , wherein the biomarker of iron status is a serum concentration of iron, ferritin or a transferrin iron saturation.
13. The method of claim 11 , wherein the transport rate or total amount of chelated iron complex transported is titrated.
14. A method for the iontophoretic transdermal delivery of a chelated iron complex, the method comprising:
applying a patch to the skin of a subject, the patch comprising an electrode and iron comprising a chelated iron complex comprising ferric pyrophosphate;
delivering an electrical current to the skin using the electrode; and
thus transporting the chelated iron complex across the skin, wherein the complex is transported across the skin without precipitation of iron in the skin, thereby reducing chromogenic reactions with the skin relative to the transport of non-chelated iron.
15. The method of claim 14 , wherein the complex is transported without producing injury or irritation to the skin.
16. The method of claim 15 , wherein the injury or irritation is erythema.
17. The method of claim 14 , wherein the complex is transported without producing a cosmetic change to the skin.
18. The method of claim 17 , wherein the cosmetic change is a tattoo.
19. The method of claim 14 , wherein the iron complex is dissociated by phagocytosis.
20. The method of claim 14 , wherein the iron is delivered to a sub-dermal tissue layer.
21. The method of claim 14 , wherein the patch comprises a therapeutically effective amount of iron for the treatment of iron deficiency.
22. The method of claim 14 , wherein the complex is transported without precipitation of iron in the skin.
23. The method of claim 14 , wherein the complex is transported without an increase in the electrical impedance in the skin from precipitation of iron in the skin.
24. The method of claim 14 , wherein the complex is transported without a temperature increase in the skin from ohmic heating resulting from precipitation of iron in the skin.
25. The method of claim 14 , wherein up to about 10 mg of elemental iron is transported across the skin.
26. The method of claim 14 , wherein up to about 20 mg of elemental iron is transported across the skin.
27. The method of claim 14 , wherein up to about 30 mg of elemental iron is transported across the skin.
28. The method of claim 14 , wherein the current comprises an alternating current.
29. The method of claim 14 , wherein the current has a waveform having a square wave, sine wave, saw tooth or trapezoidal shape.
30. The method of claim 14 , wherein the current comprises an alternating current component and a direct current component.
31. The method of claim 30 , wherein the alternating current component is configured to break down capacitive charge build up in the skin.
32. The method of claim 30 , wherein the alternating current component is configured to oscillate the chelated iron complex during transport through the skin.
33. The method of claim 14 , wherein the current is modulated.
34. The method of claim 33 , wherein the current is modulated in frequency.
35. The method of claim 33 , wherein the current is modulated by a controller.
36. The method of claim 33 , wherein the current is modulated to minimize pain perception.
37. The method of claim 33 , wherein the current is modulated to minimize thermal injury to the skin.
38. The method of claim 33 , wherein the current is modulated to reduce discoloration of the skin.
39. The method of claim 33 , wherein the current is modulated to enhance transport of the chelated iron complex across the skin.
40. The method of claim 33 , wherein the current is modulated to titrate the transport of the chelated iron complex across the skin.
41. The method of claim 14 , wherein the complex releases iron available for heme synthesis.