EP0600914A1 - Procede et appareil de traitement de tissus - Google Patents
Procede et appareil de traitement de tissusInfo
- Publication number
- EP0600914A1 EP0600914A1 EP92915713A EP92915713A EP0600914A1 EP 0600914 A1 EP0600914 A1 EP 0600914A1 EP 92915713 A EP92915713 A EP 92915713A EP 92915713 A EP92915713 A EP 92915713A EP 0600914 A1 EP0600914 A1 EP 0600914A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- electrode device
- tissue
- electrode
- treated
- area
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 238000000034 method Methods 0.000 title claims abstract description 44
- 239000003814 drug Substances 0.000 claims abstract description 52
- 229940079593 drug Drugs 0.000 claims abstract description 51
- 230000005684 electric field Effects 0.000 claims abstract description 22
- 230000000699 topical effect Effects 0.000 claims abstract description 15
- 230000003779 hair growth Effects 0.000 claims description 13
- 239000000976 ink Substances 0.000 claims description 6
- 230000000638 stimulation Effects 0.000 claims description 4
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- 210000003491 skin Anatomy 0.000 description 38
- 210000001519 tissue Anatomy 0.000 description 25
- ZFMITUMMTDLWHR-UHFFFAOYSA-N Minoxidil Chemical compound NC1=[N+]([O-])C(N)=CC(N2CCCCC2)=N1 ZFMITUMMTDLWHR-UHFFFAOYSA-N 0.000 description 12
- 229940107889 rogaine Drugs 0.000 description 11
- 210000004761 scalp Anatomy 0.000 description 11
- 238000012377 drug delivery Methods 0.000 description 8
- 108090000623 proteins and genes Proteins 0.000 description 5
- 210000003128 head Anatomy 0.000 description 4
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- 108020004707 nucleic acids Proteins 0.000 description 3
- 102000039446 nucleic acids Human genes 0.000 description 3
- 150000007523 nucleic acids Chemical class 0.000 description 3
- 102000004169 proteins and genes Human genes 0.000 description 3
- 230000037317 transdermal delivery Effects 0.000 description 3
- 201000004384 Alopecia Diseases 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 201000004681 Psoriasis Diseases 0.000 description 2
- 230000002745 absorbent Effects 0.000 description 2
- 239000002250 absorbent Substances 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- SHGAZHPCJJPHSC-YCNIQYBTSA-N all-trans-retinoic acid Chemical compound OC(=O)\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C SHGAZHPCJJPHSC-YCNIQYBTSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 230000007812 deficiency Effects 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 210000001652 frontal lobe Anatomy 0.000 description 2
- 230000001939 inductive effect Effects 0.000 description 2
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 210000005036 nerve Anatomy 0.000 description 2
- 239000012811 non-conductive material Substances 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 108090000765 processed proteins & peptides Proteins 0.000 description 2
- 150000003431 steroids Chemical class 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229960001727 tretinoin Drugs 0.000 description 2
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 1
- 101710169336 5'-deoxyadenosine deaminase Proteins 0.000 description 1
- 208000002874 Acne Vulgaris Diseases 0.000 description 1
- 102000055025 Adenosine deaminases Human genes 0.000 description 1
- 208000035285 Allergic Seasonal Rhinitis Diseases 0.000 description 1
- 108020005544 Antisense RNA Proteins 0.000 description 1
- 208000004434 Calcinosis Diseases 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 201000003883 Cystic fibrosis Diseases 0.000 description 1
- 102000001690 Factor VIII Human genes 0.000 description 1
- 108010054218 Factor VIII Proteins 0.000 description 1
- GHASVSINZRGABV-UHFFFAOYSA-N Fluorouracil Chemical compound FC1=CNC(=O)NC1=O GHASVSINZRGABV-UHFFFAOYSA-N 0.000 description 1
- 208000008454 Hyperhidrosis Diseases 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- 102000004877 Insulin Human genes 0.000 description 1
- 108090001061 Insulin Proteins 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 206010030113 Oedema Diseases 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 208000000453 Skin Neoplasms Diseases 0.000 description 1
- 206010000496 acne Diseases 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- -1 all Chemical compound 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 206010068168 androgenetic alopecia Diseases 0.000 description 1
- 238000010171 animal model Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000017531 blood circulation Effects 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000003184 complementary RNA Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000003246 corticosteroid Substances 0.000 description 1
- 238000012217 deletion Methods 0.000 description 1
- 230000037430 deletion Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 239000007772 electrode material Substances 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229960000301 factor viii Drugs 0.000 description 1
- 229960002949 fluorouracil Drugs 0.000 description 1
- 210000000245 forearm Anatomy 0.000 description 1
- 238000001415 gene therapy Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 208000024963 hair loss Diseases 0.000 description 1
- 230000003676 hair loss Effects 0.000 description 1
- 230000037315 hyperhidrosis Effects 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 229940125396 insulin Drugs 0.000 description 1
- 239000002648 laminated material Substances 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 238000002690 local anesthesia Methods 0.000 description 1
- 239000003589 local anesthetic agent Substances 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002483 medication Methods 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 238000001465 metallisation Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 229960003632 minoxidil Drugs 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 210000000214 mouth Anatomy 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 230000007383 nerve stimulation Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 230000036407 pain Effects 0.000 description 1
- 229940124641 pain reliever Drugs 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229930002330 retinoic acid Natural products 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 231100000075 skin burn Toxicity 0.000 description 1
- 201000000849 skin cancer Diseases 0.000 description 1
- 210000004927 skin cell Anatomy 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 210000002435 tendon Anatomy 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 230000000451 tissue damage Effects 0.000 description 1
- 231100000827 tissue damage Toxicity 0.000 description 1
- 229940100613 topical solution Drugs 0.000 description 1
- 238000001890 transfection Methods 0.000 description 1
- 238000013519 translation Methods 0.000 description 1
- 229940124549 vasodilator Drugs 0.000 description 1
- 239000003071 vasodilator agent Substances 0.000 description 1
- 210000001835 viscera Anatomy 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N1/00—Electrotherapy; Circuits therefor
- A61N1/02—Details
- A61N1/04—Electrodes
- A61N1/0404—Electrodes for external use
- A61N1/0408—Use-related aspects
- A61N1/0428—Specially adapted for iontophoresis, e.g. AC, DC or including drug reservoirs
- A61N1/0432—Anode and cathode
- A61N1/044—Shape of the electrode
Definitions
- This invention relates to a novel method and apparatus for treating tissue, including the application of an electric field to tissue surfaces as well as the delivery of topical drugs to an area of tissue to be treated using such electric field. More specifically, the invention relates to methods of delivering topical drugs, including proteins and nucleic acids, to skin by electrically stimulating the skin. Further, the invention relates to the transdermal delivery of electrical stimulation across the skin boundary to treat the underlying tissue. Such treatment can include the delivery of a drug or other compound to such tissue.
- Iontophoresis is a well known .technique for delivering drugs through the skin which involves applying an electric potential gradient at the skin surface to enhance the permeability of the skin to the drug molecules.
- Research has been conducted on iontophoretic transdermal delivery of peptide and protein drugs (Chien, Yie W., et al., (1989) J. of Pharm. Sci. 78. 376-383); nonpeptide drugs (Sanderson, et al., (1989) J. of Pharm. Sci. 78. 361-364); and polypeptide drugs (Srinivasan, V., et al., (1989) J. of Pharm. Sci. 78. 370-375).
- Iontophoresis has proven effective for transdermal delivery of local anesthesia, metallic and nonmetallic ions, vasodilators, dermatological medications, and steroids (Behl, et al. (1989) J. of Pharm. Sci. 78. 355- 360).
- One of the earliest uses of iontophoresis involved introducing a sweat-inducing drug through the skin to diagnose cystic fibrosis (Chien, Yie W., et al. (1989) J. of Pharm. Sci. 78. 353-354).
- Other biomedical applications of iontophoresis include treatment for hyperhidrosis, edema formation, calcium deposits, and hay fever (Behl, et al., (1989) J. of Pharm. Sci. 78, 355-360).
- An iontophoretic drug delivery system generally includes a power source, control circuitry, and two electrode pads.
- One of the electrode pads contains a solution of an ionic drug and the other electrode pad contains an electrolyte.
- the electrode pads are placed on the skin, and an electric current is supplied to the pads to induce an electric field at the skin surface.
- the power supply is connected to the electrode pads so that the charge of the pole connected to the drug-containing electrode is the same as the charge of the ionic drug.
- the application of an electric potential at the drug-containing electrode will drive the drug ions through the skin and into the body (Sanderson, John E. et al. (1987) J. of Pharm. Sci. 76. 215-218; Phipps, J. B., et al. (1989) J. of Pharm. Sci. 78. 365-369).
- One such iontophoretic drug delivery system marketed by Iomed, Inc. under the trademark TransQl, includes a dispersive electrode and a drug delivery electrode.
- the drug delivery electrode is mounted to a plastic holding tray which includes an absorbent pad for receiving the drug. Once the pad is fully hydrated with the drug, the drug delivery electrode and absorbent pad are separated from the holding tray and placed on the skin at the treatment site.
- the dispersive electrode is placed on the skin spaced from the drug delivery electrode, and leads are attached to the pair of electrodes to generate an electric potential gradient at the treatment site.
- This drug delivery system is primarily used to deliver a water soluble medication, such as a local anesthetic and/or corticosteroid, through a patient's skin. A disadvantage of this system is the excessive length of time required for treatment.
- Rogaine (Minoxidil, 2% topical solution) is a topically applied drug, marketed by the Upjohn Company, which has proven effective in treating male pattern baldness involving the top, or vertex, of the head. Although Rogaine has successfully stimulated hair growth on the top of the head, no clinically significant effect has been seen in patients with predominantly frontal hair loss.
- a preferred method of delivering topical drugs to the skin which is intended to accomphsh at least some of the foregoing objects includes the step of applying the drug to be delivered to one of an area of skin to be treated and an electrode device.
- the drug is applied to the electrode device.
- the electrode device which is formed to generate a multiplicity of simultaneous and directionally distinct electrical fields, is then placed in contact with the area of skin to be treated. Finally, voltage is delivered to the electrode device to generate simultaneous and directionally distinct electric fields at the skin surface.
- Such methods and apparatus may be readily applied to similar treatment of other tissue surfaces. Further, such methods and apparatus may be readily adapted to apply unique electric fields to the surface of tissue and to tissue underlying such tissue surfaces to enhance circulation or the delivery of drugs to such tissue.
- FIGURE 1 is a top plan view of an electrode device for use with the subject method of delivering topical drugs to the skin;
- FIGURE 2 is an enlarged top view of a section of the electrode device of Figure 1; and FIGURES 3a-c are photographs of enhanced hair growth using the methods and apparatus of the invention.
- FIGURE 1 Before describing the subject methods of applying novel electric fields and the delivery of drugs to a tissue surface or underlying tissue, it may be helpful to describe the electrode device for use with the subject method. Referring to the drawings, wherein like numerals indicate like parts, and initially to FIGURE 1, there will be seen an electrode device
- substantially planar support member 12 composed of a substantially non-conductive material.
- This device in general is made of a flexible planar support member to accommodate the contours of the tissue surface to be treated.
- Suitable non-conductive materials for forming support member 12 include mica, polyester, and polystyrene.
- Support member 12 has a main portion 14, preferably circular in shape, and a tab portion 16 extending from the perimeter of main portion 14. Tab portion 16 facilitates connection of lead lines to electrode device 10.
- a first electrode pattern 18a and a second electrode pattern 18b are disposed on main portion 14 of electrode device 10.
- First electrode pattern 18a and second electrode pattern 18b each include a set of substantially parallel electrodes 20a and 20b, respectively, which extend across main portion 14 in an alternating arrangement. Electrodes 20a and 20b are uniformly spaced across main portion 14 to ensure an even distribution of current density beneath electrode device 10, thereby reducing the likelihood of skin burns.
- a pair of electrode leads 22a and 22b extend along opposite sides of tab portion 16 and halfway around the perimeter of main portion 14. Electrodes 20a are electrically coupled together by electrode lead 22a, and electrodes 20b are electrically interconnected by electrode lead 22b. Each set of electrodes 20a and 20b are electrically connected to one another so that a voltage applied to the corresponding electrode leads 22a and 22b is uniformly distributed across each of the electrodes.
- first and second electrode patterns 18a and 18b respectively, generates multiple directionally distinct electrical fields when opposite charges are applied to electrode leads 22a and 22b.
- the arrows represent electric field lines generated by connecting lead lines of opposite polarity to electrode leads 22a and 22b.
- support member 12 may be fabricated in different shapes according to the area of tissue to be treated and according to the specific medical application.
- Electrode patterns may be formed by screen printing a conductive ink on support member 12.
- a technique for printing a conductive ink on a flexible substrate is disclosed by M. Martel in "The Basics of Area Source IR", SITE Magazine, pgs. 60-64.
- Suitable conductive inks for forming the electrode patterns of the subject invention include E-1400 ink marketed by Ercon Incorporated and Electrodag
- the electrode patterns may be formed by selectively depositing a metallic material, such as aluminum, on main portion 14.
- the electrode patterns may be formed by using a masking technique to deposit copper vapor or other metallic vapor such as aluminum, gold, platinum, and nickel, on main portion 14.
- E SHEET The methods used to produce such vapor deposited electrode devices and selectively etched electrode devices are well known. Metal deposition may be carried out according to the methods disclosed by P. Gise and R. Blanchard in "Modern Semiconductor Fabrication
- the electrode material preferably ranges in thickness from approximately .001 inches to 1 inch.
- Each electrode has a width of approximately lO ⁇ m to 2mm, preferably between 0.1mm and 1mm.
- the spacing between the electrodes ranges from approximately lO ⁇ m to 2mm, preferably 0.1mm to 1mm.
- first and second electrode leads 22a and 22b may be applied across first and second electrode leads 22a and 22b to generate an appropriate voltage gradient or sufficient electrical current.
- 10 to 100 volts DC are applied across electrode leads 22a and 22b; however, the applied voltage may range from approximately 1 to 500 volts DC. It is preferable to deliver a pulsed voltage, as opposed to a continuous voltage, to electrode device 10 to prevent the build-up of charge on the skin.
- Tissue includes but is not
- SUBSTITUTE SHEET limited to skin, tendons, muscles, nerves, internal organs and tissues of the oral cavity.
- the drug is applied to a localized area of skin to ensure even distribution of the drug across the skin surface. If the drug is applied directly to electrode device 10, the drug should be spread evenly across the surface of device 10 on which electrode patterns 18a and 18b are disposed, or the conductive surface of device 10. Once the drug has been applied, the conductive surface of device 10 is placed in contact with the area of skin to be treated. A voltage is then applied across electrode leads 22a and 22b to generate simultaneous and directionally distinct electric fields between electrodes 20a and 20b. The electric fields electrically stimulate the area of skin being treated.
- the subject method of the invention may be used in combination with the topical hair growth drug Rogaine, commercially marketed by The Upjohn Company.
- Rogaine has only been successful in promoting hair growth on the vertex of the head.
- Rogaine has been shown to stimulate hair growth on the front of the scalp.
- a user applies a full dose of Rogaine, specifically lmL, to the front of the scalp per the directions found in the literature accompanying a Rogaine prescription. After the full dose has been applied to the user's scalp with the supplied rub-
- the user places the conductive surface of electrode device 10 in contact with the area of the scalp to be treated.
- the user then turns on the power supply to electrode device 10 which is preferably set to deliver approximately fifty to one hundred 100 volt DC pulses of 1 ampere of current over a period of 15 to 30 seconds, each pulse lasting approximately 1 to 10 msec.
- the user may move electrode device 10 over the area of skin being treated.
- the user may selectively apply pressure to electrode device 10 to adjust the contact of electrode device 10 with the skin.
- the user may feel a sensation of mild tingling. After approximately four months of treatment, hair growth becomes apparent. This was repeated twice daily over 60 days.
- FIGURES 3a-c The results of applying Rogaine to the frontal lobe of the scalp and treating the scalp with the electrode device as described above over a 60 day period are shown in FIGURES 3a-c.
- FIGURE 3a shows the condition of the scalp on day 0 prior to the start of the experiment.
- FIGURES 3b and 3c show the same scalp after 20 and 60 days, respectively.
- the right side of the scalp (left side in the figures) is the area treated with Rogaine and the electrode device 10.
- the left side of the scalp (right side in the figures) is the control area, i.e., treated only with Rogaine.
- FIGURE 3b new hair growth is seen at 20 days.
- FIGURE 3c hair growth after just 60 days was substantial.
- the subject electrode device 10 may also be used in combination with other topical drugs to treat a variety of skin maladies including: (i) Retin A (Tretinoin, all, trans Retinoic Acid), commercially marketed by Ortho
- compositions for treatment of brown spots, acne, and wrinkles, (ii) steroids to treat inflammation and psoriasis, (iii) topical pain relievers for treatment of aberrations of the skin and underlying tissue, and (iv) 5-fluorouracil to treat skin cancer and psoriasis.
- electrode device 10 may also be used without an accompanying topical drug. Electrical stimulation alone has therapeutic and diagnostic value. Electrode device 10 may be used to electrically stimulate the skin of a user to, for example, increase blood flow, induce secretions, and stimulate nerves.
- tests were performed where the electrode device 10 was applied to the inner forearm area of a human.
- the same protocol as previously described was used except no topical drug was applied to the skin or electrode device 10.
- the test produced a region of redness indicating increased circulation to the area.
- the increased circulation is useful for enhancing the delivery of drugs to the localized skin area which are administered IV or orally.
- An advantage of using the apparatus and method of the invention lies in the fact that treatment can be effected without significant discomfort of tissue damage (even after twice daily treatment for almost six months).
- the only feeling sensed by the user is a mere tingling of the scalp which is believed to be evidence of subcutaneous nerve stimulation.
- Electrode device 10 may also provide gene therapy to skin or other tissue by transfecting nucleic acid into the cells of the skin or tissue or cells underlying such surfaces for treating gene deficiencies or inducing such deficiencies in laboratory animals.
- Nucleic acids which may be used for transfection include DNA capable of expressing an antisense RNA transcript which is capable of down modulating translation of endogenous RNA transcripts.
- Proteinaceous gene products may also be delivered to the skin cells by the subject method. Such proteins include Factor VIII, insulin, and adenosine deaminase.
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biomedical Technology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Radiology & Medical Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Electrotherapy Devices (AREA)
- General Preparation And Processing Of Foods (AREA)
Abstract
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US72527991A | 1991-07-03 | 1991-07-03 | |
| US725279 | 1991-07-03 | ||
| PCT/US1992/005587 WO1993000959A1 (fr) | 1991-07-03 | 1992-07-02 | Procede et appareil de traitement de tissus |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0600914A1 true EP0600914A1 (fr) | 1994-06-15 |
| EP0600914A4 EP0600914A4 (fr) | 1994-11-02 |
Family
ID=24913891
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP9292915713A Withdrawn EP0600914A4 (fr) | 1991-07-03 | 1992-07-02 | Procede et appareil de traitement de tissus. |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP0600914A4 (fr) |
| JP (1) | JPH06508783A (fr) |
| AU (1) | AU2336992A (fr) |
| CA (1) | CA2112366A1 (fr) |
| IL (1) | IL102406A0 (fr) |
| WO (1) | WO1993000959A1 (fr) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7643874B2 (en) | 2001-10-24 | 2010-01-05 | Power Paper Ltd. | Dermal patch |
| JP2003210591A (ja) * | 2002-01-24 | 2003-07-29 | Hisamitsu Pharmaceut Co Inc | エレクトロポレーション用経皮経粘膜適用製剤 |
| US7479133B2 (en) | 2003-06-30 | 2009-01-20 | Johnson & Johnson Consumer Companies, Inc. | Methods of treating acne and rosacea with galvanic generated electricity |
| US7477938B2 (en) | 2003-06-30 | 2009-01-13 | Johnson & Johnson Cosumer Companies, Inc. | Device for delivery of active agents to barrier membranes |
| US7477940B2 (en) | 2003-06-30 | 2009-01-13 | J&J Consumer Companies, Inc. | Methods of administering an active agent to a human barrier membrane with galvanic generated electricity |
| US7486989B2 (en) | 2003-06-30 | 2009-02-03 | Johnson & Johnson Consumer Companies, Inc. | Device for delivery of oxidizing agents to barrier membranes |
| US7477941B2 (en) | 2003-06-30 | 2009-01-13 | Johnson & Johnson Consumer Companies, Inc. | Methods of exfoliating the skin with electricity |
| US8734421B2 (en) | 2003-06-30 | 2014-05-27 | Johnson & Johnson Consumer Companies, Inc. | Methods of treating pores on the skin with electricity |
| US7507228B2 (en) | 2003-06-30 | 2009-03-24 | Johnson & Johnson Consumer Companies, Inc. | Device containing a light emitting diode for treatment of barrier membranes |
| US7480530B2 (en) | 2003-06-30 | 2009-01-20 | Johnson & Johnson Consumer Companies, Inc. | Device for treatment of barrier membranes |
| US7476222B2 (en) | 2003-06-30 | 2009-01-13 | Johnson & Johnson Consumer Companies, Inc. | Methods of reducing the appearance of pigmentation with galvanic generated electricity |
| WO2010088914A1 (fr) * | 2009-02-05 | 2010-08-12 | Aalborg Universitet | Dispositif de régulation du débit sanguin sous-cutané |
| US20120089232A1 (en) | 2009-03-27 | 2012-04-12 | Jennifer Hagyoung Kang Choi | Medical devices with galvanic particulates |
| US11110272B2 (en) | 2011-12-08 | 2021-09-07 | Pilogics L.P. | Apparatus for stimulating hair growth and/or preventing hair loss |
| US9566431B2 (en) | 2014-04-07 | 2017-02-14 | Pilogics L.P. | Method of forming a large number of metal-ion-deposition islands on the scalp by a rapid series of brief electrode-contact events |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2322615A1 (fr) * | 1975-09-02 | 1977-04-01 | Le Goaster Jacqueline | Procede d'application cutanee en vue d'une penetration sous-cutanee de divers produits et produit pour sa mise en oeuvre |
| US4164226A (en) * | 1976-08-25 | 1979-08-14 | Robert Tapper | Iontophoretic burn-protection electrode structure |
| GB2132892B (en) * | 1983-01-10 | 1986-10-08 | Hayashibara Ken | Device for stimulating growth and regeneration of hair |
| US4736752A (en) * | 1986-11-28 | 1988-04-12 | Axelgaard Manufacturing Co., Ltd. | Transcutaneous medical electrode |
| DE3736072A1 (de) * | 1987-09-24 | 1989-04-13 | Soft Electrics & Cosmetics Ver | Verfahren und geraet zur foerderung des wohlbefindens des menschen und zur kosmetischen behandlung der haut |
| IL86076A (en) * | 1988-04-14 | 1992-12-01 | Inventor S Funding Corp Ltd | Transdermal drug delivery device |
| EP0419473A1 (fr) * | 1988-11-28 | 1991-04-03 | Innofinance Altalanos Innovacios Penzintetet | Appareil d'iontophorese |
-
1992
- 1992-07-02 CA CA002112366A patent/CA2112366A1/fr not_active Abandoned
- 1992-07-02 AU AU23369/92A patent/AU2336992A/en not_active Abandoned
- 1992-07-02 EP EP9292915713A patent/EP0600914A4/fr not_active Withdrawn
- 1992-07-02 JP JP5502332A patent/JPH06508783A/ja active Pending
- 1992-07-02 WO PCT/US1992/005587 patent/WO1993000959A1/fr not_active Ceased
- 1992-07-03 IL IL102406A patent/IL102406A0/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2112366A1 (fr) | 1993-01-21 |
| WO1993000959A1 (fr) | 1993-01-21 |
| EP0600914A4 (fr) | 1994-11-02 |
| IL102406A0 (en) | 1993-01-14 |
| JPH06508783A (ja) | 1994-10-06 |
| AU2336992A (en) | 1993-02-11 |
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