CA2485271A1 - Electrical stimulation unit and waterbath system - Google Patents

Abstract

A method of treating onychomycosis in humans by exposing the area of a patie nt that is infected with a mycotic infection with an aqueous solution and providing a low voltage direct current across the infected area for a period of at least five minutes.

Description

ELECTRICAL STIMULATION UNIT AND WATERBATH SYSTEM
Field of the Invention For use as a fungicidal/fungistatic treatment system for toenail fungus, dermatological fungi, and fungal infections.
Background Toenail fungus alone affects 2-13% of the general population of the United States; over 30% of the population over 60 years of age are affected. Current systemic treatment consists of the use of an expensive drugs or pharmaceutical agents many of which have complications and associated interactions. These pharmaceutical treatments are less than ideal for many patients because of the cost and danger associated With it.
Various approaches to treating this disease have been attempted and employed, and most involve pharmaceutical agents applied topically or systematically. For instance, U.S. Pat. No. 6,319,957 describes the use of compositions based on glyco-alcohol, hydro-alcohol or glyco-hydro-alcohol solutions of a glycol or glyceric ester of retinoic acid, preferably in association with the ethyl ester of retinoic acid and with hydroquinone, treat unsightly skin disorders such as acne, wrinkles, scars, stretch marks, dark spots, etc., and in treating mycotic skin diseases and psoriasis.
U.S. Patent No. 6,303,140 teaches a plaster preparation comprising a synthetic rubber; a reinforcing agent based on silica or random styrene-butadiene, copolymer; a tackifier; salicylic acid or a pharmaceutically acceptable salt or ester thereof to treat mycotic infections.
U.S. Patent No. 6,290,950 describes a new class of Mycosis vaccines comprising homogenised inactivated yeast blastospores and homogenised inactivated def~naatoplzyte micYOCOnidia or antigenic material of said spores, methods for their production and their use for the prophylaxis and/or treatment of mycoses in mammals, preferably humans. The vaccines according to the present invention are especially useful for the prophylaxis and/or treatment of skin mycosis, preferably Dermatomycosis and/ox Candidosis and/or Onychomycosis.
U.S. Patent No. 6,287,276 describes a set depth nail notcher and method for treating nail fungus that is used to cut a notch to a predetermined depth in a nail or a toe of finger infected with fungus arid then apply a topical anti-fungal medication to the toe or finger through the notch.
U.S. Patent No. 6,281,239 teaches a method of treating onychomycosis by administering to an infected area around a nail of a patient a tissue softening composition containing urea and an antifungal composition in one or separate compositions, concurrently or non-concurrently.
Summary of the Invention The present invention relates to a method for treating onychomycosis in humans comprising the steps of exposing an area of a patient that is infected with a mycotic infection with a solution; and providing a low voltage direct current to said infected area. The invention also relates to apparatus for treating onychomycosis that comprises:a reservoir means fox providing an aqueous solution to a patient; a means for securing said reservoir means to an mycotically infected area; and a means for providing a low voltage current to said reservoir mean across said mycotically infected area. 'This method of treatment may also be used to treat other viral skin infection including molluscum contagium;
papilloma virus; warts; epiermodysplasia verruciformis; herpes virus, and the like.
Brief Description of the Figures Figure 1 shows a patient's feet disposed in a state of the art bath with a source of low voltage current available.
Figure 2 show a apparatus or apparel that allows for treatment of mycotic infection with immersion in a bath.
Description Several studies have reported that electrical stimulation augments wound healing, Electrical stimulation has been reported to improve blood flow, decrease edema, and inhibit bacterial growth. Numerous studies have reported that high-voltage monophasic pulsed current (HVPC) augments wound healing.
Additional studies have shown significant increases in transcutaneous partial pressure of oxygen (tCP02) in diabetic individuals following use of electrical stimulation. HVPC has been used to successfully treat diabetic foot ulcers.

Several studies have demonstrated that electrical currents exist in living organisms. Cells follow the path of this current flow, which is referred to as the galvanotaxic effect. It is theorized that electrical stimulation augments the endogenous bioelectric system in the body. The increase in the rate of wound healing with electrical stimulation is also theorized to be a result of attraction of different cell types. Studies have shown that migration of macrophages, fibroblasts, mast cells, neutrophils, and epidermal cells is influenced by electrical stimulation. Electrical stimulation has also been shown to increase the proliferation of fibroblasts and protein synthesis, as well as the growth of neurites. These factors play a significant role in healing. Furthermore, the tensile strength of the collagen has been shown to increase upon application of such electrical fields, thus increasing the strength of the wound scars. For these reasons, the use of electrical stimulation for the treatment of chronic wounds has been used increasingly during the last several years.
Thxough ifZ vitro experiments in our laboratory and clinical experience, we have discovered and shown that both high-voltage monophasic pulsed current (HVPC) and direct current electrical stimulation are fungicidal/fungistatic.
Humans treated with HVPC electrical stimulation in a waterbath displayed markedly diminished fungal infection, and sound normal nail growth. The growth of Trichophyton meiitagrophytes fungi and Trichophyton rubru fungi can be inhibited with low voltage direct current electrical stimulation. We have demonstrated the fungicidal/fungistatic properties of electrical stimulation on toenail fungus, dermatological fungi, and other fungal infections.
Based on these experiments and our discovery of electrical stimulation's fungicidal/fungistaitic properties, it is logical that a therapeutic device could be fashioned consisting of a small electrical stimulation unit and a foot waterbath system. An appliance used to treat toenail fungus will comprise a waterbath designed to allow either one or both feet to fit comfortably and be immersed in solution.
An electrode on either side of the bath will allow a safe current to pass through the solution and over and around the toes and the nails. The current will be supplied by an electrical stimulation unit, which will be a small device easily attachable to, or built into, the bath. The electrical stimulation unit will have leads, which attach to the electrodes. The system used to treat toenail fungus will have leads on either side of the bath, lateral and medial or front and back (see Figure 1 ). The therapeutic device will be adapted to treating other parts of the body which can be easily immersed, for example, hands, The device delivers a pulsed current of 0 to 300 Volts at peak and an exponential waveform at 100-200 Hz, and pulse pairs with intervals of 255 microseconds or greater (Figure 2). This device is connected to the waterbath by way of electrodes, thus allowing electrical current to travel in the solution arid cover the affected area. This unit will be as safe as a transcutaneous electrical nerve stimulator (TENS) unit pxesently used for pain modulation, but will be potentiated to deliver a distinct type of current.
Based on our findings of the fungicidal/fungistatic properties of both pulsed and direct current electrical stimulation, many additional applications are possible. In addition to toe nail fungus, dermatological fungi, fungi in wounds and fungal infections are additional fungi, which could be treated with this system.
Also, veterinary applications are possible for animals and livestock with fungal infections are anticipated.
Examples In order to demonstrate the efficacy of Low Voltage Direct Current (LVDC) or electrostimulation (E-stim) as an antifungal agent for clinical use in the treatment of onychomycosis pure cultures of Trichophyton rubrum attd Tricltophyton metztagrophytes grown on a solid agar medium were subjected to clinically relevant doses of LVDC. To determine antifungal effects due to germicidal and/or fungistatic activity of LVDC E-stim, the diameters of any zones in the agar around the electrodes which lacked fungal growth after E-stun were measured and compared to control cultures.
Zones devoid of fungal growth were observed for both Trichophyton i~ubrutn and Tricltophytott ntetttagt-opltytes at~ourtd both the anode and cathode when clinically relevant doses of LVDC from 500 microamperes to 3 milliamperes were applied. In this dose range, LVDC E-stim acted fungicidally in a dose dependent manner.
The term onychomycosis refers to any fungal infection of one or more elements of the nail system, which consists of the nail matrix, the nail bed and the nail plate. Several studies suggest that onychomycosis affects between 2 % and 18 % (or possibly more) of the world's population. In North America, onychomycosis accounts for approximately 50 % of all nail disease, is an infection several times more common in the toenail than the fingernail, and is most commonly found among older individuals (some studies suggest that nearly 50 % of the population over 70 years of age may be affected). The incidence of onychomycosis in the United States and other countries of the developed world has been increasing in recent years. This is thought to be most likely the result of several contributing factors including: the general aging of the population;
the possible higher incidence of diabetes mellitus; the greater use of immunosuppressive drugs and antibiotics; the increased exposure of the general population to the etiologic fungi; the HIV epidemiC4-5.
Onychomycosis can be caused by three different groups of fungi: the dennatophytes, the yeasts and the nondermatophytic moldSI-7 . The dennatophytes are the most common etiology, accounting for between 85% and 90% of all cases. Just two dennatophyte species, Ti~iclaophyton rubrum (T.
rubf~um) and Trichophyton fnentagf°ophytes (T. nzentagrophyte), are responsible themselves for nearly 80% of all cases of onychomycosis. Several different yeast species can also cause onychomycosis. These species are together responsible for between 5% and 10% all cases. In approximately 70% of these cases, the etiological agent is Candida albicans. Finally, several different species of the nonderniatophyte molds can also cause onychomycosis. As a group, these are responsible for approximately 3 to 5% of all cases.
Although onychomycosis is not a fatal infection, and is usually not a very debilitating condition in most afflicted individuals, it can still have serious emotional and/or physical consequences. The condition can be associated with significant pain and discomfort, and in severe cases, it may sometimes lead to disfigurement and/or to various degrees of functional loss. In addition to physical impairment, the psychological and social consequences of onychomycosis can also be significant. Thus, onychomycosis represents far more than a mere cosmetic problem for many afflicted individuals, and professional treatment from health care providers is very often sought.
The treatment of onychomycosis, however, has proven difficult. The three traditional approaches to treatment are debridement of the nail unit, topical medication and systemic chemotherapy. The most successful of these approaches has been the use of systemic antifungal drugs. Over the last 40 years, oral systemic antifungal agents have been the mainstay of onychomycosis therapy.
However, because of several negative factors that include drug toxicity, possible adverse interactions of antifungal agents with other drugs in the body, and the prolonged course of treatment required with many of these antifungal therapeutic regimes, the search for new, alternative treatments, which are both efficacious and which present minimal side effects, is still an important research goal.
During the past ten years, new treatment protocols which employ electrical stimulation (E-stim) have begun to be used in the treatment of certain types of wounds. The clinical efficacy of such treatment is now well documented. One of the ways in which E-stim probably plays a role in enhancing wound healing is by its antimicrobial effect. Several in vitro studies have conclusively demonstrated that E-stim application is antibacterial to most of the pathogenic bacteria commonly found in wounds. In the course of our own clinical use of low voltage direct current electrostimulation (LVDC E-stirn) in wound treatment during the last 10 years, we coincidently noticed that, in addition to its enhancement of the would healing process, E-stim also seemed to significantly ameliorate many cases of onychomycosis of the toenail (Michael Brogan, personal communication).
Subsequently, we began to regularly employ this modality in the treatment of onychomycosis and have had very good clinical success.
In order to begin determining the factors responsible for the observed efficacy of this modality in the treatment of onychomycosis, we conducted in vitf°o experiments to evaluated the antifungal effects of LVDC E-stim in the control and/or eradication of the two primary etiologies of onychomycosis, T. YubYUrn and T. mentagf~ophytes. In this paper, we describe the methods used and results obtained in this investigation, and we discuss the clinical significance of using LVDC E-stim in the treatment of onychomycosis in conjunction with or alternative to other current therapies.
Materials and Methods Of gafaisms:
The medium employed to culture all fungi was Sabouraud Dextrose Agar (SDA) in 100 ml petri plates obtained from Becton Dickinson Microbiology Systems. (Becton Dickinson Microbiology Systems, PO Box 243, Cockeysville, NM 21030) Pure cultures of the dermatophyte fungi T. z~ubz~um azzd T.
mentagroplzytes were obtained from Presque Isle Culturest. Permanent stock cultures of T z~ubrunz were established by inoculation of the organism onto a solid growth medium consisting of SDA in petri plates, and subsequent incubation of these SDA plates at 25°C for 7 days. After this time period, each SDA
plate was covered by numerous colonies of T rubrunz which had coalesced into a homogeneous, fluffy fimgal "lawn" (or continuous mass of gowth) along the entire surface of the agar. Pen-nanent stock cultures of T znezztagz~oplzytes were established in the manner described above for T rubruzzz. The stock cultures of .
both fungi were maintained at 4°C for the entire time period of these experiments and were weekly monitored for viability.
Expei~iznental Pz°ocedure and Izzstz°umerztatiozz:
All of the LVDC E-stim experiments described in this report were performed in a NUAIRE Class 11, Type AlB3 biological safety cabinet using standard aseptic techniques. All LVDC E-stim was performed using a Rich-Mar VI LIDC Stimulator. Independent current readings were made with a BIB
Precision amp-meter from I Dynascon Corporation.
For each E-stun experiment, a 1.0 cm section of agar containing either T
rubz~azza oz- T znezztagz°ophytes growing on the surface was removed aseptically from the respective SDA stock culture plates using a sterile dissecting needle. The 1.0 CM2 piece of SDA containing either T r~ubrum or T mentagroplaytes was then transferred to 5 ml of sterile 0.9 % saline. The sterile saline tube was mixed by vortexing for 10 sec in order to dislodge the fungal hyphae, conidia and spores from the surface of the agar. Using a sterile micropipeter, 250 ml of the fungal-saline solution were transferred to a new, sterile SDA petri plate. If multiple SDA
plates were to be inoculated in a given experiment, this procedure was performed multiple times from the same fungal-saline solution. The fungal-saline solution was evenly distributed over the entire surface of each of the inoculated SDA
plates) using a sterile glass spreading rod. The SDA plates were then incubated at 25°C for 24 hr. At the end of this period, a barely visible film of fungal growth covered the entire growth medium surface of the SDA plates. Non inoculated control SDA plates were included in each experimental group to insure the sterility of the medium.

After 24 hr of incubation, electrical current was applied to each experimental SDA plate containing either T rubYUna or T nzentagroplaytes by a Rich Mar VI LIDC Stimulator. The electrodes used to accomplish this consisted of 2 pieces of stainless steel (1 mm diameter and 2.5 cm long) which were permanently inserted through the top portion of a sterile petri plate 1.9 cm apart from each other, and which were secured with epoxy cement on the outer surface.
The electrodes were disinfected and stored in 95 % ethanol prior to and between experiments. Just prior to each experiment, the top portion containing the electrodes was removed from the 95 % ethanol storage unit, the ethanol was allowed to evaporate, and the electrodes were inserted into the agar of the bottom portion of a SDA plate containing 24 hr growth of either fungus by closing the top portion over the lower portion of a petri plate. Then, either the electrodes remained in the agar for 30 min at room temperature (22-24°C) without LVDC
application (O amperes), or LVDC was applied using the E-stim apparatus described above. A current of either 500 microamperes, 1 milliamperes, 2 milliamperes or 3 milliarnperes LVDC was applied for 30 minutes at room temperature (22-24°C). All amperages were confirmed by the use of an independent amp-meter connected in series. In each experiment, in order to confirm fungal viability and media soundness, a control SDA plate containing the particular fungus used in the experiment, but which was not subjected to either E-stim or electrode intrusion, was also included. This plate was inoculated at the same time, in the same manner and from the same saline tube as the experimental plates.
After LVDC E-stim, each SDA petri plate was incubated at 25°C for 24 hr to allow for additional fungal growth which could then be easily visualized.
Following this 24 hr incubation, the diameter of any zones lacking fungal growth (where no additional fungal growth occurred after application of E-stim) at the location of both the positive and negative electrodes was measured to the nearest 0. 1 mm using a millimeter ruler and a dissecting microscope. The SDA plates were then incubated for an additional 3 to 5 days, with additional observations and measurements made daily.
To determine if the electrode material itself was toxic to either of the two fungi, or if any ethanol (used in disinfection) remained on the electrodes during the E-stim application (which might kill the fungus or inhibit its growth), SDA

plates were inoculated with either T rubuf°rn or T mentagYOplZytes and incubated for 24 hr as described above. Following this, the electrodes were inserted into the SDA plate containing either of the fungi and allowed to remain for 30 minutes (as previously described), but no electric current was applied (O amperes). The SDA
plates were then incubated for 7 days as described previously, and then checked for the presence of any zones lacking fungal growth during each of these seven days.
To determine if any toxic or inhibitory antifungal metabolites were generated in the SDA growth medium as a result of the application of electric current, LVDC of either 3 or S milliamperes was applied to a SDA plates (as described) for 30 min prior to inoculation of either T. rubYUn2 0~ T.
naentagf~ophytes. Immediately following this, 250 microlitre of fungal-saline solution of either T. rubf~una of~ T. rnentagroplaytes was evenly distributed over the surface as described previously. The SDA plates were then incubated at 25°C for 7 days, and the presence of any zones lacking fungal growth near the site of the electrode contacts (or elsewhere) was observed and/or measured each day.
To determine if LVDC E-stim is acting primarily in a fungistatic manner (inhibited fungal growth but did not kill fungal cells) or a fungicidal manner (killed fungal cells), the following was done during each experiment with either T.
rubf~urn or T. me~ctagf°opl~ytes. LVDC E-stim was applied as described above, and after 24 hr incubation at 25°C, samplings were carefully taken in the areas lacking fungal growth around each electrode with a sterile swab in order to determine if viable fungal cells were present in these zones. This swab was then used to inoculate fresh, sterile SDA plates. These plates were incubated for 7 days at 25°C and daily observed for the presence of any fungal growth that would result from the transfer of any viable fungal hyphae or spores from an experimental plate to the new SDA plate. A control plate inoculated with fungi taken from the same experimental plate, but from a region away from the electrodes and containing fungal growth, was also included with each of these experiments.
Results In this investigation, several clinically relevant doses of LVDC E-stim were applied to 24 hr pure cultures of T. rubrum or T naentagroplaytes growing on SDA plates. Following this, the diameter of any zones around each electrode lacking fungal growth were observed and measured. For each fungus, each experiment was replicated three times at the specified current and time settings.
The size of the zones around each electrode that lacked fungal growth for T.rubrum of° T. rneratagropl~yte due to the application of LVDC E-stun at the various amperages used. For all amperages except 0 amperes, circular or roughly circular zones devoid of fungal growth were observed around both the positive (anode) and negative (cathode) electrodes. In addition, we observed an increase in the diameter of the zones with increasing amperages for both fungi (Figure 1).
Because we inserted 1 mm electrodes into the semi-solid agar surface during each experiment in order to generate a current, there was a depression produced in the agar surface at the location of these electrodes on all SDA plates. This was due, most likely, to compression and/or liquefaction of the agar. Consequently, the absence of growth observed directly under each electrode in this study, as noted in a previous was not considered to be indicative of fungicidal or fungistatic activity.
In order to confirm that the antifungal effects on T. rubrum arad T.
mentagrop7~ytes observed in this study were due to the application of LVDC E-stim and not to other possible causes, the following controls were done. To rule out the possibility that the observed antifungal effects were due to the electrode material itself, in each round of experiments, a SDA plate was inoculated with either fungus and incubated for 24 hr. After this, the electrodes were inserted in the same manner and for the same time period as we would in a typical experiment using LVDC, but no current was applied (O amperage). The plates were then incubated and observed as described above. On these SDA plates, no areas devoid of fungal growth around either electrode were ever observed with either T. rubrunZ or T. mentagrophytes. This same experiment was also used to determine if the lack of fungal growth around the two electrodes was due to any remaining ethanol (used to disinfect the electrodes between experiments) on the electrodes. If this were the case, some area devoid of fungal growth should have been observed around the region where the electrodes were inserted into the agar plates, even without the application of LVDC (O amperes). No such region was observed.
Another possible reason for the antifungal effects observed in this investigation was that changes produced in the fungal growth medium (SDA) as a result of LVDC E-stim application made the medium no longer supportive of fungal growth. To investigate this possibility we did the following set of experiments. Prior to the inoculation of either fungus onto the SDA medium, LVDC of either 3 milliamperes (the highest clinical amperage used in this study) or 8 milliamperes (beyond the clinical range used) was applied to 8 SDA plates for 30 min each (4 plates at 3 milliamperes, and 4 plates at 8 milliamperes).
T.
s°ubf~um was then inoculated on 2 of the 3 milliarnpere and 2 of the 8 milliampere plates and incubated for 7 days. T. naentagrophytes was inoculated similarly.
If the medium was indeed changed by LVDC E-stun application in such a way as to prevent or inhibit fungal growth, this should be observed as a lack of growth in the agar in the region around the electrodes (or possibly some other region of the agar). No such region lacking fungal growth was observed for either T. rubYmn or T. mentagf~ophytes in the areas surrounding either of the electrodes (or any other area) when we inoculated the fungi onto a SDA plate after 3 milliamperes of LVDC application. At 8 milliamperes, no region lacking fungal growth was observed for either fungus at the cathode. However, at this amperage, some discoloration, liquefaction and subsequent depression of the agar was observed in the area in which the anode was placed. Neither fungus was able to grow very well over this discolored, depressed anode region at 8 milliamperes.
Otherwise, growth occurred throughout the remainder of the plate.
In order to determine if the range of LVDC E-stim application used in these experiments was acting primarily as an fungicidal agent or fungistatic agent, the areas around each electrode that lacked fungal growth were sampled with a sterile swab 24 hr after E-stun application for the presence of viable fungal cells or spores. A total of 24 samplings for T rubruna and 24 samplings for T
mentagrophytes were made. A sampling was taken from the area around each electrode on all plates which received a dose of 500 microamperes,l milliampere, 2 milliamperes and 3 milliamperes. Growth was observed on the fresh SDA
plates inoculated with a swab after sampling an experimental plate. In the remaining 22 samplings, no growth was observed.
Finally, as has previously been reported, we also observed the production of gas bubbles at the cathode during all experiments, and occasionally, also at the anode. In addition, a blue discoloration was observed around the cathode, possible due to a pH change.

Discussion This investigation was undertaken in order to determine if the clinically observed efficacy of LVDC E-stun in the treatment of onychomycosis is due (at least in part) to an antifungal effect of the modality. Antibacterial effects against many of the common bacterial wound pathogens have been demonstrated ira vitro for both low voltage direct current and high voltage pulsed current in several studies. However, such ifa vitf°o documentation is negligible with respect to the effect of electric current on the common fungal pathogens, the yeast Gahdida albicaT~s being one of the few exceptions. Clinically relevant doses of LVDC E-stim are antifungal ira vitro to the two primary causes of onychomycosis, the fungi T Yub~uua and T nzeratagroplaytes. The antifungal effects of LVDC E-stim occur in a dose dependent manner in the clinically relevant ranges that we chose to use (500 microamperes to 3 milliamperes) in our iTa vitro experiments.
A second and related determination we desired to make was whether LVDC E-stim in the dose range we used was acting primarily as a fungistatic agents or a fungicidal agent. To determine this, we carefully sampled the areas devoid of fungal growth around the electrodes in each of our experiments 24 hr after E-stim with a sterile swab to assay for any viable fungal cells or spores which could give rise to fungal colonies on new SDA plates. Similar methodologies have been used to determine if E-stun is bactericidal or bacteriostatic . In 46 of the total of 48 samplings, we observed no fungal growth on the newly inoculated SDA plates. The two plates that did show some growth were both from the cathode region of the 3 milliampere dose plate. These zones had the largest diameter, and it is possible that the sampling swab may have inadvertently touched some viable fungal cells at the periphery of the zone.
As such, they would represent an artifact of these experiments, rather than actual lack of fungicidal activity. We strongly believe that such is the case.
Consequently, the data strongly suggest that LVDC E-stun is acting fungicidally in the amperage range used in this study.
Cellular death can be brought about by a number of factors that include:
damage or denaturation of key cellular enzymes; damage to DNA; damage or disruption of the cell membrane; damage or destruction of key cellular transport systems. Electricity is believed to most likely kill cells by affecting the molecular structure of the cell membrane, leading to fatal changes in cell membrane permeability . Such cell membrane damage could explain the antifungal effects of LVDC E-stim that we observed both in vivo arad in vitro. However, other factors might also play a role. Application of electric current to the agar medium can result in changes in the pH of the medium, increases in temperature and the generation of toxic metabolites. All of these (and possibly others still) could act antimicrobially to one degree or another. Such factors have been considered in other studies looking at the antibacterial effects of electricity . We did not look individually at these factors in this study because we were mainly concerned with determining if LVDC E-stim application itself was antifungal. If the application of electricity to a fungus growing on a toenail or agar surface results in the death of all or some of those fungal cells, then whether that fungicidal activity was due to fatal changes in the cell membrane of fungal cells and also to changes in pH or increases in cellular temperature is secondary to our present interest. Such aspects will hopefully be addressed in subsequent investigations.
However, in this present investigation, we were concerned to demonstrate that any antifungal effects of LVDC E-stim on the two major etiologies of onychomycosis were due to the application of E-stim itself (due to the effects of electrical current), and not due to any artifacts produced as a result of our experimental methodology. Because we did not observe any fungal inhibition around either electrode during any trial when the electrodes were inserted but when current was not applied (O amperes), we are confident that the electrode material itself (stainless steel) is not antifungal. Another concern we had was that some of the ethanol, which we used to disinfect the electrodes before and in between experiments, might remain on the electrodes upon insertion into the SDA
medium. Since ethanol is a disinfectant, it can kill and or inhibit fungal and bacterial cells. Thus, we might see areas around each electrode lacking fungal growth which were due to the disinfection action of ethanol, rather than the antifungal effects of the LVDC E-stim. To minimize the possibility of this, after we removed the electrodes from their ethanol storage unit (stored in our biological hood), we allowed them to dry for a minimum of 30 seconds before they were inserted into any SDA experimental plates. No anti-fungal activity was observed at the 0 amperage setting as described above, we are confident that insufficient (or no) ethanol remained on the electrodes upon insertion into any SDA plate. It is clear that all the ethanol had evaporated and was not a cause of the observed zones lacking fungal growth.
Another possible reason for any observed areas lacking fungal growth around either electrode was that the application of LVDC E-stim in the current range we used changed the SDA medium in some way so that is could no longer support the growth of either T. rubrum or T. rnentag~oplaytes. This could result from the production of toxic and or inhibitory products in the medium as a result of the LVDC application, or from changes in the pH of the medium due to LVDC, or from the denaturation and degeneration of necessary nutrients in the medium without which the fungi could not grow. To investigate this possibility, we first applied either 3 milliamperes or 8 milliamperes of LVDC E-stim to several SDA
plates before we inoculated them with either T. ~°ubrurra or T.
naentagrophytes. If the SDA medium was indeed changed by LVDC application so that it now prevented or inhibited fungal growth, this should be observed as a lack of growth in/on the agar in the regions) around the electrodes (or possibly some other region of the agar). As the data show, no such region was observed at 3 milliamperes around either the cathode or the anode, or anywhere else on the plates. Growth occurred throughout each SDA plate. At 8 milliamperes, more than twice the highest amperage used in our study, growth occurred at the cathode, but not the anode, where liquefaction and depression was observed. It is probable that at this amperage, lack of growth was due to some physical changes produced in the medium (i.e. liquefaction), or to the generation of toxic metabolites, or the denaturation of vital nutrients, or a combination of several factors. However, because 3 milliamperes was the highest dose of LVDC E-stun that we used in our antifungal studies, we feel confident that at this amperage and at the lower amperages, the media was not altered in a significant way so as to negatively affect the growth of either fungus. To further support this assertion, we noted that in our experiments involving 500 microamperes, 1 milliampere, 2 milliamperes and 3 milliamperes of LVDC E-stim, the areas of the agar lacking fungal growth due to the LVDC application were still capable of supporting the growth of both fungi. This is evidenced by the fact that if these agar plates were incubated at 25'C for 7 to 10 days, we would eventually clearly see viable fungi from outside the diameter of the fungicidal zone begin to re-colonize that zone until a solid fungal lawn was again formed over the entire area. Together, these results strongly support the assertion that any possible changes produced in the SDA medium were not responsible for the observed zones lacking fungal growth around the electrodes in the clinically relevant dose range of LVDC that we employed in our study.
Apparatus In other embodiments of the invention, apparel like devices can be used to treat the fungal infection by providing a wearable fluid reservoir to the area to be treated which also incorporates a first electrode means and a second electrode means. In some instances this device could have the general form of a bandage or the like with an adhesive portion along the periphery of the reservoir means to provide a seal with the contact area to be treated. Then a DC power source can be hooked up to the first and second electrode to provide the electronic field across the electrodes and the surface to be treated. This "bandage" like apparatus allows the treatment method to be undertaken without limiting the activity of the patient. A person being treated with such an apparatus will be able to be active during treatment and will hence be more likely to participate in complete treatment regimens.
Those skilled in the art will recognize that besides patches, a localized reservoir similar to the "bandage" reservoir means can be made into part of a piece of apparel. Depending upon the sites of the fungal infection the apparel could be in the form of a sock, sweat-pant, or shirt.
Solutions It has also been found that certain additives to the aqueous solution in the reservoir can increase the efficacy of the treatment regimen. For instance, it has been found that an oxygenating source such as hydrogen peroxide accelerates the reduction of onchymycotis. Preferably the concentration of hydrogen peroxide is in the range of 0.01 to about 2 weight percent. The solution at those concentrations can be pre-prepared, or can be freshly prepared just prior to treatment. Solution can also be adjusted for slat concentration so that they are isotonic, and additionally buffer systems can be added so that the pH of the solutions remains close to physiological conditions of the tissue being treated.

Claims (6)

What is claimed is:

1. A method for treating onychomycosis in humans comprising the steps of:
exposing an area of a patient that is infected with a mycotic infection with an aqueous solution; and providing a low voltage direct current across said infected area for a period of at least 5 minutes.

2. An apparatus for treating onychomycosis comprising:
a reservoir means for providing an aqueous solution to a patient; and means for providing a low voltage current to said reservoir mean across said mycotically infected area.

3. An apparatus for the treatment of onychomycosis that is wearable comprising:
a reservoir membrane made of a material that is impervious to aqueous solutions and where said reservoir membrane has a periphery portion;
a sealing means disposed on said periphery portion of said sealing membrane;
a first electrode means sealably affixed to said reservoir membrane that communicates through said membrane to provide an electrode surface and a means for being connected to a direct voltage source; and a second electrode means sealably affixed to said reservoir membrane that communicates through said membrane to provide an electrode surface and a means for being connected to a direct voltage source.

4. The apparatus of claim 3 further comprising a liquid filler opening that allows said apparatus to be sealably placed against a skin area to be treated to form a pocket which is capable of holding an amount of an aqueous liquid.

5. The method of claim 1 wherein said aqueous solution comprises 0.01 to 1.0 weight percent hydrogen peroxide.

6. The method of claim 1 wherein said direct current is between about 1 mill ampere and about 25 mill ampere.