Patent Application
20130253412
This application relates to the transdermal administration of ionic solutions, drugs and cosmetics.
More particularly, this application relates to active iontophoretic delivery systems in which a hand-held roller-ball applicator forming an electrical contact applied to the surface of the skin of a subject for the purpose of delivering agents through the surface of the skin into underlying tissues.
Iontophoresis uses electrical current through a body, such as human or animal, to drive charged ionic particles into the skin. Some ionic particles may be drugs or cosmetic solution. During active iontophoresis, direct electrical current is used to cause ions of a solution, such as a medicament, to move across the surface of the skin and to diffuse into underlying tissue. The surface of the skin is not broken by the iontophoresis. When conducted within appropriate parameters, the sensations experienced by a subject during the delivery of the ionic solution in this manner are not unpleasant. Therefore, active iontophoresis presents an attractive alternative to hypodermic injections and to intravascular catheterization.
Iontophoresis has been used with patches that allow a current flow and ionic treatment of a particular area of the body. As such, conventional iontophoresis has used patches to allow sufficient time for the current to drive an ionic solution into a particular part of the body. Due to the limitations of current and patch size, only specific, discrete areas of skin covered by an iontophoretic patch accept the transdermal ionic solution transfer.
Embodiments of iontophoretic devices are disclosed which may include a reservoir; a roller-ball applicator coupled to the reservoir and configured to dispense contents of the reservoir; a power supply; a first electrode electrically coupled to a pole of the power supply; and a second electrode coupled to the other pole of the power supply. The devices may be configured such that a current travels between the first electrode and the second electrode through the skin of a subject when the device is used.
In some embodiments, the roller-ball applicator may include the first electrode, a roller-ball, and a fitment, the roller-ball comprising a conductive material. In such embodiments, the roller-ball may function as the first electrode. Similarly, some embodiments may include a handle, wherein the second electrode is included on the handle, such that the second electrode may be configured to be grasped by the hand of the subject. The reservoir may contain an ionic solution. Iontophoretic devices may also include a control circuit disposed between the power supply and one of the first and second electrodes. The device may be configured for a single use only, or the reservoir may be refillable or replaceable. The device may also include a cap to fit over the roller-ball applicator.
Some exemplary methods of iontophoretic application may include placing ionic fluid in a reservoir; coupling the reservoir to a roller-ball applicator, the roller-ball applicator having a roller-ball and a handle; grasping the handle; placing the roller-ball against the skin of an individual; dispensing the ionic fluid by way of the roller-ball onto the skin of the individual; and applying current between the roller-ball and the skin of the individual such that the ionic fluid is delivered iontophoretic ally into the skin of the individual.
The following description can be better understood in light of Figures, in which:
b illustrates schematic view of an exemplary iontophoretic roller-ball applicator being used;
a and 2b illustrate an exemplary iontophoretic roller-ball applicator;
Together with the following description, the Figures demonstrate and explain the principles of iontophoretic roller-ball applicators and methods for making and using the iontophoretic roller-ball applicator. In the Figures, the thickness and configuration of components may be exaggerated for clarity. The same reference numerals in different Figures represent the same component.
The following description supplies specific details in order to provide a thorough understanding. Nevertheless, the skilled artisan would understand that the apparatus and associated methods of using the apparatus can be implemented and used without employing these specific details. Indeed, the apparatus and associated methods can be placed into practice by modifying the illustrated apparatus and associated methods and can be used in conjunction with any other apparatus and techniques conventionally used in the industry. For example, while the description below focuses on iontophoretic roller-ball applicators powered with a battery, applicators may also be powered from a wall socket.
Iontophoretic roller-ball applicators described below may provide a user with a manipulable device that may used to apply ionic solution, such as a medicament, to treat an area of skin with iontophoresis. Iontophoretic roller-ball applicators may provide additional massaging or stimulation to skin to facilitate the iontophoresis and to provide the iontophoresis to a larger area of skin than traditional attached patches, which are placed and held in a single location. Additionally, the ionic solution applied to the skin may be conductive and continue with iontophoresis over a broad area when in conductive contact with the roller-ball of an iontophoretic roller-ball applicator, which may function as an electrode in the iontophoresis process, as will be explained in more detail below.
The direct current employed in active iontophoresis systems may be obtained from a variety of electrical power sources. These may include electrical equipment that ultimately receives power from a wall socket, paired regions of contrasting galvanic materials that when coupled by a fluid or a gel medium produce minute electrical currents, capacitors, consumable and rechargeable batteries, etc. A flow of electrical current may require an uninterrupted, electrically-conductive pathway from the positive pole of a power source to the other, negative pole of the power source. Living tissue may be made up primarily of fluid and may be, therefore, a conductor of electrical current. In an iontophoretic circuit, the opposite poles of a power source may be electrically coupled to respective, separated contact locations on the skin of the subject. The difference in electrical potential created by the power source between those contact locations may cause a movement of electrons and electrically charged molecules, or ions, through the tissue between the contact locations.
In an active iontophoretic delivery system, the polarity of the net overall electrical charge on dissolved molecules of an ionic solution, including solutions with medicaments and/or cosmetics, may determine the contact location on the skin at which a supply of the ionic solution of must be positioned. A positively charged ionic solution in a reservoir against the skin of a patient may be coupled to the positive pole of any power source that is to be used to administer the ionic solution iontophoretically. Correspondingly, a reservoir on the skin of a patient containing a negatively charged ionic solution may be coupled to the negative pole of such a power source. Examples of common iontophoretically administrable ionic solutions of positive polarity include Bupivacaine hydrochloride, Calcium chloride, Lidocaine hydrochloride, Zinc chloride, and Lidocaine. Examples of common iontophoretically administrable ionic solutions of negative polarity include Betamethasone sodium phosphate, Dexamethasone sodium phosphate, Fentinol, Copper sulfate, Acetic acid, Magnesium sulfate, Naproxen sodium, Sodium chloride, and Sodium salicylate.
The ionic solution supply may be housed in a fluid reservoir that is positioned electrically conductively engaging the skin of the subject at an anatomical location overlying the tissue to which ionic solution is to be administered. The ionic solution reservoir can take the form of a gel suspension of the ionic solution or of a pad of an absorbent matrix, such as gauze or cotton, which is saturated with fluid containing the ionic solution. In some instances the fluid containing the ionic solution is provided from the manufacturer in the absorbent matrix. More commonly, the fluid is added to the absorbent matrix by a medical practitioner at the time that the ionic solution is about to be administered to a subject.
As shown in
The coupling of each pole of power source 12 may be affected by the electrical connection of each pole to a respective electrode. The electrode forming the roller-ball and delivering the ionic solution from reservoir 30 may be referred to as an active electrode; the electrode 16 at the location on skin 5 distanced from the roller-ball 70 may be referred to as a return electrode. The electrical potential that is imposed across ionic solution reservoir 30 of an iontophoretic circuit may produce electrical current flow Is by causing electrolysis in some of the molecules of the water (H2O) in the solution in reservoir 30. Skin 5 provides resistance Rs for circuit 10 between electrode 16 and roller-ball 70. Control circuit 20 may regulate and control current through circuit 10.
In some embodiments, such as when a person is using the applicator 100 to treat another person, a separate contact (not shown) between the skin 5 of the individual being treated and the other person performing the treatment may be provided to close the circuit between the electrode 16 and the skin 5 of the individual being treated. In some embodiments, this may simply be the person performing the treatment touching in a skin-to-skin manner the person being treated, or a cord extending from the applicator 100 with a remote electrode may be placed on or attached to the skin 5 of the individual being treated.
In electrolysis, the positively-charged hydrogen ion (H30 ) of a water molecule may then becomes separated from the negatively-charged hydroxyl radical (HO−) of that same molecule. These ions and radicals may then migrate in respective opposite directions through the solution in the ionic solution reservoir. The hydrogen ions (H+) may then move toward the negative pole of the electrical potential being imposed on the solution, while the hydroxyl radicals (HO−) move toward the positive pole. This may in turn drive the treatment solution ions M+ into skin 5.
Ionic solution reservoir 30 may be contained within a roller-ball applicator, with an associated active electrode conveniently retained against skin 5 by contact with roller-ball 70, with roller-ball 70 functioning as the electrode as described in detail below, while return electrode 16 may be retained against skin 5 through the handle of the roller-ball applicator.
a and 2b illustrate an embodiment of iontophoretic roller-ball applicator 100 Iontophoretic roller-ball applicator 100 may include body 110 with electrode 116, base 112, solution fitment 160 with roller-ball 170, and cap 150.
In the embodiments of
Base 112 may be formed of any suitable material, such as a conductive material, or a non-conductive material with a conductor to connect power source 122 to electrode 116. Some suitable materials may include metals, a plastic with a conductive coating, conductive plastic, conductive ceramic, conductive carbon etc. Power source 122 may be any suitable power source such as batteries, which may also include board circuitry to control current output, a connection to a wall outlet, capacitors, etc., to provide sufficient current over time to affect an iontophoretic process, for example between about 0.00001-100 mAmps. Power source 122 may be DC to provide a steady current to drive an ionic solution into the skin of a subject using iontophoretic roller-ball applicator 100. Lead 126 may connect power source 122 to control circuit 120. Control circuit 120 may function to provide and maintain the correct current flow between electrode 116 and roller-ball 170 when being used.
Lead 124 may connect control circuit 120 to conductive post 128 through plate 114. Plate 114 may function to separate and protect the electronic components in the lower portion of body 110 from the upper portion of body 110, which houses reservoir 130 of ionic solution. Plate 114 may be formed of a non-conductive material, such as plastic, or any other suitable material. In some embodiments, control circuit 120 may be directly connected to power source 122 external to base 112.
In the embodiment of
As such, in some embodiments the fluid in reservoir 130 may function as the conductor. In such embodiments, roller-ball 170 may be formed of a non-conductive material, the current being conveyed by the fluid flowing from reservoir 130 to skin 5. Iontophoresis may cease when the fluid is depleted, by breaking the circuit and thereby automatically stopping the iontophoresis treatment.
Reservoir 130 may be replaceable or removable in some embodiments where iontophoretic roller-ball applicator 100 is reusable. In other embodiments, reservoir 130 may be affixed to the upper portion of body 110. Similarly, reservoir 130 may fit snugly in body 110 as a selectively removable attachment. As shown, fitment 160 may be coupled to reservoir 130 through cooperative connection of complimentary threads 134 of reservoir 130 and threads 164 of fitment 160.
In some embodiments where iontophoretic roller-ball applicator 100 is not reusable, fitment and reservoir 130 may be permanently affixed using adhesive or other suitable affixment. Similarly, fitment 160 may be permanently affixed to body 110 such that when reservoir 130 is empty, iontophoretic roller-ball applicator 100 may cease to function and would no longer be useful. In such embodiments and other reusable embodiments, no current would flow when iontophoretic roller-ball applicator 100 is in an upright position and no fluid is present outside of reservoir 130, or when the fluid level in reservoir 130 does not permit an electrical connection between roller-ball 170 and conductive post 128.
Ring 172 may be located in fitment 160 and on top of reservoir 130 to provide a seat for roller-ball 170. Ring 172 may be formed as part of fitment 160, or it may be compressed between reservoir 130 and fitment 160 when assembled. Ring 172 may be conductive and attach to a conductive portion of reservoir 130 to allow current to flow to roller-ball 170. In some embodiments, fitment 160 may be formed of a non conductive material having sufficient elasticity that roller-ball 170 may be press-fit into fitment 160 and retained by the top portion of fitment 160, as the top portion returns to its diameter. The diameter of the top portion of fitment 160 may be smaller than the diameter of roller-ball 170 to keep roller-ball 170 from falling out.
In other embodiments, fitment 160 may be formed of a conductive material, such as metal, that would not permit press-fitting of roller-ball 170. In such embodiments, roller-ball 170 may be placed inside of fitment 160 through the bottom prior to attachment with reservoir 130 and body 110, and held in place with ring 172. Roller-ball 170 may fit relatively loosely within fitment 160 to allow for free rotation and to convey ionic fluid from reservoir 130 to skin 5 when in use.
Roller-ball 170 may be formed of a conductive material that forms part of the electrical circuit, or it may be formed of a non-conductive material, allowing the current to pass through the fluid as described above. Cap 150 may connect to fitment through fitment threads 162 and cap threads 152 to reduce evaporation, leaking, and spillage of a fluid in reservoir 130. Cap 150 may be formed of any suitable material, such as metal, plastic, etc.
In
In
In
Turning now to
Additionally, body 510 may be shaped in a different ergonomic configuration than iontophoretic roller-ball applicator 100, as shown in other figures and described above. Similarly, electrode 516 may be contoured to fit a hand and body 510 may be angled to give a gentler wrist position of an individual holding the applicator. The various components of iontophoretic roller-ball applicator 500 may be formed and function similarly to those of the various embodiments as described above with respect to the similar components of iontophoretic roller-ball applicator 100. In some embodiments, a single reservoir 536 may be positioned as shown in
In some embodiments, multiple roller-balls may be employed to engage a broader region. The bodies and handles of various iontophoretic roller-ball applicators may be formed and shaped to be of varying sizes and shapes depending on the desired aesthetic and ergonomic considerations of the applicator being used. Similarly, iontophoretic roller-ball applicators may be formed with specific shapes and sizes to accommodate particular areas of the body. For example, very small roller-balls may be used with iontophoretic roller-ball applicators for treating areas under the eyes, or fine wrinkles around the mouth and eyes, while a large ball may be used to treat large muscle groups such as those in legs, arms, and torso.
In other embodiments, iontophoretic roller-ball applicators may include a display in the body to indicate the amount of charge, time, and/or reservoir capacity used or remaining. Similarly, the iontophoretic roller-ball applicators may include switches to turn on the applicators and/or adjust the current to a desired level. Iontophoretic roller-ball applicators may turn on automatically with a circuit is completed between the electrodes and described above.
The various iontophoretic roller-ball applicators described may be used to provide several advantages over previous iontophoretic application systems. For example, medications or treatments may be made over a larger area of skin and a user may concentrate with varying intensities of particular trouble spots of on a region with an irregular shape that would be difficult to treat effectively with an iontophoretic patch.
Additionally, medications delivered by an active iontophoretic system may bypass the digestive system, which reduces digestive tract irritation. In many cases, ionic solutions administered orally may less potent than if administered transcutaneously. In compensation, it may be necessary in achieving a target effective dosage level to administer orally larger quantities of ionic solution than would be administered transcutaneously.
Active iontophoretic systems may not require intensive skin site sanitation to avoid infections. Equipment used in active iontophoresis may not interact with bodily fluids and, accordingly, need not be disposed as hazardous biological materials following use. Being a noninvasive procedure, the administration of ionic solution using an active iontophoretic system may not cause tissue injury of the types observed with hypodermic injections and with intravenous catheterizations. Repeated needle punctures in a single anatomical region, or long term catheter residence, can adversely affect the health of surrounding tissue. Needle punctures and catheter implantations inherently involve the experience of some degree of pain. These unintended consequences of invasive transcutaneous ionic solution administration are particularly undesirable in an area of the body that, being already injured, is to be treated directly for that injury with an ionic solution. Such might be the case, for example, in the treatment of a strained muscle or tendon.
The dosage of an ionic solution delivered iontophoretically may be conveniently and accurately measured by monitoring the amount and the duration of the current flowing during the administration. Similarly, the application may be completed with fluid contained in the reservoirs is depleted and the system stops. As such, the successful operation of an active iontophoretic system is not reliant on the medical skills of nurses or doctors. Foregoing the involvement of such medical personnel in the administration of ionic solutions whenever appropriate favors the convenience of patients and reduces the costs associated with the delivery of such types of therapy.
In addition to any previously indicated modification, numerous other variations and alternative arrangements may be devised by those skilled in the art without departing from the spirit and scope of this description, and appended claims are intended to cover such modifications and arrangements. Thus, while the information has been described above with particularity and detail in connection with what is presently deemed to be the most practical and preferred aspects, it will be apparent to those of ordinary skill in the art that numerous modifications, including, but not limited to, form, function, manner of operation and use may be made without departing from the principles and concepts set forth herein. Also, as used herein, examples are meant to be illustrative only and should not be construed to be limiting in any manner.
