The invention relates to the field of transdermal devices for delivering drugs or obtaining samples through the skin of a human or animal subject. In particular, the invention relates to a patch that is applied first to the skin in order to facilitate preparation of the skin for the transdermal procedure.
It is well known to use transdermal procedures for obtaining fluid samples or other analytes from a subject by withdrawal through the skin without the use of hypodermic needles. One example is the monitoring of glucose levels by persons who are diabetic. It is similarly known to use transdermal procedures to deliver drugs or other biologically active substances into the body of a subject. Electrochemical techniques such as iontophoresis or reverse iontophoresis may be used to enhance the transport of the substances or analytes in question across the skin.
Before the device that will carry out the transdermal procedure is applied to the skin, it is typically necessary to prepare the skin in some way to increase the effectiveness, safety or reliability of the procedure. Most simply, the skin may need to be cleaned or sterilized to prevent infection when transdermal channels are opened. Other preparation techniques can be used to enhance the permeability of the skin, for example by abrading the skin or applying a chemical permeant. A variety of poration techniques can also be used to open channels through the stratum corneum, for example by electroporation or applying microneedles to the surface of the skin. If electrochemical techniques are to be used, then it may be necessary to apply a liquid or gel electrolyte to the skin to improve conductivity between the skin and the electrodes of the device.
The working area of a transdermal device, within which the transdermal process occurs, is typically quite small relative to the total area of the device that is placed in contact with the skin. It is therefore important to ensure that the device is correctly located so that the working area of the device is aligned with the area of the skin in which the preparation process has been carried out. Misalignment between the prepared skin area and the electrodes or other components in the working area of the device can result in poor transdermal transport and/or unreliable measurement of analyte levels by the device. The working area of a transdermal device is typically somewhere in the centre of the face that is applied to the skin so that, while it is being applied, the body of the device hides both the working area and the skin preparation area from view, making difficult the accurate location of the device on the skin.
The invention provides a kit comprising a skin preparation patch and a transdermal device, as defined in claim 1.
The invention further provides a skin preparation patch as defined in claim 10.
The invention further provides a method of preparing an area of skin for a transdermal procedure as defined in claim 15 or claim 17.
Preferred but non-essential features of the invention are defined in the dependent claims.
The two-part skin preparation patch according to the invention serves a dual purpose. The second part defines the area of the skin in which the required preparation process should be carried out. The second part can then be removed to leave the first part adhered to the skin, which can be used as a guide for correctly locating the transdermal device with the working area of the device and the prepared area of the skin in alignment.
The skin treatment device may itself be in the form of a patch and its periphery may need to be hermetically sealed against the skin so as to prevent the loss of moisture from the working area, which could lead to a detrimental impact on the ability of an analyte to diffuse through or react in the working area. The patch according to the invention can ensure that sufficient area is provided around the working area of the device to accommodate such a seal.
In this specification, the term “underside” and cognate words are used to refer to the side of a patch or device that, in use, is closest to the skin of a subject. It will be understood that the patch and device may be used in any orientation, depending on the body part to which they are applied, and may similarly be manufactured, transported or stored in any orientation, without departing from the scope of the invention defined by the claims.
The skin preparation patch shown in claim 1 is formed from a thin, flexible material such as a polymer foam, or other polymeric membrane, produced from a range of materials such as silicone, acrylic polymers, cellulose acetate, etc. It has an adhesive layer over the entire area of its underside. Suitable adhesives for temporarily attaching patches to skin, so that they can be peeled off after use, are well known. The adhesive layer is protected by a backing sheet/release liner (not shown) that is peeled off immediately before use of the patch.
The patch is divided by cut lines into two or three parts 1,2,3. The adhesive layer will generally be sufficient to hold the respective parts together by their edges after removal of the backing sheet but small connections between the parts could be left for this purpose, provided that they can easily be torn when separation of the parts is desired.
A first part 1 follows the perimeter of the patch and surrounds the second and third parts 2,3. The first part 1 may form a continuous loop or may be cut by one or more lines or tabs 4 to make easier the eventual removal of any of the parts from the skin. A second part 2 comprises the whole interior of the patch, except for a central area that is formed by the third part 3.
Following the preparation step, the user removes the second part 2 of the patch by unpeeling it from anywhere on its perimeter. (One of the free edges where the strip 6 has been removed is likely to be easiest.) That leaves just the first part 1 of the patch adhered to the skin, forming a frame, with the treated area of skin 8 at a defined location inside it, as shown in
In the case of physical means such as micro-protrusions, the skin preparation area may be identified as subsections, such as two semi-circles for example, either with lettering or numbering to identify where the skin preparation means is to be applied. This is significant in the case of the use of a micro-protrusion patch for example, where it is known that application of force directly in the centre of a skin-prep patch greater than 5 mm in diameter leads to minimal effect on the periphery as compared to the centre or the region where the most pressure is applied. Therefore demarcating the area into two or more areas can allow the skin-prep to be applied in more than one step, in the case where the skin-prep patch is applied to the underside of the aforementioned device. This will allow a user to apply force with a finger or thumb, or an implement provided, over smaller regions, thus providing a higher and more concentrated force over smaller areas, significantly enhancing the effectiveness of the skin-prep step. The second part 2 of the patch may thereafter be removed to reveal a situation identical to
The reader will understand that the shape of the patch is not important in itself but it should be matched to the shape and configuration of the transdermal device with which the patch is to be used. In particular, the internal contour of the first part of the patch should match some or all of the outline of the device, while the second part of the patch should define an opening or an area of skin preparation means that substantially matches the shape, size and location of the working area of the device.
It is not essential that the third part 3 of the patch (if present) should be provided with a strip 6 extending to the perimeter of the second part 2 but it is preferred that some sort of tab should be provided to make the part 3 easy to grip. Similar tabs may be provided on the other parts 1,2 if desired. It is strongly preferred but not essential that the third part 3 (if present) should be completely detachable from the second part. One can imagine that if the third part 3 were peeled back from the circular end, the long strip 6 would allow the third part 3 to be held well clear of the skin preparation area 8 without removing it completely. Any of the first, second or third parts may be subdivided for ease of use or manufacture. An example of a cut line 16 subdividing the first part 1 is shown in
It is not essential for the adhesive layer to cover the entire area of the underside of the patch. As the final part of the patch to be removed, the first part 1 does need to be provided with an adhesive layer. However, if the adhesion of the first part 1 is sufficiently strong, and if there is sufficient mutual attachment between the various parts 1,2,3, e.g. by the provision of small connecting links, then it might be possible to omit the adhesive layer from the second and/or third parts 2,3.
Number | Date | Country | Kind |
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1819737.6 | Dec 2018 | GB | national |
Filing Document | Filing Date | Country | Kind |
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PCT/GB2019/053408 | 12/3/2019 | WO | 00 |