1. Field of the Invention
The present invention relates to a device and a method for storing and administering active substances, e.g., medical or biochemical active substances.
2. Description of Related Art
Many variants are known for administering medications of various forms, e.g. medical or biochemical active substances. In addition to the use of commonly known syringes, microneedles are also, for example, proposed as a transfer means for the active substance into a skin.
There are in principle several important criteria that must be taken into account in this context. Among the important criteria are the mechanical stability and biocompatibility of the microneedles, but also the capability of storing sufficient quantities of active substances and administering them via the microneedles. Structures such as cavities or depressions can be disposed for this purpose inside the microneedles in order to store active substances.
U.S. Pat. No. 6,334,856 B1, for example, describes microneedles that have reservoirs for the storage of active substances. The reservoir is preferably disposed under the needles on the substrate side and connected via internal ducts, such as holes, to the internal region of the microneedles, with the result that active substances can be guided out of the reservoir and delivered through microneedles to a body that is to be treated.
To allow even relatively large quantities of active substances to be stored reliably, German patent application DE 10 2006 028782.7 (not previously published and therefore not prior art) proposes to dispose microneedles inside a package that forms the reservoir. The reservoir contains a carrier medium in which the active substance is present in dissolved form. The microneedles are thus embedded in the carrier medium having the active substance, and are thereby supplied with the active substance. Storage of the active substance in dissolved form can lead to problems, however, when the solubility limit of the carrier medium is reached. When the solubility limit of the carrier medium is reached and exceeded, precipitation of the solution then occurs and the active substance settles in solid form in the reservoir. In solid form, however, the active substance cannot be administered through the microneedles. The above-described concept thus comes up against a natural limit to the quantity of active substance that can be absorbed.
It is an object of the present invention to make available an apparatus and a method that make possible storage of larger quantities of active substance as compared with proposals from the existing art.
The present invention has the advantage of avoiding any exceedance of the solubility limit of the carrier medium. Oversaturation of the carrier medium is, advantageously, not reached. A relatively large quantity of active substance can consequently be stored, as compared with previously known approaches. Rapid and convenient administration can thereby be achieved, even with large and very large quantities of active substance.
At the same time, sterile storage of the transfer means continues to be ensured. The previously observed so-called leakage problem, in which active substances slowly emerge or evaporate from the reservoir in unintended fashion, is also avoided. The transfer means can thus also be safely transported.
An apparatus 8 for storing and transporting microneedles 1a, 1b is proposed, providing firstly a first reservoir 3, 3a, 3b having a carrier medium, and at least one active substance dissolved therein for administration by way of at least one transfer means 1.
Such transfer means 1 can be, by way of example, a microneedle 1a, 1b. In the following exemplifying embodiments it is assumed that transfer means 1 is constituted by a microneedle 1a, 1b, other suitable transfer means 1 also being suitable in principle, instead of a microneedle 1a, 1b, for the inventive concept.
Microneedles 1a, 1b are advantageously disposed inside a package 4, 4a, 4b enclosing reservoir 3, 3a, 3b (
A very wide variety of embodiments of microneedles 1a, 1b themselves is known from the existing art. Advantageously, they are disposed in an array and have needle tips 1a on a substrate 1b. Microneedles 1a, 1b are made, as required, from a semiconductor material such as silicon, or else from plastic or metal.
In this exemplifying embodiment, microneedles 1a, 1b are mounted on a carrier 2 that is permeable to active substance. Carrier 2 can be implemented by way of a thin film having fine openings. Carrier 2 that is permeable to active substance extends through first reservoir 3, 3a, 3b, advantageously through the entire first reservoir 3, 3a, 3b. First reservoir 3, 3a, 3b is subdivided by carrier 2 into a first reservoir region 3a having microneedles 1a, 1b, and a second reservoir region 3b without microneedles 1a, 1b.
Package 4, 4a, 4b itself is formed by an elastic film 4a that can be pierced with microneedles 1a, 1b and by an outer layer 4b, which are connected to one another at their edge regions 7. In this case the upper region between film 4a and outer layer 4b, inside the connected edge regions 7, therefore forms first reservoir 3, 3a, 3b. Microneedles 1a, 1b are in turn carried by carrier 2 and are covered by elastic film 4a. The latter protects microneedles 1a, 1b during transport and storage, and moreover keeps microneedles 1a, 1b and the active substance sterile. Package 4, 4a, 4b, in particular film 4a, moreover prevents “leakage” or evaporation of the active substance.
Elastic film 4a and/or carrier 2 preferably have adhesive properties at least in their edge regions 7, thus making it possible to adhere film 4a and carrier 2 together by the exertion of pressure.
According to the present invention, a second reservoir 5 having the active substance in solid form is now provided in addition to first reservoir 3, 3a, 3b. Second reservoir 5 is preferably located adjacent to first reservoir 3; 3a, 3b, so that the first reservoir 3; 3a, 3b and second reservoir 5 adjoin one another.
A separating layer 6 can also advantageously be disposed between first reservoir 3; 3a, 3b and second reservoir 5. Separating layer 6 can be constituted by a porous elastic membrane, or by a film that is permeable to active substance.
In the exemplifying embodiment according to
Because the additional active substance is present in solid form in a separate second reservoir 5, the solubility limit of the carrier medium in first reservoir 3; 3a, 3b is not exceeded. Driven by the concentration gradient, only as much active substance as permitted by its solubility limit diffuses into the carrier medium. The dissolved active substance can then diffuse via microneedles 1a, 1b into the skin.
A method for administering active substances using the apparatus described above will now be explained with the aid of
Upon exertion of pressure onto apparatus 8, package 4; 4a, 4b ensures coverage of the remainder of the structure, and surrounds microneedles 1a, 1b laterally so that “leakage” is further minimized and the active substance emerges only through microneedles 1a, 1b and directly below the outermost skin layers. Active substance transport is ensured in this context by a process of diffusion out of the reservoir into the skin or body.
When a package 4a, 4b having an elastic film 4a and an outer layer 4b that are connected to one another at their edge regions 8 is used, and when microneedles 1a, 1b that are mounted on a carrier 2 that is permeable to active substance and extends through reservoir 3; 3a, 3b are used, upon exertion of pressure onto apparatus 8, carrier 2 is pressed against elastic film 4a and film 4a is pierced or penetrated by microneedles 1a, 1b. The active substance can now diffuse into skin 5 through microneedles 1a, 1b. As a result, the concentration of the active substance in the carrier medium drops, and new active substance can diffuse out of second reservoir 5 up to the solubility limit.
In a further embodiment, a film 4a and/or carrier 2 having adhesive properties at least in their edge regions 8 are used, with the result that upon the exertion of pressure onto apparatus 8, film 4a and carrier 2 adhere to one another and thus immobilize microneedles 1a, 1b and hold them in place. Microneedles 1a, 1b are thus immovably clamped in stable fashion between film 4a and carrier 2, and thus ensure controlled administration of the active substance.
It is noted in supplementary fashion that apparatus 8 as described above can be used as an active-substance patch. Apparatus 8 according to the present invention is suitable in general for use in the (bio)chemical, medical, and clinical sectors. Simple and also reliable utilization of the above-described apparatus 8 for the storage and administration of even very large quantities of active substances is made possible, without exceeding the solubility limit of the carrier medium.
Number | Date | Country | Kind |
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10 2007 030 710 | Jul 2007 | DE | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/EP2008/058227 | 6/27/2008 | WO | 00 | 3/9/2010 |
Publishing Document | Publishing Date | Country | Kind |
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WO2009/003923 | 1/8/2009 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
3964482 | Gerstel et al. | Jun 1976 | A |
4687481 | Nuwayser | Aug 1987 | A |
6334856 | Allen et al. | Jan 2002 | B1 |
6611707 | Prausnitz et al. | Aug 2003 | B1 |
20060024358 | Santini, Jr. et al. | Feb 2006 | A1 |
Number | Date | Country |
---|---|---|
10 2006 028 782 | Dec 2007 | DE |
WO 0228471 | Apr 2002 | WO |
WO 2005056103 | Jun 2005 | WO |
WO2006015299 | Feb 2006 | WO |
WO 2006015299 | Feb 2006 | WO |
WO2006015299 | Feb 2006 | WO |
Number | Date | Country | |
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20100168715 A1 | Jul 2010 | US |