This disclosure relates generally to dispensers of medical supplies. This disclosure relates more specifically to a dispenser of medical supplies, such as pills, that provides for a reduced risk of cross-contamination of the medical supplies being dispensed.
Existing automated systems for dispensing medical supplies, such as pills or capsules, are often used to expedite the filling of containers, such as bottles with pills. A problem with many of these systems is a risk of cross-contamination of the different medical supplies. For example, when the automated system dispenses a first drug A, a powder residue from the first drug A may adhere to certain components in the dispensing system. Subsequently when a second drug B is dispensed, part of the powder residue from drug A may adhere to drug B, and as a result the patient taking drug B will unknowingly also be taking trace amounts of drug A. Often the amount of cross-contamination is so minimal as to be inconsequential, but for some drugs and for some patients any cross-contamination should be avoided.
The disclosure describes one or more embodiments of medical supply dispensing systems. These and other advantages of the disclosure, as well as additional inventive features, will be apparent from the description of the invention provided herein.
In one aspect, the disclosure provides a medical dispensing system. The medical dispensing system includes dispensing and pathway components. The dispensing component includes several dispensers for medications. The pathway component includes a corresponding number of pathways to facilitate the dispensers placing medication in a container. Both the dispensing and pathway components are circular and the dispensers and pathways are arranged around the periphery of the respective components.
The circular dispensing and pathway components are arranged above and on either side of a conveyer for medication containers. The conveyer for medication containers receives empty containers and moves them to a filling area. The dispensing and pathway components overlap above the conveyer, in the filling area, from opposite sides of the conveyer.
In another aspect, the filling area is hermetically sealed from an external environment. The sealed area encompasses the filling area and most of the dispensing and pathway components, which are collectively referred to as the contaminated area. Individual dispensers and pathways rotate into and out of the contaminated area as the dispensing and pathway components are rotated. The contaminated area is maintained with a slight negative air pressure relative to the external environment, thus reducing the likelihood of contaminants leaving the contaminated area.
In yet another aspect, multiple conveyers, dispensing and pathway components are vertically arranged with respect to each other. Such an arrangement reduces the volume needed for multiple embodiments of this disclosure, thus providing a space-efficient structure.
The accompanying drawings incorporated in and forming a part of the specification illustrate several aspects of the present invention and, together with the description, serve to explain the principles of the invention. In the drawings:
While the disclosure will be described in connection with certain preferred embodiments, there is no intent to limit it to those embodiments. On the contrary, the intent is to cover all alternatives, modifications and equivalents as included within the spirit and scope of the invention as defined by the appended claims.
Automated medication dispensers are being increasingly used by pharmacists to improve their responsiveness to receiving orders for medication. An important issue when dispensing medication, via manual or automated means, is to minimize contamination to or from the medication being dispensed. The medications that are placed into these containers may be classified as hazardous. Dust and other particulates from the dispensing system may become airborne. This can be a risk to people around medication dispensing systems.
Additionally there is also a risk of dust or other particulate entering the dispensed containers either through airborne particulates, particulates from conveyors or other equipment, or tablets (partial or whole) that may have been left from other operations. These cross-contaminating particulates may remain in shared pathways or common funnels or chutes. These types of particulates can represent a risk to end users and recipients of the medication containers.
It is the intent of this disclosure to provide a design that can achieve high speed high volume container filling, while eliminating or reducing exposure and risk to both operators and those receiving the dispensed/filled containers.
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Dispensing disc 20 comprises multiple dispensers 22 arranged around periphery 40 of dispensing disc 20. Arc distance 26 separates dispensers 22. In use, dispensing disc 20 may rotate around center 24 in either clockwise direction 36 or the reverse rotational direction.
Similarly, pathway disc 50 comprises multiple pathways 52 around periphery 70 of pathway disc 50. Arc distance 56 separates pathways 52. In use, pathway disc 50 may rotate around center 54 in either clockwise direction 66 or the reverse rotational direction.
As medication is dispensed, particulates from the medication (e.g., airborne particles, dust) may be created. Controlling the distribution of the contaminating particulates is a goal of this disclosure. A specific pathway 52 is restricted to interact with (e.g., dispense medication for) dispensers 22 carrying a given medication (e.g., medication X). In a particular use, each dispenser 22 carries a different medication, and as a result each pathway 52 only interacts with a single dispenser. However, it is contemplated that for popular medications multiple dispensers 22 may include the same medication, thus allowing a single pathway 52 to interact with multiple dispensers 22.
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In use, pathway disc 50 and dispensing disc 20, including pathways 52 and dispensers 22, are cleaned in cleaning area 94. Additionally, dispensers 22 are filled and refilled in cleaning area 94.
Top surface 62 of pathway disc 50 is generally co-planar with top surface 58 of pathways 52, and bottom surface 64 of pathway disc 50 is generally co-planar with bottom surface 60 of pathways 52. Outer periphery 68 of pathways 52 is arcuately co-planar with periphery 70 of pathway disc 50 (best shown in
Similarly, top surface 32 of dispensing disc 20 is generally co-planar with top surface 28 of dispensers 22, and bottom surface 34 of dispensing disc 20 is generally co-planar with bottom surface 30 of dispensers 22. Outer periphery 38 of dispensing disc 20 is arcuately co-planar with periphery 40 of dispensing disc 20 (best shown in
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All references, including publications, patent applications, and patents cited herein are hereby incorporated by reference to the same extent as if each reference were individually and specifically indicated to be incorporated by reference and were set forth in its entirety herein.
The use of the terms “a” and “an” and “the” and similar referents in the context of describing the invention (especially in the context of the following claims) is to be construed to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context. The terms “comprising,” “having,” “including,” and “containing” are to be construed as open-ended terms (i.e., meaning “including, but not limited to,”) unless otherwise noted. Recitation of ranges of values herein are merely intended to serve as a shorthand method of referring individually to each separate value falling within the range, unless otherwise indicated herein, and each separate value is incorporated into the specification as if it were individually recited herein. All methods described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context. The use of any and all examples, or exemplary language (e.g., “such as”) provided herein, is intended merely to better illuminate the invention and does not pose a limitation on the scope of the invention unless otherwise claimed. No language in the specification should be construed as indicating any non-claimed element as essential to the practice of the invention.
Preferred embodiments of this invention are described herein, including the best mode known to the inventors for carrying out the invention. Variations of those preferred embodiments may become apparent to those of ordinary skill in the art upon reading the foregoing description. The inventors expect skilled artisans to employ such variations as appropriate, and the inventors intend for the invention to be practiced otherwise than as specifically described herein. Accordingly, this invention includes all modifications and equivalents of the subject matter recited in the claims appended hereto as permitted by applicable law. Moreover, any combination of the above-described elements in all possible variations thereof is encompassed by the invention unless otherwise indicated herein or otherwise clearly contradicted by context.