Oral solid packagers are well known as equipment that can produce bar-coded packets of oral solids (including liquids and powders), such as medications, pills, vitamins, candy, nuts, etc. With the bar codes provided on the package, it is possible to track the packets of oral solids dispensed. For instance, if the packager is used to dispense medications, the bar codes are used to track medication so that the hospital knows which patient was given what medication and at what time. This helps reduce the medication error rate in hospital settings.
The newest generation of packagers is referred to as high-speed packagers because they are able to produce bar-coded packages at much higher rates. A high-speed packager can produce unit dosed (one oral solid per package) packages at rates near or above 60 packets a minute or a multi-dose package (more than one oral solid per package) at rates near or above 50 packages a minute.
In a packager, each oral solid is placed in a singulating device that is calibrated specifically for that oral solid. Typically, upon command from the software, an oral solid drops from the singulating device and travels down a common chute or pathway, which leads to the packaging mechanism. The oral solid is then inserted into the package, which is then sealed. Either prior or subsequent to receiving the oral solid, information, including the bar code, is printed on the package.
Using a common pathway to dispense the oral solids causes several problems. Residue from one or more oral solids may remain in the pathway. Subsequent oral solids traveling along the same pathway will be contaminated by the residues from the previous oral solids. This may cause problems when, for instance, an end user receives an oral solid that is contaminated by residue from another oral solid and the end user cannot tolerate the residue. For example, a patient receiving a drug contaminated by the residues of other drugs can have unpredictable reactions for the patient due to allergies or drug interactions. The dust may also be dangerous to the technicians who have to clean the pathways, since daily cleaning is usually a requirement. The same problems occur when the packager delivers liquid medications or medications in powdered form. Oral solids can also jam in common pathways, requiring user intervention. If a jam condition is undetected, an opportunity exists for a package to not receive its intended medication, potentially endangering patients.
A device may be used to deliver each oral solid separately into the packaging mechanism to eliminate any cross-contamination. However, a collection device must often be used to channel the oral solids into a package, which is thereafter sealed by the packaging mechanism. The collection device therefore becomes contaminated with the residues from each oral solid. The collection device may be cleaned, reused or discarded as required, fostering a clean, zero cross-contaminated oral solid delivery path. Thus, there is a need for a device that allows for the delivery of oral solids from multiple, separate points of origin into a single common destination without cross-contamination.
The present disclosure provides a collection device having a base with at least first and second openings and at least first and second collector tubes in communication with the at least first and second openings in the base. The collector tubes each have a curvature configured to define a trajectory path for an object descending in the collector tube toward a common target region below the collection device. The collector tubes are configured to be placed into communication with corresponding unique transport tubes/channels/paths, etc., originating at a singulating device,
This summary is provided to introduce a selection of concepts in a simplified form that are further described below in the Detailed Description. This summary is not intended to identify key features of the claimed subject matter, nor is it intended to be used as an aid in determining the scope of the claimed subject matter.
The foregoing aspects and many of the attendant advantages of the present disclosure will become more readily appreciated by reference to the following detailed description, when taken in conjunction with the accompanying drawings, wherein:
Referring to
The common area may be defined by an intermediate collection device such as a package supplied by a packaging mechanism (not shown) or a funnel F or other suitable device for delivering the oral solids to the packaging mechanism. The common area or intermediate collection device will hereinafter be referred to as a “funnel F” for ease of description. The zero cross-contamination collector 10 receives the oral solids from unique, separate oral solid transport tubes T of the dispensing device D and delivers the oral solids into the funnel F.
The zero cross-contamination collector 10 eliminates the physical interaction of the channels of the dispensing device, thereby providing a means to collect the oral solids without cross-contamination. It should be appreciated that the zero cross-contamination collector 10 may be used to deliver any suitable object into a common area where zero cross-contamination is desired. Moreover, although the collector 100 is referred to throughout this specification as a “zero cross-contamination collector,” it should be apparent that such reference is merely a matter of convenience and is not intended to be limiting.
Referring to
The base 14, when in use with the dispensing device, is positioned relative to a support surface (not shown), such as the ground, such that the upper and lower surfaces 16 and 20 of the base 14 are substantially horizontal with respect to the support surface. Thus, directional terms will be used throughout the disclosure with reference to the position of the base 14, such as upwardly, downwardly, vertically, horizontally, etc. It should be appreciated that these directional terms are used for reference only, and should not be seen as limiting the scope of the present disclosure.
A plurality of openings 18 are formed in the base 14 that extend from the upper surface 16 to the lower surface 20 with the axis of each opening 18 substantially transverse to the upper and lower surfaces 16 and 20. A suitable number of openings 18 are arranged in any preferred pattern on the base 14. Preferably, the openings 18 are arranged in a concentric circular pattern on the base 14 starting with a single opening 18 formed in the center of the base 14. The openings 18 may be any suitable shape and size to be placed into communication with a corresponding oral solid transport tube T of the dispensing device D to accept different medications from the different oral solid transport tubes (see
The openings 18 may all be the same diameter to provide a uniform interface for mating with oral solid transport tubes T of uniform cross section. In the alternative, the openings 18 may vary in diameter to increase the versatility and/or reduce the footprint of the zero cross-contamination collector 10. For instance, the diameter of the openings 18 may gradually decrease in size from the center of the base 14 towards the outer circumference of the base 14. In this manner, smaller oral solid transport tubes T may be used to dispense smaller oral solids, thereby reducing the overall size of the zero cross-contamination collector 10 and increasing its versatility.
Each of the openings 18 are in communication with a collector tube 22 that extends downwardly from the lower surface of the base 14. The collector tubes 22 provide a curved interface for directing an oral solid traveling down a vertical or substantially vertical oral solid transport tube toward the funnel F. The collector tubes 22 may be formed from any suitable material such as a chemically inert plastic material or other suitable material that can be easily formed and produced.
The collector tubes 22 are substantially circular in cross section, and the outer diameter of the collector tubes 22 are substantially equal to the inner diameter of the openings 18 such that the collector tubes 22 may be tightly received within the openings 18. A notch may be formed within each of the openings 18 that defines a shoulder 24 between the upper and lower surfaces 16 and 20 of the base 14. Each collector tube 22 may include a cantilevered finger 28 extending along an end portion of the collector tubes 22 that passes over the shoulder 24 such that the collector tube 22 is snap fit into the opening 18. A shoulder 32 may also be formed on the exterior surface of each collector tube 22 that engages the lower surface 20 of the base 14 to help ensure that the end of the collector tube 22 is flush with the upper surface 16 of the base 14. However, it should be appreciated that the collector tubes 22 may instead be placed into communication with the openings 18 in any other suitable manner. For instance, the collector tubes 22 may instead be integrally formed with the base 14 during a molding process or other suitable manufacturing process.
Each collector tube 22 preferably includes a vertical portion 30 extending downwardly from the opening 18 and a curved portion 26 extending downwardly and inwardly from the vertical portion 30. Each of the vertical portions 30 of the collector tubes 22 are preferably in substantial vertical alignment when received within the openings 18 such that the collector tubes 22 can be easily placed into communication with corresponding vertical oral solid transport tubes T of a dispensing device D for the delivery of a specific oral solid into the funnel F (see
Each collector tube 22 is adapted to be placed into communication with the end of a dedicated oral solid transport tube T in any suitable manner. For instance, referring to
As the oral solids descend into the collector tubes 22, the curved portions 26 direct the oral solids toward the funnel F through an end opening 40. The curved portions 26 also define a smooth travel path to help eliminate shattering or lodging of the oral solids after a gravity-driven descent through the oral solid transport tube. The curved portions 26 of the collector tubes 22 gradually increase in radial curvature from the center of the base 14 toward the outer circumference of the base 14. More specifically, the collector tube 22 mated with the center opening 18 has a substantially vertical curved portion 26 (or no curved portion 26) to define an end opening 40 with a substantially vertical axis of opening such that the descending oral solids are dropped directly below into the funnel F. Accordingly, it should be appreciated that the center opening 18 may instead dispense oral solids without the use of a collector tube 22; i.e., the oral solid may instead drop through the opening 18 and directly into the funnel F.
The curved portions 26 of the collector tubes 22 mated with the openings 18 near the outer circumference of the base 14 have a radius of curvature to define an end opening 40 with a substantially horizontal axis of opening. The curved portions 26 of the collector tubes 22 mated with the openings 18 between the center and the outer circumference of the base 14 gradually increase in radial curvature to define end openings 40 increasing from a vertical axis of opening to a horizontal axis of opening.
The collector tubes 22 also increase in length from the center of the base 14 toward the outer circumference of the base 14. In this manner, the ends of the collector tubes 22 collectively define an interior substantially hemispherical cavity 42. The interior substantially hemispherical cavity 42 defines half of a target sphere having a center. The axes of each of the collector tube openings 40 are directed toward the center of the target sphere such that oral solids are ejected through the end openings 40 toward the target sphere center, or toward a common “target region.”
The target region is defined by the trajectory path of the oral solids as they are guided by the collector tubes 22 and exit the end openings 40. Thus, the target region is located just below the target sphere center since the oral solids are pulled downwardly by gravitational effects as they are ejected from the openings 40 toward the target sphere center. As shown in
Referring to
Although any suitable drop sensor assembly may be used, the assembly is preferably defined by a plurality of light sensors or other suitable sensors that can detect the oral solid without contacting the oral solid. For instance, the sensor assembly may be comprised of opto-reflective or interrupt sensors, a photodiode array, a light curtain, etc.
Referring to
The oral solid S drops downwardly into the funnel F due to gravitational effects. As the oral solid S is dropped down into the funnel F, the oral solid S trips a sensor in the sensor assembly. If an error occurs (i.e., more than one oral solid is dispensed), a signal is sent to the computer for processing and notifying a user of the error. After the predetermined quantity of oral solids are dispensed into the funnel F (either for a specific individual or for a specific type of oral solid), the funnel F is moved to deliver the dose of oral solids to a packaging mechanism or other suitable device. The funnel F may be disposed of or reused for the same individual or type of medication. In this manner, the oral solids are delivered to the packaging mechanism without any cross-contamination between types of oral solids or between doses of oral solids.
The zero cross-contamination collector 10 eliminates the physical interaction of the oral solid transport tubes of the dispensing device, thereby providing a means to collect the oral solids without cross-contamination. Moreover, the zero cross-contamination collector 10 converges the oral solid transport tubes for delivery of the oral solids into a funnel F of usable size. It should be appreciated that without the use of the zero cross-contamination collector 10, the funnel F would need to be sized to catch an oral solid being dropped from all the dispensing oral solid transport tubes. Thus, the zero cross-contamination collector also reduces the footprint of the collection device required to funnel the oral solids into the packaging mechanism.
Referring to
The hollow base 114, when in use with the dispensing device, is positioned relative to a support surface (not shown), such as the ground, such that the lower circular edge 124 is substantially horizontal with respect to the support surface and the substantially hemispherical interior cavity 142 opens toward the support surface. Thus, directional terms will be used throughout the disclosure with reference to the position of the hollow base 114, such as upwardly, downwardly, vertical, horizontal, etc. It should be appreciated that these directional terms are used for reference only, and should not be seen as limiting the scope of the present disclosure.
A plurality of openings 118 are formed in the hollow base 114 and are arranged in any suitable pattern. Preferably, the openings 118 are arranged in a concentric circular pattern on the hollow base 114 starting with a single opening 118 formed centrally in the flattened circular top portion 116 of the base 114. Moreover, the openings 118 may be any suitable shape and size to accept different medications from different oral solid transport tubes. As described above with reference to the preferred embodiment, the openings 118 are preferably circular in cross section and vary in diameter to be mated with different oral solid transport tubes of the dispensing device.
As can best be seen by referring to
A majority of the openings 118 are preferably in communication with a collector tube 122 that extends outwardly and upwardly from the exterior surface of the hollow base 114. The collector tubes 122 provide a curved interface for mating the openings 118 with a substantially vertical oral solid transport tube of the dispensing device and guiding the oral solids toward a common area as they exit the openings 118. However, it should be appreciated that the openings 118 may instead be placed into direct communication with a curved oral solid transport tube of the dispensing device without the need for a collector tube 122. In this case, the curved oral solid transport tube of the dispensing device would be considered a “collector tube.”
The collector tubes 122 may be formed from any suitable material such as a chemically inert plastic material or other suitable material that can be easily formed and produced. However, it is preferred that the collector tubes 122 are formed from the same material as the hollow base 114. Moreover, the collector tubes 122 may be formed independently and thereafter mated with the hollow base 114 in any suitable manner, or the collector tubes 122 may instead be integrally formed with the hollow base 114 during a molding process or other suitable manufacturing process.
Each collector tube 122 preferably includes a curved portion 126 extending from the opening 118 and a vertical portion 130 extending upwardly from the curved portion 126. The curved portions 126 of the collector tubes 122 have a smooth curvature to help eliminate shattering or lodging of oral solids after a gravity-driven descent through the channels. The vertical portions 130 of each of the collector tubes 122 are preferably in substantial vertical alignment such that the collector tubes 122 can be easily mated with corresponding vertical oral solid transport tubes of a dispensing device. However, it should be appreciated that the collector tubes 122 may instead extend outwardly from the base 114 at any suitable angle to be mated with the oral solid transport tubes of the dispensing device.
With the vertical portions 130 of the collector tubes 122 in substantial vertical alignment, and with the axis of the openings 118 changing from vertical to horizontal as described above, the curved portions 126 of the collector tubes 122 gradually increase in radial curvature from the top center of the base 114 toward the lower circular edge 124 of the base 114. As described above, the openings 118 defined on the substantially flat circular portion 116 have a substantially vertical axis of opening. Thus, the curved portions 126 of the collector tubes 122 mated with the openings 118 formed on the substantially flat circular portion 116 would have substantially no radius of curvature. Accordingly, the top openings 118 formed on the substantially flat circular portion 116 may instead be placed into direct communication with the oral solid transport tubes of the dispensing device without the use of a collector tube 122.
Each collector tube 122 may be placed into communication with a corresponding oral solid transport tube of the dispensing device in a substantially similar manner as that described above with reference to the preferred embodiment or any other suitable manner to provide a smooth, continuous path for the dispensed oral solid as it travels downwardly towards the common area. Each channel of the dispensing device dispenses only one specific type of oral solid, eliminating the cross-contamination of “oral solid dust” or other residue.
The oral solids are delivered to the collector tubes 122 and are ejected from the bottom of the openings 118 toward the center of the target sphere defined by the substantially hemispherical interior cavity 142, or a common “target region.” The target region is defined by the trajectory path of the oral solids as they are guided by the collector tubes 122 and exit the openings 118. The target region of each collector tube 122 is preferably just below the center of the target sphere since the oral solids are pulled downwardly by gravitational effects as they are ejected from the openings 118 toward the center of the target sphere.
A collection device, package, funnel, etc., specific to an individual or type of oral solid is located in the common area below the target region to receive a single oral solid or combination of oral solids passing through the zero cross-contamination collector 110. In this manner, only oral solids for one individual or oral solids of the same type are cross-contaminated within the collection device or package.
While the preferred embodiment of the present disclosure has been illustrated and described, it will be appreciated that various changes can be made therein without departing from its spirit and scope.
This application claims the benefit of U.S. Provisional Patent Application No. 61/017,133, filed on Dec. 27, 2007, the disclosure of which is hereby expressly incorporated by reference.
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Number | Date | Country | |
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20090194559 A1 | Aug 2009 | US |
Number | Date | Country | |
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61017133 | Dec 2007 | US |