US20140048430A1 - Cap and container assembly for a dosage product - Google Patents
Cap and container assembly for a dosage product Download PDFInfo
- Publication number
- US20140048430A1 US20140048430A1 US14/000,536 US201214000536A US2014048430A1 US 20140048430 A1 US20140048430 A1 US 20140048430A1 US 201214000536 A US201214000536 A US 201214000536A US 2014048430 A1 US2014048430 A1 US 2014048430A1
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- US
- United States
- Prior art keywords
- plunger
- assembly
- cap
- channel
- container
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/14—Details; Accessories therefor
- A61J1/20—Arrangements for transferring or mixing fluids, e.g. from vial to syringe
- A61J1/2003—Accessories used in combination with means for transfer or mixing of fluids, e.g. for activating fluid flow, separating fluids, filtering fluid or venting
- A61J1/2006—Piercing means
- A61J1/201—Piercing means having one piercing end
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/14—Details; Accessories therefor
- A61J1/18—Arrangements for indicating condition of container contents, e.g. sterile condition
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D43/00—Lids or covers for rigid or semi-rigid containers
- B65D43/02—Removable lids or covers
- B65D43/0235—Removable lids or covers with integral tamper element
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D51/00—Closures not otherwise provided for
- B65D51/24—Closures not otherwise provided for combined or co-operating with auxiliary devices for non-closing purposes
- B65D51/28—Closures not otherwise provided for combined or co-operating with auxiliary devices for non-closing purposes with auxiliary containers for additional articles or materials
- B65D51/2807—Closures not otherwise provided for combined or co-operating with auxiliary devices for non-closing purposes with auxiliary containers for additional articles or materials the closure presenting means for placing the additional articles or materials in contact with the main contents by acting on a part of the closure without removing the closure, e.g. by pushing down, pulling up, rotating or turning a part of the closure, or upon initial opening of the container
- B65D51/2814—Closures not otherwise provided for combined or co-operating with auxiliary devices for non-closing purposes with auxiliary containers for additional articles or materials the closure presenting means for placing the additional articles or materials in contact with the main contents by acting on a part of the closure without removing the closure, e.g. by pushing down, pulling up, rotating or turning a part of the closure, or upon initial opening of the container the additional article or materials being released by piercing, cutting or tearing an element enclosing it
- B65D51/2828—Closures not otherwise provided for combined or co-operating with auxiliary devices for non-closing purposes with auxiliary containers for additional articles or materials the closure presenting means for placing the additional articles or materials in contact with the main contents by acting on a part of the closure without removing the closure, e.g. by pushing down, pulling up, rotating or turning a part of the closure, or upon initial opening of the container the additional article or materials being released by piercing, cutting or tearing an element enclosing it said element being a film or a foil
- B65D51/2835—Closures not otherwise provided for combined or co-operating with auxiliary devices for non-closing purposes with auxiliary containers for additional articles or materials the closure presenting means for placing the additional articles or materials in contact with the main contents by acting on a part of the closure without removing the closure, e.g. by pushing down, pulling up, rotating or turning a part of the closure, or upon initial opening of the container the additional article or materials being released by piercing, cutting or tearing an element enclosing it said element being a film or a foil ruptured by a sharp element, e.g. a cutter or a piercer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D51/00—Closures not otherwise provided for
- B65D51/24—Closures not otherwise provided for combined or co-operating with auxiliary devices for non-closing purposes
- B65D51/28—Closures not otherwise provided for combined or co-operating with auxiliary devices for non-closing purposes with auxiliary containers for additional articles or materials
- B65D51/30—Closures not otherwise provided for combined or co-operating with auxiliary devices for non-closing purposes with auxiliary containers for additional articles or materials for desiccators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/14—Details; Accessories therefor
- A61J1/1412—Containers with closing means, e.g. caps
- A61J1/1418—Threaded type
Definitions
- the invention pertains to a cap and container assembly for mixing and/or storage of a dosage material and carrier.
- dosage products may be, for example, in solid or concentrated liquid form.
- Solid dosage products can be provided in a variety of forms including powders, granules, pucks, tablets and capsules.
- the carrier is often in liquid form but may take on a solid form as well.
- Dosage products have the advantage of delaying interaction between the dosage product and the carrier, which can extend shelf life.
- Such products may include consumables and nonconsumables. Examples of consumable dosage products include food or beverage mixes, nutritional supplements, and pharmaceuticals.
- Dosage products may be sold as two component systems including the dosage product and the carrier, or alternatively the dosage product may be sold alone where, for example, the carrier is a readily available substance, such as water.
- Two component systems have the advantage of providing all necessary ingredients in a single system or package, whereas dosage product only systems have the advantage of compactness and ease of transport.
- Typical steps for use of a dosage product include placing the carrier in a suitable receptacle, unpackaging the dosage product and adding it to the receptacle, and mixing the dosage product with the carrier by agitating or stifling with a utensil.
- This process involves numerous steps and often a suitable receptacle is not available.
- a suitable carrier may not always be available.
- many dosage product systems cannot be mixed in the same receptacle as that which the carrier was initially stored in.
- the present invention is directed to a dosage dispensing cap and container assembly.
- the assembly includes a container defining an opening that leads to an interior space.
- a cap is removably affixed over the opening and defines a channel that leads to the interior space.
- the cap includes a puncturing structure positioned at a bottom region of the channel.
- a plunger is slidably disposed within the channel and includes a sleeve portion and a dosage product housed within the sleeve portion. The plunger slides within the channel between a first position in which the plunger is located in an upper region of the channel, and a second position in which the plunger is located in a lower region of the channel and the dosage product contacts the puncturing structure.
- the present invention is further directed to a method of dispensing a dosage product within a carrier.
- the method includes providing a dosage dispensing cap and container assembly including a container defining an opening that leads to an interior space, a cap removably affixed over the opening, and a plunger slidably disposed within the channel.
- the cap defines a channel that leads to the interior space of the container and includes a puncturing structure positioned at a bottom region of the channel.
- the plunger includes a sleeve portion and a dosage product housed within the sleeve portion.
- the method further includes sliding the plunger within the channel from a first position in which the plunger is located in an upper region of the channel, to a second position in which the plunger is located in a lower region of the channel and the dosage product is in contact with the puncturing structure.
- FIG. 1 shows a perspective view of a first embodiment of the dosage dispensing cap and container assembly
- FIG. 2 shows a cross sectional view of the assembly of FIG. 1 in the starting position
- FIG. 3 shows a cross sectional view of the assembly of FIG. 1 in the dispensing position
- FIG. 4 shows a top view of an embodiment of a cap for the dosage dispensing cap and container assembly shown in FIG. 1 ;
- FIG. 5 shows a side view of an embodiment of a plunger for the dosage dispensing cap and container assembly shown in FIG. 1 ;
- FIG. 6 shows a perspective view of a second embodiment of the dosage dispensing cap and container assembly having a tamper evident device
- FIG. 7 shows a cross sectional view of the assembly of FIG. 6 in the starting position
- FIG. 8 shows a cross sectional view of the assembly of FIG. 7 in the dispensing position.
- FIGS. 1-3 A first embodiment of a dosage dispensing cap and container assembly 10 is shown in FIGS. 1-3 .
- the assembly includes a container 20 , a cap 40 , and a plunger 60 .
- the container 20 , cap 40 , and/or plunger 60 may be injection molded from a polymeric material, such as a thermoplastic material, such as, for example, a polypropylene, such as a moisture blocking polymeric material.
- an active agent such as a desiccating agent, and channeling agent may be blended into the polymer to produce an active material. Examples of such active materials are disclosed in one or more of U.S. Pat. Nos.
- the container 20 , cap 40 , and/or plunger 60 may contain a desiccant material, wherein the desiccant material is separately injection molded and assembled or formed in two shots in one injection mold.
- the container 20 includes a housing portion 22 for housing a carrier 14 and configured for receiving a dispensed dosage product 12 .
- the carrier 14 may be any type of liquid suitable for mixture with the dosage product 12 .
- suitable carriers include consumable liquids such as water, juice, or milk.
- suitable carriers include nonconsumable liquids such as solvents, as well as both consumable and nonconsumable solid materials such as powders and granules.
- the dosage product 12 can be any type of dosage product suitable for mixture with a carrier.
- suitable dosages 12 include consumable materials for mixture with consumable carriers, such as pharmaceutical products, supplements, and food products.
- Other examples of suitable dosages include nonconsumable materials for mixture with nonconsumable carriers, including colorants and fragrances.
- the dosage product 12 can be provided in any form that allows it to be mixed with the carrier, including solid forms such as powders, granules, puck, pill or tablet forms.
- the dosage product may also be provided in liquid form.
- the dosage product 12 Prior to dispensing, the dosage product 12 can optionally be housed in a rupturable package, such as a foil, paper or plastic package, or may be provided free of packaging.
- the housing portion 22 has a generally tubular body 24 with a base 26 portion for seating the container 20 on a surface.
- the container 20 may take on other shapes suitable for housing the carrier 14 and receiving the dosage product 12 as well, including, square, rectangular, trapezoidal, circular, and non-circular, among others.
- a generally cylindrical neck 28 extends upward from the housing portion 22 and defines an opening 30 .
- the neck 28 has a smaller diameter than the cylindrical body 24 of the housing portion 22 , but this is not required.
- the neck 28 is configured for attachment of the cap 40 , as described in detail below.
- the cap 40 of the assembly 10 is shown.
- the cap 40 includes an inner tubular body 42 and an outer tubular body 44 .
- the inner tubular body 42 is located within the neck 28 and the outer tubular body 44 is located outside of the neck 28 .
- the inner tubular body 42 and the outer tubular body 44 are joined at their respective upper ends by a connecting wall 46 , forming a substantially inverted U-shaped cross section, as shown in FIGS. 2 and 3 .
- the connecting wall 46 sits on the upper end of the neck 28 in the configuration shown in FIGS. 2 and 3 , though the connecting wall 46 need not actually contact the upper end of the neck 28 .
- the cap 40 can be affixed to the container 20 in a variety of ways.
- the cap 40 and container 20 are affixed by a threaded connection.
- Outer threads 32 are defined on an outer surface of the neck 28 and engage inner threads 48 defined on an inner surface of the outer tubular body 44 of the cap 40 .
- other types of connections can be used to affix the cap 40 to the container 20 , for example, other types of mechanical connections such as a snap fit or interference fit.
- the cap 40 further includes an inner base portion 50 located at the bottom of the inner tubular body 42 . As shown in FIG. 2 , the inner base portion 50 sits within the container 20 when the cap 40 is affixed over the opening 30 . The inner base portion 50 preferably sits above the carrier 14 located within the container 20 when the container 20 is in an upright position.
- the inner base portion 50 includes a puncturing structure 76 having a projection 52 that assists in dispensing the dosage product 12 , as described in detail below.
- a lower channel 56 is defined between the projection 52 and a portion of the inner tubular body 42 for passage of the dosage product 12 during dispensing.
- the inner base portion 50 includes at least one arm 70 that inwardly extends from the inner tubular body 42 and to the puncturing structure 76 .
- the inner base portion 50 includes three arms 70 a , 70 b , 70 c .
- the arms 70 a , 70 b , 70 c may be spaced apart from each other so as to provide one or more lower channels 56 a , 56 b , 56 c for the dosage 12 to be dispensed to the carrier 14 .
- the arms may include one or more orifices that form the lower channel 56 or other openings that allow for the passage of the dosage 12 through the inner base portion 50 and to the carrier 14 .
- at least a portion of the inner base portion 50 may be configured to direct dosage product 12 toward the lower channel 56 .
- the arms 70 a , 70 b , 70 c may include one or more angled upper surfaces beneath at least a portion of the projection 52 that is/are angled to direct the dosage 12 toward the lower channel 56 .
- the puncturing structure 76 may have puncturing arms 78 a , 78 b , 78 c , that are extend toward the projection 52 . Further, according to certain embodiments, the puncturing arms 78 a , 78 b , 78 c may have angled upper walls that provide an apex 80 a , 80 b , 80 c along the puncturing arms 78 a , 78 b , 78 c that assist in the puncturing or breakage of the dosage product 12 or the packaging for the dosage product 12 , and/or assist in directing the dosage product 12 toward the lower channels 56 .
- the plunger 60 includes a plunger tube 62 and an upper wall 64 .
- the plunger tube 62 is slidably disposed within the inner tubular body 42 of the cap 40 .
- the plunger 60 slides between a first or starting position, shown in FIG. 2 , and a second or dispensing position, shown in FIG. 3 .
- the upper wall 64 may extend beyond the plunger tube 62 , as shown in the illustrated embodiment, so as to define a flange 66 .
- the flange 66 prevents the plunger 60 from sliding further downward than when in the dispensing position.
- the plunger 60 may include at least one protrusion 72 , such as a rib, flange, or thread, among others, that mate with a recess 74 in the inner tubular body 42 so as to prevent the inadvertent movement of the plunger 60 from the starting position. Moreover, the mating engagement of the protrusion 72 and recess 74 may prevent the plunger 60 from being moved from the starting position before the dosage product 12 is intended to be dispensed into the carrier 14 . According to an embodiment, in use, a user may depress the plunger 60 with sufficient force to disengage the protrusion 72 from the recess 74 , and allow the plunger 60 to be displaced from the starting position.
- a protrusion 72 such as a rib, flange, or thread, among others
- the protrusion 72 and recess 74 may be mating external and internal threads, respectively, that require the user to, at least initially, turn of the plunger 60 relative to the inner wall member 60 to move the plunger 60 from the starting position.
- the plunger 60 may also be at least partially held or retained in the starting position through the use of other mechanisms, including, for example, a removable collar or tampering evident device positioned between a portion of the plunger 60 and the cap 40 , such as the first tamper evidence device 170 discussed below, among others.
- An interior space 68 that houses the dosage product 12 prior to dispensing is defined within the plunger tube 62 .
- the interior space 68 is closed off at a top portion thereof by the upper wall 64 and optionally at a bottom portion by a lower frangible wall 58 .
- the lower frangible wall 58 may be formed of any material that is easily ruptured by manual force, such as foil, paper or a thin sheet of plastic.
- the lower frangible wall 58 supports the dosage product 12 , but in embodiments where the lower frangible wall 58 is omitted, other structures could be provided for supporting the dosage product 12 , such as a wall that extends within the plunger tube 62 for only a portion of the diameter thereof. Such structures should be sufficient in extent to support the dosage product 12 , while still allowing the projection 52 to contact the dosage product 12 when the plunger 60 is depressed, as shown in FIG. 3 .
- the dosage product 12 is distributed within the carrier 14 by sliding the plunger 60 from the starting position shown in FIG. 2 to the dispensing position shown in FIG. 3 . This causes the projection 52 to contact the dosage product 12 .
- the lower frangible wall 58 it is ruptured by the projection 52 during sliding.
- this package is ruptured by the projection during sliding.
- the dosage product 12 may be ruptured by the projection during sliding, however this is not required, and in other embodiments the pill or tablet may remain in-tact and be subsequently dissolved by the carrier 14 .
- Rupture of one or more of the dosage product 12 , lower frangible wall 58 , or packaging of the dosage product 12 by the projection 52 allows the dosage product 12 to exit the interior space 68 of the plunger tube 62 .
- the dosage product 12 then passes downward through the lower channel(s) 56 of the cap 40 and into the housing portion 22 of the container for mixing with the carrier 14 .
- the assembly 10 can optionally be shaken by a user to optimally distribute the dosage product 12 within the carrier 14 .
- the cap 40 can then be removed from the container 20 , by unscrewing in the illustrated example, allowing a user to access the mixture of dosage product 12 and carrier 14 , or the mixture may flow out of the housing portion 22 through the lower channel(s) 56 .
- FIGS. 6-8 A second embodiment of a dosage dispensing cap and container assembly 110 is shown in FIGS. 6-8 .
- the second embodiment of the assembly 110 includes many of the same features as the first embodiment, and such features should be considered the same or structurally equivalent unless otherwise described or shown in the drawings.
- the second embodiment of the assembly differs from the first embodiment in that it includes a first tamper evident device 170 .
- the first tamper evident device 170 includes a tubular sleeve 172 that extends between a portion of the plunger 160 and a portion of the cap 140 to prevent depression of the plunger 160 .
- the sleeve 172 extends between the flange 166 of the plunger 160 and the connecting wall 146 of the cap 140 .
- the sleeve 172 is preferably dimensioned such that it cannot be removed from the assembly 110 without breakage.
- the sleeve 172 can be configured to allow for removal without breakage, but not for replacement on the assembly 110 once removed therefrom. In this respect, absence of the sleeve 172 on the assembly 110 indicates that the plunger 160 may have been previously depressed, and the dosage 112 distributed in the carrier 114 .
- the first tamper evident device 170 may optionally include removal structures including a pull tab 174 and perforations 176 .
- removal structures including a pull tab 174 and perforations 176 .
- the sleeve 172 can be split along the perforations 176 , permitting removal of the sleeve 172 .
- Alternative types of removal structures may include devices that allow the sleeve 172 to be removed from the assembly 110 in-tact, but not replaced thereon.
- the cap 140 , plunger 160 , or both, may optionally be provided with centering structures to retain the first tamper evident device 170 in a centered position on the assembly 110 .
- the cap 140 and plunger 160 each include outwardly projecting collars 141 , 161 , having outer diameters slightly less than the inner diameter of the sleeve 172 .
- the second embodiment of the assembly 110 may further include a second tamper evident device 180 .
- the second tamper evident device 180 includes a ring 182 attached to the cap 140 by a severable attachment mechanism.
- the attachment mechanism includes a plurality of attachment tabs 184 that affix the ring 182 on the neck 128 of the container 120 at a position directly below the outer tubular body 144 of the cap 140 .
- the ring 182 is configured to remain in position on the neck 128 , even when the cap 140 is removed. In the illustrated embodiment, this is achieved by way of a lower abutment 186 provided on the ring 182 that engages an upper abutment 134 provided on the neck 128 .
- the lower abutment 186 extends inward from an inner surface of the ring 182
- the upper abutment extends outward from an outer surface of the neck 128 .
- the lower abutment 186 contacts the upper abutment 134 , preventing the ring 182 from moving upwards and being removed from the neck 128 , and causing breakage of the attachment tabs 182 .
- Broken attachment tabs 182 thus indicate that the cap 140 has previously been removed from the assembly 110 , and that possible tampering has occurred, such as addition to or removal from the contents of the container 120 .
- a third optional feature of the assembly shown in the embodiment of FIGS. 7-8 is a recessed upper wall 164 of the plunger 160 .
- the upper wall 164 and the flange 166 are separated, and instead of being positioned at an upper end of the plunger tube 162 , the upper wall 164 extends within the plunger tube 162 at a location below the upper end thereof. This permits the dosage 112 to be dispensed with a smaller downward depression of the plunger 160 , as the upper wall 164 forces the dosage 112 to come into contact with the projection 152 .
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Abstract
Description
- The invention pertains to a cap and container assembly for mixing and/or storage of a dosage material and carrier.
- Many consumer products are sold in forms intended to be mixed with a carrier to produce an end product. Such products (hereinafter referred to as “dosage products”) may be, for example, in solid or concentrated liquid form. Solid dosage products can be provided in a variety of forms including powders, granules, pucks, tablets and capsules. The carrier is often in liquid form but may take on a solid form as well. Dosage products have the advantage of delaying interaction between the dosage product and the carrier, which can extend shelf life. Such products may include consumables and nonconsumables. Examples of consumable dosage products include food or beverage mixes, nutritional supplements, and pharmaceuticals.
- Dosage products may be sold as two component systems including the dosage product and the carrier, or alternatively the dosage product may be sold alone where, for example, the carrier is a readily available substance, such as water. Two component systems have the advantage of providing all necessary ingredients in a single system or package, whereas dosage product only systems have the advantage of compactness and ease of transport.
- Typical steps for use of a dosage product include placing the carrier in a suitable receptacle, unpackaging the dosage product and adding it to the receptacle, and mixing the dosage product with the carrier by agitating or stifling with a utensil. This process involves numerous steps and often a suitable receptacle is not available. In dosage product only systems, a suitable carrier may not always be available. Additionally, many dosage product systems cannot be mixed in the same receptacle as that which the carrier was initially stored in. A need exists for a dosage product system including all necessary components for preparation, as well as a suitable receptacle for storage of the carrier, mixing of the dosage product and carrier, and storage of the mixed end product.
- The present invention is directed to a dosage dispensing cap and container assembly. The assembly includes a container defining an opening that leads to an interior space. A cap is removably affixed over the opening and defines a channel that leads to the interior space. The cap includes a puncturing structure positioned at a bottom region of the channel. A plunger is slidably disposed within the channel and includes a sleeve portion and a dosage product housed within the sleeve portion. The plunger slides within the channel between a first position in which the plunger is located in an upper region of the channel, and a second position in which the plunger is located in a lower region of the channel and the dosage product contacts the puncturing structure.
- The present invention is further directed to a method of dispensing a dosage product within a carrier. The method includes providing a dosage dispensing cap and container assembly including a container defining an opening that leads to an interior space, a cap removably affixed over the opening, and a plunger slidably disposed within the channel. The cap defines a channel that leads to the interior space of the container and includes a puncturing structure positioned at a bottom region of the channel. The plunger includes a sleeve portion and a dosage product housed within the sleeve portion. The method further includes sliding the plunger within the channel from a first position in which the plunger is located in an upper region of the channel, to a second position in which the plunger is located in a lower region of the channel and the dosage product is in contact with the puncturing structure.
-
FIG. 1 shows a perspective view of a first embodiment of the dosage dispensing cap and container assembly; -
FIG. 2 shows a cross sectional view of the assembly ofFIG. 1 in the starting position; -
FIG. 3 shows a cross sectional view of the assembly ofFIG. 1 in the dispensing position; -
FIG. 4 shows a top view of an embodiment of a cap for the dosage dispensing cap and container assembly shown inFIG. 1 ; -
FIG. 5 shows a side view of an embodiment of a plunger for the dosage dispensing cap and container assembly shown inFIG. 1 ; -
FIG. 6 shows a perspective view of a second embodiment of the dosage dispensing cap and container assembly having a tamper evident device; -
FIG. 7 shows a cross sectional view of the assembly ofFIG. 6 in the starting position; and -
FIG. 8 shows a cross sectional view of the assembly ofFIG. 7 in the dispensing position. - Certain terminology is used in the foregoing description for convenience and is not intended to be limiting. Words such as “front,” “back,” “top,” and “bottom” designate directions in the drawings to which reference is made. This terminology includes the words specifically noted above, derivatives thereof, and words of similar import. Additionally, the words “a” and “one” are defined as including one or more of the referenced item unless specifically noted. The phrase “at least one of” followed by a list of two or more items, such as “A, B or C,” means any individual one of A, B or C, as well as any combination thereof.
- A first embodiment of a dosage dispensing cap and
container assembly 10 is shown inFIGS. 1-3 . The assembly includes acontainer 20, acap 40, and aplunger 60. According to certain embodiments, thecontainer 20,cap 40, and/orplunger 60, or any particular component thereof, may be injection molded from a polymeric material, such as a thermoplastic material, such as, for example, a polypropylene, such as a moisture blocking polymeric material. Additionally, an active agent, such as a desiccating agent, and channeling agent may be blended into the polymer to produce an active material. Examples of such active materials are disclosed in one or more of U.S. Pat. Nos. 6,130,263, 6,080,350, 6,221,446, 6,124,006, 6,214,255, 6,194,079, 6,316,520, 6,465,532, 5,911,937, 6,174,952, 6,177,183, 6,486,231, 6,696,002, 6,460,271, 6,613,405, 6,852,783, RE40,941, and U.S. Pat. No. 7,005,459, which are incorporated herein by reference as if fully set forth. Alternatively, according to other embodiments, thecontainer 20,cap 40, and/orplunger 60 may contain a desiccant material, wherein the desiccant material is separately injection molded and assembled or formed in two shots in one injection mold. - The
container 20 includes ahousing portion 22 for housing acarrier 14 and configured for receiving a dispenseddosage product 12. Thecarrier 14 may be any type of liquid suitable for mixture with thedosage product 12. Examples of suitable carriers include consumable liquids such as water, juice, or milk. Other examples of suitable carriers include nonconsumable liquids such as solvents, as well as both consumable and nonconsumable solid materials such as powders and granules. Thedosage product 12 can be any type of dosage product suitable for mixture with a carrier. Examples ofsuitable dosages 12 include consumable materials for mixture with consumable carriers, such as pharmaceutical products, supplements, and food products. Other examples of suitable dosages include nonconsumable materials for mixture with nonconsumable carriers, including colorants and fragrances. Thedosage product 12 can be provided in any form that allows it to be mixed with the carrier, including solid forms such as powders, granules, puck, pill or tablet forms. The dosage product may also be provided in liquid form. Prior to dispensing, thedosage product 12 can optionally be housed in a rupturable package, such as a foil, paper or plastic package, or may be provided free of packaging. - In the illustrated embodiment, the
housing portion 22 has a generallytubular body 24 with abase 26 portion for seating thecontainer 20 on a surface. However, thecontainer 20 may take on other shapes suitable for housing thecarrier 14 and receiving thedosage product 12 as well, including, square, rectangular, trapezoidal, circular, and non-circular, among others. - A generally
cylindrical neck 28 extends upward from thehousing portion 22 and defines anopening 30. In the illustrated embodiment, theneck 28 has a smaller diameter than thecylindrical body 24 of thehousing portion 22, but this is not required. Theneck 28 is configured for attachment of thecap 40, as described in detail below. - Still referring to
FIGS. 1-3 , thecap 40 of theassembly 10 is shown. Thecap 40 includes an innertubular body 42 and an outertubular body 44. When thecap 40 is affixed over the opening 30 of thecontainer 20, the innertubular body 42 is located within theneck 28 and the outertubular body 44 is located outside of theneck 28. The innertubular body 42 and the outertubular body 44 are joined at their respective upper ends by a connectingwall 46, forming a substantially inverted U-shaped cross section, as shown inFIGS. 2 and 3 . The connectingwall 46 sits on the upper end of theneck 28 in the configuration shown inFIGS. 2 and 3 , though the connectingwall 46 need not actually contact the upper end of theneck 28. - The
cap 40 can be affixed to thecontainer 20 in a variety of ways. In the illustrated embodiment, thecap 40 andcontainer 20 are affixed by a threaded connection.Outer threads 32 are defined on an outer surface of theneck 28 and engageinner threads 48 defined on an inner surface of the outertubular body 44 of thecap 40. In alternative embodiments, other types of connections can be used to affix thecap 40 to thecontainer 20, for example, other types of mechanical connections such as a snap fit or interference fit. - The
cap 40 further includes aninner base portion 50 located at the bottom of the innertubular body 42. As shown inFIG. 2 , theinner base portion 50 sits within thecontainer 20 when thecap 40 is affixed over theopening 30. Theinner base portion 50 preferably sits above thecarrier 14 located within thecontainer 20 when thecontainer 20 is in an upright position. Theinner base portion 50 includes a puncturingstructure 76 having aprojection 52 that assists in dispensing thedosage product 12, as described in detail below. Alower channel 56 is defined between theprojection 52 and a portion of the innertubular body 42 for passage of thedosage product 12 during dispensing. - As shown in
FIG. 4 , according to an embodiment, theinner base portion 50 includes at least one arm 70 that inwardly extends from the innertubular body 42 and to the puncturingstructure 76. For example, as shown inFIG. 4 , according to certain embodiments, theinner base portion 50 includes threearms arms lower channels dosage 12 to be dispensed to thecarrier 14. Alternatively, the arms may include one or more orifices that form thelower channel 56 or other openings that allow for the passage of thedosage 12 through theinner base portion 50 and to thecarrier 14. Additionally, at least a portion of theinner base portion 50 may be configured to directdosage product 12 toward thelower channel 56. For example, thearms projection 52 that is/are angled to direct thedosage 12 toward thelower channel 56. - According to certain embodiments, the puncturing
structure 76 may have puncturingarms projection 52. Further, according to certain embodiments, the puncturingarms arms dosage product 12 or the packaging for thedosage product 12, and/or assist in directing thedosage product 12 toward thelower channels 56. - As shown in
FIGS. 2 and 3 , theplunger 60 includes aplunger tube 62 and anupper wall 64. Theplunger tube 62 is slidably disposed within the innertubular body 42 of thecap 40. Theplunger 60 slides between a first or starting position, shown inFIG. 2 , and a second or dispensing position, shown inFIG. 3 . Theupper wall 64 may extend beyond theplunger tube 62, as shown in the illustrated embodiment, so as to define aflange 66. As shown inFIG. 3 , theflange 66 prevents theplunger 60 from sliding further downward than when in the dispensing position. - As shown in
FIGS. 2 and 5 , according to an embodiment, theplunger 60 may include at least oneprotrusion 72, such as a rib, flange, or thread, among others, that mate with arecess 74 in the innertubular body 42 so as to prevent the inadvertent movement of theplunger 60 from the starting position. Moreover, the mating engagement of theprotrusion 72 andrecess 74 may prevent theplunger 60 from being moved from the starting position before thedosage product 12 is intended to be dispensed into thecarrier 14. According to an embodiment, in use, a user may depress theplunger 60 with sufficient force to disengage theprotrusion 72 from therecess 74, and allow theplunger 60 to be displaced from the starting position. According to another embodiment, theprotrusion 72 andrecess 74 may be mating external and internal threads, respectively, that require the user to, at least initially, turn of theplunger 60 relative to theinner wall member 60 to move theplunger 60 from the starting position. However, theplunger 60 may also be at least partially held or retained in the starting position through the use of other mechanisms, including, for example, a removable collar or tampering evident device positioned between a portion of theplunger 60 and thecap 40, such as the firsttamper evidence device 170 discussed below, among others. - An
interior space 68 that houses thedosage product 12 prior to dispensing is defined within theplunger tube 62. Theinterior space 68 is closed off at a top portion thereof by theupper wall 64 and optionally at a bottom portion by a lowerfrangible wall 58. The lowerfrangible wall 58 may be formed of any material that is easily ruptured by manual force, such as foil, paper or a thin sheet of plastic. In the illustrated embodiment, the lowerfrangible wall 58 supports thedosage product 12, but in embodiments where the lowerfrangible wall 58 is omitted, other structures could be provided for supporting thedosage product 12, such as a wall that extends within theplunger tube 62 for only a portion of the diameter thereof. Such structures should be sufficient in extent to support thedosage product 12, while still allowing theprojection 52 to contact thedosage product 12 when theplunger 60 is depressed, as shown inFIG. 3 . - The
dosage product 12 is distributed within thecarrier 14 by sliding theplunger 60 from the starting position shown inFIG. 2 to the dispensing position shown inFIG. 3 . This causes theprojection 52 to contact thedosage product 12. In embodiments where the lowerfrangible wall 58 is provided, it is ruptured by theprojection 52 during sliding. In embodiments where thedosage product 12 is provided with a rupturable package, this package is ruptured by the projection during sliding. In embodiments where the dosage product is provided in the form of a pill or tablet, with our without the lowerfrangible wall 58 and the rupturable package, thedosage product 12 may be ruptured by the projection during sliding, however this is not required, and in other embodiments the pill or tablet may remain in-tact and be subsequently dissolved by thecarrier 14. - Rupture of one or more of the
dosage product 12, lowerfrangible wall 58, or packaging of thedosage product 12 by theprojection 52 allows thedosage product 12 to exit theinterior space 68 of theplunger tube 62. Thedosage product 12 then passes downward through the lower channel(s) 56 of thecap 40 and into thehousing portion 22 of the container for mixing with thecarrier 14. Theassembly 10 can optionally be shaken by a user to optimally distribute thedosage product 12 within thecarrier 14. Thecap 40 can then be removed from thecontainer 20, by unscrewing in the illustrated example, allowing a user to access the mixture ofdosage product 12 andcarrier 14, or the mixture may flow out of thehousing portion 22 through the lower channel(s) 56. - A second embodiment of a dosage dispensing cap and
container assembly 110 is shown inFIGS. 6-8 . The second embodiment of theassembly 110 includes many of the same features as the first embodiment, and such features should be considered the same or structurally equivalent unless otherwise described or shown in the drawings. - The second embodiment of the assembly differs from the first embodiment in that it includes a first tamper
evident device 170. The first tamperevident device 170 includes atubular sleeve 172 that extends between a portion of theplunger 160 and a portion of thecap 140 to prevent depression of theplunger 160. In the illustrated embodiment, thesleeve 172 extends between theflange 166 of theplunger 160 and the connectingwall 146 of thecap 140. Thesleeve 172 is preferably dimensioned such that it cannot be removed from theassembly 110 without breakage. Alternatively, thesleeve 172 can be configured to allow for removal without breakage, but not for replacement on theassembly 110 once removed therefrom. In this respect, absence of thesleeve 172 on theassembly 110 indicates that theplunger 160 may have been previously depressed, and thedosage 112 distributed in thecarrier 114. - The first tamper
evident device 170 may optionally include removal structures including apull tab 174 andperforations 176. When tension is applied to thepull tab 174, thesleeve 172 can be split along theperforations 176, permitting removal of thesleeve 172. Alternative types of removal structures may include devices that allow thesleeve 172 to be removed from theassembly 110 in-tact, but not replaced thereon. - The
cap 140,plunger 160, or both, may optionally be provided with centering structures to retain the first tamperevident device 170 in a centered position on theassembly 110. In the illustrated embodiment thecap 140 andplunger 160 each include outwardly projectingcollars sleeve 172. - The second embodiment of the
assembly 110 may further include a second tamperevident device 180. The second tamperevident device 180 includes aring 182 attached to thecap 140 by a severable attachment mechanism. In the embodiment shown, the attachment mechanism includes a plurality ofattachment tabs 184 that affix thering 182 on theneck 128 of thecontainer 120 at a position directly below the outertubular body 144 of thecap 140. - The
ring 182 is configured to remain in position on theneck 128, even when thecap 140 is removed. In the illustrated embodiment, this is achieved by way of alower abutment 186 provided on thering 182 that engages anupper abutment 134 provided on theneck 128. Thelower abutment 186 extends inward from an inner surface of thering 182, and the upper abutment extends outward from an outer surface of theneck 128. When thecap 140 is removed from thecontainer 120, by rotating to disengage thethreads cap 140 is moved in an upward direction on theneck 128, prior to being completely removed therefrom. Thelower abutment 186 contacts theupper abutment 134, preventing thering 182 from moving upwards and being removed from theneck 128, and causing breakage of theattachment tabs 182.Broken attachment tabs 182 thus indicate that thecap 140 has previously been removed from theassembly 110, and that possible tampering has occurred, such as addition to or removal from the contents of thecontainer 120. - A third optional feature of the assembly shown in the embodiment of
FIGS. 7-8 is a recessedupper wall 164 of theplunger 160. In this embodiment theupper wall 164 and theflange 166 are separated, and instead of being positioned at an upper end of theplunger tube 162, theupper wall 164 extends within theplunger tube 162 at a location below the upper end thereof. This permits thedosage 112 to be dispensed with a smaller downward depression of theplunger 160, as theupper wall 164 forces thedosage 112 to come into contact with theprojection 152. - Further embodiments of the assembly could include only one of or any combination of the first or second tamper
evident devices upper wall 164 of the plunger. - While the preferred embodiments of the invention have been described in detail above, the invention is not limited to the specific embodiments described, which should be considered as merely exemplary.
-
-
10 Cap and Container Assembly 12 Dosage 14 Carrier 20 Container 22 Housing Portion 24 Body 26 Base 28 Neck 30 Opening 32 Outer Threads 40 Cap 42 Inner Tubular Body 44 Outer Tubular Body 46 Connecting Wall 48 Inner Threads 50 Inner Base Portion 52 Projection 56 Lower Channel 58 Lower Frangible Wall 60 Plunger 62 Plunger Tube 64 Upper Wall 66 Flange 68 Interior Space 70 Arm 72 Protrusion 74 Recess 76 Puncturing structure 78 Puncturing arms 80 Apex 110 Cap and Container Assembly 112 Dosage 114 Carrier 120 Container 122 Housing Portion 124 Body 126 Base 128 Neck 130 Opening 132 Outer Threads 134 Upper Abutment 140 Cap 141 Collar 142 Inner Tubular Body 144 Outer Tubular Body 146 Connecting Wall 148 Inner Threads 150 Inner Base Portion 152 Projection 156 Lower Channel 158 Lower Frangible Wall 160 Plunger 161 Collar 162 Plunger Tube 164 Upper Wall 166 Flange 168 Interior Space 170 First Tamper Evident Device 172 Sleeve 174 Pull Tab 176 Perforations 180 Second Tamper Evident Device 182 Ring 184 Attachment Tabs 186 Lower Abutment
Claims (20)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US14/000,536 US20140048430A1 (en) | 2011-03-08 | 2012-01-04 | Cap and container assembly for a dosage product |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161450386P | 2011-03-08 | 2011-03-08 | |
US14/000,536 US20140048430A1 (en) | 2011-03-08 | 2012-01-04 | Cap and container assembly for a dosage product |
PCT/US2012/020164 WO2012121796A2 (en) | 2011-03-08 | 2012-01-04 | Cap and container assembly for a dosage product |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2012/020164 A-371-Of-International WO2012121796A2 (en) | 2011-03-08 | 2012-01-04 | Cap and container assembly for a dosage product |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US15/178,792 Continuation US10524981B2 (en) | 2011-03-08 | 2016-06-10 | Cap and container assembly for a dosage product |
Publications (1)
Publication Number | Publication Date |
---|---|
US20140048430A1 true US20140048430A1 (en) | 2014-02-20 |
Family
ID=46798685
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
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US14/000,536 Abandoned US20140048430A1 (en) | 2011-03-08 | 2012-01-04 | Cap and container assembly for a dosage product |
US15/178,792 Active US10524981B2 (en) | 2011-03-08 | 2016-06-10 | Cap and container assembly for a dosage product |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
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US15/178,792 Active US10524981B2 (en) | 2011-03-08 | 2016-06-10 | Cap and container assembly for a dosage product |
Country Status (6)
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US (2) | US20140048430A1 (en) |
EP (1) | EP2683621B1 (en) |
JP (1) | JP6111205B2 (en) |
CN (1) | CN103391887A (en) |
CA (1) | CA2829022A1 (en) |
WO (1) | WO2012121796A2 (en) |
Cited By (6)
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WO2018174429A1 (en) * | 2017-03-23 | 2018-09-27 | (주)황초원 | Portable beverage container including portion pack and fixing cap |
KR20180107971A (en) * | 2017-03-23 | 2018-10-04 | (주)황초원 | Portable drink container including portion pack and holdercap |
US10899510B2 (en) * | 2018-10-17 | 2021-01-26 | Nicole Thomas | Vial assembly with cap with disinfectant and related methods |
WO2020256451A3 (en) * | 2019-06-21 | 2021-04-15 | (주)황초원 | Portion pack fixing cap having improved liquid fluidity |
US11027898B2 (en) * | 2018-11-15 | 2021-06-08 | Silgan Dispensing Systems Corporation | Two-part dispensing closure system with internal seal and methods of using the same |
US11767153B2 (en) | 2017-05-02 | 2023-09-26 | Csp Technologies, Inc. | Mineral entrained plastic formulations as puncturing elements |
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JP6419430B2 (en) * | 2014-01-29 | 2018-11-07 | 竹本容器株式会社 | Volatilization amount adjustment cap |
KR101592816B1 (en) * | 2014-11-10 | 2016-02-05 | 임효빈 | Container cap having reusable containers and Container having its cap |
CN105984644A (en) * | 2015-06-25 | 2016-10-05 | 中山鼎晟生物科技有限公司 | Blood sample storage kit and using method thereof |
EP3190062A1 (en) * | 2016-01-07 | 2017-07-12 | Pont Packaging B.V. | A cap construction with a storage space and a container provided therewith as well as a method of using same |
US10494164B2 (en) * | 2016-03-09 | 2019-12-03 | Fifth Third Bank, an Ohio Banking | Dispensable containment vessel and dispensing system |
JP2017194324A (en) * | 2016-04-19 | 2017-10-26 | 株式会社DeNAライフサイエンス | Saliva preservation kit |
US10537892B2 (en) * | 2017-01-03 | 2020-01-21 | Illumina, Inc. | Sample tube with integrated mixing plunger head |
US11883817B2 (en) * | 2017-01-25 | 2024-01-30 | Yantai Ausbio Laboratories Co., Ltd. | Equipment and methods for automated sample processing for diagnostic purposes |
KR101972880B1 (en) * | 2017-11-30 | 2019-04-26 | (주)황초원 | Holdercap for portion pack |
GB2574480A (en) * | 2018-06-08 | 2019-12-11 | Dexos Drinks Ltd | Bottle closure with first liquid dispenser |
CN110514819A (en) * | 2019-09-06 | 2019-11-29 | 安徽福贸生物科技有限公司 | A kind of detachable sample liquid detection device |
CN112027343A (en) * | 2020-08-06 | 2020-12-04 | 东莞市晶森包装制品有限公司 | Bottle cap and bottle |
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- 2012-01-04 EP EP12754965.7A patent/EP2683621B1/en active Active
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Also Published As
Publication number | Publication date |
---|---|
US20160279030A1 (en) | 2016-09-29 |
EP2683621A2 (en) | 2014-01-15 |
EP2683621B1 (en) | 2016-07-27 |
CA2829022A1 (en) | 2012-09-13 |
WO2012121796A2 (en) | 2012-09-13 |
JP2014511319A (en) | 2014-05-15 |
JP6111205B2 (en) | 2017-04-05 |
EP2683621A4 (en) | 2014-07-30 |
CN103391887A (en) | 2013-11-13 |
WO2012121796A3 (en) | 2012-11-22 |
US10524981B2 (en) | 2020-01-07 |
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