WO2015063849A1 - 分包体、分包体の製造方法および分包体の製造装置 - Google Patents
分包体、分包体の製造方法および分包体の製造装置 Download PDFInfo
- Publication number
- WO2015063849A1 WO2015063849A1 PCT/JP2013/079214 JP2013079214W WO2015063849A1 WO 2015063849 A1 WO2015063849 A1 WO 2015063849A1 JP 2013079214 W JP2013079214 W JP 2013079214W WO 2015063849 A1 WO2015063849 A1 WO 2015063849A1
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- WIPO (PCT)
- Prior art keywords
- package
- sealed
- packaging bag
- medicine
- swallowing
- Prior art date
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Classifications
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- 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
- A61J1/2093—Containers having several compartments for products to be mixed
-
- 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
- A61J1/03—Containers specially adapted for medical or pharmaceutical purposes for pills or tablets
-
- 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
- A61J1/03—Containers specially adapted for medical or pharmaceutical purposes for pills or tablets
- A61J1/035—Blister-type containers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
- B65B29/00—Packaging of materials presenting special problems
- B65B29/10—Packaging two or more different substances isolated from one another in the package but capable of being mixed without opening the package, e.g. forming packages containing a resin and hardener isolated by a frangible partition
-
- 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
- B65D75/00—Packages comprising articles or materials partially or wholly enclosed in strips, sheets, blanks, tubes, or webs of flexible sheet material, e.g. in folded wrappers
- B65D75/28—Articles or materials wholly enclosed in composite wrappers, i.e. wrappers formed by associating or interconnecting two or more sheets or blanks
-
- 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
- B65D75/00—Packages comprising articles or materials partially or wholly enclosed in strips, sheets, blanks, tubes, or webs of flexible sheet material, e.g. in folded wrappers
- B65D75/52—Details
- B65D75/58—Opening or contents-removing devices added or incorporated during package manufacture
-
- 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
- B65D81/00—Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents
- B65D81/32—Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents for packaging two or more different materials which must be maintained separate prior to use in admixture
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- 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
- A61J1/05—Containers specially adapted for medical or pharmaceutical purposes for collecting, storing or administering blood, plasma or medical fluids ; Infusion or perfusion containers
-
- 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
- B65D2217/00—Details of mixing containers or closures
Definitions
- the present invention relates to a packaging body, a method for producing a packaging body and an apparatus for producing a packaging body, and more particularly, a packaging body having a packaging body in which a swallowing aid substance is sealed, a packaging body
- the present invention relates to a method of manufacturing the same and a manufacturing apparatus of a packaged body.
- Patent Document 1 a powder / particle body containing chamber for containing powdery / powdered substances, a swallowing auxiliary material chamber containing the substance for swallowing assistance such as jelly, and the like;
- a dose storage container is described in which an introduction channel communicating the storage chamber and the swallowing auxiliary substance storage chamber is formed.
- the introduction path is sealed by an openable easy opening portion.
- the easy-opening portion is opened by pressing the swallowing auxiliary substance storage chamber, and the jelly is guided to the powder particle storage chamber and wraps the powdery dose.
- the powdered and granular dose encased in the jelly is taken out from the dose container. Therefore, if the above-mentioned dose substance storage container is used, even an elderly person who is not good at swallowing the drug can easily take the drug.
- Patent Document 2 JP-A-2011-206150 (Patent Document 2) describes a drug preparation container for dissolving a drug in a dissolved substance.
- the drug preparation container for example, a storage bag containing a dissolved substance such as sterilized purified water is disposed in the drug preparation container.
- the drug is inserted into the drug chamber.
- the dissolved substance is filled in the drug chamber where the drug is inserted, and the drug is dissolved in the dissolved substance.
- a three-way valve is attached to the drug passage, and the dissolved substance is infused into the patient's body through the three-way valve.
- Patent Document 3 describes a sachet in which a drug dispensed based on a doctor's prescription is packaged at a single dose. According to the packaging bag, fine scratches are formed on the medicine packaging paper made of polyethylene terephthalate or the like. Therefore, even the elderly or children can easily open the packaging bag with bare hands.
- This invention is made in view of the said subject,
- the objective provides the manufacturing method of the package body which can assist the swallowing of a chemical
- the packaging body according to the present invention includes a package, a medicine, and a packaging bag.
- the package seals the swallowing aid substance.
- the drug is disposed outside the package.
- the sachets seal the package and drug with the swallowing aid substance sealed.
- the package and the drug are sealed by sachets.
- the packaging body in accordance with the present invention the packaging body in which the swallowing auxiliary substance is sealed and the medicine are sealed by the commonly used packaging bag. Therefore, it is possible to provide a packaged body capable of assisting the swallowing of a drug by a simple method without using a special-shaped dose container. Also, the swallowing auxiliary substance is sealed by the package, and the package is sealed by the sachet. Therefore, the deterioration of the swallowing aid can be effectively suppressed.
- the package is configured such that the swallowing auxiliary substance can flow out from the inside of the package to the outside of the package and into the inside of the packaging bag by external pressure. This allows the swallowing aid substance to be introduced into the interior of the sachet in a simple manner and mixed with the drug.
- the package includes a first seal portion on which the superposed films are welded.
- the swallowing auxiliary substance is configured to be able to flow out of the interior of the package, inside the package, inside the package and inside the sachet by breaking the first seal portion.
- breaking the first seal portion By forming the first seal portion, it is possible to adjust the load when introducing the swallowing auxiliary substance into the inside of the sachet.
- the package is provided on the side opposite to the direction in which the swallowing auxiliary substance is disposed with respect to the first seal portion, and the second seal has a seal strength higher than that of the first seal portion. Further includes a seal portion of The second seal portion is provided to divide the flow path when the swallowing auxiliary substance flows out from the inside of the package to the outside of the package and into the inside of the sachet. The second sealing portion can grind the swallowing aid, so that the swallowing aid can be crushed to a size that is easy to swallow.
- the method for producing a packet according to the present invention comprises the following steps.
- a package having an opening and in which a swallowing aid is sealed, and a sachet containing a medicine are prepared.
- the package in which the swallowing auxiliary substance is sealed and the medicine are sealed by the sachet.
- the package in which the swallowing auxiliary substance is sealed and the medicine are sealed by the packet.
- the swallowing auxiliary substance is sealed by the package, and the package is sealed by the sachet. Therefore, it is possible to manufacture a packaged body capable of effectively suppressing the deterioration of the swallowing aid substance.
- the step of preparing the package body and the package bag in which the drug is disposed includes the steps of preparing the package bag in which the drug is sealed, opening the package bag and Placing the package with the swallowing aid substance sealed inside the opened sachet.
- the package bag in which the drug is sealed is opened, and the package in which the swallowing aid substance is sealed is disposed inside the opened packet package, whereby the package body capable of assisting in swallowing the drug is obtained. It can be manufactured.
- the apparatus for manufacturing a package according to the present invention includes a package insertion portion and a package sealing portion.
- the package insertion portion is configured to be able to place a package in which the swallowing auxiliary substance is sealed, inside a packaging bag having an opening.
- the packing bag sealing portion is configured to be able to seal the packing bag by closing the opening of the packing bag in which the packaging body 2 in which the medicine and the swallowing auxiliary substance are sealed is disposed.
- the package insertion portion is configured to be able to dispose a package in which the swallowing auxiliary substance is sealed, inside the packet having the opening.
- a manufacturing apparatus capable of manufacturing a packaged body capable of assisting the swallowing of a drug by a simple method without using a special-shaped dose container.
- the swallowing auxiliary substance is sealed by the package, and the package is sealed by the sachet. Therefore, it is possible to provide a manufacturing apparatus capable of manufacturing a packaged body capable of effectively suppressing the deterioration of the swallowing aid substance.
- the apparatus for manufacturing a package according to the above further includes a package opening part configured to be able to open a package containing a medicine sealed therein.
- a package body capable of assisting the swallowing of the drug 3 by opening the package bag in which the drug is sealed and arranging the package 2 in which the swallowing auxiliary substance 1 is sealed inside the package package 4 which is opened. Can be provided.
- the present invention it is possible to provide a packaged body capable of assisting swallowing of a drug, a method of manufacturing the packaged body, and a manufacturing apparatus of the packaged body by a simple method.
- FIG. 1 is a schematic perspective view showing a configuration of a packaging body according to Embodiment 1 of the present invention.
- FIG. 2 is a schematic cross-sectional view in a region II-II of FIG. It is a cross-sectional schematic diagram in area
- Embodiment 1 First, the configuration of the packaging body 10 according to the first embodiment of the present invention will be described.
- the packaging body 10 mainly includes a packaging body 2 in which a swallowing auxiliary substance 1 is sealed, a medicine 3 and a packaging bag 4.
- the swallowing aid substance 1 is a substance capable of assisting the swallowing of the drug 3, for example, an orally available edible jelly.
- the swallowing aid 1 is in the form of a gel and has a viscosity that allows it to be attached to the drug 3 so as to enclose the drug 3.
- the swallowing auxiliary substance 1 enters the oral cavity in a state of being attached to the drug 3 so as to enclose the drug 3 and is transported to the stomach through the throat and esophagus. Therefore, it is preferable that the swallowing auxiliary substance 1 have a viscosity that allows it to pass smoothly through the inner wall of each of the throat and esophagus.
- the swallowing auxiliary substance 1 is a liquid, a liquid or a semisolid, and preferably contains water. Also, the swallowing aid substance 1 may be water. Preferably, swallowing aid 1 is more viscous, more cohesive and more adhesive to drug 3 than water.
- the swallowing auxiliary substance 1 may contain a substance (eg, lactic acid bacteria etc.) containing a pharmaceutically active ingredient or an active ingredient.
- the package 2 seals the swallowing aid 1.
- the package 2 seals the swallowing auxiliary substance 1 in a liquid tight manner.
- the film 2a which comprises the package body 2 consists of a material which can seal the swallowing auxiliary substance 1, for example, contains polyethylene.
- the package body 2 arrange
- the swallowing auxiliary substance 1 is configured to be able to flow out from the inside of the package 2 to the outside of the package 2 and to the inside of the sachet 4 by breaking the first seal portion S1.
- package 2 is provided on the side opposite to the direction in which swallowing auxiliary substance 1 is arranged with respect to first seal portion S1, and a first seal portion It further includes a second seal portion S2 having a seal strength higher than that of S1. The dimension of the second seal portion S2 along the direction in which the first seal portion S1 extends is smaller than the dimension of the first seal portion S1.
- the seal strength of the first seal portion S1 is, for example, about 50 gf / 15 mm to 300 gf / 15 mm, preferably about 100 gf / 15 mm to 200 gf / 15 mm.
- the seal strength of the second seal portion S2 is, for example, about 500 gf / 15 mm or more, and preferably about 600 gf / 15 mm or more.
- the seal strength can be measured by the method described in JIS Z 0238.
- the second seal portion S2 is a flow path of the swallowing aid substance 1 when the swallowing aid substance 1 flows out from the inside of the package 2 to the outside of the package 2 and into the inside of the sachet 4 It is provided to be divided. Furthermore, preferably, the second seal portion S2 is configured to be able to grind the swallowing aid 1 when an external pressure is applied to the swallowing aid 1.
- an interval x between two adjacent second seal parts S2 is, for example, about 5 mm or more and 15 mm or less, preferably about 7 mm or more and 13 mm or less.
- the load required to break the first seal portion S1 can be significantly reduced.
- interval x is 13 mm or less, the jelly which has a magnitude
- the distance y between the first seal portion S1 and the second seal portion S2 along the direction perpendicular to the direction in which the first seal portion S1 extends is, for example, about 3 mm, preferably 3 mm or more. It is.
- the package 2 has a third seal portion S3 at one end and the other end in a direction along the direction in which the first seal portion S1 extends.
- the seal strength of the third seal portion S3 is higher than the seal strength of the first seal portion S1, and is substantially the same as the seal strength of the second seal portion S2. That is, the package 2 seals the swallowing aid substance 1 by the first seal portion S1 and the third seal portion S3. The package 2 may seal the swallowing aid substance 1 by sealing the entire outer peripheral portion by the first seal portion S1.
- the medicine 3 is, for example, a solid medicine such as a tablet and a capsule, and is disposed outside the package 2 and inside the sachet 4.
- the medicine 3 is used, for example, for diagnosis, treatment or prevention of human plague, and is prescribed at a pharmacy based on a doctor's or dentist's prescription.
- Drug 3 may be, for example, a non-prescription drug other than a medical drug.
- the medicine 3 may be, for example, a supplement such as a vitamin.
- the packaging bag 4 is made of a general medicine package such as, for example, glassine paper or cellopoly paper, and the package 2 and the medicine 3 in which the swallowing auxiliary substance 1 is sealed are contained and sealed therein. That is, the package 2 and the medicine 3 in which the swallowing auxiliary substance 1 is sealed are sealed by the packing bag 4. That the package 2 and the drug 3 are sealed by the package 4 does not mean that the package 2 and the drug 3 are sealed using members other than the package 4 but by the package 4 itself The package 2 and the medicine 3 are in a sealed state.
- the packaging bag 4 has a substantially rectangular outer shape in a plan view (a view in which the packaging body 10 is viewed from the vertical direction when the packaging body 10 is placed on a horizontal surface).
- the package 2 and the medicine 3 may be sealed by the packing bag 4 by forming a seal along the entire outer circumference of the packing bag 4 in a plan view. Also, the packaging bag 4 does not have to be completely hermetically sealed, and the drug 3 is sealed to an extent that the deterioration of the drug 3 can be substantially suppressed by being exposed to the air outside the packaging bag 4 It should just be.
- the medicine packing paper may have a higher water absorbability than the film 2a constituting the package 2 because it is used for the purpose of containing the package 2 and the medicine 3 instead of sealing the liquid.
- sachet 4 includes a first medicine package 4a, a second medicine package 4b, a fourth seal portion S4, and a fifth seal portion S5.
- One end of the first medicine package 4a is thermally welded by one end of the second medicine package 4b and the fourth seal portion S4, and the other end of the first medicine package 4a is manufactured as the other of the second medicine package 4b. Thermal welding is performed by the end portion and the fifth seal portion S5.
- a space surrounded by the first medicine package 4a, the second medicine package 4b, the fourth seal portion S4, and the fifth seal portion S5 is formed, and the swallowing auxiliary substance 1 is sealed in the space.
- Each of the packaged body 2 and the medicine 3 is contained and sealed.
- Each of the fourth seal portion S4 and the fifth seal portion S5 has a seal strength higher than the seal strength of the first seal portion S1.
- the seal strength of each of the fourth seal portion S4 and the fifth seal portion S5 is, for example, about 400 gf / 15 mm or more, and preferably about 500 gf / 15 mm or more.
- the fifth seal portion S5 is a seal portion formed by closing the opening formed in the packaging bag 4 by heat welding.
- the opening scheduled portion 5 is a portion scheduled to cut the packaging bag 4 when the packaging bag 4 is opened.
- the portion to be opened 5 is, for example, a printing portion printed with ink on the outer surface (the surface opposite to the direction in which the package 2 and the medicine 3 are disposed) of the first medicine package 4a of the packaging bag 4.
- the opening scheduled portion 5 may be, for example, a notch provided in the first medicine package 4a or the second medicine package 4b.
- the notches are for example of type I or V.
- the direction in which the portion to be opened 5 extends is a direction intersecting both the longitudinal direction and the lateral direction of the packaging bag 4.
- the dimension of the portion to be opened 5 is smaller than the dimension in the lateral direction of the packaging bag 4 in plan view.
- the opening scheduled portion 5 may be, for example, a minute through hole provided by a sewing needle on the first medicine package 4a or the second medicine package 4b.
- the portion to be opened 5 is provided on the opposite side to the first sealing portion S1 with respect to the swallowing auxiliary substance 1.
- the package 2 may have a substantially trapezoidal external shape in a plan view.
- the package 2 may not have the second seal portion S2 received on the side opposite to the side on which the swallowing auxiliary substance 1 is disposed with respect to the first seal portion S1.
- a third seal portion S3 is provided at one end and the other end in the direction in which the first seal portion S1 extends.
- the third seal portion S3 has a seal strength higher than that of the first seal portion S1.
- the distance x between the third seal parts S3 along the direction in which the first seal parts S1 extend is, for example, about 5 mm or more and 15 mm or less, and preferably about 7 mm or more and 13 mm or less.
- the swallowing auxiliary substance 1 is configured to be able to flow out from the inside of the package 2 to the outside of the package 2 and to the inside of the sachet 4 by breaking the first seal portion S1.
- the first seal portion S1 is formed by laminating and bending one sheet of film 2a so that one end and the other end face each other, and the laminated film 2a is heat-welded. May be Further, in plan view, the entire outer periphery of the package 2 may be sealed only by the first seal portion S1.
- each of the film 2a constituting the package 2 and the medicine package constituting the packaging bag 4 includes a sealant layer capable of heat welding.
- each of the film 2a constituting the package 2 and the medicine package constituting the packaging bag 4 includes the sealant layer and another layer having a higher melting point than the sealant layer.
- the film 2a constituting the package 2 contains a material capable of sealing the swallowing auxiliary substance 1 in a liquid tight manner.
- the film 2a which comprises the package body 2 may contain the multilayer film which laminated plastics, such as polyethylene terephthalate, polybutylene terephthalate, nylon, a polypropylene, or polyethylene, for example.
- a packaging body 10 is prepared in which a packaging body 2 in which the swallowing auxiliary substance 1 is sealed and a medicine 3 disposed outside the packaging body 2 are sealed by a packaging bag 4. Ru.
- a packaging bag 4 by applying load F from the outside of the packaging bag 4 from the outside with, for example, a finger or the like, the swallowing aid substance 1 contained in the inside of the package 2 is inserted through the package 2. Is pushed toward the first seal portion S1. When the force applied to the first seal portion S1 exceeds the seal strength of the first seal portion S1, the first seal portion S1 is broken and the package 2 is unsealed.
- a load F is applied to swallowing aid 1 from the outside through film 2a, so that swallowing aid 1 is provided with two adjacent second seal portions S2. And squeezed out from between the third seal portion S3 and the second seal portion S2 to flow into the interior of the sachet 4.
- the swallowing auxiliary substance 1 is crushed and granulated by passing between the two adjacent second seal parts S2 or between the third seal part S3 and the second seal part S2. That is, a plurality of granular swallowing aid substances 1 a are formed outside the package 2 and inside the packaging bag 4.
- load F is applied to swallowing aid substance 1 from the outside through package 2 so that swallowing aid substance 1 b remaining inside package 2 is outside package 2 and is divided into bags It is squeezed out to the inside of 4.
- swallowing aid substance 1 is mixed with medicine 3 so that granular swallowing aid substance 1 wraps medicine 3 with a finger from the outside of sachet 4.
- the packaging bag 4 is opened by cutting the packaging bag 4 along the portion to be opened 5.
- the medicine 3 with the swallowing aid 1 attached thereto is taken out of the packing bag 4 and taken through the opening 6 of the packing bag 4.
- the swallowing auxiliary substance 1 enters the oral cavity in a state of being attached to the drug 3 so as to enclose the drug 3 and is transported to the stomach through the throat and esophagus.
- the swallowing auxiliary substance 1 adheres so as to enclose the drug 3, the drug 3 can pass smoothly through the inner wall of the throat and esophagus. Therefore, even a person having dysphagia can take the drug 3 without difficulty. Moreover, since the swallowing auxiliary substance 1 adheres to the drug 3 so as to enclose the drug 3, when taking the drug 3, the drug 3 can be taken without feeling bitterness peculiar to the drug.
- the manufacturing apparatus 100 of the packaging body 10 which concerns on Embodiment 1 of this invention is demonstrated.
- the manufacturing apparatus 100 of the packet 10 according to the present invention includes the package insert portion 101, the height adjustment unit 102, the cut line print unit 103, and the package open portion.
- the apparatus mainly includes a package insertion portion 105, a suction pad 106, a packing bag sealing part 107, a motor 108, a packing bag collection part 109, and a feeding belt 110.
- the packaging bag insertion portion 101 is configured to be capable of inserting a medicine package in which a plurality of packaging bags 4 in which the medicine 3 is sealed are connected.
- the packaging bag recovery unit 109 is configured to be able to recover a medicine package in which a plurality of packaging bags 4 in which the package 2 in which the swallowing auxiliary substance 1 is sealed and the medicine 3 are connected are connected.
- the medicine package in which a plurality of sachets 4 are connected is wound in a roll and disposed in a sachet inserting section 101.
- medicine packaging paper in which a plurality of sachets 4 are connected is collected in a sachet collecting portion 109 so as to be wound in a roll.
- the packaging bag insertion part 101 and the packaging bag recovery part 109 are respectively disposed on one side and the other side of the manufacturing apparatus 100 of the packaging body 10.
- the feed belt 110 is configured to be able to move a plurality of connected sachets 4 from the sachet insertion portion 101 to the sachet collecting portion 109.
- the feed belt 110 has an annular shape, and is configured to be rotatable by the motor 108 along the annular shape.
- the feed belt 110 is provided so as to extend from the position at which the height adjustment portion 102 is disposed to the position at which the sachet packaging portion 107 is disposed.
- the feed belt 110 is disposed in contact with a part of the outer surface of the packaging bag 4, and the packaging bag 4 moves as the feeding belt 110 rotates.
- the height adjustment unit 102 adjusts the height of the packing bag 4 along a direction perpendicular to each of the connection direction of the plurality of connected packing bags 4 and the normal direction of the outer surface of the packing bag 4. It is configured to be possible.
- the cutting line printing unit 103 is provided closer to the packing bag recovery unit 109 than the height adjustment unit 102, and is configured to be able to print a cutting line to be the opening scheduled part 5 on the outer surface of the packing bag 4.
- the cut line printing unit 103 may be configured to be able to form a cut portion (notch portion) to be the opening planned portion 5 in the packaging bag 4 or may be configured to be able to form each of a cut line and a cut portion.
- the packaging bag opening unit 104 is provided closer to the packaging bag recovery unit 109 than the tear line printing unit 103, and is configured to be able to open the packaging bag 4 in which the medicine 3 is sealed.
- the cutter is configured to be in contact with the vicinity of the upper portion of the outer surface of the packaging bag 4, and the packaging bag 4 moves from the packaging bag insertion part 101 toward the packaging bag recovery part 109.
- An opening can be formed in the upper part of the outer surface of the packaging bag 4 by cutting the vicinity of the upper part of the outer surface of the packaging bag 4.
- the package inserting portion 105 is provided on the side of the bag collection portion 109 with respect to the bag opening portion 104, and the swallowing aid is provided in the inside of the bag 4 having the opening formed by the bag opening portion 104.
- the package 2 in which the substance 1 is sealed is configured to be arrangeable.
- the package insertion portion 105 has a cassette capable of containing the package 2 in which a plurality of swallowing auxiliary substances 1 are sealed.
- the package insertion portion 105 is disposed above the packaging bag 4 (the side opposite to the side on which the feeding belt 110 is disposed with respect to the packaging bag 4), and the packaging bag 2 is packaged by gravity.
- the packaging body 2 can be disposed inside the packaging bag 4 by dropping it into the inside of the packaging bag 4.
- a position detection sensor (not shown) for detecting the position of the packaging bag 4 is provided at a position facing the outer surface of the packaging bag 4, and the packaging bag 4 having an opening is the package insertion portion 105
- the package insertion portion 105 may be configured such that the package 2 is inserted from the package insertion portion 105 into the interior of the packaging bag 4 when being disposed directly under the As shown in FIG. 12, the plurality of packages 2 are accommodated in the cassette of the package insertion portion 105 along a direction perpendicular to the traveling direction of the packaging bag 4 and the height direction of the packaging bag 4. .
- the package insertion portion 105 may have a plurality of package insertion portions disposed along the traveling direction of the packaging bag 4.
- the package insertion portion 105 may have, for example, a first package insertion portion 105a, a second package insertion portion 105b, and a third package insertion portion 105c.
- the package 2 for the morning is disposed in the first package insertion portion 105a
- the package 2 for the day is disposed in the second package insertion portion 105b
- the package 2 for the third package insertion portion 105c A night package 2 may be arranged. For example, forgetting to drink the medicine 3 can be prevented by making the morning, day and night packages 2 different colors. As shown in FIG.
- the package insertion portion 105 is formed in a ring shape, and a plurality of packages 2 may be accommodated in a ring shape.
- the manufacturing apparatus 100 of the package 10 can be made more compact than when the package insertion portion 105 is formed in a straight line.
- the suction pad 106 is disposed to face the outer surface of the packaging bag 4 and is configured to be capable of adsorbing to the outer surface of the packaging bag 4.
- the suction pad 106 can expand the opening formed by the bag opening portion 104 by moving in a direction along the normal to the outer surface of the suction pad 106 while being adsorbed to the outer surface of the bag 4. It is. Thereby, the package 2 can be inserted into the interior of the packaging bag 4 with high accuracy.
- the package insertion portion 105 is preferably configured to insert the package 2 into the packaging bag 4 while the suction pad 106 expands the opening of the packaging bag 4.
- the packing bag sealing part 107 is provided closer to the packing bag recovery part 109 than the packing body insertion part 105 and the suction pad 106, and the packing body 2 in which the medicine 3 and the swallowing aid substance 1 are sealed is disposed.
- the opening of the packaging bag 4 is closed to seal the packaging bag 4.
- the packaging bag sealing portion 107 is, for example, a heater for heat welding, is disposed to face the upper part of the outer surface of the packaging bag 4 and is configured to be able to seal the opening of the packaging bag 4 by heat welding There is.
- the sachet 4 sealed by heat welding is sent to the sachet recovery unit 109 and recovered.
- the cut line printing unit 103 is disposed between the packaging bag insertion unit 101 and the packaging bag opening unit 104 in the manufacturing apparatus 100 of the packaging body 10 according to the first embodiment.
- the cut line printing unit 103 may be disposed between the packing bag sealing unit 107 and the packing bag collection unit 109.
- the packaging bag preparation step (S1: FIG. 14) is performed.
- the packaging bag 4 in which the medicine 3 is sealed is prepared.
- a medicine 3 prepared by a pharmacist based on a doctor's prescription is placed in the sachet 4 and the sachet 4 is sealed.
- the packaging bag 4 in which the medicine 3 is sealed is disposed in the packaging bag insertion part 101.
- an opening scheduled portion forming step (S2: FIG. 14) is performed.
- a score line as the planned opening portion 5 is printed on the outer surface of the packaging bag 4 in which the medicine 3 is sealed.
- the packaging bag 4 is moved by the feeding belt 110 along the direction (feeding direction) from the packaging bag insertion unit 101 to the packaging bag recovery unit 109, and is sent to the tear line printing unit 103.
- the cutting line printing unit 103 a cut line is printed on the outer surface of the packaging bag 4. The cut line may be printed, and a cutout (notch) as the opening scheduled portion 5 may be formed in the packaging bag 4.
- an opening formation step (S3: FIG. 14) is performed.
- the opening 4d is formed in the packaging bag 4 in which the medicine 3 is sealed.
- the packaging bag 4 is sent from the cut line printing unit 103 to the packaging bag opening unit 104 by the feed belt 110.
- the package opening section 104 the package 4 is moved along the moving direction of the package 4 with the cutter pressed against the upper part of the outer surface of the package 4 in which the medicine 3 is sealed. By doing this, the upper part of the outer surface of the packaging bag 4 is cut to form the opening 4 d.
- the package inserting step (S4-6: FIG. 14) is performed.
- the package 2 in which the swallowing auxiliary substance 1 is sealed is disposed inside the opened package 4 through the opening 4 d of the package 4.
- the packaging bag 4 is sent from the packaging bag opening unit 104 to the package insertion unit 105 by the feed belt 110.
- the package 2 accommodated in the cassette of the package inserting portion 105 is inserted into the interior of the package 4 from above the package 4 through the opening 4 d.
- the suction pad 106 preferably spreads the opening 4 d of the packaging bag 4.
- the opening 4 d of the packaging bag 4 is expanded.
- the package 2 in which the swallowing auxiliary substance 1 is sealed at the same time from different package inserts 105 is inserted into each of the three linked sachets 4.
- the package 2 having the opening 4 d and having the swallowing auxiliary substance 1 sealed therein and the sachet 4 in which the medicine 3 is disposed are prepared.
- the packaging bag sealing step (S7: FIG. 14) is performed.
- the packaging body 2 and the medicine 3 in which the swallowing auxiliary substance 1 is sealed are sealed by the packaging bag 4.
- the packaging bag 4 is sent from the package insertion part 105 to the packaging bag sealing part 107 by the feed belt 110.
- the opening 4d of the packing bag 4 is heated by a heater to close the opening 4d of the packing bag 4 by heat welding.
- the package 2 and the medicine 3 in which the swallowing auxiliary substance 1 is sealed are sealed by the packing bag 4.
- the opening 4 d is heat-welded while pressing the roller against the outer surface of the packing bag 4 so as to push out the air inside the packing bag 4 to the outside. May be closed.
- the opening 4 d of the packaging bag 4 is closed by heat welding to form a fifth sealed portion S5.
- the packaging bag recovery step (S8: FIG. 14) is performed.
- the packing bag 4 is sent from the packing bag sealing unit 107 by the feeding belt 110 to the packing bag collection unit 109.
- the packaging bag recovery unit 109 the packaging body 2 in which the swallowing auxiliary substance 1 is sealed and the packaging body 10 in which the medicine 3 is sealed by the packaging bag 4 are recovered.
- the planned opening part formation step (S2: FIG. 14) may be performed after the opening part formation step (S3: FIG. 14). Specifically, as shown in FIG. 15, after the opening forming step (S2: FIG. 15), the package inserting step (S4-6: FIG. 15) and the packaging bag sealing step (S6: FIG. 15) And in order. After the packing bag sealing step (S6: FIG. 15), the planned opening part forming step (S7: FIG. 15) may be performed. Forming the opening scheduled portion 5 in the fifth sealed portion S5 of the packaging bag 4 by performing the opening scheduled part forming step (S7: FIG. 15) after the packaging bag sealing step (S6: FIG. 15) Can.
- the opening forming step (S3: FIG. 14) may be omitted.
- a sachet 4 having an opening is prepared.
- the package 2 in which the medicine 3 and the swallowing auxiliary substance 1 are sealed is inserted into the inside of the packaging bag 4 having the opening.
- the opening of the packaging bag 4 is closed by heat welding so as to seal the package 2 in which the medicine 3 and the swallowing auxiliary substance 1 are sealed.
- the package 2 in which the swallowing auxiliary substance 1 is sealed, the medicine 3 disposed outside the package 2, and the package 2 in which the swallowing auxiliary substance 1 is sealed and the medicine package 3 are sealed.
- the package 2 and the medicine 3 may be manufactured in the package 10 in which the package 2 and the medicine 3 are sealed by the package 4.
- packaging body 10 mainly includes packaging body 2 in which swallowing aid substance 1 is sealed, medicine 3 and packaging bag 4.
- the material for swallowing auxiliary substance 1, the material for package 2, the drug 3 and the material for sachet 4 according to Embodiment 2 are the same as the material for swallowing auxiliary substance 1 described in Embodiment 1, the material for package 2, the drug 3 and It is the same as the material of the packaging 4.
- the packaging bag 4 encloses and seals each of the package 2 and the medicine 3 in which the swallowing auxiliary substance 1 is sealed.
- the package 2 and the medicine 3 in which the swallowing auxiliary substance 1 is sealed are sealed by the packing bag 4.
- the sachet 4 has a polygonal outer shape.
- the packaging bag 4 may have an octagonal outer shape, and as shown in FIG. 17, the packaging bag 4 may have a hexagonal shape.
- the dimension in the lateral direction of the packaging bag 4 near the center in the longitudinal direction of the packaging bag 4 is smaller than the dimension in the lateral direction of the packaging bag 4 near the longitudinal end of the packaging bag 4.
- the packaging bag 4 may be formed by folding a sheet of medicine package 4a so that one end and the other end of the medicine package 4a face each other.
- the periphery other than the portion where the medicine package 4a is folded is welded by the fourth seal portion S4.
- the entire outer periphery of the packaging bag 4 may be welded by the fourth seal portion S4.
- a sixth seal portion S6 is formed so as to weld the overlapped medicine wrapping paper 4a in the vicinity of the center of the packaging bag 4.
- the sixth seal portion S6 is a substantially circular seal portion in a plan view.
- each of the fourth seal portion S4 and the sixth seal portion S6 is, for example, about 400 gf / 15 mm or more, and preferably about 500 gf / 15 mm or more.
- a mixing chamber 4c is formed in the inside of the sachet 4 on the opposite side to the side where the package 2 is disposed with respect to the sixth seal portion S6.
- the medicine 3 is disposed in the mixing chamber 4c.
- the mixing chamber 4c has a wide space to such an extent that the swallowing aid substance 1 and the medicine 3 can be sufficiently mixed.
- the package 2 has a hexagonal shape in a plan view, and a first seal portion S1 and a third seal portion S3 having a seal strength higher than that of the first seal portion S1. have.
- the swallowing auxiliary substance 1 is accommodated inside the package 2.
- the package 2 seals the swallowing aid substance 1.
- the swallowing auxiliary substance 1 is configured to be able to flow out from the inside of the package 2 to the outside of the package 2 and to the inside of the sachet 4 by breaking the first seal portion S1.
- the first seal portion S1 may have a first weak seal portion S11 and a second weak seal portion S12.
- the first weak seal portion S11 is spaced apart from and in parallel with the second weak seal portion S12.
- the extending direction of each of the first weak seal portion S11 and the second weak seal portion S12 is a direction intersecting the outflow direction of the swallowing auxiliary substance 1.
- a sixth seal portion S6 is disposed on the opposite side of the first seal portion S1 from the side on which the swallowing auxiliary substance 1 is disposed.
- the dimension of the sixth seal portion S6 along the direction in which the first seal portion S1 extends is smaller than the dimension of the first seal portion S1.
- the seal strength of each of the first weakly sealed portion S11 and the second weakly sealed portion S12 is, for example, about 50 gf / 15 mm or more and 300 gf / 15 mm or less, preferably about 100 gf / 15 mm or more and 200 gf / 15 mm or less.
- the seal strength of the second seal portion S2 is, for example, about 500 gf / 15 mm or more, and preferably about 600 gf / 15 mm or more.
- the opening scheduled portion 5 is a position at which the packaging bag 4 is cut when the packaging bag 4 is opened.
- the portion to be opened 5 is formed such that the medicine 3 is taken out of the packaging bag 4 along the short direction of the packaging bag 4 in the mixing chamber 4 c of the packaging bag 4.
- the opening planned portion 5 may be, for example, a notch provided in the medicine package 4a.
- the opening scheduled portion 5 may be, for example, a small through hole provided by a sewing needle in the first medicine package 4a.
- the configuration of the packaging body 10 according to the third embodiment of the present invention will be described.
- the configuration of the packaging body 10 according to the third embodiment is different from the configuration of the packaging body 10 according to the second embodiment in the outer shape of the packaging bag 4 and the position of the portion 5 to be opened in plan view.
- the configuration is substantially the same as that of the packaging body 10 according to the second embodiment.
- differences from the configuration of the second embodiment will be mainly described.
- the packaging bag 4 of the packaging body 10 has a rectangular outer shape in plan view. Near the center in the longitudinal direction of the packaging bag 4, a seventh seal portion S7 extending along the short direction is provided.
- the seventh seal portion S ⁇ b> 7 and the sixth seal portion S ⁇ b> 6 function as stoppers so that the package 2 does not move to the mixing chamber 4 c of the sachet 4.
- the portion to be opened 5 is formed on the outer surface of the mixing chamber of the packaging bag 4 so as to extend in a direction intersecting both the longitudinal direction and the lateral direction of the packaging bag 4.
- the part to be opened 5 is cut, it is possible to form an opening through which the medicine 3 can be taken out in a direction intersecting both the longitudinal direction and the lateral direction of the packaging bag 4.
- Embodiment 4 Next, the configuration of the packaging body 10 according to the fourth embodiment of the present invention will be described.
- the configuration of the package 10 according to the fourth embodiment is different from the configuration of the package 10 according to the second embodiment at the position of the portion to be opened 5, and the other configuration is the same as that according to the second embodiment. It is almost the same as the configuration of the envelope 10.
- differences from the configuration of the second embodiment will be mainly described.
- the portion to be opened 5 of the packet 10 according to the fourth embodiment extends along the short direction of the packet 4 near the center in the longitudinal direction of the packet 4. It is formed as. Further, the sixth seal portion S6 is not formed in the packaging bag 4.
- the swallowing auxiliary substance 1 is introduced from the inside of the package 2 into the mixing chamber 4c of the packaging bag 4 by breaking the first seal portion S1. After the swallowing auxiliary substance 1 is mixed with the medicine 3 in the mixing chamber 4 c, the sachet 4 is cut at the opening planned portion 5. As shown in FIG. 20, by removing the part on the opposite side to the mixing chamber 4c of the packaging bag 4 and the package 2 from which the swallowing auxiliary substance 1 has been discharged, the longitudinal center of the packaging bag 4 is removed. The opening 6 is formed at. The opening 6 is formed so that the medicine 3 can be taken out along the longitudinal direction of the sachet 4.
- the configuration of the packaging body 10 according to the fifth embodiment is different from the configuration of the packaging body 10 according to the second embodiment in the shape of the outer shape of the packaging bag 4 and the position of the portion 5 to be opened Is substantially the same as that of the packaging body 10 according to the second embodiment.
- differences from the configuration of the second embodiment will be mainly described.
- the incisions are formed in the direction inclined from the long side to the long side and the short side of the packaging bag 4. After being cut, a notch is subsequently formed along the longitudinal direction and has a decagonal outline.
- a folding position 7 capable of folding the packaging bag 4 in the longitudinal direction is formed in the vicinity of a central position along the longitudinal direction of the packaging bag 4, and a sixth seal portion S6 is formed with respect to the folding position 7.
- An opening scheduled portion 5 is formed on the side opposite to the side where the user is looking.
- packaging bag 4 is folded at folding position 7.
- the packaging bag 4 is cut at the opening scheduled portion 5.
- An opening 6 is formed near the longitudinal center of the packaging bag 4.
- the opening 6 is formed so that the medicine 3 can be taken out along the longitudinal direction of the sachet 4.
- the packaging bag 4 of the packaging body 10 according to the sixth embodiment has a projecting portion in which a part of the short side of the rectangle protrudes along the longitudinal direction, and has a hexagonal outer shape. Have. An opening scheduled portion 5 is formed at an end of the projecting portion. A seventh seal portion S7 is formed in the vicinity of the longitudinal center of the packaging bag 4 so as to extend from the long side of the packaging bag 4 to each of the long side and the short side. There is. Seventh Embodiment Next, the configuration of the packaging body 10 according to the seventh embodiment of the present invention will be described.
- the configuration of the packaging body 10 according to the seventh embodiment is different from the configuration of the packaging body 10 according to the second embodiment in the shape of the outer shape of the packaging bag 4 and the position of the portion 5 to be opened Is substantially the same as that of the packaging body 10 according to the second embodiment.
- differences from the configuration of the second embodiment will be mainly described.
- the short side of packaging bag 4 of packaging body 10 according to the seventh embodiment is formed to be inclined with respect to the long side.
- a cut is formed in the longitudinal central portion of the packaging bag 4.
- a seventh seal portion S7 is formed in the vicinity of the longitudinal center of the packaging bag 4 so as to extend from the long side of the packaging bag 4 to each of the long side and the short side.
- the package 2 has a heptagonal outer shape in a plan view.
- the portion of the package 2 in which the first seal portion S1 is formed is bent at the central portion in the longitudinal direction of the sachet 4.
- the opening scheduled portion 5 is formed to extend along a direction perpendicular to the short side of the packaging bag 4.
- the configuration of the package 10 according to the eighth embodiment is the configuration of the package 10 according to the second embodiment in the shape of the outer shape of the packet 4, the position of the portion 5 to be opened and the shape of the outer shape of the package 2.
- the other configuration is substantially the same as that of the packaging body 10 according to the second embodiment.
- differences from the configuration of the second embodiment will be mainly described.
- the packaging bag 4 of the packaging body 10 has a hexagonal outer shape formed such that one side of a trapezoidal portion is in contact with one side of a square portion in plan view.
- the package 2 has a hexagonal outer shape in plan view, and is disposed in the square portion of the sachet 4.
- the medicine 3 is disposed in the trapezoidal portion of the packaging bag 4.
- the portion to be opened 5 is formed on the outer surface of the packaging bag 4 on the side opposite to the side where the package 2 is disposed with respect to the sixth seal portion S6.
- the package 2 and the medicine 3 in which the swallowing auxiliary substance 1 is sealed are sealed by the generally used packet 4. Therefore, it is possible to provide the packaging body 10 capable of assisting the swallowing of the medicine 3 by a simple method without using a special-shaped dose container.
- the swallowing auxiliary substance 1 is sealed by the package 2, and the package 2 is sealed by the packing bag 4. Therefore, the deterioration of the swallowing auxiliary substance 1 can be effectively suppressed.
- the package 2 is such that the swallowing auxiliary substance 1 is from the inside of the package 2 by the pressure from the outside, and the package 2 is outside the package 2. It is configured to be leakable inside. Thereby, the swallowing auxiliary substance 1 can be introduced into the inside of the packaging bag 4 by a simple method and mixed with the medicine 3.
- the packaging body 2 contains 1st seal
- the swallowing auxiliary substance 1 is configured to be able to flow out from the inside of the package 2 to the outside of the package 2 and to the inside of the sachet 4 by breaking the first seal portion S1.
- the first seal portion S ⁇ b> 1 it is possible to adjust the load at the time of introducing the swallowing auxiliary substance 1 into the inside of the packaging bag 4.
- the package 2 is provided on the side opposite to the direction in which the swallowing auxiliary substance 1 is disposed with respect to the first seal portion S1, and the first seal It further includes a second seal portion S2 having a seal strength higher than that of the portion S1.
- the second seal portion S2 is provided so as to divide the flow path when the swallowing auxiliary substance 1 flows out from the inside of the package 2 to the outside of the package 2 and into the inside of the packaging bag 4. Since the swallowing aid substance 1 can be crushed by the second seal portion S2, the swallowing aid substance 1 can be crushed to a size easy to swallow.
- the package 2 and the medicine 3 in which the swallowing auxiliary substance 1 is sealed are sealed by the packet 4.
- the swallowing auxiliary substance 1 is sealed by the package 2, and the package 2 is sealed by the packing bag 4. Therefore, it is possible to manufacture the packaging body 10 capable of effectively suppressing the deterioration of the swallowing auxiliary substance 1.
- the packet bag 4 in which the drug 3 is sealed is prepared.
- the process includes the steps of: opening the packaging bag 4; and disposing the package 2 in which the swallowing aid substance 1 is sealed inside the opened packaging bag 4.
- the package bag 4 in which the medicine 3 is sealed is opened, and the package body 2 in which the swallowing auxiliary substance 1 is sealed is disposed inside the opened package bag 4, thereby assisting the swallowing of the medicine 3 Possible packages can be produced.
- the package insertion portion 105 can arrange the package 2 in which the swallowing auxiliary substance 1 is sealed inside the packet 4 having the opening. Is configured.
- the manufacturing apparatus 100 which can manufacture the package 10 which can assist swallowing of the chemical
- the swallowing auxiliary substance 1 is sealed by the package 2, and the package 2 is sealed by the packing bag 4. Therefore, the manufacturing apparatus 100 which can manufacture the package 10 which can suppress deterioration of the swallowing auxiliary substance 1 effectively can be provided.
- the packet opening unit 104 is further provided with the package opening unit 104 configured to be able to open the packet 4 in which the medicine 3 is sealed.
- the package opening unit 104 configured to be able to open the packet 4 in which the medicine 3 is sealed.
- the package 2 has a first seal portion S1 and a plurality of second seal portions S2.
- the intervals (slit widths) of the adjacent second seal parts S2 of the package 2 are 6 mm, 7 mm, 8 mm, 9 mm, 10 mm, 11 mm, 12 mm, 13 mm, 14 mm, 15 mm, 16 mm, 17 mm, 18 mm and 19 mm. .
- the relationship between the slit width and the load F necessary for breaking the first seal portion S1 of the package 2 will be described.
- the load F that breaks the first seal portion S1 is 83.1 N.
- the load F that breaks the first seal portion S1 is 48.9 N.
- the load F for breaking the first seal portion S1 is 50 N or less. That is, it was confirmed that the load capable of breaking the first seal portion S1 when the slit width is 7 mm or more is significantly reduced compared to the case where the slit width is 6 mm. In other words, by setting the slit width to 7 mm or more, the first seal portion S1 can be broken with a small load.
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- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
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- Animal Behavior & Ethology (AREA)
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- Engineering & Computer Science (AREA)
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Abstract
Description
(実施の形態1)
まず、本発明の実施の形態1に係る分包体10の構成について説明する。
まず、図1に示すように、嚥下補助物質1が密封された包装体2と、包装体2の外部に配置された薬剤3とが分包袋4によって密封された分包体10が準備される。次に、図5を参照して、分包袋4の外部からたとえば指などにより外部から荷重Fを加えることにより、包装体2の内部に収容されている嚥下補助物質1が包装体2を介して第1のシール部S1に向かって押圧される。第1のシール部S1に加えられた力が第1のシール部S1のシール強度を超えると、第1のシール部S1が破壊され、包装体2が開封される。図6および図7を参照して、引き続き、外部からフィルム2aを介して嚥下補助物質1に対して荷重Fが加えられることにより、嚥下補助物質1は、隣り合う2つの第2のシール部S2の間と、第3のシール部S3および第2のシール部S2の間とから絞り出されることにより、分包袋4の内部に流出する。嚥下補助物質1は、隣り合う2つの第2のシール部S2の間または第3のシール部S3および第2のシール部S2の間を通過することにより粉砕されて粒状になる。つまり、包装体2の外部であって、かつ分包袋4の内部において、粒状の嚥下補助物質1aが複数形成される。さらに、外部から包装体2を介して嚥下補助物質1に対して荷重Fが加えられることにより、包装体2の内部に残っている嚥下補助物質1bが包装体2の外部であって分包袋4の内部に絞り出される。
図11および図12を参照して、本発明に係る分包体10の製造装置100は、分包袋挿入部101と、高さ調整部102と、切取線印字部103と、分包袋開封部104と、包装体挿入部105と、吸着パッド106と、分包袋密封部107と、モータ108と、分包袋回収部109と、送りベルト110とを主に有している。
図14を参照して、分包袋準備工程(S1:図14)が実施される。分包袋準備工程(S1:図14)において、内部に薬剤3が密封された分包袋4が準備される。たとえば医師の処方箋に基づいて薬剤師が準備した薬剤3が分包袋4に配置され、当該分包袋4が密封される。薬剤3が密封された分包袋4は、分包袋挿入部101内に配置される。
(実施の形態2)
次に、本発明の実施の形態2に係る分包体10の構成について説明する。
(実施の形態3)
次に、本発明の実施の形態3に係る分包体10の構成について説明する。実施の形態3に係る分包体10の構成は、平面視における分包袋4の外形および開封予定部5の位置において実施の形態2に係る分包体10の構成と異なっており、他の構成に関しては実施の形態2に係る分包体10の構成とほぼ同じである。以下、実施の形態2の構成と異なる点を中心に説明する。
(実施の形態4)
次に、本発明の実施の形態4に係る分包体10の構成について説明する。実施の形態4に係る分包体10の構成は、開封予定部5の位置において実施の形態2に係る分包体10の構成と異なっており、他の構成に関しては実施の形態2に係る分包体10の構成とほぼ同じである。以下、実施の形態2の構成と異なる点を中心に説明する。
(実施の形態5)
次に、本発明の実施の形態5に係る分包体10の構成について説明する。実施の形態5に係る分包体10の構成は、分包袋4の外形の形状および開封予定部5の位置において実施の形態2に係る分包体10の構成と異なっており、他の構成に関しては実施の形態2に係る分包体10の構成とほぼ同じである。以下、実施の形態2の構成と異なる点を中心に説明する。
(実施の形態6)
次に、本発明の実施の形態6に係る分包体10の構成について説明する。実施の形態6に係る分包体10の構成は、分包袋4の外形の形状および開封予定部5の位置において実施の形態2に係る分包体10の構成と異なっており、他の構成に関しては実施の形態2に係る分包体10の構成とほぼ同じである。以下、実施の形態2の構成と異なる点を中心に説明する。
(実施の形態7)
次に、本発明の実施の形態7に係る分包体10の構成について説明する。実施の形態7に係る分包体10の構成は、分包袋4の外形の形状および開封予定部5の位置において実施の形態2に係る分包体10の構成と異なっており、他の構成に関しては実施の形態2に係る分包体10の構成とほぼ同じである。以下、実施の形態2の構成と異なる点を中心に説明する。
(実施の形態8)
次に、本発明の実施の形態8に係る分包体10の構成について説明する。実施の形態8に係る分包体10の構成は、分包袋4の外形の形状、開封予定部5の位置および包装体2の外形の形状において実施の形態2に係る分包体10の構成と異なっており、他の構成に関しては実施の形態2に係る分包体10の構成とほぼ同じである。以下、実施の形態2の構成と異なる点を中心に説明する。
Claims (8)
- 嚥下補助物質が密封された包装体と、
前記包装体の外部に配置されている薬剤と、
前記嚥下補助物質が密封された前記包装体および前記薬剤を密封する分包袋とを備え、
前記包装体および前記薬剤は前記分包袋によって密封されている、分包体。 - 前記包装体は、外部からの圧力によって前記嚥下補助物質が前記包装体の内部から、前記包装体の外部であってかつ前記分包袋の内部に流出可能に構成されている、請求項1に記載の分包体。
- 前記包装体は、重ね合わせたフィルムが溶着された第1のシール部を含み、
前記嚥下補助物質は、前記第1のシール部を破壊して前記包装体の内部から、前記包装体の外部であってかつ前記分包袋の内部に流出可能に構成されている、請求項1または請求項2に記載の分包体。 - 前記包装体は、前記第1のシール部に対して前記嚥下補助物質が配置されている方向と反対側に設けられ、かつ前記第1のシール部よりもシール強度の高い第2のシール部をさらに含み、
前記第2のシール部は、前記嚥下補助物質が前記包装体の内部から前記包装体の外部であってかつ前記分包袋の内部に流出する際の流路を分けるように設けられている、請求項3に記載の分包体。 - 開口部を有し、かつ内部に嚥下補助物質が密封された包装体および薬剤が配置された分包袋を準備する工程と、
前記嚥下補助物質が密封された前記包装体および前記薬剤を前記分包袋により密封する工程とを備えた、分包体の製造方法。 - 前記包装体および前記薬剤が配置された前記分包袋を準備する工程は、前記薬剤が密封された前記分包袋を準備する工程と、前記分包袋を開封する工程と、開封された前記分包袋の内部に前記嚥下補助物質が密封された前記包装体を配置する工程とを含む、請求項5に記載の分包体の製造方法。
- 開口部を有する分包袋の内部に、嚥下補助物質が密封された包装体を配置可能に構成された包装体挿入部と、
薬剤および前記嚥下補助物質が密封された前記包装体が配置された前記分包袋の前記開口部を閉じて前記分包袋を密封可能に構成された分包袋密封部とを備えた、分包体の製造装置。 - 前記薬剤が密封された前記分包袋を開封可能に構成された分包袋開封部をさらに備えた、請求項7に記載の分包体の製造装置。
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JP2015510531A JP5931280B2 (ja) | 2013-10-29 | 2013-10-29 | 分包体、分包体の製造方法および分包体の製造装置 |
CN201380080590.7A CN105722492B (zh) | 2013-10-29 | 2013-10-29 | 分包体、分包体的制造方法以及分包体的制造装置 |
PCT/JP2013/079214 WO2015063849A1 (ja) | 2013-10-29 | 2013-10-29 | 分包体、分包体の製造方法および分包体の製造装置 |
EP13896379.8A EP3064189B1 (en) | 2013-10-29 | 2013-10-29 | Divided packet, method of manufacturing divided packet, and device for manufacturing divided packet |
KR1020167013846A KR101996841B1 (ko) | 2013-10-29 | 2013-10-29 | 분포체, 분포체의 제조방법 및 분포체의 제조장치 |
US15/140,493 US20160235627A1 (en) | 2013-10-29 | 2016-04-28 | Divided packet, method of manufacturing divided packet, and device for manufacturing divided packet |
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Citations (4)
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JP2003000677A (ja) | 2001-06-18 | 2003-01-07 | Nishimura Chemical Co Ltd | 薬包紙及び分包袋 |
WO2010110366A1 (ja) * | 2009-03-25 | 2010-09-30 | 株式会社モリモト医薬 | 医薬組成物容器 |
JP2011200261A (ja) | 2008-07-22 | 2011-10-13 | Morimoto Iyaku:Kk | 服用物収容容器 |
JP2011206150A (ja) | 2010-03-29 | 2011-10-20 | Morimoto Iyaku:Kk | 薬物調製容器および薬物の混合方法 |
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US5195658A (en) * | 1991-03-12 | 1993-03-23 | Toyo Bussan Kabushiki Kaisha | Disposable container |
JPH10234820A (ja) * | 1996-12-25 | 1998-09-08 | Takeda Chem Ind Ltd | 濃厚流動物質を併用する粉粒状剤及びこれらの複室型容器 |
JP5896897B2 (ja) * | 2010-03-29 | 2016-03-30 | 株式会社モリモト医薬 | 経口摂取用の医薬組成物容器 |
CN203079042U (zh) * | 2012-12-31 | 2013-07-24 | 白洁 | 一种果冻盛杯 |
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Publication number | Priority date | Publication date | Assignee | Title |
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JP2003000677A (ja) | 2001-06-18 | 2003-01-07 | Nishimura Chemical Co Ltd | 薬包紙及び分包袋 |
JP2011200261A (ja) | 2008-07-22 | 2011-10-13 | Morimoto Iyaku:Kk | 服用物収容容器 |
WO2010110366A1 (ja) * | 2009-03-25 | 2010-09-30 | 株式会社モリモト医薬 | 医薬組成物容器 |
JP2011206150A (ja) | 2010-03-29 | 2011-10-20 | Morimoto Iyaku:Kk | 薬物調製容器および薬物の混合方法 |
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CN105722492B (zh) | 2019-12-27 |
EP3064189A1 (en) | 2016-09-07 |
US20160235627A1 (en) | 2016-08-18 |
KR101996841B1 (ko) | 2019-07-05 |
JPWO2015063849A1 (ja) | 2017-03-09 |
EP3064189B1 (en) | 2022-04-20 |
EP3064189A4 (en) | 2016-11-16 |
CN105722492A (zh) | 2016-06-29 |
JP5931280B2 (ja) | 2016-06-08 |
KR20160079829A (ko) | 2016-07-06 |
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