This application is a 371 of PCT/JP02/09407 filed Sep. 13, 2002, and claims priority to Japanese patent applications 2001-279182 filed Sep. 14, 2001, and 2002-231489 filed Aug. 8, 2002.
The present invention relates to a liquid-medicine injection port device, which is used for injecting and mixing liquid medicines, specifically mixing a liquid medicine into a liquid to be injected such as a transfusion solution, aseptically and simply, and a liquid-medicine container provided with the liquid-medicine injection port device.
Clinically, it is a matter of common practice that various medicines are simultaneously given to a patient. For example, in the case of injecting vitamins or the like into a vein, they must not be stored in a liquid-medicine container such as a transfusion-solution pack and conduct high-pressure steam sterilization processing beforehand. This is because vitamins deteriorate upon heated. When using it, therefore, it is necessary to inject and mix (referred to as injection-mix) it into a liquid-medicine container which stores another liquid medicine in advance. In short, mixing needs to be conducted in the liquid-medicine container.
If the above described liquid medicine is injection-mixed into a liquid-medicine container, conventionally, there has been used the injection-mixing method of piercing a rubber stopper of a liquid-medicine discharge port in the liquid-medicine container with an injection needle. In this method, however, it has been hard to ensure asepsis when an injection-mixing operation is conducted. If microorganisms (or germs) get mixed from the outside when the injection-mixing operation is conducted, the microorganisms propagate themselves in a mixed injection solution while the mixed injection solution is given to a patient. Especially, if an injection solution is, for example, a transfusion solution for nutrition, such as a high-calorie transfusion solution, there is a risk that microorganisms may propagate themselves while it is given, even though only a small number of microorganisms get mixed inside. Thus, there is a possibility that numerous microorganisms may be injected, together with the transfusion solution, into the body of a patient during the latter part of the time when the transfusion solution is given. If such a mixed injection solution is given, that produces some serious side effects such as septicemia and endotoxin shock on the patient. Hence, it is necessary to take the safety of a patient sufficiently into account, so that asepsis can be secured when an injection-mixing operation is conducted.
It is an object of the present invention to provide a liquid-medicine injection port device which is capable of injecting a liquid medicine aseptically and has a smaller number of component parts and a smaller and simpler structure than in any conventional ones, and a liquid-medicine container provided with this liquid-medicine injection port device.
A liquid-medicine injection port device according to the present invention, as the gist thereof, comprising: a liquid-medicine inlet which is formed at an upper end thereof; a liquid-medicine outlet which is formed at a lower end thereof, the liquid-medicine outlet being connected to a liquid-medicine container; a liquid passageway which connects the liquid-medicine inlet and the liquid-medicine outlet; a germ-removal filter which is provided in the liquid passageway; and a closure which closes the liquid passageway underneath the germ-removal filter and opens the liquid passageway easily.
Furthermore, in this liquid-medicine injection port device, the closure may be used which is opened by the injection pressure of a liquid medicine which is injected from the liquid-medicine inlet.
Furthermore, this closure may be a film which blocks the liquid passageway. The film has a weak part which is broken by a liquid-medicine injection pressure.
Furthermore, this closure may be a film which blocks the liquid-medicine outlet. The film is melted and attached, or is glued, to the periphery of the liquid-medicine outlet to cover the liquid-medicine outlet; and the strength of the melting-attachment or gluing is such a degree that the film is peeled by a liquid-medicine injection pressure.
Furthermore, this closure may be a cylindrical film which blocks the liquid-medicine outlet. One end of the film is fixed with kept open on the periphery of the liquid-medicine outlet to cover the liquid-medicine outlet; and the interior surfaces of the other end thereof are melted and attached, or are glued, to each other to close the other end, at such a strength that it is broken by a liquid-medicine injection pressure.
Furthermore, this closure may be an elastic member which blocks the liquid-medicine outlet. The elastic member is deformed by receiving a liquid-medicine injection pressure to open the liquid-medicine outlet.
Furthermore, this closure may be a closure member which is inserted into the liquid-medicine outlet. The closure member clings to the inside of the liquid-medicine outlet, at such a strength that it comes off the liquid-medicine outlet by a liquid-medicine injection pressure.
Furthermore, in this closure, a means may be provided which receives the closure member that comes off the liquid-medicine outlet when a liquid medicine is injected.
Furthermore, in a liquid-medicine injection port device provided with such a closure, the liquid-medicine inlet is sealed up with a rubber elastic body which is pierced with an injection needle to form a liquid-medicine storage space between the liquid-medicine inlet and the germ-removal filter; a compressor may be provided which compresses the inner volume of the liquid-medicine storage space; and the liquid-medicine injection pressure of a liquid medicine which is once injected into the liquid-medicine storage space is heightened by the compressor to compressively send the liquid medicine to the side of the germ-removal filter.
Furthermore, particularly, in this liquid-medicine injection port device, the closure may be used which is opened by a movement of a main-body member provided with the liquid-medicine inlet and the germ-removal filter.
Furthermore, in this closure, an up-and-down movement of the main-body member may allow the closure member to be moved or broken to open the closure.
Furthermore, in this closure, the main-body member may be slid up and down. The liquid-medicine outlet which is formed in a side of a hanging portion of the main-body member is blocked with a slide surface when the main-body member is in an upper position; and it is away from the slide surface and opened when it is slid downward.
Furthermore, in this closure, a turning operation of the main-body member may allow the closure member to be moved or broken to open the closure.
Furthermore, in this closure, the main-body member may be made turnable. The liquid-medicine outlet is formed in the side of a hanging portion of the main-body member; and an opening portion which leads to the outside is provided at a part of a turning-and-rubbing surface with which the liquid-medicine outlet is in contact.
Furthermore, in this closure, underneath the main-body member, an inner-lid member may be provided which engages with the main-body member so as to turn together with the main-body member. The inner-lid member is housed in the liquid passageway which is relatively widened; at least two liquid-medicine outlets are provided which are in contact with the lower surface of the inner-lid member and are away from the turning-center axis of the main-body member; and the inner-lid member has blind parts which cover the liquid-medicine outlets from the inside and has such a shape that the liquid-medicine outlets are opened by turning of the inner-lid member.
Furthermore, particularly, in this liquid-medicine injection port device, the closure may be an open-and-close valve which blocks the liquid passageway. The open-and-close valve is opened by an operation of an operation member, which penetrates the side wall of the liquid-medicine injection port device and is connected to the open-and-close valve.
Furthermore, in this closure, the open-and-close valve may be opened by turning the operation member.
Furthermore, in this closure, the open-and-close valve may be opened with a slide of the operation member, the slide crossing the liquid passageway.
Furthermore, particularly, in this liquid-medicine injection port device, the closure may be a partition wall which blocks the liquid-medicine outlet. The partition wall is broken and opened by an operation of an operation member which penetrates the side wall of the liquid-medicine injection port device.
Furthermore, a liquid-medicine container provided with the liquid-medicine injection port device according to the present invention, as the gist thereof, comprising a liquid-medicine injection port device according to any of the above described ones.
Furthermore, a liquid-medicine container provided with the liquid-medicine injection port device according to the present invention, as another gist thereof, which includes a liquid-medicine injection port device and a liquid-medicine discharge port device, is provided with two front and back sheets and is shaped like a bag, in which: an injection chamber provided with a liquid-medicine injection port device and a storage chamber storing a liquid medicine in advance are divided by a weak seal portion which is formed by melting and attaching, or gluing, the two front and back sheets to each other at such a strength that they are easily peeled.
Furthermore, particularly, this weak seal portion may be peeled by receiving the injection pressure of a liquid medicine which is injected from the liquid-medicine injection port device to allow the injection chamber to lead to the storage chamber.
Particularly, a projection may be formed in either or both of the front and back surfaces of this weak seal portion. The projection is picked up and pulled so that the weak seal portion is peeled and separated into the two front and back sheets.
Next, embodiments of a liquid-medicine injection port device and a liquid-medicine container according to the present invention will be described in detail with reference to drawings.
In the liquid-medicine injection port device 10 according to the present invention, the upside means the side on which the liquid-medicine inlet 24 is provided, and the downside means the side on which the liquid-medicine outlet 28 is provided in the direction where it is connected to the liquid-medicine container 12. The liquid-medicine inlet 24 is shaped so as to be connected to a syringe which stores a liquid medicine to be injection-mixed, and it is gently tapered off downward. The germ-removal filter 16 is disposed with its front surface wide open, so that a liquid medicine can be filtrated over an area as large as possible. As shown in
In the lower surface of the outlet member 18, there are formed twelve projections 42 which doubly surround the liquid-medicine outlet 28, and in addition, a circular projection 44 which surrounds them. The closure film 30 is melted and attached to the circular projection 44 to block the liquid-medicine outlet 28. The twelve projections 42 have the function of supporting the closure film 30 against the pressure applied on the closure film 30 from behind. The projections 42 are suitably away from each other, so that a liquid medicine can move freely between these projections 42.
In the closure film 30 is formed a weak part which is broken by a liquid-medicine injection pressure. The weak part is formed with scratches engraved by a Thomson blade, a heat press or the like, perforations, or the like. For example, a weak part 46 shown in
In the closure film 30 shown in
With respect to the liquid-medicine injection port device 10 according to the present invention which has such a structure as described above, as shown in
As the germ-removal filter 16, especially, limitations are not necessarily placed, but each type of filter usually used in the art may be suitably used, for example, a membrane type, a screen type, a depth type, an anisotropic type, or the like. Among them, the membrane-type filter is especially preferable. If the germ-removal filter 16 is realized with the membrane-type, its hole diameter (or mesh fineness) should preferably be chosen to be 0.01 μm to 1.0 μm, so that it can cut off the passage of germs. More preferably, it should be chosen 0.01 μm to 0.5 μm. In addition, as a material forming the germ-removal filter 16, there are enumerated cellulose acetate, regenerated cellulose, cellulose ester, nylon, polytetrafluoroethylene, polystyrene, polycarbonate, acrylic-system resin, polyolefin, polyvinylidene difluoride, polyether sulfone, and the like. However, it is not limited to these.
The material of the inlet member 14, the outlet member 18, the cylindrical member 22, the cap 26 and the like, is not limited especially. However, plastics having superior moldability are used preferably. Above all, it is especially preferable that materials having great chemical-resistance to a liquid medicine to be injection-mixed, great heat-resistance to high-pressure steam sterilization, superior melting-and-attaching properties useful for the connection between each member or their connection to the liquid-medicine container 12, and the like, are used, such as polyethylene, polypropylene, polyvinyl chloride, polyester, polycarbonate, and the like. Preferably, the outlet member 18 should be the same material as the liquid-medicine container 12, so that they can be easily connected by melting attachment.
In addition, the closure film 30 is not especially limited, as long as it has chemical-resistance and a suitable thickness for forming the weak part 46. Preferably, it should be melted and attached to the circular projection 44. To do this, it is preferable that a film is used which is made of the same material as the outlet member 18, or a material blended with the material of the outlet member 18. For example, if the outlet member 18 is made of polyethylene, then polyethylene, a polymer blend of polyethylene and polypropylene, or the like, is used preferably. However, a film which is difficult to melt and attach to the outlet member 18 may also be used and glued to the circular projection 44 to close the liquid-medicine outlet 28.
The liquid-medicine container 12 provided with the liquid-medicine injection port device 10 according to the present invention is sterilized in advance before it is used (or injection-mixing is conducted). Specifically, with storing a liquid medicine in the liquid-medicine container 12, it undergoes processing, such as high-pressure steam sterilization, ethylene-oxide gas sterilization, and γ-ray sterilization. Then, it is sealed with the cap 26 to be kept aseptic. When injection-mixing is conducted, first, the cap 26 is removed, and then, using a syringe or an injection needle, a liquid medicine is injected from the liquid-medicine inlet 24. The germs which have got mixed into the injected liquid medicine are hindered from passing through the germ-removal filter 16, and thus, stop short of the inside of the liquid-medicine container 12. Therefore, the injection-mixed injection solution remains aseptic, allowing it to be safely given to a patient.
A closure in the liquid-medicine injection port device 10 shown in
In this liquid-medicine injection port device 10, the liquid-medicine outlet 28 is formed in the lowermost side wall of the cylindrical member 22 and is blocked with the closure film 30. The closure film 30 is melted and attached, or glued, to the periphery of the liquid-medicine outlet 28. The strength of the melting-attachment or gluing is such a degree that it is peeled by a liquid-medicine injection pressure applied when a liquid medicine has been injected from the liquid-medicine inlet 24. Thus, before it is used, the liquid-medicine outlet 28 is blocked with the closure film 30, thereby preventing a liquid medicine in the liquid-medicine container 12 from going into the liquid-medicine injection port device 10. If injection-mixing is conducted, the closure film 30 is peeled to open the liquid-medicine outlet 28 automatically. Then, the injected liquid medicine goes into the liquid-medicine container 12 and is mixed with a liquid medicine already stored in the liquid-medicine container 12.
According to this embodiment in which the liquid-medicine outlet 28 is blocked with the film at such a strength that it is peeled by a liquid-medicine injection pressure, the location or shape of the liquid-medicine outlet 28 is not limited especially.
The liquid-medicine injection port device 10 shown in
In another example shown in
The liquid-medicine injection port device 10 shown in
In the liquid-medicine injection port device 10 shown in
In this example, a receiving member 54 is attached to the bottom of the liquid-medicine outlet 28. It receives the closure member 58 which comes off and is released by the liquid-medicine injection pressure, thereby preventing it from falling into the liquid-medicine container 12 (refer to
In the liquid-medicine injection port device 10 shown in
If it is used in the liquid-medicine injection port device 10 provided with a closure which is opened by a liquid-medicine injection pressure, this contrivance for heightening the liquid-medicine injection pressure secondarily helps open the closure more certainly. This is especially effective in the case where a liquid medicine is injected using an injection needle under relatively-low injection pressure. As the closure used together, any one may be used, as long as it is opened by a liquid-medicine injection pressure. It includes the closure already described using
The liquid-medicine injection port device 10 shown in
In the liquid-medicine injection port device 10 shown in
The liquid-medicine injection port device 10 shown in each of
In the liquid-medicine injection port device 10 shown in
In the liquid-medicine injection port device 10 shown in
In the liquid-medicine injection port device 10 shown in
As shown in
In this embodiment, the lower surfaces of the blind parts 88 of the inner-lid member 82 which cover the liquid-medicine outlets 28 may also be melted and attached, or glued, to the upper surface of the bottom member 80, at such a strength that it is peeled when you turn the main-body member 20 manually. Furthermore, the flat-plate portion 94 of the inner-lid member 82 may also be circular which has two openings leading to the liquid-medicine outlets 28. Alternatively, the cylindrical member 22 and the bottom member 80 may also be united, so that only the main-body member 20 and the inner-lid member 82 can be turned. Alternatively, three or more liquid-medicine outlets 28 may also be formed. In that case, the inner-lid member 82 is produced which can open and close all those liquid-medicine outlets 28.
The liquid-medicine injection port device 10 shown in
The liquid-medicine injection port device 10 shown in
In the liquid-medicine injection port device 10 shown in
Next, the liquid-medicine container 12 according to the present invention will be described in detail. In one of its embodiments is provided with some of the above described liquid-medicine injection port devices 10. Where or how the liquid-medicine injection port device 10 is attached is not limited especially. For example, it can be attached to the end or center of the liquid-medicine container 12. The liquid-medicine injection port device 10 may be attached to the main body of the liquid-medicine container 12, preferably, by melting-attachment, gluing or the like.
The means of peeling the weak seal portion 61 is not limited especially, but preferably, it should be peeled automatically by a liquid-medicine injection pressure. Therefore, in the embodiment especially useful according to the present invention, the weak seal portion 61 is melted and attached, or glued, at such a strength that it is peeled by receiving a liquid-medicine injection pressure. In the liquid-medicine container 12 shown in
Some projections are also effective in peeling the weak seal portion 61. For example, a projection for picking up and pulling may be formed in either or both of the front and back surfaces of the weak seal portion 61. In the weak seal portion 61 shown in
In the weak seal portion 61 shown in
Hereinbefore, the liquid-medicine injection port device and the liquid-medicine container which this is attached to according to the present invention have been described in detail. However, the present invention is not limited to the above described citations and illustrations. The shape or configuration of the liquid-medicine injection port device, the material quality of the inlet member, the outlet member, the bottom member, the cap or the like, the type or configuration of the germ-removal filter, the method of attaching the liquid-medicine injection port device to the liquid-medicine container, the type or configuration of the liquid-medicine container, the type or quantity of a liquid medicine, the method of sterilization, or the like, can be implemented from aspects including various improvements, modifications and variations, based on the knowledge of those skilled in the art, within the scope which does not depart from the spirit of the present invention.
For example, the shape of the liquid-medicine container is not limited to a rectangle, e.g., it may also be an ellipse or the like. In addition, the position in which the liquid-medicine injection port device is attached is not limited to the edge of the liquid-medicine container, e.g., it may also be attached to the side thereof. Besides, the weak seal portion may also be peeled by applying pressure on it by compulsion via the storage chamber. Furthermore, as a similar structure to the liquid-medicine injection port device 10 shown in
In the liquid-medicine injection port device according to the present invention, a germ-removal filter is provided, thereby making injection-mixing safe. This is because even if germs or the like get mixed into a liquid medicine to be injected for the injection-mixing, they are removed with the germ-removal filter, and then, the liquid medicine goes into the liquid-medicine container. Furthermore, a closure is provided which blocks the liquid passageway downstream from the germ-removal filter. This prevents a liquid medicine stored in the liquid-medicine container from going into the liquid-medicine injection port device before its use. Thereby, the germ-removal filter is kept from deteriorating, clogging up or the like, and thus, the capability of the germ-removal filter 16 is normally maintained. Furthermore, the closure is easily opened, allowing it to be used (or injection-mixing to be conducted) conveniently by a simple operation.
Furthermore, the closure is opened by a liquid-medicine injection pressure. Hence, the liquid-medicine injection port device can be obtained which is capable of conducting injection-mixing easily, simply by injecting a liquid medicine. In other words, there is no need to conduct any other operation.
Furthermore, the closure is opened by a movement of the main-body member. Accordingly, there is no need for any new members which open the main-body member. This allows the liquid-medicine injection port device to have a simple structure.
Furthermore, the closure is an open-and-close valve which is opened by an operation of the operation member which penetrates the side wall of the liquid-medicine injection port device. Hence, the liquid-medicine injection port device can be obtained which is capable of opening the closure surely.
Furthermore, in the liquid-medicine container which is provided with the liquid-medicine injection port device according to the present invention, injection-mixing can be conducted by an easy operation, and a safe liquid medicine which does not include any germs or the like can be obtained. This makes it possible to give it to a patient at ease, without worrying about any side effects such as septicemia and endotoxin shock.
Number | Date | Country | Kind |
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2001-279182 | Sep 2001 | JP | national |
2002-231489 | Aug 2002 | JP | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/JP02/09407 | 9/13/2002 | WO | 00 | 3/4/2004 |
Publishing Document | Publishing Date | Country | Kind |
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WO03/028617 | 4/10/2003 | WO | A |
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