Plunger rod comprising at least three annular elements for a prefilled syringe
11571520 · 2023-02-07
Assignee
Inventors
Cpc classification
A61M5/002
HUMAN NECESSITIES
A61M5/28
HUMAN NECESSITIES
A61M5/31511
HUMAN NECESSITIES
International classification
A61M5/00
HUMAN NECESSITIES
B65D75/36
PERFORMING OPERATIONS; TRANSPORTING
A61M5/28
HUMAN NECESSITIES
Abstract
A prefilled syringe includes a syringe body filled with a medical fluid, which has a nozzle at a front side, the nozzle being closed with a cap, and which is closed at a rear side with a displaceable plunger; and a plunger rod that can be inserted into the syringe body via the rear side. The plunger rod has a connecting portion at a front side, via whi9ch the plunger rod can be connected to the plunger. At least three annular elements, which extend at least in some sections about a longitudinal axis of the rod, are arranged on a rear side of the connecting portion on the plunger rod in such a manner that they are located in the syringe body when the plunger rod is fully connected to the plunger. The three annular elements support a coaxial connection of the rod to the plunger positioned in the syringe.
Claims
1. A prefilled syringe comprising a syringe body which is filled with a medical fluid and comprises, on a front end thereof, a nozzle, which is closed by way of a cap, wherein the syringe body is closed, on a rear end thereof, by way of a displaceable plunger, and a plunger rod, which is insertable into the syringe body via the rear end of the syringe body and comprises, on a front end thereof, a connecting portion by means of which the plunger rod is connectable to the plunger, wherein at least three annular elements extend along a portion of a longitudinal axis of the plunger rod, the portion being next to a rear end of the connecting portion, wherein the portion extends from a proximal-most annular element to a distal-most annular element, wherein, when the connecting portion of the plunger rod is fully connected to the plunger, the at least three annular elements are situated in the syringe body, wherein the annular elements engage the syringe body to promote maintenance of a coaxial position of the plunger rod relative to the plunger while the connecting portion is being connected to the plunger, wherein wing elements, extend radially outwardly and connect the at least three annular elements together, the wing elements being distributed along a circumference of the plunger rod, wherein an outside diameter (D.sub.F) of the wing elements within the portion along which the three annular elements extend is smaller than an outside diameter (D) of the at least three annular elements, and wherein the rear end of the plunger rod is closed off by a flange.
2. The prefilled syringe as claimed in claim 1, wherein a position of the plunger in the prefilled syringe body and the position of the at least three annular elements on the plunger rod are matched to one another such that in a first step, when the plunger rod is placed by way of its connecting portion on the plunger, two of the at least three annular elements are arranged in the interior of the syringe body.
3. The prefilled syringe as claimed in claim 2, wherein the outside diameter (D) of the at least three annular elements and an inside diameter of the syringe body are selected to enable the at least three annular elements to engage the syringe body.
4. The prefilled syringe as claimed in claim 2, wherein the outside diameter (D) of the at least three annular elements is identical.
5. The prefilled syringe as claimed in claim 2, wherein at least four wing elements are arranged to form angles therebetween, each angle being 90°, wherein the at least four of the wing elements are arranged between two of the at least three annular elements.
6. The prefilled syringe as claimed in claim 1, wherein the outside diameter (D) of the at least three annular elements and an inside diameter of the syringe body are selected to enable the at least three annular elements to engage the syringe body to permit guiding the plunger rod in the syringe body.
7. The prefilled syringe as claimed in claim 1, wherein the outside diameter (D) of the at least three annular elements is identical.
8. The prefilled syringe as claimed in claim 1, wherein at least four of the wing elements are arranged, to form angles therebetween, each angle being 90°, wherein the at least four of the wing elements are arranged between two of the at least three annular elements.
9. The prefilled syringe as claimed in claim 1, wherein the outside diameter (D.sub.F) of the wing elements is selected to enable the wing elements to engage the syringe body.
10. The prefilled syringe as claimed in claim 1, wherein the outside diameter (D.sub.F) of the wing elements is substantially the same as the outside diameter (D) of the at least three annular elements.
11. The prefilled syringe as claimed in claim 1, wherein the outside diameter (D.sub.F) of the wing elements is less than the outside diameter (D) of the at least three annular elements by between 1 mm and 10 mm.
12. The prefilled syringe as claimed in claim 1, wherein the plunger rod is premounted on the plunger.
13. The prefilled syringe as claimed in claim 1, wherein the plunger rod is located next to the syringe body in an oxygen-impermeable, over pack.
14. An oxygen-impermeable over pack having an interior in which the syringe as claimed in claim 1, wherein it is hermetically enclosed.
15. A plunger rod for a prefilled syringe as claimed in claim 1, including a front-end connecting portion, the plunger rod being connectable to a plunger, wherein the at least three annular elements, extend at least in portions about a longitudinal axis of the plunger rod and are arranged at a distance R, wherein 0.5 mm≤R≤20 mm.
16. A pre-filled syringe as claimed in claim 1, the pre-filled syringe including a plunger positionable in the syringe body and the at least three annular elements are arranged on the plunger rod such that, when the plunger rod is fully connected to the plunger, the at least three annular elements are situated in the syringe body.
17. The prefilled syringe as claimed in claim 1, wherein the wing elements are individually arranged between the at least three annular elements.
18. The prefilled syringe as claimed in claim 1, wherein the outside diameter (D.sub.F) of the wing elements is less than the outside diameter (D) of the at least three annular elements by between 4 mm and 8 mm.
19. A plunger rod for a prefilled syringe as claimed claim 1, including a front-end connecting portion, the plunger rod being connectable to a plunger, wherein the at least three annular elements extend at least in portions about a longitudinal axis of the plunger rod and are arranged at a distance R, wherein 1 mm≤R≤10 mm.
20. An oxygen-impermeable overpack comprising: a prefilled syringe and a plunger rod; wherein the prefilled syringe and the plunger rod are hermetically enclosed within an interior of the oxygen impermeable overpack; the plunger rod including a front-end connecting portion by means of which the plunger rod is connectable to a plunger, wherein at least three annular elements which extend at least in portions about a longitudinal axis of the plunger rod and which are arranged on a rear end of the connecting portion at a distance R, wherein 0.5 mm≤R≤20 mm, wherein wing elements, extend radially outwardly and connect the at least three annular elements together, the wing elements being arranged distributed over a circumference of the plunger rod, an outside diameter (D.sub.F) of the wing elements is smaller than an outside diameter (D) of the at least three annular elements, wherein the rear end of the plunger rod is closed off by a flange.
21. A plunger rod for a prefilled syringe, the plunger rod comprising a front end connecting portion, by means of which the plunger rod is connectable to a plunger, wherein at least three annular elements which extend at least in portions about a longitudinal axis of the plunger rod and which are arranged on a rear end of the connecting portion at a distance R, wherein 0.5 mm≤R≤20 mm, wherein wing elements, extend radially outwardly and connect the at least three annular elements together, the wing elements being arranged distributed over a circumference of the plunger rod, an outside diameter (D.sub.F) of the wing elements is smaller than an outside diameter (D) of the at least three annular elements, wherein the rear end of the plunger rod is closed off by a flange.
22. A prefilled syringe comprising a syringe body having a front end and a rear end, said syringe body being filled with a medical fluid, a displaceable plunger that closes said body at said rear end, a nozzle at said front end, a cap that closes said nozzle, and a plunger rod that is insertable into said syringe body at said rear end thereof, wherein said plunger rod that extends along a longitudinal axis, said plunger rod comprising wing elements distributed along a circumference of said plunger rod and extending radially outward from said longitudinal axis, a connecting portion that is configured to connect to said displaceable plunger at said rear end, and three annular elements that extend along a portion of said longitudinal axis, said portion being next to a rear end of said connecting portion, said portion extending from a proximal-most annular element to a distal-most annular element, said three annular elements being connected to each other by said wing elements, wherein, when said connecting portion of said plunger rod is fully connected to said displaceable plunger, said three annular elements are situated in said syringe body, wherein the annular elements engage the syringe body to promote maintenance of a coaxial position of the plunger rod relative to the plunger while the connecting portion is being screwed into the plunger, wherein an outside diameter of the wing elements within the portion along which the three annular elements extend is smaller than an outside diameter of the at least three annular elements, and wherein the rear end of the plunger rod is closed off by a flange.
Description
(1) The invention is described in detail below by way of exemplary embodiments in connection with the drawings, in which:
(2)
(3)
(4)
(5)
(6)
(7)
(8)
(9)
(10) The front end of the plunger rod 15′ is provided by a connecting portion 1, by means of which the plunger rod 15′ is connected to a plunger 12, not shown here, (see
(11) The cross-shaped cross section of the plunger rod 15′ is also continued between the three annular elements 2a, 2b, 2c. Ignoring the flange 4 and the connecting portion 1, the diameter D of the plunger rod is identical or substantially identical along the longitudinal axis. As a result, so-called wing elements 3a, 3b or ribs are formed between the three annular elements 2a, 2b, 2c. The front, here four, wing elements 3a connect the front ring 2a to the central ring 2b. The rear, here four, wing elements 3b connect the central ring 2b to the rear ring 2b. The annular elements 2a, 2b, 2c and the wing elements 3a, 3b enable the plunger rod 15′ to be guided into the syringe body 8 in as coaxial a manner as possible and, as a result, enable the plunger rod 15′ to be screwed into the plunger 12 in as coaxial a manner as possible (see
(12)
(13) The outside diameter D or D.sub.F of the plunger rod 15′ and/or of the annular elements 2a, 2b, 2c and/or of the wing elements 3a, 3b can be identical to the inside diameter of the syringe body 8. In order to make it easier for the plunger rod 15′ to move in the syringe body 8, the outside diameter D or D.sub.F of the plunger rod 15′ and/or of the annular elements 2a, 2b, 2c and/or of the wing elements 3a, 3b is, in particular, smaller than the inside diameter of the syringe body 8. The outside diameter D or D.sub.F is preferably reduced in relation to the inside diameter of the syringe body 8 by approximately between 0.5 mm and 5 mm.
(14) The prefilled syringe 20 can be filled, for example, via its initially open rear end and then can be closed by way of the plunger 12. The plunger rod 15′ can then be connected to the plunger 12 at a later point in time, for example shortly before the application. However, the plunger 12 can also, for example, be inserted into the syringe body 8 with the plunger rod 15′ already screwed into the plunger 12.
(15) The position of the plunger 12 in the prefilled syringe body 8 and the position of the three annular elements 2a, 2b, 2c on the plunger rod 15′ are preferably matched to one another in such a manner that in a first step, when the plunger rod 15′ is placed on the plunger 12 by way of its connecting portion 1, the two front rings 2a, 2b are already arranged in the interior of the syringe body 8 and are preferably guided by the inner side of the syringe body 8. When being screwed in, the plunger rod 15′ is initially guided by the two front annular elements 2a, 2b and the front wing elements 3a and then also by the rear wing elements 3b in the syringe body 8. The rear third ring 2c supports the guiding of the plunger rod 15′ in the final, fixed connection between the plunger rod 15′ and the plunger 12. The three rings 2a, 2b, 2c are positioned in the interior of the syringe body 8 no later than in the state in which the plunger rod 15′ is fully connected to the plunger 12, preferably is screwed into the plunger 12. The annular elements 2a, 2b, 2c prove to be advantageous as they prevent tilting over the entire circumference of 360°. The wing elements 3a, 3b prove to be advantageous as they enable longer guidance along the longitudinal axis of the plunger rod 15′. The present invention joins said advantages together.
(16)
(17) As a result, when screwing the plunger rod 15″ into the plunger 12, it is possible, in particular, for the user to have haptic and/or acoustic control. If the user screws the plunger rod 15″ correctly into the plunger 12 immediately, he does not receive a haptic and/or acoustic message. If, in contrast, the user tries, unintentionally, to screw the plunger rod 15″ into the plunger 12 incorrectly askew, he is able to perceive, in particular, the transition of the plunger rod 15″ from the central annular element 2b to the rear annular element 2c on the edge 14 in the rear syringe body opening (see
(18) In addition,
(19) Finally,
(20) It is clear to the person skilled in the art that the described embodiments are to be understood as examples. The invention is not limited to said embodiments but can be varied in many different ways without departing from the essence of the invention. Features of individual embodiments and the features named in the general part of the description can be combined with one another both individually and together.