Patent Application
20240131273
The present invention relates, in general, to the technical field of syringe caps. More particularly, the present invention relates to an air-tight and unintentional anti-unscrewing closure cap for a disposable syringe with Luer-lock connector. The invention also relates to a syringe with Luer-lock connector provided with such a cap.
Syringes, in particular pre-filled ones, are widely used to inject medicinal products in a person such as, among others, anticoagulants, for example heparin and the like, vaccines, small sized molecules, and cosmetic products, for example hyaluronic acid. They represent a growing market, as they make it possible to effectively reduce errors in the dosage of a product to be injected and help to reduce packaging costs.
A syringe typically comprises a transparent cylindrical body, on which measurement notches are indicated, a plunger sliding inside the transparent cylindrical body and a hollow and frusto-conical tip, extending from the transparent cylindrical body and onto which a needle, it also being hollow, is subsequently fitted through which the product to be injected, contained in the hollow cylindrical body, passes. The plunger is provided, at one end thereof, with a rubber ring or capsule to ensure the controlled and constant sliding of the plunger inside the transparent cylindrical body. The tip of the syringe can be provided with a Luer-lock connector, i.e. a screwing system that locks the needle connection to prevent the unintentional removal thereof.
Syringes, particularly pre-filled ones, may also be provided with a closure cap, the function of which is to prevent the leakage of the product with which the syringe was previously filled, when the syringe is not in use.
With particular reference to pre-filled syringes, they must guarantee the sterility of the product inside them for several years, typically up to five years, i.e. they must prevent the product from coming into contact with air. In fact, if air enters the pre-filled syringe, the product inside it could undergo such deteriorations as to compromise the effectiveness thereof.
The entry of air into a pre-filled syringe typically occurs following repeated thermal cycles and/or unintentional impacts, which phenomena might cause the partial or total separation of the cap from the syringe. The entry of air into the pre-filled syringe might also occur during the syringe sterilization process, for example in an autoclave, or in the centrifugation phase, during which a pressure drop is generated in the syringe that promotes the entry of air.
The closure caps for the syringes, in particular for pre-filled syringes, with a Luer-lock connector must therefore have sealing properties, i.e. ensure air-tightness, and anti-unscrewing properties, i.e. be configured so as not to separate unintentionally and in an unwanted manner from the syringe, when the syringe is not in use, typically during storage.
A closure cap for pre-filled syringe with Luer-lock connector of known type comprises a rigid and relatively non-deformable portion for handling and coupling with the Luer-lock connector, and a softer and hollow portion, typically made of rubber, which is housed in the rigid portion and is designed to come into contact, by wrapping it, with the frusto-conical tip of the syringe.
The known cap briefly described above has some drawbacks.
Firstly, this cap, even if correctly positioned at the tip and at the Luer-lock connector of the syringe, does not guarantee a sufficient sealing and unintentional anti-unscrewing action, as the contact force between the rubber portion and the tip of the syringe is distributed over a surface, namely the frusto-conical external side surface of the tip, which is relatively extended. The soft rubber portion of the cap therefore exerts a relatively low pressure on the external side surface of the tip, with consequent possibility of air entering the pre-filled syringe and simultaneous reduction of the anti-unscrewing effect exerted by the cap at the Luer-lock connector, under storage conditions of the pre-filled syringe. This anti-unscrewing effect is in fact due to the frictional forces generated between the external frusto-conical surface of the syringe tip and the soft rubber portion of the cap.
Secondly, when mounting the cap onto the tip of the pre-filled syringe, air can remain trapped between the soft rubber portion of the cap and the tip of the pre-filled syringe, which trapped air is inevitably forced into the pre-filled syringe, as the soft rubber portion is fitted onto the pre-filled syringe.
Furthermore, in the step of inserting the cap onto the pre-filled syringe, a creeping action of the cap is generated on the external side surface of the tip. This creeping, in addition to being annoying for the operator, can cause the generation of unwanted microparticles that might contaminate the product contained in the syringe.
Finally, the closure caps for syringes of the known type are difficult to assemble for the manufacturer and have a relatively high cost.
Patent documents US 2019/344017 A1, EP 2 862 587 A1 and US 2006/178627 A1 describe closure caps for syringes according to the prior art.
The main object of the present invention is therefore to provide a cap for a syringe with Luer-lock connector capable of overcoming the drawbacks mentioned above with reference to the caps for a syringe of the known type.
More specifically, the main object of the present invention is to provide a cap for a syringe with Luer-lock connector configured in such a way as to considerably increase the sealing and unintentional anti-unscrewing properties, in particular during the step of the autoclave sterilization of the syringe, a step during which high pressure, humidity and temperature values are reached, so as to guarantee perfect preservation of the product contained in the syringe, at least for a period of five years.
Still another object of the present invention is to provide a cap for a syringe with Luer-lock connector configured to facilitate the screwing operation onto the syringe, as well as the unscrewing operation when the syringe is to be used to inject the product contained therein.
Not the least object of the present invention is to provide a cap for a syringe with Luer-lock connector, which can be produced in times and at costs lower than those for producing traditional caps.
These and other objects, which will become clearer in the following of the present description, are achieved by a cap for a syringe with Luer-lock connector and by a syringe according to independent claims 1 and 10. Preferred characteristics of the cap are disclosed in dependent claims 2 to 9.
The invention thus relates, in a first aspect thereof, to a cap of a syringe with Luer-lock connector comprising:
The cap is characterized in that raised elements are formed at respective crests of the threads of the external threading of the second coupling portion and in that the raised elements are dimensioned so as to frictionally couple with a bottom of respective threads of the internal threading of the Luer-lock connector.
In a second aspect thereof, the invention relates to a syringe, preferably a pre-filled syringe, with a Luer-lock connector provided with a cap as defined above.
When the cap is mounted onto the syringe, friction is generated between the raised elements provided on the external threading of the cap and the threading of the Luer-lock connector of the syringe and the rubber abuts against the tip of the syringe, suitably compressed inside of the axial cavity. The unintentional anti-unscrewing and air-tight closure of the syringe is thus ensured for long periods of time.
In other words, the sealing and anti-unscrewing characteristics of the cap according to the invention are ensured by two factors, namely the friction force generated between the raised elements of the cap and the internal threading of the Luer-lock connector of the syringe, a force which is added to the friction between the flanks of the threads of the external threading of the cap and the flanks of the threads of the internal threading of the Luer-lock connector, and the elastic reaction of the rubber, compressed inside the axial cavity. In fact, the rubber, in addition to air-tightly closing the tip of the syringe, increases, due to its elastic reaction, the frictional force between the second coupling portion of the main body and the Luer-lock connector to which the cap is coupled.
Yet, since the rubber abuts against the tip of the syringe and is constantly compressed inside the axial cavity of the main body, the elastic reaction of the rubber remains in an interval such as to guarantee the anti-unscrewing effect and the sealing power of the cap. It is therefore avoided that the rubber undergoes a plastic deformation over time, which would affect the efficiency of the tight closure of the free open end of the syringe tip.
Further characteristics and advantages of the present invention will become clearer from the following detailed description of a preferred embodiment thereof, given below, by way of non-limiting example, with reference to the attached drawings. In the drawings:
With reference to
The cap, generally indicated with the reference number 100, comprises a main body 10, substantially cylindrical, including a first portion 14 for handling the cap 100 and a second portion 15 for coupling the cap 100 with a syringe with Luer-lock connector.
As shown in detail in
The first handle portion 14 preferably has a faceted external surface 16 to facilitate the gripping of the cap 100 by a user in the step of screwing/unscrewing the cap 100 onto/from the syringe 1.
Preferably, the second coupling portion 15 has an external diameter smaller than the external diameter of the first handle portion 14, so that an annular surface 19 is delimited between the first handle portion 14 and the second coupling portion 15, which is designed to abut against a corresponding annular surface 7 of the Luer-lock connector 5, when the cap 100 is mounted on the syringe 1.
The second coupling portion 15 also has a conical mouth 18 at a free end thereof, which advantageously facilitates the insertion of the cap 100 into the space S comprised between the tip 4 and the Luer-lock connector 5 of the syringe 1.
The second coupling portion 15 has, in addition, an external threading 17 for coupling with the internal threading 6 of the Luer-lock connector 5 of the syringe 1.
In the external threading 17 of the second coupling portion 15, preferably at a crest portion of the threads, raised elements 30 are formed, preferably having a substantially rectangular or trapezoidal section, the function of which is to generate friction with corresponding threads of the internal threading 6 of the Luer-lock connector 5 in order to ensure a tight and unintentional anti-unscrewing closure of the cap 100 on the syringe 1.
In the illustrated embodiment, two sets of raised elements 30 are provided, each comprising at least one raised element, preferably three raised elements 30, provided on the external threading 17 in a diametrically opposite position. Alternatively, only one set of raised elements may be provided, or a number of sets of raised elements 30 greater than two, suitably distributed on the external threading 17 along the circumference of the second coupling portion 15, each set being composed of a number of raised elements less than or greater than three. For example, if three sets of raised elements are provided, these sets are preferably arranged at 120 degrees around the circumference of the second coupling portion 15 of the cap 100.
Preferably, the raised elements 30 of each set of raised elements are aligned with each other along the external threading 17 of the second coupling portion 15 of the cap 100 according to a longitudinal axis of the cap 100.
Preferably, the raised elements 30 are recessed or aligned, but never protruding, with respect to an edge of the external threading 17 of the second coupling portion 15 of the cap 100.
In particular, and as shown in detail in
This localised static friction is added to the one generated between the flanks 6a and 17a, respectively, of the internal threading 6 of the Luer-lock connector and the external threading 17 of the cap 100, advantageously avoiding that, in particularly extreme conditions, for example during the step of sterilisation of the syringe 1 in an autoclave, where high values of pressure, humidity and temperature are reached, a loosening of the cap 100 occurs, with consequent reduced tightness of the same and penetration of air into the cylindrical body of the syringe 1.
In fact, this configuration of the external threading 17 of the second coupling portion 15, in particular the presence of the raised elements 30, ensures that the interference between the cap 100 and the Luer-lock connector 5 is contained in a well-defined region, thus obtaining an effective unintentional anti-unscrewing effect and, at the same time, allowing the Luer-lock connector to deform elastically just enough to avoid cracks and breakage.
Preferably, the threads of the cap 100 and the threads of the Luer-lock connector 5 are slightly tapered, thereby further facilitating the operations of screwing and unscrewing the cap 100 on the syringe 1. In fact, the contact forces between the cap 100 and the Luer-lock connector 5 do not persist for the entire duration of the screwing and unscrewing steps of the cap—that is, they are present in the final part of the screwing and in the initial part of the unscrewing. Furthermore, the contact forces between cap 100 and Luer-lock connector 5 are also generated at the raised elements 30.
As clearly visible in
The main body 10 is made of a rigid and non-deformable material, for example compact polycarbonate (Makrolon®), cyclic-olefin polymer (COP), or cyclic-olefin copolymer (COC), and the plane bottom surface 13 of the axial cylindrical cavity 11 is also rigid and non-deformable.
The cap 100 also comprises a rubber 20, which is housed in the axial cylindrical cavity 11 of the main body 10.
The rubber 20 is substantially cylindrical in shape and has a surface 21, a surface 22, opposite to the surface 21 and facing the aperture 11a of the axial cavity 11 so as to abut, in use, against a free end 4a of the tip 4 of the syringe 1, and a side surface 23.
The surfaces 21 and 22 are preferably plane, while, at the side surface 23, at least one longitudinal groove 24, preferably a pair of opposed longitudinal grooves 24, more preferably a series of longitudinal grooves 24 are formed, which allow the user to deform the rubber 20 to advantageously facilitate the insertion thereof into the axial cylindrical cavity 11 of the main body 10, during the assembly of the cap 100. The longitudinal grooves 24 also advantageously allow air to escape when inserting the rubber 20 into the axial cavity 11 during the assembly phase of the cap 100, so that no air is trapped between the bottom surface 13 and the surface 21 of the rubber 20.
Alternatively, instead of being plane, the surface 22 of the rubber 20 designed to abut, in use, against the free end 4a of the tip 4 of the syringe 1 can be convex, with convexity facing the tip 4. In this case, as the cap is screwed onto the syringe, the convex surface 22 of the rubber 20 flattens, thus abutting against the free end 4a of the syringe 1, air-tightly closing the opening thereof.
In the assembled condition of the cap 100, shown in detail in
In the illustrated embodiment, the bottom surface 13 of the axial cylindrical cavity 11 is a plane, rigid surface. Alternatively, recesses may be formed at the bottom surface 13, between which an abutment surface 21 of the rubber 20 is delimited.
In yet another alternative embodiment, a seat for housing a pin extending from the bottom surface 13 of the axial cylindrical cavity 11 of the main body 10 may be formed in the surface 21 of the rubber 20.
With reference to
In the mounting condition of the cap 100 on the syringe 1, the second coupling portion 15 of the main body 10 is screwed onto the Luer-lock connector 5 by coupling the corresponding threadings 17 and 6.
In particular, each raised element 30 formed on the external threading 17 of the second coupling portion 15 is frictionally coupled with the bottom 8 of a corresponding thread of the internal threading 6 of the Luer-lock connector 5 and this localised static friction is added to that produced by the coupling between flanks 6a and 17a, respectively, of the internal threading 6 of the Luer-lock connector and of the external threading 17 of the cap 100.
The advantage given by the frictional coupling between each raised element 30 and the bottom 8 of a corresponding thread of the threading of the Luer-lock connector is that it does not have such a tangential component as to unscrew the cap. The tangential component is instead always present in the friction between the flanks of the threads, since the threads are helical, and therefore the friction tangent to the flanks of the threads has a component that tends to unscrew the cap from the syringe. This aspect is of fundamental importance when the syringe, e.g. pre-filled with acid and placed in an autoclave, is subject to internal pressure. Indeed, the internal pressure pushes the cap axially and the tangential component of the friction between the flanks of the threads would tend to unscrew the cap. However, thanks to the friction between each raised element 30 and the bottom 8 of a corresponding thread of the threading of the Luer-lock connector 5, which has no such a tangential component as to unscrew the cap, the cap is prevented from unscrewing from the syringe 1.
Furthermore, the annular surface 19 of the cap 100 abuts against the corresponding annular surface 7 of the Luer-lock connector 5, thus providing a mechanical stop and at the same time ensuring a suitable elastic deformation of the rubber 20. In fact, when the annular surface 19 is in abutment against the Luer-lock connector 5, the rubber 20 has the plane surface 22 in abutment against the free end 4a of the tip 4 of the syringe 1 and the surface 21 against the plane, rigid bottom surface 13 of the axial cylindrical cavity 11 of the main body 10. The rubber 20 is therefore suitably elastically compressed between the free end 4a of the syringe 1 and the bottom surface 13 of the main body 10 of the cap 100.
Under its compressed condition, the rubber 20 generates an appropriate elastic reaction force, which acts on the threaded coupling between the second coupling portion 15 and the Luer-lock connector 5, so that the threadings 6 and 17 of the Luer-lock connector 5 and of the cap 100 press between them, completely eliminating any clearance between the threads, generating friction between them and therefore eliminating any possibility of unintentional unscrewing of the cap 100 from the syringe 1.
Furthermore, since the contact between rubber 20 and tip 4 of the syringe 1 is essentially frontal, that is, between the plane surface 22 of the rubber 20 and the free end 4a of the tip 4 of the syringe 1, there is no friction between the rubber 20 and the external surface of the tip 4. It follows that the operations of screwing and unscrewing the cap 100 by the operator are facilitated.
Under this mounted condition, the cap according to the invention achieves the desired air-tight and anti-unscrewing effect.
In fact, the rubber 20, in addition to air-tightly closing the free end 4a of the tip 4 of the syringe 1, due to the effect of the elastic deformation, increases the degree of coupling between the threadings 6 and 17, of the Luer-lock connector 5 and of the second coupling portion 15, respectively, with an anti-unscrewing effect which is very similar to that obtained by inserting an elastic washer between screw and nut, tightening the latter.
The localised static friction force generated between the surface 32 of each raised element 30 of the external threading 17 of the second coupling portion and the bottom 8 of the corresponding thread of the internal threading 6 also contributes to increase the anti-unscrewing effect of the Luer-lock connector 5 of the syringe 1.
Furthermore, the presence of the rubber 20 eliminates the anti-unscrewing effects due to thermal cycles and/or vibrations since the elastic material is able to absorb these effects, always guaranteeing an adequate elastic reaction force.
From the above description, the characteristics of the cap for a syringe with Luer-lock connector, and of the syringe comprising it, of the present invention are clear, as well as are the relative advantages.
Finally, it is clear that the cap as conceived herein is susceptible to many modifications and variations; furthermore, all the details are replaceable by technically equivalent elements. In practice, the materials used, as well as their dimensions, can be of any type according to the technical requirements. For example, the cap and the cylindrical body of the syringe can be made of the same material, so as to advantageously have the same thermal expansion coefficient.
| Number | Date | Country | Kind |
|---|---|---|---|
| 102021000003320 | Feb 2021 | IT | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IB2022/051234 | 2/11/2022 | WO |
