The present disclosure relates to single-use lancing devices, for example for use in providing a sample of blood.
Lancing devices are used to obtain blood samples from a person by piercing the skin on a finger or other body part with a small needle or blade. Such blood samples are required for many medical tests, for example glucose tests for diabetes management. To make the process of drawing the blood sample convenient and safe to the user, lancing devices need to satisfy high standards. For example, in order to avoid infection and contamination, lancing devices are preferable single-use disposable products. They must therefore be small and simple, to be economic, and preferably should use a sustainable design to minimise waste and environmental impact through their life cycle.
Disposable lancing devices typically include a needle connected to a holder, collectively referred to as a lancet, and a trigger mechanism. When the trigger is activated the lancet is propelled from a retracted position within the housing of the device to an extended position wherein the needle projects from the housing to prick the subject's skin. Usually the lancet is driven by a metal spring which is cocked during the assembly of the device and released by the trigger. A problem with these devices is that the use of metal springs contributes to the device's environmental impact during disposal. Furthermore, metal springs require additional space within the device, increasing the amount of plastic required and the size of the packaging. Another problem with current designs is that storing a lancing device with a cocked spring can cause parts to become misshapen through tension, impairing its operation.
The present invention has been devised to overcome the problems described above; in particular, to address the need for a lancing device which is more sustainable than current designs.
According to a first aspect of the present invention there is provided a lancing device comprising a housing and a lancet. The lancet comprises a needle and is configured to be movable rearwardly within the housing from an initial operational position to a retracted position. The lancing device further comprises a shroud coupled movably to the housing and at least partially covering and extending forwards beyond a forward end of the needle before use of the lancing device, and a biasing member coupled between the lancet and the shroud. The shroud is configured to, when pressed against skin around a sampling site, move rearwards relative to the housing, prime the biasing member during the rearward movement, and, at a first point of the rearward movement, allow the needle to contact the sampling site and subsequently, at a second point of the rearward movement, release energy stored in the biasing member to drive the lancet from the operational position to the retracted position. The housing comprises one or more deflectable legs. The or each deflectable legs extend from an inner surface of the housing and are configured to engage with a shoulder of the lancet to restrict a rearward movement of the lancet with respect to the housing until the shroud reaches the second point of the rearward movement. The shroud is further configured to, at the second point of the rearward movement, deflect the legs so that rearward movement of the lancet is no longer restricted and energy stored in the biasing member is released to drive the lancet from the operational position to the retracted position.
The biasing member may comprise one or more springs that are compressed during the rearward movement. The or each spring may be a plastic spring. The or each plastic spring may be formed integrally with the shroud. The or each plastic spring may be a flexible leg.
The housing may comprise one or more fingers configured to resist an initial rearward movement of the shroud until a level of force applied by the user exceeds a predefined threshold force. The housing and the shroud may comprise cooperating snap-fit fastening features for preventing resetting of the shroud, after the shroud reaches the second point of the rearward movement.
The housing may comprise a lower housing part and an upper housing part in snap-fit engagement with one another. The lower housing part may be configured to couple the shroud moveably to the lower housing. The lower housing part may comprise the or each deflectable legs, one or more fingers configured to resist an initial rearward movement of the shroud until a level of force applied by the user exceeds a predefined threshold force, and snap-fit fastening features for cooperatively engaging with features of the shroud for preventing resetting of the shroud, after the shroud reaches the second point of the rearward movement.
Components of the device may be configured to facilitate assembly of the device by installing the shroud into the lower housing part by inserting the shroud from a lower end of the lower housing part and pushing the shroud rearwards into the lower housing part until the or each finger restricts further rearward movement of the shroud; installing the lancet into the lower housing part by inserting the lancet from an upper end of the lower housing part and fastening the lancet into the or each deflectable legs, and joining the upper housing part with the lower housing part by snap-fit engagement.
The Figures illustrate the components and operation of a single use lancing device designed for pricking a person's skin to, for example, provide a blood sample. The references to “lower”, “upper”, “horizontal” and “vertical” have been chosen for convenience, and refer to the orientations as shown in
Referring to
Referring to
Referring to
The lower housing part 13 also provides two legs 14 which extend upwards from the inner surface of the lower housing part 13 (fewer or more than two legs may also be envisaged). The upper end of each leg 14 is shaped to serve as a hook of a snap-fit fastener. At the upper end of each leg 14, a generally triangular shaped hook protrudes towards the central axis of the lower housing part 13, providing a generally flat and horizontal surface at its lower end.
The legs 14 are deflectable such that the unsupported upper ends of the legs flex away from the central axis of the lower housing part 13 when the legs 14 are deflected. Each of the legs 14 comprises a section 26 which protrudes towards the central axis of the lower housing part 13. As discussed in more detail below, the protruding section 26 is configured to enable an interaction with the shroud 17 such that the shroud 17 deflects the legs 14 during operation of the lancing device. At its lower end, the inner surface of the lower housing part 13 further includes a tapered region 30. As discussed in further detail below, this tapered region 30 is configured to match the tapered lip 29 of the shroud 17.
Referring to
The upper housing part 2 is closed at its upper end and defines a generally circular opening 3 at its lower end. The lateral extent of the upper housing part 2 is greater at its lower end than at its upper end. The upper housing part 2 includes two portions of convex shape and two portions of concave shape with respect to the central axis, as illustrated respectively in the side and front views shown in
The lower housing part 13, the upper housing part 2, the shroud 17 and the lancet body 8 are moulded components. Considering the lancet, the needle 12 is embedded into the lancet body 8 by over-moulding. It is an advantage that the main components of the lancing device 1, including the spring legs 18, are manufactured from plastic materials. Moulded plastic springs enable designs which are highly compact and reduce waste.
The assembly of the lancing device comprises three simple steps. First, the shroud 17 is pushed into the passage 16 from the lower end of the lower housing part 13 until the fingers 23 restrict further rearward movement of the shroud 17. Second, the lancet 7 is installed in its operating position in the lower housing part 13 by inserting it into the passage 16 from the upper end of the lower housing part 13 and fastening the shoulder 9 into the two legs 14. Third, the upper housing part 2 is connected to the lower housing 13 part via the corresponding annular snap fit features 15, 22. NB. The lancet is sterilised prior to assembly.
In an assembled lancing device, as shown in
In an assembled lancing device, an upper end of the shroud 17 is located inside the lower housing part 13 and the shroud 17 extends outwardly from the passageway 16 of the lower housing part 13. The ribs 21 of the shroud 17 cooperatively engage with pockets in the lower housing part 13, preventing rotational movement of the shroud 17. The hooks 24 of the shroud 17 are cooperatively engaged with recesses in the lower housing part 13, preventing forward movement of the shroud 17. The fingers 23 are engaged with the tapered portions 25 of the shroud 17. The fingers 23 restrict the rearward movement of the shroud 17 until a level of force applied by the user exceeds a predefined threshold force and thereby prevent an accidental activation of the lancing device.
With reference to
After removal of the cap 11, the user places the skin contacting surface 19 with projections 20 against skin 27 around a sampling site, as illustrated in
The user then continues to press the lancing device 1 against the skin 27 and, as illustrated in
The legs 14 are now flexed away from the central axis of the lower housing part 13 by the shroud 17 engaging with the protruding section 26 of the legs 14. The upper ends of the legs 14 are no longer engaged with the lancet shoulder 9. The rearward movement of the lancet 7 is no longer restricted within the housing and the energy stored in the spring legs 18 is released to drive the lancet 7 from the operational position to a retracted position. As shown in
Next, the user removes the lancing device from the sampling site and collects the blood sample, e.g. with a suitable swab. As the lancet 7 is now in the retracted position, the risk of accidental needle injuries is greatly reduced. The lancing device is now in a “used” state and can be disposed of. The retracted shroud 17 serves as a visual indicator to the user that the device has been used and thereby prevents any confusion by the user as to the state of the lancing device.
It is an advantage of the lancing device 1 that the shroud 17 engages directly with the legs 14 to release the lancet 7 since this allows precise control over the maximum skin penetration depth without requiring overly tight (and thus expensive) manufacturing tolerances. As described above, the needle 12 penetrates further into the skin until the lancet is retracted, i.e. until the shroud 17 engages with the protruding section 26 of the legs 14 to flex the legs 14 away from the central axis of the housing. This simple release mechanism may be less sensitive to manufacturing variations than known release mechanisms which employ intermediate parts to realise a coupling between the shroud and the lancet retaining features. In particular, the maximum skin penetration depth of the lancing device 1 does not depend on the stiffness of the deflectable legs 14 but only on the dimensions of the protruding section 26 of the legs 14 and the corresponding engaging section of the shroud 17. Thus, the lancing device 1 described with respect to the accompanying figures provides a very simple and elegant solution to the problem of manufacturing disposable lancing devices with a consistent and well-defined skin penetration depth.
Those skilled in the art will appreciate that various modifications may be made to the above described embodiment without departing from the scope of the present invention.
In the embodiment shown in
In the above description, the pricking member that pierces the skin has been described as a “needle”. Those skilled in the art will appreciate that this term encompasses conventional needles, blades etc.
Number | Date | Country | Kind |
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2204315.2 | Mar 2022 | GB | national |
Filing Document | Filing Date | Country | Kind |
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PCT/EP2023/057771 | 3/27/2023 | WO |