Automatic Lancet Device and Method of Using the Same

For a better understanding of the present invention, reference may be had to the following detailed description taken in conjunction with the accompanying drawings in which:

FIGS. 1A, 1B, and 1C are front elevation views of an automatic lancet apparatus in accordance with the present invention;

FIG. 2 is an elevation view of a lancet needle for use with the lancet apparatus of FIG. 1A;

FIG. 3 is an exploded perspective view of a portion of the lancet apparatus of FIG. 1A;

FIG. 4 is a cross-sectional view taken through the slot 46 of the lancet apparatus of FIG. 3;

FIG. 5 is a perspective view of the device 30 of FIG. 4;

FIG. 6 is a top plan view of the lancet apparatus of FIG. 1A with top portion 16 removed; and

FIG. 7 is an elevation view of the release and trigger mechanism of FIG. 4.

Referring first to FIGS. 1A, 1B, and 1C, there is shown a simplified elevation view of a front end of an automatic lancet device in accordance with the teaching of the present invention. The device comprises a casing 12 preferably formed of plastic or other lightweight material and having a lower portion 14 and an upper portion 16. Between the lower portion 14 and the upper portion 16, there is provided a spacing in which there is positioned a slide member 18. The slide member 18 includes a first slot 20 and a second parallel slot 22. A plurality of lancet needles 24 is stored within the housing 12. Spring device 26 biases the needles upward toward the slide member 18.

In the operation of the illustrative device, as the needles 24 are biased upward, one of the needles enters the slot 20, FIG. 1A, where it is captured by the slide member 18. The slide member 18 is thereafter moved to the right hand direction into the position shown in FIG. 1B to transport one of the needles 24 into the location indicated at 28. In this injecting location, the needle is captured by an injecting device 30. In order to utilize the needle in the injecting position 28, the slide member 18 must be moved to the position indicated in FIG. 1C. In so doing, the slide member rides upward over the needle in the injecting position by means of the inclined plane 32 formed on the slide member between the slots 20 and 22. The slide member 18 is moved to the left until the slot 22 overlays the needle in the position 28. In this position, the needle can be driven forward, i.e., in a direction out of the plane of the paper, in order to puncture a finger of a person whose blood is to be tested. Once the needle has been used, the slide member 18 is again moved towards the right hand edge into the position shown in FIG. 1B such that the used needle captured in the slot 22 is pushed laterally out of the injecting position. By tipping the device towards its front surface after pushing slide 18 to the position of FIG. 1B, the used needle can be caused to simply fall out of the slot 22 and thereby be disposed of. The slide 18 can then be moved back to the position of FIG. 1A to capture a new needle in the slot 20 for transport into the injecting position 28 so that the device is again ready to be used. Referring briefly to FIG. 2, there is shown a side view of one of the needles 24. The needle is captured in a plastic needle holder 34 and has a tip end 36 enclosed within a plastic cover 38. A small notch 39 separates holder 34 from cover 38 and is defined by a reduced thickness of plastic which is easily removed. When the needles 24 are transported from the loading position at the extreme left side of the device, the plastic portion 38 is automatically separated by an element 40 located on the lower portion of the case 14. The method of separation will become apparent from the description of the figures to follow.

It will be appreciated from the above description of operation that a used needle is ejected before a fresh needle can be loaded. This process assures sterility of the needles and prevents the protective cover 38 of the fresh needle from being removed before the used needle is ejected. The slide 18 is spring loaded to return to the position of FIG. 1C when a needle is positioned in the injecting location. The spring action is chosen so as to prevent the slide 18 from pushing the needle to the left side, i.e., the spring is sufficiently weak that it cannot force the needle out of the injecting position. As will become apparent, the needle is held tightly in the injecting position so as to require manual force to remove it.

Turning now to FIG. 3, there is shown a simplified partial perspective view of the lancet device of FIG. 1 with the upper section 16 removed from the lower section 14 and with the slide member 18 and injection device 30 omitted. In this view, it can be seen that the needles 24 are positioned within a slot 42 on the side of the case 12. Spring means 26 biases the needles 24 upwardly until it contacts with the slide member 18. The needles are preferably held together in a continuous chain of needles by means of a flexible plastic member 45 (shown oversized for clarity) which is easily severed as the needles are picked up by the slide member 18. The lower section 14 and upper section 16 have mating slots 46 within which the injection device 30 slides. The element 40 which removes the plastic cover 38 from the needle tip ends 36 is shown as a triangular member attached to the upper surface of case portion 14. A mating triangular section is also preferably formed on a lower surface of the upper section 16 to assist in pulling the covers 38 from the needles. When one of the needles 24 is picked up by the slide member 18 and the slide member is moved laterally to transfer the needle to the injecting position, the needle tip is forced past the triangular member 40 which fits into the slot or spacing 39 between the needle cover 34 and the tip cover 38. As the needle is moved from left to right across the device 12, the triangular portion separates the cover 38 from the needle and forces it to be discarded out the front of the device 12. Thus, when the needle is in the injecting position within the injecting device 30, the cover 38 has been removed from the needle and the tip of the needle is exposed.

FIG. 3 also shows a slot 48 running vertically up the front face 50 of the housing 12. The upper portion of the slot 48 is sized to accept a platform 52. The platform 52 is provided with a center aperture 54 and a tapered bowl-like depression 56 leading to the aperture 54. The platform 52 provides a convenient place for positioning a person's finger at the front of the device 12 in preparation for puncturing the finger with one of the needles 24. The lower portion of the slot 48 is not as deep as the upper portion which receives the platform 52. The remainder of the slot 48 is designed to pass a flexible strip of material which can be pulled through the slot and overlay the platform 52 to provide a degree of isolation between the platform 52 and a person's finger. The strip may be pulled up and overlay the platform for each person to be examined. After a person's finger is punctured, the strip may be pulled upward to present a new section to the platform 52 and allow a used section to be torn off and discarded.

Referring now to FIG. 4, there is shown a cross-sectional view taken through the slot 46 of FIG. 3. In this figure, the upper section 16 has been omitted and the injection device 30 included. The injection device 30 is designed to capture and hold one of the needles 24 using opposed teeth 58. Referring briefly to FIG. 5, there is shown a perspective view of an injection device 30. The teeth 58 are relatively sharp and are designed to puncture the plastic material encompassing the needle Referring again to FIG. 4, the injection device is propelled forward by spring 60 compressed between a portion of the lower housing 14 and the device 30. The device 30 is held in a cocked position by means of a trigger mechanism including a trigger 62 and a release 64. A spring 66 biases the release 64 towards the member 30 while a spring 68 biases the trigger 62 into a ready position. When the trigger 62 is pressed inward, the release 64 is forced downward retracting it from a notch 70 in the device 30 and allowing the device 30 to be propelled forward. As can be seen, the trigger 62 has a relatively narrow portion 72 which fits through an aperture 74 (see FIG. 7) in the release 64. A larger diameter shaft section 76 connects a head 78 of the trigger to the narrow portion 72. The connection between the shaft section 76 and the narrow portion 72 is provided by a tapered segment which operates against a tapered entry into the aperture 74 and release 64 in a manner to force the release member 64 in a downward direction in order to center the aperture 74 on the shaft portion 76.

FIG. 4 also illustrates the use of a roll of continuous flexible material 80 positioned within an aperture 82 in the lower portion of the casing 14. The strip material is pulled off of the roll and fed through the slot 48 along the face 50 of the device 12. The material extends upward and overlays the platform 52.

As was previously stated, the slide member 18 functions not only to transport the needles from the loading position and into the injecting device 30 but also serves to position the device 30 in its cocked position in preparation for use of one of the needles 24. Referring now to FIG. 6, there is shown a top view of the device 12 with the upper housing section 16 removed. The slide member 18 can be seen to have a cam section 84 which operates against a surface 86 (see FIG. 4) on member 30. As the slide member 18 is moved in the direction indicated by the arrow 88, the cam surface 84 operates against the surface 86 to force the injector device 30 in the direction indicated by arrow 90. As the member 30 is pushed in the indicated direction, it reaches a point at which the release 64 can be pushed into the slot 70 thereby retaining the member 30 in the cocked position. It will be noted that the lancet device cannot be fired until the slide member 18 has been returned to the position indicated in FIG. 6. This is the position shown in the illustration of FIG. 1C. The spring 92 drives the member 18 to this position.

In the operation of the illustrated automatic lancet device, the needles 24 are loaded into the slot 42 on the side of the housing section 14. The slide member is then moved to its extreme left hand position (FIG. 1A) in order to place the slot 20 over the needles and enable one of the needles to enter into the slot. The slide member is then moved to its extreme right hand position (FIG. 1B) in order to transport the needle 24 to the injecting position within the injecting device 30. The slide member is then moved to the left again (FIG. 1C) such that the slot 22 overlays the needle in the injecting position. When the trigger 62 is depressed, the release 64 is forced downward thereby releasing the injecting mechanism 30 so that the spring 60 pushes the mechanism 30 forward to cause the needle tip 36 to project through the aperture 54 within the platform 52. If the strip material 80 is being used, a person's finger will have depressed the strip material against the aperture 54 so that the needle will puncture both the strip material and the person's finger. After use, the slide member 18 is again moved towards the right hand position in order to transport the used needle out of the injecting position and allow it to be discarded by falling out of the front of the device. When it is desired to use the device again, the slide member 18 is pushed fully to the left hand position of FIG. 1A and a fresh needle is transported into the injecting device while the cover 38 is removed from the needle by the stripping mechanism 40 during such transport. Because the slide member 18 which serves to transport needles between the storage position, the injection position, and the discarding position is also utilized to effect cocking of the injecting mechanism, it will be appreciated that the device cannot be cocked and reused until a used needle has been removed from the injecting position and into a discarding position.

While the invention has been described in what is presently considered to be a preferred embodiment, many modifications and variations will become apparent to those skilled in the art. It is intended therefore that the invention not be limited to the disclosed embodiment but be interpreted within the full spirit and scope of the appended claims.