1. Field of the Invention
The present invention relates to a disposable safety syringe, and more particularly, to a disposable safety syringe whose needle is retracted after injection to prevent reuse and needle stick injuries.
2. Description of the Prior Art
Due to the serious risk of contamination to various diseases by using infected needles, virtually all syringes in use nowadays are disposable. Furthermore, some of these also possess a retractable mechanism, which retracts the needle inside the syringe after use so that the person administering the injection is prevented from impaling himself and others with a potentially infected needle.
Accordingly, the needle retraction mechanism is considered an especially critical component. Issues such as minimizing the quantity of medicinal fluid being trapped inside the syringe after needle retraction, the amount of pressure required to engage the hooking mechanism and the robustness of the hooking mechanism itself are essential to the creation of an excellent needle retraction mechanism.
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Note that the hooking mechanism's 120 detent 122 and stem 124, the pulling member 202 and the clamps 118 and 118′ constitute the needle retraction mechanism.
The needle retraction mechanism becomes engaged when the plunger rod is fully inserted inside the syringe barrel by additional pressure on the thumb press, so that the hooking mechanism goes passed the clamps and the detent latches on to them.
This type of needle retraction mechanism, which uses the two clamps 118 and 118′, has two serious shortcomings. First of all, the clamps 118 and 118′ are protruding components that are latched on to the wall of pulling member 202. As such, they are not sufficiently robust and can, henceforth, as protrusions can generally break easily. Secondly, using the hooking mechanism 120, as suggested by prior art, does not minimize the loss of medicinal fluid. While it is true that the space between the clamps 118 and 118′ allows the free passage of fluid, this does not prevent fluid to be caught that between the detent 122 and plunger crown 126 after the detent 122 has latched on to the clamps 118 and 118′, as the hooking mechanism 120 does not have the ability expel fluid trapped between itself and the crown 126.
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This kind of hooking mechanism has its own drawbacks, which are as follows. First of all, in order for the detent 316 to go through the central hollow 400, an unreasonable amount of pressure is required to push the plunger. Consequently, it is probable that the individual administering the injection does not have the sufficient strength to generate sufficient pressure on the thumb press in order to get the detent through the central hollow 400 of the ring 314. Furthermore, the large force applied on the plunger will cause the syringe and the needle to shake while the needle is still in the patient, which is dangerous and uncomfortable for the patient.
Another disadvantage of the prior art is that this type of hooking mechanism does not minimize fluid loss to the maximum extent possible. As the detent 316 latches on to the ring 314, some fluid becomes trapped below the face 402 of the ring 314, between the face 402 and the plunger crown 322. This occurs due to the fact that the neck 318 acts as an obstacle that prevents the face 402 of the ring 314 from touching the crown 322, hence creating an area that will be filled with fluid even after the hooking mechanism has been engaged.
It is therefore a primary objective of the claimed invention to provide a disposable retractable safety syringe that solves the above-mentioned problems of the prior art.
According to the claimed invention, a retractable safety syringe comprises a syringe barrel, a needle mount, a plunger rod and a needle. The needle mount is assembled at an upper end of the syringe barrel and formed with an inner hub, and a hollow truncated cone extending inward and upward with a completely surrounded lower conical portion. The hollow truncated cone includes a slit cutting from a ridge of the truncated cone. The plunger rod includes a rod and a plunger formed at one end of the rod. The plunger has a plunger crown and a detent connected to the plunger crown. The needle includes a needle cannula coupled to an upper portion of the inner hub.
These and other objectives of the present invention will no doubt become obvious to those of ordinary skill in the art after reading the following detailed description of the preferred embodiment that is illustrated in the various figures and drawings.
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Subsequently, the needle mount 510 comprises the inner hub 508, an outer hub 509, a fluid passage 507 and a retaining groove 512. The needle mount 510 is air tightly installed inside the syringe barrel 504, at its upper end, so that the syringe barrel's 504 retaining edge 502 retains the needle mount's 510 retaining groove 512, preventing the needle mount 510 from coming out at the upper end of the syringe barrel 504. It is to be noted that the outer hub 509 is an optional element, meaning that the retractable safety syringe 550 could be manufactured with or without an outer hub.
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Furthermore, a plunger rod 528 comprises at an upper end a detent 520, which is made up of a connector 518 that continues with a truncated cone-shaped neck 516. The truncated cone-shaped neck 516 contains on its upper end a detent lip 515. The detent 520 is connected to a crown 522, which is the terminating upper layer of a plunger 524. The plunger 524 contains on its upper end a color band 532 that serves for identification of the fluid level in the syringe barrel 504. The plunger 524 is further connected to a rod 526, which terminates at a lower end with a thumb press 540. The rod 526 further comprises a V-notch 530 that facilitates the breaking of the rod 526 after use, for the purpose of recycling the rod 526 separately from the rest of the syringe and preventing the needle from being pushed out of the injecting end of the syringe barrel 504 after retraction.
Note that the detent's 520 truncated cone-shaped neck 516, detent lip 515, connector 518, plus the needle mount's 510 hollow truncated cone 600 constitute the needle retraction mechanism.
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The difference between the retractable safety syringes 850 and 550 is in the structure of the plunger rods 830 and 528. The plunger rod 830 of the retractable safety syringe 850 comprises at an upper end a detent 820, which is made up of a connector 816 and a detent lip 815. The detent 820 is connected to a crown 522, which is the terminating upper layer of a plunger 524. The plunger 524 contains on its upper end a color band 532. The plunger 524 is further connected to a rod 526, which terminates at a lower end with a thumb press 540. The rod 526 further comprises a V-notch 530.
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A needle mount 130 comprises an inner hub 140 and a retaining groove 144. The inner hub 140 includes a fluid passage 138 and a hollow truncated cone 132, which has its base attached to the inside of the inner hub 140. The hollow truncated cone 132 includes at its upper opening a ridge 136. Also forming at the hollow truncated cone's 132 upper opening there is one or more slits 134.
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Minimizing the quantity of medicinal fluid being trapped inside the syringe after needle retraction and reducing the amount of pressure required to engage the hooking mechanism while increasing the robustness of the hooking mechanism are issues not adequately addressed by the prior art. However, the present invention manages to address and to solve many of these problems that were left unsolved in prior art retractable safety syringes.
First of all, as it has been discussed above, the prior art has not been able to minimize the amount of the fluid trapped in the syringe to the same degree as the present invention. In the present invention, due to the shape of the detent, which hermetically hugs the inside of the hollow truncated cone as the hooking mechanism is engaged, the amount of little fluid being trapped is insignificant, since being only limited to small portions of the inner hub of the needle mount. However, in the prior art, fluid is also being caught between the plunger crown and the detent itself, making this aspect of the prior art inferior to the current invention.
Also different from the prior art, the present invention is successful in maximizing the robustness of the hooking mechanism, while at the same time minimizing the pressure required to drive the detent lip past the hollow truncated cone's upper opening ridge.
Robustness is primarily attained by using the hollow truncated cone, which unlike the prior art's clamps or ring, is inherently a sturdier shape that is capable to bear more pressure on its upper opening than a mechanism employing either a ring or clamps.
Moreover, in the present invention, the pressure required to engage the hooking mechanism is not unreasonable, and fortunately, it does not come at the expense of robustness. To ensure that everybody can engage the syringe's hooking mechanism without undue effort and to prevent excessive movement of the needle while it is still inside the patients body, the present invention has procured the hollow truncated cone with a slit. The slit permits the upper opening of the hollow truncated cone to expand more readily than it would be possible if there was no slit and the detent lip would have had to force its way through a rigid upper opening of the hollow truncated cone.
Those skilled in the art will readily observe that numerous modifications and alterations of the device and method may be made while retaining the teachings of the invention. Accordingly, the above disclosure should be construed as limited only by the metes and bounds of the appended claims.