The present invention relates to a hypodermic syringe. More particularly this invention concerns a syringe preloaded with the desired amount of medicament that is ready to be injected into a patient. After the needle of the syringe is forced into the patient, a plunger automatically pushes the medicament into the patient through the needle.
A hypodermic syringe is described as having a generally cylindrical syringe tube centered on a longitudinal axis and having a hollow needle with an open tip attached to the front end. A plunger is slidable inside the tube and define the liquid compartment into which the medicament is placed. When the plunger is moved forward toward the needle, the medicament is pushed though the needle and out the open tip of the needle so that the medicament is injected into the patient.
Hypodermic syringes are primarily used to effect subcutaneous injections. It is well known in the art that many patients are injected with the same dosage of the same medicament. Thus, in preparation, medical professionals often pre-load multiple syringes with the same dosage of the same medicament. When the syringes are pre-loaded, the plunger is left in the retracted position ready to be pushed toward the needle so as to inject the medicament. However, a common problem encountered is that the plunger can be moved forward or backward inadvertently before it is injected into a patient. As this occurs, some of the medicament is pushed out or air is pulled into the tube of the syringe. Either of these scenarios is highly undesirable because it results in the medicament to be contaminated with air or the dosage of the medicament in the syringe to be reduced. Whether air enters the tube of the syringe or some of the medicament is pushed out of the syringe, such pre-loaded syringe becomes unusable and must often be discarded. This problem is primarily caused by the plunger that is unprotected and susceptible to inadvertent movement forward or backward relative to the tube of the syringe.
Accordingly, there is a need for a syringe with a plunger that is protected or encased so that it does not move forward or backward inadvertently until the medicament is ready to be injected into the patient.
Accordingly, the present invention has been made in view of the above-mentioned disadvantages occurring in the prior art. The present invention is an automatic injection syringe that is pre-loaded with the desired dosage of a medicament and can be stored for extended periods of time without fear that the plunger will inadvertently be pushed or pulled rendering the syringe useless.
It is therefore the primary object of the present invention to provide a syringe with a plunger that is encapsulated or encased so that it may not be inadvertently pushed or pulled.
Another object of the present invention is to provide a syringe that can be pre-loaded with the desired amount of medicament.
Yet another object of the present invention is to provide a syringe that automatically injects the medicament into the patient once the needle is forced into the patient.
A still further object of the present invention is to provide a syringe with components that can be varied so as to control the rate by which the medicament injected into the patient.
A yet further object of the present invention is to provide a syringe that is cost effective to manufacture.
The above objects and other features and advantages of the present invention, as well as the structure and operation of various embodiments of the present invention described in detail with reference to the accompanying drawings.
The accompanying drawings which are incorporated by reference herein and form part of the specification, illustrate various embodiments of the present invention and, together with the description, further serve to explain the principles of the invention and to enable a person skilled in the pertinent art to make and use the invention. In the drawings, like reference lumbers indicate identical or functional similar elements. A more complete appreciation of the invention and many of the attendant advantages thereof will be readily obtained as the same becomes better understood by reference to the following detailed description when considered in connection with the accompanying drawings, wherein:
Reference will now be made to the drawings in which various elements of the present invention will be given numerical designations and in which the invention will be discussed so as to enable one skilled in the art and make use the invention.
The present invention comprises an automatic injection syringe 100 comprising a syringe tube 10, a shell 20, a shell cap 30, a needle 40, a sleeve 45, a needle cap 43, and a plunger assembly 90 which comprises a plunger 50, a spring 60, a retainer 70, and a retainer sleeve 80. It is well known that in the treatment of patients, medical professionals often inject the same dosage of the same medicament. Thus, as a time saving exercise, it is customary for medical professionals to pre-load multiple syringes with the same dosage of the same medicament ready for use. However, conventional syringes comprise a plunger that is exposed and can be manually displaced inadvertently so as to release some of the medicament and render the pre-loaded syringe useless. The automatic injection syringe 100 of the present invention allows a syringe to be pre-loaded with medicament and encapsulates the plunger so as to eliminate the risk that it will be inadvertently displaced. Then when needed, the medical professional can inject the medicament into a patient without pressing or even touching the plunger.
Once the plunger assembly 90 is assembled, it is coupled with the tube 10 through the opening 11 so that the plunger 50 is inside the tube 10 and the base 81 of the retainer sleeve 80 rests on the annular flange 12 of the tube 10. With the plunger assembly 90 in place, the tube 10 is inserted into the shell 20 through the rear opening 22 until the annular flange 12 rests against the rear opening 22 and a portion of the sleeve 45 is exposed and protrudes past the front opening 21 of the shell 20. Finally, the shell cap 30 is attached to the rear opening 22 of the shell 20 so as to cover or encapsulate the entire tube 10 and plunger assembly 90 within the shell 20 and the shell cap 30. Once the shell cap 30 is attached to the shell 20, the automatic injection syringe 100 of the present invention is ready for use, as shown in
When the automatic injection syringe 100 of the present invention is ready for use to inject medicament into a patient, the needle cap 43 is removed and the needle 40 is forced into the patient in such a manner and to such extent as to press against, the portion of the sleeve 45 that is exposed and protrudes past the front opening 21 of the shell 20. In doing this, the tube 10 is pushed back so as to longitudinally compress the retainer sleeve 80. As the retainer sleeve 80 is pushed back longitudinally, the large section 81a of the base 81 is aligned with the outer pegs 75 so as to allow the flexing elements 73 to displace to its natural position, thus, releasing, the inner pegs 74 that are held within the groove 55. This allows the spring 60 to extend to its natural uncompressed length, thus, pushing the plunger 50 toward the needle 40, as shown in
It is well known in the field of art that different medicaments have to be injected with different injection rates. Thus, the automatic injection syringe 100 of the present invention can be configured with a spring 60 having a compressibility ration that corresponds the desired injection rate. This way, when the spring 60 is released, the stiffness of the spring 60 will allow the plunger 50 to be pushed forward at the desired injection rate. For example, the stiffer the spring 60, the greater the force with which the plunger 50 will be pushed, thus, resulting in a greater injection rate. Similarly, the less stiff the spring 60, the lower the force with which the plunger 50 will be pushed, thus, resulting in a lower injection rate.
Therefore, the automatic injection syringe 100 of the present invention is superior in design and functionality than any existing prior art. It is understood that the described embodiments of the present invention are illustrative only, and that the modifications thereof may occur to those skilled in the art. Accordingly, this invention is not to be regarded as limited to the embodiments disclosed, but to be limited only as defined, by the appended claims herein.