US2673561A - Disposable double-action syringe - Google Patents

Description

March 30. 1954 c. B. Pr nbu. JR 2,673,561

DISPOSABLE DOUBLE-ACTION SYRINGE Filed March 22, 1951 INVENTOR m &

" BY W q/ ATTORNEY Patented Mar. 30, 1954 UNITED STATES PATENT OFFICE 2,673,561 DISPOSABLE DOUBLE-ACTION SYRINGE Charles B. Peterson, Jr., Lancaster, Pa. Application March 22, 1951, Serial N 0. 216,997

8 Claims.

This invention relates to a disposable double action syringe or blood specimen receptacle and is concerned particularly with a unit which may be produced at low cost and will perform the functions of a. more expensive glass or metal plunger type of syringe.

- It is an object of the present invention to provide a disposable double action syringe which includes a resilient bellows or the like which is capable of being expanded or contracted to create either a positive or a negative pressure at the end of the hollow needle associated theremanufacture at low cost.

Another object of the invention is to provide a double action disposable syringe which may be actuated in use in essentially the same manner drawing, in which Figure l is a view partly in elevation and partly in section of a disposable double action syringe embodying my invention;

Figure 2 is a longitudinal sectional view of a disposable double action syringe of modified construction;

Figure 3 is a diagrammatic illustration showing the syringe of 'gure 2 in use with the bellows extended to provide a negative pressure at the pointof the hollow needle;

Figure 4 is a view similar to Figure 3 show- Figure 5 is a view similar to Figure 2 of a further modification of. my invention.

Referring to Figure 1, the syringe includes a body orreceptacle portion 2 of resilient material which is provided with a plurality of pleats orfolds 3 and 4 to provide ready compressibility of the'body portion 2 along the central axis thereof. A head orclosure member 5 is secured to thebody portion 2, and it receives a needle 6 which is preferably rigidly and permanently secured to thehead member 5. A wire stylet I may be inserted within the opening in the needle in the customary manner, and aprotective cover cap 8 may be provided to maintain the needle in sterile condition.

The syringe of Figure 1 may be made wholly of moldable plastic materials, except for the needle and stylet. The body orreceptacle portion 2 may be formed in a manner similar to the formation of plastic bottles made of polyethylene or similar yieldable and resilient plastic materials. Such materials are frequently formed by processes similar to those employed in glass blowing, the 'body of polyethylene being blown within a forming mold. Thereceptacle portion 2 is of ing use of the syringe. The base 9 of the receptacle may be of somewhat thicker Wall section to prevent collapse of the receptacle portion dureffect may be achieved by providing a concave portion w in the base. A fiat annular surface H may be provided upon which the unit may rest in an upright position.

The mouth of thereceptacle portion 2 terminatesin an annular flange [2 to which the head ene or other resinous material. This part is preferably formed with a somewhat heavier wall thickness than the body of thereceptacle 2 to provide a measure of rigidity for proper support of the needle and to facilitate the operation of injecting or withdrawing fluids from the body. Theclosure member 5 may in fact be formed of a hard resinous molding composition such as urea or phenol with formaldehyde. Theclosure member 5 includes a top portion it and. a epending flange portion M. The flange M is provided with an annular recess i5 which receives the annular flange E2 of thereceptacle portion 2. This provides a structure in which the closure member is firmly secured to the receptacle member with a fiuid and airtight seal which may be effected by frictionally fitting the parts together, preferably supplemented by an adhesive bond,

the adhesive being disposed within the recess prior to assembly of the parts.

An annular upwardly projecting flange i6 is provided on theclosure 5, the flange being disposed inwardly from the outer circumference of theclosure 5 to provide a shoulder ll for the reception of the plasticprotective cover 8. Thiscover member 8 may be molded of polyethylene, polystyrene, or other moldable material, flexible or rigid.

A central reinforcing and securing projection orboss 18 is molded in theclosure 5, and it is preferred to dispose the needle 6 within an open ing in the mold disposed centrally of the mold opening in which the boss i8 is formed and to mold the closure men ber 5 about the needle 6, thus insuring an adequate bond between the two parts. An enhanced bonding action may be secured by providing barbs, ribs or other projections on the outer surface of the needle in the area disposed within the boss it, although this is not essential for a secure bond may be obtained, particularly where theclosure 5 is formed of urea formaldehyde or phenol formaldehyde molding compositions. As an alternative, the boss [8 may be provided with a central opening for the reception of the needle 6 and the same may be frictionally fitted therein or may be adhesively secured in position.

As will be observed by reference to Figure 1, the needle 6 may be disposed a short distance from the inner head surface E9 of theclosure 5 so that theclosure 5 forms a complete seal for the contents of thereceptacle 2. ihe stylct i may be pressed downwardly to perforate the head surface IS. If desired, of course, the medle 6 may extend completely through th: top l3 of the closure, in which event no piercing of the head member will be required at the point of use, or a separate sealing diaphragm may be provided, interposed between the niedle and the container contents.

Preferably, the cover cap onto theclosure 5, but if desired, th's may be supplemented by providing interlocking projections 2i on the inside of thecover cap 8 and the outside of the flange it, such as screw threads, lugs, or the like, as shown in Figure 2.

A permanent liruiid-tight and airtight seal should be obtained between theclosure 5 and thereceptacle 2. By close frictional fittng of the flange l2 within therecess 25, a satisfactory seal may generally be obtained; and, as mentioned above, this may be supplemented by the use of an adhesive. Mechanical securing arrangements such as screw thread projections or the like 22 on theclosure member 23 and thereceptacle 2 as shown in Figure 2, may also be employed to secure the desired seal. In this embodiment, thereceptacle portion 24 is molded as a separate unit as are theclosure member 23 and abase member 25. Complementary screw threads are formed on thebase member 25 and the lower end of thereceptacle portion 2 3 and the two parts are firmly sealed together by screwing the base member onto the receptacle portion in the same manner as the closure member is secured to the receptacle. The particular method of joining the closure to the receptacle is not critical and many different types of structures may be employed, two simple types of joints being shown for purposes of illustration in Figures 1 and 2.

Figure 5 shows a structure in which theclosure member 25 is integral with the body or receptacle portion 21 and aseparate base member 8 is frictionally held 28 is secured to the body or receptacle portion 21 byscrew thread projections 29 formed on the parts. This unit may be readily formed of polyethylene resin and theneedle 30 joined thereto in the formation of the closure and receptacle portions, or it may be otherwise secured in position.

Also as shown in Figure 2,digital members 3| may be provided on the closure portion to assist in the positioning of the device in use.

As shown in Figure 3, the syringe is preferably grasped adjacent to the base portion by the thumb and index finger, and one or more fingers are applied to the digital members or to the closure portion if no digital members are provided. An upward force may then be applied to the receptacle, and because of its plicated structure the capacity of the receptacle will be increased and a negative pressure will result at the needle. This action is essential in the intramu cular inection of certain me v.icaments which should not be injected into the blond str: am. In this operation, the neezfle is fnsertcd and negatt've pressure is applied by expanding the receptacle. If the blood stream is cisposed. at the needle point, H506, will be drawn into the receptacle and will be observed there through the transparent or transl zent body thereof. In :uch event a repositionng ol' the needle will be effected: and, w en in proper p sitian, force may be app'ied, a: ldl ated in figure 4 where the digital port'on: are fisposcd betwen the in'lex and second in er an force appliej. by the thumb to cornthc pii ate-d r'cz-piac'e and thus compress ""16, re .iuclng the volume thereof, ap;l ing ve pressure to the contents, andv in eating Ls of the receptacle through the needle c the body of the 1:at':nt.

Where the syringe is to be used as a blood specilllTn rece;tacle, the nee-d1: 6 will be preferably iiriosed eccentric with respect to theclosure member 5 so that the ne'dle may be inserted wth faci'iity into a vein and then negative pressure ill be applied in the manner illustrated in Figure 3 to withdraw a specimen of blood into thereceptacle 2. Thecover cap 8 may then be appl ed and sealed in posi't'on and the specimen trnsferred. to the laboratory for analysis. Where a removable closure is provided as shown in Figure 2, or where the base member is removable as shown in Figures 2 and 5, the rerrovable member may be detached for the di char e of the specimen. Where the parts are integrally formed or adhesively joined, the receptacle porton may be severed with a blade and the contents discharged through the severed. opening.

The provision of a removable closure is particularly desirable where the syringe is for use in blood chemistry, for it permits an operator to decant the supernatant portion of the specimen with the receptacle disposed in an upright p'sition on its base. It also facilitates ready removal of clotted blood. Of course, a srrall quantity of crystals of sodium citrate, sodium oxalate, or other anticoagulant may be disposed within the receptacle prior to use, and under such circumstances the uncoagulated blood may be discharged from the receptacle through the needle. This is not possible, obviously, with clotted or coagulated blood.

The size of thereceptacle 2 will vary depending upon the service for which it is intended. For many physiological injections, a volume of 1 cc. will be adequate; whereas, for blood specimens,

a size of cc. or 20 cc. may be required. The size of the unit is not critical and the invention will be applicable to units of all sizes from the smallest for conventional medicament injections to the larger sizes for blood specimen and similar uses.

Should it be desired to utilize thereceptacle 2 for retaining a blood specimen without the needle, a separate sealing cover cap may be provided therefor similar to the cap of Figure 2 without the needle and without the digital portions. The cover cap preferably will be provided with screw threads or the like complementary to theelements 22 of Figure 2. However, the unit may be sealed by pinching the needle with a hemostat or forceps or by bending it upon itself to thereby seal oil? the opening therein.

From the foregoing it will be clear that by this invention there is provided a disposable injection syringe and blood specimen receptacle which may be produced at low cost with conventional equipment. The unit is simple to operate and is extremely compact, facilitating its packaging and shipment. The operator may readily visualize the functon of the device and the contents of the receptacle and a completely sterile package may be provided with the contents fully sealed. The device will perform all of the functions of the more complicated and expensive conventional plunger type syringes.

I claim:

1. A double action syringe comprising a hollow receptacle including an impervious body portion of yieldable plicated form which is readily expansible and contractible digitally to increase and de- I crease the volume thereof, a relatively rigid head portion at one end of said body portion and forming an hermetic seal therewith, a relatively rigid closure member at the other end of said body por-- tion at one end of said body portion and forming an hermetic seal therewith, a relatively rigid closure member at the other end of said body portion, and a hollow needle carried by said closure member and constituting the sole passageway for communication with said body portion, whereby said head portion and closure member may be digitally grasped and axial forces applied therethrough to effect collapse and expansion of said plicated body portion and fluid transfer with respect to said receptacle will be effected solely through said needle.

2. A double action syringe or the like in accordance with claim 1 in which the closure member is joined to the body portion and carries the needle.

3. A double action syringe or the like in accordance with claim 1 in which the closure member is integral with the body portion and the needle is disposed therein and in which a base member is removably secured to the body portion.

4. A double action syringe or the like in accordance with claim 1 in which there are separate base and closure members joined to the body member at opposite ends thereof, one of which carries the needle.

5. A double action syringe in accordance with claim 1 in which the body is formed of translucent plastic material.

6. A double action syringe comprising a hollow receptacle including an impervious body portion of generally cylindrical yieldable plicated form which is readily expansible and contractible generally along the axis thereof by digital forces to increase and decrease the volume thereof, a relatively rigid head portion at one end of said body portion and forming an hermetic seal therewith, a relatively rigid closure member secured to the other end of said body portion and sealed thereto, and a hollow needle carried by said closure member and constituting the sole passageway for communication with said body portion, whereby said head portion and closure member may be digitally grasped and axial forces applied therethrough to effect collapse and expansion of said plicated body portion and fluid transfer with respect to said receptacle will be effected solely through said needle.

7. A double action syringe comprising a hollow receptacle including an impervious outer body wall portion of yieldable plicated form which is readily expansible and contractible digitally to increase and decrease the volume thereof, a relatively rigid reinforcing head portion integral with the outer body wall portion and of greater thickness than the body wall portion and hermetically sealing one end thereof, a separate relatively rigid closure member sealingly attached to the opposite end of said body wall portion, and a hollow needle carried by said closure member and constituting the sole passageway for communication with said body portion, whereby said head portion and closure member may be digitally grasped and axial forces applied therethrough to effect collapse and expansion of said plicated body portion and fluid transfer with respect to said receptacle will be effected solely through said needle.

8. A disposable blood specimen retractor comprising a hollow receptacle including a thin impervious body wall portion of yieldable plicated form which is readily expansible digitally to increase the volume thereof, a relatively rigid reinforcing head portion at one end of said body portion and forming an hermetic seal therewith, a relatively rigid closure member at the other end of said body portion, and a hollow needle carried by said closure member and constituting the sole passageway for communication with said body portion for application of negative pressure to said passageway upon expansion of said plicated body wall portion to effect transfer of blood through said needle to said receptacle upon insertion of said needle into a blood stream.

CHARLES E. PETERSON, JR.

References Cited in the file of this patent UNITED STATES PATENTS Number Name Date 2,258,883 Cressler Oct. 14, 1941 2,353,153 Ferrel July 11, 1944 2,388,323 Henderson Nov. 6, 1945 2,403,074 Goldsmith July 2, 1946 2,514,575 Hein July 11, 1950 FOREIGN PATENTS Number Country Date 573,611 Great Britain Nov. 28, 1945

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