U.S. patent number 3,557,787 [Application Number 04/732,622] was granted by the patent office on 1971-01-26 for disposable syringe.
Invention is credited to Milton J. Cohen.
United States Patent |
3,557,787 |
Cohen |
January 26, 1971 |
DISPOSABLE SYRINGE
Abstract
A syringe device formed of inner and outer tubular members with
the inner member adapted to be telescoped within the outer member
and sealed therefrom by a resilient, thin seal. The inner member
has a planar flange surface on its forward end and across which the
thin seal extends. The thin seal has passage means therethrough in
sealing relation to the flange surface. The outer member is formed
with a rupturable seal having an injection needle in alignment
therewith for rupture in use with the inner tubular member. The
inner member is adapted to contain a liquid carrier and the outer
tubular member a dry medicant to be taken up with the carrier for
injection whereby the materials are freshly mixed immediately prior
to injection for operation of the device.
Inventors: |
Cohen; Milton J. (Washington,
DC) |
Family
ID: |
24944314 |
Appl.
No.: |
04/732,622 |
Filed: |
May 28, 1968 |
Current U.S.
Class: |
604/90 |
Current CPC
Class: |
A61M
5/32 (20130101); A61M 5/31596 (20130101); A61M
5/34 (20130101); A61M 5/284 (20130101); A61M
5/288 (20130101); A61M 5/286 (20130101); A61M
2005/31598 (20130101) |
Current International
Class: |
A61M
5/28 (20060101); A61M 5/32 (20060101); A61M
5/34 (20060101); A61M 5/315 (20060101); A61m
005/22 () |
Field of
Search: |
;128/220,218M,218NV,215,218 |
References Cited
[Referenced By]
U.S. Patent Documents
Primary Examiner: Koren; Samuel
Assistant Examiner: Czerwonky; James H.
Claims
I claim:
1. A syringe assembly for injection comprising inner and outer
tubular members with the inner members having an outer wall to wall
dimension less than the inner wall to wall dimension of the outer
tubular member to enable the inner tubular member to be telescoped
within the outer tubular member, said inner tubular member defining
a planar flange surface on the forward end thereof, a rupturable
closure sealing the forward end of the outer tubular member, a
flexible closure having a resilient, thin web means across said
flange surface and sealing the forward end of the inner tubular
member, said thin web means including passage means therethrough
seated on said flange surface in sealing relation thereto whereby
said passage means are unseated to communicate with the interior of
the inner tubular member in response to internal pressure therein,
a piston ring portion on the forward end of the inner tubular
member in sliding engagement with the inner walls of the outer
tubular member, a piston plug dimensioned slidably to be received
within the inner tubular member, and means for actuating the piston
plug axially relative to the inner tubular member, a hypodermic
needle, and collapsible means on the forward end portion of the
outer tubular member supporting the needle with the rearward end
terminating a short distance in advance of the rupturable closure
when in uncollapsed position and penetrating through the rupturable
closure when in collapsed position.
2. A syringe as claimed in claim 1 which includes a removable cover
for the needle.
3. A syringe as claimed in claim 1 in which the inner tubular
member is adapted to contain a liquid carrier and in which the
outer tubular member is adapted to contain a dry material to be
taken up by the liquid carrier when the latter is forced from the
inner tubular member into the outer tubular member in response to
movement of the piston plug axially in the inner tubular
member.
4. A syringe as claimed in claim 1 in which the collapsible means
comprises a hub member secured at its rearward end portion onto the
forward end of the outer tubular member and a forward end having an
opening through which the needle extends with a flexible portion
between the ends to enable displacement of the forward end between
normal and collapsed position.
5. A syringe as claimed in claim 1 in which the piston ring portion
on the forward end of the inner tubular member comprises ring
members of rubberlike material in sealing engagement with the outer
walls of the inner tubular member and extending into sealing
engagement with the inner walls of the outer tubular member.
6. A syringe as claimed in claim 1 in which the piston ring portion
and flexible closure are of a unitary construction mounted onto the
forward end portion of the inner tubular member and in which the
means in the flexible sealing closure comprises openings extending
through the sealing member in a position offset outwardly from
axial alignment with the passage through the inner tubular
member.
7. A syringe as claimed in claim 1 in which the piston plug within
the inner tubular member is formed of rubberlike material having
circular ribs dimensioned to extend into sealing engagement with
the inner walls of the inner tubular member.
8. A syringe as claimed in claim 1 which includes means on the
rearward end of the piston plug for attachment of an actuator and
which includes an elongate actuator dimensioned to exceed the
length of travel of the piston plug through the inner tubular
member.
9. A syringe as claimed in claim 8 in which the actuator comprises
an elongate rod dimensioned to be received in telescoping relation
within the inner tubular member and with means for attachment of
the actuator to the piston plug.
10. A syringe as claimed in claim 1 which includes flanged members
extending radially outwardly from the rearward end portions of the
inner and outer tubular members for use as finger grips.
Description
This invention relates to a device for the administration of
parenteral solutions and more particularly to a hypodermic syringe
adapted to contain dry solids separate and apart from the
dissolving or carrier liquids until, immediately prior to
administration, the liquid is caused to flow into the compartment
containing the solids for injection of the formed mixture.
To the present, it has been the practice to make use of stock
solutions housed within a container of relatively large capacity,
from which increments can be removed, as desired, for
administration by a suitable syringe. This procedure is deemed to
be unsatisfactory because most such solutions are of insufficient
stability to militate against change before the stock solution has
been used up. With a solution of short "shelf life," its utility
may become dissipated before the solution has been completely
utilized.
The most effective means for maintaining the "shelf life" over
extended periods of time is to maintain complete separation between
the liquid carrier and the solids to be incorporated therein, until
immediately prior to use. Maintenance of solid-liquid separation
until time of use presents other problems with respect to ejecting
and administering the solution containing the necessary
concentration of ingredients and under the most sanitary
conditions. The usual practice is to introduce the solids into the
liquid for solution in a suitable container from which the solution
can be withdrawn into a syringe for injection. This procedure
required the use of at least three separate containers and
maintenance under sterile conditions as well as accurate
measurement of the ingredients.
It is an object of this invention to provide a single device in
which accurately measured amounts of solid medicants and liquid
carrier can be maintained in a completely separated relation, in
which the measured amounts of liquid carrier and solid material can
be brought together and in which the freshly formed mixture can be
injected, all while maintaining the ingredients in a sealed and
sanitary state, without exposure to the outside atmosphere, and in
which the entire operation for mixture and administration can be
carried out with one hand.
It is another object to provide a disposable syringe which houses
the liquid and solids in separately sealed compartments and in
which admixture of the liquid and solid can be effected entirely
within the confines of the syringe to make a freshly prepared
solution of the measured ingredients and from which the freshly
prepared solution can be injected in the manner desired for
use.
Other objects and advantages of this invention will hereinafter
appear and, for purposes of illustration but not of limitation, an
embodiment of the invention is shown in the accompanying drawings
in which:
FIG. 1 is a sectional elevational view of the syringe embodying the
features of this invention, with the elements illustrated prior to
use;
FIG. 2 is a sectional elevational view of the syringe shown in FIG.
1 with the syringe partially actuated to effect displacement of the
liquid carrier from the liquid chamber to the solids chamber for
solution or admixture;
FIG. 3 is a sectional elevational view of the syringe shown in
FIGS. 1 and 2 with the syringe in fully actuated position to effect
displacement of the freshly prepared solution from the solids
compartment for injection;
FIG. 4 is a sectional elevational view of a portion of the syringe
shown in FIGS. 1 to 3 and showing a modification in the closure for
the liquid containing compartment; and
FIG. 5 is a sectional elevational view of the actuator which may
also be used as a needle cover.
With reference now to the drawings, the syringe of this invention
is formed with an outer casing 1 in the form of a tubular member,
formed of glass, plastic or the like, having a continuous bore 2
extending therethrough from an open rearward end portion 3 to a
neck portion 4 of smaller cross section, at the forward end. The
forward end is sealed by means of a disc member 5 held in place in
sealing relationship across the open neck 6 of the tubular member 1
by means of a metal cap 7 which is crimped about the outer neck end
portion of the tubular member while the inner portions 8 of the cap
overlap the outer edge portions of the sealing disc member
overlying the flattened end surface 9 of the tubular member. The
rearward end of the tubular member is formed with an outwardly
extending annular flange 10 which serves as a finger grip. A hub
member 11 has a skirt portion 12 crimped about the skirt portion of
the cap for securing the hub onto the neck end portion of the
tubular member. The hub is also formed with an intermediate
collapsible or corrugated portion 13 extending forwardly in axial
alignment with the forward end of the tubular member with a hub 14
on the forward end through which a hollow needle 15 extends with a
sharpened end portion of the needle projecting into the interior of
the hub member 11 for a distance less than the spaced relationship
between the hub end and the diaphragm 5, when in normal position,
thereby to locate the rearward end of the needle immediately in
advance of the center of the diaphragm.
A second tubular member 20 of glass, plastic or the like material
is dimensioned to have an outer wall to wall dimension which is
less than the inner wall to wall dimension of the tubular member 1
to enable the former to be telescoped through the interior of the
outer tubular member 1. The second tubular member is similarly
formed with a passage 21 extending from the open rearward end 22
through a neck portion 23 of smaller cross section at the forward
end. The forward neck end portion of the second tubular member is
fitted with a rubber stopper 24 including an outer ribbed portion
25 fitted in gripping relationship about the neck and extending
laterally beyond the walls of the second tubular member for a
distance to effect sealing engagement with the inner walls of the
outer tubular member 1 whereby the second tubular member is capable
of the function of a piston movable axially relative the outer
tubular member 1 thereby to provide a piston and cylinder
arrangement between the two tubular members.
The rubber stopper 25 has a disc portion 26 which normally spans
the forward end of the passage to seal the tubular member. It is
further formed with one or more openings 27 in the lateral portions
beyond the passage to enable flow of liquid from the second tubular
member into the first when the sealing disc 26 is flexed for
displacement for sealing engagement with the end of the second
tubular member. Again, the rearward end portion of the second
tubular member is formed with an outwardly extending flanged
portion 28 for use as a finger grip, as will hereinafter be
described. The rearward end of the passage 21 is sealed with a
rubber plug 30 mounted for axial displacement through the passage
21 as a piston within the cylinder defined by the second tubular
member. Means, such as a threaded stud 31, is provided on the
rearward end of the plug type piston for connection of an actuator
32 for displacement of the piston relative the cylinder. In the
illustrated modification, the actuator 32 is in the form of a third
elongate tubular member dimensioned to have a cross section less
than the cross section of the passage 21 through the second tubular
member and formed at one end with an internally threaded female
portion 33 for threaded engagement onto the threaded plug 31. The
rearward end of the actuator is formed with an outwardly extending
flanged portion 34, for use as a finger grip.
In the modification shown in FIG. 5, the actuator is capable of use
as a needle cover to protect the needle when other than in position
of use and which can be removed from the hub to expose the needle
and for attachment to the plug for operation of the device, when in
position of use. Thus the element supplies the dual function of a
needle protector during nonuse and as an actuator in use.
In the assembled relation, illustrated in FIG. 1, fluid 35 is
housed in sealing relationship within the second tubular member
while the dry medicant is housed in sealing relationship within the
first tubular member. The loaded device can be shipped and stored
for extended periods of time without deterioration of the
ingredients and without exposure of the elements to nonsanitary
conditions.
In use, the needle cover 32 is removed to expose the needle 15 and
the cover is screwed onto the end of the piston plug 30 for use as
an actuator. The device is held with the two needle fingers under
the flanged members 28 of the second tubular member and the
actuator is pressed by the thumb to effect displacement of the plug
30 through the cylindrical passage 21. This operates to place the
liquid 35 under pressure which transfers to the resilient closure
disc 26 to cause flexure and unset the disc for establishing
communication between the chambers 21 and 2 through the openings 27
to enable flow of fluid under pressure from the chamber 21 in the
second tubular member into the chamber 2 of the first tubular
member for admixture with the dry medicant 36. This intermediate
position is illustrated in FIG. 2. The liquid carries the medicant
into solution or suspension, with shaking when necessary, to
provide a freshly prepared fluid system ready for administration by
injection.
Administration is made without change of devices and without
exposure of the freshly prepared solution or suspension by
inserting the needle into the vessel or tissue. For this purpose,
the outer casing is grasped with the one hand with the needle
fingers beneath the flanged portion 10. The needle is inserted and
the hub is compressed to effect relative movement between the
needle 15 and the rubber sealing diaphragm 5 whereby the rearward
end of the needle punctures the diaphragm to bring the end of the
needle into the chamber 2 for direct communication with the freshly
prepared liquid system. Thereafter, the thumb is pressed down onto
the actuator which, at the end of its travel in the second tubular
member, causes displacement of the second tubular member for
movement as a piston through the cylindrical passage 2 of the first
tubular member thereby forcibly to displace the freshly prepared
liquid system from the interior of the first tubular member through
the needle and into the tissue.
Upon administration of the freshly prepared solution, the entire
device can be discarded.
In the modification shown in FIG. 4, the sealing disc 26 extends
continuously in sealing engagement across the neck of the second
tubular member but is provided with a slit 40 which maintains a
sealing relationship until opened in response to the application of
fluid pressure as the plug 30 is displaced forwardly through the
passage 21.
It will be apparent from the foregoing that I have provided a
simple disposable syringe capable of operation with one hand in
which liquids and solids are maintained in separately sealed
chambers and mixed immediately prior to injection by a simple
operation of the device.
It will be understood that changes may be made in the details of
construction, arrangement and operation without departing from the
spirit of the invention, especially as defined in the following
claims.
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