U.S. patent number 3,566,859 [Application Number 04/854,090] was granted by the patent office on 1971-03-02 for vacuum syringe.
Invention is credited to Boris Schwartz.
United States Patent |
3,566,859 |
Schwartz |
March 2, 1971 |
VACUUM SYRINGE
Abstract
A syringe combination having an outer housing and a hollow
plunger providing a pair of chambers of determined size. The
plunger is provided with a piston having three or more spaced,
ringlike sealing surfaces and with a fluid passageway from the
interior of the plunger which is flow-connected to the outer piston
surface and between ringlike sealing surfaces. The outer housing
has one or more recesses of determined size formed in its inner
surface with the recesses positioned near the open end of the
housing and of a length so that the rearmost sealing surface of the
plunger piston engages the housing between the recesses and the
rear end of the housing when the flow-connection is brought into a
fluid-conducting position with the recess.
Inventors: |
Schwartz; Boris (Paterson,
NJ) |
Family
ID: |
27094663 |
Appl.
No.: |
04/854,090 |
Filed: |
August 29, 1969 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
Issue Date |
|
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645264 |
Jun 12, 1967 |
3464412 |
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Current U.S.
Class: |
600/578; 604/82;
604/222 |
Current CPC
Class: |
A61B
5/150755 (20130101); A61M 5/31596 (20130101); A61B
5/150236 (20130101); A61B 5/153 (20130101); A61B
5/150389 (20130101); A61B 5/150213 (20130101); A61B
5/150267 (20130101); A61B 5/150251 (20130101); A61B
5/150519 (20130101); A61B 5/15003 (20130101); A61B
5/150244 (20130101); A61M 2005/3104 (20130101); A61M
2005/3106 (20130101); A61B 5/150099 (20130101); A61B
5/150259 (20130101); A61M 2005/31598 (20130101) |
Current International
Class: |
A61B
5/15 (20060101); A61M 5/315 (20060101); A61M
5/31 (20060101); A61b 005/14 (); A61m 005/22 () |
Field of
Search: |
;128/218,218 (M)/
;128/22 (D)/ ;128/2 ;251/205 |
References Cited
[Referenced By]
U.S. Patent Documents
Foreign Patent Documents
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705,392 |
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Mar 1954 |
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GB |
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1,105,113 |
|
Apr 1961 |
|
DT |
|
Primary Examiner: Gaudet; Richard A.
Assistant Examiner: Pace; Channing L.
Parent Case Text
REFERENCE TO RELATED APPLICATION
This Application is a division of application Ser. No. 645,264
filed Jun. 12, 1967 now U.S. Pat. No. 3,464,412.
Claims
I claim:
1. A sampling syringe for the withdrawal and storage of blood and
the like, the syringe including: (a) an outer housing of generally
tubular configuration and having an inner bore of a generally
constant cross section and with at least one bypass recess formed
in the inner bore, said bypass recess positioned at a determined
distance from and near an open rear end of the housing, the housing
having a front partially closed other end and a passageway
therethrough; (b) means for selectively closing the passageway of
the partially closed front end of the housing so as to prevent the
passage of air, fluids and the like; (c) a test tube of integral
construction and having a closed rear end and having a main portion
of generally tubular configuration, the test tube slidable in the
bore of the outer housing, and (d) a resilient piston mounted in
and closing the front end of the test tube, said piston having a
plurality of ringlike sealing surfaces sized so as to be slidable
in the bore of the outer housing while engaging said bore in a
fluid-flow sealing manner, the piston having at least one
fluid-flow passageway provided through the wall of the piston with
one end of the passageway opening to the interior of the plunger
and the other end terminating at the piston outer surface and
between adjacent ringlike sealing surfaces, said sealing surfaces
disposed to provide a sealing extent to the rear of the outer
surface flow passageway termination of the piston so that when this
passageway termination is brought in way of the housing bypass
recess this sealing extent of the piston to the rear of the
termination extends beyond the bypass and into the bore of the
outer housing so as to seal the bore from any unwanted flow of air,
fluid and the like from and to the open end of the outer
housing.
2. A sampling syringe as in claim 1 in which the test tube is made
of heat resistant glass.
3. A sampling syringe as in claim 1 in which the means for closing
the passageway in the housing front end is a resilient plug of
plastic, rubber and the like, the plug having a shank portion sized
for removable insertion into and closing of said passageway, and
the front end of the housing is formed with a hub portion adapted
to receive and retain a needle, and in which the housing bore at
its open end is formed with a small internal lip providing a stop
shoulder engaged by the rearward ringlike sealing surface of the
piston to position the piston axially in the housing bore so as to
bring the flow passageway of the piston into a flow conducting
relationship with the bypass recess in the housing.
4. A sampling syringe as in claim 1 in which the piston is a
separate member and in which there is provided a separate plug to
close the end of the test tube and in which there is provided means
for retaining the piston in an aligned and contiguous relationship
to the plug during and while the test tube is in the housing.
5. A sampling syringe as in claim 4 in which the plug has a closed
end and in which there is provided a needlelike member providing a
portion of the flow passageway from the piston to and through the
plug and to the interior of the test tube.
Description
BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates to the general class of surgery and more
particularly to the subclass of syringes.
2. Description of the Prior Art
Syringes are well known in the general field of surgery and those
for storing and intermixing various ingredients are represented in
patents as to PIERICK, U.S. Pat. No. 3,279,654 of Oct. 1966; to
BROWN, U.S. Pat. No. 2,591,046 of Apr. 1952; and to CAMBER, Great
Britain No. 746,057 of Jan. 1959. These and other patents use
gravity to induce a flow from one chamber to another. This method
of transfer is often uncertain and sometimes is incomplete or
requires an exact manipulation by the user who may not have the
required skill or training. The precise and exact mixing of the
various components comprising some of the new medicants is an
absolute necessity. Ease of mixing by any potential administrator
of the medicant is necessary and desirable, and an easily
manipulative device is an object of this invention.
The syringe of present invention provides a means for bringing the
interior of the housing of the syringe into a condition of reduced
pressure, whereupon as a flow-conducting portion of a piston of a
hollow plunger is brought into a fluid-passing or-mixing position,
the fluid which is preferably stored in the plunger is sucked from
the plunger interior to flow to the housing chamber for a
controlled mixing of the stored ingredients.
SUMMARY OF THE INVENTION
This invention provides a syringe-type apparatus having an outer
housing of generally tubular construction which is formed with an
open end and a closed end. This closed end has an aperture or
passageway for the passage of medicants and the like which is
usually to and through a needle. The plunger is slidable in the
bore of the housing and is formed having a fluid-flow passageway
extending from between a pair of ring-type sealing surfaces and to
the interior of the plunger. The inner surface of the barrel
portion of the outer housing has formed therein at least one recess
of a determined length, width and depth and adapted to provide a
fluid passageway from the interior of the plunger to and around one
of the sealing rings and thence to the foreportion of the
housing.
The other embodiment of the invention the syringe is intended to be
used as a vacuum container in which the hollow plunger portion is a
test tube which may be furnished with small predetermined
quantities of various blood-treating fluids stored in the test
tube. By manipulation, the test tube or plunger and the interior of
the housing is caused to be brought into a condition of reduced
pressure after which the plunger in the reduced pressure condition
is moved to a storing position after which the interior of the
housing is opened to the atmosphere to bring the interior of the
housing to atmospheric pressure. At the time of use, the fore end
or closed end of the housing has a needle mounted on a hub
portion.
The apparatus with the needle attached is used as a syringe to
withdraw a blood sample from the patient and to secure and store a
determined quantity of blood within the syringe. After the desired
amount of blood is drawn into the housing, the syringe is
manipulated to draw the blood into the test tube. When the transfer
of the blood to the test tube is completed the needle is discarded
and the test tube may be moved fully into the housing for shipment
to the laboratory. In other embodiments there are shown means
whereby the test tube and housing may be separated with the test
tube sealed with a rubber plug and the housing substantially closed
with a rubber plug.
It is an object of this invention to provide a syringe apparatus in
which the plunger is a test tube having a piston portion on its
open end and adapted to slide within a housing so that the test
tube may be brought to a condition of reduced pressure. The closed
end of the housing is adapted to mount a needle for the drawing of
blood from a patient and after the drawing of a determined quantity
of blood into the housing this blood is transferred by manipulation
of the plunger into the test tube for storage and transport.
There has been outlined rather broadly the most important features
of the syringe apparatus of this invention in order that the
present contribution to the art may be more fully appreciated. The
chosen embodiments are provided for the purposes of illustration
and description of the principles of this invention and are shown
in the accompanying drawings forming a part of the specification
wherein:
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 represents a sectional view of an intermixing syringe in
which the components to be mixed are shown as stored in two
separate compartments or members of the syringe;
FIG. 2 represents the syringe of FIG. 1 with the components brought
into mixing relationship within the housing member;
FIG. 3 represents the syringe of FIG. 1 and showing a needle
attached to the housing and the syringe after the contents have
been expelled therefrom;
FIG. 4 represents a sectional view taken on the line 4-4 of FIG. 1
and showing one embodiment of a fluid bypass recess as formed in
the outer housing member;
FIG. 5 represents a sectional view through an alternate embodiment
in which the hollow plunger is a test tube;
FIG. 6 represents a sectional view through yet another embodiment
in which the plunger outer end is provided with a resilient bulb
and the plunger and housing are adapted for mixing and for
dispensing of a medicant in the manner of a dropper;
FIG. 7 represents a sectional view showing an end closure or cap
for mounting on the discharge end of the housing of FIG. 6;
FIG. 8 represents a side view of an outer housing with a portion of
the sidewall broken away to show yet another form of a fluid bypass
formed in the housing inner wall;
FIG. 9 represents a fragmentary and sectional side view of the
fluid bypass of FIG. 8, the view taken on the line 9-9 of FIG.
10;
FIG. 10 represents a sectional view of the housing as taken on the
line 10-10 of FIG. 8;
FIG. 11 represents a fragmentary sectional view of an alternate
stopper and piston arrangement as mounted in the test tube
member;
FIG. 12 represents a fragmentary sectional view of yet another
alternate stopper and piston arrangement as mounted in the test
tube member;
FIG. 13 represents a plan view of the needlelike member as used in
the assembly of FIG. 11 and providing a flow passageway from the
piston interior to and through the stopper; and
FIG. 14 represents a side view of the member of FIG. 13.
In the following description and in the claims various details will
be identified by specific names for convenience; these names,
however, are intended to be generic in their application.
Corresponding reference characters refer to like members throughout
the several FIGS. of the drawings.
The drawings accompanying, and forming part of, this specification
disclose certain details of construction for the purpose of
explanation of the broader aspects of the invention, but it should
be understood that structural details may be modified in various
respects without departure from the concept and principles of this
invention and that the invention may be incorporated in other
structural forms than shown.
DESCRIPTION OF THE SYRINGE OF FIGS. 1--4
Referring now in particular to the intermixing syringe shown in
FIGS. 1 through 4, in which is shown an outer housing 20 of
conventional configuration and including a reduced front end 21
sized so as to retain a needle on its outer tapered end. This
housing has an open rear end with an outer flange portion 22
providing a shoulder or strap for the user's fingers. The interior
diameter of this housing 20 is substantially round and constant
with the exception of a portion near the rear in which is provided
a fluid bypass in the form of outwardly extending scallops 24.
These scallops are particularly seen in FIG. 1 and 4 and, as
reduced to practice, are in the form of arcuate cuts approximately
one-quarter of an inch long and with a depth and width of
one-sixteenth of an inch at their maximum. At the rear end of the
housing 20 it is to be noted that a small internal lip 25 is formed
in order to provide a limit means or stop for the outward movement
of a plunger member 30.
Referring now to the movable plunger member generally identified as
30, it is to be noted that a generally tubular portion 31 has a
reduced front end upon which is fitted a piston plunger preferably
of rubber and identified as 32. This piston plunger, in the
preferred instance, is formed with three outwardly extending
like-sized resilient ringlike portions 33. Between the front first
and second ringlike portions 33 there is formed a fluid passageway
34 extending from the inner portion of the plunger to and through
the outer peripheral surface of the piston.
At the open or rearward end of the plunger 30 (as seen in FIG. 1)
there is carried a movable piston 35 slidable within the interior
diameter of the barrel 31. This piston is sized to provide a
fluidtight slip fit and, in the present instance, is formed with
two outwardly extending ring portions adapted to provide a fluid
sealing means as well as sliding surfaces. At the rear end of the
tubular portion 31, it is to be noted that there is a small
internal shoulder or lip 36 provided to prevent or limit the
unwanted outer movement of the piston 35.
It is also to be noted that the rear end of plunger 30 is provided
with a small grasping flange 38 for the easy gripping thereof by
the fingers of the operator. Still referring to FIG. 1 it is to be
noted that the reduced end of the outer housing 20 is provided with
a vacuum or fluid seal in the form of a rubber or plastic plug 40
which is adapted to enter into a passageway 42 and seal this
passageway both from the unwanted loss or entry of or plugging by
powder and also to prevent the flow of air in and out of this
passageway.
Referring next to FIG. 3, it is to be noted that a needle 44 is
shown as mounted on the front end of the outer housing 20 after the
plug 40 has been removed. This needle is of standard and
conventional construction. After mounting on the syringe the
insertion of this needle into the flesh or vein of the patient is
in the manner of conventional practice.
DESCRIPTION OF VACUUM SYRINGE
Referring now to FIG. 5 and a syringe in which the plunger is a
test tube and in which an outer housing 60 is similar to the
housing 20 above described, this housing 60 is formed with a closed
and reduced front end 62 sized to receive and retain a needle, not
shown, but which may be the needle 44 (FIG. 3) above described.
Within the front end of this housing is shown a plug 40 as
previously described which plug seals a passageway 64 within the
housing 60. The rear end of the housing is open and has a small
internally formed lip 65 providing a stop means in the manner of
lip 25 above. The outer portion of the housing 60 is formed with
ribs 66 and 67 which provide means for easy grasping and retaining
of the housing in the hands of the user.
Within this housing there is plunger member which, in this
embodiment, includes a glass tube 70 whose open end is closed by a
rubber stopper and piston combination 72. The rear or left end
portion of the stopper-piston is sized to close and seal the open
end of the test tube 70 while the foreportion of any piston is
formed with three fluid-sealing ring portions preferably
substantially equally spaced. A fluid passageway 74 is provided
between the first and second rings 75 reading from the right to the
left as seen the FIG. 5 and a third ring adjacent the test tube
provides an extended sealing means. The fluid passageway extends
from the interior of the test tube to the outer surface between the
first and second sealing rings.
In use, the test tube 70 may have stored within it one or more
fluids or other materials used for making blood determinations.
Among such materials are potassium oxalate; sodium heparin; lithium
oxalate; sodium oxalate; potassium oxalate and sodium fluoride;
ammonium oxalate or mixtures of the above, and mineral oil may be
used for other determinations. The quantities and selection of
material that may be combined within the test tube 70 is merely a
suggestion of the various anticoagulants or other materials used
for determining blood tests. These materials are now customarily
provided in measured quantities in test tubes so as to be combined
with blood at the time of taking of the blood sample specimens. The
test tube, of course, in many tests is sterilized in the customary
manner and has nothing in it and may be used for other tests. The
storing of anticoagulants, etc., in a test tube for use in certain
test determinations is not to be implied as novel but is
illustrative of one use for this embodiment.
OPERATION OF THE TEST TUBE SYRINGE
It is contemplated that the syringe apparatus of FIG. 5 will be
shipped assembled for use and with the stopper-piston portion 72
moved to the forward part of the outer housing 60 and with the plug
40 in an air-sealing relationship with the passageway 64. Whether
the test tube 70 also contains anticoagulants and the like or not
is merely a matter of selection as determined by the intended use
of the syringe. Prior to the use of this assembly as a syringe the
test tube is grasped and moved leftwardly until piston 72
approaches the rear of the housing and the passageway 74 is brought
in the way of a fluid bypass in the housing. As the piston moves
leftwardly the air in the housing expands so that reduced pressure
is developed in the forepart of the outer housing 60. As the front
ring 75 of the piston comes in the way of the fluid bypass, the
reduced pressure in the housing is allowed to communicate itself to
the test tube 70 to provide a determined vacuum or reduced pressure
in the test tube. The test tube is then pushed forward or
rightwardly into the closed position, whence, as the front sealing
ring is moved forwardly of the bypass, the vacuum within the test
tube 70 is maintained. The test tube is advanced forwardly into the
forward end of the housing after which the plug 40 is removed and a
needle is mounted on the reduced front end 62.
The needle may then be inserted into a vein and, in the manner of a
syringe and with the test tube acting as the plunger, it is pulled
rearwardly so that the piston 72 acts in a usual manner to draw
blood from the vein. After the desired amount of blood is drawn
within the outer housing 60 the plunger is stopped and the needle
is withdrawn from the vein. The plunger then may be moved to
provide an exact determination of the amount of blood within the
forward portion of the housing 60, as for example, by expelling a
small amount of blood through the needle. After the quantity of
blood is provided in the housing portion, the test tube is pulled
rearwardly until the passageway 74 of the plunger is brought in the
way of the fluid bypass, whereupon the reduced pressure in the test
tube causes the blood to be drawn from the housing 60 and into the
test tube 70.
After the transfer of blood from the housing to the test tube is
completed, the piston portion and test tube is pushed forwardly
within the container housing 60 and in this condition the test tube
with the outer housing 60 acting as a shield may be transferred to
the laboratory for the determination of the blood test. At the
laboratory, with the housing passageway 64 open, the test tube is
drawn to the back end of the housing 60. The piston is moved past a
shoulder 77 of the rear of the housing and is removed therefrom
with the housing 60 being discarded. The stopper and piston portion
72 is drawn from the test tube opening and discarded after which
the material in the test tube is tested in the usual manner. The
test tube is preferably of conventional fire-resistant glass and
after the test may be discarded.
It is to be noted in FIG. 8, 9 and 10, that a preferred fluid
bypass as formed in the outer housing is a triangular shape recess
which is embossed in only one portion of the interior surface of
the housing. The housing may be the housing 60 of FIG. 5 with this
embossure extending about one-quarter of an inch along the axis of
the barrel and at its base at the rear of the housing being
approximately one-quarter of an inch wide. The recess if preferably
about ten or fifteen thousandths of an inch below the normal
housing bore and generally throughout the triangular shape as
shown. This fluid bypass provides the passage area generally
necessary for the blood to be transferred from the housing to the
interior of the test tube.
This triangular shape also provides a variable passageway whereby
if the transfer to the test tube is to be very slow, the exposure
of the forward ring to the triangular portion is made at the apex
or forward end which is very small. When the piston is drawn
further back its forward sealing ring portion is in the way of a
larger portion of the bypass 80 and the blood or fluid will flow in
a more rapid manner.
DESCRIPTION OF THE STOPPER-PISTON OF FIGS. 11, 13 AND 14
Referring next to FIGS. 11, 13 and 14 there is shown a two piece
stopper-piston assembly which also may be used with the test tube
70 of FIG. 5. A stopper 150 is preferably made of rubber and, as
shown, has a center relief 152 formed in one end so as to provide a
closed other end of relative thinness. In the outer diameter of
this stopper which is adapted to extend beyond the inturned end of
the test tube there is formed one or more recess portions adapted
to engage the inwardly extending leg portion of a clip 154. This
clip may be in the nature of a wire staple or may be one or more
band segments of arcuate configuration and selected length. The
other leg portion of clip 154 is engaged in a recess formed in a
rubber piston 156.
The outer surface of the piston has three ribs 158, 159 and 160 and
the inner portion of the piston is provided with a bore 162 having
an enlarged inner end. Transverse passageways 164 extend from the
outer surface between ribs 158 and 159 to flow connect the outside
of the piston to the bore 162.
A needlelike member 170 may be of metal or plastic and from a loop
end 171 legs 172 and 173 converge to form a pointed other end. As
seen in FIGS. 13 and 14 the member 170 is of relatively little
width and when the loop end is inserted into bore 162 the
protruding ends of the legs form a pointed member which may be
pushed through the closed end of the stopper 150. The space between
the legs 172 and 173 provide a flow passage from bore 162 to and
into the relief 152. This flow passage becomes closed by the self
closing action of the rubber as and after the member 170 is
withdrawn from the stopper end.
Clip or clips 154 insure that the stopper and piston are retained
in a contiguous flow sealing face-to-face relationship until these
clips are removed. The removal of the clips is not accomplished
until the test tube 70 (FIG. 5) has been drawn from housing 60
after which the clips may be easily removed with the piston 156
remaining in the housing to close the large end of the housing and
the stopper 150 remains in the test tube 70 to seal the tube.
DESCRIPTION OF THE STOPPER-PISTON OF FIG. 12
Referring finally to the assembly of FIG. 12 there is shown a
stopper 180 having a center relief 182 disposed to provide a closed
end of relative thinness. The outer diameter extending beyond the
end of test tube 70 is formed with an outwardly extending rib
portion 184. A piston 186 having three outwardly extending ribs
188, 189 and 190 has a shouldered recess formed in the open end of
piston 184. This recess is sized to snugly engage and retain the
stopper rib 184. Piston 184 has a bore 192 formed therein and this
bore is flow-connected to the outside of the piston by means of
transverse passageways 194 formed in the piston. The outer ends of
these passageways terminate between ribs 188 and 189.
A needlelike member 196 is mounted with its loop end retained in
bore 192. The legs of member 196 are contemplated as being arcuate
in cross section facing and mating with the other to form a fluid
passageway from the open loop to the other end which is beveled to
provide a sharp point. This member 196 when pushed through the
stopper provides a flow passageway from bore 192 to relief 182.
While the ribs of the piston 186 are in the housing 60 (FIG. 5) the
stopper is retained in the piston by means of engaged rib 184. When
the rib 190 has been brought outside the housing 60 the stopper may
be tilted to cause the rib 184 to disengage from the piston and
then needlelike member 196 is pulled from the stopper. The rubber
in the stopper is sufficiently resilient to be self-sealing and
when the needle is removed the stopper 180 seals the end of the
test tube while piston 184 closes the large end of the housing
60.
Terms such as "left," "right," "in," "out," "fore," "rear" and the
like are applicable to the embodiment as shown and described in
conjunction with the drawings. These terms are merely for the
purpose of description and do not necessarily apply to the various
syringe embodiments shown and described and the manner in which
they may be constructed or used.
The conception of the vacuum syringe and its many applications is
not limited to the specific embodiments shown but departures
therefrom may be made and without sacrificing its chief advantages
and protection is sought to the broadest extent the prior art
allows.
* * * * *