U.S. patent number 3,659,602 [Application Number 05/094,942] was granted by the patent office on 1972-05-02 for two component syringe.
This patent grant is currently assigned to Nosco Plastics, Incorporated. Invention is credited to Harold S. Cloyd.
United States Patent |
3,659,602 |
Cloyd |
May 2, 1972 |
TWO COMPONENT SYRINGE
Abstract
A two component syringe having two vials each containing a
single component. A needle is mounted in the syringe and is
arranged to interconnect the vials prior to mixing the contents
thereof. One vial is mounted on a holder having a needle hub. The
other vial is mounted on an adapter sleeve removably mounted on the
needle hub. The adapter sleeve and the other vial are removed after
the ingredients have been mixed, leaving the first vial with the
associated needle in readiness for injection.
Inventors: |
Cloyd; Harold S. (Erie,
PA) |
Assignee: |
Nosco Plastics, Incorporated
(Erie, PA)
|
Family
ID: |
22248079 |
Appl.
No.: |
05/094,942 |
Filed: |
December 30, 1970 |
Related U.S. Patent Documents
|
|
|
|
|
|
|
Application
Number |
Filing Date |
Patent Number |
Issue Date |
|
|
848446 |
Aug 8, 1969 |
|
|
|
|
Current U.S.
Class: |
604/88 |
Current CPC
Class: |
A61M
5/2429 (20130101); A61J 1/2096 (20130101); A61J
1/201 (20150501); A61M 5/2448 (20130101); A61J
1/2051 (20150501); A61J 1/2013 (20150501) |
Current International
Class: |
A61J
1/00 (20060101); A61M 5/24 (20060101); A61m
005/18 () |
Field of
Search: |
;128/218,218P,218M,218D,218N,220 |
References Cited
[Referenced By]
U.S. Patent Documents
Foreign Patent Documents
|
|
|
|
|
|
|
526,191 |
|
Feb 1954 |
|
BE |
|
1,167,766 |
|
Aug 1958 |
|
FR |
|
1,074,027 |
|
May 1960 |
|
DT |
|
Primary Examiner: Reich; Joseph S.
Parent Case Text
This application is a streamline continuation of application Ser.
No. 848,446, filed Aug. 8, 1969 and now abandoned.
Claims
What is claimed is:
1. A syringe assembly having a solid plastic post with a needle hub
at one end of the post and a first part of a coupling at the other
end of the post, a double ended needle having one end of the needle
projecting from the first coupling part and the other end of the
needle projecting out through the hub and the intermediate portion
of the needle embedded and anchored in the post, a first vial
having a closed end remote from the first coupling part and a
cylindrical wall telescoped over the first coupling part and post,
a first piston in sliding sealing relation to the cylindrical wall
of the first vial, said first piston having a second coupling part,
said first and second coupling parts having interlocking means for
connecting the parts to stand axial forces in opposite direction
whereby after connecting the parts subsequent reciprocation of the
first vial relative to the post causes corresponding reciprocation
of the first vial relative to the first piston, said first piston
having a portion penetrated by said one end of the needle as its
said second coupling part is connected with said first coupling
part to establish communication between the needle and the first
vial, a second vial having a closed end remote from the needle hub
and a cylindrical wall and means for removably telescoping said
second vial over said other end of the needle, a second piston in
sliding sealing relation to the cylindrical wall of the second
vial, said second piston having a portion penetrated by said other
end of the needle to establish communication between the needle and
the second vial as the cylindrical wall of the second vial is
telescoped over said other end of the needle, one of said vials
containing a first ingredient and the other of the vials containing
a second ingredient which may be mixed with the first ingredient by
reciprocating the vials after establishing communication between
the needle and both vials, a holder fixed to the post having a
cylindrical wall surrounding the first vial in telescoping
relation, said assembly being conditioned for injection by
expelling into the first vial the contents of the second vial and
then removing the second vial from the assembly.
2. The assembly of claim 1 having a sleeve with one end surrounding
and telescopically receiving the open end of the first vial and the
other end surrounding and telescopically receiving the first
coupling part to provide a sliding telescoping seal between the
post and the cylindrical wall of the first vial.
3. The assembly of claim 1 having a sleeve with one end surrounding
and telescopically receiving the open end of the second vial and
the other end surrounding and telescopically receiving a member
associated with the needle hub to provide a sliding telescoping
seal between the hub and the cylindrical wall of the second
vial.
4. The assembly of claim 3 in which said member is an intermediate
sleeve removably seated on the needle hub and surrounding said
other end of the needle.
5. The assembly of claim 4 in which the intermediate sleeve has a
socket adjacent said other end of the needle receiving said portion
of the second piston as the cylindrical wall of the second vial is
telescoped over said other end of the needle.
6. The assembly of claim 1 in which one of the coupling parts is a
socket and the other of the coupling parts is a projection on the
piston adapted to be received in said socket.
Description
This invention is intended to provide a syringe assembly in which
two vials of the type forming an inverted syringe are initially
connected by a holder having a double ended needle for establishing
communication between the vials. The holder is provided with means
for attaching the plunger of the first vial so as to resist thrust
in both directions and thereby permit aspiration. The plunger of
the second vial is connected to the holder through a removable
sleeve so that when the contents of the vials have been mixed and
discharged into the first vial, the sleeve and second vial may be
removed, leaving the first vial and holder in condition for
injection.
In the drawing,
FIG. 1 is a longitudinal section through a two component syringe
assembly prior to mixing of the components, and
FIG. 2 is a longitudinal section through the syringe in readiness
for injection.
FIG. 1 at its upper end shows the glass vial 1 which is to be used
for the injection of a mixture of two ingredients. The lower end of
the vial is closed by a rubber or other suitable piston 2 having a
diaphragm 3 normally sealing a needle passageway 4, 5. The vial 1
contains one of the ingredients to be mixed.
At the lower end of FIG. 1 is a substantially identical vial 1a
having its lower end sealed by a rubber piston 2a and having a
diaphragm 3a normally sealing a needle passageway 4a. The vial 1a
contains the other ingredient to be mixed with the ingredient
contained in vial 1 prior to administration. The vials so far
described are or may be of common construction.
Between the vials 1 and 1a is a plastic holder 6 such as shown in
my copending application Ser. No. 749,448 filed Aug. 1, 1968,
incorporated by reference, for receiving the vial 1 and an
associated adapter sleeve 7 for receiving the vial 1a.
The holder 6 has a cylindrical body 6 with finger gripping
projections 8 at its upper end and a needle hub 9 at its lower end.
The body 6a telescopically receives the vial 1 and is integral with
a solid plastic post 10 having longitudinal external guide ribs
10a. The needle hub 9 is at the lower end of the post 10 in which
is embedded and anchored a double ended needle 11 with the lower
end 12 projecting out through the needle hub 9 and with the upper
end 13 terminating within or slightly above an upwardly presented
socket 14. The socket 14 and a projection 16 at the lower end of
the piston 2 are provided with interlocking means such as screw
threads 17, 18 which, when engaged, connect the piston 2 and the
socket 14 in axial thrust resisting relation so that reciprocation
of the vial 1 relative to the post causes corresponding
reciprocation of the vial 1 relative to the piston 2. This means
that the reciprocation of the vial relative to the post can cause
both suction to aspirate into the needle or pressure to expel out
through the needle.
The adapter sleeve 7 has its upper end removably received on a Luer
taper 19 on the lower end of the needle hub 9 and has its lower end
provided with a socket 20 for receiving the upper end 21 of the
piston 2a. The socket 20 and the piston end 21 could be of the same
construction as the socket 14 and projection 16. That is not
necessary since the vial 1a is to be thrown away prior to use of
the syrings for injection. Prior to use, the pointed end 12 of the
needle 11 is normally partially within the passageway 5a short of
the diaphragm 3a. When the vial 1a is pushed toward the needle hub
9, the pointed end 12 of the needle punctures the diaphragm 3a.
The parts are normally shipped in the partially assembled condition
shown in FIG. 1 with the vials 1 and 1a containing the separate
ingredients which are to be mixed prior to injection. One of these
ingredients is usually a solution and the other may be a
concentrate or a powder. The ingredients are such that the mixture
must be used promptly after mixing.
In the partially assembled condition, a sealing sleeve 22 for vial
1 has one end in sealing engagement with the open end of vial 1 and
has the opposite or reduced diameter end 23 telescoped over the
socket 14. The telescoping engagement with the vial and socket
provides a seal. In this position, the pointed end 13 of the needle
11 partially enters the needle passageway 5 but does not enter the
sealing diaphragm 3. A similar sealing sleeve 22a is telescoped
over the open end of vial 1a and has its reduced diameter end 23a
telescoped over the socket 20 on the adapter sleeve 7. The
telescoping engagement of the sealing sleeve 22a with the vial 1a
and socket 20 provides a seal protecting the needle point 12 and
the adjacent portion of the vial 1a from contamination. The adapter
sleeve 7 is seated on the Luer taper on the needle hub 9 so that
the needle point 12 partially enters the passageway 5a, but does
not puncture the diaphragm 3a. The assembly so far described, and
shown in FIG. 1, is shipped as a sterile package which insures
arrival at the point of use of the proper ingredients to be mixed
for injection.
Upon arrival of the package at the point of use, the first step is
to connect the projection 16 of the piston 2 to the socket 14. For
the particular type of connection illustrated, this merely requires
pushing the vial 1 toward the socket so that the projection 16
starts to enter the socket and then rotating the vial to screw the
projection into the socket and thereby establish a connection
between the piston and the socket which will stand axial thrust in
opposite directions. As the projection 16 is screwed into the
socket 14, the pointed end 13 of the needle 11 penetrates the
diaphragm 3 and establishes communication between the needle 11 and
the contents of the vial 1. The second step is to push the vial 1a
into the socket 20 until it bottoms. As the needle end 12
penetrates the diaphragm 3a and thereby establishes communication
between the needle and the contents of the vial 1a. With the
establishment of communication through the needle of the contents
of vials 1 and 1a, the ingredients may now be mixed. This may be
done by first expelling the contents of vial 1a into vial 1 by
pressure exerted on vial 1a and then by expelling the contents of
vial 1 back into vial 1a by pressure exerted on vial 1. This
sequence may be repeated as many times as necessary to insure
thorough mixing. The guide ribs 10a on the post 10 cooperate with
the sealing sleeve 22 and similar guide ribs 21 on adapter sleeve 7
cooperate with the sealing sleeve 22a to guide the reciprocation of
the vials 1 and 1a and the associated sleeves 22 and 22a. The final
step should end with expulsion of the contents of vial 1a back into
vial 1. Then, by removing the adapter sleeve 7 from Luer taper 19
on needle hub 9 and throwing away the adapter sleeve 7 and the
associated vial 1a, the remaining parts consisting of the vial 1
and the holder 6 are now in condition for injection of the mixed
ingredients as shown in FIG. 2.
* * * * *