Information
-
Patent Grant
-
6746438
-
Patent Number
6,746,438
-
Date Filed
Wednesday, August 15, 200123 years ago
-
Date Issued
Tuesday, June 8, 200420 years ago
-
Inventors
-
Original Assignees
-
Examiners
Agents
-
CPC
-
US Classifications
Field of Search
US
- 604 181
- 604 533
- 604 198
- 604 263
- 604 905
- 604 244
- 604 83
- 604 86
- 604 192
- 604 199
- 604 256
- 604 239
- 604 264
- 604 272
- 604 537
- 604 538
- 141 329
- 141 369
- 141 370
- 141 374
- 141 382
- 141 383
-
International Classifications
-
Abstract
The invention concerns a device for the two-way transfer of a liquid (38) between a bottle (14) provided with a cap (44) capable of being perforated at a cartridge (12) comprising a cylindrical reservoir (26) wherein slides a piston (34) capable of being perforated. It comprises: a body (16) including means to be fixed on the bottle (14); a member (24) linking the piston (34) capable of being perforated to the body (16); a shuttle (20) relative to the body (16) and said linking member (24), the shuttle bearing a hollow needle (22) whereof one first end (112) is adapted to pierce the piston (34) and whereof the second end (114) is adapted to pierce the cap (44). The shuttle (20) is mobile between a piston wherein the needle ends (112, 114) are spaced apart from the piston (34) capable of being perforated and the cap (44) capable of being perforated and an end-of-stroke transferring position wherein the needle ends (112, 114) are received in the cartridge (12) and the bottle (14).
Description
BACKGROUND OF THE INVENTION
The present invention relates to a device for two-way transfer of a liquid between a bottle, provided with a perforable stopper, and a cartridge, comprising a cylindrical reservoir in which a perforable piston slides.
Before proceeding with an injection using a syringe, it is common for the practitioner to have to mix the liquid contained initially in the syringe with a lyophilisate which is contained initially in a bottle provided with a perforable stopper.
To mix these extemporaneously, the practitioner first injects all of the liquid contained in the syringe into the bottle. To this end, he perforates the stopper of the bottle with the aid of the needle which is provided on the syringe and is intended for the injection proper.
After the lyophilisate has dissolved in the liquid, the mixture obtained is reaspirated into the syringe through the injection needle. After the needle has been removed from the bottle, the injection proper on the patient is carried out.
Carrying out this extemporaneous mixing using such means is relatively awkward, and it also poses the risk of the injection needle being contaminated upon its introduction into the bottle.
Devices are also known for transferring fluid between a bottle and a flexible bag intended in particular for transfusion. However, these devices are not designed to permit two-way transfer of a liquid between a bottle and a syringe.
SUMMARY OF THE INVENTION
It is an object of the invention to make available a solution to the problem of two-way transfer of a liquid between a bottle and an injection syringe by making available a device which is easy to use and which guarantees satisfactory aseptic conditions.
To this end, the subject of the invention is a device for two-way transfer of a liquid between a bottle, provided with a perforable stopper, and a cartridge, comprising a cylindrical reservoir in which a perforable piston slides, characterized in that it includes a body having means for fixing to the bottle, a member for connecting the perforable piston to the body, and a shuttle which is displaceable relative to the body and to said connecting member, the shuttle bearing a hollow needle of which a first end is adapted to perforate the piston and of which the second end is adapted to perforate the stopper, and in that the shuttle is displaceable between an initial position, in which the needle ends are spaced apart from the perforable piston and the perforable stopper, and a final transfer position, in which the needle ends are received in the cartridge and the bottle.
According to particular embodiments, the transfer device includes one or more of the following characteristics:
said member for connecting the piston to the body comprises means for fixing to the body and is movable relative to the body from an initial position, in which the fixing means are not in engagement with the body, and a final position, in which the fixing means are in engagement with the body, thus ensuring that the piston is connected to the body;
said member for connecting the piston to the body comprises a threaded protuberance for fixing it in a tapped recess in the piston;
said shuttle is mounted so as to slide in a conduit of said member for connecting the piston to the body;
said conduit has on the inside an abutment limiting the displacement travel of the shuttle;
it comprises a protective cap initially mounted on the body, which protective cap has means for fixing it to the reservoir of the cartridge;
the body has a continuation surrounding said shuttle and extending beyond the first end of the needle;
it comprises at least one abutment limiting the axial displacement of the reservoir relative to the connecting member, preventing removal of the piston from the reservoir; and
it comprises a cartridge support on which the reservoir of the cartridge bears axially, and in that one of the cartridge support and connecting member has at least one projection, forming said abutment, received in a longitudinal slit of the other of the cartridge support and connecting member, in order to limit their relative axial displacement between the reservoir and the connecting member.
The invention also relates to an injection kit including a device for two-way transfer as defined above, and a cartridge and a bottle, in which the cartridge is initially connected to the attachment member and the bottle is initially connected to the body.
BRIEF DESCRIPTION OF THE DRAWINGS
The invention will be better understood on reading the following description which is given solely by way of example and in which reference is made to the drawings, in which:
FIG. 1
is a longitudinal cross-sectional view of the transfer device according to the invention in its storage position;
FIGS. 2 and 3
are a longitudinal cross-sectional view and a perspective and partially cutaway view, respectively, of the transfer device in its initial phase of use;
FIG. 4
is a longitudinal cross-sectional view of the transfer device after the needle ends have penetrated into the bottle and the cartridge;
FIG. 5
is a longitudinal cross-sectional view of the transfer device during the phase of transfer of the fluid from the cartridge to the bottle;
FIG. 6
is a longitudinal cross-sectional view of the transfer device once all the liquid has been transferred to the bottle;
FIG. 7
is a longitudinal cross-sectional view of the transfer device when returning the mixture from the bottle to the cartridge;
FIG. 8
is a cross-sectional view of an alternative embodiment of the transfer device according to the invention; and
FIG. 9
is a partial perspective view of the connecting member of the device in FIG.
8
.
DETAILED DESCRIPTION OF THE INVENTION
The transfer device
10
shown in
FIG. 1
is designed for two-way transfer of fluid bet ween a cartridge
12
and a bottle
14
. This device is generally of revolution about its longitudinal axis. It mainly comprises a body
16
, a protective cap
18
, a shuttle
20
bearing a hollow needle
22
, and a screw pusher or connecting member
24
intended to ensure axial securing of the movable piston of the cartridge
12
and the body
16
.
In
FIG. 1
, the transfer device
10
, equipped with the cartridge
12
and the bottle
14
, is shown in its storage position before use.
The cartridge
12
is intended for carrying out an injection after it has been withdrawn from the transfer device and is equipped with an injection needle and an actuating pusher. It comprises a cylindrical reservoir
26
which at the front has a narrowed neck
28
closed off by a perforable cap
30
supported by an a head
31
. The cap
30
is designed to be perforated by an injection needle mounted on the head
31
of the cartridge with a view to proceeding with an injection.
The rear end
32
of the reservoir
26
, at the opposite end from the head
31
, is closed of by a perforable piston
34
mounted so as to slide in a leaktight manner inside the reservoir
26
. The piston
34
has axially a recess
36
opening to the outside of the cartridge. This recess is tapped internally in order subsequently to allow screwed insertion of an actuating pusher with a view to injecting the liquid contained in the cartridge.
The piston
34
is made of a polymer material of given Shore hardness.
The cartridge
12
is initially filled with an injectable liquid
38
.
The bottle
14
comprises a glass body
40
with a neck
42
closed off by a perforable stopper
44
. The neck
42
has a peripheral rim
46
defining a shoulder
48
.
The perforable stopper
44
is made of a polymer material having substantially the same Shore hardness as the material from which the piston
34
is made. Thus, the piston
34
and the stopper
44
have the same resistance to engagement of a sharp point. The materials from which the stopper
44
and the piston
34
are made are advantageously the same. Moreover, their thicknesses measured on the axis X—X are substantially identical.
The bottle
14
is initially filled with a lyophilisate
50
constituting a medicinal substance in powder form. The oyophilisate
50
only partially fills the bottle. As is known per se, the bottle is sealed under vacuum so that the pressure inside the bottle is very much lower than the atmospheric pressure.
The body
16
has a conduit
60
passing axially through it from one end to the other. At one end, called the lower end, the conduit
60
defines a seat
62
for receiving the bottle. This seat has a countersink
64
for receiving the rim
46
of the bottle
14
in order to fix the latter. In particular, the countersink
64
is delimited by projections
66
defining profiles for fixing the bottle. They are designed to cooperate with the shoulder
48
delimited by the neck of the bottle. The projections
66
have ramps converging from the open end of the seat
62
so as to make it easier to introduce the bottle into the body.
At its other end, called the upper end, the conduit
60
has a cylindrical chamber
70
in which the shuttle
20
and the connecting member
24
are received. The chambers
62
and
70
are linked via an intermediate portion
74
of smaller diameter.
The chamber
70
has a diameter which is sufficient to allow the passage of the reservoir
26
. The total length of the chamber
70
and of the portion
74
is advantageously greater than that of the hollow needle
22
.
The portion
74
is partially closed, at its end which opens into the chamber
62
, by a membrane
75
which delimits an opening sufficient for the passage of the needle
22
. This membrane
75
partially covers the membrane
44
of the bottle
14
.
At its upper end, the body
16
has on the outside a shoulder
76
reducing the thickness of the body. This is designed for fitting the protective cap
18
.
The protective cap
18
generally has the form of a sleeve and defines a seat
78
which is able to receive the cartridge
16
and to be engaged from its open end partially about the body
16
.
It additionally comprises, on the outside, at its blind end, means
80
for fixing on the head
31
of the cartridge. As is shown in perspective in
FIG. 3
, the means
80
comprise a fork
82
delimited by two arms which define a notch
84
which extends radially and whose width corresponds to the diameter of the narrowed neck
28
. Behind the fork
82
, a chamber
86
is provided in the protective cap
80
for the purpose of receiving the head
31
.
The connecting member
24
has a tubular shape. It comprises a cylindrical side wall
90
delimiting a conduit
91
. It is closed off at an upper end by a threaded protuberance
92
projecting outward. This protuberance
92
is screwed inside the tapped recess
36
and thus ensures that the connecting member
24
and the piston
34
are axially secured.
The protuberance
92
is provided with an axial conduit
94
whose diameter corresponds substantially to the external diameter of the needle
22
.
At its lower end, the connecting member
24
has, on the outer surface of its wall
90
, two successive grooves
96
A,
96
B which are spaced axially apart. They are separated by a distance I
1
. The grooves
96
A and
96
B are designed to cooperate with a peripheral flange
98
formed in the conduit
60
of the body. The flange is provided at the end of the intermediate portion
74
opening into the chamber
70
.
The groove
96
and the peripheral flange
98
are designed to secure the connecting member
24
and the body
16
. The flange
98
is initially engaged in the lower groove
96
A.
The distance I
1
is chosen to be smaller than the length of the intermediate portion
74
, less the thickness of the membrane
75
.
The wall
90
of the connecting member
24
has on the inside a peripheral flange
100
which delimits, in the space circumscribed by the wall
90
, a chamber
102
confining the shuttle
20
. Thus, the flange
100
forms an axial abutment for stopping the shuttle
20
.
The shuttle
20
is made up of a cylindrical slide
110
, with the hollow needle
22
passing axially through the latter from one end to the other. Thus, a first end
112
of the needle protrudes beyond the slide
110
and is received initially in the passage
94
. The second end
114
of the needle
22
protrudes rearward of the slide
110
and is initially arranged facing the stopper
44
of the bottle.
The two ends of the needles have analogous bevels, so that they have sharp points with the same profiles facing the piston
34
and the stopper
44
.
The diameter of the slide
110
is greater than the diameter of the passage defined by the membrane
75
.
The cylindrical slide
110
has, along a part of its length received in the confinement chamber
102
, longitudinal ribs
116
(
FIG. 3
) which define a shoulder
118
which is designed to cooperate with the peripheral flange
11
forming an abutment. The longitudinal ribs
116
guide the shuttle
20
in translation inside the connecting member
24
.
The length of the ribs
116
is smaller than the length of the confinement chamber
112
defined between the protuberance
92
and the flange
100
. This difference in length is labeled I
2
.
Initially, as is shown in
FIG. 1
, the connecting member
24
is free from the body
16
, so that the fixing means formed by the groove
96
A and the flange
98
are in engagement. Likewise, the shuttle
20
initially bears on the peripheral flange
100
by way of the shoulder
118
, so that the end
112
of the needle extends inside the protuberance
92
. It is thus spaced apart from the perforable piston
34
. The shuttle is then spaced apart by the distance I
2
from the protuberance
92
.
Likewise, the end
114
of the hollow needle is kept spaced apart from the stopper
44
by the lower end of the connecting member
24
bearing on the peripheral flange
98
and the shuttle
20
bearing on the flange
100
. The lower end of the slide
11
is then separated from the stopper
44
by a distance I
3
.
The distances I
1
, I
2
and I
3
are advantageously related to each other such that I
1
=I
2
+I
3
.
The transfer devise
10
is used in the following way.
The protective cap
18
is first pulled off and turned. The fixing means
80
are engaged about the head
31
of the cartridge, as is shown in
FIGS. 2 and 3
.
The protective cap
18
and the body
16
are then moved together in the direction of the arrow F
4
, as is shown in FIG.
4
. Upon this axial displacement, the shuttle
20
moves relative to the body
16
until a transfer position is reached in which the end
112
protrudes inside the cartridge
12
after passing through the piston
34
and the end
114
protrudes inside the bottle
14
after passing through the stopper
44
.
The displacement of the protective cap
18
in fact brings about the engagement of the cartridge
12
in the chamber
70
of the body. Upon this displacement, the connecting member
24
is displaced toward the bottle
14
by being pushed by the cartridge. The groove
96
A disengages from the peripheral flange
98
and the lower end of the member
24
is displaced until the flange
98
is received in the peripheral groove
96
B. The elastic engagement of the flange
98
in the groove
96
B ensures definitive axial securing of the connecting member
24
and the body
16
.
Upon displacement of the connecting member
24
along the course I
1
, the shuttle
20
, mounted so as to slide inside the connecting member
24
along a course of length I
2
, is also displaced relative to the body
16
and the member
24
.
In fact, at the start of the sliding of the connecting member
24
, the ends
112
and
114
of the needle come to bear respectively on the piston
34
and the stopper
44
. These latter then perforate the piston
34
and the stopper
44
simultaneously as the cartridge
12
and the bottle
14
are brought together. The ends of the needle then penetrate into the cartridge
12
and the bottle
14
.
As the Shore hardness values for the piston
34
and for the stopper
44
are identical, and likewise the two profiles of the ends
112
and
114
of the needle, the initial perforations of the piston and of the membrane are effected simultaneously, the needle being stressed only at these two ends.
At the end of displacement of the connecting member
24
, the slide
110
comes into abutment, on the one hand, on the end protuberance
92
of the connecting member and, on the other hand, against the membrane
75
extending over the stopper
44
which closes the bottle. In this position, shown in
FIG. 4
, the hollow needle
22
ensures communication between the bottle
14
and the cartridge
12
.
As is illustrated in
FIG. 5
, when the reservoir
26
is subsequently engaged in the body
16
under the action of the protective cap
18
displaced toward the body
16
in the direction of the arrow F
5
, the liquid
38
initially contained in the cartridge
12
is gradually transferred into the bottle
14
.
This transfer results from the engagement of the piston
34
inside the cylindrical reservoir
26
, the piston
34
being held fixed in relation to the body by way of the connecting member
24
which thus forms an abutment while the reservoir
26
is displaced toward the body
16
.
Filling the bottle
14
is made possible because it is initially at a pressure below atmospheric pressure.
When, as is shown in
FIG. 6
, the piston
34
is bearing against the neck
28
of the cartridge, most of the liquid initially contained in it is transferred into the bottle
14
.
After sufficient shaking, the lyophilisate
50
dissolves in the liquid
38
inside the bottle
14
.
To transfer the extemporaneous mixture thus formed to the inside of the cartridge
12
, the transfer device
10
is turned around, as is shown in
FIG. 7
, then the protective cap
18
is removed from the body
16
and the extemporaneous mixture is aspirated into the cartridge.
During the pull exerted on the cylindrical reservoir
26
of the cartridge in the direction of the arrow F
7
, the piston
34
is kept integral with the body
16
by way of the connecting member
24
fixed to the body through the cooperation of the groove
96
B and the peripheral flange
98
.
The mixture is aspirated under the action of the movement of the cylindrical reservoir
26
relative to the piston
34
. The relative movement of the piston and of the reservoir in fact creates an underpressure inside it, which leads to aspiration of the mixture contained in the bottle
14
.
After the cartridge
12
has been filled completely with the extemporaneous mixture, the cartridge
12
is detached from the connecting member
24
by being unscrewed. It can then be used for injection purposes after being fitted with an injection needle and an actuating pusher.
The transfer device thus without the cartridge is then discarded. It should be noted that in this position the end
112
of the needle is protected on account of the continuation of the body
16
, thereby avoiding any risk of accidental needle stick injuries. To this end, the length of the body
16
is chosen to be sufficient to continue beyond the end
112
of the hollow needle.
The device according to the invention permits a transfer of the liquid between the cartridge and the bottle without any risk of contamination of the liquid. This is because the two ends of the hollow needle are at all times protected inside the closed space delimited by the connecting member
24
, the body
16
and the bottle
14
.
This protection is further reinforced by the presence of the protective cap
18
during storage of the device.
Moreover, the simultaneous penetration of the two ends of the needles avoids any risk of ambient air entering the cartridge or the bottle.
When the transfer device is pre-fitted with a bottle
14
and a cartridge
12
before delivery, the transfer can be carried out without any need for the cartridge or the bottle to come back into contact with the hand. This eliminates any risk of contamination from the hands.
An alternative embodiment of the transfer device according to the invention is shown in
FIGS. 8 and 9
. In this figure, the elements which are analogous or identical to those of the embodiment in
FIGS. 1 through 7
are designated by the same reference numbers.
This figure shows a transfer device
200
combined with a cartridge
12
and a bottle
14
containing a lyophilisate.
The transfer device
200
comprises a body
16
in which the bottle
14
is axially immobilized, a connecting member
24
which slides relative to the body, and a needle-holedr shuttle
20
which slides freely along the axis of the connecting member
24
.
The transfer device
200
additionally comprises a cartridge support
202
which has means
203
for axially fixing the cap
18
.
In this embodiment, the connecting member
24
includes, in addition to the cylindrical wall
90
, a coaxial outer sleeve
204
which surrounds the cylindrical wall
90
and is connected to it by an annular wall
206
. The sleeve
204
is mounted so as to slide inside the body
16
. It has raised and recessed profiles
208
designed to cooperate with complementary profiles provided on the side wall of the body
16
in order to axially secure these after perforation of the stopper
44
by the end
114
of the hollow needle.
The sleeve
204
continues beyond the threaded protuberance
92
screwed into the piston
34
of the cartridge.
As is shown in
FIG. 9
, the sleeve
204
has, in its side wall, two pairs of longitudinal slits
210
,
212
offset by an angle of 90°. The slits
210
have a length twice that of the slits
212
. The lower end of the two pairs of slits
210
,
212
, arranged toward the bottle
14
, extend at the same level on the sleeve
204
.
The cartridge support
202
comprises an inner tube
220
for receiving the body
26
of the cartridge. It is partially closed at its lower end by a shoulder
222
on which the open end of the reservoir
26
of the cartridge bears axially. The shoulder
222
is continued by a tubular portion
224
sliding along the cylindrical wall
90
of the connecting member. In addition, the tube
220
is surrounded in its lower part by a coaxial sleeve
230
bearing two diametrically opposite projections
232
which are designed to slide inside one or other of the pair of slits
210
,
212
.
Depending on the capacity of the cartridge
12
used with the transfer device, the projections
232
are introduced into one or other of the pairs of slits. For a cartridge with a capacity of 1.3 mm, that is to say a cartridge having a body of reduced length, the projections
232
are arranged in the short slits
212
.
By contrast, when the transfer device is used with a cartridge having a capacity of 2.3 ml, that is to say a cartridge in which the length of the body is twice that of a cartridge of 1.3 ml, the projections
232
are engaged in the slits
210
.
It will be appreciated that the cartridge support
202
guides the cartridge
12
axially as it slides relative to the connecting member
24
. The presence of the two pairs of slits on the sleeve
204
of the connecting member makes it possible to use the same transfer device with cartridges of two different capacities.
After the liquid contained initially in the cartridge has been transferred to the inside of the bottle and it has been mixed with the lyophilisate, the mixture thus obtained is reaspirated into the cartridge
12
through the needle. For this purpose, the reservoir of the cartridge is pulled using the cap fixed to the needle support
202
. When the mixture is transferred to the cartridge
12
, the projections
232
slide along the slits
210
or
212
. When the projections
232
come into contact with the end of these slits, the latter form an abutment and oppose subsequent displacement of the cartridge
12
. Thus, any risk of the piston
34
being withdrawn from the reservoir of the cartridge on account of too great a displacement of the latter is avoided by the presence of the projections
232
forming an abutment. This is because these limit the course of displacement of the reservoir of the cartridge relative to the connecting member
24
secured to the piston.
Claims
- 1. A device for two-way transfer of a liquid (38) between a bottle (14), provided with a perforable stopper (44), and a cartridge (12), comprising a cylindrical reservoir (26) in which a perforable piston (34) slides, characterized in that it includes:a body (16) having means for fixing to the bottle (14), a member (24) for connecting the perforable piston (34) to the body (16), a shuttle (20) which is displaceable relative to the body (16) and to said connecting member (24), the shuttle (20) bearing a hollow needle (22) of which a first end (112) is adapted to perforate the piston (34) and of which the second end (114) is adapted to perforate the stopper (44), and in that the shuttle (20) is displaceable between an initial position, in which the needle ends (112, 14) are spaced apart from the perforable piston (34) and the perforable stopper (44), and a final transfer position, in which the needle ends (112, 114) are received in the cartridge (12) and the bottle (14).
- 2. The device as claimed in claim 1, characterized in that said member (24) for connecting the piston to the body comprises means (96) for fixing to the body (16) and is movable relative to the body (16) from an initial position, in which the fixing means (96) are not in engagement with the body (16), and a final position, in which the fixing means (96, 98) are in engagement with the body, thus ensuring that the piston is connected to the body.
- 3. The device as claimed in claim 1, characterized in that said member (24) for connecting the piston to the body comprises a threaded protuberance (92) for fixing it in a tapped recess (36) in the piston (34).
- 4. The device as claimed in claim 1, characterized in that said shuttle (20) is mounted so as to slide in a conduit (91) of said member (24) for connecting the piston to the body.
- 5. The device as claimed in claim 4, characterized in that said conduit (91) has on the inside an abutment (100) limiting the displacement travel of the shuttle (20).
- 6. The device as claimed in claim 1, characterized in that it comprises a protective cap (18) initially mounted on the body (16), which protective cap (18) has means (80) for fixing it to the reservoir (26) of the cartridge.
- 7. The device as claimed in claim 1, characterized in that the body (16) has a continuation surrounding said shuttle (20) and extending beyond the first end (112) of the needle.
- 8. The device as claimed in claim 1, characterized in that it comprises at least one abutment (232) limiting the axial displacement of the reservoir (26) relative to the connecting member (24), preventing removal of the piston (34) from the reservoir (26).
- 9. The device as claimed in claim 8, characterized in that it comprises a cartridge support (202) on which the reservoir (26) of the cartridge (12) bears axially, and in that one of the cartridge support (202) and connecting member (24) has at least one projection, forming said abutment (232), received in a longitudinal slit (210, 212) of the other of the cartridge support (202) and connecting member (24), in order to limit their relative axial displacement between the reservoir (26) and the connecting member (24).
- 10. An injection kit including a device (10) for two-way transfer according to claim 1, and a cartridge (12) and a bottle (14), in which the cartridge (12) is initially connected to the connecting member (24) and the bottle (14) is initially connected to the body (16).
Priority Claims (1)
Number |
Date |
Country |
Kind |
99 03392 |
Mar 1999 |
FR |
|
PCT Information
Filing Document |
Filing Date |
Country |
Kind |
PCT/FR00/00671 |
|
WO |
00 |
Publishing Document |
Publishing Date |
Country |
Kind |
WO00/54723 |
9/21/2000 |
WO |
A |
US Referenced Citations (6)
Foreign Referenced Citations (2)
Number |
Date |
Country |
676548 |
Apr 1988 |
CH |
676 548 |
Feb 1991 |
CH |