Title of Invention

DEVICE FOR AUTOMATICALLY INJECTING INJECTION LIQUIDS

Abstract Device for automatically injecting injection liquids In a device (1) for automatically injecting injection liquids, including an axially subdivided housing whose parts are connectable with each other, wherein an axially displaceable pressure pin (5) is guided in a first housing part (2), which pin is capable of being inserted against a force accumulator (6) and locked in the inserted position and extended upon relief of the force accumulator (6), wherein an injection needle (15) fixed in a needle guide (14) and an ampoule (13) are mounted in a second housing part (3) so as to be axially displaceable relative to each other, wherein the injection needle (15) on its side facing the ampoule (13) is designed as a perforation piece (32), for the ampoule (13), the ampoule (13) with its end facing the injection needle (15) is mounted to reach into a sleeve (16) fixed within the second housing part (3) and whose inner diameter substantially corresponds to the outer diameter of the ampoule (13). Radially inwardly protruding projections (17) are formed on the inner periphery of the sleeve (16), and the sleeve (16) comprises locking members cooperating with locking members (20) of the needle guide (14), whereby an axial displacement of the ampoule (13) in the direction to the needle guide (14) while overcoming the displacement resistance exerted by the projections (17) causes the release of the locking members (20) and the axial displaceability of the needle guide (14).
Full Text Device for automatically injecting injection liquids
The invention relates to a device for automatically injecting
injection liquids, including an axially subdivided housing whose
parts are connectable with each other, wherein an axially
displaceable pressure pin is guided in a first housing part,
which pin is capable of being inserted against a force
accumulator and locked in the inserted position and extended
upon relief of the force accumulator, and an injection needle
fixed in a needle guide and an ampoule are mounted in a second
housing part so as to be axially displaceable relative to each
other, wherein the injection needle on its side facing the
ampoule is designed as a perforation piece for the ampoule.
Devices of the initially defined kind have become known under
the name of autoinjector. The known devices are instruments
which facilitate the injection of an emergency drug into the
body in case of emergency. Autoinjectors are, for instance, used
in allergic emergencies, e.g. after insect bites, snake bites
etc., yet also in the military field, for instance, in order to
quickly counteract intoxications by chemical warfare agents. The
known devices in most cases are devised as disposable devices
and, therefore, disposed of after one-time use.
From AT 303 251, an injection device is known, which comprises
two housing parts capable of being screwed one into the other,
an activator containing a spring-loadable pressure pin, and an
injector containing the ampoule and the injection needle as an
inseparable unit. After having been unlocked, the spring-loaded
pressure pin exerts a force on the piston plug of the ampoule,
whereupon the ampoule is, at first, displaced along with the
injection needle in the axial direction within the injector
housing so that the injection needle penetrates into the
patient's body and the liquid contained in the ampoule is

subsequently set under such a high pressure that a sealing
membrane provided between the ampoule and the injection needle
will break, thus causing the liquid to be ejected. That known
configuration, however, involves the drawback that the broken
membrane may obstruct the injection needle, thus preventing the
rapid ejection of the injection liquid.
From WO 01/07104, an advanced injection device has already
become known, in which the ampoule and the injection needle are
arranged within the housing so as to be relatively displaceable
in the axial direction, and the injection needle end facing the
ampoule is designed as a perforation piece for the ampoule. The
ampoule is, in fact, mounted in the interior of the housing
without being firmly connected with the injection needle. It is
only during application that the ampoule is displaced in the
direction of the injection needle under the force of the
pressure pin extending upon relief of the force accumulator and
pierced by the injection needle end designed as a perforation
piece.
The previously known autoinjectors, however, are only
insufficiently able to meet the recent demands as are prescribed
for use in the military field. Autoinjectors that are to be
suitable for military purposes must, in fact, safeguard a
longer-than-average storability and sterility of the respective
injection devices and be designed extremely robust. On a trial
basis, autoinjectors for military purposes are, for instance,
dropped on a stone floor from a height of two meters in order to
check whether the ampoule has broken or whether the mechanical
impact has caused slipping of the ampoule and/or injection
needle in a manner that the sealing disc of the ampoule is
pierced by the injection needle. Similar tests are also carried
out under extreme temperature conditions.

The invention aims to provide a device of the initially defined
kind, which complies with the demands set out above for use in
the military field in a satisfactory manner. To solve this
object, the device according to the invention essentially
consists in that the ampoule with its end facing the injection
needle is mounted to reach into a sleeve fixed within the second
housing part and whose inner diameter substantially corresponds
to the outer diameter of the ampoule, that radially inwardly
protruding projections are formed on the inner periphery of the
sleeve, and that the sleeve comprises locking members
cooperating with locking members of the needle guide, whereby an
axial displacement of the ampoule in the direction to the needle
guide while overcoming the displacement resistance exerted by
the projections causes the release of the locking members and
the axial displaceability of the needle guide. By the ampoule
with its end facing the injection needle being mounted so as to
reach into a sleeve fixed within the second housing part, the
radially inwardly protruding projections provided on the inner
periphery of the sleeve and defining a smaller diameter than the
ampoule are able to prevent the ampoule from slipping in the
direction to the injection needle. The energy set free by an
impact or other mechanical action at worst is absorbed by the
inwardly protruding projections while expanding the wall of the
sleeve. After a short displacement, the ampoule will, thus, be
stuck between the inwardly protruding projections with any
further displacement being prevented.
In accordance with the invention, the sleeve is equipped with
locking members which cooperate with respective locking members
of the needle guide such that the needle guide too, along with
the injection needle fixed therein, will be secured against
axial displacement. Both the ampoule reaching into the sleeve
and the needle guide connected with the sleeve are, hence,
coupled to the sleeve, with the sleeve being, in turn, immovably

retained in the second housing part, to which end the end-side
annular sleeve surface facing the needle guide preferably rests
on a radially inwardly protruding projection of the second
housing part. This is to ensure that the ampoule or the needle
guide will not be detached, and the injection needle will be
unable to emerge from the injector housing, even if the
injection device falls from an extreme height on hard ground.
To activate the injection device, it is provided according to
the invention that an axial displacement of the ampoule in the
direction to the needle guide while overcoming the displacement
resistance exerted by the projections causes the release of the
locking members and the axial displaceability of the needle
guide. Thereby, the locking members will only be released if the
ampoule in the injector housing is pushed towards the injection
needle by the spring force of the unlocked pressure pin, whereby
such high forces are released that the displacement resistance
exerted on the ampoule by the projections of the sleeve will be
overcome. The release of the locking members fixing the needle
guide may advantageously be effected in that the locking members
of the sleeve are formed on arms capable of excursing outwardly
in a resilient manner, said arms each carrying an inwardly
protruding projection in the region of their coupling site,
which cooperates with the ampoule under the excursion of the
arms and release of the locking members. In this case, the
locking members may be comprised of snap-in noses engaging in
reception openings. An axial displacement of the ampoule, thus,
causes the ampoule to run up inwardly protruding projections
formed on outwardly resilient arms in a manner that further
axial displacement causes an excursion of the arms and the
locking members formed on said arms to disengage and release the
needle guide.


After having released the needle guide, the ampoule is able to
pass through the sleeve unhampered and approach the injection
needle end designed as a perforation piece. In order to cushion
the hard impact of the ampoule on the injection needle to be
expected subsequently, a spring element acting in the axial
direction is preferably arranged between the needle guide and
the ampoule. The spring action causes the absorption of the
impact energy, thus preventing a possible fracture of the glass
ampoule. The spring element may be designed in one piece with
the needle guide, as a spring basket compressible in the axial
direction such that the spring basket can be additionally used
as a spacer in order to prevent the ampoule from striking
against the bottom of the needle guide. The ampoule will
consequently reach its end position closely in front of the
bottom of the needle guide, whereby a rupture of the ampoule
head will be safely prevented.
In order to prevent the injection liquid from escaping
prematurely, the configuration is advantageously further
developed such that the injection needle includes a radial
passage opening at an axial distance from its end designed as a
perforation piece for the ampoule. The channel of the injection
needle, thus, will not enter into fluid connection with the
injection liquid immediately upon piercing of the ampoule, but
only after a further axial displacement which causes the radial
passage opening of the injection needle to reach into the
ampoule. In order to ensure that the injection liquid be pressed
into the injection needle through the radial passage opening
rather than emerging around the injection needle laterally from
the pierced rubber sealing disc or the ampoule head, the
configuration is preferably further developed such that the
radial passage opening in the axial direction is arranged
between the injection needle end designed as a perforation piece
and an annular web arranged on the needle guide and surrounding

the injection needle, said annular web defining a closed annular
space between the web and the injection needle reaching into the
ampoule.
In order to enhance the security against fracture of the
ampoule, which is mostly made of glass, the configuration is
preferably further developed such that the ampoule with its end
facing away from the injection needle is arranged to reach into
a sleeve-shaped ampoule socket which comprises a plurality of
lamellar guide ribs extending in the longitudinal direction. In
this case, the ampoule is positioned centrally within the
sleeve-shaped ampoule socket. The elastic guide ribs of the
ampoule socket protect the glass ampoule from fracture, since
the vibrations acting on the injection device from outside are
to the major extent absorbed by the guide ribs rather than
transmitted to the ampoule. It is, thus, safeguarded that the
glass ampoule is mounted in a fracture-proof manner even under
heavy vibrations.
In order to ensure the reguired sterility, the ampoule reception
opening facing the first housing part including the pressure pin
is advantageously closed by a gas-permeable sealing foil. This
gas-permeable sealing foil enables the interior of the fully
equipped, bilaterally closed injection part to be sterilized by
the aid of a gas so as to guarantee the sterility of the
injection part over years. To provide complete tightness, a seal
and, in particular, an O-ring seal may be arranged between the
outer periphery of the ampoule socket and the inner periphery of
the second housing part.
In the following, the invention will be explained in more detail
by way of an exemplary embodiment schematically illustrated in
the drawing. Therein:

Fig. 1 depicts a longitudinal section through the device
according to the invention;
Fig. 2 is an enlarged sectional illustration of the activator
part;
Fig. 3 is an enlarged illustration of the injector part;
Fig. 4 is partially sectioned partial illustration of the
injector unit;
Fig. 5 is an exploded view of the injector part;
Fig. 6 shows a modified configuration of the injector part; and
Figs. 7a to 7h illustrate the operation seguence of the device
according to the invention.
Fig. 1 depicts an injection device 1 whose housing is subdivided
in the axial direction. The first housing part 2 encloses the
activator part and the second housing part 3 encloses the
injection part of the device according to the invention, the two
housing parts being connectable by means of a thread 4. The
activator part, which is illustrated in more detail in Fig. 2,
comprises a pressure pin 5 that is axially displaceable within
the housing 2 and insertable against a spring 6. The pressure
pin 5 comprises inwardly resilient snap-in projections 7 forming
the conical termination of the pressure pin 5. In the locked
position, a pin 9 of a cap 8 keeps the snap-in projections 7 in
a radially outwardly excursed position such that the snap-in
connections 7 overlap the annular part 10. Upon removal of the
cap 8, the activator part can be triggered by actuating the
safety sleeve 11 in the sense of arrow 12, whereby the snap-in
projections 7 are pressed inwardly and the pressure pin 5 is
catapulted in the sense of arrow 12 by the force of the spring
6, thus causing the conical end formed by the snap-in
projections 7 to pass through the clear cross section of the
ring 10.


Fig. 3 illustrates the injector part, in which an ampoule 13 and
an injection needle 15 fixed in a needle guide 14 are mounted.
The ampoule 13 in this case reaches into a sleeve 16 which is,
in turn, secured against axial displacement in the housing 3. As
is apparent from Fig. 4, the sleeve 16 on its inner periphery
comprises radially inwardly protruding projections 17 defining a
smaller diameter than the outer diameter of the ampoule 13. They
are dimensioned such that the ampoule 13 rests on the wedge-
shaped run-up surfaces of the projections 17. It is only under a
strong mechanical action on the injector part occurring, for
instance, as the latter is dropped from a great height, that an
axial displacement of the ampoule 13 in the sense of arrow 18 is
effected, which causes the ampoule 13 to be further displaced in
the axial direction along the wedge-shaped run-up surfaces of
the projections 17 under the expansion of the sleeve 16 and,
consequently, be jammed between the projections 17, thus being
secured against further axial displacement.
The sleeve 16 comprises radially outwardly resilient arms 19,
which are provided with recesses into which respective snap-in
noses 20 of the needle guide 14 engage. The needle guide 14 is
thereby coupled to the sleeve 16 and likewise secured against
axial displacement. It is only upon actuation of the injection
device by triggering the pressure pin 5 that the needle guide
will be released. The spring 6 of the activator part in this
case is devised such that the pressure pin 5 exerts a force on
the piston plug 21, thus causing a further displacement of the
ampoule 13 in the sense of arrow 18 against the displacement
resistance created by the projections 17. After this, the
ampoule 13, via wedge-shaped run-up surfaces 22, impinges on
projections 23 formed on the resilient arms 19 of the sleeve 16.
This causes an excursion of the resilient arms 19 in the sense
of arrows 24 such that the recesses will no longer be engaged

from behind by the snap-in noses 20 and the needle guide 14 will
be released.
In order to dampen the impact of the ampoule 13 on the needle
guide 14, a spring element and, in particular, a spring basket
25 is provided, which is formed in one piece with the needle
guide 14. The ampoule 13 can subsequently be further moved on in
the axial direction along with the needle guide 14, and the
injection needle can emerge from the housing 3. From Fig. 3, it
is apparent that the housing 3 is closed by a needle protection
cap 26, which is held firmly in a clamping ring 27. From Fig. 3,
it is further apparent that the ampoule 13 is retained in an
ampoule socket 28, which protects the ampoule 13 against
fracture. In the exploded view according to Fig. 5, the
individual elements of the injector part are clearly
illustrated, it being also apparent that the ampoule socket 28
is closed by a sealing foil 29 and sealed relative to the inner
side of the housing 3 by a sealing ring 30. In this manner, the
whole interior of the injector part is encapsulated so as to
safeguard the permanent sterility of the injection unit
including the ampoule. The sealing of the injector interior may,
however, also be effected in another way, as illustrated in Fig.
6. There, the ampoule socket 28 on its outer periphery comprises
a labyrinth seal which ensures the tightness of the ampoule
socket relative to the housing 3. The labyrinth seal has a
plurality of peripherally extending lamellas which are slit at a
point along their peripheries, the slits of axially adjacent
lamellas being each offset by 180°. The thus formed labyrinth is
permeable for a gas that serves to sterilize the injector part
so as to enable its introduction into the injector part through
the labyrinth seal. The labyrinth seal, however, is impermeable
to bacteria. Besides, the sealing ring 30 is to be seen, which,
as opposed to the configuration according to Fig. 5, is not
arranged between the ampoule socket 28 and the inner periphery

of the housing 3, but between the ampoule socket 28 and the
ampoule 13. With this configuration, a separate sealing disc is
no longer necessary.
Figs. 7a to 7h illustrate the operation sequence during the
actuation of the injection device. Fig. 7a shows the starting
position prior to the triggering of the activator. In Fig. 7b,
the securing cap 8 has already been removed and the activator is
triggered, with the snap-in projections 7 being compressed and
the pressure pin 5 being released. In Fig. 7c, the pressure pin
5 extends, with the pressure pin end provided with a sprocket 31
punching the sealing foil 29. In Fig. 7d, the ampoule 13 is
displaced forwardly in the axial direction against the displace-
ment resistance exerted by the projections 17, running onto the
projections 23 of the resilient arms 19. In Fig. 7e, the two
spring arms 19 of the sleeve 16 are pivoted outwardly, thus
releasing the needle guide 14. In Fig. 7f the ampoule-side
injection needle end, which is designed as a perforation piece
32, pierces the needle protection cap of the ampoule 13. The
ampoule is, thus, moved forwardly as far as to the end position
along with the needle guide 14, with the injection needle 15
leaving the injection part with its full length. In Fig. 7g, the
spring basket 25 is compressed while further displacing the
ampoule 13 such that the injection needle 15 will pass
completely through the sealing disc of the ampoule 13 and the
radial opening 33 of the injection needle 15 will enter into
communication with the injection liquid contained in the ampoule
13. At the same time, the annular web 34 illustrated in Fig. 3
penetrates the sealing disc of the ampoule 13, thus causing a
closed annular space to form between the annular web 34 and the
injection needle 15 reaching into the ampoule 13, which annular-
space prevents the injection liquid from leaving the ampoule 13
laterally outside of the injection needle 15. By enabling the
injection liquid to emerge through the radial opening 33 and the

injection needle 15, the piston plug 21 is driven forwardly as
far as to the stop by the pressure pin 5 so as to cause all of
the injection liquid to be ejected.

WE CLAIM:
1. A device for automatically injecting injection liquids, including an axially
subdivided housing whose parts are connectable with each other, wherein an
axially displaceable pressure pin (5) is guided in a first housing part (2), which
pin is capable of being inserted against a force accumulator (6) and locked in
the inserted position and extended upon relief of the force accumulator (6), and
an injection needle (15) fixed in a needle guide (14) and an ampoule (13) are
mounted in a second housing part (3) so as to be axially displaceable relative to
each other, wherein the injection needle (15) on its side facing the ampoule (13)
is designed as a perforation piece for the ampoule (13), wherein the ampoule
(13) with its end facing the injection needle (15) is mounted to reach into a
sleeve (16) fixed within the second housing part (3) and whose inner diameter
substantially corresponds to the outer diameter of the ampoule (13), that radially
inwardly protruding projections (17) are formed on the inner periphery of the
sleeve (16), and that the sleeve (16) comprises locking members cooperating
with locking members (20) of the needle guide (14), whereby an axial
displacement of the ampoule (13) in the direction to the needle guide (14) while
overcoming the displacement resistance exerted by the projections (17) causes
the release of the locking members (20) and the axial displaceability of the
needle guide (14).
2. A device as claimed in claim 1, wherein the locking members of the sleeve (16)
are formed on arms (19) capable of excursing outwardly in a resilient manner,
said arms (19) each carrying an inwardly protruding projection (23) in the
region of their coupling site, which cooperates with the ampoule (13) under the
excursion of the arms (19) and release of the locking members (20).

3. A device as claimed in 1 or 2, wherein the end-side annular surface of the sleeve
(16) facing the needle guide (14) rests on a radially inwardly protruding
projection of the second housing part (3).
4. A device as claimed in claim 1, 2 or 3, wherein the locking members are
comprised of snap-in noses (20) engaging in reception openings, said snap-in
noses (20) being preferably formed on the needle guide (14).
5. A device as claimed in any one of claims 1 to 4, wherein a spring element acting
in the axial direction is arranged between the needle guide (14) and the ampoule
(13).
6. A device as claimed in claim 5, wherein the spring element is designed in one
piece with the needle guide (14), as a spring basket (25) compressible in the
axial direction.
7. A device as claimed in any one of claims 1 to 6, wherein the injection needle
(15) includes a radial passage opening (33) at an axial distance from its end
designed as a perforation piece (32) for the ampoule (13).
8. A device as claimed in claim 7, wherein the radical passage opening (33) in the
axial direction is arranged between the injection needle end designed as a
perforation piece (32) and an annular web (34) arranged on the needle guide
(14) and surrounding the injection needle (15), said annular web (34) defining a
closed annular space between the web (34) and the injection needle (15)
reaching into the ampoule (13).

9. A device as claimed in any one of claims 1 to 8, wherein the ampoule (13) with
its end facing away from the injection needle (15) is arranged to reach into a
sleeve-shaped ampoule socket (28) which comprises a plurality of lamellar
guide ribs extending in the longitudinal direction.
10. A device as claimed in claim 8, wherein the ampoule reception opening facing
the first housing part (2) including the pressure pin (5) is closed by a gas-
permeable sealing foil (29).
11. A device as claimed in claim 9 or 10, wherein a seal and, in particular, an O-
ring seal (30) is arranged between the outer periphery of the ampoule socket
(28) and the inner periphery of the second housing part (3).
12. A device as claimed in claim 8, wherein the outer periphery of the ampoule
socket (28) comprises a labyrinth seal, and that a seal and, in particular, an O-
ring seal (30) is arranged between the ampoule socket (28) and the ampoule
(13).


Device for automatically injecting injection liquids
In a device (1) for automatically injecting injection liquids, including an axially
subdivided housing whose parts are connectable with each other, wherein an axially
displaceable pressure pin (5) is guided in a first housing part (2), which pin is
capable of being inserted against a force accumulator (6) and locked in the inserted
position and extended upon relief of the force accumulator (6), wherein an injection
needle (15) fixed in a needle guide (14) and an ampoule (13) are mounted in a
second housing part (3) so as to be axially displaceable relative to each other,
wherein the injection needle (15) on its side facing the ampoule (13) is designed as
a perforation piece (32), for the ampoule (13), the ampoule (13) with its end facing
the injection needle (15) is mounted to reach into a sleeve (16) fixed within the
second housing part (3) and whose inner diameter substantially corresponds to the
outer diameter of the ampoule (13). Radially inwardly protruding projections (17)
are formed on the inner periphery of the sleeve (16), and the sleeve (16) comprises
locking members cooperating with locking members (20) of the needle guide (14),
whereby an axial displacement of the ampoule (13) in the direction to the needle
guide (14) while overcoming the displacement resistance exerted by the projections
(17) causes the release of the locking members (20) and the axial displaceability of
the needle guide (14).

Documents:

00645-kolnp-2006-abstract.pdf

00645-kolnp-2006-claims.pdf

00645-kolnp-2006-description complete.pdf

00645-kolnp-2006-drawings.pdf

00645-kolnp-2006-form 1.pdf

00645-kolnp-2006-form 2.pdf

00645-kolnp-2006-form 3.pdf

00645-kolnp-2006-form 5.pdf

00645-kolnp-2006-international publication.pdf

00645-kolnp-2006-international search report.pdf

00645-kolnp-2006-pct request.pdf

645-KOLNP-2006-CORRESPONDENCE.pdf

645-KOLNP-2006-EXAMINATION REPORT.pdf

645-KOLNP-2006-FORM 18.pdf

645-KOLNP-2006-FORM 26.pdf

645-KOLNP-2006-FORM 3.pdf

645-KOLNP-2006-FORM 5.pdf

645-KOLNP-2006-GRANTED-ABSTRACT.pdf

645-KOLNP-2006-GRANTED-CLAIMS.pdf

645-KOLNP-2006-GRANTED-DESCRIPTION (COMPLETE).pdf

645-KOLNP-2006-GRANTED-DRAWINGS.pdf

645-KOLNP-2006-GRANTED-FORM 1.pdf

645-KOLNP-2006-GRANTED-FORM 2.pdf

645-KOLNP-2006-GRANTED-SPECIFICATION.pdf

645-KOLNP-2006-OTHERS.pdf

645-KOLNP-2006-REPLY TO EXAMINATION REPORT.pdf

645-KOLNP-2006-TRANSLATED COPY OF PRIORITY DOCUMENT.pdf

abstract-00645-kolnp-2006.jpg


Patent Number 252749
Indian Patent Application Number 645/KOLNP/2006
PG Journal Number 22/2012
Publication Date 01-Jun-2012
Grant Date 30-May-2012
Date of Filing 20-Mar-2006
Name of Patentee PHARMA CONSULT GES. M.B.H. & CO. NFG KG.
Applicant Address DIVISCHGASSE 4 A-1210 WIEN AUSTRIA
Inventors:
# Inventor's Name Inventor's Address
1 PICKHARD,EWALD KLRCHENPLATZ 4 A-2203 GROSSEBERSDORF AUSTRIA
PCT International Classification Number A61M 5/20,A61M 5/24
PCT International Application Number PCT/AT04/000295
PCT International Filing date 2004-08-27
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 GM 593/2003 2003-08-29 Austria