# US 7,744,580 B2 · Device and procedure for the extemporaneous preparation of an individual quantity of sterile liquid

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- Number: US 7,744,580 B2
- Document ID: US7744580B2
- Status: Granted
- Kind: B2
- Application number: 10/771,325
- Filed: 2004-02-05
- Published: 2004-08-12
- Granted: 2010-06-29
- Earliest claimed: 2003-02-05
- Assignees: Arcadophta
- Inventors: Gerard Reboul
- Web page: https://patentgrep.com/patent/US7744580B2

## CPC

- A61J 1/2096: {Combination of a vial and a syringe for transferring or mixing their contents}
- A61M 5/002: {Packages specially adapted therefor, e.g. packages for syringes or needles or kits for diabetics}
- A61M 5/1782: {Devices aiding filling of syringes in situ (combination of a vial and a syringe for transferring or mixing their contents A61J1/2096, filling of medical containers in general B65B3/003)}
- A61J 1/145: {using air filters}
- A61J 1/1456: {using liquid filters}
- A61J 1/2037: {having valve means}
- A61J 1/2082: {for gas filtration}
- A61J 1/2086: {for fluid filtration}
- A61M 5/3145: {Filters incorporated in syringes}
- A61M 39/26: Valves closing automatically on disconnecting the line and opening on reconnection thereof {(check valves A61M39/24)}
- A61M 2005/312: {comprising sealing means, e.g. severable caps, to be removed prior to injection by, e.g. tearing or twisting}
- A61M 2209/06: Packaging for specific medical equipment
- A61J: CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61M: DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY (introducing media into or onto the bodies of animals A61D7/00; means for inserting tampons A61F13/26; devices for administering food or medicines orally A61J; containers for collecting, storing or administering blood or medical fluids A61J1/05); DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY (surgery A61B; chemical aspects of surgical articles A61L); DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR {(Electrotherapy, e.g. producing anaesthesia by the use of alternating or intermittent currents A61N1/36021)}

## Abstract

A device and a procedure for the extemporaneous preparation of an individual quantity of sterile treatment fluid that may be compressible, in particular a treatment gas, the device comprising a rigid cartridge (3) with an outlet valve, an administration syringe (4) and a filtration-type connection/sterilization device (5, 6). The cartridge (3) simply contains an individual quantity of treatment fluid under pressure, and the cylinder of the syringe (4) is adapted to contain this individual quantity.

## Claims

### Claim 1

A device for the extemporaneous preparation of an individual quantity of sterile treatment fluid that may be compressible, for the purposes of administration to a patient, comprising:
a syringe (4) for administering a dose of treatment fluid, comprising a piston (42) sliding in a cylinder (44) provided with an open distribution end (41);
a reservoir (3) containing a quantity of treatment fluid under pressure, formed by a rigid cartridge (3) equipped with an outlet valve (10) capable of being hermetically connected in fluid communication with the distribution end (41) of the syringe (4), and capable of being opened in order to release the treatment fluid under pressure into the cylinder of the syringe; and
a connection/sterilisation device (5, 6) containing a filtration-type sterilisation device (5) provided with a fluid inlet (38) and a fluid outlet (40), and capable of sterilising the treatment fluid flowing between the inlet (38) and the outlet (40), this connection/sterilisation device (5, 6) being capable of permitting the assembly and hermetic connection of the cartridge (3) and syringe (4) for the purposes of filling the syringe (4), with the sterilisation device (5) interposed between the cartridge (3) and the syringe (4), so that the fluid outlet (40) of the sterilisation device (5) can deliver, into the syringe (4), sterile fluid leaving the cartridge (3),
wherein the reservoir (3) contains a quantity of treatment fluid under pressure such that the total quantity of treatment fluid that can be released at atmospheric pressure by the cartridge (3) during the opening of the valve (10) corresponds to an individual quantity of treatment fluid that can be contained completely in the cylinder (44) of the syringe (4),
wherein the outlet valve (10) is of the type that can be axially and elastically displaced towards the exterior in the sealing position and can be axially urged towards the interior in order to open the valve so as to release the treatment fluid, and wherein the connection/sterilisation device (5, 6) is capable of effecting an axial assembly of the syringe (4), this connection/sterilisation device (5,6), and the valve (10) of the cartridge, and of permitting the filling of the syringe (4) without loss of treatment fluid by simply axially bringing together the syringe (4) and the cartridge (3), and
wherein the connection/sterilisation device (5, 6) comprises a connection portion (26) to the valve (10) of the cartridge (3), and wherein this connection portion (26) and this valve (10) are adapted so that:
in a first relative axial bringing together of the components, an hermetic connection may be formed between them without actuating the valve (10) of the cartridge (3), which remains closed, and
in a second relative axial bringing together of the components subsequent to the first bringing together, the valve (10) is open.

### Claim 2 (depends on 1)

A device as claimed in claim 1, wherein:
the valve (10) of the cartridge (3) is a female valve provided with a distribution orifice (14), a peripheral gasket (17), and an actuating cavity (24) capable of receiving an end (24) of a bifunctional delivery tube (26) for actuating the valve (10) and ejecting the treatment fluid,
the said connecting portion (26) of the connection/sterilisation device (5, 6) forms a bifunctional delivery tube (26) compatible with the female valve (10) of the cartridge (3).

### Claim 3 (depends on 2)

A device as claimed in claim 2, wherein the connection/sterilising device (5, 6) comprises an upstream hermetic connection device (6) having, on one side, the said bifunctional delivery tube (26) compatible with the female valve (10) of the cartridge (3) and, on the other side, a connection (36) compatible with the inlet (38) of the filtration-type sterilisation device (5).

### Claim 4 (depends on 3)

A device as claimed in claim 3, wherein the said connection (36) of the upstream hermetic connection device (6) is a truncated conical connection paired with a truncated conical connection (37) formed by the inlet of the filtration-type sterilisation device (5).

### Claim 5 (depends on 2)

A device as claimed in claim 2, wherein the cartridge (3) comprises a cap (31) for the hermetic closure of the orifice (14) of the female valve (10) adapted to prevent any penetration of sterilisation fluid into the valve (10) and the cartridge (3), and that can be broken by introduction of the bifunctional delivery tube (26) into the orifice (14) of the valve (10).

### Claim 6 (depends on 1)

A device as claimed in claim 1, wherein the outlet (40) of the filtration-type sterilisation device (5) is capable of being able to be connected directly to the axial end (41) of the administration syringe (4).

### Claim 7 (depends on 1)

A device as claimed in claim 1, wherein the outlet (40) of the filtration-type sterilisation device (5) is a female truncated conical connection paired with a male truncated conical connection formed by the axial end (1) of the administration syringe (4).

### Claim 8 (depends on 1)

A device as claimed in claim 1, wherein the cartridge (3) comprises a flexible internal pocket (11) containing the said individual quantity of treatment fluid under pressure connected to the outlet valve (10) and to the exterior of the pocket (11), a quantity of thrust gas capable of pressurising the treatment fluid contained in the pocket (11).

### Claim 9 (depends on 8)

A device as claimed in claim 8, wherein the thrust gas is a physiologically acceptable gas.

### Claim 10 (depends on 8)

A device as claimed in claim 8, wherein the thrust gas is of the same type as the treatment fluid.

### Claim 11 (depends on 8)

A device as claimed in claim 8, wherein the quantity of thrust gas is capable of maintaining in the pocket (11) an excess pressure of treatment fluid of less than 2000 hPa, in particular of the order of 600 to 1800 hPa.

### Claim 12 (depends on 1)

A device as claimed in claim 1, wherein the treatment fluid is a treatment gas.

### Claim 13 (depends on 1)

A device as claimed in claim 1, wherein the cartridge (3) comprises a volume of treatment fluid between 10 ml and 100 ml, in particular of the order of 40 ml.

### Claim 14 (depends on 1)

A device as claimed in claim 1, further comprising a sterile needle (7) capable of being connected to the end (41) of the syringe (4) for the administration of the treatment fluid to the patient.

### Claim 15 (depends on 1)

A device as claimed in claim 1, further comprising a label (46), in particular in the form of a bracelet (8), designed to be associated with the patient.

### Claim 16 (depends on 1)

A device as claimed in claim 1, further comprising a sterile external packaging (2) containing all the constituent elements (3, 4, 5, 6, 7, 8) of the device in the sterile state, the whole device adapted to be sterilized with ethylene oxide after packaging.

### Claim 17 (depends on 16)

A device as claimed in claim 16, wherein the syringe (4) and the sterilisation device (5) are assembled beforehand in the sterile state in the packaging (2).

### Claim 18

A procedure for the extemporaneous preparation of an individual quantity of sterile treatment fluid that may be compressible, for the purposes of administration of the fluid to a patient, the procedure comprising the steps of:
with a device (1) for the extemporaneous preparation of an individual quantity of sterile treatment fluid that may be compressible, for the purposes of administration to a patient, comprising i) a syringe (4) for administering a dose of treatment fluid, comprising a piston (42) sliding in a cylinder (44) provided with an open distribution end (41), ii) a reservoir (3) containing a quantity of treatment fluid under pressure, formed by a rigid cartridge (3) equipped with an outlet valve (10) capable of being hermetically connected in fluid communication with the distribution end (41) of the syringe (4), and capable of being opened in order to release the treatment fluid under pressure into the cylinder of the syringe; and iii) a connection/sterilisation device (5, 6) containing a filtration-type sterilisation device (5) provided with a fluid inlet (38) and a fluid outlet (40), and capable of sterilising the treatment fluid flowing between the inlet (38) and the outlet (40), this connection/sterilisation device (5, 6) being capable of permitting the assembly and hermetic connection of the cartridge (3) and syringe (4) for the purposes of filling the syringe (4), with the sterilisation device (5) interposed between the cartridge (3) and the syringe (4), so that the fluid outlet (40) of the sterilisation device (5) can deliver, into the syringe (4), sterile fluid leaving the cartridge (3), wherein the reservoir (3) contains a quantity of treatment fluid under pressure such that the total quantity of treatment fluid that can be released at atmospheric pressure by the cartridge (3) during the opening of the valve (10) corresponds to an individual quantity of treatment fluid that can be contained completely in the cylinder (44) of the syringe (4),
initially assembling the syringe (4) and the sterilisation device (5); and
axially asemblying the sterilisation device to the valve (10) of the cartridge (3) by connecting the inlet of the sterilisation device to the valve (10) of the cartridge (3), wherein,
the syringe (4), the connection/sterilisation device (5, 6), and the valve (10) of the cartridge (3) are axially assembled so as to form between them a communication that is hermetically sealed from the surroundings, and
the syringe (4) and the cartridge (3) axially brought together so as to open the valve (10) and introduce into the syringe (4) a predetermined dose of sterile treatment fluid, by equilibration of the pressures.

### Claim 19 (depends on 18)

A procedure as claimed in claim 18, wherein the treatment fluid is diluted in the syringe (4).

### Claim 20 (depends on 18)

A procedure as claimed in claim 18, wherein the filtration-type sterilisation device (5) is next disconnected from the syringe (4), to which an administration needle (7) is then connected.
