Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
  • B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
  • B65B3/00—Packaging plastic material, semiliquids, liquids or mixed solids and liquids, in individual containers or receptacles, e.g. bags, sacks, boxes, cartons, cans, or jars
  • B65B3/003—Filling medical containers such as ampoules, vials, syringes or the like
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • 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
  • A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
  • A61J1/05—Containers specially adapted for medical or pharmaceutical purposes for collecting, storing or administering blood, plasma or medical fluids ; Infusion or perfusion containers
  • A61J1/06—Ampoules or carpules
  • A61J1/062—Carpules
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M2207/00—Methods of manufacture, assembly or production

Definitions

• the present invention relates to a method for manufacturing a prefilled syringe with a unit dose, comprising on the one hand a cartridge open at one of its ends, provided with a neck of narrowed section, intended to contain a drug to be injected, and d on the other hand, an injector composed of a capsule adaptable on the neck of the carpule and a piston-valve integral with the capsule and intended to be inserted inside the carpule, into which it is brought in by two different routes, in the same assembly station, the cartridge containing the drug to be injected and the injector, these two components are positioned one above the other and are approached to assemble them, and in which one proceeds before the assembly of the components, in said assembly station, at a gassing of the cartridge or of the cartridge and of the injector.
• the filling requirements are extremely strict, since the objective to be achieved consists in introducing the medicament into the syringe and hermetically sealing the latter in such a way that the atmosphere surmounting the medicament in the syringe consists exclusively of a gas chosen according to the medicament, for example neutral, i.e. free of solid particles, contaminants, oxygen and oxygenated substances.
• Another technique has been used to gass the cartridge after filling and during the placement of the plunger in certain pre-filled syringes comprising a carpule which in fact constitutes the body of the syringe and a plunger which closes one of the extremities of this body.
• This technique consists of pinching the plunger between two jaws so as to reduce its diameter, and blowing a chosen gas between the inner wall of the syringe body and the plunger, on one of the sides of the latter, in such a way that this gas can escape on the other side.
• This procedure does not provide guarantees that the gassing does not drain solid particles or oxygen towards the inside of the syringe body and does not allow to generate an overpressure of the gas inside the syringe. .
• the present invention proposes to overcome the drawbacks of known systems and to develop a simple and effective method for manufacturing pre-filled syringes in unit dose, satisfying both the most stringent filling requirements as well as those relating to control. during manufacturing and final product control.
• the method according to the invention is characterized in that the gassing is carried out by generating inside a cavity entirely containing said cartridge, a stream of gas flowing from bottom to top by sweeping the outer walls of the cartridge, and by causing a flow of purge gas through the injector channels, in that a qualitative and / or quantitative control of the gas is carried out during or after the gassing, and in that a final control of the syringe after assembly of the components, by pushing on one of these components and controlling at least the return of this component to its initial position.
• At least one phase of gassing of the injector comprises scanning the channels by an ascending flow of gas initially surmounting the liquid contained in the cartridge, which is forced back towards the channels during setting up the injector.
• the gas stream sweeping the outer walls of the cartridge preferably has a speed greater than the speed of a laminar flow. in which the installation is located, and likely to cause contaminating particles.
• the current of sweeping gas is caused by discharging into the cavity containing the cartridge, a predetermined quantity of chosen gas stored in a metering chamber.
• the current of sweeping gas is caused by continuously supplying the cavity containing the cartridge by means of a chosen gas.
• the cavity containing the cartridge can be closed and the current of sweeping gas is generated at a pressure higher than atmospheric pressure.
• a downward flow of sweeping gas is generated, during at least one phase of the operation, through the channels of this injector.
• the gas is carried out in static form by punctual interventions at a determined frequency.
• the final control of the syringes is preferably carried out by exerting a determined force, axially on the carpule or on the injector previously assembled, and both the value of the relative sinking of these two components and the value of the return of these components in their original position.
• Said determined force is preferably exerted by a counterweight of predetermined mass.
• the gassing cavity has a depth greater than the height of the cartridge, and the device comprises means for bringing a chosen gas into this cavity and means for generating a current of scanning of this gas, flowing from bottom to top between the walls of the cavity and those of the carpule.
• the gassing cavity advantageously comprises a metering chamber formed under the gassing cavity, this metering chamber being supplied with selected gas and initially containing a predetermined volume of this gas at a given pressure.
• the gassing cavity is formed in a central support and transfer unit, and this central unit is in the form of a rotary or rectilinear circular table with linear movement.
• the central support and transfer unit preferably comprises several cavities, each of these cavities being constituted by a notch formed at the periphery of said unit and comprising means for selectively closing this notch to produce a cylindrical cavity.
• the central support and transfer unit is broken down into two adjacent blocks, one of which is fixed and the other of which is movable in translation, each of these blocks comprising a series of notches arranged at so as to be able to be brought opposite each other so that the cartridges and / or injectors and / or syringes can be transferred from one notch to another and moved linearly with the movable block in translation.
• the central support and transfer is associated with a second transport unit, and comprises a series of peripheral notches each comprising a rotary door arranged to cooperate with the corresponding notch to form said gassing cavity.
• the final control means preferably comprise two dimensional sensors mounted one on a fixed frame, the other on a slide movable axially with respect to this fixed frame.
• These final control means advantageously include three indicators arranged to respectively indicate the relative depression of the carpule and the injector, the return of the injector relative to the carpule and the algebraic sum of the two preceding values.
• the means for carrying out a quantitative control of the gas contained in the cartridge preferably comprises a volumetric sensor and means for putting the interior of the cartridge into communication with this sensor.
• the means for carrying out a qualitative control of the gas contained in the cartridge preferably comprises a particle counter and / or a detector at partial pressure of gas.
• the gassing cavity is advantageously connected to a partial pressure gas detector and / or to a particle counter.
• FIG. 1A represents a view in axial section of a first embodiment of a prefilled syringe in unit dose which the method and the device according to the invention propose to assemble
• FIG. 1B represents a view in axial section of a second embodiment of a prefilled syringe with unit dose which the method and the device according to the invention propose to assemble
• FIG. 2 represents a schematic view of a first embodiment of the device according to the invention
• FIG. 3 represents a schematic view of another embodiment of the device according to the invention.
• FIGS. 4A, 4B and 4C illustrate the three main phases of the positioning of the injector on the cartridge
• FIG. 5 is a partial section view of an embodiment of the central support and transfer unit illustrating more particularly the receptor cavity of the cartridges
• FIG. 6 represents a sectional view of another embodiment of the receptor cavities of carpules
• FIG. 7 represents a variant of the clipping mechanism associated with the receptor cavities of carpules
• FIG. 8 represents a cross-sectional view of a particular embodiment of the central support and transfer unit for the cartridges
• FIG. 9 represents a variant of this central support and transfer unit
• FIG. 10 represents another embodiment of this central unit for supporting and transferring the cartridges, illustrating more particularly a method of supplying the gas chosen in the cavity containing the cartridges,
• FIG. 11 illustrates an embodiment of the device according to the invention, and more particularly a variant in which a protective cover is provided covering the injector,
• FIG. 12 illustrates an embodiment in which the central support and transfer unit for the components is constituted by a rotary table
• FIG. 13 represents another embodiment in which this unit is constituted by a linear transfer table
• FIG. 13A represents an intermediate phase of work of the central support and transfer unit shown in FIG. 13,
• FIG. 14 represents a mode of transfer of the cartridges from a first central unit to a second transport unit
• FIG. 15 represents a schematic view of a preferred embodiment of the dynamic control unit carrying out the final control of the syringes
• FIG. 16 illustrates a device making it possible to carry out quantitative control of the gassing
• FIG. 17 illustrates a device making it possible to carry out a qualitative control of the gassing.
• FIG. 1A represents a first embodiment of a prefilled syringe 1 in unit dose which it is proposed to produce by the method defined above. It essentially consists of a cartridge 2, an injector 3 and a needle holder bit cover 4.
• the cartridge 2 has a neck 5 of narrowed section.
• the injector comprises a piston-valve 6 essentially consisting of a flexible closure member 7 mounted on a rigid stiffening member 8 and a capsule 9 integral with the piston-valve 6 and adaptable over the neck of the cartridge.
• the flexible closure member 7 comprises a piston head 7a integral with an annular skirt 7b provided with at least one sealing bead 7c.
• a radial channel 7d, formed through the annular skirt communicates with an axial channel 8a formed in the rigid stiffening member 8.
• a cap 4 'carpule protector can be adapted to the carpule and fixed by removable means (not shown) capsule 9.
• Fig. 1B shows a second embodiment of a prefilled syringe with a unit dose which it is proposed to produce by the above method. It essentially consists of a cartridge 2 containing a liquid medicine under pressure of a chosen gas.
• the flexible sealing member 7 is directly mounted on a short stiffening end piece 9a integral with the capsule 9 and extended by a needle holder end piece 9b.
• FIG. 2 illustrates in schematic form the device 10 for manufacturing a pre-filled syringe with unit dose as defined above.
• This device essentially comprises a central unit 11 for supporting and transferring the components brought in and treated in a series of work stations which, in the example illustrated by the figure are as follows: a) a station 12 for feeding the cartridges 2 , b) a station 13 for pre-purging the cartridges 2, c) a station 14 for filling-gassing the cartridges 2, d) a station 15 for supplying the injectors 3, coupled with a station 15 'for gassing the injectors, e) a station 16 for assembling the cartridges 2 and the injectors 3, f) a station 17 for supplying the needle holder bit covers 4, g) a station 18 for placing said needle holder bit covers 4, h ) a station 19 for final control of the syringe 1, and i) a station 20 for discharging the syringes accepted by the final control station.
• the cartridges 2 are housed in cavities 21 formed along the periphery of the central support and transfer unit 11.
• the cartridges are therefore the governing bodies which drive the injectors after passing through station 16. This choice makes it possible, as will be described in more detail below, to perform a gassing of the cartridges during the entire phase of setting up the injector, and, in certain cases, maintaining a gas pressure above atmospheric pressure above the liquid drug.
• the purpose of pre-gasing in station 13 is to "wash" the cartridges using a chosen gas such as, for example, CO2, the most commonly used.
• the filling-gassing carried out in the station 14 is preferably carried out by means of a double needle 22 whose central channel 22a is used for filling the cartridge and whose peripheral annular channel 22b provides gas for gassing of the carpule.
• FIG. 3 A variant of this device is illustrated in FIG. 3.
• This device comprises, as previously, a central unit 11 for supporting and transferring the components, as well as the following stations: a) a station 12 for feeding the cartridges 2, b) a station 13 for pre-gasing the cartridges 2, c) a station 14 for filling-gassing the cartridges 2, d) a station 15 for supplying the injectors 3, equipped with their needle-holder cover caps 4, (this station is therefore, in this case, not coupled with a station for gassing of the injectors), e) a station 16 for assembling the cartridges 2 and the injectors 3, f) a station 19 for final control of the syringe 1, g) a station 20 for quantitative control of the gassing of the syringes h) a station 21 for quality control of the gassing of syringes i) a syringe disposal station 22 accepted by the final control station.
• Figs. 4A, 4B and 4C illustrate the three main phases of the installation of the injector on the cartridge in the case where only the cartridge is gassed and in the case where the two components, namely the cartridge and the injector, are simultaneously gassed.
• These figures show the syringe 1 shown partially.
• the cartridge 2 pre-gased in station 13 is filled and gassed in station 14.
• station 12 it has been previously introduced into a cavity which is also gassed (see detailed description below), so that a flow the chosen gas flows from bottom to top around the cartridge, preventing any penetration of particles and air and in particular oxygen into the cartridge.
• the piston head 7a engages in the area of the neck with diameter narrowed to reach the second sealing point illustrated in fig. 4C. From this point, the relative displacement of the cartridge and the injector, which generates a decrease in the volume of gas overcoming the medicated liquid, results in an increase in the pressure of this gas inside the cartridge. In fact, as soon as the second sealing point is reached, the radial channel is closed, which prevents any leakage of gas by this route.
• the injector will continue to be pushed into a position in which the head of the piston 7a is compressed to the maximum in the region of narrowed section of the neck of the carpule, while the bead or sealing lip 7c remains positioned in the wide area extending this narrowed neck, in order to avoid excessive compression of this bead during the storage phase.
• This strong compression of the piston head constitutes in practice an excellent protection against the migration of undesirable gases such as for example oxygen towards the interior of the cartridge during the storage of the syringe.
• the chosen gas is injected into the axial channel 8a.
• This gas "rinses” the axial channel then the radial channel 7d and initially escapes in the direction of the arrow C.
• the chosen gas injected through the axial channel is forced to penetrate inside the cartridge in the direction of arrow D.
• This means makes it possible, among other things, to create an adjustable overpressure which can be relatively large at inside this cartridge.
• the piston head 7a reaches the position illustrated in FIG. 4C, the injection of gas chosen inside the cartridge through the axial channel 8a and the channel 7d is stopped.
• the central support and transfer unit 11 illustrated in FIG. 5, also called a rotary or linear table, comprises cavities 30 in which are housed the cartridges 2 suspended from lateral stops 31. Each of these cavities communicates with a chamber. 32 supplied with selected gas, represented by arrow 33, coming from a source of this pressurized gas.
• This chamber 32 contains a piston 34 arranged to be actuated by a rod 35 provided with a support plate 36 on which a thrust spring 37 acts and a force symbolized by the arrow 38.
• the piston 34 When the piston 34 is pushed upwards, it cuts off the chosen gas supply and discharges the gas from the chamber into the cavity 30, causing a sweeping flow around the walls of the cartridge.
• the injector When the injector is brought above the carpule, we find the configurations of fig. 4A, 4B and 4C. Seals 39 are provided around the upper opening of the cavities 30, to ensure sealing between the capsule 9 and the table 11, and to allow the chosen gas to be injected under overpressure in the cartridge. The tightness is maintained by pressing in the direction of the arrows 40 on the fins 9a of the capsule 9.
• the piston 34 has a double purpose: in a first phase it generates a chosen flow of gas around the cartridge and in in a second phase, it pushes back the cartridge to cause the injector and the cartridge to be clipped.
• the cavity 30 formed in the table 11 and illustrated in FIG. 6, differs from the previous one in that it comprises a pressure relief valve communicating with the chamber 32.
• This valve comprises a ball 41 held in abutment against a seat 42 by a spring 43 blocked in a bore 44 by a screw 45 traversed by a channel 46.
• the pressure of the spring 43 adjustable by the screw 45 makes it possible to define a maximum pressure of the gas contained in the chamber 32, at the end of the piston stroke, and consequently the maximum pressure of the gas contained in the cartridge. It also differs in that it comprises a device of the type described in detail with reference to FIG. 17, to allow the partial pressure of oxygen and / or solid particles to be detected.
• Fig. 7 illustrates another embodiment of the cavity 30 containing the cartridge 2 and of the mechanism for clipping the latter onto the injector.
• the cavity does not include a stop for retaining the cartridge, which rests on a pusher 50 housed inside the chamber 32.
• This chamber contains, as before, a piston 34, which, in this case, comprises a cavity 51 in which the pusher 50 is partially housed.
• a compression spring 52 is placed in the chamber 32 bearing, on the one hand against the upper surface piston 34, and secondly against the upper surface of the chamber 32.
• the pusher 50 rests on a fixed vertical rod 53 secured to a base plate 54 or supported on the latter.
• This base plate is preferably crossed by two rods 55 provided as before with a support plate 36 on which a force symbolized by the arrow 38 can act.
• the cartridge 2 is initially housed in the cavity 30 bearing on the pusher 50.
• the force 38 acting on the support plate 36 pushes the piston 34 upward, the supply of CO2 represented by the arrow 33 is completely first cut, then the gas contained in the chamber 32 is progressively discharged between the outer walls of the cartridge 2 and the inner walls of the cavity 30.
• the piston 34 When the piston 34 is lifted enough so that the bottom of the cavity 51 comes in pressing against the base of the pusher 50, the piston 34 drives the pusher 50 and exerts a vertical upward thrust on the cartridge 2, this thrust being sufficient to cause the clipping of the cartridge and the injector (not shown).
• the spring 52 plays the role of return spring intended to push the piston 34 back into its initial position, the pusher automatically returning to its starting position.
• the central unit 11 for supporting and transferring the cartridges 2 and the injectors 3 comprises a central cavity 60 delimited by a base plate 61, a cover plate 62 and an annular block 63 in which the cavities 30 intended for receive the cartridges 2.
• a central cavity 60 delimited by a base plate 61, a cover plate 62 and an annular block 63 in which the cavities 30 intended for receive the cartridges 2.
• an annular cavity 64 formed on the upper surface of the piston 34 a cavity serving to partially house the compression spring 52, the mechanism for clipping the cartridges and the injectors, which constitutes simultaneously the gas delivery device chosen is identical to that described above with reference to FIG. 7.
• the chosen gas is injected into the central cavity through a conduit 65 passing through the cover plate 62.
• a conduit 66 is formed through the annular block 63 to make the cavity 60 communicate with the chamber 32 located under the cavity 30.
• Fig. 9 illustrates a variant of the embodiment according to FIG. 8 in which the metering chamber 32 of the gas used to cause a laminar flow around the walls of the cartridge, has been eliminated.
• the chosen gas is introduced into the central cavity
• the mechanism for clipping the cartridges and the injectors consists in this case of a pusher 70 passing through the base plate 61 of the central support and transfer unit 11.
• Fig. 10 illustrates another embodiment in which the central cavity 60 for storing the chosen gas has been eliminated and replaced by external supply means 71 connected to a conduit 72 which communicates with the cavity 30 formed in the annular block 63 of the central unit 11.
• FIG. 11 An interesting variant of the device as illustrated in FIG. 3 is shown in FIG. 11.
• a bell 80 is disposed over the injector 3, to hold the latter in an enclosure containing essentially the chosen gas.
• This enclosure advantageously has an opening 81 allowing the excess gas contained inside the enclosure 80 to leak.
• Seals 82 are provided under the rim of this enclosure in order to ensure a tight closure between this rim 83 and the upper surface of the central unit 11.
• no seal is provided at the fins 9a of the capsule 9, which allows the flow of the chosen gas contained in the enclosure 30 towards the inside of enclosure 80 in the direction of arrow E.
• This enclosure 80 has been reported by way of example to a device according to the embodiment according to FIG. 5. It is however obvious that such an enclosure could be attached to any other device described above, since the presence of this enclosure is intended to create an atmosphere of gas chosen around the injector during the clip-on phase of the carpule and this injector.
• the purpose of the gassing of the cartridges, as well as the possible gassing of the injectors is to prevent particles or oxygen from the air from entering the atmosphere of chosen gas overcoming the liquid drug contained in the cartridge.
• an upward flow of a selected, sterile, filtered and clean gas is created in the cavity containing the cartridge, and the speed of this upward flow is determined so that it is greater than that of the downward laminar flow in which the entire installation is located.
• Current regulations on the control of injectable drugs require a final optical check to determine the possible presence of particles in the drug liquid.
• Gassing as described in detail above constitutes an effective means guaranteeing the absence of solid particles in the medicament, a guarantee which, combined with the presence of a filter which the liquid medicament is forced to pass through before being injected, makes it possible to safely remove this obligation of final optical inspection.
• the device as described may include a particle probe integrated into the installation as well as a probe for measuring the partial pressure of oxygen contained in the atmosphere which is introduced into the cartridge, when the filling of the drug must be done in an anaerobic medium, in such a way that at the time of filling and mounting of the syringe there are all the indications necessary to make this final optical control particularly superfluous, particularly costly in terms of time and material.
• FIG. 12 illustrates an embodiment in which the central unit 11 for supporting and transferring the components is constituted by a rotary table whose peripheral surface is equipped with a series of notches 90 designed to contain the cartridges 2, the latter being retained in the notches by a fixed guide 91 which closes these notches.
• Fig. 13 illustrates another embodiment in which the central support and transfer unit 11 is constituted by a linear transfer table consisting of a first fixed block 92 and a second block 93 movable in the direction of the double arrow K.
• the two blocks 92 and 93 respectively comprise a series of notches 92a and 93a, each of which cooperates with a pusher 92b and 93b respectively, each series of plungers being connected by a strip respectively 92c and 93c.
• the cooperation between the different elements makes it possible to advance the cartridges 2 in a direction parallel to the direction of movement of the block 93 by passing them alternately from a notch 93a to a notch 92a and vice versa.
• a cartridge 2a initially housed in a notch 93a is brought in, when the block 93 moves from the left to the right opposite a notch 92a of the block 92.
• the corresponding pusher 93b pushes the cartridge 2a into the cavity 92a disposed opposite where it will occupy the position 2 ′ shown in broken lines.
• the block 93 will reverse move from right to left until the next notch 93a will be opposite the notch 92a containing the cartridge 2'a.
• the corresponding pusher 92b will push the cartridge 2'a into this notch where it will occupy the position 2''a.
• This alternative movement therefore makes it possible to generate a linear or rotary movement of the cartridges, and their routing in the various treatment stations.
• Fig. 13A represents an intermediate phase in which all of the pushers 93b actuated by the corresponding slide 93c pushes back all of the cartridges 2 from the notches 93a towards the notches 92a arranged opposite.
• Fig. 14 illustrates a means of transferring the cartridges 2 from a central support unit and of transfer 11a to a second transport unit 11b.
• each of the two elements 11a and 11b has peripheral notches 11'a and 11'b respectively.
• the notches 11a must be equipped with means allowing them to be closed.
• These means can be constituted by rotary doors 100 shown in the closed position (reference 100a) and in the open position (reference 100b).
• a pusher 101 acts on the cartridge 2 to push it back from the notch 11'a into the notch 11'b brought opposite the notch 11'a by the play of reverse rotations of the two elements 11a and 11b.
• the revolving doors 100 can also be replaced by any other closing device, for example a flap or guillotine door, an external fixed guide, etc.
• the doors can be opened and the ejector controlled by any means. mechanical known per se such as cam, guide ramp, electromagnetic device, etc.
• the installation of the injector on the cartridge, and more particularly the phase which begins when the second sealing point is reached generates a reduction in the internal volume reserved for the chosen gas overcoming the drug liquid. This reduction in volume results in compression of this chosen gas. If the reduction in volume due to the insertion of the injector is not sufficient to induce a significant overpressure inside the cartridge, it is possible, as mentioned above, to increase the overpressure either during or after filling the carpule, during a pressurization phase.
• the overpressure is justified because it makes it possible to obtain and maintain the saturation of the liquid medicinal product with the chosen gas, which is usually carbon dioxide.
• the chosen gas which is usually carbon dioxide.
• the drug is generally saturated with carbon dioxide at ambient temperature in the region of 18 to 20 ° C. This gives a known fixed saturation. Knowing that the medication behaves approximately like water and that the water appreciably absorbs its own volume of carbon dioxide at 15oC, to increase saturation the medication can be cooled when it is filled.
• this solution is not applicable to all medicines, some of which cannot be stored at temperatures below 15oC.
• the other solution to increase saturation is to increase the pressure.
• Another object of the overpressure is to obtain a crushing of the shutter member which results in a reinforced tightening of this member against the walls of the neck of the carpule.
• This tightening has the consequence of increasing the tightness of the cartridge and therefore of increasing the shelf life of the medicament which it contains, since the conditions of supersaturation in the chosen gas are maintained longer.
• the final syringe control station 19 or dynamic control station is illustrated in detail in FIG. 15.
• the device 110 comprises a vertical frame 111, a slide 112 movable along this frame, and two dimensional sensors 113 and 114 carried respectively by two brackets 113 'and 114' secured respectively to the frame and the slide.
• the vertical frame is mounted on a support 115 arranged to receive the syringe for said control.
• a cam 116 controls the movements of the slide relative to the frame.
• the principle of control is based on the existence inside any conforming syringe, of an overpressure of which one knows the value.
• a force exerted on the cartridge, the injector being supported on the support 115, or on the injector, the cartridge being supported on this support, causes a relative depression of the injector relative to the cartridge. Thanks to the overpressure prevailing in the cartridge, the removal of the force which caused this depression has the consequence of returning the injector to its initial position.
• This principle makes it possible to control a whole series of parameters relating to the components of the syringe, their assembly and their content. Thanks to this dynamic control, 100% syringe operation is guaranteed, which allows you to confidently suppress the visual control of syringes as it is currently practiced on ampoules. Additional safety, mentioned for the record, is obtained by the presence of a filter in each syringe, a filter which allows the pharmaceutical industry to guarantee a compliant product even after very long-term storage.
• the control device operates as follows: the slide 112 descends until the sensor or probe 114 comes into contact with the injector. At this time, the sensor 114 sinks relative to the bracket 114 'of the slide. The sensor 113 being in abutment against the slide, gradually comes out as the slide goes down relative to the bracket 113 '. During the travel of the sensor 114, a data processing unit, connected to this sensor, clears the memory which records the difference in values previously recorded by the two dimensional sensors. When the sensor 114 has completely penetrated inside the bracket 114 ', this bracket comes into contact with the injector.
• An indicator C displays the value of the algebraic sum of the respective values displayed by the indicators A and B, which makes it possible to control by direct reading the possible difference between the descent and the ascent of the injector having undergone a determined axial thrust.
• the dynamic control device described above makes it possible to control: a) the presence of each of the components of the syringe, b) the filling volume, c) the leakage due to loss of gas, d) the siliconization of the components, e) the tolerances of the obturation member f) the tolerances of the cartridge g) the clipping of the injector h) the sliding of the injector relative to the cartridge.
• the insufficient insertion which causes an automatic rejection of the syringe can be due to the following reasons: a) to the absence of one of the components b) to the bad siliconization of the cartridge, c) to a tightening due to the internal diameter of the cartridge too small, d) a tightening due to the outside diameter of the cartridge too large e) the outside diameter too large of the closure member f) the inside diameter too small of the capsule g) a filling volume too important h) improper sliding of the injector in relation to the cartridge.
• Too much sinking of the injector relative to the cartridge may be due to the following reasons: a) the inside diameter of the cartridge is too large b) the outside diameter of the closure member is too small c) a defect of the obturation member d) a defect in the cartridge, e) an insufficient filling volume, f) incorrect insertion of the injector onto the cartridge.
• control station 19 is equipped with means making it possible to automatically deliver all the syringes which do not correspond to the predetermined criteria. Accepted syringes meet the most stringent requirements, so they are ready to use and no longer require any additional testing.
• control device based on the use of dimensional sensors and a weight of determined mass acting on the injector, could be replaced by other measurement principles based on the use of pressure sensors, sensors optical or the like.
• Fig. 16 illustrates a device allowing statistical control of the quantity of gas contained in the cartridge after assembly of the components.
• the corresponding station is designated by the reference 20 in FIG. 3.
• This control is carried out in the following manner: from time to time a syringe is withdrawn 1.
• a needle 120 is introduced into the axial channel of the injector, and the obturation member is pierced so that the end free of the needle ends in the space arranged above the liquid and containing the selected gas under pressure.
• This needle is connected by flexible tubing 121 to a volumetric sensor 122, or more simply to a column of water, making it possible to measure the quantity of gas contained in the cartridge.
• Fig. 17 illustrates a device making it possible to carry out a statistical control of the quality of the gas contained in the cartridge.
• This device comprises a particle counter 130 and a detector 131 at partial gas pressure.
• the particle counter 130 of the optical or filter type, makes it possible to check the possible existence of solid particles in the chosen gas contained in the cartridge.
• the detector 131 is used, in this case, to detect the possible presence of oxygen. It can be of the type marketed under the names ORBISPHERE Model 2715 by ORBISPHERE LABORATORIES (GENEVA - Switzerland).
• This device can be mounted in station 21 shown schematically in FIG. 3.
• the two detectors are mounted in a support block 132 comprising a valve 133, a connection channel 134 of this valve with a chosen gas supply, used to purge the installation, suggested by the double arrow 135, a connection conduit 136 making this valve communicate with the two detectors, and a pipe 137 for connecting the syringe 1 with the sensors.
• the valve 133 makes it possible to purge the installation.
• a pusher 138 exerts a thrust on the cartridge to allow the gas to escape through the channels of the injector successively towards the two detectors.
• the only method of detecting the presence of oxygen currently used is that of the KOH bath, which cannot be used on a syringe assembly line in an automatic control station. The use of the above method makes it possible to carry out an effective, immediately exploitable control, of the quality of the gas contained in the cartridges.

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• 1985
  • 1985-05-14 JP JP60502069A patent/JPS61502099A/ja active Pending
  • 1985-05-14 DE DE8585901962T patent/DE3579893D1/de not_active Expired - Fee Related
  • 1985-05-14 EP EP85901962A patent/EP0185027B1/fr not_active Expired - Lifetime
  • 1985-05-14 WO PCT/CH1985/000080 patent/WO1985005269A1/fr not_active Ceased
  • 1985-05-15 US US06/833,392 patent/US4703781A/en not_active Expired - Fee Related

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