CA2404360C - Needle-less injector of miniature type - Google Patents
Needle-less injector of miniature type Download PDFInfo
- Publication number
- CA2404360C CA2404360C CA002404360A CA2404360A CA2404360C CA 2404360 C CA2404360 C CA 2404360C CA 002404360 A CA002404360 A CA 002404360A CA 2404360 A CA2404360 A CA 2404360A CA 2404360 C CA2404360 C CA 2404360C
- Authority
- CA
- Canada
- Prior art keywords
- needle
- less injector
- liquid
- nozzle
- hollow plunger
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Classifications
-
- 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
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/178—Syringes
- A61M5/30—Syringes for injection by jet action, without needle, e.g. for use with replaceable ampoules or 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
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/178—Syringes
- A61M5/31—Details
- A61M2005/3103—Leak prevention means for distal end of syringes, i.e. syringe end for mounting a needle
- A61M2005/3104—Caps for syringes without needle
-
- 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
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/178—Syringes
- A61M5/31—Details
- A61M2005/3128—Incorporating one-way valves, e.g. pressure-relief or non-return valves
-
- 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
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/178—Syringes
- A61M5/20—Automatic syringes, e.g. with automatically actuated piston rod, with automatic needle injection, filling automatically
- A61M5/204—Automatic syringes, e.g. with automatically actuated piston rod, with automatic needle injection, filling automatically connected to external reservoirs for multiple refilling
-
- 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
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/178—Syringes
- A61M5/31—Details
- A61M5/3145—Filters incorporated in syringes
-
- 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
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/178—Syringes
- A61M5/31—Details
- A61M5/315—Pistons; Piston-rods; Guiding, blocking or restricting the movement of the rod or piston; Appliances on the rod for facilitating dosing ; Dosing mechanisms
- A61M5/31525—Dosing
- A61M5/31531—Microsyringes, e.g. having piston bore diameter close or equal to needle shaft diameter
-
- 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
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/178—Syringes
- A61M5/31—Details
- A61M5/315—Pistons; Piston-rods; Guiding, blocking or restricting the movement of the rod or piston; Appliances on the rod for facilitating dosing ; Dosing mechanisms
- A61M5/31533—Dosing mechanisms, i.e. setting a dose
- A61M5/31545—Setting modes for dosing
- A61M5/31548—Mechanically operated dose setting member
- A61M5/31555—Mechanically operated dose setting member by purely axial movement of dose setting member, e.g. during setting or filling of a syringe
-
- 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
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/178—Syringes
- A61M5/31—Details
- A61M5/315—Pistons; Piston-rods; Guiding, blocking or restricting the movement of the rod or piston; Appliances on the rod for facilitating dosing ; Dosing mechanisms
- A61M5/31533—Dosing mechanisms, i.e. setting a dose
- A61M5/31545—Setting modes for dosing
- A61M5/31548—Mechanically operated dose setting member
- A61M5/31563—Mechanically operated dose setting member interacting with a displaceable stop member
Landscapes
- Health & Medical Sciences (AREA)
- Vascular Medicine (AREA)
- Engineering & Computer Science (AREA)
- Anesthesiology (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Infusion, Injection, And Reservoir Apparatuses (AREA)
Abstract
Needleless injectors for liquids are known from the art in a variety of designs that are adapted to different conditions of application. The inventive needle-less injector is designed as a hand-held device. It comprises a lockable tensioning system, an energy-storing spring (36), a hollow piston (37) displaceable within a cylinder (38), and a nozzle (39). The hollow piston is provided with a valve body on its one end. The storage container (44) for the liquid is disposed within the hous-ing. The lockable tensioning system is tensioned by counterrotating the two housing parts (31; 32), thereby withdrawing the hollow piston (37) from the cylinder (38).
At the same time the amount of liquid required for the injection is withdrawn from the storage container (44) and transported through the hollow piston to the pump chamber (34). When the lockable tensioning system is released, the amount of liq-uid is ejected from the pump chamber through the nozzle. The needleless injector is easy and reliable to handle also for unpracticed people. It is used for intracutaneous injections of a medical liquid into biological tissue, for injecting a liquid containing an active substance into a plant or for injecting a liquid through a membrane into the space behind said membrane.
At the same time the amount of liquid required for the injection is withdrawn from the storage container (44) and transported through the hollow piston to the pump chamber (34). When the lockable tensioning system is released, the amount of liq-uid is ejected from the pump chamber through the nozzle. The needleless injector is easy and reliable to handle also for unpracticed people. It is used for intracutaneous injections of a medical liquid into biological tissue, for injecting a liquid containing an active substance into a plant or for injecting a liquid through a membrane into the space behind said membrane.
Description
Boehringer Ingelheim International GmbH
Needle-less injector of miniature type The invention concerns a needle-less injector in the form of a hand-held unit, preferably of miniature type, with which a liquid is intracutaneously injected for example into human or animal tissue. The invention aims to expand the area of use of an injector of that kind.
Liquids in the sense of the present invention are preferably solutions, suspensions or dispersions which contain an active substance. Active substances can be pharmacologically active substances for treatment of the human or animal body or they may be substances for diagnostic or cosmetic uses.
Active substances for non-pharmaceutical uses can be for example in the area of plant protection insecticides, fungicides, growth-promoting or growth-inhibiting agents or fertilisers. The needle-less injector according to the invention permits the environmentally friendly application of agents with a systemic action, as the active substance is applied directly to the plant.
EP 0 063 341 and EP 0 063 342 disclose a needle-less injector which includes a piston pump for expelling the liquid to be injected, which is driven by a motor by means of a pressure agent. The liquid container is mounted laterally to the piston pump.
The amount of liquid required for an injection is sucked into the pump chamber by way of an inlet passage and a flap check valve when the piston is retracted. As soon as the piston is moved in the direction of the nozzle body the liquid is urged through the outlet passage to the nozzle and expelled. The piston of the piston pump is a solid round piston.
EP 0 133 471 describes a needle-less vaccination unit which is operated with carbon dioxide under pressure, from a siphon cartridge by way of a special valve.
EP 0 347 190 discloses a vacuum compressed gas injector in which the depth of penetration of the injected drug can be adjusted by means of the gas pressure and the volume of the drug can be adjusted by way of the piston stroke.
EP 0 427 457 discloses a needle-less hypodermic syringe which is operated by means of compressed gas by way of a two-stage valve. The injection agent is disposed in an ampoule which is fitted into a protective casing which is secured to the injector housing. The ampoule is fitted on to the end of the piston rod. Disposed at the other end of the ampoule is the nozzle whose diameter decreases towards the end of the ampoule.
WO 89/08469 discloses a needle-less injector for one-off use. WO 92/08508 sets forth a needle-less injector which is designed for three injections. The ampoule containing the drug is screwed into one end of the drive unit, with the piston rod being fitted into the open end of the ampoule. At its one end, the ampoule contains the nozzle through which the drug is expelled. A displaceable closure plug is provided approximately at the centre of the length of the ampoule. The dose to be injected can be adjusted by way of the screwing-in depth of the ampoule. The piston rod which projects from the drive unit after actuation of the injector is pushed back by hand.
Both units are operated with compressed gas.
WO 93/03779 discloses a needle-less injector with a two-part housing and a liquid container which is fitted laterally to the unit. The drive spring for the piston is stressed by means of a drive motor. The spring is released as soon as the two parts of the housing are displaced relative to each other by pressing the nozzle against the injection location. Respective valves are provided in the intake passage for the liquid and in the outlet of the metering chamber.
WO 95/03844 discloses a further needle-less injector. It includes a liquid-filled cartridge which at one end includes a nozzle through which the liquid is expelled. At the other end the cartridge is closed by a cap-type piston which can be pushed into the cartridge. A piston which is loaded by a prestressed spring, after release of the spring, displaces the cap-type piston into the cartridge by a predetermined distance, with the amount of liquid to be injected being expelled in that case. The spring is triggered as soon as the nozzle is pressed sufficiently firmly against the injection location. This injector is intended for one-off or repeated use. The cartridge is arranged in front of the spring-loaded piston and is a fixed component of the injector. The position of the piston of the injector which is intended for a plurality of uses is displaced after each use by a distance in a direction towards the nozzle. The piston and the drive spring cannot be reset. The prestressing of the spring is initially sufficiently great to expel the entire amount of liquid in the cartridge all at once. The spring can only be stressed again if the injector is dismantled and the drive portion of the injector assembled with a fresh, completely filled cartridge.
In FR-2 629 706, two embodiments of a needle-less injector for use in dentistry are described, with which a pre-determined amount of liquid can be injected into the gum. Both injectors are respectively composed of two portions that are assembled together coaxially and are releasably connected to one another. Compressed air serves as the operating medium, and is supplied from the outside to the injector.
When the injector is triggered by means of a trigger button, an operating piston is suddenly pushed by a pre-determined arnount by means of a combination of compressed air, coil springs and locking mechanisms, wherein the amount of liquid to be injected is expelled through a nozzle. At the same time, several coil springs are tensioned which push several axially displaceable parts within the injector back into their original position as soon as the compressed air applied is no longer effective. The liquid to be injected is housed within the injector in a tubular, rigid container that is provided at one end with a plug moveable within the container, which keeps the liquid in the container constantly under pressure by means of a spring-tensioned piston. When some of the liquid is pushed out of the container into the liquid chamber within the pump cylinder, the pressure spring pushes the plug, via the piston, by a corresponding amount into the liquid container.
In some known design configurations of the needle-less injector the supply container for the liquid to be injected is arranged laterally beside the drive unit. The amount of liquid to be injected is sucked into the pump chamber when the solid piston of the piston pump is retracted. The inlet passage includes an inlet valve and the outlet passage includes an outlet valve. Both valves operate with an auxiliary force.
In other design configurations of the needle-less injector the supply container for the liquid to be injected serves directly as a pump chamber and is subjected to the sudden application of force which occurs upon expulsion of the amount of liquid to be injected.
Needle-less injector of miniature type The invention concerns a needle-less injector in the form of a hand-held unit, preferably of miniature type, with which a liquid is intracutaneously injected for example into human or animal tissue. The invention aims to expand the area of use of an injector of that kind.
Liquids in the sense of the present invention are preferably solutions, suspensions or dispersions which contain an active substance. Active substances can be pharmacologically active substances for treatment of the human or animal body or they may be substances for diagnostic or cosmetic uses.
Active substances for non-pharmaceutical uses can be for example in the area of plant protection insecticides, fungicides, growth-promoting or growth-inhibiting agents or fertilisers. The needle-less injector according to the invention permits the environmentally friendly application of agents with a systemic action, as the active substance is applied directly to the plant.
EP 0 063 341 and EP 0 063 342 disclose a needle-less injector which includes a piston pump for expelling the liquid to be injected, which is driven by a motor by means of a pressure agent. The liquid container is mounted laterally to the piston pump.
The amount of liquid required for an injection is sucked into the pump chamber by way of an inlet passage and a flap check valve when the piston is retracted. As soon as the piston is moved in the direction of the nozzle body the liquid is urged through the outlet passage to the nozzle and expelled. The piston of the piston pump is a solid round piston.
EP 0 133 471 describes a needle-less vaccination unit which is operated with carbon dioxide under pressure, from a siphon cartridge by way of a special valve.
EP 0 347 190 discloses a vacuum compressed gas injector in which the depth of penetration of the injected drug can be adjusted by means of the gas pressure and the volume of the drug can be adjusted by way of the piston stroke.
EP 0 427 457 discloses a needle-less hypodermic syringe which is operated by means of compressed gas by way of a two-stage valve. The injection agent is disposed in an ampoule which is fitted into a protective casing which is secured to the injector housing. The ampoule is fitted on to the end of the piston rod. Disposed at the other end of the ampoule is the nozzle whose diameter decreases towards the end of the ampoule.
WO 89/08469 discloses a needle-less injector for one-off use. WO 92/08508 sets forth a needle-less injector which is designed for three injections. The ampoule containing the drug is screwed into one end of the drive unit, with the piston rod being fitted into the open end of the ampoule. At its one end, the ampoule contains the nozzle through which the drug is expelled. A displaceable closure plug is provided approximately at the centre of the length of the ampoule. The dose to be injected can be adjusted by way of the screwing-in depth of the ampoule. The piston rod which projects from the drive unit after actuation of the injector is pushed back by hand.
Both units are operated with compressed gas.
WO 93/03779 discloses a needle-less injector with a two-part housing and a liquid container which is fitted laterally to the unit. The drive spring for the piston is stressed by means of a drive motor. The spring is released as soon as the two parts of the housing are displaced relative to each other by pressing the nozzle against the injection location. Respective valves are provided in the intake passage for the liquid and in the outlet of the metering chamber.
WO 95/03844 discloses a further needle-less injector. It includes a liquid-filled cartridge which at one end includes a nozzle through which the liquid is expelled. At the other end the cartridge is closed by a cap-type piston which can be pushed into the cartridge. A piston which is loaded by a prestressed spring, after release of the spring, displaces the cap-type piston into the cartridge by a predetermined distance, with the amount of liquid to be injected being expelled in that case. The spring is triggered as soon as the nozzle is pressed sufficiently firmly against the injection location. This injector is intended for one-off or repeated use. The cartridge is arranged in front of the spring-loaded piston and is a fixed component of the injector. The position of the piston of the injector which is intended for a plurality of uses is displaced after each use by a distance in a direction towards the nozzle. The piston and the drive spring cannot be reset. The prestressing of the spring is initially sufficiently great to expel the entire amount of liquid in the cartridge all at once. The spring can only be stressed again if the injector is dismantled and the drive portion of the injector assembled with a fresh, completely filled cartridge.
In FR-2 629 706, two embodiments of a needle-less injector for use in dentistry are described, with which a pre-determined amount of liquid can be injected into the gum. Both injectors are respectively composed of two portions that are assembled together coaxially and are releasably connected to one another. Compressed air serves as the operating medium, and is supplied from the outside to the injector.
When the injector is triggered by means of a trigger button, an operating piston is suddenly pushed by a pre-determined arnount by means of a combination of compressed air, coil springs and locking mechanisms, wherein the amount of liquid to be injected is expelled through a nozzle. At the same time, several coil springs are tensioned which push several axially displaceable parts within the injector back into their original position as soon as the compressed air applied is no longer effective. The liquid to be injected is housed within the injector in a tubular, rigid container that is provided at one end with a plug moveable within the container, which keeps the liquid in the container constantly under pressure by means of a spring-tensioned piston. When some of the liquid is pushed out of the container into the liquid chamber within the pump cylinder, the pressure spring pushes the plug, via the piston, by a corresponding amount into the liquid container.
In some known design configurations of the needle-less injector the supply container for the liquid to be injected is arranged laterally beside the drive unit. The amount of liquid to be injected is sucked into the pump chamber when the solid piston of the piston pump is retracted. The inlet passage includes an inlet valve and the outlet passage includes an outlet valve. Both valves operate with an auxiliary force.
In other design configurations of the needle-less injector the supply container for the liquid to be injected serves directly as a pump chamber and is subjected to the sudden application of force which occurs upon expulsion of the amount of liquid to be injected.
3~
-i~}es~as dismantIed and the_ e wi a es,. sn completely filled cartridge.
In some known design configurations of the needle-less-ifijector the supply container for the liquid to be injected is arranged later eside the drive unit. The amount of liquid to be injected is sucked into th mp chamber when the solid piston of the piston pump is retracted. The inlet ssage includes an inlet valve and the outlet passage includes an outlet valve. valves operate with an auxiliary force.
In other design zgurations of the needle-less injector the supply container for the liquid e injected serves directly as a pump chamber and is subjected to the sudd pplication of force which occurs upon expulsion of the amount of liquid to be In the case of the needle-less injectors which are operated with compressed gas, a part of the compressed gas escapes after each injection. The compressed gas container is possibly replaceable but it cannot be directly filled with compressed gas again. With such injectors, the drive unit has to be replaced as soon as the compressed gas container is empty.
Accordingly the object is that of providing a multi-use needle-less injector of a simple design, which is preferably suited for repeated expulsion of a predetermined amount of liquid. The amount of liquid which is expelled overall after many uses should preferably be greater than the amount of liquid contained in a supply container.
It should be possible for either a plurality of partial amounts of the liquid to be successively dispensed from the supply container or for the amount of liquid contained in a supply container to be taken as a whole and expelled all at once. The supply container should be able to be replaced in a simple manner. A sufficiently great mechanical thrust force (impulse) is to be imparted to the predetermined amount of liquid so that the predetermined amount of liquid penetrates a membrane, a foil or biological tissue.
In accordance with the invention that object is attained by a needle-less injector for a liquid, which is arranged in the form of a hand-held unit in a cylindrical housing and which includes a supply container for the liquid. The housing substantially comprises two portions. The two portions are releasably or non-releasably connected together and are arranged rotatably relative to each other. The needle-less injector includes a locking stressing mechanism for a spring-actuated drive, which is stressed prior to the expulsion of a predetermined amount of the liquid and which is provided with a triggering device. Fixed in the sprung portion of the locking stressing mechanism is a hollow plunger which is driven by the locking stressing mechanism.
The hollow plunger is arranged slidably within a cylinder. It projects with its one end out of the cylinder. Preferably at its other end there is mounted a valve body which is the single valve body of the needle-less injector. A nozzle with at least one opening is disposed at the end of the cylinder. The space between the nozzle and the end of the hollow plunger is the pump chamber. A supply container for the liquid is provided within the housing. The supply container is in the form of a container which is separate from the needle-less injector and which - preferably by means of a press fit -is releasably connected to the end of the hollow plunger which projects out of the cylinder. The predetermined amount of the liquid which has been conveyed into the pump chamber upon retraction movement of the sprung portion and the hollow plunger connected thereto, through the hollow plunger, is determined by the stroke movement and the cross-section of the hollow plunger.
The locking stressing mechanism comprises a spring-loaded drive flange as the sprung portion, a drive for stressing the spring, a locking member, two abutments for the drive flange, between which the drive flange can move with a reciprocating movement, and a device for triggering the locking member. The travel of the drive portion is limited precisely by the two abutments. A force-transmitting transmission arrangement is disposed between the energy-storing spring and the drive for stressing the spring. The locking member is annular and has interengaging locking surfaces. A
preferably cylindrical coil spring or a disk spring or a leaf spring, which acts as a tension spring or as a compression spring, can be used as the energy storage means.
The energy-storing spring can be stressed by means of a direct drive. For that purpose the drive flange is displaced by an axially acting external force.
When a high level of spring force is involved, a force-stepup transmission arrangement is advantageous, for example a worm-thrust transmission arrangement, by means of which the spring is stressed by an external torque. A transmission arrangement of that kind is a single-speed or multi-speed transmission arrangement which is disposed between the spring and the drive for stressing the spring.
The drive flange can be of a cup-shaped configuration. The collar of the drive flange may include for example two sawtooth-shaped openings, against which two sawteeth in the upper part of the housing slide.
The average spring force can be between 10 N and 150 N. Between the two positions of the sprung portion of the locking stressing mechanism the spring force changes approximately by 10% of the average spring force.
The locking member can be a ring which in itself is radially elastically deformable or a rigid ring with displacement projections or a rigid ring with leaf springs formed thereon or a ring which is subjected to prestressing by one or more metal springs. The ring can be closed or open; it can comprise a plurality of portions.
The locking member is arranged displaceably in a plane perpendicular to the axis of the housing, or it is deformable in that plane.
Further details relating to the locking stressing mechanism for a spring-actuated drive are described in DE 195 45 226.
Fixed in the sprung portion of the locking stressing mechanism is a hollow plunger which is driven by the locking stressing mechanism. The hollow plunger engages into the cylinder and projects with a part of its length out of the cylinder; it is arranged slidably within the cylinder.
A nozzle is fitted to the end of the cylinder. The nozzle opening can have a hydraulic diameter of 10 m to 500 m, preferably 50 m to 150 m. The nozzle opening can have a length of 50 m to 500 m, preferably 100 m to 300 m.
When the nozzle has a plurality of openings, the longitudinal axes of the nozzle openings can run parallel to one another, or they can be inclined divergently with respect to one another. When the nozzle has a plurality of openings, the hydraulic diameters thereof can be different.
The nozzle can comprise a parallelepiped which is composed of two silicon plates and which for example is 1.1 mm wide, 1.5 mm long and 2.0 mm high. In the contact surface between the plates the parallelepiped can have a shallow triangular opening which is about 400 m thick and which terminates in a single nozzle opening which is 50 m wide, 50 m thick and 200 m long. It may be desirable for the nozzle to be surrounded over its entire periphery with an accurately fitting elastomer shaped portion. The internal contour of the elastomer shaped portion is matched to the external contour of the nozzle and the external contour of the elastomer shaped portion is matched to the internal contour of a nozzle holder which preferably comprises metal. A
'floating mounting' of that kind means that the nozzle which is of brittle material is insensitive to loadings which act in a shock-like fashion and which occur in regular use of the needle-less injector.
A valve body which preferably consists of one piece is mounted preferably to the end of the hollow plunger which is disposed within the cylinder, which valve body is guided by the hollow plunger and is arranged axially displaceably with respect to the hollow plunger. The valve body moves substantially with the hollow body. The valve body is preferably of a shape which is rotationally symmetrical about a single axis, such as for example a circular cylinder or a truncated cone. Its diameter can be smaller than the diameter of the space in which the valve body is displaceably arranged. The valve body can rotate about its axis. The axis of the valve body always remains parallel to the axis of the hollow plunger. That therefore affords a defined sealing surface on the inlet side of the valve body. The distance over which the valve body can be displaced relative to the hollow plunger is limited by an abutment. The valve is closed in the position in which the valve body bears against the defined sealing surface.
The space between the nozzle and the valve body mounted to the hollow plunger is the pump chamber. It is possible to arrange a filter which is preferably in the form of a depth filter in front of the nozzle end of the pump chamber, that is to say in the expulsion passage for the liquid. If the liquid to be injected contains suspended particles, the pore width of the filter has to be matched to the size of the particles.
Further details relating to the hollow plunger and the valve body are set forth in DE 195 36 902.
The locking stressing mechanism and the energy-storing spring are preferably stressed relative to each other by rotation of the two housing portions, preferably by way of a worm-thrust transmission arrangement. The torque can be produced by hand or by means of a motor.
The cylinder diameter is preferably practically identical over its entire length to the outside diameter of the hollow plunger. The cylinder can be fixedly mounted in the one portion of the housing. In addition the cylinder can be axially displaceably mounted in the one portion of the housing. The displaceable cylinder is held in its rest position by a return spring.
The two abutments for the sprung portion can be fixedly positioned in the housing. Furthermore the position of one of those abutments can be variable in the axial direction. In that way it is possible to alter the volume of the pump chamber while the outside diameter of the hollow plunger is constant. In an otherwise unaltered design configuration of the needle-less injector the amount of expelled liquid can be altered by varying the position of an abutment.
The position of the travel movement of the sprung portion and thus the stroke movement of the hollow plunger within the needle-less injector is delimited by the two abutments. With a given position for the abutments the position of the travel movement of the sprung portion and therewith the stroke travel of the hollow plunger is constant for each injection.
The locking member is displaced parallel to the plane of the ring or is radially deformed in the plane of the ring, by means of a triggering device. When the cylinder is fixedly mounted in the housing the triggering device is actuated by means of a triggering button which can be depressed with a finger and the locking member is released. When the cylinder is mounted slidably in the housing the triggering device is actuated when the cylinder is pressed in against the force of the return spring and the locking member is disengaged.
A supply container for the liquid is provided within the housing. That supply container is in the form of a container which is separate from the needle-less injector; it is connected to the end of the hollow plunger which is in opposite relationship to the pump chamber. The end of the hollow plunger is covered by the liquid which is disposed in the supply container.
The supply container which is connected to the hollow plunger can additionally be connected to the sprung portion. That connection can be a releasable or non-releasable push-in connection in which the sprung portion is provided with a plurality of snap hooks which engage into a peripherally extending groove in the supply container after the supply container has been pushed into the needle-less injector.
The predetermined amount of the liquid to be expelled is determined by the stroke movement and the cross-section of the hollow plunger. The stroke movement of the hollow plunger is delimited by the two abutments for the drive flange.
It is desirable to provide in front of the nozzle a removable closure cap for protecting the nozzle opening during storage of the needle-less injector prior to and during the period of use thereof from contamination and evaporation of the liquid.
The two portions of the housing, the locking stressing mechanism, the cylinder and the supply container preferably comprise plastics material, for example polybutyleneterephthalate. The hollow plunger preferably comprises metal, for example high-quality steel.
The valve body can comprise metal, ceramic, glass, precious stone, plastics material or elastomer.
The nozzle can comprise metal, plastics material, glass, silicon or precious stone such as sapphire, ruby or corundum.
The filter preferably comprises sintered metal or sintered plastics material.
The needle-less injector is preferably produced in the form of a hand-held unit.
It can be held and operated with one hand in the injection procedure. The cylinder, the hollow plunger, the valve body, the nozzle and possibly the filter are miniaturised components.
The mode of operation of the needle-less injector is described hereinafter.
During storage of the needle-less injector which has not been used or which has already been put to use and between two injections, the needle-less injector is in the rest condition. The energy-storing spring is in a prestressed condition. The sprung portion bears against the abutment which limits the travel of the sprung portion in the rest condition. The hollow plunger engages deeply into the cylinder. There is only a small spacing between the end of the hollow plunger and the inside of the nozzle.
The locking member is in the disengaged position.
The locking stressing mechanism is stressed when the two housing portions are rotated relative to each other. The sprung portion is displaced in the axial direction away from the cylinder, in which case the stressing of the energy-storing spring is increased. At the same time the hollow plunger is pulled a distance out of the cylinder and the pump chamber is increased in size. The hollow plunger still projects with a part of its length into the cylinder. At the same time a part of the liquid contained in the storage container is conveyed through the hollow plunger and past the valve body into the pump chamber and the pump chamber is filled with liquid. The amount of liquid in the pump chamber is practically the same as the amount of liquid expelled upon an injection being administered. The sprung portion is displaced until the locking member jumps into its engaged position. In the case of a needle-less injector with a triggering button that button protrudes somewhat out of the housing.
The nozzle end of the needle-less injector is applied to and pressed against the injection location. In the case of a needle-less injector with triggering button the triggering button is actuated with a finger and pressed into the housing. In that way the locking member is pushed into the disengaged position and the injection is triggered. In the case of a needle-less injector with slidably arranged cylinder the injector is pressed with its nozzle end by hand with increasing force against the force of the return spring, against the injection location. In that situation the cylinder is pushed into the housing, the locking member is pushed into its disengaged position and the injection is triggered.
When the needle-less injector is lifted off the injection location the return spring urges the cylinder back into its rest position.
As soon as the locking member has assumed the disengaged position the force K of the stressed energy-storing spring acts by way of the sprung portion, the hollow plunger and the closed valve at the end of the hollow plunger, during the period of time At, on the liquid in the pump chamber, whereby the mass of liquid m has imparted thereto the speed Av and thus a mechanical impulse K' At = m* Av, and it issues from the nozzle at high speed and intracutaneously penetrates into the tissue. The needle-less injector is in the rest condition again after the injection.
The needle-less injector according to the invention can serve in human medicine and in veterinary medicine for intracutaneous injection of an active substance in liquid form, for example, a medicinal preparation, into human or animal tissue.
Examples of suitable pharmaceutical preparations are inter alia analgesics, vaccines, anti-diabetic agents, horrnones, contraceptives, vitamins, antibiotics, sedatives, antimicrobial substances, amino acids and coronary agents.
The preparation of the drug can be in the form of a solution, a s spension or an emulsion. In the case of suspensions the mean particle size should not exceed 15 m, preferably 10 m.
Suitable agents for dissolving, suspending or emulsifying active substances and possibly required additives are for example water, alcohols, alcohol-wa er mixtures and emulsions of oil in water or water in oil. They include purified, terilised water, ethanol, propane diol, benzyl alcohols, ethanol-water mixtures, oils ( uch as coconut oil, peanut oil, soya oil, castor oil, sunflower oil), fatty acid esters (s ch as isopropyl myristate, isopropyl palmitate and ethyloleate), triglycerides, triaceti , solketal, and propylene glycol. The formulations may also contain additives such as for example preserving agents as well as acids or bases for adjusting the pH-value.
The predetermined amount of a liquid can be injected by me s of the needle-less injector into a leaf or the stalk of a plant through a membrane into he space behind the membrane.
The needle-less injector according to the invention enjoy~ the following advantages:
= It is of an easily manageable shape. The supply container for the liquid is disposed in the injector housing.
= It can be used for many - up to several hundred - injections which can be taken from one or more supply containers.
= Besides the valve at the end of the hollow plunger it does not have any further valves.
= The locking stressing mechanism can be easily handled, even when high spring forces are involved, even by unskilled persons, and can be stressed with the application of a relatively small amount of force by way of a worm-thrust transmission arrangement.
= The locking stressing mechanism is triggered by hand by pressing the trigger button with a finger or when the needle-less injector is pressed against the injection location.
= The drive unit is not replaced but only the supply container for the liquid.
= The valve mounted at the end of the hollow plunger operates without ancillary force and closes very quickly.
= The volume of the pump chamber can be varied by varying the position of one of the two abutments.
= The mechanical impulse of the amount of liquid to be injected can be adapted to the desired depth of penetration into the tissue or to the thickness of the membrane to be penetrated.
= The supply container for the liquid is adapted to the conditions involved upon storage of the container - possibly for years - and to the connection thereof to the injector. Its design configuration is independent of the demands which are made on the pump chamber in front of the nozzle.
= The supply container for the liquid is not exposed to the thrust force upon injection.
= The supply container for the liquid can be replaced in a simple manner.
= The amount of liquid to be delivered that is necessary for a given application can be injected in a simple manner consecutively in several partial amounts in different places in the area of injection.
= Needle-less injection affects the place injected considerably less than injection by means of a hypodermic syringe.
In one broad aspect, there is provided a needle-less injector for a liquid, which is in the form of a hand unit, comprising a housing and a supply container for the liquid, wherein the housing includes two portions which are connected together and are arranged rotatably relative to each other, and the needle-less injector includes a locking stressing mechanism with a sprung portion which is displaceable between two abutments and which is provided with a triggering device, and a hollow plunger which is fixed in the sprung portion and which is driven by the locking stressing mechanism, wherein the hollow plunger is arranged slidably within a cylinder and includes a single valve body and mounted at the end of the cylinder is a nozzle with at least one opening and the space between the nozzle and the valve body forms a pump chamber, and the supply container for the liquid is arranged within the housing and is in the form of a container separate from the needle-less injector and is connected to the end of the hollow plunger which projects out of the cylinder, and the amount of liquid which has been conveyed through the hollow plunger into the pump chamber when the hollow plunger is pulled out of the cylinder is determined by the stroke travel a and the cross-section of the hollow plunger, and the position of the hollow plunger stroke travel a within the needle-less injector is determined by the position of the two abutments.
The invention will now be described in greater detail with reference to the Figures.
Figure 1 is a view in longitudinal section through a needle-less injector with triggering button in the rest condition, in which the cylinder is fixedly arranged in the one housing portion.
Figure 2 is a view in longitudinal section through a needle-less injector without triggering button in the stressed condition of the energy-storing spring, in which the cylinder is arranged displaceably in the one housing portion.
Figures 3 and 4 show one end of the supply container and the sprung portion in a further embodiment.
In Figure 3 the hollow plunger has been introduced into the supply container but not yet connected to the hollow plunger.
Referring to Figure 1 shown therein are the two housing portions (1) and (2) which are releasably connected together and which are arranged rotatably relative to each other. Of the locking stressing arrangement which is in the rest condition, the Figure shows the sprung portion (3), the locking member (4) in the disengaged condition, the triggering button (5) which acts on the locking member, and the energy-storing coil spring (6) in the form of a compression spring. Fixed in the sprung portion (3) is the hollow plunger (7) which engages into the cylinder (8).
Mounted to the end of the cylinder is the nozzle (9) with the nozzle opening (10). The filter (11) is disposed in front of the nozzle. The nozzle end of the hollow plunger is provided with the valve body (12). The pump chamber (13) is disposed between the valve body and the filter. The supply container (14) is arranged in the otherwise free space within the coil spring; it is fitted in the flange (15) on to the hollow plunger and is held on the hollow plunger by the press fit (19). The cage (16) which surrounds the coil spring is connected in positively locking relationship to the housing portion (1). The sprung portion (3) bears against the abutment (17). The nozzle is protected by the removable closure cap (18).
13a Referring to Figure 2, shown therein are the two housing portions (31) and (32) which are releasably connected together and which are arranged rotatably relative to each other. Of the locking stressing mechanism in the stressed condition, the Figure shows the sprung portion (33), the locking member (34) in the engaged condition and the energy-storing coil spring (36) in the stressed condition. Fixed in the sprung portion (33) is the hollow plunger (37) which engages into the cylinder (38). Mounted at the end of the cylinder is the nozzle (39) having the nozzle opening (40). The nozzle end of the hollow plunger is provided with the valve body (42). The pump chamber (43) is disposed between the valve body and the nozzle. The supply container (44) is arranged in the otherwise free space within the coil spring; it is fitted in the flange (45) on to the hollow plunger and is held on the hollow plunger by the press fit 49. The cage (46) which surrounds the coil spring is connected in positively locking relationship to the housing portion (31). The sprung portion (33) bears against the abutment (47) on the engaged locking member (34). The cylinder (38) is arranged axially slidably in the housing portion (31); it is held in its rest position by the helical return spring (48) which acts as a compression spring. The cylinder (38) is provided with a triggering device (not shown) which disengages the locking member (34) as soon as the cylinder (38) is pushed into the housing portion (31) against the force of the return spring when the needle-less injector is pressed against the injection location. Reference (a) denotes the travel of the drive portion between the two abutments. The stroke movement of the hollow plunger is identical to that travel.
Figure 2 shows the needle-less injector used for injection. The nozzle (39) is pressed against the 13b schematically shown tightly stretched skin (35); with further pressure on the point of injection, the needle-less injector is triggered and the liquid is injected from the pump chamber (43) into the skin.
Figure 3 is a view in longitudinal section of part of the (triple-shell) supply container (54). The outer shell of the supply container is a stiff casing (55) which is provided with a peripherally extending groove (52). The supply container is closed by the plug (56) which goes into the immersion connection portion (58) with a press fit (59).
A part of the sprung portion (53) with the hollow plunger (57) fixed therein is shown in longitudinal section. On its side towards the supply container the sprung portion is provided with a plurality of snap hooks (51).
In Figure 4 the supply container is connected to the hollow plunger and the sprung portion, more specifically to the hollow plunger by the press fit (59) and to the sprung portion by way of the snap hooks (51) which engage into the peripherally extending groove (52) in the supply container.
The connection between the supply container and the sprung portion, which is shown in Figures 3 and 4, comprises snap hooks (51) with round shoulders and a peripherally extending groove (52) of semicircular cross-section. That connection is a releasable plug-in connection.
To provide a non-releasable plug-in connection, it is possible to adopt snap hooks with sawtooth-shaped shoulders and a peripherally extending groove of triangular cross-section.
13c Example 1: Structure of a needle-less injector according to the invention.
A needle-less injector for intracutaneous injection into biological tissue has the following features:
The housing is of an outside diameter of about 20 mm and a length of about 70 mm. Both portions of the housing, the locking stressing mechanism and the spring cage, are made from polybutyleneterephthalate. The cylinder also comprises polybutyleneterephthalate; it is of an outside diameter of 5 mm and an inside diameter of 1.60 mm.
The nozzle comprises quartz. The nozzle opening is of a diameter of 140 m and a length of 220 m. The hollow plunger of high-quality steel is of an outside diameter of 1.59 mm and an inside diameter of 0.35 mm. The piston stroke travel is 12 mm. The valve body comprises elastomer;
it is in the form of a 2 mm thick disc with an outside diameter of 1.60 mm. The disc is provided on its peripheral surface with axial openings through which the liquid can flow past the valve body into the pump chamber. The end of the hollow plunger is provided with a groove into which the valve body engages. The amount of liquid expelled is about 23 mm3. The interchangeable supply container is of a volume of about 11 cm3.
Example 2: Intracutaneous application of a liquid An injection solution comprising 20g of dextran fluorescein (UW 3000) per litre of distilled water was injected through the skin of two dogs under anaesthetic using the needle-less injector according to the invention. For that purpose 4.5 ml of the dextran fluorescein solution was introduced into the supply container of the needle-less injector and the supply container was connected to the hollow plunger of the injector.
The injector was actuated by stressing and triggering the locking stressing mechanism a plurality of times in order to expel the air from the hollow plunger, the pump chamber and the nozzle. The needle-less injector was then applied to a previously shaved part of the skin in the region of the stomach of the dogs and triggered. That procedure was repeated a plurality of times.
Blood samples were taken from the dogs at regular intervals and the content of dextran fluorescein in the blood plasma was determined. The results demonstrate the operability of the needle-less injector according to the invention.
Example 3: In-vitro examination of a viral suspension In laboratory experiments using the needle-less injector, it was determined whether the viability of suspended live viruses was decreased when the suspension was expelled through the valve of the needle-less injector.
From the viral suspension obtained after expulsion from the needle-less injector, a yield of only approximately 1 logio PFU (plaque forming units) in the case of relatively large DNA viruses (test virus: vaccinia virus) and less (approximately 0.5 logio PFU) with small RNA viruses (test virus: bovine viral diarrhoea virus) was determined.
Example 4: In-vivo application of a vaccine with modified live viruses In an animal experiment, the applicability of the needle-less injector for delivering a vaccine suspension with modified live viruses was tested. In this experiment, both the safety and the tolerability of vaccination by means of the needle-less injector, as well as the effectiveness of this method of delivery were determined.
Six healthy dogs of the same age were assigned to two groups. Group 1 comprised two dogs, group 2 comprised four dogs. The animals in both groups were each vaccinated three times, in each case at an interval of three weeks, with a modified live vaccine for canine adenovirus.
In group 1, in each case 1 millilitre of the canine adenovirus vaccine (CAV-1) (Galaxy DA2ppvL+Cv, SNo 610041; Solvay Animal Health Inc.) was delivered intramuscularly in accordance with the manufacturer's recommendations by means of a hypodermic syringe. In group 2, an experimental canine adenovirus was delivered by means of the needle-less injector.
The experimental vaccine (CAV-2) used for vaccinating the animals in group 2 was manufactured from a weakened strain of the canine adenovirus. The titre was 7.2 logio TCID50 per 60 microlitres (TCID = tissue culture infective dose). At each injection site, six individual shots were administered (six times 10 microlitres = 60 microlitres for each vaccination). The injection area on the back of the dogs was shaved and the respective six injection sites were marked with a ball-point pen.
The effectiveness of the vaccination was established by determining the number of virus neutralising antibodies in the serum of the dogs, in each case three weeks after each vaccination.
Tolerability was determined by observation of the injection sites six seconds after the vaccination and subsequently daily until the end of the animal experiment.
The injection sites were photographed and the results after palpating the injection sites were noted.
This experiment showed:
In the animals in group 2 a very slight reddening of the injection sites was evident during the first 2 to 3 days. A temporary swelling lasting 1 to 2 days could be determined only by palpation. This slight and entirely tolerable local reaction is very probably connected with the local amplification of the depleted modified live virus, and is therefore viewed as necessary for the proper effectiveness of the vaccine.
This explanation is supported by the fact that after the injection of physiological common salt solution, using the needle-less injector, absolutely no colouration and also not even a slight, temporary swelling was to be noted.
Effectiveness is determined by the virus neutralisation test. The results are shown in Table 1. The largest titres are still capable of neutralising canine adenoviruses.
In the serum of all the animals from the two groups, virus neutralising antibodies were evident three weeks after the first vaccination. After the second and third vaccination, a small intensification effect was shown.
The vaccination with the experimental canine adenovirus vaccine by means of the needle-less injector is exactly as effective as intramuscular vaccination with the conventional vaccination by means of a hypodermic syringe.
Table 1: Canine adenovirus neutralisation titres of canine serum Dog VN titre of canine serum Test number Reference 21days after first 21 days after second 21 days after third vaccination vaccination vaccination CAV-1 conventional vaccine intramuscular by means of hypodermic syringe CAV-2 experimental vaccine Subcutaneous by means of needle-less injector
-i~}es~as dismantIed and the_ e wi a es,. sn completely filled cartridge.
In some known design configurations of the needle-less-ifijector the supply container for the liquid to be injected is arranged later eside the drive unit. The amount of liquid to be injected is sucked into th mp chamber when the solid piston of the piston pump is retracted. The inlet ssage includes an inlet valve and the outlet passage includes an outlet valve. valves operate with an auxiliary force.
In other design zgurations of the needle-less injector the supply container for the liquid e injected serves directly as a pump chamber and is subjected to the sudd pplication of force which occurs upon expulsion of the amount of liquid to be In the case of the needle-less injectors which are operated with compressed gas, a part of the compressed gas escapes after each injection. The compressed gas container is possibly replaceable but it cannot be directly filled with compressed gas again. With such injectors, the drive unit has to be replaced as soon as the compressed gas container is empty.
Accordingly the object is that of providing a multi-use needle-less injector of a simple design, which is preferably suited for repeated expulsion of a predetermined amount of liquid. The amount of liquid which is expelled overall after many uses should preferably be greater than the amount of liquid contained in a supply container.
It should be possible for either a plurality of partial amounts of the liquid to be successively dispensed from the supply container or for the amount of liquid contained in a supply container to be taken as a whole and expelled all at once. The supply container should be able to be replaced in a simple manner. A sufficiently great mechanical thrust force (impulse) is to be imparted to the predetermined amount of liquid so that the predetermined amount of liquid penetrates a membrane, a foil or biological tissue.
In accordance with the invention that object is attained by a needle-less injector for a liquid, which is arranged in the form of a hand-held unit in a cylindrical housing and which includes a supply container for the liquid. The housing substantially comprises two portions. The two portions are releasably or non-releasably connected together and are arranged rotatably relative to each other. The needle-less injector includes a locking stressing mechanism for a spring-actuated drive, which is stressed prior to the expulsion of a predetermined amount of the liquid and which is provided with a triggering device. Fixed in the sprung portion of the locking stressing mechanism is a hollow plunger which is driven by the locking stressing mechanism.
The hollow plunger is arranged slidably within a cylinder. It projects with its one end out of the cylinder. Preferably at its other end there is mounted a valve body which is the single valve body of the needle-less injector. A nozzle with at least one opening is disposed at the end of the cylinder. The space between the nozzle and the end of the hollow plunger is the pump chamber. A supply container for the liquid is provided within the housing. The supply container is in the form of a container which is separate from the needle-less injector and which - preferably by means of a press fit -is releasably connected to the end of the hollow plunger which projects out of the cylinder. The predetermined amount of the liquid which has been conveyed into the pump chamber upon retraction movement of the sprung portion and the hollow plunger connected thereto, through the hollow plunger, is determined by the stroke movement and the cross-section of the hollow plunger.
The locking stressing mechanism comprises a spring-loaded drive flange as the sprung portion, a drive for stressing the spring, a locking member, two abutments for the drive flange, between which the drive flange can move with a reciprocating movement, and a device for triggering the locking member. The travel of the drive portion is limited precisely by the two abutments. A force-transmitting transmission arrangement is disposed between the energy-storing spring and the drive for stressing the spring. The locking member is annular and has interengaging locking surfaces. A
preferably cylindrical coil spring or a disk spring or a leaf spring, which acts as a tension spring or as a compression spring, can be used as the energy storage means.
The energy-storing spring can be stressed by means of a direct drive. For that purpose the drive flange is displaced by an axially acting external force.
When a high level of spring force is involved, a force-stepup transmission arrangement is advantageous, for example a worm-thrust transmission arrangement, by means of which the spring is stressed by an external torque. A transmission arrangement of that kind is a single-speed or multi-speed transmission arrangement which is disposed between the spring and the drive for stressing the spring.
The drive flange can be of a cup-shaped configuration. The collar of the drive flange may include for example two sawtooth-shaped openings, against which two sawteeth in the upper part of the housing slide.
The average spring force can be between 10 N and 150 N. Between the two positions of the sprung portion of the locking stressing mechanism the spring force changes approximately by 10% of the average spring force.
The locking member can be a ring which in itself is radially elastically deformable or a rigid ring with displacement projections or a rigid ring with leaf springs formed thereon or a ring which is subjected to prestressing by one or more metal springs. The ring can be closed or open; it can comprise a plurality of portions.
The locking member is arranged displaceably in a plane perpendicular to the axis of the housing, or it is deformable in that plane.
Further details relating to the locking stressing mechanism for a spring-actuated drive are described in DE 195 45 226.
Fixed in the sprung portion of the locking stressing mechanism is a hollow plunger which is driven by the locking stressing mechanism. The hollow plunger engages into the cylinder and projects with a part of its length out of the cylinder; it is arranged slidably within the cylinder.
A nozzle is fitted to the end of the cylinder. The nozzle opening can have a hydraulic diameter of 10 m to 500 m, preferably 50 m to 150 m. The nozzle opening can have a length of 50 m to 500 m, preferably 100 m to 300 m.
When the nozzle has a plurality of openings, the longitudinal axes of the nozzle openings can run parallel to one another, or they can be inclined divergently with respect to one another. When the nozzle has a plurality of openings, the hydraulic diameters thereof can be different.
The nozzle can comprise a parallelepiped which is composed of two silicon plates and which for example is 1.1 mm wide, 1.5 mm long and 2.0 mm high. In the contact surface between the plates the parallelepiped can have a shallow triangular opening which is about 400 m thick and which terminates in a single nozzle opening which is 50 m wide, 50 m thick and 200 m long. It may be desirable for the nozzle to be surrounded over its entire periphery with an accurately fitting elastomer shaped portion. The internal contour of the elastomer shaped portion is matched to the external contour of the nozzle and the external contour of the elastomer shaped portion is matched to the internal contour of a nozzle holder which preferably comprises metal. A
'floating mounting' of that kind means that the nozzle which is of brittle material is insensitive to loadings which act in a shock-like fashion and which occur in regular use of the needle-less injector.
A valve body which preferably consists of one piece is mounted preferably to the end of the hollow plunger which is disposed within the cylinder, which valve body is guided by the hollow plunger and is arranged axially displaceably with respect to the hollow plunger. The valve body moves substantially with the hollow body. The valve body is preferably of a shape which is rotationally symmetrical about a single axis, such as for example a circular cylinder or a truncated cone. Its diameter can be smaller than the diameter of the space in which the valve body is displaceably arranged. The valve body can rotate about its axis. The axis of the valve body always remains parallel to the axis of the hollow plunger. That therefore affords a defined sealing surface on the inlet side of the valve body. The distance over which the valve body can be displaced relative to the hollow plunger is limited by an abutment. The valve is closed in the position in which the valve body bears against the defined sealing surface.
The space between the nozzle and the valve body mounted to the hollow plunger is the pump chamber. It is possible to arrange a filter which is preferably in the form of a depth filter in front of the nozzle end of the pump chamber, that is to say in the expulsion passage for the liquid. If the liquid to be injected contains suspended particles, the pore width of the filter has to be matched to the size of the particles.
Further details relating to the hollow plunger and the valve body are set forth in DE 195 36 902.
The locking stressing mechanism and the energy-storing spring are preferably stressed relative to each other by rotation of the two housing portions, preferably by way of a worm-thrust transmission arrangement. The torque can be produced by hand or by means of a motor.
The cylinder diameter is preferably practically identical over its entire length to the outside diameter of the hollow plunger. The cylinder can be fixedly mounted in the one portion of the housing. In addition the cylinder can be axially displaceably mounted in the one portion of the housing. The displaceable cylinder is held in its rest position by a return spring.
The two abutments for the sprung portion can be fixedly positioned in the housing. Furthermore the position of one of those abutments can be variable in the axial direction. In that way it is possible to alter the volume of the pump chamber while the outside diameter of the hollow plunger is constant. In an otherwise unaltered design configuration of the needle-less injector the amount of expelled liquid can be altered by varying the position of an abutment.
The position of the travel movement of the sprung portion and thus the stroke movement of the hollow plunger within the needle-less injector is delimited by the two abutments. With a given position for the abutments the position of the travel movement of the sprung portion and therewith the stroke travel of the hollow plunger is constant for each injection.
The locking member is displaced parallel to the plane of the ring or is radially deformed in the plane of the ring, by means of a triggering device. When the cylinder is fixedly mounted in the housing the triggering device is actuated by means of a triggering button which can be depressed with a finger and the locking member is released. When the cylinder is mounted slidably in the housing the triggering device is actuated when the cylinder is pressed in against the force of the return spring and the locking member is disengaged.
A supply container for the liquid is provided within the housing. That supply container is in the form of a container which is separate from the needle-less injector; it is connected to the end of the hollow plunger which is in opposite relationship to the pump chamber. The end of the hollow plunger is covered by the liquid which is disposed in the supply container.
The supply container which is connected to the hollow plunger can additionally be connected to the sprung portion. That connection can be a releasable or non-releasable push-in connection in which the sprung portion is provided with a plurality of snap hooks which engage into a peripherally extending groove in the supply container after the supply container has been pushed into the needle-less injector.
The predetermined amount of the liquid to be expelled is determined by the stroke movement and the cross-section of the hollow plunger. The stroke movement of the hollow plunger is delimited by the two abutments for the drive flange.
It is desirable to provide in front of the nozzle a removable closure cap for protecting the nozzle opening during storage of the needle-less injector prior to and during the period of use thereof from contamination and evaporation of the liquid.
The two portions of the housing, the locking stressing mechanism, the cylinder and the supply container preferably comprise plastics material, for example polybutyleneterephthalate. The hollow plunger preferably comprises metal, for example high-quality steel.
The valve body can comprise metal, ceramic, glass, precious stone, plastics material or elastomer.
The nozzle can comprise metal, plastics material, glass, silicon or precious stone such as sapphire, ruby or corundum.
The filter preferably comprises sintered metal or sintered plastics material.
The needle-less injector is preferably produced in the form of a hand-held unit.
It can be held and operated with one hand in the injection procedure. The cylinder, the hollow plunger, the valve body, the nozzle and possibly the filter are miniaturised components.
The mode of operation of the needle-less injector is described hereinafter.
During storage of the needle-less injector which has not been used or which has already been put to use and between two injections, the needle-less injector is in the rest condition. The energy-storing spring is in a prestressed condition. The sprung portion bears against the abutment which limits the travel of the sprung portion in the rest condition. The hollow plunger engages deeply into the cylinder. There is only a small spacing between the end of the hollow plunger and the inside of the nozzle.
The locking member is in the disengaged position.
The locking stressing mechanism is stressed when the two housing portions are rotated relative to each other. The sprung portion is displaced in the axial direction away from the cylinder, in which case the stressing of the energy-storing spring is increased. At the same time the hollow plunger is pulled a distance out of the cylinder and the pump chamber is increased in size. The hollow plunger still projects with a part of its length into the cylinder. At the same time a part of the liquid contained in the storage container is conveyed through the hollow plunger and past the valve body into the pump chamber and the pump chamber is filled with liquid. The amount of liquid in the pump chamber is practically the same as the amount of liquid expelled upon an injection being administered. The sprung portion is displaced until the locking member jumps into its engaged position. In the case of a needle-less injector with a triggering button that button protrudes somewhat out of the housing.
The nozzle end of the needle-less injector is applied to and pressed against the injection location. In the case of a needle-less injector with triggering button the triggering button is actuated with a finger and pressed into the housing. In that way the locking member is pushed into the disengaged position and the injection is triggered. In the case of a needle-less injector with slidably arranged cylinder the injector is pressed with its nozzle end by hand with increasing force against the force of the return spring, against the injection location. In that situation the cylinder is pushed into the housing, the locking member is pushed into its disengaged position and the injection is triggered.
When the needle-less injector is lifted off the injection location the return spring urges the cylinder back into its rest position.
As soon as the locking member has assumed the disengaged position the force K of the stressed energy-storing spring acts by way of the sprung portion, the hollow plunger and the closed valve at the end of the hollow plunger, during the period of time At, on the liquid in the pump chamber, whereby the mass of liquid m has imparted thereto the speed Av and thus a mechanical impulse K' At = m* Av, and it issues from the nozzle at high speed and intracutaneously penetrates into the tissue. The needle-less injector is in the rest condition again after the injection.
The needle-less injector according to the invention can serve in human medicine and in veterinary medicine for intracutaneous injection of an active substance in liquid form, for example, a medicinal preparation, into human or animal tissue.
Examples of suitable pharmaceutical preparations are inter alia analgesics, vaccines, anti-diabetic agents, horrnones, contraceptives, vitamins, antibiotics, sedatives, antimicrobial substances, amino acids and coronary agents.
The preparation of the drug can be in the form of a solution, a s spension or an emulsion. In the case of suspensions the mean particle size should not exceed 15 m, preferably 10 m.
Suitable agents for dissolving, suspending or emulsifying active substances and possibly required additives are for example water, alcohols, alcohol-wa er mixtures and emulsions of oil in water or water in oil. They include purified, terilised water, ethanol, propane diol, benzyl alcohols, ethanol-water mixtures, oils ( uch as coconut oil, peanut oil, soya oil, castor oil, sunflower oil), fatty acid esters (s ch as isopropyl myristate, isopropyl palmitate and ethyloleate), triglycerides, triaceti , solketal, and propylene glycol. The formulations may also contain additives such as for example preserving agents as well as acids or bases for adjusting the pH-value.
The predetermined amount of a liquid can be injected by me s of the needle-less injector into a leaf or the stalk of a plant through a membrane into he space behind the membrane.
The needle-less injector according to the invention enjoy~ the following advantages:
= It is of an easily manageable shape. The supply container for the liquid is disposed in the injector housing.
= It can be used for many - up to several hundred - injections which can be taken from one or more supply containers.
= Besides the valve at the end of the hollow plunger it does not have any further valves.
= The locking stressing mechanism can be easily handled, even when high spring forces are involved, even by unskilled persons, and can be stressed with the application of a relatively small amount of force by way of a worm-thrust transmission arrangement.
= The locking stressing mechanism is triggered by hand by pressing the trigger button with a finger or when the needle-less injector is pressed against the injection location.
= The drive unit is not replaced but only the supply container for the liquid.
= The valve mounted at the end of the hollow plunger operates without ancillary force and closes very quickly.
= The volume of the pump chamber can be varied by varying the position of one of the two abutments.
= The mechanical impulse of the amount of liquid to be injected can be adapted to the desired depth of penetration into the tissue or to the thickness of the membrane to be penetrated.
= The supply container for the liquid is adapted to the conditions involved upon storage of the container - possibly for years - and to the connection thereof to the injector. Its design configuration is independent of the demands which are made on the pump chamber in front of the nozzle.
= The supply container for the liquid is not exposed to the thrust force upon injection.
= The supply container for the liquid can be replaced in a simple manner.
= The amount of liquid to be delivered that is necessary for a given application can be injected in a simple manner consecutively in several partial amounts in different places in the area of injection.
= Needle-less injection affects the place injected considerably less than injection by means of a hypodermic syringe.
In one broad aspect, there is provided a needle-less injector for a liquid, which is in the form of a hand unit, comprising a housing and a supply container for the liquid, wherein the housing includes two portions which are connected together and are arranged rotatably relative to each other, and the needle-less injector includes a locking stressing mechanism with a sprung portion which is displaceable between two abutments and which is provided with a triggering device, and a hollow plunger which is fixed in the sprung portion and which is driven by the locking stressing mechanism, wherein the hollow plunger is arranged slidably within a cylinder and includes a single valve body and mounted at the end of the cylinder is a nozzle with at least one opening and the space between the nozzle and the valve body forms a pump chamber, and the supply container for the liquid is arranged within the housing and is in the form of a container separate from the needle-less injector and is connected to the end of the hollow plunger which projects out of the cylinder, and the amount of liquid which has been conveyed through the hollow plunger into the pump chamber when the hollow plunger is pulled out of the cylinder is determined by the stroke travel a and the cross-section of the hollow plunger, and the position of the hollow plunger stroke travel a within the needle-less injector is determined by the position of the two abutments.
The invention will now be described in greater detail with reference to the Figures.
Figure 1 is a view in longitudinal section through a needle-less injector with triggering button in the rest condition, in which the cylinder is fixedly arranged in the one housing portion.
Figure 2 is a view in longitudinal section through a needle-less injector without triggering button in the stressed condition of the energy-storing spring, in which the cylinder is arranged displaceably in the one housing portion.
Figures 3 and 4 show one end of the supply container and the sprung portion in a further embodiment.
In Figure 3 the hollow plunger has been introduced into the supply container but not yet connected to the hollow plunger.
Referring to Figure 1 shown therein are the two housing portions (1) and (2) which are releasably connected together and which are arranged rotatably relative to each other. Of the locking stressing arrangement which is in the rest condition, the Figure shows the sprung portion (3), the locking member (4) in the disengaged condition, the triggering button (5) which acts on the locking member, and the energy-storing coil spring (6) in the form of a compression spring. Fixed in the sprung portion (3) is the hollow plunger (7) which engages into the cylinder (8).
Mounted to the end of the cylinder is the nozzle (9) with the nozzle opening (10). The filter (11) is disposed in front of the nozzle. The nozzle end of the hollow plunger is provided with the valve body (12). The pump chamber (13) is disposed between the valve body and the filter. The supply container (14) is arranged in the otherwise free space within the coil spring; it is fitted in the flange (15) on to the hollow plunger and is held on the hollow plunger by the press fit (19). The cage (16) which surrounds the coil spring is connected in positively locking relationship to the housing portion (1). The sprung portion (3) bears against the abutment (17). The nozzle is protected by the removable closure cap (18).
13a Referring to Figure 2, shown therein are the two housing portions (31) and (32) which are releasably connected together and which are arranged rotatably relative to each other. Of the locking stressing mechanism in the stressed condition, the Figure shows the sprung portion (33), the locking member (34) in the engaged condition and the energy-storing coil spring (36) in the stressed condition. Fixed in the sprung portion (33) is the hollow plunger (37) which engages into the cylinder (38). Mounted at the end of the cylinder is the nozzle (39) having the nozzle opening (40). The nozzle end of the hollow plunger is provided with the valve body (42). The pump chamber (43) is disposed between the valve body and the nozzle. The supply container (44) is arranged in the otherwise free space within the coil spring; it is fitted in the flange (45) on to the hollow plunger and is held on the hollow plunger by the press fit 49. The cage (46) which surrounds the coil spring is connected in positively locking relationship to the housing portion (31). The sprung portion (33) bears against the abutment (47) on the engaged locking member (34). The cylinder (38) is arranged axially slidably in the housing portion (31); it is held in its rest position by the helical return spring (48) which acts as a compression spring. The cylinder (38) is provided with a triggering device (not shown) which disengages the locking member (34) as soon as the cylinder (38) is pushed into the housing portion (31) against the force of the return spring when the needle-less injector is pressed against the injection location. Reference (a) denotes the travel of the drive portion between the two abutments. The stroke movement of the hollow plunger is identical to that travel.
Figure 2 shows the needle-less injector used for injection. The nozzle (39) is pressed against the 13b schematically shown tightly stretched skin (35); with further pressure on the point of injection, the needle-less injector is triggered and the liquid is injected from the pump chamber (43) into the skin.
Figure 3 is a view in longitudinal section of part of the (triple-shell) supply container (54). The outer shell of the supply container is a stiff casing (55) which is provided with a peripherally extending groove (52). The supply container is closed by the plug (56) which goes into the immersion connection portion (58) with a press fit (59).
A part of the sprung portion (53) with the hollow plunger (57) fixed therein is shown in longitudinal section. On its side towards the supply container the sprung portion is provided with a plurality of snap hooks (51).
In Figure 4 the supply container is connected to the hollow plunger and the sprung portion, more specifically to the hollow plunger by the press fit (59) and to the sprung portion by way of the snap hooks (51) which engage into the peripherally extending groove (52) in the supply container.
The connection between the supply container and the sprung portion, which is shown in Figures 3 and 4, comprises snap hooks (51) with round shoulders and a peripherally extending groove (52) of semicircular cross-section. That connection is a releasable plug-in connection.
To provide a non-releasable plug-in connection, it is possible to adopt snap hooks with sawtooth-shaped shoulders and a peripherally extending groove of triangular cross-section.
13c Example 1: Structure of a needle-less injector according to the invention.
A needle-less injector for intracutaneous injection into biological tissue has the following features:
The housing is of an outside diameter of about 20 mm and a length of about 70 mm. Both portions of the housing, the locking stressing mechanism and the spring cage, are made from polybutyleneterephthalate. The cylinder also comprises polybutyleneterephthalate; it is of an outside diameter of 5 mm and an inside diameter of 1.60 mm.
The nozzle comprises quartz. The nozzle opening is of a diameter of 140 m and a length of 220 m. The hollow plunger of high-quality steel is of an outside diameter of 1.59 mm and an inside diameter of 0.35 mm. The piston stroke travel is 12 mm. The valve body comprises elastomer;
it is in the form of a 2 mm thick disc with an outside diameter of 1.60 mm. The disc is provided on its peripheral surface with axial openings through which the liquid can flow past the valve body into the pump chamber. The end of the hollow plunger is provided with a groove into which the valve body engages. The amount of liquid expelled is about 23 mm3. The interchangeable supply container is of a volume of about 11 cm3.
Example 2: Intracutaneous application of a liquid An injection solution comprising 20g of dextran fluorescein (UW 3000) per litre of distilled water was injected through the skin of two dogs under anaesthetic using the needle-less injector according to the invention. For that purpose 4.5 ml of the dextran fluorescein solution was introduced into the supply container of the needle-less injector and the supply container was connected to the hollow plunger of the injector.
The injector was actuated by stressing and triggering the locking stressing mechanism a plurality of times in order to expel the air from the hollow plunger, the pump chamber and the nozzle. The needle-less injector was then applied to a previously shaved part of the skin in the region of the stomach of the dogs and triggered. That procedure was repeated a plurality of times.
Blood samples were taken from the dogs at regular intervals and the content of dextran fluorescein in the blood plasma was determined. The results demonstrate the operability of the needle-less injector according to the invention.
Example 3: In-vitro examination of a viral suspension In laboratory experiments using the needle-less injector, it was determined whether the viability of suspended live viruses was decreased when the suspension was expelled through the valve of the needle-less injector.
From the viral suspension obtained after expulsion from the needle-less injector, a yield of only approximately 1 logio PFU (plaque forming units) in the case of relatively large DNA viruses (test virus: vaccinia virus) and less (approximately 0.5 logio PFU) with small RNA viruses (test virus: bovine viral diarrhoea virus) was determined.
Example 4: In-vivo application of a vaccine with modified live viruses In an animal experiment, the applicability of the needle-less injector for delivering a vaccine suspension with modified live viruses was tested. In this experiment, both the safety and the tolerability of vaccination by means of the needle-less injector, as well as the effectiveness of this method of delivery were determined.
Six healthy dogs of the same age were assigned to two groups. Group 1 comprised two dogs, group 2 comprised four dogs. The animals in both groups were each vaccinated three times, in each case at an interval of three weeks, with a modified live vaccine for canine adenovirus.
In group 1, in each case 1 millilitre of the canine adenovirus vaccine (CAV-1) (Galaxy DA2ppvL+Cv, SNo 610041; Solvay Animal Health Inc.) was delivered intramuscularly in accordance with the manufacturer's recommendations by means of a hypodermic syringe. In group 2, an experimental canine adenovirus was delivered by means of the needle-less injector.
The experimental vaccine (CAV-2) used for vaccinating the animals in group 2 was manufactured from a weakened strain of the canine adenovirus. The titre was 7.2 logio TCID50 per 60 microlitres (TCID = tissue culture infective dose). At each injection site, six individual shots were administered (six times 10 microlitres = 60 microlitres for each vaccination). The injection area on the back of the dogs was shaved and the respective six injection sites were marked with a ball-point pen.
The effectiveness of the vaccination was established by determining the number of virus neutralising antibodies in the serum of the dogs, in each case three weeks after each vaccination.
Tolerability was determined by observation of the injection sites six seconds after the vaccination and subsequently daily until the end of the animal experiment.
The injection sites were photographed and the results after palpating the injection sites were noted.
This experiment showed:
In the animals in group 2 a very slight reddening of the injection sites was evident during the first 2 to 3 days. A temporary swelling lasting 1 to 2 days could be determined only by palpation. This slight and entirely tolerable local reaction is very probably connected with the local amplification of the depleted modified live virus, and is therefore viewed as necessary for the proper effectiveness of the vaccine.
This explanation is supported by the fact that after the injection of physiological common salt solution, using the needle-less injector, absolutely no colouration and also not even a slight, temporary swelling was to be noted.
Effectiveness is determined by the virus neutralisation test. The results are shown in Table 1. The largest titres are still capable of neutralising canine adenoviruses.
In the serum of all the animals from the two groups, virus neutralising antibodies were evident three weeks after the first vaccination. After the second and third vaccination, a small intensification effect was shown.
The vaccination with the experimental canine adenovirus vaccine by means of the needle-less injector is exactly as effective as intramuscular vaccination with the conventional vaccination by means of a hypodermic syringe.
Table 1: Canine adenovirus neutralisation titres of canine serum Dog VN titre of canine serum Test number Reference 21days after first 21 days after second 21 days after third vaccination vaccination vaccination CAV-1 conventional vaccine intramuscular by means of hypodermic syringe CAV-2 experimental vaccine Subcutaneous by means of needle-less injector
Claims (24)
1. A needle-less injector for a liquid, which is in the form of a hand unit, comprising a housing and a supply container for the liquid, wherein - the housing includes two portions which are connected together and are arranged rotatably relative to each other, and - the needle-less injector includes a locking stressing mechanism with a sprung portion which is displaceable between two abutments and which is provided with a triggering device, and a hollow plunger which is fixed in the sprung portion and which is driven by the locking stressing mechanism, wherein the hollow plunger is arranged slidably within a cylinder and includes a single valve body and mounted at the end of the cylinder is a nozzle with at least one opening and the space between the nozzle and the valve body forms a pump chamber, and - the supply container for the liquid is arranged within the housing and is in the form of a container separate from the needle-less injector and is connected to the end of the hollow plunger which projects out of the cylinder, and - the amount of liquid which has been conveyed through the hollow plunger into the pump chamber when the hollow plunger is pulled out of the cylinder is determined by the stroke travel a and the cross-section of the hollow plunger, and - the position of the hollow plunger stroke travel a within the needle-less injector is determined by the position of the two abutments.
2. A needle-less injector according to claim 1 wherein - the two portions of the housing are releasably connected together.
3. A needle-less injector according to claim 1 or claim 2 wherein - the nozzle includes only one opening of a hydraulic diameter of 10 µm to 500 µm, and - the nozzle opening is of a length of 50 µm to 500 µm.
4. A needle-less injector according to claim 1 or claim 2 wherein - the nozzle includes a plurality of nozzle openings whose hydraulic diameters are different.
5. A needle-less injector according to claim 1 or claim 2 wherein - the nozzle includes a plurality of nozzle openings whose longitudinal axes extend in mutually parallel relationship or are inclined divergently relative to each other.
6. A needle-less injector according to any one of claims 1 to 5 wherein - the position of the abutments and thus the hollow plunger stroke travel a is variable.
7. A needle-less injector according to any one of claims 1 to 6 wherein - the locking stressing mechanism is stressed by rotating the two housing portions relative to each other by hand.
8. A needle-less injector according to any one of claims 1 to 7 wherein - the locking stressing mechanism is stressed by way of a worm-thrust transmission by rotation of the two housing portions relative to each other.
9. A needle-less injector according to any one of claims 1 to 8 wherein - the locking stressing mechanism includes one of a coil spring, a plate spring, and a leaf spring as an energy storage means.
10. A needle-less injector according to any one of claims 1 to 9 wherein - the nozzle comprises one of metal, plastic material, glass, silicon and precious stone.
11. A needle-less injector according to any one of claims 1 to 10 wherein - the separate supply container for the liquid is releasably connected by means of a press fit to the end of the hollow plunger which projects out of the cylinder.
12. A needle-less injector according to any one of claims 1 to 11 wherein - the separate supply container for the liquid is releasably connected to the hollow plunger and is displaceable with the stroke movement of the hollow plunger within the housing.
13. A needle-less injector according to any one of claims 1 to 12 wherein - the separate supply container for the liquid is in the form of a replaceable supply container and the sprung portion is adapted to receive the separate supply container.
14. A needle-less injector according to any one of claims 1 and 13 wherein - the separate supply container for the liquid is releasably connected to the hollow plunger and the sprung portion, and - the sprung portion is provided with snap hooks which engage into a peripherally extending groove in the supply container.
15. A needle-less injector according to any one of claims 1 to 14 wherein - the nozzle end of the nozzle-less injector is provided with a closure cap.
16. A needle-less injector according to any one of claims 1 to 15 wherein - a filter is provided in front of the side of the nozzle, which is towards the pump chamber.
17. A needle-less injector according to any one of claims 1 to 16 wherein - the separate supply container for the liquid is filled with a liquid drug.
18. A needle-less injector according to any one of claims 1 to 3 for a liquid, which is in the form of a hand unit, comprising a housing and a supply container for the liquid, wherein - the locking stressing mechanism includes a coil spring, the locking stressing mechanism is stressed by way of a worm-thrust transmission by rotation of the two housing portions relative to each other, and the locking stressing mechanism is provided with a triggering device, and - a nozzle having a single opening is mounted at the end of the cylinder, and - the supply container is connected by means of a press fit to the end of the hollow plunger and is connected to the sprung portion by means of snap hooks which engage into a peripherally extending groove in the supply container, and - the separate supply container is filled with a liquid drug.
19. A needle-less injector according to claim 18 wherein - a filter is disposed in front of the side of the nozzle, which is towards the pump chamber.
20. Use of the needle-less injector according to any one of claims 1 to 19 for injecting a liquid containing active substance into vegetable tissue.
21. The needle-less injector of claim 3, wherein the diameter of the opening is from 50 µm to 150 µm.
22. The needle-less injector of claim 3, wherein the length of the nozzle opening is from 100 µm to 300 µm.
23. The needle-less injector of claim 10, wherein the precious stone comprises one of sapphire, ruby and corundum.
24. The needle-less injector of claim 17, wherein the liquid drug is selected from the group consisting of analgesics, vaccines, antidiabetic agents, hormones, contraceptives, vitamins, antibiotics, sedatives, anti-microbial substances, amino acids and coronary agents.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10010123.2 | 2000-03-03 | ||
| DE10010123A DE10010123A1 (en) | 2000-03-03 | 2000-03-03 | Needle-less injector for liquids comprises a tensioning system, an energy storing spring, a hollow piston in a cylinder, and a nozzle |
| PCT/EP2001/002356 WO2001064268A1 (en) | 2000-03-03 | 2001-03-02 | Miniaturized needleless injector |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2404360A1 CA2404360A1 (en) | 2001-09-07 |
| CA2404360C true CA2404360C (en) | 2007-12-18 |
Family
ID=7633206
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002404360A Expired - Fee Related CA2404360C (en) | 2000-03-03 | 2001-03-02 | Needle-less injector of miniature type |
Country Status (35)
| Country | Link |
|---|---|
| EP (1) | EP1263490B1 (en) |
| JP (1) | JP2003525086A (en) |
| KR (1) | KR100777146B1 (en) |
| CN (1) | CN1179763C (en) |
| AR (1) | AR027595A1 (en) |
| AT (1) | ATE300325T1 (en) |
| AU (2) | AU2001250347B2 (en) |
| BG (1) | BG64726B1 (en) |
| BR (1) | BR0108914A (en) |
| CA (1) | CA2404360C (en) |
| CZ (1) | CZ20022970A3 (en) |
| DE (2) | DE10010123A1 (en) |
| DK (1) | DK1263490T3 (en) |
| EA (1) | EA200200877A1 (en) |
| EE (1) | EE04583B1 (en) |
| EG (1) | EG22864A (en) |
| ES (1) | ES2247092T3 (en) |
| HK (1) | HK1053990A1 (en) |
| HR (1) | HRP20020720A2 (en) |
| HU (1) | HU226578B1 (en) |
| IL (2) | IL151465A0 (en) |
| MX (1) | MXPA02008581A (en) |
| MY (1) | MY126848A (en) |
| NO (1) | NO20024170D0 (en) |
| NZ (1) | NZ521723A (en) |
| PE (1) | PE20011111A1 (en) |
| PL (1) | PL200838B1 (en) |
| PT (1) | PT1263490E (en) |
| RS (1) | RS49509B (en) |
| SA (1) | SA01220003B1 (en) |
| SK (1) | SK12502002A3 (en) |
| TW (1) | TW541185B (en) |
| UA (1) | UA70409C2 (en) |
| WO (1) | WO2001064268A1 (en) |
| ZA (1) | ZA200206987B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8221347B2 (en) | 2004-12-01 | 2012-07-17 | Acushot, Inc. | Needle-free injector |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20020035107A1 (en) | 2000-06-20 | 2002-03-21 | Stefan Henke | Highly concentrated stable meloxicam solutions |
| US6945472B2 (en) | 2001-09-04 | 2005-09-20 | Boehringer Ingelheim International Gmbh | Locking-stressing mechanism for a miniaturised high pressuriser |
| DE10143350A1 (en) * | 2001-09-04 | 2003-03-20 | Boehringer Ingelheim Int | Locking mechanism for a miniaturized high pressure generator |
| WO2003041768A1 (en) * | 2001-11-14 | 2003-05-22 | Riemser Arzneimittel Ag | Injection device and ampoule, particularly for an injection device |
| DE10161077A1 (en) | 2001-12-12 | 2003-06-18 | Boehringer Ingelheim Vetmed | Highly concentrated stable meloxicam solutions for needleless injection |
| DE10226537A1 (en) | 2002-06-14 | 2004-01-08 | Peter Eichhorst | pre-injection device |
| US7699052B2 (en) | 2002-09-05 | 2010-04-20 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Apparatus for the dispensing of liquids, container cartridge suitable for this, and system comprising the apparatus for the dispensing of liquids, and the container cartridge |
| US8992980B2 (en) | 2002-10-25 | 2015-03-31 | Boehringer Ingelheim Vetmedica Gmbh | Water-soluble meloxicam granules |
| DE10252917A1 (en) * | 2002-11-12 | 2004-05-27 | Lothar Bode | Device used for applying substances under pressure to skin comprises main component with pressure medium container, controllable stop valve, pressure reducer and nozzle |
| DE20218974U1 (en) * | 2002-12-07 | 2003-07-10 | Boehringer Ingelheim Pharma | Atomizers for liquids |
| DE10340586A1 (en) * | 2003-09-03 | 2005-04-07 | Tecpharma Licensing Ag | Mixing device for multi-chamber ampoule |
| DE102004001451A1 (en) | 2004-01-08 | 2005-08-11 | Boehringer Ingelheim International Gmbh | Device for holding a fluidic component |
| EP1568369A1 (en) | 2004-02-23 | 2005-08-31 | Boehringer Ingelheim Vetmedica Gmbh | Use of meloxicam for the treatment of respiratory diseases in pigs |
| US20070055200A1 (en) * | 2005-08-10 | 2007-03-08 | Gilbert Scott J | Needle-free jet injection drug delivery device |
| DE202006018609U1 (en) * | 2006-08-29 | 2007-05-16 | Euro-Celtique S.A. | Needle-free apparatus for administrating pharmaceutical composition in humans, comprises a housing; auxiliary substance to force a pharmaceutical composition from a package into human body; a composition comprising analgesic, e.g. opioids |
| KR100876650B1 (en) * | 2007-04-13 | 2009-01-09 | (주) 비에이치케이 | Apparatus for vascular access |
| DE102009002826A1 (en) | 2009-05-05 | 2010-11-11 | Beiersdorf Ag | Needle-free injection system for delivering cosmetic active ingredients in dermis or epidermis for restructuring connective tissue, improving skin aging, reducing scar tissue and modulating sweating, comprises injector and drug formulations |
| CA2777366C (en) | 2009-10-12 | 2023-11-14 | Boehringer Ingelheim Vetmedica Gmbh | Containers for compositions comprising meloxicam |
| US8932398B2 (en) | 2009-10-29 | 2015-01-13 | Mylan Group | Gallotannic compounds for lithographic printing plate coating compositions |
| AU2010347598B2 (en) | 2010-03-03 | 2014-11-27 | Boehringer Ingelheim Vetmedica Gmbh | Use of meloxicam for the long-term treatment of musculoskeletal disorders in cats |
| US9795568B2 (en) | 2010-05-05 | 2017-10-24 | Boehringer Ingelheim Vetmedica Gmbh | Low concentration meloxicam tablets |
| KR101313632B1 (en) | 2013-01-18 | 2013-10-02 | 한국기계연구원 | Needle free injector |
| KR20160094037A (en) | 2015-01-30 | 2016-08-09 | 권은미 | Assembly type Pallet |
| CN105413024A (en) * | 2016-01-07 | 2016-03-23 | 深圳市赫拉铂氢时代科技有限公司 | Nanometer/micrometer hydrogen water needle-free injector and injection method thereof |
| KR101939061B1 (en) | 2017-06-22 | 2019-01-17 | (주)엠큐어 | Injector capable of metering |
| KR102107578B1 (en) | 2018-05-02 | 2020-05-07 | 주식회사 피테크 | Constant velocity infusion device for painless syringe and painless sylinge having the same |
| KR102104080B1 (en) | 2018-05-02 | 2020-04-23 | 주식회사 피테크 | Sonic vibration device for painless syringe and painless sylinge having the same |
| KR101907552B1 (en) | 2018-05-03 | 2018-10-12 | 주식회사 피테크 | Painless injection device without needle |
| DE202018102738U1 (en) * | 2018-05-16 | 2018-09-10 | Ira Yasmin Lehmann | Needle-free injection system |
| KR102199724B1 (en) | 2018-10-05 | 2021-01-07 | 주식회사 피테크 | Painless injection device without needle |
| CN109432553B (en) * | 2018-11-19 | 2024-04-16 | 北京快舒尔医疗技术有限公司 | Syringe head assembly of medicine storage tube of needleless injector, medicine storage tube and needleless injector |
| KR102248430B1 (en) | 2019-04-22 | 2021-05-06 | 주식회사 피테크 | Portable painless injection device without needle |
| JP7039703B2 (en) * | 2019-06-19 | 2022-03-22 | ジウン イ | Nozzle assembly, syringe body, and needleless syringe containing it |
| CN111110958B (en) * | 2020-02-06 | 2021-08-17 | 唐文珍 | Syringe used in medical field |
| CN111558112B (en) * | 2020-04-30 | 2021-09-24 | 北京快舒尔医疗技术有限公司 | Injection head of needleless injector, needleless injector body and needleless injector |
| WO2021218108A1 (en) * | 2020-04-30 | 2021-11-04 | 北京快舒尔医疗技术有限公司 | Injection nozzle for needle-free injector, needle-free injector body, and needle-free injector |
| CN111870456B (en) * | 2020-08-04 | 2021-09-07 | 张家港江苏科技大学产业技术研究院 | Labor-saving mechanical device |
| KR102463473B1 (en) * | 2020-10-26 | 2022-11-04 | 미라클스코프(주) | Needleless syringe with portable drug inlet |
| KR102244030B1 (en) | 2021-02-16 | 2021-04-23 | 주식회사 피테크 | Assistannt kits for injecting liquid medicine of painless injection device without needle |
| CN113767773B (en) * | 2021-08-16 | 2022-11-04 | 北京农业智能装备技术研究中心 | Embedded device for slowly releasing liquid from plant tissue |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3115375A1 (en) | 1981-04-16 | 1982-11-11 | Hoechst Ag, 6000 Frankfurt | PISTON PUMP FOR NEEDLE-FREE INJECTION EQUIPMENT |
| DE3115376A1 (en) | 1981-04-16 | 1982-12-16 | Hoechst Ag, 6000 Frankfurt | NEEDLE-FREE INJECTION DEVICE |
| HU186718B (en) * | 1983-06-29 | 1985-09-30 | Radelkis Electrokemiai | Automatic needleless syringe operable by cardox cylinder suitable for personal giving injection e.g. insulin |
| FR2629706B1 (en) * | 1988-04-11 | 1992-05-22 | Accaries Claude | LIQUID INJECTION APPARATUS, PARTICULARLY FOR USE IN DENTAL CARE |
| US4913699A (en) | 1988-03-14 | 1990-04-03 | Parsons James S | Disposable needleless injection system |
| JPH0284962A (en) * | 1988-06-14 | 1990-03-26 | Vci Corp | Negative pressure press contact needle free syringe |
| AU6550990A (en) * | 1989-11-09 | 1991-05-16 | Bioject, Inc. | Needleless hypodermic injection device |
| CA2095858A1 (en) | 1990-11-09 | 1992-05-10 | Peter Elliott Rosenzweig | Needleless hypodermic jet injector device |
| GB9118204D0 (en) | 1991-08-23 | 1991-10-09 | Weston Terence E | Needle-less injector |
| RU2179864C2 (en) | 1993-07-31 | 2002-02-27 | Вестон Медикал Лимитед | Needleless injector |
| DE19536902A1 (en) * | 1995-10-04 | 1997-04-10 | Boehringer Ingelheim Int | Miniature fluid pressure generating device |
| DE19545226C1 (en) | 1995-12-05 | 1997-06-19 | Boehringer Ingelheim Int | Locking mechanism for a spring-operated output |
-
2000
- 2000-03-03 DE DE10010123A patent/DE10010123A1/en not_active Withdrawn
-
2001
- 2001-02-03 UA UA2002107806A patent/UA70409C2/en unknown
- 2001-03-01 PE PE2001000210A patent/PE20011111A1/en not_active Application Discontinuation
- 2001-03-01 EG EG20010223A patent/EG22864A/en active
- 2001-03-02 HU HU0300550A patent/HU226578B1/en not_active IP Right Cessation
- 2001-03-02 AU AU2001250347A patent/AU2001250347B2/en not_active Ceased
- 2001-03-02 EE EEP200200494A patent/EE04583B1/en not_active IP Right Cessation
- 2001-03-02 KR KR1020027011544A patent/KR100777146B1/en not_active IP Right Cessation
- 2001-03-02 AR ARP010100998A patent/AR027595A1/en active IP Right Grant
- 2001-03-02 DE DE50106892T patent/DE50106892D1/en not_active Expired - Lifetime
- 2001-03-02 EA EA200200877A patent/EA200200877A1/en not_active IP Right Cessation
- 2001-03-02 MX MXPA02008581A patent/MXPA02008581A/en active IP Right Grant
- 2001-03-02 MY MYPI20010966A patent/MY126848A/en unknown
- 2001-03-02 ES ES01923619T patent/ES2247092T3/en not_active Expired - Lifetime
- 2001-03-02 PT PT01923619T patent/PT1263490E/en unknown
- 2001-03-02 RS YU64502A patent/RS49509B/en unknown
- 2001-03-02 AU AU5034701A patent/AU5034701A/en active Pending
- 2001-03-02 EP EP01923619A patent/EP1263490B1/en not_active Expired - Lifetime
- 2001-03-02 CN CNB018059465A patent/CN1179763C/en not_active Expired - Fee Related
- 2001-03-02 CZ CZ20022970A patent/CZ20022970A3/en unknown
- 2001-03-02 PL PL357343A patent/PL200838B1/en unknown
- 2001-03-02 JP JP2001563164A patent/JP2003525086A/en active Pending
- 2001-03-02 TW TW090104904A patent/TW541185B/en not_active IP Right Cessation
- 2001-03-02 IL IL15146501A patent/IL151465A0/en active IP Right Grant
- 2001-03-02 CA CA002404360A patent/CA2404360C/en not_active Expired - Fee Related
- 2001-03-02 SK SK1250-2002A patent/SK12502002A3/en unknown
- 2001-03-02 AT AT01923619T patent/ATE300325T1/en active
- 2001-03-02 NZ NZ521723A patent/NZ521723A/en not_active IP Right Cessation
- 2001-03-02 BR BR0108914-5A patent/BR0108914A/en not_active Application Discontinuation
- 2001-03-02 WO PCT/EP2001/002356 patent/WO2001064268A1/en active IP Right Grant
- 2001-03-02 DK DK01923619T patent/DK1263490T3/en active
- 2001-03-28 SA SA01220003A patent/SA01220003B1/en unknown
-
2002
- 2002-08-08 BG BG106987A patent/BG64726B1/en unknown
- 2002-08-26 IL IL151465A patent/IL151465A/en not_active IP Right Cessation
- 2002-08-30 ZA ZA200206987A patent/ZA200206987B/en unknown
- 2002-09-02 NO NO20024170A patent/NO20024170D0/en not_active Application Discontinuation
- 2002-09-02 HR HRP20020720 patent/HRP20020720A2/en not_active Application Discontinuation
-
2003
- 2003-09-01 HK HK03106240A patent/HK1053990A1/en not_active IP Right Cessation
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8221347B2 (en) | 2004-12-01 | 2012-07-17 | Acushot, Inc. | Needle-free injector |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2404360C (en) | Needle-less injector of miniature type | |
| US6689092B2 (en) | Needle-less injector of miniature type | |
| JP3260375B2 (en) | Particle input | |
| US10099011B2 (en) | Needle-less injector and method of fluid delivery | |
| JP4035127B2 (en) | Needleless syringe | |
| CA1295902C (en) | Automatic injector and cartridge or ampoule for use in injectors | |
| EP0686053B1 (en) | Apparatus for injecting a pharmaceutical preparation in solid form | |
| JPH09512719A (en) | Needleless injection syringe | |
| WO1996024398A1 (en) | Needle-less injector |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| MKLA | Lapsed |
Effective date: 20160302 |