Systems, devices and methods
The device addresses fluid loss and contamination issues in needle-free injection by using two fluids with controlled release and a detachable dosing unit, ensuring precise and sterile delivery of therapeutic fluids.
Patent Information
- Application Number
- JP2022122986
- Authority / Receiving Office
- JP · JP
- Patent Type
- Patents
- Current Assignee / Owner
- Priority Date
- 2021-08-10
- Filing Date
- 2022-08-01
- Publication Date
- 2026-02-10
- Estimated Expiration
- 2042-08-01
AI Technical Summary
Existing needle-free injection devices require complete filling of treatment fluid channels, leading to unwanted fluid losses and contamination risks, especially when using patient-specific treatments, and lack controlled fluid release mechanisms for sensitive fluids like biological cells.
A device utilizing two fluids, where a first fluid opens a channel with a high-pressure impulse and a second fluid is released gradually by a dosing unit with a drive mechanism, minimizing dead volumes and allowing controlled release of therapeutic fluids, with a detachable dosing unit for sterilization and reuse.
Minimizes fluid loss and contamination risks, enables precise administration of sensitive fluids, and allows for sterilization and reuse of the device components, ensuring efficient and sterile treatment fluid delivery.
Smart Images

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Abstract
Description
[Technical Field]
[0001] The present invention relates to a device for administering medicinal fluids to the animal or human body, and further to an apparatus for operating the device and a method for generating a fluid flow from two different fluids. [Background technology]
[0002] For example, for needle-free injection of drugs and other medically effective fluids into tissues of the human or animal body, devices are used that use fluid delivered under high pressure to penetrate the patient's skin and needle-free create a through channel through which therapeutic fluid under lower pressure is subsequently introduced.
[0003] Patent document 1 discloses an applicator in which a therapeutic fluid, such as a hemostatic agent, can be atomized by pressurized air or another pressurized gas and applied in this way to the area to be treated. The applicator comprises a holder having a fluid channel in which a valve is arranged and which can be connected to a gas pressure source. The fluid channel opens at a spray nozzle. A conventional syringe can be attached to the applicator. When holding the applicator in the hand, the user can open the valve for the air channel with one finger and activate the syringe plunger with their thumb, so that the liquid contained in the syringe is guided to the spray nozzle and released there in the form of a mist.
[0004] Furthermore, Patent Document 2 discloses an instrument for needleless injection of a substance into the body. The instrument comprises a reservoir for storing the substance to be injected, connected to an injection nozzle via a fluid channel. To expel the therapeutic fluid in a short, sharp jet, a plunger disposed in the reservoir is assigned an electrodynamic drive that generates a fluid pressure transition with a very steep front flank at the injection nozzle. The pressure increase generates a sharp liquid jet suitable for penetrating the skin. After the sudden pressure increase, the pressure decreases to a lower level to inject the liquid into the tissue and finally returns to zero after the end of the operating cycle.
[0005] Furthermore, for needleless injection of a therapeutic liquid, Patent Document 3 proposes an instrument having a plurality of fluid channels for delivering different liquids to an injection nozzle, in particular a central channel for the injection fluid for opening the through-channels, the central channel being surrounded by a second channel for delivering the therapeutic liquid towards the injection nozzle.
[0006] The device is basically well suited for use on a patient. However, for this purpose, the channels provided for the treatment fluid must be completely filled with this fluid. If a patient-specific treatment fluid is used, a larger volume of treatment fluid must be provided than the volume of fluid to be administered to the patient.
[0007] This also applies to the system according to US Pat. No. 5,699,499, in which an instrument with two fluid channels is known: the first channel conducts the injection fluid and the second channel conducts the treatment fluid to the application nozzle. For supply, a device is provided which has a pressure accumulator and a number of valves, and in particular supplies the instrument with the injection fluid at a predetermined pressure. [Prior art documents] [Patent documents]
[0008] [Patent Document 1] European Patent Application Publication No. 3015076 [Patent Document 2] US Patent Application Publication No. 2013 / 0102957 [Patent Document 3] European Patent Application Publication No. 3714926 [Patent Document 4] European Patent No. 3040101 Summary of the Invention [Problem to be solved by the invention]
[0009] It is an object of the present invention to provide an improved concept for needle-free administration of therapeutic fluids. [Means for solving the problem]
[0010] This object is achieved by an appliance according to claim 1, a device according to claim 12 and a method according to claim 15.
[0011] The device according to the present invention is useful for injecting a medicinal solution into an animal or human body. To this end, the device utilizes two different fluids. The first fluid serves for needleless opening of a channel (through channel) in the tissue to be treated and is released with a pressure impulse having a sudden pressure rise at the front flank. The device further comprises a dosing unit having a compartment for a fluid container containing a second fluid. The second fluid is preferably a therapeutic fluid, such as a medicinal solution, a cell suspension, or any other liquid useful for treating the human or animal body or tissue. The dosing unit includes a drive unit capable of pressurizing the fluid container or, specifically, reducing its volume. For example, the drive unit can act on the fluid container to reduce its volume so as to gradually release the second fluid.
[0012] When the fluid container is placed in a dispensing unit directly attached to the device, dead volumes are minimized. This avoids unwanted losses of treatment fluid, especially during patient-specific treatment fluid use. Furthermore, the preparation of the device and the preparation of the supply device are simplified. The risk of treatment fluid residues from the previous treatment remaining in channels, pumps, or valves, and thus contaminating the treatment fluid for the next patient, is minimized.
[0013] Controlling and releasing the first and second fluids with the same device allows for a regulated and careful release of the fluids, for example, the second fluid may contain biological cells that must not be subjected to high pressure fluctuations or shear forces, and can be administered particularly carefully with the aid of the device according to the invention using the instrument according to the invention.
[0014] The dispensing unit can be detachably attached to the device. This is therefore particularly advantageous when the dispensing unit itself does not include any part that comes into contact with the first or second fluid. For example, the dispensing unit can consist of a housing having a compartment for a fluid container and a drive unit that applies force or pressure to the fluid container. When the dispensing unit is detached from the device, the device can be sterilized or completely replaced without the need to replace the dispensing unit. The dispensing unit can be reused. If necessary, the dispensing unit can also be washed and further sterilized.
[0015] The instrument can have a shank including a bendable portion at its distal end, and a manipulation element can be provided on the housing to control bending of the shank. Such an instrument is suitable, for example, for insertion into the ureter or another body cavity and for injection of a carrier liquid containing biological cells, for example, into a sphincter. For this purpose, the fluid channel can include a jet focus outlet opening at its distal end.
[0016] A valve arrangement may be provided within the housing of the instrument for generating a high pressure fluid impulse within the fluid channel, however, this valve arrangement may also be part of the device providing the instrument.
[0017] The first fluid is delivered from the device via a hose to the appliance, and the dosing unit can be connected to the appliance via an electrical line, with control of the dosing unit then being performed by the device to which the appliance is connected.
[0018] The housing of the device can include a fluid connector for the fluid container and a mechanical plug connector for the plug device provided on the dosing part. The fluid container, for example in the form of a cartridge or syringe, can then be fluidly connected to the housing and protrude into the dosing part for mechanical operation. This is advantageous if the plug device and the plug connector have corresponding directions of movement. As a result, when the fluid container is inserted into the compartment, the dosing part simultaneously presses the fluid container against the fluid connector when it is plugged into the housing, thereby establishing a fluid connection. For example, the fluid container can be a cartridge or any other container with a movable plunger.
[0019] The drive of the dosing unit preferably comprises an actuation motor, e.g., a stepper motor, configured to act on the fluid container via a gear. For example, the gear is a spindle-type gear that converts the rotational movement of the actuation motor into a linear movement, which in turn allows a plunger, which is part of the fluid container, to move in a specifically controlled manner. By controlling each of the actuation motors, the output of the drive acting on the fluid container can move along a defined distance length, thereby discharging a defined amount of liquid.
[0020] To provide the device, a device can be provided that includes a control unit that initiates the ejection of a first fluid with a first high pressure impulse followed by a lower pressure, and further activates the dosing unit after the high pressure impulse to generate a lower pressure impulse to eject a second fluid through the fluid channel at a lower pressure.
[0021] Using this concept, a channel is opened in the tissue by a first fluid. After the first pressure impulse decays, and after a further period of time, a therapeutic liquid (second fluid) is delivered into the first fluid so as to be carefully introduced into the tissue. The device can supply the first fluid into a pressure vessel, and the first fluid can be output from the pressure vessel in an impulse by a rapidly switching valve. Furthermore, the device can have an electrical connector for the dispensing portion of the instrument.
[0022] Further details of advantageous embodiments of the invention follow from the drawings or the description and the dependent claims. [Brief explanation of the drawings]
[0023] [Figure 1] FIG. 1 is a schematic basic diagram of an instrument and delivery device according to the present invention. [Figure 2] FIG. 2 is a schematic basic diagram of a variation of the device. [Figure 3] FIG. 3 is a partial longitudinal cutaway view of the dispensing part of the device according to FIG. 1 or FIG. [Figure 4] FIG. 4 is a basic longitudinal cross-sectional view of the interface between the device and the administration part. [Figure 5] FIG. 5 is a functional design diagram of the instrument and device according to FIGS. [Figure 6] FIG. 6 is an idealized diagram of the pressure rise during the ejection of the first and second fluids. DETAILED DESCRIPTION OF THE INVENTION
[0024] 1 shows a device 10 for injecting medicinal fluids into the human or animal body, in particular for needleless injection of such fluids into bodily tissues. The device 10 is connected to a supply device 11 useful for supplying energy and / or a medium, for example a sodium chloride solution, to the device.
[0025] The instrument 10 comprises a housing 12 from which a shank 13 extends distally to its distal end 14 at which an injection opening 14a is disposed for outputting a fluid jet. The housing 12 may be provided with a handle 15 for manual guidance of the instrument 10.
[0026] To treat a patient, for example to output a medicinal solution to be injected into the patient's tissue, the device 10 is further provided for this purpose with a dispensing portion 16. The dispensing portion 16 may be located in any suitable location on the housing 12, for example, on the side, on the top, in the handle 15, or on the proximal rear surface opposite the shank 13 as shown in FIG.
[0027] An instrument 10 provided for needleless injection of a medical solution into living tissue uses a first fluid to open a through channel in the tissue, the first fluid being a liquid dispensed at high pressure that can be supplied by a device 11 via a fluid line 17, by which the device 11 is connected to the instrument 10.
[0028] A second fluid, e.g., a medically effective liquid, is introduced into the patient's tissues by means of a dosing unit 16. To control the dosing unit 16, the device 11 can be connected to the instrument 10 via an electrical line 18, e.g., realized by a two-core or multi-core cable.
[0029] To activate the instrument 10, a switch may be provided on the instrument 10, which in turn is connected to the device 11 via a control line or another control connection, not shown. Alternatively, other switches, such as a foot switch, may also be used.
[0030] The instrument 10 shown in Fig. 1 in a particularly simple form can have additional functionality, such as a bendable distal end 14, so that bending can be effected, for example, by means of a control lever 19. The control lever 19 can be arranged near the handle 15 or even at another location on the instrument 10. Furthermore, the shank 13 can be rotatably arranged on the housing 12, for which purpose a respective swivel connector 20 can be provided. Otherwise, the description referring to the instrument 10 according to Fig. 1 also applies to the instrument 10 according to Fig. 2.
[0031] The dispensing portion 16 of the device 10 includes a compartment 21 for a fluid container 22 containing a medical treatment liquid, such as a cell suspension containing biological cells or a drug solution. The compartment 21 can extend into the housing 12. For example, the fluid container 22 can be configured like a piston syringe and, to this end, can include a cylinder 23 in which a piston 24 is arranged, the piston rod of the piston 24 protruding from the cylinder 23.
[0032] 3, the dosing unit 16 includes a drive unit 25, which may be configured as a motor having a rotatable rotor 25a that linearly moves a plunger 26 via gears, e.g., a spindle-type lifting device 25b. The drive unit 25 thereby gradually moves the plunger 26 in order to (slowly) displace a piston in the cylinder 23 by the plunger 26 via the piston rod 24. Thus, a "slow" displacement of the piston rod 24 refers to a movement that does not result in a pressure increase in the fluid container 22 that would adversely affect the treatment fluid.
[0033] The compartment 21 extends with a portion 21' entering the housing 12, as shown in Figure 4. Inside the housing 12, a connecting branch 27 suitable for connecting a fluid container 22 can be provided at the bottom of the compartment 21, 21'. The connecting branch 27 is shown only diagrammatically in Figure 4. In either case, the connecting branch 27 matches the connection of the fluid container 22 so as to establish a fluid-tight connection as soon as the fluid container 22 is inserted into the compartment 21 and moves towards the connecting branch 27. This allows it to penetrate a potential closure or seal of the fluid container 22.
[0034] The dosing part 16 is provided in particular so that the fluid container 22 can be exchanged. According to Figure 4, for this purpose, a special interface can be provided between the housing 12 and the dosing part 16, which in particular allows the dosing part 16 to remain in abutment against the housing 12, to be only slightly displaced from the housing 12 or to be completely removed from the housing 12.
[0035] For this purpose, the dispensing part 16 can be attached to the housing 12 by a latch coupling 28. In a simple and convenient embodiment, the latch coupling 28 can comprise, for example, two latch pins 29, 30, each assigned with a latch opening 31, 32 configured in the housing 12. The latch pins 29, 30 can have a circular cross section or any other suitable cross section, for example an oval or polygonal cross section, and can each be provided with a recess, i.e., for example, a flat area 33, 34, 35, along part of their length. For example, the latch pin 29 can have a long flat area, while the latch pin 30 can be provided with two short, groove-like flat areas 34, 35 arranged at an axial distance from each other. Latch sliders 36, 37 can be assigned to the flat areas 33-35 for selectively locking or releasing the latch pins 29, 30 inside the latch openings 31, 32. The latch sliders 36, 37 and flat areas 33-35 are thereby arranged relative to one another such that release of the latch slider 37 allows movement of the dosing part 16 away from the housing 12 within the axial length of the flat area 33. When the slider 37 is locked within the flat area 35, the latch slider 36 is located on the proximal side of the flat area 33. When the latch slider 37 is locked within the flat area 34, the latch slider 36 is located on the distal side of the flat area 33. Only by releasing both latch sliders 36, 37 can the dosing part 16 be removed from the housing 12. However, the flat areas and latch slider are not required.
[0036] The ability to detach the dispensing portion 16 from the device 10 allows the device 10 to be configured as a disposable or sterilizable device, although the dispensing portion 16 is essentially reusable. However, in variants, the reusable part can also include the housing, the handle 15 or parts thereof. The device can also be completely sterilizable.
[0037] 5 shows the cooperating functional units and components of the tool 10 and the device 11. It is noted hereby that some or all of the components and units of the device 11 described below may also be fully or partially integrated into the tool 10. However, the tool 10 comprises at least a shank 13, a housing 12 and a dispensing part 16.
[0038] The device 10 includes a first fluid channel 40 that emits a first fluid at the distal end 14 as a concentrated jet at a pressure high enough to penetrate biological tissue without the aid of an injection needle and open a channel therein. The first fluid is preferably an aqueous sodium chloride solution, by way of example, although other fluids can be used. The first fluid is supplied under pressure by a pump 41 from a reservoir (not shown) to a pressure vessel 42 that is connected to the first fluid channel 40 via a valve 43. The pressure vessel 42 can also consist of only a supply line, allowing a separate pressure vessel to be optionally omitted.
[0039] Valve 43 is controlled by a controller 44, i.e., open-loop controlled, and can therefore be selectively opened or closed. In a rest state (at the start of administration), valve 43 is closed. A further valve 45, which is closed in a rest state, branches off from fluid channel 40. Valve 45 serves to relieve pressure in fluid channel 40 and selectively connects fluid channel 40 to an outlet via a throttle 46. Valve 45, and optionally throttle 46, can be connected to controller 44 so as to be controlled by controller 44.
[0040] The dosing part 16 includes as functional components, in particular, a drive part 25 and a fluid reservoir 22 that functions as a piston pump. The fluid reservoir 22 is connected to a second fluid channel 47 that extends from the branch connection 17 to the distal end 14 of the shank 13. The fluid channels 40, 47 can alternatively be joined inside the shank 13 at the distal end 14 of the shank 13 or inside the housing 12.
[0041] The instrument 10 and device 11 described thus far both operate as follows.
[0042] To initiate and prepare the injection of the therapeutic liquid into the tissue, the first dosing part 16 is supplied with the therapeutic liquid. For this purpose, the fluid container 22 is inserted into the compartment 21. To simplify or enable this process, the drive 25 moves the plunger 26 to a proximal position, which can be initiated by the control device 44 accordingly. The user can now partially remove the dosing part 16 from the housing 12 by operating at least the latch slider 37, and thus insert the fluid container 22 into the compartment 21 with the piston rod of the piston 24 protruding from the fluid container 22. When this is done, the slider 37, which was previously locked in the flat area 34, can be released, and the dosing part 16 can be pressed against the housing 12 until the slider 37 locks in the flat area 35. The fluid container 22 then connects to the connecting branch 27 so as to communicate with the second channel 47.
[0043] Additionally, the controller 44 operates the pump 41 to fill the pressure vessel 42 with the infusion fluid and to pressurize the pressure vessel 42. Filling the pressure vessel can be part of the dispensing process. As a further preparation step, the first fluid channel 40 can be filled with the first fluid, i.e., the infusion fluid, and thus the first fluid channel 40 can be vented. Once this is done, the device 10 is ready for use.
[0044] To administer the treatment fluid, the shank 13 is now inserted into the patient's body, for example into a patient's lumen, such as the ureter or another natural channel. The tissue portion to which the treatment fluid is to be administered is located by the distal end 14. Once at that location, the first fluid (infusion fluid) and the second fluid (treatment fluid) are output by the mechanism according to Figure 6. The time-dependent pressure profiles of the two fluids are ideally shown in Figure 6.
[0045] Initially, the first fluid is ejected at a steep pressure flank 50 by opening valve 43 while valve 45 is closed. This creates a sharp liquid jet at distal tip 14 that penetrates the tissue layers and enters the tissue. After a short period (a few milliseconds), valve 45 opens, causing a reduction in the pressure of the infusion fluid by back flank 51. The first fluid is then continuously supplied with a reduced pressure, as shown by curve 52 in FIG. 6 . Meanwhile, controller 44 activates drive 25 to eject the second fluid (the therapeutic liquid) at distal tip 14 at a lower pressure, ideally shown by curve 53. The therapeutic fluid is then carried by the infusion fluid and introduced into the tissue.
[0046] The injection treatment is then completed: the drive 25 is deactivated and first the valve 43 is closed, followed immediately or simultaneously by the valve 45.
[0047] The injection process can be repeated in a similar or identical manner at the same or another location until fluid container 22 is empty. Alternatively, the pressure reduction can be achieved by reducing the pump's delivery capacity. In this case, valve 45 is opened for a short period of time to reduce the pressure quickly, i.e., with a steep backflank. Following the backflank, valve 45 is closed, while valve 43 remains open.
[0048] To continue treatment, the dispensing portion 16 can be partially or completely removed from the housing 12 using the latch sliders 36, 37 as appropriate to replace the fluid container 22. Treatment can then continue as described.
[0049] The device 10 according to the present invention includes a dosing unit 16 connected to the handle or housing 12 of the device 10. The length of the supply line for the administered medically effective substance is significantly reduced compared to solutions in which the dosing unit is part of the delivery device. The dosing unit 16 can essentially consist of a reusable actuator including a drive unit 25 and a disposable cartridge including a cylinder and a piston, e.g., a medical syringe. The disposable cartridge can be filled by the user immediately before the intervention or prefilled by the manufacturer. The disposable cartridge is simply inserted into the device. For this purpose, the dosing unit 16 is brought into an open position, offset from the housing 12. This is achieved by operating the latch slider 37, which pulls the dosing unit proximally. After insertion of the cartridge (fluid container 22), the dosing unit can be brought into a closed position, i.e., moved toward the housing 12. This establishes a fluid-tight connection between the cartridge and the second fluid channel 47. The latch slider 37 then locks the dosing unit 16 in this position. [Explanation of symbols]
[0050] 10. Equipment 11 Equipment 12. Case 13 Shank 14 Distal end of shank 13 14a Injection opening 15 Handle 16 Administration site 17 Fluid Lines 18 Electrical Lines 19 Control lever 20 Swivel Connector 21 compartments Part of a 21' compartment 22 Fluid container 23 cylinders 24 Piston with piston rod 25 Drive unit 25a rotor 25b Spindle-type lifting device 26 Plunger 27 Connecting Branches 28 Latch coupling / plug device 29, 30 Latch pin 31, 32 Latch opening 33~35 Flat area / recess 36, 37 Latch slider 40 First fluid channel 41 Pump 42 Pressure Vessels 43 Valve 44 Control device 45 valve 46 Throttle 47 Second Fluid Channel 50 Sudden pressure increase 51 Back Flank 52, 53 curve
Claims
1. A system comprising an instrument (10) for injecting a medicinal solution into the body of an animal or a human, and a supply device (11) for operating said instrument (10), The device (10) comprises: a housing (12) provided with a handle (15) for holding and guiding the instrument (10); a distally extending shank (13) including at least one fluid channel (40); a fluid line (17) connected to a supply device (11) that supplies a first fluid under pressure to said device (10); a dosing part (16) including a compartment (21) for a fluid container (22) containing a second fluid and including a drive part (25) for pressurizing said fluid container (22); The supply device (11) a control device (44) for actuating the dosing portion (16) during the ejection of the first fluid at a lower pressure after the first high pressure impulse to generate a low pressure impulse to initiate the ejection of the first fluid at a lower pressure and to eject the second fluid through the fluid channel (47) at a lower pressure. system.
2. The dispensing part (16) is detachably attached to the housing (12). The system of claim 1 .
3. The shank (13) includes a bendable portion at its distal end (14), and at least one operating element (19) for controlling bending of the shank (13) is provided on the housing (12) of the instrument (10). The system of claim 2 .
4. The fluid channel (40) includes a jet focus outlet opening at its distal end. The system of claim 1 .
5. The instrument (10) or the device (11) comprises a valve device (43, 45) for generating a high pressure impulse (50) in the fluid channel (40). The system of claim 1 .
6. The dispensing portion (16) includes an electrical line (18) that can be connected to the control device (44). The system of claim 1 .
7. The housing (12) includes a fluid connection (27) for the fluid container (22) and mechanical plug connections (31, 32) for a plug device (28) provided on the dosing part (16). The system of claim 1 .
8. The fluid connection (27) and the plug device (28) have a coincident direction of operation. The system of claim 7.
9. The fluid container (22) includes a movable piston (24). The system of claim 1 .
10. The fluid container (22) includes a movable piston (24), and the direction of movement of the piston (24) coincides with the direction of movement. The system of claim 8.
11. The drive (25) includes a servo motor configured to act on the fluid container (22) via gears. The system of claim 1 .
12. A device (11) for operating an instrument (10) for injecting a medicinal solution into the body of an animal or a human, comprising: The device (10) comprises: a housing (12) provided with a handle (15) for holding and guiding the instrument (10); a distally extending shank (13) including at least one fluid channel (40); a fluid line (17) connected to a supply device (11) that supplies a first fluid under pressure to said device (10); a dosing part (16) including a compartment (21) for a fluid container (22) containing a second fluid and including a drive part (25) for pressurizing said fluid container (22); The device (11) comprises: Initially, a first high pressure impulse (50) followed by a lower pressure initiates the ejection of said first fluid through said fluid channel (40); activating the dosing portion (16) to generate a low-pressure impulse (53) during the ejection of the first fluid at a lower pressure after the high-pressure impulse (50) to eject the second fluid through the fluid channel (47) at a lower pressure; Equipped with a control device (44) Device.
13. The device (11) comprises a pressure vessel (42) capable of being filled under high pressure with the first fluid by a pump (41) and capable of generating the high pressure impulse (50) connectable to the instrument (10) via a release valve (43).
13. The apparatus of claim 12.
14. The device (11) comprises a fluid output for connecting the fluid line (17) of the device (10) and an electrical connection for the dosing part (16).
13. The apparatus of claim 12.
15. 1. A method for producing a fluid stream from two different fluids, comprising: a first fluid is provided in a pressure vessel (42) under a first pressure and is directed into a fluid line (40) by a quick-open valve (43), followed by a lower pressure to initiate the discharge of said first fluid through said fluid line (40); a second fluid is supplied into the container (22) at atmospheric pressure and is passed into the fluid line (47) during the discharge of the first fluid at a lower pressure after the valve (43) is opened by reducing the volume of the container (22) under a second pressure less than the first pressure; A drive unit (25) having a servo motor is provided to reduce the volume of the container (22), and the drive unit (25) and the valve (43) are controlled by a common control device (44). method.
Citation Information
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