AMBULATORY INFUSION SYSTEM WITH DETACHABLE DRUG CONTAINER

• US 20140378943A1
• Filed: 06/20/2014
• Published: 12/25/2014
• Est. Priority Date: 06/21/2013
• Status: Active Application

• Current Assignee: Roche Diabetes Care Inc. (Roche Holding AG)
• Original Assignee: Roche Diagnostics International AG (Roche Holding AG)
• Inventors: Geipel, Andreas
• Application Number:
  US14/310,462
• Publication Number:
  US 20140378943A1
• Time in Patent Office: Days
• US Class Current: 604/506
• CPC Class Codes: A61M 2005/14268 with a reusable and a disposable component
• CPC Class Codes: A61M 2005/16868 Downstream occlusion sensors
• CPC Class Codes: A61M 2005/3114 Filling or refilling
• CPC Class Codes: A61M 2205/14 Detection of the presence or absence of a tube, a connector or a container in an apparatus
• CPC Class Codes: A61M 2205/18 with alarm
• CPC Class Codes: A61M 2205/3355 Controlling downstream pump pressure
• CPC Class Codes: A61M 2205/3368 Temperature
• CPC Class Codes: A61M 2205/3561 local, e.g. within room or hospital
• CPC Class Codes: A61M 2205/3569 sublocal, e.g. between console and disposable
• CPC Class Codes: A61M 2205/3584 using modem, internet or bluetooth
• CPC Class Codes: A61M 2205/3592 using telemetric means, e.g. radio or optical transmission
• CPC Class Codes: A61M 2205/36 related to heating or cooling
• CPC Class Codes: A61M 2205/3606 cooled
• CPC Class Codes: A61M 2205/3653 by Joule effect, i.e. electric resistance
• CPC Class Codes: A61M 2205/3673 thermo-electric, e.g. Peltier effect, thermocouples, semi-conductors
• CPC Class Codes: A61M 2205/6054 Magnetic identification systems
• CPC Class Codes: A61M 2209/01 Remote controllers for specific apparatus
• CPC Class Codes: A61M 2209/045 for filling, e.g. for filling reservoirs
• CPC Class Codes: A61M 5/1413 Modular systems comprising interconnecting elements
• CPC Class Codes: A61M 5/14216 Reciprocating piston type
• CPC Class Codes: A61M 5/14248 : of the skin patch type
• CPC Class Codes: A61M 5/14276 : specially adapted for implantation
• CPC Class Codes: A61M 5/16809 : by repeated filling and emptying of an intermediate volume pressure infusion using positive displacement pumps A61M5/142
• CPC Class Codes: A61M 5/1684 : by detecting the amount of infusate remaining, e.g. signalling end of infusion
• CPC Class Codes: A61M 5/16881 : Regulating valves on-off valves, e.g. clamps A61M39/28
• CPC Class Codes: A61M 5/5086 : for indicating if defective, used, tampered with or unsterile

Abstract

Methods and devices for drug infusion and for storing a drug container. The methods and devices can include ambulatory infusion systems and dosing units. The dosing units can have and an inlet port for attachment to an external liquid drug container, an outlet port, a pump kernel, and a control valve.

Claims

1. A dosing unit for an ambulatory infusion system, the ambulatory infusion system designed for the infusion of a liquid drug into a patient'"'"'s body over an extended time period, the dosing unit comprising:

an inlet port;

an outlet port, the outlet port being configured to couple to the patient'"'"'s body; and

a pump kernel, the pump kernel comprising a kernel body, the kernel body forming a limiting surface of a stepwise or continuously variable dosing volume;

a control valve, the control valve being configured to couple the variable dosing volume alternatively, in a filling state, to the inlet port for filling or refilling the dosing unit by increasing the dosing volume, or, in a infusing state, to the outlet port for dosing liquid drug out off the dosing unit by decreasing the dosing volume;

wherein the inlet port is configured for being repeatedly manually attached to and detached from an external liquid drug container, thus enabling a repeated sequence of attaching the external liquid drug container to the inlet port, filling the dosing unit with the control valve being in the filling state, detaching the liquid drug container from the inlet port and infusing drug from the dosing unit with the control valve being in the infusing state.

2. The dosing unit according to claim 1 wherein the inlet port comprises at least one of a self-sealing piercable septum, a self-closing fluidic coupler, and a check-valve.

3. The dosing unit of claim 2 wherein the dosing unit is configured to be continuously coupled, via the outlet port, to the patient'"'"'s body during the filling of the dosing unit.

4. The dosing unit of claim 3 wherein the dosing unit is designed for fluidic decoupling of the outlet port from the patient'"'"'s body prior to filling the dosing unit and re-establishing the fluidic coupling to the patient'"'"'s body after the filling.

5. The dosing unit of claim 1, wherein the dosing unit has a maximum filling volume corresponding to the total daily dose of insulin of a diabetic infant, in particular a maximum filling volume in a range of 8 to 15 International Units (IU) of liquid insulin.

6. The dosing unit according to claim 1 wherein the control valve is designed as a rotary valve or a slide valve.

7. The dosing unit according to claim 6, wherein the control valve includes the kernel body as a movable valve member and a further stationary valve member, the control valve being switchable between the filling state and the infusing state by moving the kernel body with respect to the stationary valve member.

8. The dosing unit of claim 1 wherein the pump kernel is a piston pump, with the kernel body being a pump cylinder and the pump kernel further including a piston, the piston being displaceable, in particular linearly displaceable, arranged in a cavity of the pump cylinder, such that the surfaces of the cavity and the piston, in combination, define the dosing volume.

9. The dosing unit according to claim 1, wherein the pump kernel includes a drive coupler for releasable coupling to a drive unit with a single drive, the dosing unit being designed to control force and/or torque transmission such that operation of the single drive alternatively effects both varying the dosing volume and switching the control valve between the filling state and the infusing state.

10. The dosing unit of claim 1 wherein the pump kernel includes a drive coupler for releasable coupling to a drive unit with a dosing drive for varying the dosing volume and a valve drive for switching the control valve between the filling state and the infusing state, the valve drive being separate from the dosing drive.

11. The dosing unit of to claim 1, wherein the dosing unit includes a user-operable cradle-coupler, the cradle coupler being designed to engage a dosing unit coupler of a separate skin-mountable cradle, thus enabling attachment of the dosing unit to the patient'"'"'s body via the cradle.

12. The dosing unit of claim 1 wherein the dosing unit is coupled to a base unit, the base unit comprising a drive unit, the drive unit being designed to releasable couple to the dosing unit, an electronic unit, the control unit being coupled to the drive unit for controlling operation of the infusion system alternatively in a filling mode for filling, by increasing the dosing volume, the dosing unit with liquid drug from the liquid drug container, and in an infusing mode for infusing, by decreasing the dosing volume, the liquid drug into the patient'"'"'s body.

13. The dosing unit of claim 12, wherein the control unit is further designed to activate an alarming device when, during operation of the ambulatory infusion system in the infusing mode, a filling state of the dosing kernel approaches emptiness.

14. The dosing unit of claim 12, wherein the control unit is further designed, before switching the ambulatory infusion system to the infusing mode, to request a user confirmation input.

15. The dosing unit of claim 12, wherein the control unit is designed to operate the drive unit to switch the valve arrangement from the infusing state into the filling state prior to increasing the dosing volume in the filling mode and from the filling state to the infusing state prior to decreasing the dosing volume in the dosing mode.

16. The dosing unit of claim 12, wherein the base unit includes a coupling detector, the coupling detector being coupled to the control unit to provide a signal indicating whether or not a drug container is coupled to the inlet port.

17. A method for storing a drug container comprising:

providing;

a container storage box having a storage box housing, the container storage box being a self-contained unit, the container storage box comprising a compartment for replaceably receiving a liquid drug container,

a temperature control unit housed within the storage box housing, the temperature control unit being designed to vary a temperature of a liquid drug that is stored inside the liquid drug container by actuating an electrically driven heating element and a cooling element to maintain a pre-set temperature within the container storage box;

a temperature sensor housed within the storage box housing;

the liquid drug; and

the liquid drug container storing the liquid drug; and

storing the liquid drug container inside the container storage box;

storing the container storage box inside a refrigerator;

sensing a temperature with the temperature sensor;

actuating the electrically driven heating element to maintain the pre-set temperature.

18. The method of claim 17 further comprising detecting a steep ambient temperature increase by the sensor, determining by the temperature controller the steep temperature increase is removal of the container storage box from the refrigerator, and actuating the electrically driven cooling element to maintain the pre-set temperature.

19. The method of claim 17 further comprising controlling the heating element with a clock relay.

20. A method for drug infusion comprising:

providing;

a dosing unit for an ambulatory infusion system, the ambulatory infusion system being designed for the infusion of a liquid drug into a patient'"'"'s body over an extended time period, the dosing unit comprising;

an inlet port configured for being repeatedly manually attached to and detached from an external liquid drug container;

an outlet port, the outlet port being configured to couple to the patient'"'"'s body;

a pump kernel, the pump kernel comprising a kernel body, the kernel body forming a limiting surface of a stepwise or continuously variable dosing volume,

a control valve, the control valve being configured to couple the variable dosing volume alternatively, in a filling state, to the inlet port for filling or refilling the dosing unit by increasing the dosing volume, or, in an infusing state, to the outlet port for dosing liquid drug out off the dosing unit by decreasing the dosing volume; and

attaching the external liquid drug container to the inlet port,

filling the dosing unit with the control valve in the filling state,

detaching the liquid drug container from the inlet port;

infusing the liquid drug from the dosing unit with the control valve being in the infusing state; and

repeating the attaching, filling, detaching, and infusing.