The present invention relates to components, methods, devices and systems adapted for capturing information in respect of rotational movement. In a specific aspect the invention addresses issues relating to electronic dose data capturing in and for a drug delivery device.
In the disclosure of the present invention reference is mostly made to the treatment of diabetes using a drug delivery device, however, this is only an exemplary use of the present invention.
Drug injection devices have greatly improved the lives of patients who must self-administer drugs and biological agents. Drug injection devices may take many forms, including simple disposable devices that are little more than an ampoule with an injection means or they may be durable devices adapted to be used with pre-filled cartridges. Regardless of their form and type, they have proven to be great aids in assisting patients to self-administer injectable drugs and biological agents. They also greatly assist care givers in administering injectable medicines to those incapable of performing self-injections.
Performing the necessary drug injection at the right time and in the right size is essential for managing diabetes, i.e. compliance with the specified drug regimen is important. In order to make it possible for medical personnel to determine the effectiveness of a prescribed dosage pattern, diabetes patients are encouraged to keep a log of the size and time of each injection. However, such logs are normally kept in handwritten notebooks, from the logged information may not be easily uploaded to a computer for data processing. Furthermore, as only events, which are noted by the patient, are logged, the note book system requires that the patient remembers to log each injection, if the logged information is to have any value in the treatment of the patient's disease. A missing or erroneous record in the log results in a misleading picture of the injection history and thus a misleading basis for the medical personnel's decision making with respect to future medication. Accordingly, it may be desirable to automate the logging of ejection information from medication delivery systems.
Correspondingly, a number of injection devices with a dose monitoring/acquisition feature has been provided, see e.g. in US 2009/0318865, WO 2010/052275 and U.S. Pat. No. 7,008,399. However, most devices of today are without it.
Having regard to the above, it is an object of the present invention to provide a drug delivery device as well as components, assemblies and methods therefore which in a safe, accurate, user-friendly, cost-effective and reliable way allows detection and storage of dose data related to use of a drug delivery device. It is a further object to provide such components and assemblies which could be used also in other applications having the same types of input.
In the disclosure of the present invention, embodiments and aspects will be described which will address one or more of the above objects or which will address objects apparent from the below disclosure as well as from the description of exemplary embodiments.
Thus, in a first aspect of the invention a method of manufacturing a sensor member is provided. The method comprises the step of (i) providing a sensor member in an initial state, wherein the sensor member comprises a carrier having a surface and an alignment portion, as well as at least one conducting sensor layer area formed on a portion of the carrier surface. The method comprises the further steps of (ii) providing a material-removing tool adapted to remove material from the carrier alignment portion and the sensor layer, (iii) arranging the sensor member in a fixed position relative to the tool, and (iv) control the tool to remove material from the carrier alignment portion to thereby create an alignment structure, and remove material from at least one sensor layer area to thereby create a code segment pattern, each code segment thereby being aligned with the alignment structure. More than one alignment structure may be created.
By combining the two process activities in one step, the tolerances inherent when aligning the surfaces between the two process activities are eliminated, and only the inherent tolerances in the single process of creating the pattern and alignment structure are present. The tool may for example be an ablation laser.
In an exemplary embodiment the created alignment structure is an edge portion of the carrier. The carrier is in the form of a planar board, and the at least one conducting sensor layer area may be formed on the carrier surface by a plating process to thereby create a traditional printed circuit board (PCB).
In exemplary embodiments at least one conducting sensor layer area is ring-formed, the created code segments being in the form of a plurality of annular segments each spanning a given number of degrees.
The provided carrier may have one or more additional surfaces each comprising at least one conducting sensor layer area, the tool being controlled to remove material from at least one further sensor layer area to thereby create at least one further code segment pattern. A further surface may be the opposed surface on a disc-formed carrier or the circumferential edge surface.
As used herein, the term “drug” is meant to encompass any flowable medicine formulation capable of being passed through a delivery means such as a cannula or hollow needle in a controlled manner, such as a liquid, solution, gel or fine suspension, and containing one or more drug agents. The drug may be a single drug compound or a premixed or co-formulated multiple drug compounds drug agent from a single reservoir. Representative drugs include pharmaceuticals such as peptides (e.g. insulins, insulin containing drugs, GLP-1 containing drugs as well as derivatives thereof), proteins, and hormones, biologically derived or active agents, hormonal and gene based agents, nutritional formulas and other substances in both solid (dispensed) or liquid form. In the description of the exemplary embodiments reference will be made to the use of insulin and GLP-1 containing drugs, this including analogues thereof as well as combinations with one or more other drugs.
In the following embodiments of the invention will be described with reference to the drawings, wherein
In the figures like structures are mainly identified by like reference numerals.
When in the following terms such as “upper” and “lower”, “right” and “left”, “horizontal” and “vertical” or similar relative expressions are used, these only refer to the appended figures and not necessarily to an actual situation of use. The shown figures are schematic representations for which reason the configuration of the different structures as well as their relative dimensions are intended to serve illustrative purposes only. When the term member or element is used for a given component it generally indicates that in the described embodiment the component is a unitary component, however, the same member or element may alternatively comprise a number of sub-components just as two or more of the described components could be provided as unitary components, e.g. manufactured as a single injection moulded part. When it is defined that members are mounted axially free to each other it generally indicates that they can be moved relative to each other, typically between defined stop positions whereas when it is defined that members are mounted rotationally free to each other it generally indicates that they can be rotated relative to each other either freely or between defined stop positions. The terms “assembly” and “subassembly” do not imply that the described components necessary can be assembled to provide a unitary or functional assembly or subassembly during a given assembly procedure but is merely used to describe components grouped together as being functionally more closely related.
Referring to
More specifically, the pen device comprises a cap part (not shown) and a main part having a proximal body or drive assembly portion 120 with a housing 121 in which a drug expelling mechanism is arranged or integrated, and a distal cartridge holder portion in which a drug-filled transparent cartridge 180 with a distal needle-penetrable septum can be arranged and retained in place by a cartridge holder 110 attached to the proximal portion, the cartridge holder having openings allowing a portion of the cartridge to be inspected. The cartridge may for example contain an insulin, GLP-1 or growth hormone formulation. The device is designed to be loaded by the user with a new cartridge through a distal receiving opening in the cartridge holder, the cartridge being provided with a piston driven by a piston rod 128 forming part of the expelling mechanism. A proximal-most rotatable dose ring member 125 serves to manually set a desired dose of drug shown in display window 126 and which can then be expelled when the release button 127 is actuated. Depending on the type of expelling mechanism embodied in the drug delivery device, the expelling mechanism may comprise a spring which is strained during dose setting and then released to drive the piston rod when the release button is actuated. Alternatively the expelling mechanism may be fully manual in which case the dose ring member and the release button moves proximally during dose setting corresponding to the set dose size, and then moved distally by the user to expel the set dose.
The cartridge is provided with distal coupling means in the form of a needle hub mount 182 having, in the shown example, an external thread 185 adapted to engage an inner thread of a corresponding hub of a needle assembly. In alternative embodiments the thread may be combined with or replaced by other connection means, e.g. a bayonet coupling.
The cartridge holder comprises a distal opening adapted to receive a cartridge. More specifically, the cartridge holder comprises an outer rotatable tube member 170 operated by the user to control movement of gripping means to thereby open and close gripping shoulders 145 configured to grip and hold a cartridge.
As appears,
With reference to
The different components of the logging module 300 are shown in
The second rotary sensor part 330 shown in
In this way a given pair of contact arms provides a combined contact structure adapted to create electric contact between two contact segments. In the shown embodiment the two inner ground contact arms 331 are provided to be in contact with the single ground contact area 321 of the inner concentric ring, the three position contacts arms 332 are provided to be in contact with the four position contact segments 322 of the intermediate concentric ring, and the two outer switch contact arms 333 are provided to be in contact with the three switch contact segments 323 of the outer concentric ring, the outer switch contact arms carrying a laterally extending projection 334. Indeed, for the intermediate and outer contact arms the rotational position between the two sensor parts will determine which contact segment is engaged with a given contact arm.
In the shown embodiment the gaps between two neighbouring outer contact segments are dimensioned such that the dome-formed contact point will be in contact with both segments as it moves from one segment to the next, this being explained in greater detail below. The second rotary sensor part further comprises a gripping part 336 adapted to engage the projection 337 on the rotary sensor holder 339 to prevent rotational movement there between.
In the shown embodiment the intermediate arms and contact segments provide the rotary sensor contacts whereas the outer arms and contact segments provide an axial switch as will be described in greater detail below.
When manufacturing a rotary sensor part of the type shown in
Turning to
By combining the two process activities in one step, the tolerances inherent when aligning the surface between the two process activities are eliminated, and only the inherent tolerances in the single process of creating the pattern and alignment structure are present, e.g. the accuracy/precision of a laser ablation system.
The initial alignment portion has been cut to a final alignment portion 421 having an alignment structure in the form of well-defined edges 422, and with the ring-formed conducting sensor layer cut into a number of individual segments 431. If desired the specific sensor member of
In alternative embodiments the carrier member may be provided with conducting sensor layers on additional surfaces, e.g. the opposed surface or the edge surface. Indeed, if the outer circumferential edge should be used for sensor purposes the alignment structure should be arranged at an alternative location, e.g. as shown in
In the above description of exemplary embodiments, the different structures and means providing the described functionality for the different components have been described to a degree to which the concept of the present invention will be apparent to the skilled reader. The detailed construction and specification for the different components are considered the object of a normal design procedure performed by the skilled person along the lines set out in the present specification.
Number | Date | Country | Kind |
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14188039.3 | Oct 2014 | EP | regional |
Filing Document | Filing Date | Country | Kind |
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PCT/EP2015/073157 | 10/7/2015 | WO | 00 |