Surgery – Liquid medicament atomizer or sprayer
Reexamination Certificate
2000-07-14
2002-07-16
Weiss, John G. (Department: 3761)
Surgery
Liquid medicament atomizer or sprayer
C128S200170, C128S200180, C128S203120, C128S203150
Reexamination Certificate
active
06418924
ABSTRACT:
FIELD OF THE INVENTION
The invention relates to a control means for a drug delivery device and also a drug delivery device including a control means.
BACKGROUND OF THE INVENTION
A number of therapeutic treatments are administered by inhalation and thus, primarily, are directed to the upper respiratory tract ie the nose and throat. Accordingly, a number of conventional devices exist for this purpose. In some instances, for example where a therapeutic agent may be dangerous when a given dose is exceeded, or alternatively where a therapeutic agent may be potentially addictive, it is important to regulate the administered dose or dose regime. It is therefore important to try and prevent the inadvertent overdosing of a given therapeutic agent or the inadvertent addiction to a given therapeutic agent.
Conventional dispensers typically include a dispensing means which controls the amount of therapeutic agent delivered per use, or application, of the dispense. For example, a pump and associated chamber can be used to control the delivery of a selected amount of therapeutic agent, typically in the form of a therapeutic fluid, thus the volume of fluid dispensed is determined by the geometry of the chamber on which the pump acts and therefore for each pumping action a given volume of fluid is dispensed. In this provided an individual only uses the dispenser, or pump, a specified number of times over a given period, the dose of therapeutic agent should fall within a dose regime.
However, it is not uncommon for individuals to forget how much of a given quantity of therapeutic agent has been inhaled in any given period and therefore to inadvertently exceed a dosage. Additionally, given that pump operated dispensers sometimes need to be primed for a correct amount of therapeutic agent to be dispensed an individual may not receive a correct dosage of therapeutic agent. And indeed in these circumstances it is possible for an individual to inadvertently exceed his or her recommended dose by following this partial dose, with a full dose and thus run the risk of inadvertent overdose or addiction.
A further complication concerns the fact that increasingly new and effective therapeutic agents are becoming hazardous and therefore if a partial dose, due to inadequate priming, is not taken it is not always advisable to simply dispense into the atmosphere by a technique known as air priming the partial dose. Additionally, it is not always advisable to air prime because of the considerable expense that may be associated with the use of certain therapeutic agents in this way.
It can therefore be seen that there is a need to provide a means for controlling the dispensing of therapeutic agents; and a device including same.
SUMMARY OF THE INVENTION
It is therefore an object of the invention to provide a control means in, or for use in a dispensing device whereby the dose regime of a dispensed therapeutic can be reliably controlled.
According to a first aspect of the invention there is provided a drug delivery device for the delivery of a fluid carrying or, comprising a therapeutic agent said device comprising: a reservoir for storing said fluid, and in fluid connection therewith a regulatable pump means for dispensing said fluid via an outlet means; wherein a control means is further provided for selectively controlling the pumping mode of said pump means such that in a first mode said pump means acts to dispense said fluid and in a second mode said pump means acts such that substantially no fluid is dispensed.
In a preferred embodiment of the invention said reservoir comprises an exit portion comprising a dispensing chamber and associated dispensing channel which is in fluid connection with a storage portion of said reservoir.
In a preferred embodiment of the invention said pump means comprises a selectively controllable bypass valve which has a dual mode of operation. In a first mode when the bypass valve is closed fluid in said reservoir can be dispensed from said device. Alternatively, or additionally, in a second mode when said bypass valve is opened fluid in said reservoir is diverted from an exit portion of said reservoir to a storage portion of said reservoir.
More preferably still said bypass valve comprises an aperture covered by a flexibly membrane that allows the passage therethrough or thereby of therapeutic fluid when said bypass valve is in said second mode.
In yet a further preferred embodiment of the invention said bypass valve comprises an aperture in said dispensing chamber and/or said dispensing channel and a means for releasably sealing same such that when the device is to dispense a dosage of therapeutic agent said aperture is closed; and when the device is to prevent dispensing of said therapeutic agent the aperture of the bypass valve is opened thus enabling therapeutic agent in said dispensing chamber to be diverted to the storage portion of said reservoir. Ideally, said releasable sealing means comprises an urging means which is ideally controlled using electrical means, and most ideally comprises a solenoid.
It will therefore be apparent that when the urging means acts so as to apply sufficient pressure to the releasable sealing means the aperture in the dispensing chamber is sealed and this ensures that therapeutic agent can be dispensed from the device. Alternatively, when the urging means does not act to apply sufficient pressure to the releasable sealing means the aperture in the dispensing chamber is opened and the therapeutic agent is therefore directed towards the reservoir storage portion.
It therefore follows that the selective control of the urging means status will determine the pumping mode of the pump and so the ability of the deliverer device to dispense medication.
In yet a further preferred embodiment of the invention control means ideally in the form of an electronic circuit with at least one microchip is provided so that the number of times the device can dispense a therapeutic agent can be controlled over a set period of time. Additionally, and advantageously, said control means is adapted to record information relating to use of the dispensing device and also to respond to interrogation of same so that, with the provision and use of a suitable display means, an individual can enquire as to how frequently the device may be used over a remaining period of time or how much medication has already been administered. Additionally further still an interface means is provided whereby data stored on said control means can be down-loaded to another compatible device for further use/analysis. This is useful for determining drug regime compliance either from the perspective of a GP or clinical trials coordinator.
An additional advantage intrinsic in the device of the invention concerns an ability to prime the pump means without dispensing the therapeutic agent. As will be well known to those skilled in the art, the loss of prime in pumps is a consequence of fluid leaking out of the relevant chamber, in this instance the dispensing chamber. This typically occurs when the device is jostled or laid on its side. Thus the amount of fluid in the dispensing chamber is decreased and an insufficient dose is administered on use. In order to ensure that a correct dose is administered the conventional device is repeatedly operated at least once, to refill the dispensing chamber. This involves effecting additional cycles of the device and thus dispensing some therapeutic agent to the atmosphere. However with the device of the invention it is possible to prime the pump with the bypass valve open and thus divert the therapeutic fluid in the dispensing chamber to the reservoir storage portion. In this way, the device can be primed without loss of medication or fluid.
It therefore follows that the control means could be further programmed to enable a user to prime the device each time before usage. For example, it is possible to program the control means so that at least one pump operation is provided, for the purpose of priming with the bypass valve open, and then a further pump operatio
Poley John
Seeney Philip
Erezo Darwin
P A Knowledge Limited
Weiss John G.
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