The present patent application claims priority from United Kingdom Patent Application No. 0711997.7, filed on Jun. 21, 2007.
The present invention is concerned with testing of inhalers used for medicament delivery, and more particularly with devices for automatically shaking and firing an inhaler for testing purposes.
Inhalers for pharmaceutical delivery are in themselves well known and widely used for the treatment of various conditions including asthma. An inhaler typically has a mouthpiece (or in some cases a nasal nozzle), some form of storage for the medicament itself, and a manually actuable mechanism for releasing a dose of the medicament. Some inhalers are intended to be shaken before the dose of medicament is dispensed. This is the case for so-called “metered dose inhalers” (MDIs), which have a manually actuated mechanism for releasing a controlled dose from a larger reservoir of the medicament, and which typically also use a compressed propellant to eject this dose through the inhaler's mouthpiece. One such inhaler is described in detail in international patent application PCT/GB2006/000966, filed in the name of Glaxo Group Limited and published under WO 2006/097747. It has a housing which serves to mount the mouthpiece and which contains a cylinder of pressurised propellant, and a valve mechanism which is actuated by the user by means of two pivotally mounted arms which are squeezed together in one hand to release a dose of medicament into the user's mouth for inhalation.
Testing of sample inhalers is carried out routinely by manufacturers to ensure that they consistently meet certain requirements with regard to dispensed dose, etc. The procedure involves test firing the inhaler and collecting the dispensed dose for analysis. In some cases the test will specify that the dose chosen for analysis is not the first dispensed by the inhaler but, say, the fiftieth. In this case, forty nine waste doses will have to be fired from the inhaler before the fiftieth dose is collected. Testing can in principle be carried out manually, which requires an operative to repeatedly shake and fire inhaler devices. This of course is labour intensive, particularly as significant numbers of sample inhalers may need to be tested. There is consequently a need to automate the test firing process, which involves both shaking the inhaler and then suitably actuating it to cause firing, as well as arranging for collection of the test doses.
It is also desirable to be able to closely monitor, adjust and record the conditions of such tests—the shaking motion of the inhaler in particular—to ensure that the tests are being carried out in a reproducible manner and provide a meaningful simulation of real operating conditions. There have been devices constructed in the past which were capable of shaking inhalers, but these are believed typically to have used mechanisms using an electric motor and belt drive so that accurate control and recordal of the shake profile was not available.
In accordance with the first aspect of the present invention, there is a device for automatically shaking and firing an inhaler for medicament delivery, the device comprising a guideway, a carriage mounted upon the guideway for linear movement upon it, the carriage being adapted to receive and releasably mount the inhaler, and a linear motor operatively coupled to the carriage for reciprocally driving it to shake the inhaler.
Specific embodiments of the present invention will now be described, by way of example only, with reference to the accompanying drawings in which:—
a is a side view of a shake device embodying the present invention;
b is a plan view of the same shake device;
The system illustrated serves to simulate the action of an inhaler user by first putting the inhaler through a shaking process in which it is moved reciprocally along a linear path, and then actuating the release device of the inhaler to cause it to fire a dose of medicament. These functions are carried out by separate mechanisms: an inhaler shake device 10 and an inhaler fire device 10a. In the illustrated embodiment the two devices are constructed and mounted independently of one another, and can operate independently. However their motions are coordinated by a control system.
The inhalers themselves are not seen in the drawings but are to be received in respective mounting frames 12 carried upon a movable carriage 14. The carriage is supported by an upright pillar 16 which is in this embodiment directly floor mountable by means of bolts 20 passing into a floor mounted plate 22. The upright pillar 16 incorporates plate 18 and an arrangement of studs, spherical seat nuts and spherical seat washers (collectively identified 24) which allows pillar 16 to be adjusted in position and angle.
Mounting the shaking device directly upon the floor in this way reduces any tendency for it to cause undesirable vibration of adjacent pieces of apparatus during the shake operation.
The carriage 14 is mounted upon a guideway carried on the pillar 16 to provide for linear motion, which in the illustrated embodiment is along the vertical direction. The guideway in this embodiment is formed as part of a linear motor 26, a traveler part 28 of which serves both to mount the carriage and to drive it during the shake operation. Linear motors are in themselves well known and are electric devices which provide controlled linear movement, when suitably driven through associated electronics.
A distance transducer is used in monitoring and recording motion of the carriage during the shake operation, inter alia in order to provide confirmation that a suitable shake profile was achieved. In this case the relevant transducer takes the form of a low voltage distance transducer which reads off a reflective strip within the linear motor 26.
In use, the shake device 10 is first loaded with a set of five inhalers which are then subject to a controlled shake operation by reciprocally driving the carriage 14. The actual shake profile can be closely controlled by means of the software used to drive the linear motor 26. The device is not for example limited to providing sinusoidal motion but could provide an approximation to a square wave, a saw tooth wave, etc., and nor need the wave form of the motion be consistently repeated—it could for example vary in amplitude or wave shape over time.
The carriage 14 is best seen in
The firing device 10a is seen in
By moving the carriage 14 downward into alignment with the fire device 10a, each inhaler, still mounted in its frame 12, is positioned between a respective pair of movable arms such as 32 and 34. Each such pair comprises one arm 32 which is carried on a first sliding beam 36 and another arm 34 carried upon a second sliding beam 38. A rack and pinion mechanism is provided for driving the first and second sliding beams 36, 38 concurrently and in opposite directions.
Motion of the sliding beams 36, 38 is monitored by means of a distance transducer 52, formed in this embodiment as a low voltage distance transducer.
Each of the movable arms such as 32 and 34 carries a respective actuating finger such as 54, 56, and it is these fingers which engage with the respective inhalers to fire them. The illustrated device is intended for use with the type of inhaler described in PCT/GB2006/000966. Recall that firing of this particular device requires it to be squeezed, to move a pair of pivotally mounted arms inwardly. When the pinion 42 is driven to move the arms such as 32 and 34 toward each other, a suitable squeezing action is provided. Provision is made to monitor the force thereby applied to the inhaler. In the present embodiment, one of each opposed pair of actuating fingers 54 is movably mounted, and the force applied to it is reacted to the corresponding arm such as 32 through a load cell.
The monitoring of both the positions of the actuating fingers 54, 56 and the forces they exert makes it possible to record a complete profile of the actuation of the device, and to detect anomalies which might be indicative of a malfunction. Modern inhalers are typically intended to provide a predetermined, characteristic force/displacement profile. Deviation from the intended force profile is likely to be indicative of a malfunction and could be detected by the illustrated device. Recordal and analysis of the force profile is carried out by an associated digital computer which receives signals from the relevant transducers.
The fire device 10a has sensors for detecting whether inhalers are actually present at all in five of the sites where they are expected. In the illustrated embodiment these are formed as reflective optical sensors 64, which are carried upon the channel member 50 and face toward the sites between pairs of movable arms such as 32 and 34.
Trials have shown that is desirable to electrically isolate the electric motor/gearbox 44 to prevent electrical noise which might otherwise disrupt readings from the load cells 62, etc. The motor's electrically isolating components 66 and 66a are illustrated in
In order to automate the entire process of taking the required samples from the inhalers, an arrangement is needed not only to shake and fire them, but also to collect the dose of medicament which they discharge.
As noted above, test protocols may stipulate that only certain doses are required for analysis—say the fiftieth discharged from the inhalers—so that other, waste, doses need to be fired and safely disposed of before the chosen doses can be collected for analysis. For this purpose, robotic actuators are provided for moving the collection intakes away from the area of the carriage 14 and aligning instead the waste intakes 74 with the inhaler mouthpieces in this area. The waste intakes 74 function in essentially the same manner as the collection intakes 72 except that the material withdrawn through them is not collected for analysis but is simply discharged into a waste collection receptacle for disposal.
For the sake of safety, the entire apparatus is housed in a transparent-walled enclosure 76.
Number | Date | Country | Kind |
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0711997.7 | Jun 2007 | GB | national |
Number | Name | Date | Kind |
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20020081748 | Roberts et al. | Jun 2002 | A1 |
20040226555 | Scarrott et al. | Nov 2004 | A1 |
20040231667 | Horton et al. | Nov 2004 | A1 |
Number | Date | Country |
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2371861 | Aug 2002 | GB |
WO-01-28615 | Apr 2001 | WO |
WO 2006097747 | Sep 2006 | WO |
Number | Date | Country | |
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20080316857 A1 | Dec 2008 | US |