The present invention relates to the art of environmental detectors, and in particular to a detector, a system and a method for detecting environmental conditions inside pharmaceutical product packets.
Many pharmaceutical products are sensitive to environmental influence such as temperature and/or humidity, and are therefore provided in sealable containers or product packages that shields the products from the ambient environment. Such product packages for pharmaceutical products can be of many different types, such as tablet pots of various forms with re-sealable lids of screw on type or snap-on type, small or large blister packs that cannot be re-sealed, etc. One common feature for all types of product packages is that they provide an essentially sealed environment for the pharmaceutical product placed inside. Even though the basic designs of available product packages are relatively similar, the performance and robustness due to external environmental influence varies.
When determining best before date for pharmaceutical products in a specific product package, one main parameter to be investigated is therefore the shielding capacity of the product package. In the prior art this has been performed by placing one or more environmental sensors inside the product package, the sensors being connected to a control unit by wire or wireless connection for real time registration of the environmental parameters inside the package, and by placing the packet in an environmental chamber. When the sensors are connected to the control unit by wires, there must be provided a through-connection through the wall of the package, which therefore must be adequately sealed in order to not influence the shielding performance. WO 0391679A1 discloses a wireless sensor for registering temperature within a pharmaceutical package in the form of a blister pack. This sensor requires wireless connection to a control unit to function, but it provides detection of temperature within a sealed package without the need for any through-connections. Thereafter, the registered data is evaluated, and the shelf life for a specific product and product package combination is estimated. Such estimation is limited to an estimation of the external environmental conditions that the product package is subjected to during e.g. shipping and/or storage.
As an alternative to the estimation of shelf life in accordance with above, there are also devices for registering the actual external conditions that the product packages are subjected to. U.S. Pat. No. 6,810,350 and EP 1262161 disclose pharmaceutical product packages with integrated sensor units for registration of environmental parameters within the package. More in detail, U.S. Pat. No. 6,810,350 discloses a system for active determination of pharmaceutical expiration date, which registers temperature and bases a calculation of expiration date upon registered temperature history. U.S. Pat. No. 4,972,099, EP 0511807 A1, EP1319928 A1 and WO8903020 all disclose examples of stand alone environmental sensor units with data logging capability. The sensor units are intended to be used for automated supervision of environmental conditions, e.g., during shipping of temperature-sensitive goods such as food or pharmaceutical products. The stored environmental data is thereafter transferred to a computer for analysis.
However, the estimations of external environmental influence using the above sensor units and systems have limitations in accuracy and do not provide fully reliable internal environmental data corresponding to real conditions.
A new environmental sensor device, a system for determining best before date and a method of evaluating the environmental protection provided by a pharmaceutical product package are described.
One advantage of the stand alone sensor device is that it is small enough to be placed fully inside a pharmaceutical product package, and can be used to record real environmental conditions inside the package.
Another advantage is that it is small enough to be placed inside the product package together with a quantity of a medical product, whereby the recorded environmental data will be even more realistic. Still another advantage is that no through-connection for connection wires has to be furnished in the package, nor is any direct wireless connection needed during the evaluation period, as the sensor device is provided with a memory circuit for storing data.
Still another advantage is that the method according to one embodiment provides more accurate determination of best before date for pharmaceutical products that are sensitive to environmental influence.
The sensor system 2 further comprises a control unit 14 being arranged to communicate with the sensor device 1 via the communication interface to receive environmental parameter data for evaluation.
Preferably, as is shown in
In order to save power and to avoid excessive data registration, the device 1 is arranged to log temperature and humidity at predetermined intervals. According to one embodiment, the duration of the intervals is random. According to another embodiment, the logging of environmental parameters is initiated by one or more readings of temperature and/or humidity that meets a predetermined criteria. The criteria for initialization of the logging may, e.g., be a slope of temperature and/or humidity increase.
The environmental sensor device 1 is preferably used for evaluating the environmental protection provided by a pharmaceutical package 11. It may also be used for evaluating the function of drying agent in a pharmaceutical package 11, or for evaluating environmental influence on pharmaceutical products 10 during transport, or for determining best before date of products 10 in a pharmaceutical product package 11.
According to another embodiment, there is provided a system 2 for determining best before date for pharmaceutical products 10 contained in a pharmaceutical package 11. The system 2 includes a stand alone environmental sensor device 1 for detecting environmental parameters inside the pharmaceutical product package 11 during a predefined external environmental evaluation cycle. The sensor device 1 is sized to fully fit inside the pharmaceutical product package 11, and a control unit 14 is arranged to communicate with the sensor device 1 via the communication interface 8 to receive environmental parameter data for evaluation.
According to one embodiment of the system 2, the sensor device includes a memory 6 for storing environmental parameter data, and the control unit 14 is arranged to read the stored environmental data from the sensor device 1 after the evaluation cycle. Alternatively, the communication interface 8 is wireless, and the control unit 14 is arranged to read environmental data from the sensor device 1 in real-time during the evaluation cycle.
A method of evaluating the environmental protection provided by a pharmaceutical product package 11 includes:
placing an environmental parameter sensor device 1 capable of storing registered environmental data in the product package 11,
exposing the product package 11 containing the sensor device 1 to environmental changes,
retrieving the registered environmental data to a control unit 14, and evaluating the protection.
In order to register as realistic environmental data as possible, the above method can also include one or more of the steps:—placing a quantity of a pharmaceutical product 10 in the product package 11,
By these measures any influences from the product itself, a drying agent or the filling process are recorded and can therefore be evaluated. Such measures are especially useful to detect potential residual water content in the pharmaceutical product, and to optimize the amount of drying agent that is needed to keep the humidity at a predefined level. Moreover, the method effectively identifies any problems in the filling process, when the environmental data for packages closed in real filling situations are compared with data from packages closed under optimum conditions.
As is mentioned above, it is a complex task to set the best before date for pharmaceutical products, depending on the environmental parameters that the products often are exposed to during transport, storing etc. Due to such uncertainties, the best before date is most often based on worst case scenarios that are not likely to occur. However, a method that can be used for evaluation of best before date after transport and/or storing etc., includes:
By such a method, the best before date can be remarkably postponed as the estimation errors are much smaller when the environmental history is complete.
As discussed above, there are product packages/dispensers for pharmaceutical products with integrated sensor units for registration of environmental parameters within the package and even systems for active determination of pharmaceutical expiration date. However, many pharmaceutical products are intended for use under a very limited period of time, such as antibiotics prescribed due to a bacterial infection at a dose of two pills per day during one week or 10 days. In order to achieve a more efficient determination of the best before date for such products (especially for sensitive products), the above method can be used.
Number | Date | Country | Kind |
---|---|---|---|
0501541-7 | Jun 2005 | SE | national |
This application is a national phase application under 35 U.S.C. §371 of PCT International Application No. PCT/SE2006/000792, filed Jun. 28, 2006, which claims priority to Swedish Application Serial No. 0501541-7, filed Jun. 30, 2005. The contents of each of these applications are incorporated herein by reference in their entirety.
Filing Document | Filing Date | Country | Kind | 371c Date |
---|---|---|---|---|
PCT/SE06/00792 | 6/28/2006 | WO | 00 | 6/24/2008 |