The present invention relates to a blister pack for housing pharmaceutical products. A method for manufacturing such blister packs is also disclosed.
In medication, drug or dietary supplements blister packs are well known for packaging pharmaceutical products such as tablets, capsules, powders and liquids. Further, packages providing for a once-a-day regimen appear to be more effective than a multiple-doses-a-day regimen. Indeed, patients more readily follow a single daily medical administration than multiple daily medical administrations.
Multiple packaging combining different pharmaceutical compositions or dietary supplements are thus useful to ensure adherence to an optimal daily regimen.
However, combining and storing different pharmaceutical compositions or different components of a pharmaceutical composition in a common package is not simple as it may lead to undesired reactions or interactions between the chemical compounds present in the different compositions and/or supplements.
In particular, during storage a reaction between the bioactive substances in the formulation may occur, leading to degradation of one or more bioactive substances. Further, a bioactive substance may have a very limited stability when it is stored as aqueous solution, whereas when stored as lyophilized powder it possesses a much greater stability, such that no further freezing or cooling is necessary during storage. Degradation of one or more components or undesired reactions between different components may limit the combination of components in the final product, and/or the shelf life period of the product. It is thus challenging to decide on blending of substances in a final product and still keep good stability.
One possibility to avoid direct contact between different components or compositions may be achieved by packaging said components or compositions separately in different containers, such as bottles. This is, however, not convenient for patients and usually requires additional handling by the patient. The latter is prominent source of errors leading to an inefficient medication.
Hence, an improved blister package would be advantageous, and in particular, a blister package providing simple storage and facilitating convenient administration would be advantageous.
An object of the present invention is to provide a solution for holding different pharmaceutical components or compositions in a single use package. A further object of the invention is to provide a single use package that is able to hold different pharmaceutical components or compositions and that is easy to open.
Another object of the present invention is to provide an alternative to the prior art.
It is an object of the present invention to wholly or partly overcome the above disadvantages and drawbacks of the prior art.
The object is achieved by a blister pack according to the present invention as defined in claim 1. A method for manufacturing a blister pack according present invention is also provided as defined in claim 9. Further preferred embodiments are subject to the dependent claims.
A blister pack according to the present invention comprises a base laminate with a sealing layer and a lid laminate with a sealing layer. The base laminate has at least one cavity for housing a product. The base laminate and the lid laminate are sealed to each other via their sealing layers whereby the seal comprises two different sealing subzones, a first sealing subzone that provides a permanent seal and a second sealing subzone that provides a peelable seal.
In a further preferred embodiment a blister pack according to the present invention comprises a base laminate with a sealing layer and a lid laminate with a sealing layer. The base laminate has at least one cavity for housing a product. The base laminate and the lid laminate are directly sealed to each other via their identical sealing layers whereby the seal comprises two different sealing subzones, a first sealing subzone providing a permanent seal and a second sealing subzone providing a peelable seal. The sealing layer comprises a blend of polyethylene and of several functionalized ethylene copolymers.
The blister pack according to the present invention provides a simple possibility to achieve different sealing zones having different seal strength which allows forming peelable and permanent seals. There is no need to use different sealing materials as the different seals may be achieved with the blend of polyethylene and several functionalized ethlyene copolymers.
In a further embodiment the base laminate has at least two cavities, a first cavity housing a first product, and a second cavity housing a second product. The first sealing subzone defines a sealed perimeter forming the closed blister pack whereas the second sealing subzone is internal to the first sealing subzone and at least partly separates the first and second cavity. The second sealing subzone is generally arranged between the at least two cavities in the form of a strip. However, different shapes of the second sealing subzone arranged between the cavities are also possible, e.g., an arched strip.
In another embodiment the second sealing subzone delaminates upon sustained manual pressure applied on one of the cavities. When the peelable seal provided by the second sealing subzone is broken by application of sustained manual pressure a communicating passage between the first and the second cavity is created which allows the mixture of the first and the second product.
In a further embodiment the first sealing subzone and the second sealing subzone define a sealed perimeter having a first end and a second end and two opposed sides forming the closed blister pack. The first sealing subzone is arranged at the second end and provides a peel stop and thereby prevents the complete separation of the lid laminate and the base laminate in an opened state of the blister pack.
In preferred embodiment the base laminate and the lid laminate comprise an identical sealing layer.
In another embodiment the sealing layer comprises a blend of polyethylene and several functionalized ethylene copolymers.
In a preferred embodiment the blend of the sealing layer comprises 10 to 80 weight percent polyethylene and 90 to 20 weight percent of functionalized ethylene copolymers.
The polyethylene component of the sealing layer preferably is a low density polyethylene, preferably having a density in the range of 0.921 g/cm3 to 0.924 g/cm3.
Blister pack according to claim 6, characterized in that the functionalized ethylene copolymers are copolymers of ethylene and an unsaturated co-monomer having an organic functional group containing a carbon atom double bonded oxygen atom and being linked to an additional oxygen atom. Examples of such copolymers are ionomers, acrylic acid polymers, acrylic acid and methacrylic acid ester copolymers, and ethlylene vinyl acetate copolymers.
In a preferred embodiment the functionalized ethylene copolymers, in particular the ionomers are derived from acid copolymers by partially neutralizing the acid moiety of the acid copolymer with a cation. A suitable synthesis is disclosed e.g. in U.S. Pat. No. 3,264,272. The preferred ionomers are sodium neutralized ionomers derived from at least (i) ethylene and (ii) acrylic acid or methacrylic acid and the zinc neutralized ionomers derived from at least (i) ethylene and (ii) acrylic acid or methacrylic acid and (iii) a mono-ethylenically unsaturated monomer as described in U.S. Pat. No. 5,891,500.
In another embodiment the ethylene acrylic acid copolymers (EAA) are non-cation neutralized copolymers synthesized from (i) ethylene and (ii) an acid comonomer (such as acrylic acid or methacrylic acid).
In another embodiment the acrylic and methacrylic ester copolymers (EMA, EBA) are copolymerized from (i) ethylene and (ii) non-symmetrically substituted ethylene in which the ester function contains an n-alkyl chain; and more specifically methyl in the case of EMA and n-butyl in the case of EBA.
In a further embodiment the functionalized ethylene copolymer is ethylene vinyl acetate copolymer having a vinyl acetate content of up to 30 weight percent based on the weight of the ethylene vinyl acetate copolymer. The ethylene vinyl acetate copolymers (EVA) with a vinyl acetate (VA) copolymer level up to 30% are typically prepared by high pressure radical copolymerization of (i) ethylene and (ii) vinyl acetate as diclosed in U.S. Pat. No. 5,135,988.
In another embodiment the blend of the sealing layer comprises ethylene functionalized copolymers selected from the group of ionomers, ethylene acrylic acid copolymer (EAA), ethylene butyl acrylate copolymer (EBA), ethylene methacrylic acid copolymer (EMA), and ethlyene vinyl acetate copolymer (EVA). A suitable ionomer is for instance the commercially available Surlyn® of Dupont.
In another embodiment the base laminate comprises three adhesively bonded layers, an outer layer of oriented polyamide, an optional primer layer, an intermediate layer of aluminum and an inner sealing layer made of a blend of polyethylene and several functionalized ethylene copolymers.
The base laminate may also comprise different multi-layer structures, it may comprise for instance additional intermediate layers either made of plastics or metal, metal alloys, e.g. aluminum and aluminum alloys. The intermediate layer may also comprise suitable plastics instead of metal and metal alloys. The outer layer of the base laminate may comprise oriented polyamide, oriented polypropylene, oriented polyethyleneterephtalat or further suitable plastics.
In a further embodiment of the blister pack the outer layer of the base laminate has a thickness in the range 10 μm to 40 μm, preferably 15 μm to 35 μm and more preferably 20 μm to 30 μm. The intermediate layer of the base laminate has thickness in the range of 30 μm to 60 μm, preferably 35 μm to 55 μm and more preferably 40 μm to 50 μm. Further, the inner sealing layer of the base laminate has a thickness in the range of 30 μm to 90 μm, preferably 40 μm to 80 μm and more preferably 50 μm to 70 μm.
In a further embodiment the lid laminate comprises of three adhesively bonded layers, an outer layer made of polyethylene terephthalate, an intermediate layer made of aluminium and an inner sealing layer made of a blend of polyethylene and several functionalized ethylene copolymers.
Other embodiments of the lid laminate wherein the lid laminate comprises additional layers are also conceivable. It may comprise multi-layer structures that made of adhesively bonded or coextruded plastics layers.
In yet another embodiment of the blister pack the outer layer of the lid laminate has a thickness in the range of 6 μm to 18 μm, preferably 8 μm to 16 μm and more preferably 10 μm to 14 μm. The intermediate layer of the lid laminate has thickness in the range of 10 μm to 30 μm, preferably 14 μm to 26 μm and more preferably 18 μm to 22 μm. Further, the inner sealing layer of the lid laminate has a thickness in the range of 30 μm to 90 μm, preferably 40 μm to 80 μm and more preferably 50 μm to 70 μm.
A method for manufacturing a blister pack according to the present invention comprises the step that the first sealing subzone is sealed at a first temperature and the second sealing subzone is sealed at a lower second temperature. The difference between the first sealing temperature and the second sealing temperature is at least 30° C., preferably 40° C. and more preferably 50° C.
In a further method for manufacturing a blister pack the first sealing subzone is sealed at a first temperature in the range of 170° C. to 200° C. and the second sealing subzone is sealed at a lower second temperature in the range of 110° C. to 140° C.
It is also possible to achieve the first and the second sealing subzone by sealing in two consecutive steps. In a first sealing step the base laminate and the lid laminate are sealed and form a peelable seal throughout the entire sealed area. That is, the second sealing subzone is formed in a first sealing step. In a subsequent sealing step those parts of the sealed area where a permanent seal is required are sealed a second time thereby achieving a permanent seal forming the first sealing subzone.
The method for forming packaging materials and the packaging materials according to the present invention are explained in more detail below with reference to exemplary embodiments in the drawings, in which, purely schematically:
Number | Date | Country | Kind |
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16020318.8 | Aug 2016 | EP | regional |
Filing Document | Filing Date | Country | Kind |
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PCT/EP2017/025246 | 8/30/2017 | WO | 00 |