Method for producing blister packs for medicinal products and blister pack
10828234 ยท 2020-11-10
Assignee
Inventors
- Kurt Laemmle (Ehingen, DE)
- Christian Link (Baustetten, DE)
- Peter Rafensteiner (Laupheim, DE)
- Martin Seiffert (Schelklingen, DE)
- Michael Schultes (Ehingen, DE)
Cpc classification
B65B5/02
PERFORMING OPERATIONS; TRANSPORTING
B65D81/267
PERFORMING OPERATIONS; TRANSPORTING
B65B47/00
PERFORMING OPERATIONS; TRANSPORTING
B65B9/045
PERFORMING OPERATIONS; TRANSPORTING
International classification
B65B5/02
PERFORMING OPERATIONS; TRANSPORTING
B65B47/00
PERFORMING OPERATIONS; TRANSPORTING
B65B7/16
PERFORMING OPERATIONS; TRANSPORTING
Abstract
The method for producing blister packs for medicinal products comprises the steps of forming blister pockets in a bottom film, wherein each blister pocket has an at least two-level shape with a first recess and a second, lower recess, filling the second recesses of the blister pockets with the medicinal products, placing a strip of active material in the first recess of each blister pocket above the medicinal product, wherein the strip of active material rests on at least one support surface of the first recess next to the second recess, sealing a lidding film to webs of the bottom film arranged around the blister pockets and simultaneously to the strips of active material, thus forming a sealed blister web, and stamping out individual blister packs from the blister web.
Claims
1. A method for producing blister packs for medicinal products, comprising the steps of: providing a bottom film and forming a plurality of blister pockets in the bottom film, wherein each blister pocket has an at least two-level shape with a first recess, which defines a first level of the blister pocket, and a second recess, which is formed in a subsection of a two-dimensional area over which the first recess extends and is situated lower down than the first recess; filling the second recesses of the blister pockets with the medicinal products; providing strips of active material and placing a strip of active material in the first recess of each blister pocket above the medicinal product, wherein the strip of active material rests on at least one support surface of the first recess, which at least one support surface is arranged next to the second recess; providing a lidding film and sealing the lidding film to webs of the bottom film arranged around the blister pockets and simultaneously to the strips of active material, thus forming a sealed blister web; and stamping out individual blister packs from the blister web.
2. The method of claim 1, wherein providing the strips of active material is accomplished by providing a web of active material wound up into a roll and by stamping out the strips of active material from the unwound web.
3. The method of claim 1, wherein the strips of active material are sections of a film.
4. The method of claim 1, wherein the strips of active material have a thickness in the range of 0.2-2 mm.
5. The method of claim 1, wherein, as a result of its material properties, the active material has an absorption function for absorbing at least one substance or a release function for releasing at least one substance.
6. The method of claim 1, wherein placing of the strips of active material is carried out by means of a pick-and-place device.
7. The method of claim 1, wherein, after the strips of active material have been placed on the at least one support surface of the first recess, the strips of active material project above the webs of the bottom film by 0.05-0.5 mm.
8. The method of claim 1, wherein, during forming of the plurality of blister pockets in the bottom film, an upward-projecting rib extending around the second recess is, or at least two upward-projecting knobs spaced a certain distance apart are, formed in the bottom film in an area of the first recess, which rib forms, or which knobs form, the support surface or support surfaces for the strip of active material.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION
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(37) A lidding film 12, which covers at least one blister pocket 8, is sealed to the webs 10 of the bottom film 6 and closes off the at least one blister pocket 8. The lidding film 12 is shown only in
(38) Materials which can be used for the bottom film include in particular PVC, PVDC, Aclar, aluminum, PETG, and laminated films. Materials which can be used for the lidding film include in particular aluminum, polyethylene, polypropylene, paper-laminated films and other types of composite films.
(39) A strip 14 of active material is arranged in the at least one blister pocket 8 and is sealed to the lidding film 12. The entire surface of the strip 14 can be sealed to the lidding film 12, or only certain areas of the strip 14, e.g., along lines or only at certain points, can be sealed to it.
(40) As a result of its material properties, the active material usually has an absorption function for absorbing at least one substance or a release function for releasing at least one substance. The most widely encountered purpose is for the absorption of moisture. In the case of strips 14 with an absorption function, the strips 14 of active material can also absorb oxygen, CO.sub.2, reactive impurities, or odors, for example. In the case of strips 14 with a release function, the strips 14 of active material can release nitrogen or carbon dioxide, for example.
(41) A strip 14 of active material preferably has a thickness in the range of 0.2-2 mm, more preferably of 0.3-1.2 mm. The material of the strip 14 preferably has at least some stiffness to facilitate handling. The material of the strip 14 is preferably a film, more preferably a polymer, and even more preferably a three-phase polymer. The film can be produced by extrusion, for example, wherein the active particles are added to the polymer. Channels within the polymer allow the movement of gases. The active particles are preferably present in the strip 14 as spheres.
(42) In the embodiment according to
(43) As can be seen in
(44) The two support surfaces 20 for the strip 14 of active material lie on two sides of the second recess 18, diametrically opposite each other. The strip 14 of active material therefore covers a large part of the second recess 18 and rests by two opposite corner areas on the support surfaces 20.
(45) The embodiment of the blister pack 2 according to the disclosure shown in
(46) The embodiment of the blister pack 2 according to the disclosure shown in
(47) The shape of the blister pockets 8 can depart from the configurations described so far. Any geometric configuration is conceivable, as long as the blister pocket 8 has an at least two-level shape. The shape of the second recess 18 depends preferably on the shape of the product 4 to be packaged, which can have any possible geometric shape. In addition to the oblong form, the sugar-coated pill form, or the spherical form discussed so far, triangular or polygonal shapes of the medicinal products 4 can also be present.
(48) Finally, the shape of the strip 14 of active material can depart from the exemplary embodiments described so far. In addition to the rectangular base surface illustrated, the strips 14 can also have a round, an oval, or a triangular base surface. In each of these configurations, it is possible to provide an opening 22 in the strip. The strips 14 are usually cut-to-size blanks.
(49) The support surfaces 20 for the strips 14 of active material can be arranged on two opposite sides of the second recess 18, as illustrated in the previous exemplary embodiments. It is also possible, however, for more than two support surfaces 20 to be arranged around the second recess 18 or for a single continuous support surface 20 to extend all the way around the second recess 18.
(50) A method according to the disclosure for producing blister packs 2 will now be described with reference to
(51) In a feed station 28, the strips 14 of active material are then provided, and a strip 14 of active material is placed in the first recess 16 of each blister pocket 8 above the medicinal product 4, i.e., on the at least one support surface 20 of the first recess 16. The at least one support surface 20 of the first recess 16 is therefore preferably arranged above the medicinal product 4, more preferably a certain distance away from it. The step of providing the strips 14 of active material is preferably achieved by providing a web of active material wound up into a roll and by stamping out the strips 14 of active material from the unwound web. The placing of the strips 14 of active material is preferably achieved by means of a pick-and-place device. It is also possible, however, to provide other means of transferring the strips 14 of active material.
(52) The lidding film 12 is provided in a following sealing station 30 and sealed to the webs 10 of the bottom film 6. At the same time, the lidding film 12 is also sealed to the strips 14 of active material. All these steps taken together thus lead to the formation of a sealed blister web. Finally, the individual blister packs 2 are stamped out of the blister web in a downline stamping station 32. The individual blister packs 2 are then sent onward for further processing measures.
(53) A first forming tool 34 and a second forming tool 36, which cooperate in the forming station 24 to form the blister pockets 8 in the bottom film 6, are sketched in
(54) The first forming tool 34 comprises at least one, preferably a plurality, of troughs 40 for forming at least one blister pocket 8 in the bottom film 6. The at least one trough 40 has an at least two-level shape. A first recess 42 of the trough 40 defines a first level of the trough 40. A second recess 44 of the trough 40 is arranged in a subsection of a two-dimensional area over which the first recess 42 extends and is situated lower down than the first recess 42. The shape of the trough 40 corresponds to the shape of the blister pockets 8 to be formed. The shape of the trough 40 shown in
(55) A first sealing tool 54 and a second sealing tool 56, which cooperate in the sealing station 30 to seal the lidding film 12 to the webs 10 of the bottom film 6 and to the strips 14 of active material, are sketched in
(56) The first sealing tool 54 comprises at least one, preferably a plurality, of troughs 60 for accommodating at least one blister pocket 8 of the bottom film 6. The at least one trough 60 comprises an at least two-level shape. A first recess 62 of the trough 60 defines a first level of the trough 60. A second recess 64 of the trough 60 is arranged in a subsection of the two-dimensional area over which the first recess 62 extends and is situated lower down than the first recess 62. The shape of the trough 60 corresponds substantially to the shape of the blister pockets 8 previously formed in the forming station 24. In this concrete example, the shape of the trough 60 corresponds to that of the blister pack of
(57) When the strips 14 of active material are placed on the at least one support surface 20 of the first recess 16, it is advantageous for the strips 14 of active material to project upward beyond the webs 10 of the bottom film by an amount in the range of 0.05-0.5 mm, more preferably of 0.08-0.2 mm. The geometry of the blister pocket 8 and of the first recess 62 in the first sealing tool 54 is therefore to be adapted correspondingly to the thickness of the strip 14 of active material, so that the strip 14 projects by this amount prior to the sealing operation in the sealing station 30. This projection of the strip 14 guarantees that the lidding film 12 will be sealed not only to the webs 10 of the bottom film 6 but also to the strips 14 of active material.
(58) Another embodiment of the blister pack 2 according to the disclosure is shown in
(59) In a departure from the embodiment of
(60) Another possible configuration of the forming tools 34, 36 is shown in
(61) In a departure from the embodiment of
(62) Another possible configuration of the sealing tools 54, 56 is shown in
(63) As a modification of the sealing tools of
(64) The sealing tools 54, 56 shown in
(65) The knobs 50 in the bottom film 6 preferably comprise a height in the range of 0.5-5 mm, preferably of 1-3 mm. Accordingly, the projections 46 in the first forming tool 34 and possibly the projections 66 in the first sealing tool 54 have a height in the range of 0.5-5 mm, preferably of 1-3 mm. If pins 68 are being used, these project preferably by an amount in the range of 0.5-5 mm, preferably of 1-3 mm, above the bottom area of the first recess 62 of the trough 60 or are extended by this amount.
(66) In the embodiments shown, the knobs 50 are illustrated as rounded elevations. Other shapes for the knobs 50 are also conceivable; for example, the knobs 50 could have a triangular cross-sectional shape with a rounded tip or with a flat plateau surface at the top, on which the strips 14 of active material rest. The knobs 50 could also be elongated objects extending along a line (straight or curved). The shape of the projections 46, 66 and/or of the tips of the pins 68 preferably corresponds in each case to the shape of the knobs 50 in the bottom film 6.
(67) It is also possible that a peripheral rib could be formed instead of several knobs 50. This is conceivable especially in the case of the embodiment according to
(68) For the production of blister packs like those in
(69) With respect to the first sealing tool 54, the only measure to be taken is preferably to produce a similarly shaped peripheral projection 86, as can be seen in the cross-sectional view of
(70) Alternatively, it would be possible to use a peripheral, extendable support element 78 in the first sealing tool, the apex of which element would correspond to the shape of the rib 70.
(71) With respect to the cross-sectional shape of the rib 70, of the projection 76, of the projection 86, or of the apex of the support element 78, what was said concerning the cross-sectional shape of the knobs 50 also applies.