ZA200304034B - Packaging system. - Google Patents
Packaging system. Download PDFInfo
- Publication number
- ZA200304034B ZA200304034B ZA200304034A ZA200304034A ZA200304034B ZA 200304034 B ZA200304034 B ZA 200304034B ZA 200304034 A ZA200304034 A ZA 200304034A ZA 200304034 A ZA200304034 A ZA 200304034A ZA 200304034 B ZA200304034 B ZA 200304034B
- Authority
- ZA
- South Africa
- Prior art keywords
- packaging system
- chamber
- tampon
- frangible member
- crimping
- Prior art date
Links
- 238000004806 packaging method and process Methods 0.000 title claims description 79
- 239000000314 lubricant Substances 0.000 claims description 31
- 239000000463 material Substances 0.000 claims description 29
- 239000000758 substrate Substances 0.000 claims description 28
- 239000004698 Polyethylene Substances 0.000 claims description 24
- 239000000853 adhesive Substances 0.000 claims description 23
- 230000001070 adhesive effect Effects 0.000 claims description 23
- 238000002788 crimping Methods 0.000 claims description 22
- -1 polypropylene Polymers 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 17
- 229920000573 polyethylene Polymers 0.000 claims description 16
- 239000012528 membrane Substances 0.000 claims description 14
- 235000015067 sauces Nutrition 0.000 claims description 11
- 239000003814 drug Substances 0.000 claims description 10
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 10
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 235000013399 edible fruits Nutrition 0.000 claims description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 6
- 230000002745 absorbent Effects 0.000 claims description 6
- 239000002250 absorbent Substances 0.000 claims description 6
- 229920000642 polymer Polymers 0.000 claims description 6
- 239000004743 Polypropylene Substances 0.000 claims description 5
- 229920001155 polypropylene Polymers 0.000 claims description 5
- 241000196324 Embryophyta Species 0.000 claims description 4
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims description 4
- 239000000284 extract Substances 0.000 claims description 4
- 239000008274 jelly Substances 0.000 claims description 4
- 229920003023 plastic Polymers 0.000 claims description 4
- 239000004033 plastic Substances 0.000 claims description 4
- 235000013618 yogurt Nutrition 0.000 claims description 4
- 239000004952 Polyamide Substances 0.000 claims description 3
- 239000011111 cardboard Substances 0.000 claims description 3
- 238000005520 cutting process Methods 0.000 claims description 3
- 239000002648 laminated material Substances 0.000 claims description 3
- 229920002647 polyamide Polymers 0.000 claims description 3
- 229920000728 polyester Polymers 0.000 claims description 3
- 229920001223 polyethylene glycol Polymers 0.000 claims description 3
- HVYWMOMLDIMFJA-UHFFFAOYSA-N 3-cholesterol Natural products C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)CCCC(C)C)C1(C)CC2 HVYWMOMLDIMFJA-UHFFFAOYSA-N 0.000 claims description 2
- 229920001817 Agar Polymers 0.000 claims description 2
- 229920000945 Amylopectin Polymers 0.000 claims description 2
- 241000416162 Astragalus gummifer Species 0.000 claims description 2
- 241000195493 Cryptophyta Species 0.000 claims description 2
- 229920001353 Dextrin Polymers 0.000 claims description 2
- 239000004375 Dextrin Substances 0.000 claims description 2
- 239000001856 Ethyl cellulose Substances 0.000 claims description 2
- 229920000084 Gum arabic Polymers 0.000 claims description 2
- 229920001612 Hydroxyethyl starch Polymers 0.000 claims description 2
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 claims description 2
- 239000004677 Nylon Substances 0.000 claims description 2
- 239000002202 Polyethylene glycol Substances 0.000 claims description 2
- 229920002472 Starch Polymers 0.000 claims description 2
- 229920001615 Tragacanth Polymers 0.000 claims description 2
- 235000010489 acacia gum Nutrition 0.000 claims description 2
- 239000000205 acacia gum Substances 0.000 claims description 2
- 239000008272 agar Substances 0.000 claims description 2
- 235000010443 alginic acid Nutrition 0.000 claims description 2
- 229920000615 alginic acid Polymers 0.000 claims description 2
- 239000001913 cellulose Substances 0.000 claims description 2
- 229920002678 cellulose Polymers 0.000 claims description 2
- 235000010980 cellulose Nutrition 0.000 claims description 2
- 235000019425 dextrin Nutrition 0.000 claims description 2
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 2
- 235000019325 ethyl cellulose Nutrition 0.000 claims description 2
- 229920001249 ethyl cellulose Polymers 0.000 claims description 2
- 239000000194 fatty acid Substances 0.000 claims description 2
- 229930195729 fatty acid Natural products 0.000 claims description 2
- 125000005456 glyceride group Chemical group 0.000 claims description 2
- 229930195733 hydrocarbon Natural products 0.000 claims description 2
- 150000002430 hydrocarbons Chemical class 0.000 claims description 2
- 229940050526 hydroxyethylstarch Drugs 0.000 claims description 2
- 239000001863 hydroxypropyl cellulose Substances 0.000 claims description 2
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 claims description 2
- 229920000609 methyl cellulose Polymers 0.000 claims description 2
- 239000001923 methylcellulose Substances 0.000 claims description 2
- 235000010981 methylcellulose Nutrition 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 229920001778 nylon Polymers 0.000 claims description 2
- 239000003921 oil Substances 0.000 claims description 2
- 239000012188 paraffin wax Substances 0.000 claims description 2
- 239000001814 pectin Substances 0.000 claims description 2
- 229920001277 pectin Polymers 0.000 claims description 2
- 235000010987 pectin Nutrition 0.000 claims description 2
- 229920000058 polyacrylate Polymers 0.000 claims description 2
- 229920001515 polyalkylene glycol Polymers 0.000 claims description 2
- 229920001296 polysiloxane Polymers 0.000 claims description 2
- 229920002635 polyurethane Polymers 0.000 claims description 2
- 239000004814 polyurethane Substances 0.000 claims description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 2
- 235000019422 polyvinyl alcohol Nutrition 0.000 claims description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 2
- 150000004671 saturated fatty acids Chemical class 0.000 claims description 2
- 235000003441 saturated fatty acids Nutrition 0.000 claims description 2
- 239000008107 starch Substances 0.000 claims description 2
- 235000019698 starch Nutrition 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 235000010487 tragacanth Nutrition 0.000 claims description 2
- 239000000196 tragacanth Substances 0.000 claims description 2
- 229940116362 tragacanth Drugs 0.000 claims description 2
- 150000003626 triacylglycerols Chemical class 0.000 claims description 2
- 229940099259 vaseline Drugs 0.000 claims description 2
- 235000019219 chocolate Nutrition 0.000 claims 6
- 239000003999 initiator Substances 0.000 claims 3
- 235000015895 biscuits Nutrition 0.000 claims 2
- 235000008429 bread Nutrition 0.000 claims 2
- 239000006071 cream Substances 0.000 claims 2
- 235000015243 ice cream Nutrition 0.000 claims 2
- 235000013580 sausages Nutrition 0.000 claims 2
- 239000002453 shampoo Substances 0.000 claims 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 claims 1
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 claims 1
- 244000215068 Acacia senegal Species 0.000 claims 1
- 229920000742 Cotton Polymers 0.000 claims 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 claims 1
- 244000061456 Solanum tuberosum Species 0.000 claims 1
- 235000002595 Solanum tuberosum Nutrition 0.000 claims 1
- 239000012711 adhesive precursor Substances 0.000 claims 1
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 claims 1
- 230000005540 biological transmission Effects 0.000 claims 1
- 235000012970 cakes Nutrition 0.000 claims 1
- 238000004040 coloring Methods 0.000 claims 1
- 235000021185 dessert Nutrition 0.000 claims 1
- 235000011850 desserts Nutrition 0.000 claims 1
- 235000014505 dips Nutrition 0.000 claims 1
- 210000000416 exudates and transudate Anatomy 0.000 claims 1
- 235000013305 food Nutrition 0.000 claims 1
- 235000010445 lecithin Nutrition 0.000 claims 1
- 239000000787 lecithin Substances 0.000 claims 1
- 229940067606 lecithin Drugs 0.000 claims 1
- 239000000178 monomer Substances 0.000 claims 1
- 239000002243 precursor Substances 0.000 claims 1
- 235000008371 tortilla/corn chips Nutrition 0.000 claims 1
- 208000013464 vaginal disease Diseases 0.000 claims 1
- 239000012530 fluid Substances 0.000 description 4
- 229920000298 Cellophane Polymers 0.000 description 2
- 229940121375 antifungal agent Drugs 0.000 description 2
- 239000003429 antifungal agent Substances 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 210000001124 body fluid Anatomy 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
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- 229940079593 drug Drugs 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 2
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- GHXZTYHSJHQHIJ-UHFFFAOYSA-N Chlorhexidine Chemical compound C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 GHXZTYHSJHQHIJ-UHFFFAOYSA-N 0.000 description 1
- 241000252067 Megalops atlanticus Species 0.000 description 1
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- XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
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- 229960003260 chlorhexidine Drugs 0.000 description 1
- 229960004022 clotrimazole Drugs 0.000 description 1
- VNFPBHJOKIVQEB-UHFFFAOYSA-N clotrimazole Chemical compound ClC1=CC=CC=C1C(N1C=NC=C1)(C=1C=CC=CC=1)C1=CC=CC=C1 VNFPBHJOKIVQEB-UHFFFAOYSA-N 0.000 description 1
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- 239000003995 emulsifying agent Substances 0.000 description 1
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- 230000001632 homeopathic effect Effects 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000006041 probiotic Substances 0.000 description 1
- 235000018291 probiotics Nutrition 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 229960003500 triclosan Drugs 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Landscapes
- Absorbent Articles And Supports Therefor (AREA)
Description
SEA PCT/GBO1/05622 @
TAMPON PACKAGING SYSTEM
The present invention relates to a novel tampon packaging system.
In particular the invention relates to a tampon packaging system which is adapted to house a tampon and substrate which may subsequently be mixed just prior to use.
In particular embodiment the invention relate to such systems comprising means for applying medicaments and/or lubricants to tampons.
Co In the field of sanitary products, it is known that the application of a dry, absorbent sanitary product, for example a catamenial tampon, to or into moist body tissue, often causes discomfort. This is largely because the often filamentous external surfaces of the sanitary product absorb moisture and adhere to and irritate the tissue.
It is known to attempt to solve this problem by lubricating the product’s external surfaces. In one form, such lubrication consists of low-friction cover nets, meshes and webs and other perforate layers constructed to be capable of deforming resiliently, and permitting the passage of bodily fluids.
Alternative approaches have included fluid surface lubricants. However, problems
J associated with such lubricants include the fact that, over time, the sanitary article may gradually absorb the surface lubricant which may, inter alia, lead to a loss in absorbency in the article. :
US Patent No 4,428,747, attempts to overcome this problem with a blister package for holding, e.g. a sanitary tampon, which includes a trough which is adapted to act as a lubricant reservoir. In one embodiment the reservoir is provided with a removable cover. However, such a device suffers from the disadvantage that, inter alia, the trough renders the packaging bulky, and the complicated construction is difficult and expensive to manufacture. Moreover, the design requires that the tampon be
AMENDED SHEET
Co WO 02051718 PCT/GB01/05622 ® removed and dipped into the lubricant. Furthermore, the system cannot easily be incorporated in an integral tampon applicator.
The novel form of packaging which we have developed also overcomes or mitigates some of the disadvantages of prior art methods of delivering, e.g. lubricated tampons.
Thus, according to the present invention we provide a tampon packaging system comprising two strips of laminate material crimped along a first and second longitudinal edge and further crimped in a direction perpendicular to said longitudinal edges to provide at least three seals, being first and second end seals and
Co a frangible member, said three seals creating a first chamber for housing a tampon and a second chamber for housing a substrate for coating the tampon
In particular, the use of a frangible member in the packaging system of the invention allows the tampon and substrate to be brought into contact with each other without opening the packaging system. Thus, the frangible member should be such that, once ruptured, one or more apertures should be created between the first and second chambers, permitting the tampon in the first chamber to be contacted with the substrate in the second and vice versa.
The tampon may be of conventional design with coverstock and removal cord. . A
Suitable materials for the housing include at least one flexible synthetic polymer, such as a thermoplastic, for example a polyester or polyamide (e.g. nylon™), polypropylene or polyethylene or other conventionally known polymer materials.
Elastomeric materials may also be used (for example elastomeric polyurethanes) and may be incorporated together with non-elastomeric material of the film, membrane or sheet.
Preferred materials for the housing are polyethylene laminates, examples of such laminates include laminates of polyester/polyethylene, polypropylene/polyethylene, 2
AMENDED SHEET ot AWG,02/051718 PCT/GB01/05622 nylon/polyethylene and poly(ethyleneterephthalate)/polyethylene. The most preferred laminate is poly(ethyleneterephthalate)/polyethylene (PET/PE) and especially one in which the PE is a peelable PE.
S The first and second chambers, may be formed of the same, similar or different materials, the last-mentioned including at least one rigid synthetic polymer, such as a thermoplastic, for example a polyester or polyamide (e.g. nylon™), polypropylene or polyethylene, or other polymer materials. However, it is preferred that the first and second chambers comprise the same material so that, for example, they may be manufactured from a continuous strip of material.
Other materials that may be used include cellulosic materials, for example sheet materials, such as cardboard. When an absorbent surface like card is used then the substrate chamber is preferentially coated with a moisture and/or substrate resistant coating such as silicon, wax or cellophane or, alternatively, acrylic papers may be used. :
The thickness of the walls of the system may vary and may therefore be from 40 to 100 pm in thickness for each laminate. The thickness of each of the walls may be the same or different. Preferably, when the laminate comprises a PET/PE laminate, the
PE layer is of greater thickness than the PET layer. The PET layer may be from 10 to d 20 pm in thickness, preferably 10 to 15 pm. A thickness of 12 pum is most preferred.
The PE layer may be from 30 to 80 um in thickness, preferably from 35 to 70 pm and most preferably from 40 to 65 pm and especially 40 or 50 pm. A particularly preferred embodiment comprises a first wall comprising a laminate of 12 um PET and 50 pm peelable PE; and second wall of 50 pm PET and 65 pum peelable PE.
In one embodiment one or both of the walls may be metallised.
The substrate in the tampon packaging system will generally be provided only or mainly to the external surface of the tampon where it will provide the least hindrance 3
AMENDED SHEET
.1 MVO02/051718
ES b PCT/GB01/05622 to absorption of bodily fluids. An example would include the nose of a catamenial tampon.
The frangible member may be created by pressure crimping or heat crimping or a combination thereof.
In accordance with a preferred aspect of the invention we provide a process for the manufacture of a tampon packaging system as hereinbefore described which comprises the steps of; 1) heat and/or pressure crimping two strips of a laminate material along a first : longitudinal edge; (ii) heat and/or pressure crimping in a direction perpendicular to the first longitudinal edge seal to create at least three seals, being first and second end seals and a frangible member, said three seals creating first and second chambers; (iii) placing a tampon and a substrate in their respective first and second chambers; . (iv) heat and/or pressure crimping along a second longitudinal edge; and v) cutting to produce a tampon packaging system.
It may be optional to include step (v) as part of one of the earlier steps, e.g. step (i1), thus the heat and/or pressure crimping to create the first and second end seals may incorporate cutting step which may be separate, simultaneous or sequential to the sealing step.
Under laboratory conditions a preferred temperature of heat/pressure crimping is from 125 to 160°C (257 to 320F), preferably 130 to 150°C (266 to 302F), most ; 4
AMENDED SHEET
Co 9 #WO0,02/051718 } ® | PCT/GB01/05622 preferably about 140°C (284F). A preferred pressure for heat/pressure sealing is from 10 to 20 psi (0.69 to 1.38Bar), preferably 14 psi (0.966 Bar).
The duration of the crimping may vary and may be from 0.5 to 2.0 seconds, preferably 0.5t0 1.5, most preferably 1 second (under laboratory conditions).
The depth of the seal for the frangible membrane may vary and may be from 1 to 10 mm, preferably from 2 to 8 mm, more preferably from 3 to 6 mm and most preferably 3 mm.
If the periphery of the chambers are crimp sealed then the depth of the seal may be from 2 to 10 mm, more preferably 3 to 8 mm, more preferably 4 to 6 mm and especially 5 mm.
The substrate may comprise a variety of materials, such as medicaments, cosmetics, drugs, hormones, probiotics or lubricants. Examples of medicaments include antimicrobial agents, such as triclosan or chlorhexidine; or antifungal agents, such as clotrimazole. Medicaments also includes homeopathic medicines and/or aromatherapy materials. Examples of lubricants include extracts of sea algae, such as alginates, agar, cararageern, exsudates of plants, such as tragacanth, gum arabic;
Co extracts of plants, such as pectins, starch fractions and derivates, such as dextrins, ” amylopectins, hydroxyethyl starch; derivates of cellulose, such as methyl, ethyl, and hydroxypropyl cellulose; fatty substances such as mono, di, triglycerides of higher : saturated fatty acids, polyalkylene glycols and other ethoxylated products, such as polyethylene glycol 200-4000, PEG-G-capryl/caprine glyceride; hydrocarbons, such as paraffin oils, vaseline; polymers, such as polyvinyl alcohols, polyvinyl pyrrolidones, polyacrylates; alcohols, such as ethylene glycol, glycerol; emulsifiers, such as alecithin, cholesterin, or derivates of the sorbitan fatty acid esters; silicones; cellulosic polymers, e.g. KY-Jelly® (available in the UK from Johnson &
Johnson®). Mixtures of any of the aforesaid are also intended to be covered.
AMENDED SHEET co WO 021051718 PCT/GB01/05622 ® ,-
The frangible member may comprise at least one line of tear, break, fracture or breach, or other points, or at least one other line or region of brittleness, fragility or weakness. Such a member is thus capable of collapsing and/or tearing, breaking, bursting, cracking or snapping or tearing or breaking down under stress. :
In a further embodiment it may be desirable that one or more portions of the first chamber and/or the second are movable relative to the rest of the packaging system.
In use, a tampon housed in the first chamber is pushed into the second chamber, breaking the frangible member. The substrate substantially coats the nose and ! shoulder of the tampon. The two chambers may then be opened to facilitate removal of the substantially coated tampon.
The method of opening may vary depending upon, inter-alia, the method of construction employed for the chambers. However, as hereinbefore described, in a preferred embodiment, the chambers are formed by crimping the edges of the two walls of the chamber such that one wall may simply be peeled away from the other.
The chambers, and especially the first chamber, may be provided with means to facilitate peeling of the wall. Such facilitation means may comprise a liftable tab at a 70 comer of the chamber or at one end of the chamber. Alternatively, at least a portion of the periphery of the chamber may be perforated or cut away, €.g. notched to allow : an end of the chamber to be tom. Preferentially the facilitation means is provided adjacent the end of the chamber distal to the frangible member. In order to move the tampon into contact with the substrate, or vice versa. The term “movable” includes, for example, “compressible” and “squeezable” relative to the rest of the applicator and/or packaging system.
In another embodiment of the invention, the system may comprise a tampon applicator. Thus, according to a further feature of the invention we provide a tampon packaging system which comprises a first chamber for housing a tampon applicator and a second chamber for housing a substrate the first and second
AMENDED SHEET
SES ~ PCT/GB01/05622 chambers being separated by a frangible member. Means may be provided such as a piston or plunger slidable within the housing means to drive the tarpon out of the applicator.
Thus in a preferred embodiment of the invention the system comprises a cylindrical housing such that the membrane is radial to the cylinder. The substrate reservoir preferentially lies at one end of the cylinder.
In the applicator of the invention the second reservoir chamber may be provided with an openable end wall. Alternatively it may simply comprise an open wall with a ) removable cover. The cover may be a cardboard or plastics cover or may be, a plastics film, e.g. cellophane. The openable end wall is preferentially the wall distal to the membrane.
Thus it will be intended that the tampon be fluid-lubricated for application on its removal from the applicator across all or a major proportion of its absorbent surfaces by passage of the entire tampon product through the fluid lubricant.
It may be desirable that the first and second chambers are in the form of two coaxial hollow cylindrical chambers, containers or other receptacles of the same diameter but unequal axial length with a frangible or collapsible intervening wall or barrier, as hereinbefore described.
Thus, the tampon (a bullet-shaped catamenial tampon) may be housed in the larger chamber, container or other receptacle, which is the housing, with its nose towards and/or against the frangible wall or barrier, and a fluid lubricant may be held in the smaller chamber, container or other receptacle, which is thus the reservoir.
Alternatively, the first and second chambers may possess different diameters so that one may be slidable within the other.
AMENDED SHEET a . PCT/GB01/05622
The reservoir may optionally decrease in internal diameter towards end distal to the membrane. For example it may taper down and/or be domed or have at least one step change in internal diameter.
In one form, the side walls of the lubricant reservoir may extend beyond the closure membrane, film or sheet in the form of a dome covering the closure membrane.
Additionally or alternatively, the membrane may be integral with the side walls and may optionally be domed.
For an applicator tampon it may be undesirable for the tampon applicator to be
Co driven through the frangible membrane and through the fluid lubricant in the reservoir as there is a high risk that the tampon may be expelled from the applicator.
Thus, although in one embodiment an applicator tampon may be used to break the frangible membrane, it is preferred that the reservoir chamber is squeezed causing the material, eg a lubricant to rupture the frangible member and to be squeezed onto the nose of the applicator. Thus when the tampon is administered via the applicator, the nose of the tampon is coated as it is ejected from the applicator; in addition to the "lubrication of the applicator itself.
According to a further feature of the invention we provide a tampon applicator as hereinbefore described wherein said applicator also houses a tampon and a substrate.
When the applicator reservoir houses a medicament, such as an antifungal agent, the tampon and/or the applicator may be used in the treatment of certain disorders and may be used as an alternative to a pessary.
According to yet a further feature of the invention we provide the use of a cellulosic based lubricant and/or KY-Jelly® in the manufacture of a prefilled tampon packaging system as hereinbefore described. 8
AMENDED SHEET
+ WO 02/051718
Co o PCT/GB01/05622
In a further feature of the invention the packaging system may be provided with a fastening means for releasably securing the packaging in a folding arrangement. The fold may be a C or an S fold or any conventionally used fold. However, preferentially, the fold is a C fold and particularly a fold along the line of the frangible member. When the frangible member comprises the crimped walls of the chambers then a natural fold line is produced.
The fastening means may be any conventionally known fastening used in connection with, for example, sanitary articles. Thus, the fastening means may comprise an area of adhesive applied to a surface of the outer wall of one or both of the chambers.
Preferably, the fastening means comprises an adhesive tab such as is described in Us
Patent No 5,484,636, which is incorporated herein by reference.
Thus, the adhesive tab comprises a first end which is coated, on one side, with a relatively strong adhesive. The first end of the adhesive tab being fixed to an end of either the first or second chambers. Preferably the first end of the tab is fixed to the : end of the smaller of the two chambers, usually the second chamber, i.e. the substrate reservoir. The end of the chamber to which the adhesive tab is fixed is usually the end distal to the frangible member. ; A second end of the adhesive tab is coated, on one side, with a relatively weak or at
Jeast peelable adhesive. Alternatively, an adhesive may be provided with a ‘dead’ adhesive area for ease of opening.
The use of such a tab has the benefit that the tampon packaging system may present in a folded form which allows it to be carried discreetly. Moreover, once the packaging has been used it may be folded or rolled and the adhesive tab used to fasten the packaging together to aid disposal. Alternatively, the used packaging may itself be used as a receptacle for used or soiled tampon. Thus the used tampon may be placed in the first chamber and the packaging system folded or rolled as herein before described for disposal. 9
AMENDED SHEET
® }
The invention will now be described by way of example only and with reference to the accompanying drawings, in which
Figure 1 is a plain cross-section of a system of the invention housing a digital tampon and a lubricant;
Figure 2 is a plain cross-section of a system of the invention in which the tampon has broken the frangible member;
Figure 3 is a system of the invention in which the tampon has been drawn back out of the lubricant chamber;
Figure 4 is a side cross-section of a system of the invention housing a digital
Co tampon;
Figure 5 is a side cross-section of a system of the invention in which the tampon has broken the frangible member;
Figure 6 is a side cross-section of a system of the invention in which the tampon is removed from the lubricant chamber and is coated with lubricant;
Figure 7 is a side cross-section of a system of the invention in which one of the chamber walls is peeled away to expose the tampon;
Figure 8 is a close up cross-section of the liftable tab; :
Figure 9 is a plan cross-section of an applicator tampon system;
Figure 10 is a plan cross-section of an applicator tampon system in which the frangible member has been ruptured; ol Figure 11 is a plan cross-section in which the applicator tampon has been coated with lubricant; and
Figure 12 is a cross section view of the releasable folded system.
Referring to Figure 1, a packaging system (11) comprises a longitudinal cylinder and is provided with a first chamber (12) and a second chamber (13). The chambers (12 and 13) being separated by a frangible member (14). The first chamber (12) is adapted to house a tampon (15) when the article is a tampon which comprises a domed end (16) and a flat distal end (17) and the second chamber (13) houses a substrate (18), e.g. a lubricant.
AMENDED SHEET vo . : PCT/GB01/05622
Referring to Figure 2, in use, the tampon (25) is pushed via its flat end (26), either by hand or using a plunger, so that the domed end (26) breaks the frangible member (24). The tampon (25) then enters the reservoir of the second chamber (23) and contacts the substrate (28).
Referring to Figure 3, the tampon (35) is removed from the second chamber (33), by retracting it through the frangible membrane (34), the tampon (35) being coated with substrate (38). 0) Figure 3 to 6 provide a longitudinal cross-section view of the process illustrated in
Figures 1 to 3.
Referring to Figure 7, the end (711) of the first chamber (72), distal to the frangible member (not shown) is provided with a non-crimped, releasable region (710), which facilitates peeling apart the walls (711 and 712).
Referring to Figure 8, the end (811) of the first wall (89) is peeled away from the end (812) of the second wall (89).
Referring to Figure 7, the end (79) of the first chamber (72), distal to the frangible member (74) is provided with a non-crimped portion (10) which facilitates peeling apart of the walls (711 and 712) of the first chamber (72) and, optionally, the second chamber (73).
Referring to Figures 9 to 11, a packaging system (91) of the invention is used to house an applicator tampon (93). Thus, in use the second chamber (93) is squeezed causing the frangible member (94) to rupture, the lubricant (98) coats the applicator tampon (93). 11
AMENDED SHEET
Referring to Figure 12, the packaging system (121) is folded about the crimp line (124) between the first and second chambers (122 and 123). The end (125) of the second chamber (123) distal to the crimp line (124) is provided with a tab (126). A first end (127) of the tab (126) is coated with a relatively strong adhesive and is attached to the end (125) of the second chamber (123). A second end (128) of the tab (126) is coated with a relatively weak, peelable, adhesive. The second end (128) is attached to an outer wall of the first chamber (122). In use, the second end of the tab (126) may be peeled away to allow the packaging system to be used. After use, the packaging system may be rolled up and held together by re-adhering the second end (128) of the tab (126). Alternatively the used system may be used to discreetly dispose of soiled articles. 12
AMENDED SHEET
: © WO 02/051718 PCT/GB01/05622
Figure 1 is a plain cross-section of a system of the invention housing a digital tampon and a lubricant; : Figure 2 is a plain cross-section of a system of the invention in which the tampon has broken the frangible member; : 5 Figure 3 is a system of the invention in which the tampon has been drawn back out of the lubricant chamber;
Figure 4 is a side cross-section of a system of the invention housing a digital tampon,
Figure 5 is a side cross-section of a system of the invention in which the tampon has broken the frangible member;
Figure 6 is a side cross-section of a system of the invention in which the tampon is removed from the lubricant chamber and is coated with lubricant;
Figure 7 is a side cross-section of a system of the invention in which one of the chamber walls is peeled away to expose the tampon;
Figure 8 is a close up cross-section of the liftable tab;
Figure 9 is a plan cross-section of an applicator tampon system;
Figure 10 is a plan cross-section of an applicator tampon system in which the frangible member has been ruptured;
Figure 11 is a plan cross-section in which the applicator tampon has been coated with lubricant; and
Figure 12 is a cross section view of the releasable folded system.
Figure-14-is-a-plan-cross-section-of a sachet system in which the frangible member basheanuphued and
Figuret5isaplancross-section-in—whieh-the-yoghurt-and-fruit-have-been ~mixed-together.
Referring to Figure 1, a packaging system (11) comprises a longitudinal cylinder and is provided with a first chamber (12) and a second chamber (13). The chambers (12 and 13) being separated by a frangible member (14). The first chamber (12) is adapted to house an article (15), e.g. a tampon. When the article is a tampon which : comprises a domed end (16) and a flat distal end (17) and the second chamber (13) houses a substrate (18), e.g. a lubricant.
Referring to Figure 2, in use, the tampon (25) is pushed via its flat end (26), either by hand or using a plunger, so that the domed end (26) breaks the frangible member (24). The tampon (25) then enters the reservoir of the second chamber (23) and contacts the substrate (28).
Referring to Figure 3, the tampon (35) is removed from the second chamber (3 3), by retracting it through the frangible membrane (34), the tampon (35) being coated with substrate (38).
Figure 3 to 6 provide a longitudinal cross-section view of the process illustrated in
Figures 1103.
Referring to Figure 7, the end (711) of the first chamber (72), distal to the frangible member (not shown) is provided with a non-crimped, releasable region (710), which facilitates peeling apart the walls (711 and 712).
Referring to Figure 8, the end (811) of the first wall (89) is peeled away fromthe end (812) of the second wall (89).
Referring to Figure 7, the end (79) of the first chamber (72), distal to the frangible member (74) is provided with a non-crimped portion (10) which facilitates peeling apast of the walls (711 and 712) of the first chamber (72) and, optionally, the second chamber (73).
Referring to Figures 9 to 11, a packaging system (91) of the invention is used to house an applicator tampon (93). Thus, in use the second chamber (93) is squeezed causing the frangible member (94) to rupture, the lubricant (98) coats the applicator tampon (93).
Referring to Figure 12, the packaging system (121) is folded about the crimp line (124) between the first and second chambers (122 and 123). The end (125) of the second chamber (123) distal to the crimp line (124) is provided with a tab (126). A first end (127) of the tab (126) is coated with a relatively strong adhesive and is attached to the end (125) of the second chamber (123). A second end (128) of the tab (126) is coated with a relatively weak, peelable, adhesive. The second end (128) is attached to an outer wall of the first chamber (122). In use, the second end of the tab (126) may be peeled away to allow the packaging system to be used. After use, the packaging system may be rolled up and held together by re-adbering the second end (128) of the tab (126). Alternatively the used system may be used to discreetly dispose of soiled articles.
Referring to Figures 13 to 15, a packaging system (1) of the invention is used to house e.g. a yoghurt (1313) and a fruit sauce.
Thus, in use either the first (141) or the second chamber (143) is squeezed causing the frangible member (144) to rupture. The yoghurt (1513) and fruit sauce (153) are mixed around the point indicated as (155).
P36472WO.1
Claims (48)
1. A packaging system which comprises a first chamber adapted to house a first - material and a second chamber adapted to house a second material, the first and second chambers being separated by a frangible member.
2. A packaging system according to Claim 1 which comprises a first chamber for housing an article and a second chamber adapted to act as a substrate reservoir, the first and second chambers being separated by a frangible member.
3. A packaging system according to Claim 2 characterised in that the article is an absorbent article.
4. A packaging system according to Claim 3 characterised in that the absorbent article is a cotton bud.
5. A packaging system according to Claim 3 characterised in that the absorbent article is a sanitary tampon.
6. A packaging system according to Claim 1 characterised in that the frangible membrane is adapted to allow the first and second materials to be brought into contact without opening the packaging system.
7. A packaging system according to Claim 1 characterised in that the housing material comprises one or more of the following materials; a polyester, a polyamide, a polypropylene, a polyethylene, a polyurethane.
8. A packaging system according to Claim 1 characterised in that the housing material comprises a polyethylene laminate.
or WO 02/051718 PCT/GB01/05622
9. A packaging system according to Claim 8 characterised in that the polyethylene laminate is selected from polyester/polyethylene, polypropylene/polyethylene, nylon/polyethylene and polyethylene/poly (ethyleneterephthalate).
10. A packaging system according to Claim 9 characterised in that the laminate is a polyethylene/poly(ethyleneterephthalate) laminate.
11. A packaging system according to Claim 1 characterised in that the materials are selected from yoghurts and fruit sauces; polymerisable adhesive precursor and a polymer initiator; shampoos and colouring or conditioners, bread sticks and dip, sausages and dips, cake or biscuit bar and cream, chocolate or fudge sauce, e.g. ice-cream, desserts with fruit, chocolate or fudge sauce.
12. A packaging system according to Claim 1 characterised in that at least one of the materials is a foodstuff.
13. A packaging system according to Claim 1 characterised in that the materials are selected from yoghurt and fruit sauce; bread sticks and dip; sausages and dip; potato chip and dip; corn chips and dip; cake or biscuit bar and cream, chocolate or chocolate sauce or fudge sauce, frozen dessert, e.g. ice-cream, and fruit or fruit sauce, chocolate or chocolate sauce or fudge sauce. —
14. A _ packaging system_according to Claim_1_characterised_in_that_the materials comprise a shampoo and a colourant or conditioner.
15. A packaging system according to Claim 1 characterised in that the substrates are adapted to form an adhesive.
16. A packaging system according to Claim 10 characterised in that the adhesive comprises a monomeric polymer precursor and polymerisation initiator.
> WO 02/051718 PCT/GB01/05622
17. A packaging system according to Claim 3 characterised in that the substrate is a lubricant.
18. A packaging system according to Claim 17 characterised in that the lubricant is selected from one or more of; extracts of sea algae, alginates, agar, cararageen; exudates of plants, tragacanth, gum arabic; extracts of plants, pectins; starch fractions, dextrins, amylopectins, hydroxyethyl starch; derivatives of cellulose, methyl cellulose, ethyl cellulose, hydroxypropyl cellulose; fatty substances, monoglycerides, diglycerides, triglycerides of higher saturated fatty acids, polyalkylene glycols; ethoxylated products, polyethylene glycol 200-4000 (PEG), PEG-6-capryl/caprine glyceride; hydrocarbons, paraffin oils, Vaseline; polyvinyl alcohols, polyvinyl pyrrolidones, polyacrylates; ethylene glycol, glycerol; lecithin, cholesterin, sorbitan fatty acid esters; silicones; cellulosic polymers and mixtures of any of the aforesaid. : 15
19. A packaging system according to Claim 18 characterised in that the cellulosic polymer is KY-Jelly.
20. A packaging system according to Claim 1 characterised in that the substrate is a medicament. :
21. A packaging system characterised in that the frangible member is created by — bonding together the walls of the chambers. ~~ ~~
22. A packaging system according to Claim 19 characterised in that the bonding for the frangible member comprises heat and/or pressure crimping.
23. A packaging system according to Claim 22 characterised in that the crimping for the frangible member is carried out at a temperature of from 125 to 160°C.
v WO 02/051718 PCT/GB01/05622
24. A packaging system according to Claim 22 characterised in that the crimping for the frangible member is carried out by applying a pressure of from 10 to 20 psi.
25. A packaging system according to Claim 22 characterised in that the crimping for S the frangible member is carried out with a duration of 0.5 to 1.5 seconds.
26. A packaging system according to Claim 21 characterised in that the walls for the frangible member are crimped to a depth of from 2 to 10 mm.
27. A process for the manufacture of a packaging system according to Claim 1 which comprises heat and/or pressure crimping a portion of a strip material to create a first chamber for housing the sanitary article and a second chamber adapted to act as a substrate reservoir, the process of heat and/or pressure crimping crating a frangible member which separates the first and second chambers.
28. A process according to Claim 27 characterised in that the crimping is carried out at a temperature of from 120 to 160°C.
29. A process according to Claim 27 characterised in that the crimping is carried out by applying a pressure of from 10 to 20 psi.
30. A process according to Claim 27 characterised in that the crimping is carried out ~~ withaduationof0.5to LL3seconds. ~~~ ~~
31. A packaging system according to Claim 3 which comprises a first chamber for housing a sanitary article applicator and a second chamber, adapted to act as a substrate reservoir, the first and second chambers being separated by a frangible member.
32. A packaging system according to Claim 31 characterised in that the system comprises a first chamber, adapted to house a tampon applicator and a second
~ WO 02/051718 PCT/GB01/05622 chamber, adapted to act as a substrate reservoir, the first and second chambers being separated by a frangible member, the second chamber having a radial end wall, distal to the membrane which is operable to allow transmission of the tampon.
33. A packaging system according to Claim 31 characterised in that means is provided slidable within the first chamber to drive the tampon out of the applicator.
34. A packaging system according to Claim 31 characterised in that the applicator material is selected from one or more of cardboard, plastics or plastics film.
35. A packaging system according to Claim 31 characterised in that the tampon is a bullet-shaped catamenial tampon. :
36. A packaging system according to Claim 1 characterised in that the frangible member is provided with at least one line of tear or weakness to facilitate opening.
37. A packaging system according to Claim 1 characterised in that the system is provided with means for releasably securing the packaging in a folding arrangement.
38. A packaging system according to Claim 37 characterised in that the means for releasably securing the packaging in a folding arrangement is an adhesive coated tab.
39. A packaging system according to Claim 37 characterised in that the adhesive coated tab is coated with a relatively strong adhesive at a first end and a relatively weak adhesive at a second end.
thd WO 02/051718 PCT/GB01/05622
40. A method of intravaginal delivery of a lubricant or medicament which comprises the use of a sanitary article in a packaging system according to Claim 1.
41. A method of treating a vaginal disorder which comprises delivering a medicament using a sanitary article in a packaging system according to Claim 19.
42. The use of KY-Jelly in the manufacture of a sanitary article packaging system according to Claim 19.
43. A method of delivering two separate mixable components which comprises the use of a sachet system according to Claim 1.
44. The use of a food material in the manufacture of a prefilled foodstuff sachet system according to Claim 1.
45. The use of an adhesive monomer and/or a polymerisation initiator in the “manufacture of a prefilled adhesive sachet system according to Claim 1.
46. A process for the manufacture of a packaging system as hereinbefore described which comprises heat and/or pressure crimping a portion of a strip material to create a first chamber for housing a first material and a second chamber adapted to house a second material, the process of heat and/or pressure crimping creating a frangible member which separates the first and second chambers.
47. A process for the manufacture of a sanitary article packaging system as hereinbefore described which comprises the steps of; @) heat and/or pressure crimping two strips of a laminate material along a first longitudinal edge;
v WO 02/051718 PCT/GB01/05622 (iii) placing a sanitary article and a material in their respective first and second chambers; (iv) heat and/or pressure crimping along a second longitudinal edge; and (v) cutting to produce a sanitary article.
48. A sanitary article packaging system as hereinbefore described with reference to the accompanying drawings. 22 SUBSTITUTE SHEET (RULE 26)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0031655A GB0031655D0 (en) | 2000-12-23 | 2000-12-23 | Packaging system |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200304034B true ZA200304034B (en) | 2004-03-26 |
Family
ID=9905900
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200304034A ZA200304034B (en) | 2000-12-23 | 2003-05-23 | Packaging system. |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB0031655D0 (en) |
ZA (1) | ZA200304034B (en) |
-
2000
- 2000-12-23 GB GB0031655A patent/GB0031655D0/en not_active Ceased
-
2003
- 2003-05-23 ZA ZA200304034A patent/ZA200304034B/en unknown
Also Published As
Publication number | Publication date |
---|---|
GB0031655D0 (en) | 2001-02-07 |
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