WO1999062697A9 - Desiccant blended in a thermoplastic - Google Patents
Desiccant blended in a thermoplasticInfo
- Publication number
- WO1999062697A9 WO1999062697A9 PCT/US1999/011565 US9911565W WO9962697A9 WO 1999062697 A9 WO1999062697 A9 WO 1999062697A9 US 9911565 W US9911565 W US 9911565W WO 9962697 A9 WO9962697 A9 WO 9962697A9
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- desiccant
- insert
- container
- thermoplastic
- moisture
- Prior art date
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D23/00—Details of bottles or jars not otherwise provided for
- B65D23/02—Linings or internal coatings
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/26—Drying gases or vapours
- B01D53/261—Drying gases or vapours by adsorption
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D81/00—Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents
- B65D81/24—Adaptations for preventing deterioration or decay of contents; Applications to the container or packaging material of food preservatives, fungicides, pesticides or animal repellants
- B65D81/26—Adaptations for preventing deterioration or decay of contents; Applications to the container or packaging material of food preservatives, fungicides, pesticides or animal repellants with provision for draining away, or absorbing, or removing by ventilation, fluids, e.g. exuded by contents; Applications of corrosion inhibitors or desiccators
- B65D81/264—Adaptations for preventing deterioration or decay of contents; Applications to the container or packaging material of food preservatives, fungicides, pesticides or animal repellants with provision for draining away, or absorbing, or removing by ventilation, fluids, e.g. exuded by contents; Applications of corrosion inhibitors or desiccators for absorbing liquids
Definitions
- the present invention relates to packages having desiccating abilities. More particularly, the present invention relates to a thermoplastic having a desiccant blended therein.
- BACKGROUND OF THE INVENTION There are many articles that are preferably stored, shipped and/or utilized in an environment that is as moisture free as possible. Therefore, containers and/or packages having the ability to absorb excess moisture trapped therein have been recognized as desirable.
- One application in which moisture absorbing containers are desired is for the shipment and storage of medications whose efficacy is compromised by moisture.
- the initial placement of medicines into a sealed moisture free container is usually controllable.
- the container for the medicine is selected so that is has a low permeability to moisture. Therefore, the medication will normally be protected from moisture until it reaches the end user.
- the container must be repeatedly opened and closed to access the medication.
- moisture bearing air will most likely be introduced into the container and sealed therein upon closure. Unless this moisture is otherwise removed from the atmosphere or head space of the container, it may be detrimentally absorbed by the medication. For this reason, it is a well known practice to include a desiccating unit together with the medication in the container.
- moisture may be released from items that have been placed in containers or sealed in packaging wrap for shipping and/or storage. Prime examples of such items are food stuffs that release moisture during shipping and storage. In the instance of containers that are sealed and substantially impermeable to moisture, the released moisture will remain within the container.
- this released moisture may have ill effects on the very item that released the moisture. It has been found that a substantial amount of moisture is released from certain food products within the first forty-eight (48) hours after manufacture and packaging. This released moisture will remain until removed. If the moisture is not removed shortly after its release, it may cause the food to degrade into a condition that is not saleable and/or useable. In these cases, desiccants may be included together with the contained item or items to continually absorb the released moisture until the product is unpacked. In this way, a relatively dry environment is maintained about the stored item. The need to eliminate moisture from within sealed containers has been previously recognized.
- the desiccant is not integrally constructed with the container, or at least attached thereto, it may be prematurely removed while still needed for continued removal of moisture from within the container. Therefore, a need has been recognized for containers that include a desiccant as an integral component of the container's body or package. Regarding the included desiccant of the container, it is desired to enhance its capabilities of moisture absorption with respect to both rate and quantity. Still further, as in all manufacturing processes, it is desired to reduce the required steps for constructing desiccating containers and simplify the resulting structures.
- SUMMARY OF THE INVENTION In one embodiment of the present invention, a container, and process for constructing the container is provided that satisfies the need for more effective desiccating storage and shipping containers.
- the containers of the present invention provide superior desiccating abilities, while at the same time permitting efficient construction of a container that has and maintains structural integrity. Furthermore, the present invention provides a means by which the container may be formed having a substantially unitized and continuous body. In another embodiment, the present invention may be used to form an insert, integral or non-integral, for the container or package in the form of a shaped article such as a sheet, film, or pellets, for example, in the base or bottom of the container and not capable by itself of containing the contents of the container.
- Figure 1 is a cross-sectional view of a desiccating container with an insert in the form of a disc molded therein.
- Figure 2 is a cross-sectional view of a desiccating container with an insert in the form of a liner molded therein.
- Figure 3 is a partial cross-sectional view of the container body showing a lip retainer.
- Figure 4 is a side view of a mold in partial section mounted upon a rotatable table for transport between injection stations and showing a container and insert molded therein.
- Figure 5 is a side view of a mold in partial section showing a container and insert molded therein in a single station configuration with two injection ports.
- Figure 6 is a schematic of the method by which the container is co-molded.
- the containers 01 disclosed herein are not limited to vials. It is contemplated that containers 01 constructed according to the present invention may be larger or smaller than the vials of 4,783,056 and of variable shape. Furthermore, the caps 14 may be integrally formed with the bodies 12 of the containers 01 , or they may be manufactured as separate units. Still further, the present invention may be embodied exclusively within the body of a container 12 or a cap 14 for a container 01.
- the material used in the construction of these containers 01 typically provides a barrier between the interior 201 and exterior 202 of the container 01 that is substantially moisture impermeable and most often is a thermoplastic. While it is contemplated that any thermoplastic may be utilized, polypropylene is preferred for the construction of the body 12 of the container 01.
- Polypropylene is desirable because of its durability, rigidity and resistance to breakage after being molded into the form of a container 01.
- suitable thermoplastics may be selected from the following groups: polyolefm, polyethylene, polycarbonate, polyamide, ethylene-vinyl acetate copolymer, ethylene-methacrylate copolymer, polyvinyl chloride, polystyrene, polyester, polyester amide, polyacrylic ester, and polyvinylidene chloride, acrylic, polyurethane, polyacetal, and polycarbonate.
- These and other thermoplastics may be utilized either singularly, or in combinations.
- the present invention includes the manufacture of a container 01 in which the majority of the container's body 12 is constructed from the base thermoplastic, e.g.
- an insert 200 that has been formed from a desiccant entrained thermoplastic is integrally constructed with the body 12 of the container 01.
- the heat molded insert of the present invention consists essentially of the thermoplastic material with the entrained desiccant.
- the term "consisting essentially of” is used herein to denote that the molded insert may contain other materials so long as they do not materially effect the moisture removal properties of the insert.
- the heat molded insert may have also entrained carbon black or other coloring agents to provide color or other aesthetic properties to the insert.
- concentration of desiccant entrained e.g.
- the desiccant concentration in the insert 200 will fall within a range of forty to seventy- five (40-75%o) desiccant to thermoplastic, by weight. This concentration is considered to be a high concentration for most thermoplastics.
- the maximum desiccant bearable concentrations will vary among the various types of thermoplastics due to their differing characteristics. In the instance of polyethylene or polypropylene, for example, the maximum concentration of desiccant will be about seventy-five percent (75%) by weight.
- the insert 200 is located in the base or bottom 203 of the container body 12 and is exposed to the interior space 201 of the container 01.
- the configuration of this embodiment is similar to a sample vial. Because the durability and resistance to breakage is lessened in the higher ranges of desiccant content, it is advantageous to have the polypropylene used in the construction of the container's body 12 formed about the insert 200 except for at those surfaces to be exposed to the interior 201 of the container 01.
- a container 01 of this configuration provides desired structural integrity while also providing the greater desiccating ability of the high desiccant laden insert 200 that is directly exposed to the interior 201 of the container 01.
- the insert 200 may be included in the construction of the container's cap 14. In this case, the insert will be integrally formed with the cap 14 so that an exterior surface of the insert 200 is exposed to the interior 201 of the container 01 when installed thereupon.
- the insert 200 may be less localized, and extended to a greater degree about a greater portion of the interior surface 204 of the container body 12.
- the high desiccant bearing thermoplastic forms more of a liner 205 at the interior surface 204 of the container 01.
- the liner 205 may completely cover the interior surface 204 of the container 01 ; this may optionally include the interiorly exposed surfaces of a cap 14 of a closed container 01.
- One contemplated method for the manufacture of the container 01 includes the provision of a performed insert 200 about which the thermoplastic of the remainder of the body 12 of the container 01 is injection molded. In this process, it is important that the insert 200 be affixed to or within the body 12 of the container 01. This may be achieved merely by molding the body 12 about the insert 200 so that the two components are mechanically connected one to the other.
- the mechanical connection may take the form of a retaining lip 206 formed by the container body 12 about the insert 200 that effectively fixes the insert 200 with respect to the rest ofthe body Ol.
- the insert of the present invention is formed by heat molding the desiccant entrained thermoplastic of the present invention.
- the insert may be heat molded using any conventional technique such as co-extruding, extrusion blow moulding, injection blow molding, reaction injection moulding or extruding.
- a "shrink-fit" may be achieved by the body 12 forming thermoplastic about the insert 200.
- a particular example of this shrink-fit application would be the provision of a desiccant loaded insert 200 constructed from a base thermoplastic of polyethylene and a container body 12 molded thereabout from a base thermoplastic of polypropylene.
- polyethylene shrinks less than polypropylene under similar circumstances. Therefore, if a polypropylene body is injection molded about a polyethylene insert 200 that has been either previously formed, or is injection molded contemporaneously with the container body 12, the polypropylene container body 12 will shrink about the polyethylene insert 200.
- This shrink-fit method may be implemented whether or not the insert 200 is relatively small and localized with respect to the container body 12 or whether or not the insert 200 is relatively small and localized with respect to the container body 12 or whether the insert 200 takes the form of a previously described liner 205 configuration. In either case, the exteriorly formed container body 12 may shrink about the insert 200 if the thermoplastics from which the insert 200 and container body 12 are appropriately selected.
- the retaining lip 206 and shrink-fit method of affixing the insert 200 or liner 205 to the container body 12 is used primarily when the materials of construction of the insert 200 and container body 12 are not compatible. The two components will be considered incompatible if they do not automatically adhere one to the other as a result of the manufacturing process.
- the insert 200 will be constructed from a material that bonds to the body 12 of the container 01 when the body 12 is placed thereabout. Therefore, one method for constructing the insert 200 bearing container 01 of the present invention is co-molding. That is, the primary body 12 of the container 01 is molded, while the high desiccant insert 200 is also molded.
- the two portions are said to be co-molded because they are either simultaneously or sequentially injection molded in a single process.
- the process of co-molding results in the construction of a unitized container body 12 in which the insert 200 is seamlessly combined with the body 12.
- the insert 200 and container body 12 adhere one to the other as a result of a melding together of the base thermoplastics from which each is constructed at an interface therebetween.
- the melding action takes place when the insert 200 and container body 12 are each injected into the mold 10 sufficiently closely with respect to time so that each is in at least a semi-molten state while in contact one with the other.
- thermoplastic in which the desiccant is entrained is moisture permeable to the degree that moisture from the interior 201 of the container 01 may be transferred to and stored in the desiccant. It is possible that the thermoplastic from which the insert 200 is manufactured may have a higher moisture permeability than that from which the remainder of the body 12 of the container 01 is constructed.
- the insert 200 may be enclosed within the container 01 by a lower moisture permeable thermoplastic of the container's body 12. In this way, moisture will not readily be transferred from outside the container 01 to the interior.
- the two components 200, 12 may be constructed from different materials that are potentially incompatible.
- the process of the present invention in which the insert 200 is co-molded within the primary body 12 of the container 01 may vary. In a first embodiment of the molding process, it is contemplated that the mold 10 will move between two injection stations. An injection assembly that is generally designated by reference numeral 96 may be installed and withdrawn from the mold frame 24.
- the insert 200 will be injection molded.
- a ring shaped barrier will be provided that has a circumference substantially matching the perimeter of a lower end of care 48. It is desired that the thickness of the insert 200 be approximately one-eighth of an inch, therefore the thickness or height of the barrier ring will likewise be one-eighth of an inch.
- the barrier ring is the leading component. The ring contacts the lower surface of the core 48 forming a barrier within which thermoplastic may be injected. High concentrate desiccant thermoplastic is then injected into the interior of the ring thereby forming the insert 200.
- the high concentrate desiccant thermoplastic of the insert 200 may be injected at a temperature that is less than the temperature at which the thermoplastic of the container body 12 is injected.
- the lowered temperature may be required so that the desiccant contained therein does not degrade.
- the necessity of the lowered temperature may be obviated by using different and/or high-grade desiccants that are not susceptible to degradation within the normal temperature ranges of the injection process. It is anticipated that the rate of absorption into the insert 200 may be controlled by the amount of surface area of the insert 200 exposed to the container's 01 interior 201. If greater absorption rates are desired, more surface area of the insert 200 may be exposed. If it is desired that a more prolonged absorption process be achieved, then less surface area will be exposed.
- the rate of absorption by the insert 200 may be controlled by encapsulation of the insert 200. If slower rates of absorption are desired, then the insert 200 can be encased to greater degrees by the thermoplastic that forms the body 12 of the container 01 and which is less permeable to moisture. The rate of absorption may also be controlled by using different types of thermoplastics having different moisture permeability rates.
- the moisture permeability rates of the thermoplastics of the present invention are determined by ASTM test method F 1249-90, entitled "Standard Test Method for Water Vapor Transmission Rate Through Plastic Film and Sheeting Using a Modulated Infrared Sensor.”
- ASTM F 1249-90 test method the thermoplastics suitable for the present invention have a moisture vapor transmission rate of less than about 30g/mil/l 00 in2/24 hours.
- polyethylene typically has a moisture vapor transmission rate of about 3 to about 5 gm per mil per 100 square inches per 24 hours.
- the polyethylene that is suitable in the present invention is made by Dow Chemical Co. and has a tradename of polyethylene 4012.
- polypropylene homopolymer typically has a moisture vapor transmission rate below 10 gm per mil per 100 square inches per 24 hours.
- the polypropylene that is suitable in the present invention is made by Exxon Chemicals and has a tradename of Escorenea Polypropylene-PP 3505G.
- low density polyethylene butene copolymer typically has a moisture vapor transmission rate of about 1 to about 2 gm per mil per 100 square inches per 24 hours.
- the low density polyethylene butene copolymer that is suitable in the present invention is made by Union Carbide Corp. and has a tradename of GRSN-1539. The amount of moisture that can be absorbed by the insert 200 may be controlled in several ways.
- the amount of moisture absorbable by the insert 200 may be effected by changing the concentration of desiccant within acceptable ranges; the greater the concentration, the greater the amount of moisture that can be captured.
- the thermoplastic from which the body 12 is constructed may also have desiccant entrained and suspended therein, but in lesser concentrations than the insert 200. It has been found that the concentration of desiccant in the thermoplastic affects the performance characteristics of the molded container 01. As an example, it has been found that while the plastic will carry relatively high percentages of desiccant, desirable characteristics such as durability and resistance to breakage may degrade at higher desiccant concentrations.
- thermoplastic may be combined with lower concentrations of desiccant without appreciably degrading the performance of the thermoplastic material in its molded and solid state.
- a relatively low concentration will fall within the rate of five to fifteen percent (5 - 15%) desiccant by weight to thermoplastic, with a preferred concentration being approximately seven and one-half (7.5%).
- desiccant-free thermoplastic may also be considered low concentration thermoplastic.
- the thermoplastic having the lower concentration of desiccant is molded with the thermoplastic having the higher concentration of desiccant. That is, the primary body 12 of the container 01 is molded, while the high desiccant insert 200 is also molded.
- the two portions are said to be co-molded. This process results in a unitized contained body 12.
- Various concentrations of desiccant bearing thermoplastic are commercially available in pellet form. Custom concentrations may be achieved by dry blending higher concentration desiccant pellets with lower concentration or desiccant-free pellets of thermoplastic. When blended in appropriate proportions, any desiccant concentration less than that of the high concentration desiccant pellets may be accomplished. After the drying blending process, the resulting mixture of pellets may be injection molded in a typical manner.
- the type of desiccants that are suitable for use in the present invention obtain their moisture adsorbing capabilities through physical adsorption.
- the adsorption process is accomplished because of a fine capillary morphology of the desiccant particles which pulls moisture therethrough.
- the pore size of the capillaries, as well as the capillaries' density determine the absorption properties of the desiccant.
- these physical adsorption desiccants include molecular sieves, silica gels, clays and starches.
- the molecular sieve pore sizes that are suitable for use in the present invention include between about 3 to 15 Angstroms; about 3 to 5 Angstroms, about 5 to 8; 3 Angstroms; 4 Angstroms; 5 Angstroms; 8 Angstroms and 10 Angstroms.
- the pore size of silica gel is about 24 Angstroms.
- these types of physical adsorption desiccants are both inert and non-water soluble, they are preferred for many applications. Among other reasons, these innocuous characteristics are particularly compatible with food products and medicinal products such as pharmaceutical drugs and devices that may be enclosed within containers formed from the desiccant entrained polymers, or at least exposed thereto. As stated previously, however, any of the three types may be employed within the polymer bases of the present invention for the purposes of producing a desiccant entrained polymer.
- Suitable desiccating agents of the present invention include silica gel, molecular sieve and naturally occurring clay compounds which would also include montmorillimite clay.
- the desiccant that is suitable for use in the present invention is zinc chloride.
- the molded insert can be produced by mixing the components, heating and molding the mixture.
- the mixing conditions are chosen so that the desiccant is sufficiently entrained by substantially uniformly blending in the thermoplastic.
- the components are mixed using a conventional mixer, for example, a Hensehel mixer.
- the present invention does not require further processing by stretching (e.g. uniaxial or biaxial orientation method) or expanding (e.g. stretching at fast rates then exposing the material to its crystalline melt point) to produce a porous material.
- the present invention is particularly suited for applications where a product's (e.g. pharmaceutical drug or device) efficacy may be compromised by a threshold amount of moisture.
- the present heat molded insert having a combination of: (a) a thermoplastic having certain moisture vapor transmission rate characteristics; (b) a certain type of desiccant; (c) the insert having a certain minimum and maximum weight % of desiccant; and (d) the insert having a minimum moisture adsorption after 8 hours at 10%> relative humidity ("Rh") without stretching or expanding.
- Rh relative humidity
- EXAMPLE 1 This example illustrates a desiccant blended in a thermoplastic consisting essentially of a thermoplastic of polypropylene (Exxon Chemicals, tradename Escorenea Polypropylene 3505G) and a desiccant of molecular sieve (Elf Atochem, tradename Siliporitea molecular sieves; NK 10).
- the desiccant and thermoplastic were weighed to achieve the weight percent of each shown in the table.
- the desiccant and thermoplastic were then mixed in a Henschel FM-200 high intensity mixer.
- the material was then fed to a Leistritz twin screw extruder at a temperature in the ten zones ranging from about 200° to 320°F, at about 400 rpm and at about 30 lbs./hr to produce a pelletized material of about 1/8 inch diameter.
- the pelletized material was fed directly to a hot roll press. A film was formed of desired thickness (10 mil).
- the film was then evaluated for moisture adsorption of its total weight by using the following test method (a) the environmental chamber was preset for 72°F and the desired relative humidity ("Rh"); (b) the dish was weighed and the weight recorded; (c) the scale was then tared to remove the weight of the dish from the balance; (d) the film was then added to the weighed dish; (e) the material was then weighed and the weight recorded; (f) the weigh dish with the sample was placed in the environmental chamber; (g) the sample was left in the chamber for the desired time; (h) after the desired time was reached, the dish with the sample was removed, re-weighed and the weight recorded; and (i) percent of moisture absorbed per gram of material was calculated by: final weight - original weight * 100 original weight
- thermoplastic consisting essentially of a thermoplastic of a low density polyethylene butene copolymer (Union Carbide, tradename 1137) and of a desiccant of molecular sieve (Elf Atochaem, tradename Siliporitea molecular sieves, NK10).
- the desiccant and thermoplastic were prepared in a manner similar to the method discussed in Example 1 to produce a pellet.
- the pellet was then formed into a film by using a platen press.
- the pellet was placed in the press between 2 sheets of Mylar film.
- the pellet was pressed at 425°F at 25 tons for about 15-20 seconds.
- the desired thickness was achieved by placing shims inside press.
- the film was removed and allowed to cool for about 15-20 seconds and then placed in a vacuum sealed brown bag.
- the film was also evaluated by the same method as discussed in Example 1. The results are presented in Table II.
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- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Food Science & Technology (AREA)
- Packages (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP99925837A EP1112175A4 (en) | 1998-06-04 | 1999-05-25 | Desiccant blended in a thermoplastic |
JP2000551938A JP2002516917A (en) | 1998-06-04 | 1999-05-25 | Desiccant blended with thermoplastic material |
AU42047/99A AU4204799A (en) | 1998-06-04 | 1999-05-25 | Desiccant blended in a thermoplastic |
BR9910917-4A BR9910917A (en) | 1998-06-04 | 1999-05-25 | Heat molded insert |
CA002334014A CA2334014A1 (en) | 1998-06-04 | 1999-05-25 | Desiccant blended in a thermoplastic |
NO20006172A NO20006172L (en) | 1998-06-04 | 2000-12-04 | Desiccant mixed in thermoplastic |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US9063598A | 1998-06-04 | 1998-06-04 | |
US09/090,635 | 1998-06-04 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO1999062697A1 WO1999062697A1 (en) | 1999-12-09 |
WO1999062697A9 true WO1999062697A9 (en) | 2000-03-09 |
Family
ID=22223628
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1999/011565 WO1999062697A1 (en) | 1998-06-04 | 1999-05-25 | Desiccant blended in a thermoplastic |
Country Status (8)
Country | Link |
---|---|
EP (1) | EP1112175A4 (en) |
JP (1) | JP2002516917A (en) |
CN (1) | CN1308574A (en) |
AU (1) | AU4204799A (en) |
BR (1) | BR9910917A (en) |
CA (1) | CA2334014A1 (en) |
NO (1) | NO20006172L (en) |
WO (1) | WO1999062697A1 (en) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU742886B2 (en) * | 1997-03-05 | 2002-01-17 | Capitol Vial, Inc. | A method of making a desiccating container with an insert from desiccant bearing material |
US7700305B2 (en) | 1999-09-17 | 2010-04-20 | N2Itive1 Innovations | Analyte detection |
GB0015043D0 (en) † | 2000-06-21 | 2000-08-09 | Glaxo Group Ltd | Medicament dispenser |
DE10060852A1 (en) | 2000-12-06 | 2002-06-20 | Hexal Ag | Active ingredient-impermeable cover layer or removable protective layer of a transdermal therapeutic system containing absorbents and channel formers |
WO2003013843A1 (en) † | 2001-08-06 | 2003-02-20 | Csp Technologies, Inc. | Method and composition for an in-mold liner |
US7617932B2 (en) | 2003-09-19 | 2009-11-17 | Diabetes Diagnostics, Inc. | Medical device package, kit and associated methods |
US7516845B2 (en) | 2004-03-31 | 2009-04-14 | Inverness Medical Limited | Medical device package with deformable projections |
US7595278B2 (en) * | 2005-01-21 | 2009-09-29 | Multisorb Technologies, Inc. | Resin bonded sorbent |
EP1935796B8 (en) * | 2006-12-22 | 2010-10-20 | Airsec S.A.S. | Container |
EP2050334B1 (en) | 2007-10-18 | 2017-04-05 | Allflex Europe SAS | An ear tag for marking an animal and for sampling tissue from said animal |
CA2724353C (en) | 2008-05-15 | 2017-06-20 | Csp Technologies, Inc. | Vial with non-round seal |
ITMI20081374A1 (en) * | 2008-07-25 | 2010-01-26 | Getters Spa | COMPOSITE ABSORBER OF H2O FOR SEALED MEDICAL DEVICES |
WO2015106109A1 (en) | 2014-01-10 | 2015-07-16 | Medtronic, Inc. | Frames for implantable medical devices and methods |
CN105460347A (en) * | 2014-09-11 | 2016-04-06 | 钱国华 | Package bottle |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5078909A (en) * | 1989-05-23 | 1992-01-07 | Sasaki Chemicals Co., Ltd. | Moisture-absorbent compositions and molded items |
US5304419A (en) * | 1990-07-06 | 1994-04-19 | Alpha Fry Ltd | Moisture and particle getter for enclosures |
FR2698289B1 (en) * | 1992-11-20 | 1995-01-27 | Airsec Ind Sa | Desiccants based on polymers. |
WO1996037288A1 (en) * | 1995-05-26 | 1996-11-28 | Hitachi Chemical Company, Ltd. | Environment purifying material |
-
1999
- 1999-05-25 WO PCT/US1999/011565 patent/WO1999062697A1/en not_active Application Discontinuation
- 1999-05-25 CN CN 99808443 patent/CN1308574A/en active Pending
- 1999-05-25 CA CA002334014A patent/CA2334014A1/en not_active Abandoned
- 1999-05-25 AU AU42047/99A patent/AU4204799A/en not_active Abandoned
- 1999-05-25 BR BR9910917-4A patent/BR9910917A/en not_active IP Right Cessation
- 1999-05-25 JP JP2000551938A patent/JP2002516917A/en not_active Withdrawn
- 1999-05-25 EP EP99925837A patent/EP1112175A4/en not_active Withdrawn
-
2000
- 2000-12-04 NO NO20006172A patent/NO20006172L/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
NO20006172D0 (en) | 2000-12-04 |
CA2334014A1 (en) | 1999-12-09 |
WO1999062697A1 (en) | 1999-12-09 |
EP1112175A4 (en) | 2001-08-08 |
NO20006172L (en) | 2001-02-01 |
JP2002516917A (en) | 2002-06-11 |
AU4204799A (en) | 1999-12-20 |
EP1112175A1 (en) | 2001-07-04 |
CN1308574A (en) | 2001-08-15 |
BR9910917A (en) | 2001-10-16 |
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