Multilayer test pack for sterilization monitoring
12544472 ยท 2026-02-10
Assignee
Inventors
- G. Marco Bommarito (Stillwater, MN)
- Timothy J. Nies (Stillwater, MN, US)
- Paul N. Holt (St. Paul, MN, US)
Cpc classification
B32B3/266
PERFORMING OPERATIONS; TRANSPORTING
B32B7/10
PERFORMING OPERATIONS; TRANSPORTING
A61L2103/15
HUMAN NECESSITIES
B32B3/28
PERFORMING OPERATIONS; TRANSPORTING
B32B37/0076
PERFORMING OPERATIONS; TRANSPORTING
B32B37/10
PERFORMING OPERATIONS; TRANSPORTING
B32B38/18
PERFORMING OPERATIONS; TRANSPORTING
B32B37/153
PERFORMING OPERATIONS; TRANSPORTING
A61L2/28
HUMAN NECESSITIES
B32B37/12
PERFORMING OPERATIONS; TRANSPORTING
B32B3/30
PERFORMING OPERATIONS; TRANSPORTING
B32B7/12
PERFORMING OPERATIONS; TRANSPORTING
International classification
B32B3/00
PERFORMING OPERATIONS; TRANSPORTING
A61L2/28
HUMAN NECESSITIES
B01L3/00
PERFORMING OPERATIONS; TRANSPORTING
B32B3/26
PERFORMING OPERATIONS; TRANSPORTING
B32B3/28
PERFORMING OPERATIONS; TRANSPORTING
B32B3/30
PERFORMING OPERATIONS; TRANSPORTING
B32B37/00
PERFORMING OPERATIONS; TRANSPORTING
B32B37/10
PERFORMING OPERATIONS; TRANSPORTING
B32B37/15
PERFORMING OPERATIONS; TRANSPORTING
B32B38/18
PERFORMING OPERATIONS; TRANSPORTING
Abstract
The disclosed multilayer test pack comprises a channel lamina to form a recessed channel, and then a seal layer covers the recessed channel to form an embedded channel. By providing the recessed channel in a thin-film channel lamina, the recessed channel tolerances are better controlled. Further, using thin films for the channel lamina, which can be formed into a roll, allows for a continuous unrolling and continuous bonding to a seal layer.
Claims
1. A multilayer test pack for sterilization monitoring, the multilayer test pack comprising: a channel lamina configured to provide resistance for exposing a sterilant to a sterilization indicator contained within the multilayer test pack, the channel lamina comprising: a channel layer, comprising: a top surface; a bonding surface; and a recessed channel having a depth defined by an entire thickness of the channel layer and extending through the entire thickness of the channel layer, wherein the thickness of the channel layer extends from the bonding surface to the top surface; and a surface layer fixed to the top surface of the channel layer; a seal layer comprising a seal surface and an outer surface opposite from the seal surface, wherein the seal surface is bonded to the bonding surface; and a sealed cavity formed in a layer of the multilayer test pack other than the channel lamina, wherein the sealed cavity holds the sterilization indicator, wherein the recessed channel extends from an inlet port exposed to an external environment to an outlet port exposed to the sealed cavity.
2. The multilayer test pack of claim 1, wherein the channel lamina comprises a first continuous layer comprising the channel layer and a second continuous layer comprising the surface layer.
3. The multilayer test pack of claim 2, wherein the recessed channel extends entirely through the first continuous layer.
4. The multilayer test pack of claim 1, wherein the surface layer and the bonding surface are planar.
5. The multilayer test pack of claim 1, wherein the channel lamina further comprises an edge surrounding the channel layer and the surface layer.
6. The multilayer test pack of claim 1, wherein the seal layer further comprises an edge surrounding the seal surface and the outer surface.
7. The multilayer test pack of claim 1, wherein the seal layer further comprises the sealed cavity.
8. The multilayer test pack of claim 1, wherein the inlet port is located at an edge of the channel lamina, is located at the surface layer, or is at the seal layer.
9. The multilayer test pack of claim 1, wherein the outlet port is located at the channel layer or at the seal layer.
10. The multilayer test pack of claim 1, wherein the sealed cavity holds at least one of a biological indicator or a chemical indicator.
11. The multilayer test pack of claim 1, wherein the seal surface is bonded to the bonding surface by thermal bonding or adhesive bonding.
12. The multilayer test pack of claim 1, further comprising a biological indicator disposed in the sealed cavity.
13. The multilayer test pack of claim 1, wherein the sterilant comprises steam, ethylene oxide, or hydrogen peroxide.
14. The multilayer test pack of claim 1, wherein the recessed channel is configured to provide sufficient challenge to the sterilant reaching an indicator within the sealed cavity.
15. A method of making a multilayer test pack for sterilization monitoring, the method comprising: providing a channel lamina configured to provide resistance for exposing a sterilant to a sterilization indicator contained within the multilayer test pack and comprising a channel layer and a surface layer fixed to the channel layer, wherein the channel layer comprises: a top surface; a bonding surface; and a recessed channel having a depth defined by an entire thickness of the channel layer and extending through the entire thickness of the channel layer, wherein the thickness of the channel layer extends from the bonding surface to the top surface; providing a seal layer comprising a seal surface and an outer surface opposite from the seal surface; and forming a sealed cavity in a layer of the multilayer test pack other than the channel lamina; and disposing the sterilization indicator in the sealed cavity.
16. The method of claim 15, wherein the recessed channel extends from an inlet port exposed to an external environment to an outlet port exposed to the sealed cavity.
17. The method of claim 15, wherein bonding the seal surface to the bonding surface comprises thermal bonding or adhesive bonding.
18. The method of claim 15, wherein the channel lamina comprises a single, unitary structure, and wherein the method further comprises microreplicating the recessed channel into the channel layer.
19. The method of claim 15, wherein the channel lamina comprises a first continuous layer comprising the channel layer and a second continuous layer comprising the surface layer, and wherein the method further comprises bonding the first continuous layer to the second continuous layer.
20. The method of claim 15, wherein the channel lamina is provided on a first roll and the seal layer is provided on a second roll, the method further comprising: unrolling the channel lamina; unrolling the seal layer; and continuously bonding the seal surface to the bonding surface.
Description
BRIEF DESCRIPTION OF DRAWINGS
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(12) While the above-identified drawings and figures set forth embodiments of the invention, other embodiments are also contemplated, as noted in the discussion. In all cases, this disclosure presents the invention by way of representation and not limitation. It should be understood that numerous other modifications and embodiments can be devised by those skilled in the art, which fall within the scope and spirit of this invention. The figures may not be drawn to scale.
DETAILED DESCRIPTION
(13) Precisely forming a channel into a sterilization test pack will provide a definite amount of resistance for exposing sterilant to the sterilization indicators contained within the test pack. A thin-film channel lamina is used to form a recessed channel, and then a seal layer covers the recessed channel to form an embedded channel By providing the recessed channel in a thin film channel lamina, the recessed channel tolerances are better controlled. As will be described below, microreplication processes can be used, which have extremely controlled manufacturing tolerances or in embodiments where the channel lamina is a multilayer structure, the recessed channel can be entirely cut through a film layer forming the recessed channel. Further, using thin films for the channel lamina, which can be formed into a roll, allows for a continuous unrolling and continuous bonding to a seal layer. Therefore, manufacturing can be continuous, fast and efficient.
(14) Prior test packs, such as shown in U.S. Pat. Nos. 7,927,866 and 9,017,944 typically used thermoforming processing to create all of the structured surfaces, the channel as well as the sealed cavity, in a single layer. Given the large difference in size between the channel and the sealed cavity, wide variation in forming the channel can occur. Further, thermoforming or injection molding can be a slow, batch manufacturing process where parts are made one-by-one.
(15) The disclosed multilayer test pack comprises a channel lamina, a seal layer, which combine to form an embedded channel. The sealed cavity for holding the sterilization indicator is separately connected with the channel lamina.
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(17) The multilayer test pack 100 has a channel lamina 120, a seal layer 130, and a sealed cavity 150. In an assembled form, such as shown in
(18) Channel lamina 120 is a generally planar sheet comprising channel surface 122, covering surface 128, and an edge 129. The channel lamina 120 is generally much longer and wider than it is thick. Channel surface 122 comprises bonding surface 124 and recessed channel 126. In this embodiment, the recessed channel 126 extends partially into the channel lamina 120. In this embodiment, recessed channel 126 does not extend completely through channel lamina 120. In one embodiment, recessed channel 126 extends no greater than 10%, no greater than 25%, no greater than 50%, no greater than 75%, no greater than 90% into a thickness of channel lamina 120. Precise control of the dimensions (length, depth, and diameter) of recess channel 126 is important for obtaining a reliable test pack. High precision can be achieved using a method such as microreplication for manufacturing the channel lamina 120 such as shown in
(19) Seal layer 130 has a seal surface 132, an outer surface 134, and an edge 136. Seal layer 130 is generally planar and in this embodiment further comprises recess 138. Recess 138 is a space that can hold one or more indicators. Indicators include chemical indicators and biological indicators.
(20) As shown in
(21) Sealed cavity 150 is formed from the recess 138 sealed to the channel lamina 120. The sealed cavity 150 can receive one or more indicators, such as chemical or biological indicators. As shown in this embodiment, the sealed cavity 150 is integral with the seal layer 130. The sealed cavity 150, in the assembled construction such as shown in
(22) Chanel lamina 120 and seal layer 130 can be formed from materials that are able to bond together and can withstand the sterilization process. For example, the materials could be thermoplastic material, including, but not limited to, propylene, polyethylene, polystyrene, and polyvinyl chloride.
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(24) The multilayer test pack 200 has a channel lamina 220, which comprises a channel layer 221 and a surface layer 225, a seal layer 230, and a sealed cavity 250. In an assembled form, the channel lamina 220 and seal layer 230 interface to form a sealed channel 240.
(25) Channel lamina 220 comprises channel layer 221, surface layer 225, surrounded by an edge 229. Channel layer 221 comprises top surface 223 and channel surface 222 Channel surface 222 comprises bonding surface 224 and recessed channel 226. The recessed channel 226 extends through the entire thickness of channel layer 221. Top surface 223 of channel layer 221 is fixed to surface layer 225. Precise control of the depth of the recess channel 226 is achieved because control of the thickness of the channel layer 221 will define the thickness for the recessed channel 226.
(26) Seal layer 230 has a seal surface 232, an outer surface 234, and edges 236. Seal layer 230 is generally planar and further comprises recess 238. Recess 238 is a space that can hold one or more indicators, such as chemical indicators and biological indicators.
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(28) Sealed cavity 250 is formed from the recess 238 sealed to the channel lamina 220. The sealed cavity 250 can receive one or more indicators, such as chemical or biological indicators. As shown, the sealed cavity 250 is integral with the seal layer 230. The sealed cavity 250, in the assembled construction such as shown in
(29) Chanel lamina 220 and seal layer 230 can be formed from materials that are able to bond together and can withstand the sterilization process. For example, the materials could be thermoplastic material, including, but not limited to, propylene, polyethylene, polystyrene, and polyvinyl chloride.
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(31) The multilayer test pack 300 has a channel lamina 320, which comprises a channel layer 321 and a surface layer 325, a seal layer 330, and a sealed cavity 350. When assembled, the channel lamina 320 and seal layer 330 interface to form a sealed channel 340. In this embodiment, sealed cavity 350 is not integrally formed with the seal layer 330 but is instead separately connected with the seal layer 330.
(32) Channel lamina 320 comprises channel layer 321, surface layer 325, surrounded by edge 329. Similar to the construction described in
(33) Seal layer 330 has a seal surface 332, an outer surface 334, and an edge 336. Seal layer 330 is generally planar. As assembled, seal layer 330 is fixed to channel lamina 320 at the interface of bonding surface 324 with seal surface 332 with techniques such as as, ultrasonic welding, solvent welding, an adhesive, hot melt bonding, thermal bonding/lamination and combinations thereof. Recessed channel 326 forms the embedded channel 340 when seal layer 330 is fixed to channel lamina 320, and when the channel lamina 320 has surface layer 325 secured. Embedded channel 340 has first end 341 and second end 343 (exemplified in
(34) Sealed cavity 350 is formed from the recess 338 sealed to the seal layer 330. Sealed cavity 350 receives one or more indicators, such as chemical and biological indicators. As shown, the sealed cavity 350 is separately connected with the seal layer 330. In this embodiment, the sealed cavity 350 can be bonded or secured to the seal layer 330 through such techniques as ultrasonic welding, solvent welding, an adhesive, hot melt bonding, thermal bonding/lamination, or combination thereof. The sealed cavity 350, in the assembled construction such as shown in
(35) Chanel lamina 320, seal layer 330, and sealed cavity 350 can be formed from materials that are able to bond together and can withstand the sterilization process. For example, the materials could be thermoplastic material, including, but not limited to, propylene, polyethylene, polystyrene, and polyvinyl chloride. Any one of these layers may be of various thickness, flexibility, or rigidity.
(36) Inserted into the sealed cavity 350 is at least one of a biologic indicator or a chemical indicator. Following a sterilization cycle, where the sterilant travels through the embedded channel to reach the sealed cavity, the indicators must be read. If the sealed cavity is constructed of a clear material, visual indication on the indicator can be perceived. However, typically biologic indicators will need to be removed from the sealed cavity and allowed to incubate. Following incubation then the biologic indicator is read. Therefore, the various layers of the disclosed test package should be constructed to allow access into the sealed cavity following sterilization. In one example, the adhesive or lamination of the sealed cavity is removable to allow access to the contained indicator in the sealed cavity.
(37) Although the embodiments described a single embedded channel, it is understood that more than on embedded channel could be formed for providing access from the exterior environment to the sealed cavity.
(38) It is understood that for any embodiment, the location of the inlet port can be interchangeably located in the edge of the channel lamina such as shown in
(39) It is understood that for any embodiment, the channel lamina maybe a single layer, like shown in
(40) It is understood that for any embodiment, the cavity can be integrally formed as part of the seal layer such as shown in
(41) An advantage of the test packs described herein is that the overall area of the test pack can be minimized because the embedded channel can extend over an area of the sealed cavity. Alternative designs where the channel and the cavity are integrally formed into the same material have the channel adjacent to the cavity and therefore the size of the test pack is larger. In an embodiment, the cavity can be located directly beneath the embedded channel.
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(44) A method of using the test pack can include subjecting the test pack containing one or more indicators to a decontamination process such as autoclaving along with the materials being decontaminated. The sterilant, such as steam, ethylene oxide, or hydrogen peroxide, travel from the external environment, through the embedder channel, and into the sealed cavity containing the indicators. A chemical indicator will indicate exposure to the sterilant. The sterilant will kill any of the biologic material within the biologic indicator. Following sterilization, the indicators can be removed. If used, a biologic indicator may be incubated to determine whether any remaining biologic matter will grow to indicate a failed sterilization cycle.
(45) Although specific embodiments have been shown and described herein, it is understood that these embodiments are merely illustrative of the many possible specific arrangements that can be devised in application of the principles of the invention. Numerous and varied other arrangements can be devised in accordance with these principles by those of skill in the art without departing from the spirit and scope of the invention. The scope of the present invention should not be limited to the structures described in this application, but only by the structures described by the language of the claims and the equivalents of those structures.