Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
  • B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
  • B65B55/00—Preserving, protecting or purifying packages or package contents in association with packaging
  • B65B55/02—Sterilising, e.g. of complete packages
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
  • A61L12/00—Methods or apparatus for disinfecting or sterilising contact lenses; Accessories therefor
  • A61L12/02—Methods or apparatus for disinfecting or sterilising contact lenses; Accessories therefor using physical phenomena, e.g. electricity, ultrasonics or ultrafiltration
  • A61L12/04—Heat
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
  • A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
  • A61L2/02—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using physical phenomena
  • A61L2/04—Heat
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
  • A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
  • A61L2/02—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using physical phenomena
  • A61L2/04—Heat
  • A61L2/06—Hot gas
  • A61L2/07—Steam
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
  • A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
  • A61L2/24—Apparatus using programmed or automatic operation

Definitions

• the present invention relates generally to a contact lens manufacturing arts, and, in particular to a novel in-line sterilizer for an ophthalmic contact lens manufacturing system, sterilization tray and method for performing inline sterilization of packaged contact lenses more efficiently and with increased throughput.
• each lens is formed by sandwiching a monomer between back curve (upper) and front curve (lower) mold structure transported in a mold cavity.
• the monomer is polymerized (cured) to form a lens blank, and is subject to further processing including, but not limited to: removing the lens blanks from their mold structures, i.e., de-molding; subjecting the lenses to a hydration process; transferring of the lenses to an individual blister package; automatic lens inspection of the lens, e.g., while contained in their blister pack; lens sterilization; and final packaging for consumer use.
• the reader may refer to U.S. Patent No. 5,555,504 entitled PRODUCTION LINE TRACKING AND QUALITY CONTROL SYSTEM for a description of an exemplary prior art ophthalmic lens production and packaging control system.
• a manufactured ophthalmic lens in an aqueous solution is sealed in a blister pack and sterilized in a steam sterilizer.
• Example descriptions of packaged contact lenses and techniques for their sterilization are described in U.S. Pat Nos. 5,488,815 and 5,577,367. Particularly, in commonly-owned issued U.S. Patent No.
• an apparatus contemplates the utilization of a conveyor system for the conveyance of a plurality of trays, each adapted to house therein a specific quantity of interleaved pairs of arrays of blister packages, which are sequentially folded into paired interleaved positions, and then conveyed through the intermediary of a transfer conveyor into a respective metal tray so as to fill spaces in the latter arranged in specified rows and columns.
• the metal tray which is placed into an upended position in order to be able to receive the interleaved pairs of arrays of blister packages from a shuttle conveyor, upon being filled is then tilted back into a normally horizontal orientation and, if desired depending upon production requirements, up to three such array-filled metal trays may then be vertically stacked or superimposed, and also conveyed in a series of such stacked trays.
• a conveyor is adapted to convey the metal trays with the arrays of blister packages contained therein into a sterilizing chamber, such as an autoclave, in which the arrays of blister packages are collectively sterilized.
• a secondary packaging procedure is implemented where the trays together with the sterilized arrays of blister packages are transported by a further conveyor towards an unloading arrangement in which the trays are unstacked and individual trays then sequentially upended.
• This enables the contents of the trays to be transferred to an unloading shuttle conveyor which, in turn, facilitates specified quantities of interleaved pairs of arrays of blister packages to be advanced in succession into a cartoner having open-ended cartons therein adapted to receive the arrays of blister packages.
• the blister package array trays must be transferred from the manufacturing line to the sterilizer which is in a separate area off-line from the manufacturing stations.
• an in-line sterilization machine that sterilizes ophthalmic lens packages without having to offload product from the line. Furthermore, as prior attempts to segregate sterile and non-sterile product implement manual procedures, it would be highly desirable to provide for an automated contact lens manufacturing facility, an in-line sterilization machine that inherently prevents the mixing of sterile and no-sterile product. It would be highly desirable to provide for an automated contact lens manufacturing facility, an in-line sterilization machine that sterilizes ophthalmic lens packages without having to offload product from the line, and, that is of improved design and capable of sterilizing a greater number of package containing trays that can be achieved in current systems, thus increasing throughput per unit volume.
• an object of the present invention to provide an in-line sterilizing apparatus for sterilizing contact lens containing packages without off-loading the packages from the manufacturing line. It is another object of the present invention to provide a novel tray structure for carrying contact lens containing packages in an in-line sterilizing apparatus that enables increased throughput per unit volume.
• the integration of the ophthalmic lens package sterilizer within the manufacturing line provides physical separation of sterile and non-sterile product. The result is that the product cannot move the sterile packaging area without going through the sterilizer.
• the integration also allows complete tracking of the product through the lens machine by the machine controller, ensuring that the product must go through a complete sterilization cycle before unloading to the secondary packaging area.
• Figure 1 is a conceptual top plan view of a portion of the lens production facility including the various stations involved with loading of ophthalmic lens containing blister packages in novel tray units and their in-line sterilization according to the principles of the invention;
• Figure 2 is a side elevation view of the in-line sterilizer station 50 including the tray stacking, novel sterilizer machine, and tray de-stacking stations;
• Figure 3(a) is a top plan view of the novel tray unit according to the principles of the invention.
• Figure 3(b) is a detailed close-up view of the circled portion 100a of the tray 100 illustrated in Figure 3(a);
• Figure 4(a) is a side cross-sectional view of the novel tray 100 taken along line "E-E" illustrated in Figure 3(a);
• Figure 4(b) is a front cross-sectional view of a portion of the novel tray 100 taken along line "F-F" of the tray 100 illustrated in Figure 3(a);
• Figure 5 depicts the interleaved pairs of blister arrays 150 deposited in a respective cavity 120 of the novel tray 100;
• Figure 6 illustrates the front elevation view of the in-line sterilizer machine shown receiving a stack of trays from a conveyor;
• Figure 7 is a piping and instrumentation diagram illustrating the devices and operating parameters for performing steam sterilization according to the invention.
• Figure 8 is a side elevation view of the latch mechanism 175 that retains the stack of trays at the tray stacking station 25 of Figure 2.
• the invention includes an apparatus for sterilizing ophthalmic lens packages comprising a sterilizing chamber designed to accommodate a plurality of ophthalmic lens packages; a means for transporting said ophthalmic lens packages to said sterilizing chamber; a means for subjecting a plurality of ophthalmic lens packages to appropriate sterilization cycle when said ophthalmic lens packages are contained within said sterilizing chamber; wherein, said sterilizing chamber is disposed contiguously with prior processing stations and secondary packaging stations of a ophthalmic lens manufacturing line.
• ophthalmic lens includes but is not limited to hard contact lenses, soft contact lenses, rigid gas permeable contact lenses, intraocular lenses and lenses for eyeglasses.
• the ophthalmic lenses inspected in this invention may or may not contain vision correction.
• the preferred lenses are soft contact lenses with or without vision correction.
• Soft lenses may be made of conventional hydrogels and are generally prepared from monomers including but not limited to hydroxyethyl methacrylate (HEMA), vinyl pyrrolidone, glycerol methacrylate, methacrylic acid and acid esters; or silicone hydrogels.
• HEMA hydroxyethyl methacrylate
• vinyl pyrrolidone vinyl pyrrolidone
• glycerol methacrylate methacrylic acid and acid esters
• silicone hydrogels silicone hydrogels.
• soft contact lenses include but are not limited to etafilcon A, genfilcon A, lenefilcon A, polymacon, acquafilcon A, balafilcon A, lotrafilcon A and silicone hydrogels as prepared in U.S. Pat. No. 5,998,498, US Pat. App. No. 09/532,943, a continuation-in-part of US Pat App. No. 09/532,943, filed on August 30, 2000, U.S. Pat. Ser. No. 09/957, 299 filed on September 20, 2001 , U.S. Patent No. 6,087,415, U.S. Pat. No. 5,760,100, U.S. Pat. No.5,776, 999, U.S. Pat. No.
• ophthalmic lenses Numerous processes are known for making ophthalmic lenses, including various processes to make soft contact lenses. While the present invention is applicable across the board to all ophthalmic lens processes, a preferred practice, along with its correlative manufacturing line stations, will now be described in the context of a soft contact lens, it being understood that the present invention is not limited to such lenses.
• ophthalmic lens packages refers to the primary packaging for individual ophthalmic lenses, or more commonly known a blister packages. Examples of said packages include but are not limited to the packages disclosed in U.S. Patent Nos. 4,691 ,820; 5,054,610; 5,337,888; 5,375,698; 5,409,104; 5,467,868; 5,515,964; 5,609,246; 5,695,049; 5,697,495; 5,704,468; 5,711 ,416; 5,722,536; 5,573,108; 5,823,327; 5,704,468; 5,983,608; 6,029,808; 6,044,966; and 6,401 ,915, U.S. Pat. App. Ser. No. 60/436,109 filed on December 23, 2002 entitled "Contact Lens
• the term "sterilizing chamber” refers to an enclosure that is used to sterilize ophthalmic lens packages. Said chamber may be opened, automatically or manually, to permit entry and exit of said packages. Further said chamber must be constructed to allow, either or both, heating or cooling by of any of a number of methods which include but are not limited to dry heat, steam heat, jacketed cooling, and the like. Temperature modification of said chamber sterilizes ophthalmic lens packages contained therein.
• means for transporting includes but is not limited to conveyor belts, pulleys, and other mechanized system used to move items along a manufacturing line.
• means for transporting includes "sterilizing trays.” Said sterilizing trays have external walls and internal walls dividing said tray in order to enable to hold a plurality of ophthalmic lens packages in the most efficient orientation for sterilizing said packages. The preferred orientation for sterilizing said packages is with the package held vertically, as depicted in Figure 5.
• means for subjecting includes but is not limited to pressure, heat and steam sources and regulators.
• prior processing stations include but are not limited to any stations an ophthalmic lens manufacturing line such as lens formation, hydration, inspection and the like.
• the prior processing stations include any or any combination of the following means for loading said sterilizing trays with ophthalmic lens packages, means for transferring the loaded sterilizing trays to the sterilizing chamber, means for unloading said sterilizing trays, and means for transferring the sterilized ophthalmic lens packages to said second packaging station.
• the term “sterilization cycle” refers subjecting said packages to different temperatures and pressures in order to sterilize said packages and ophthalmic lenses contained therein.
• “secondary packaging” includes but is not limited to cartons, shrinking wrapping or other methods of enclosing the individually packaged ophthalmic lenses in multiple containers. Examples of such secondary packaging are disclosed in U.S. Pat. No. 5,577,367 which is hereby incorporated by reference in its entirety. An example of an embodiment of the invention is illustrated in greater detail in reference to the following figures.
• FIG. 1 there is shown a simplified diagrammatic top view of a portion 10 of a contact lens production facility including a processing station designed to enable expedient and consolidated packaging of manufactured ophthalmic lenses in an aqueous solution contained in an individual blister package, and a processing station designed to enable their expedited sterilization with increased throughput.
• a processing station designed to enable expedient and consolidated packaging of manufactured ophthalmic lenses in an aqueous solution contained in an individual blister package
• a processing station designed to enable their expedited sterilization with increased throughput.
• an individual formed ophthalmic contact lens is placed into an individual plastic "blister" package containing an aqueous solution.
• each individual blister package is removably attachable to one or more other packages to form a blister pack array comprising three blister packages, for example (not shown).
• a formed ophthalmic lens is loaded in each blister pack of the array and is sealed in accordance with techniques known in the art.
• the formed and sealed blister pack arrays 22 are transferred to a tray loading station 20, where they are loaded into a novel sterilizer tray (not shown), as will be described in greater detail herein.
• two formed and sealed blister pack arrays 22 are interleaved (nested) in a manner prior to transference to a tray loading station 20 by rotating one array and placing a second array on top of the other.
• the blister pack array has been designed to provide the interleaving feature.
• a novel sterilizing tray unit designed to receive and support the blister packs for conveyance through the in-line sterilizer unit is indexed from an empty tray stack (not shown) proximate the tray loading station 20 to receive the packages at the tray loading station 20.
• the novel in-line sterilizer tray is suitably indexed and oriented for enabling a gripper mechanism 28 to automatically pick and transfer each interleaved pair of blister arrays into a correspondingly indexed cavity formed in the tray.
• the tray is situated horizontally while the gripper mechanism picks five (5) pairs of blister pack arrays and places them vertically into one (1) row comprising five tray cavities designed to receive the nested pair.
• the tray filled with the plurality of interleaved pairs of blister arrays is automatically conveyed by a servo-controlled belt driven conveyor, for example, in the direction labeled "A", into a tray stacking station 25 where a stack of trays are formed.
• nine trays, each filled with the plurality of interleaved pairs of blister package arrays, is stacked one on top of each other and automatically conveyed, in the direction labeled "B", to an immediately adjacent in-line sterilizer 50 where they are subject to an efficient steam/heat sterilization process as will be explained in greater detail herein.
• the design of the in-line sterilization station 50 coupled with the novel sterilization tray design that permits stacking enables increased lens sterilization throughput levels heretofore unachievable.
• the novel in-line sterilizer design permits implementation of new sterilization process parameters that ensures the dryness of every blister pack array, which is essential for subsequent automated secondary packaging.
• the tray stack comprising the sterilized blister pack arrays is automatically conveyed, in the direction labeled "C", to an immediately adjacent tray de-stacking station 60 where, in an essentially a reversed process, the trays are one-by-one destacked.
• the individual de-stacked tray is then automatically conveyed, in the direction labeled "D", to an unload station 70 where the blister packs of each tray are picked-up for transference to a secondary packaging station where they are suitably placed in cartons as part of a secondary packaging procedure.
• FIG. 2 is a side elevation view of the in-line sterilizer station including the tray stacking station 25, novel sterilizer machine, and tray de-stacking stations.
• the tray stacking station 25 operates as follows: a first sterilizer tray 100 filled with the plurality of interleaved pairs of blister package arrays is automatically conveyed from the tray loading station on a tray carrier 160. This tray carrier serves to index the tray one (1) row at a time through the tray loading process and then indexes to the stacking position. Under precise program control, the stacker cylinder 170 is actuated to elevate the tray carrier carrying the tray 100, in the direction labeled "G", above the level of conveyor 180, e.g.
• the latch is actuated by an air cylinder which opens with air and closes with spring force. The spring force allows the trays to push past the latch and closes on the tray to hold it in place.
• the cylinder is then actuated to retract the tray carrier 160 to retrieve the next tray unit including the plurality of interleaved pairs of blister package arrays.
• the process repeats and the tray carrier is elevated for placement underneath the tray stack in a stackable manner.
• the latch mechanism is actuated to hold the second tray having the first tray in a stacked configuration thereon, as will described herein with respect to Figure 8.
• the latch mechanism is holding a nested stack of nine sterilizer trays 200.
• the latch is finally released and the stack 200 of sterilizer trays becomes supported by conveyor 180 which is driven to convey the stack into the in-line sterilizer machine 50 in the load direction as indicated in Figure 2.
• the sterilizer includes a motorized roller conveyor 195 which is synchronized with the conveyor 180. This allows the stack of trays to load into the sterilizer.
• the stack unloads to the conveyor 181 at the de-stacker station 60 where the top tray 100 of the stack 200 is transferred to another tray carrier 161.
• the interleaved arrays of blister packs are unloaded using a similar gripper mechanism used to load the tray as described with respect to Figure 1.
• Figure 8 is a side elevation view of the latch mechanism 175 that retains the stack of trays at the tray stacking station 25 of Figure 2.
• latching fingers 175a,b under spring control are actuated by the stacking cylinder 170 when extended ( Figure 2) to nest the next successive tray 101 at the bottom of the tray stack.
• the elevation of the stack by the tray carrier and stacking cylinder causes the latch fingers to disengage from the first tray, and catch the next upward moving tray in the stack where the latch fingers again engage the peripheral ridge portion 107 at each side of the tray 100.
• the spring is actuated so that the latch fingers will eventually engage the respective ridge portion 107 at each side of the bottommost tray 101 for supporting the stack thereon.
• Figure 6 illustrates the front elevation view of the in-line sterilizer machine Figure 6 shown receiving the stack of trays 200 on a conveyor. More particularly, as shown in Figures 5 and 6, a conveyor 195, such as a roller type conveyor provided within the sterilizer, is communicatively situated at an equal height "h" in the sterilizer as the conveyor 180 of the tray stacking station so that the tray stack 200 may be directly transported to within the confines of the sterilizer chamber 53. Prior to transference, under program control, the doors of the sterilizer are opended, e.g., vertical doors may be retracted. The stack in conveyed from conveyor 180 to 195 within the sterilizer in synchrony. After the sterilizer is loaded, the doors are closed and the sterilization cycle begins.
• a conveyor 195 such as a roller type conveyor provided within the sterilizer
• the sterilizer 50 is a jacketed pressure chamber 53 having two doors 56 with the jacket 307 surrounding the chamber 53 so as to provide extra heat during the sterilization cycle as shown in Figure 7.
• the dimensions of the in-line sterilizer chamber is approximately 650 mm in height, 450 mm wide and 650 mm deep, thus providing less than a cubic meter (1 m 3 ), which using the novel sterilization trays of the invention, is sufficient to provide a capacity per unit of chamber volume of approximately three (3) times greater than prior art versions.
• the sterilizer machine is a complete system with mechanical/electrical process components, an internal sterilizer tray conveyor 195, and control system.
• the sterilizer 50 is integrated into the manufacturing machine to provide much higher throughput per unit volume. As will be explained in greater detail, this throughput/volume is achieved by implementing the novel sterilization trays used. Meeting the requisite "dryness” criteria is achieved by the design of the sterilizer, use of the novel trays, and the sterilization process parameters implemented during the sterilization cycle, as will be explained.
• the invention includes a method of sterilizing ophthalmic lens packages comprising transporting a plurality of said ophthalmic lens packages to a sterilizing chamber; subjecting said plurality of ophthalmic lens packages at least one sterilization cycle within said sterilizing chamber; wherein, said sterilizing chamber is disposed contiguously with prior processing stations and secondary packaging stations of a ophthalmic lens manufacturing line.
• ophthalmic lens packages, sterilizing chamber, prior processing station, sterilization cycle, and secondary packaging stations all have their aforementioned meanings and preferred ranges.
• An embodiment, that illustrates, but does not limit, this invention is disclosed below.
• FIG. 7 is a piping and instrumentation diagram illustrating the major devices and controls utilized for performing steam sterilization according to the invention.
• the expedited and efficient lens package sterilization process is enabled under the programmed control and supervision of an enhanced programmable logic control system (PLC) or like equivalent control device 99.
• PLC enhanced programmable logic control system
• the function is to pre-heat product and internal chamber with dry heat only, to prevent steam condensation on product.
• the steps involved with this process includes: starting the fan motor which is indicated at 302 in Figure 7; initiating the start of the Preheat Sequence Timer with a pre-set value of 2.0 minutes in an example embodiment described.
• a jacket steam valve that is indicated at 304 in Figure 7 is opened and a Jacket Pressure Switch 308 setpoint is controlled, which, in the example embodiment described, is at a switch setpoint value of about 2.0 bar, for example.
• Air valves 310 and drain valves 320 are then actuated to control the air pressure of the chamber at air overpressure setpoint with a small percentage of the alarm limits.
• the air overpressure setpoint value is a saturated steam pressure at + 1.05 bar and is set within the overpressure alarm limits of +/- 0.2 bar, for example.
• the function is to heat the product with steam and dry heat to a sterilization temperature.
• the steps involve opening a jacket steam valve 304 and setting the jacket pressure switch to a setpoint value of approximately 2.0 bar.
• one or more air valves and drain valves 310, 320 are actuated in order to control the chamber pressure at air over-pressure setpoint within a +/- percentage of the alarm limits.
• the air overpressure setpoint value is a saturated steam pressure at + 1.05 bar and is set within the overpressure alarm limits of +/- 0.2 bar, for example.
• the Steam Control Valve that is indicated at 305 in Figure 7 is opened to achieve a temperature setpoint value plus overshoot.
• the temperature setpoint value is 124.0 ° C with an overshoot value of about 0.6 ° C.
• an Exposure Start delay timer preset to a value of 1.0 minute begins counting and when the Exposure Start timer reaches 1.0 minute, the process advances to the next phase.
• the function is to hold the product at sterilization temperature for minimum sterilization time.
• an Exposure Sequence Timer commences which is pre-set to an Exposure Timer Value of 18.0 minutes.
• one or more air valves 310 are actuated in order to control the chamber pressure at air over-pressure setpoint within a +/- percentage of the alarm limits.
• the air overpressure setpoint value is a saturated steam pressure at + 1.05 bar and is set within the overpressure alarm limits of +/- 0.2 bar, for example.
• the Steam Control Valve 305 opens to the setpoint value, which, in the example embodiment, is 124.0 ° C. In the preferred embodiment, all temperatures are maintained within no more than 1 ° C of the Exposure Temperature setpoint. Then, the jacket steam valve 304 is then closed. When the Exposure Timer reaches a pre-set value, the cycle advances to the next phase.
• a fourth sterilization cycle referred to as the Sterilization Cycle AIR COOL Phase the function is to cool the package product with air flowing into the chamber to remove steam vapor. In this phase, an Air Cool Phase Sequence Timer is commenced which is at a pre-set value of about 4.0 minutes.
• one or more air valves and drain valves 310, 320 are actuated in order to control the chamber pressure at air over-pressure setpoint within a +/- percentage of the alarm limits.
• the air overpressure type is a ramp control; ramp setpoint value is set to -0.04 bar/minute; and, an overpressure alarm limit values: +/- 0.2 bar.
• the steam valve 305 is closed; and, when Air Cool Timer reaches a preset value, the cycle advances to the next phase.
• the function is to cool the product with water flowing into the internal heat exchanger chamber indicated at 315 in Figure 7, in order to condense remaining steam vapor and cool product to final temperature for unloading to secondary packaging area.
• one or more air valves and drain valves 310, 320 are actuated in order to control the chamber pressure at air over-pressure setpoint within a +/- percentage of the alarm limits.
• the air overpressure type is a ramp control; a ramp setpoint value being set to -0.04 bar/minute; and, an overpressure alarm limit values of +/- 0.2 bar.
• a Water Valve 325 opens to fill the internal heat exchanger 315.
• the cycle advances to an Exhaust phase.
• the water cool load phase setpoint value is equal to 65.0° C.
• the Chamber drain valves 320 are opened and the Air valves 310 are closed.
• the Water valve 325 is opened.
• the cycle advances to an End of Cycle phase.
• the Exhaust phase setpoint value is 0.1 bar. The sterilization cycle is now complete.
• the total sterilization cycle time is approximately forty (40) minutes which is a fairly dramatic improvement over the sterilization cycle times in prior art sterilizer equipment.
• FIG. 3(a) there is illustrated the novel plastic tray unit 100 for carrying nested stacks of blister pack arrays carrying ophthalmic lenses for input to the sterilizer machine.
• a detailed close-up view of a portion 100a of the tray 100 is illustrated in Figure 3(b).
• the tray includes an external wall 102 bounding the perimeter of the tray, and four internal divider walls 104a - 104d, which form five tray columns 110a-110e.
• Figure 4(a) which illustrates a side cross-sectional view of the novel tray 100 taken along line "E-E" illustrated in Figure 3(a)
• the cavities 120a, 120b 120v are shown separated by the divider walls 115 formed there between.
• the tray 100 When the tray 100 is indexed for loading at the blister pack loading station 20 ( Figure 1 ), the tray is oriented horizontally with the divider walls 115 extending upward.
• the interleaved pairs of blister arrays 150 may easily be deposited in a respective cavity 120 separated from each other by the divider walls 115 in the manner illustrated, and supported by the plastic tray bottom 101.
• the configured interleaving of a nested array of packages for sterilization according to the invention is substantially similar to the configuration of the interleaved nested array of packages that will be ultimately packaged in a carton at the subsequent secondary packaging station (not shown).
• each plastic tray 100 along the perimeter of each plastic tray 100, is the external wall 102 which is shown as extending above height of the divider walls 115.
• a top portion 103 of the external wall 102 includes a recessed or "lip" portion 106 that preferably forms an internal shelf about the substantially the whole periphery of the tray and that is designed to stackably engage a bottom portion of the next tray that is to be stacked thereon.
• the bottom portion 101 of the tray is designed for easy stacking placement within the peripheral recess portion 106 of each tray for enabling nested stacking of the trays at the tray stacking station.
• Figure 3(b) further shows openings 109 formed in the bottom of the tray 100 to provide circulation of steam and air to the sealed blister pack arrays.
• the external wall is provided with a peripheral ridge or flanged portion 107 that accommodates the placement of the latch fingers for supporting the trays during at the tray stacking station, as described with respect to Figure 8.
• a single plastic tray 100 is designed to support the weight of at least a stack of nine trays for input to the sterilizer machine.
• the material of the plastic tray is not only designed for strength to support the weight of the trays but to additionally endure the temperature and pressure of the steam sterilization cycle.
• the tray is injection molded plastic such as Polyether Imide Ultem ® brand manufacture by General Electric.
• each column 110a-110e of the tray 100 formed between internal divider walls 104a - 104d includes a plurality of internal divider walls 115, which in the example embodiment shown in Figures 5, 3(a), and 3(b), amounts to twenty-one (21) dividers. Between each pair of dividers 115a,b are formed the cavity 120 for retaining an individual array of blister packs (not shown). In this embodiment, the twenty internal dividers form twenty-two (22) cavities, each cavity 120 for carrying a nested pair of interleaved packages carrying 3-pack arrays in a proper orientation for sterilization.
• the tray there are 110 cavities formed in the tray, with each cavity accommodating a total of six lens packages (interleaved pair of three blister packs each).
• the amount of packages carried per tray amounts to 660.
• the total number of blister packages that may be conveyed for simultaneous sterilization in the novel sterilizing chamber amounts to about 5,940.
• the molded plastic tray provides the additional benefit of being lightweight relative to a metal tray (for example), which makes it easier to convey in and out of the sterilizer.
• a stack of metal trays weigh approximately two (2) times the weight, which would require a larger motor, rollers and more durable system for conveying the stack.
• Another advantage of the in-line sterilizer design is a higher output per unit volume of sterilizer chamber. This capacity reduces floor space required for sterilization and in-process product inventory. The sterilization process time and use of the stacking sterilization trays provide this capacity. The process also provides a dry package following sterilization, required by immediate packing of the product following sterilization.
• the invention includes a sterilizing tray for conveying arrays of ophthalmic lens packages, each of which includes at least one ophthalmic lens immersed in a sterile aqueous solution, through a sterilizing chamber in a manufacturing line for sterilizing said packages prior to packaging in secondary packaging, said sterilizing tray comprises an external wall surrounding a perimeter of said tray and having and a number of internal divider walls forming columns therebetween, each divider wall comprising a plurality of cavities for holding a plurality of packages in a nested configuration, said cavities for holding the plurality of packages, in an orientation optimized for sterilization in a sterilizing chamber, wherein said tray is designed for strength to support the weight of a plurality of trays and endure the temperature, and pressure of the steam sterilization.
• said sterilizing tray is made of a lightweight plastic material.
• said sterilizing tray comprises openings either or both, above and below said the perimeter wall said tray to provide optimum heating or cooling, of said packages contained therein.
• An ophthalmic lens manufacturing line comprising: a first station for successively loading arrays of packaged ophthalmic lenses into respective cavities formed in a plastic tray receptacle; a second station for successively stacking a plurality of plastic tray receptacles each loaded with an array of packaged ophthalmic lenses; a third station comprising a sterilizing chamber designed to accommodate simultaneous sterilization of a plurality of ophthalmic lens packages; a conveyor means for synchronously conveying said stack of loaded plastic tray receptacles from said second station to said third station for sterilizing said ophthalmic lens included in said plastic tray; wherein, said sterilizing chamber of said third station is disposed contiguously with said second station to enable continuous sterilization of said ophthalmic lens

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Publications (1)

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• 2003
  • 2003-02-27 BR BR0308096-0A patent/BR0308096A/pt not_active IP Right Cessation
  • 2003-02-27 KR KR10-2004-7013624A patent/KR20040097140A/ko not_active Application Discontinuation
  • 2003-02-27 WO PCT/US2003/005946 patent/WO2003074093A2/en active Application Filing
  • 2003-02-27 TW TW092104197A patent/TWI292326B/zh not_active IP Right Cessation
  • 2003-02-27 AU AU2003217763A patent/AU2003217763A1/en not_active Abandoned
  • 2003-02-27 JP JP2003572606A patent/JP2005518872A/ja active Pending
  • 2003-02-27 EP EP03713726A patent/EP1482990A2/de not_active Withdrawn
  • 2003-02-27 CA CA002477905A patent/CA2477905A1/en not_active Abandoned
  • 2003-02-28 AR ARP030100674A patent/AR038633A1/es unknown
• 2009
  • 2009-03-18 AU AU2009201074A patent/AU2009201074A1/en not_active Abandoned

Non-Patent Citations (1)

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