BACKGROUND OF THE INVENTIONThe present invention relates to sterilized medical packaging. In particular, the present invention relates to packaging a sterilized writing instrument, such as a pen, and labels, which may be contained in a pen and label kit (PAL) kit.
One problem often encountered in modern medicine relates to the need to identify and correctly label medical devices and products in a sterile fashion. Such medical devices and products may include therapeutic agents, (i.e., saline infused with a medicine), tissue samples, blood samples, used medical implements, and other medically related devices and products. The use of a sterile pen in such environments can prevent infection that might otherwise occur due to handling of a non-sterile implement. Because pens are routinely used by medical personnel, the risk of unintended exposure to dangerous agents resulting from the use of a non-sterile pen has been identified as problematic in the medical field.
Similarly, using sterile labels may reduce the risk of exposure or contamination by dangerous agents in a sterile environment, or by health-care professionals wearing sterile gloves. In some instances, touching a seemingly innocuous label that is not sterile may put patients at risk of infection. Such risks may be overlooked by the medical professionals because of the common use of such labels and because such labels must be used to correctly identify certain objects and materials.
One approach to addressing this problem has been to provide sterile PAL kits or pens along with certain medical products, or alone, for use by medical personnel. Some traditional methods of sterilization may include heat, chemical dipping and/or ultrasonic treatment. These traditional methods of sterilization may cause problems when used in attempts to sterilize a pen and labels, as the heat may melt the pen and the label adhesive, chemical dipping may damage the pen and labels, and ultrasonic treatment may not be as effective as other processes in killing all dangerous agents.
Sterilization using EtO (Ethylene Oxide) gas effectively kills bacteria and has been used to sterilize medical products since the 1960's. In a typical EtO cycle, a product is placed in an air tight chamber from which the air can be evacuated. EtO gas is then pumped into the chamber for an extended period of time. Temperature (heat) and humidity are also part of the cycle to enhance the kill time. After a certain period of time, the chamber recycles and pulls the EtO out and replaces it with clean air, as EtO gas is harmful to breathe. EtO sterilization usually requires about a day to prepare for a cycle, a day to run through the sterilizer, and about a week to wait for sterilization confirmation using a Petri dish sample test, making the EtO sterilization somewhat time consuming and expensive. Another problem with sterilizing pens using EtO sterilization is that drawing a vacuum in a volume containing a pen may cause the pen to leak, creating a mess.
What is needed is a sterilized PAL kit that can be processed quickly, while minimizing losses due to damaged or leaking pens.
BRIEF SUMMARY OF EMBODIMENTS OF THE INVENTIONEmbodiments of the present invention relate to packaging a writing instruments, such as a pen, including the steps of placing the writing instrument into packaging configured to be sealed such that the writing instrument is contained in a sealed portion of the packaging, sealing the package, and sterilizing the writing instrument and the package using gamma sterilization such that all portions of the writing instrument are sterilized. Gamma sterilization is effective at sterilizing all components of the PAL kit, including the interior of any pen cap or lid and even the ink inside of a pen. Similarly, gamma irradiating labels ensures that the labels, including any adhesive layer, are sterilized throughout.
In some embodiments, the packaging is an inner packaging, and the method further includes the steps of placing the sealed inner packaging into an outer packaging, placing at least one other item into the outer packaging, sealing the outer packaging such that the sealed inner packaging and the additional items are contained in a sealed portion of the outer packaging, and sterilizing the contents of the outer packaging. In some embodiments, EtO sterilization is employed.
Another embodiment of the present invention is directed to a kit that includes packaging, a writing instrument, and labels configured to be written on by a user with the writing instrument. At least the writing instrument is sealed in the packaging, and at least the packaging and the writing instrument are sterilized using gamma sterilization.
In some embodiments, the packaging may be inner packaging, the kit further including outer packaging and at least one other item. The writing instrument is sealed in the inner packaging. The labels, and the at least one other item are sealed in the outer packaging, and the outer packaging and the contents of the outer packaging are sterilized, such as by using EtO sterilization, for example.
BRIEF DESCRIPTION OF THE DRAWINGSTo further clarify the above and other aspects of the present invention, a more particular description of the invention will be rendered by reference to specific embodiments thereof which are illustrated in the appended drawings. It is appreciated that these drawings depict only typical embodiments of the invention and are therefore not to be considered limiting of its scope. The invention will be described and explained with additional specificity and detail through the use of the accompanying drawings in which:
FIG. 1A is a top view of a PAL kit including a pen and labels in a package according to one embodiment of the invention;
FIG. 1B is a top view of the PAL kit including a pen and labels in a package ofFIG. 1A according to one embodiment of the invention;
FIG. 2 is a view of a PAL kit including a pen in a package according to one embodiment of the invention;
FIG. 3 is view of a kit including a PAL kit and additional packaging and components according to one embodiment of the invention; and
FIG. 4 is a process diagram of packaging a PAL kit according to one embodiment of the invention.
DETAILED DESCRIPTION OF EXEMPLARY EMBODIMENTSThe present invention relates to sterile packaging of writing instruments, such as pens, for use in a medical environment. The sterile packaging may include labels packaged along with a pen in a pen and label (PAL) kit. The present invention also relates to methods of packaging a pen and/or the PAL kit. In particular, the method of packaging includes the steps of placing a writing instrument into packaging configured to be sealed such that the writing instrument is contained in a sealed portion of the packaging, sealing the package, and sterilizing the writing instrument and the package using gamma sterilization such that all portions of the writing instrument are sterilized.
In some embodiments, the packaging is an inner packaging, and the method further includes the steps of placing the sealed inner packaging into an outer packaging, placing at least one other item into the outer packaging, sealing the outer packaging such that the sealed inner packaging and the additional items are contained in a sealed portion of the outer packaging, and sterilizing using EtO sterilization such that the contents of the outer package are sterilized.
Some embodiments of the present invention relate to a kit including packaging, a writing instrument, and labels configured to be written on by a user with the writing instrument. In such embodiments, at least the writing instrument is sealed in the packaging, and at least the packaging and the writing instrument are sterilized using gamma sterilization.
In some embodiments, the packaging may be inner packaging, the kit further including outer packaging and at least one other item. In such embodiments, the outer packaging is sealed to include the sealed inner packaging containing the writing instrument, labels, and the at least one other item. The outer package contents are sterilized using EtO sterilization.
FIGS. 1A and 1B show aPAL kit100 according to one embodiment of the present invention. ThePAL kit100 includespackaging110,pen120, andlabels130.Packaging110 has afirst layer112 and asecond layer114 that may be sealed together at or adjacent to their respective peripheries.First layer112 may be made of semi-permeable material such as Tyvek® or other gas-permeable material that would allow gasses to flow in and out without allowing contaminants to penetrate the material, maintaining the sterility of the interior and contents ofPAL kit100. The material offirst layer112 may also allow printing on the surface offirst layer112. Such printing may include, for example, identification and/or instructions. One example of such printing is shown inFIG. 1B.
Second layer114 may be made of a gas and liquid impermeable transparent plastic material or any other suitable material.Second layer114 may have a depression formed in the material to create a pocket or space forpen120 and labels130. Similarly a pocket may be formed infirst layer112. Alternatively, the pocket may be defined by neither layer, and may be implemented as a space defined between joinedlayers112 and114.
First layer112 andsecond layer114 ofpackaging110 may be joined at a periphery to create a hermetically sealed interior pocket capable of holding contents such aspen120, or labels130, or both. Such packaging may be multivac blister packaging. Thelayers112 and114 may be joined using any conventional joining processes including adhesives, welding, etc. In some embodiments,layers112 and114 may also be joined together to form more than one interior pocket allowing for production of several packages with continuous sheets of material, or allowingpen120 andlabels130, or other objects, to be placed in separate pockets.
Layers112 and114 may also be joined such that on at least one side, the joined portion is located in from an edge ofpackaging110 to enable a user to grasp thelayers112 and114 individually and then separate the joined layers. In other embodiments, a periphery ofpackaging110 may include a notch to allow the package to be easily torn open for use.
Pen120 may be any conventional pen, such as a fine-tip, permanent ink pen.Pen120 may be provided in a non-sterile initial state, prior to being placed and packaged inpackaging110 and sterilized. Whilepen120 is illustrated in the Figures, any suitable writing instrument may be substituted forpen120, such as a marker, pencil, electronic writing instrument, etc.
Labels130 may be any labels that would accept and hold ink frompen120, or otherwise lend themselves to being marked by a writing instrument.Labels130 may include printing directed to the anticipated use ofPAL kit100. For example, as shown inFIG. 1A, at least one oflabels130 may be pre-printed with “HEP./SALINE” or other lettering such as “CONTRAST,” “SALINE,” “PREP SOLUTION,” “LIDOCAINE,” or any other printing. Similarly, labels130 may be pre-printed with designated spaces for writing, such as spaces for date and initials to indicate when a product was prepared or administered, or when a sample was taken, and who completed the procedure. More generally, labels130 may include any printed information that may be useful to a medical professional using a PAL kit.
In preparingPAL kit100 as shown inFIGS. 1A and 1B,pen120 andlabels130 are placed inpackaging110. Packaging110 is then sealed to encapsulatepen120 orlabels130, or both, inpackaging110. Packaging110 may be hermetically sealed. After packaging110 is sealed to includepen120 orlabels130, or both, to createPAL kit100,PAL kit100 is sterilized using gamma sterilization. A printing process may also be performed to labelPAL kit100. The sealing and printing processes may be performed simultaneously to reduce production time.
Gamma sterilization requires a short cycle time, typically taking about one minute.PAL kit100 is bombarded with gamma radiation, which penetrates through all materials inpackaging110,pen120 andlabels130, sterilizing each component both internally and externally. As some materials are sensitive to gamma radiation, such that they become brittle and/or discolored, the materials selected forPAL kit100 may be selected for their resistance to damage by gamma radiation. By using gamma sterilization, each portion of the PAL kit is sterilized, including all inside portions ofpen120, or other writing instrument, including the ink and inside of any lid orcap covering pen120. Gamma sterilization also allowsPAL kit100 to be packaged without using a vacuum. This approach to packaging may limit manufacturing loss due to pen leakage and failure that can be caused by drawing a vacuum onpen120. However, in some embodiments, vacuum packaged PAL kits may also be sterilized using gamma sterilization.
InFIG. 2,PAL kit200 includespackaging210 andpen220. While labels may be included inPAL kit200,PAL kit200 as illustrated does not include labels inpackaging210 along withpen220. Packaging210 includesfirst layer212 andsecond layer214. In the embodiment illustrated inFIG. 2, layers212 and214 are made from impermeable metal foil or semi-metallic material.Layers212 and214 may also be made from any other suitable material that allows for gamma sterilization.Layers212 and214 are joined around a peripheral edge such that a hermetically sealed interior space is created for containingpen220.Layers212 and214 may by joined using any suitable conventional joining process including, for example, adhesive, pressing, crimping, melting, and welding. Similar to pen120 ofPAL kit100,pen220 may be any pen or writing instrument, such as a fine-tip, permanent ink pen.
In preparingPAL kit200 as shown inFIG. 2,pen220 may be placed inpackaging210. Excess air in the packaging may then be withdrawn by drawing a vacuum onpackaging210. The vacuum may be a relatively low vacuum sufficient to evacuate some or all of the internal air frompackaging210, while minimizing manufacturing losses due to pen failure.PAL kit200 may then be hermetically sealed and gamma radiated in a process similar to process described in connection withPAL kit100 above.
FIG. 3 showsmedical kit250. In this example embodiment,medical kit250 includesouter packaging260,PAL kit200, as discussed above, labels230 andadditional components240. Packaging260 includes a firstouter layer262 and a secondouter layer264, firstouter layer262 may be made of semi-permeable material such as Tyvek® or other suitable material to allow gasses to flow in and out without allowing contaminants to penetrate the material, thereby maintaining the sterility of the interior and contents ofmedical kit250 after performance of a sterilization process. The material of firstouter layer262 may also allow printing on the surface of firstouter layer262, so that identification and/or instruction to be printed on the packaging. The sealing and printing processes may be performed simultaneously to reduce production time.
Secondouter layer264 may be made of a non-permeable transparent plastic material or any other suitable material. Secondouter layer264 may have a depression formed in the material to create a pocket or space forPAL kit200,labels230, andadditional components240. Similarly, a pocket may be formed in firstouter layer262 or in neither layer, existing only as a space between joinedlayers262 and264.
Firstouter layer262 and secondouter layer264 ofpackaging260 may be joined at a periphery to create a hermetically sealed interior pocket capable of holding contents such asPAL kit200,labels230, andadditional components240. Such packaging may be multivac blister packaging.Outer layers262 and264 may be joined using any conventional joining processes, such as adhesives and welding. In some embodiments,layers262 and264 may also be joined to form more than one interior pocket, allowing for production of several packages with continuous sheets of material. In some embodiments, each of the items contained inmedical kit250 may be placed in a separate respective pocket.
Outer layers262 and264 may also be joined such that on at least one side, the joined portion is located in from the edge to provide a user access to graspouter layers262 and264 separately and separate the joined layers. In other embodiments, a periphery ofpackaging260 may include a notch to allow the package to be torn open for use.
In some embodiments,labels230 may be included inside ofPAL kit200, or may be included both insidePAL kit200 along withpen220 and inouter packaging260, separate fromPAL kit200.Labels230 may be conventional labels as discussed above with regard to labels130.Additional components240 may include any components for any medical kit that may require labeling, such as with a PAL kit, and may be as numerous or as few as desired in the particularmedical kit250. For example,additional components240 may include a catheter kit including an introducer sheath, syringes, tubing, guidewire, and collection receptacle.
In preparingmedical kit250 as illustrated inFIG. 3,PAL kit200, previously sterilized,labels230, andadditional components240 are placed inouter packaging260.Outer layers262 and264 are then hermetically sealed. Sterilization is then performed on themedical kit250, such as by EtO sterilization. BecausePAL kit200 includesfoil packaging210, EtO sterilization does not penetratePAL kit200, but does sterilize the external surfaces ofpackaging210. During the EtO sterilization, EtO gas penetrates throughouter layer262 and seeps through the open lumens of any tubing and other components contained inmedical kit250.
In some embodiments,medical kit250 may includePAL kit100 as described above instead ofPAL kit200.
FIG. 4 shows a process diagram ofprocess400 listing some exemplary steps to create a PAL kit. As shown, packaging is provided inbox410.Box420 includes the step of placing a writing implement in the packaging. The packaging is sealed to contain the writing instrument inbox430, creating a PAL kit. The PAL kit is sterilized inbox440. Thus, a PAL kit may be created by including at least a writing instrument in packaging, sealing the packaging to contain the writing instrument, and sterilizing the PAL kit.
The present invention may be embodied in other specific forms without departing from its spirit or essential characteristics. The described embodiments are to be considered in all respects only as illustrative and not restrictive. The scope of the invention is, therefore, indicated by the appended claims rather than by the foregoing description. All changes which come within the meaning and range of equivalency of the claims are to be embraced within their scope.