NZ236809A

NZ236809A - Vapour sterilisation device containing vaporisable antimicrobial solution connectable to lumen of medical article to be sterilised

Info

Publication number: NZ236809A
Application number: NZ236809A
Authority: NZ
Inventors: Paul T Jacobs; Ronald F Berry; Toby A Soto
Original assignee: Johnson & Johnson Medical
Priority date: 1987-07-30
Filing date: 1988-07-12
Publication date: 1997-12-19

Description

<div class="application article clearfix" id="description"> New Zealand No. International No. 236809 PCT/ TO BE ENTERED AFTER ACCEPTANCE AND PUBLICATION Priority dates: 30.07.1987; Complete Specification Filed: 12.07.1988 Classification^) A61L2/20 Publication date: 19 December 1997 Journal No.: 1423 NEW ZEALAND PATENTS ACT 1953 COMPLETE SPECIFICATION Title of Invention: DEVICE FOR VAPOR STERILIZATION OF ARTICLES HAVING LUMENS Name, address and nationality of appiicant(s) as in international application form: JOHNSON & JOHNSON MEDICAL, INC, a New Jersey corporation of 2500 Arbrook Boulevard, Arlington, Texas, United States of America 236 8 0 9 lindtor Hi# provistoM <* Wkm" 23 (1) tha ...&«$&£ ftlHuWr-Mm* Mr immvu * ji Zulu •••'•••••a Uf|**»i I « & IftMtto Patents Form No. 5 Number PATENTS ACT 1953 Dated COMPLETE SPECIFICATION -rs <3" DEVICE FOR VAPOR STERILIZATION OF ARTICLES HAVING LUMENS ftcc^coA • We, SURGIKOS. IN&. a corporation organised under the laws of the State of Taacao-, united States of Amerxca, of 2500 Arbrook Boulevard, Arlington, Texas, United States of America do hereby declare the invention for which we pray that a Patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement: - 1 - (followed by page la) % 2 3 6 8 0 -1a- .Field of Invention 5 : The invention relates to the vapor sterilization of articles such as medical instruments having long narrow lumens therein, and more particularly, to a device for delivering a gaseous sterilant directly into the lumen of 10 an article during the sterilization process. Background of Invention — The need to sterilize articles such as medical instruments 15 and others for use in the agriculture and fermentation industries is well knovn. In recent years, many methods of vapor sterilization, have been developed. .While these methods offer the advantage of being generally faster than sterilization by immersion in a sterilant solution, they 20 suffer from one major disadvantage, namely the inability to sterilize the interior of a long narrow tube in a short period of time. Thus, with regard to medical instruments such as endoscopes, the difficulty in sterilizing the lumen can often negate the general advantage of using 25 vapor sterilization. One way of overcoming "the above disadvantage is set forth in U.S. Patent Nos. 4,410,492 and 4,337,223. The apparatus described therein comprises a sterilizing 30 chamber with means for introducing a sterilant gas into the chamber and circulating the gas within the chamber. Disposed within the chamber is a socket for receiving the tubular end of a medical instrument. The socket is connected to a valve and a recirculating pump and the 35 sterilant gas is recirculated from the chamber through the JSU 67 236809 -2- lumen of the instrument. The commercial apparatus, using ethylene oxide and water as the sterilant, has had little commercial "r success which may be attributable to the extended sterilization times of about 3 hours for flexible endoscopes and about 2 hours for the shorter, rigid endoscopes, as well as to the toxicity problems associated with ethylene oxide sterilization. In addition, the method and apparatus described in these references cannot be used to sterilize an instrument within a sterile pack since one end of the instrument must be attached to the socket. Thus there is a current need for an effective method to sterilize medical instruments such as endoscopes in a reasonably short period of time, preferably in one hour or less. The device of the present invention makes vapor sterilization of such instruments practical by delivering vapor directly to the interior of the lumen in the endoscope, whether or not it is in a sterile pack. A method for vapor sterilization of an article having a narrow lumen therein is disclosed in our New Zealand patent specification No 225382 and is incorporated herein by way of reference. Summary of the Invention The present invention may in broad terms be said to be a vapor sterilization device, said device comprising a vessel for containing a vaporisable antimicrobial solution and having sin opening therein, and means to connect said opening of said vessel to said lumen. A method for vapour sterilization is also disclosed but not claimed in the present specification. The device and method are intended for use with solution vapor sterilization procedures. In these procedures, the article is placed within a sterilization chamber, the pressure in the chamber is reduced, and a liquid solution of an antimicrobial agent is introduced into the chamber where it vaporizes. Alternatively, an antimicrobial vapor may be introduced directly to the chamber after the pressure therein has been reduced. In either case, the instrument is sterilized by exposure to the vapor or an active species generated from it rather than by direct 236 8 0 9 -3- cor.tact with a liquid sterilant. The procedure may further involve the use of heat or, e.g., low pressure gas plasma to enhance the antimicrobial activity, reduce sterilization times, and/or remove residual sterilant from the instrument. In its simplest form, the device of the present invention comprises a vessel containing a small amount of the antimicrobial solution, and a means for connecting the vessel to the lumen of the instrument to provide a source of antimicrobial vapor directly to the lumen during the vapor sterilization process. The device is placed on the instrument prior to disposing the instrument in the sterilization chamber. As the pressure in the chamber is reduced, the antimicrobial solution contained in the vessel is vaporized and passes from the vessel into the lumen of the instrument. In its simplest form, the means of connecting the vessel to the end of the instrument tube may comprise something as simple as a piece of firm but flexible tubing, such as tygon tubing of appropriate diameter such that one end of the tubing may be inserted in or disposed about the opening of the vessel, and the end inserted in or disposed about the lumen of the instrument so as to be securely join the two. However, the preferred means described below provide more adjustable fastening and may be used with instruments having a wide variation in internal and external tube diameters. With the use of the device and method of the present invention, vapor sterilization times for endoscopes can be reduced to one hour or less. In addition, the method and the device may be used to sterilize endoscopes in a sterile pack since the device of the present invention may be attached to and packaged with the endoscope before the endoscope is placed within the sterilization chamber. Upon opening of the pack, the 236 8 0 9 -4- device may be retrieved for re-use or discarded with the pack. In one preferred embodiment of the device of the present 5 invention, the means fox connecting the vessel to the end of the tube comprises expandable sheath, one end of which is securely attached about an opening in the vessel, and the other end of which comprises an elastic ring for making a releasable attachment about the end of a tubular 10 instrument. Where the vessel of the device includes a rim or lip about the opening, the sheath may be attached to ; the vessel by means of a second elastic ring disposed over such lip or rim. l' , 15 In another embodiment of the device of the present invention, the means foJ: connecting the vefisel to the end of the instrument comprises a flexible bushing disposed within the opening of the vessel. The bushing may be made of a series of rings of inwardly extending plastic flaps. 20 The vessel may be provided with means for attaching a closure cap thereto, such as threads internal or external to the opening of the vessel for attaching a screw cap or plug, to maintain the antimicrobial solution in the vessel prior to use. Alternatively, the vessel may be provided 25 with an aperture for attaching a disposable cartridge containing a premeasurefi aliquot of antimicrobial solution. In another embodiment, the vessel comprises a flexible . pouch, and the means for connecting the vessel to the end 3 0 of the instrument tube comprises a drawstring disposed about the opening of the, pouch. The pouch may be provided with an airtight seal for sealing the antimicrobial solution therein prior to use, and a means for creating an opening in the sealed pouch so that the pouch may be 3 5 disposed about the end of the instrument when desired. \ 20 30 23 6 8 0 -5- Both the seal and the means for creating an opening may be achieved with, for instance, a "zip-lock" interlocking channel and ridge type fastening across the opening of the pouch. As an alternative, the pouch may be heat sealed 5 and provided with scoring, notches, or other known means for tearing open the pouch. The device and method of the present invention reduce sterilization time required for instruments having long 10 narrow lumens therein. Reduced sterilization times are also achieved with the instruments encased in a package designed to maintain sterility after the removal from the sterilized chamber. In addition, as antimicrobial vapor is provided directly into the lumen of the instrument, 15 lower concentrations of antimicrobial solutions may be used in the sterilizer, and this together with the reduced sterilization times provides improved materials compatibility with respect to both the instrument components and the'packaging or wrapping materials. Brief Description of the Drawings Figure 1 is a perspective view of one embodiment of the device of the present invention, attached to the end of a 25 tube. Figure 2 is a perspective view of another embodiment of the device of the present invention, showing the end of . the device for making a connection to a tubular member. Figure 2A is a variation of the device of Figure 2. Figure 3 is a plan view of another embodiment of a device of the present invention. 35 JSU 67 \ 236 8 0 9 -6- Figure 3A is a variation of the device of Figure 3. Detailed Description of the Invention 5 The method and device of the present invention relates to the sterilization of articles such as medical instruments having a long narrow tube therein. The term instruments as used herein applies to medical or surgical devices such as endoscopes, catheters, tubing, or similar instruments 10 or articles having an internal lumen which is preferably-used in a sterile condition as in, for example, the agricultural or fermentation industries. The method and device of the present application show particular advantages in the solution vapor sterilization of lumens 15 exceeding ten centimeters in length and having an internal diameter of about 7 millimeters or less. As endoscopes typically have lumens with internal diameters of 1 to 4 millimeters and lengths of up to 1.5 meters or more for flexible endoscopes and at least 45 centimeters for rigid 20 endoscopes, the method and device of the present application have particular applicability to the sterilization of these instruments. With the use of the device of the present invention, antimicrobial vapor is supplied directly to the lumen or interior of the tube of 25 the instrument during the vapor sterilization process. The. antimicrobials used with the method and device of the present invention include solutions of glutaraldehyde, hydrogen peroxide, chlorine dioxide or other 30 antimicrobials in an inert solvent, the only requirement being that the solution be liquid at atmospheric pressure and a vapor at the temperature and pressure of the sterilization process. Though the higher concentration solutions of antimicrobials are more effective, problems 35 with materials compatibility and shipping and handling may JSU 67 \ 236809 -7- arise at very high concentrations. For example, a 30% to 50% solution of hydrogen peroxide in water is both very effective and presents few shipping and handling problems, while higher concentrations of up to 70% become 5 increasingly more difficult and dangerous to handle. In solution vapor sterilization, the procedure'generally used is as follows: The article to be sterilized is placed within the sterilization chamber, the chamber is 10 sealed, and a vacuum is drawn on the chamber to reduce the pressure to less than about 50 torr, and preferably to 20 torr or less. An antimicrobial solution is then injected into the chamber where it vaporizes and contacts the exposed surfaces of article." The time necessary for total 15 kill of specific microbial agents varies with the type and concentration of antimicrobials present, and with the degree of exposure to the microbial agent. Microbials disposed in cracks, crevices or internal tubular structures are somewhat protected from the antimicrobial 20 agent and require more time for total kill than microbials on the external surface of the article. Heat or high frequency radiation may be used to increase the effectiveness of the antimicrobial and its penetration into remote areas of the instrument. ' 25 The device of the present invention comprises a vessel for containing a small amount of antimicrobial solution, and a means for connecting the vessel directly to the lumen or the end of the tube of the article to be sterilized. When 30 the article with device containing antimicrobial solution is disposed in the sterilization chamber and a vacuum drawn on the chamber, antimicrobial vapor generated from the solution within the vessel flows directly into the lumen. 35 JSU 67 \ 236 S O 9 -8- The effectiveness of the method and device of the present invention was demonstrated by the following experiments: 50 inch (127 centimeters) lengths of tygon tubing having a 5 2 millimeter inside diameter were used to simulate an endoscope in the sterilization test. A paper strip (2mra x 13mm) containing approximately 2.0 x 10 Bacillus subtilis (var. globigii) spores was placed in each tube equidistant from each end. A syringe containing 0.05 10 milliliters of 10% by weight hydrogen peroxide solution in water was provided for each tube. Each of the samples was individually packaged in a TYVEKm/MYLARm envelope prior to sterilization. 15 One third of the samples (three units) were placed in the package' with the syringe unattached to the end of the tube. Another one-third of the samples were packaged with the syringe attached. Individual samples were placed-within a 65 liter sterilization chamber and sent through a 20 hydrogen peroxide vapor sterilization cycle wherein the pressure within the chamber was reduced to 3 torr for the total exposure time minus 15 minutes, and 0.5 torr for the final 15 minutes of exposure. No additional hydrogen peroxide was injected into the chamber". 25 The.remaining one-third of the samples, packaged with the syringe attached to the end of the tube as described above, were sent through a hydrogen peroxide vapor sterilization cycle supplemented with high frequency 30 radiation plasma which is known to generate an active species from the hydrogen peroxide. Again a 65 liter chamber was used, and the pressure within the chamber was reduced to 3.0 torr for the totsl exposure time minus 15 minutes and 0.5 torr for the final 15 minutes of 35 exposure. Again, no additional hydrogen peroxide was JSU 67 2 3 6 8 0 injected into the chamber. Plasma was generated only during the final 15 minutes of exposure at 2.05 MHz with 320 watts of power, pulsed 0.3 milliseconds on to 1.0 milliseconds off. - '5 At the conclusion of the sterilization cycle, the paper strip was removed from each tube and placed in a glass vial containing 10 mis of a sterile pH 7.0 phosphate buffer solution. This solution contained 10 milligrams of 10 TWEEN 80 to aid in removal of any spores from the paper strip and 0.0066 milligram of catalase to neutralize any remaining hydrogen peroxide. Five glass beads were placed in the solution, and the solution was vortexed for two minutes to completely mascerate the paper strip. Three 15 decimal dilutions of the solution were made with sterile pH 7.0 phosphate buffer, and the original solution and the decimal dilutions were poured into sterile glass Petri plates. A culture medium w^s added and the plates were incubated for four days at 30°C. After incubation the 20 number of viable organisms in eiach plate was counted, and the number of spores on the paper strip calculated by multiplying the spore count by the appropriate dilution factor. 25 The results of the experiments are presented in Table I below, and plotted in Figure 4, where S/SQ represents the ratio of the number of organisms surviving the test to the initial number of organisms which were placed on the paper strip prior to the test. As shown by these data, no 30 reduction in microbial population was achieved in samples where the syringe was unattached to the tubing, even after an exposure time of 75 minutes. Attaching the syringe to the end of the tube according to the method of the present invention produced total kill in 35. riiinutes without low 35 temperature gas plasma, and in 25 minutes when the \ 236 8 0 9 -10- antimicrobial activity was enhanced by the use of low temperature gas plasma. Table I 10 Sample A Sterilization Time - Min. 35 45 75 Efficacy (S/So) .-1 8.6 x 10 8.9 x .,10 1.1 x 10( -1 15 B 20 25 35 20 25 35 7.0 x 10 5.8 x 10 0 -1 -1 8.5 x 10 0 0 -3 20 Sample A - Syringe unattached Sample B - Syringe attached Sample. C - Syringe attached plus plasma A preferred embodiment of the device to be used in 25 accordance with the teaching of the present invention is shown in Figure 1. The device indicated generally at 10 is shown attached to a tube 12. In the device depicted in Figure 1, the means for connecting the vessel 14 to the end of the tube comprises an expandable sheath 16, one end 30 of which is securely attached to the vessel, and the other end of which comprises an elastic ring 18 making a releasable attachment about the end of the tube. The sheath 16 may be attached to the vessel in any known manner and, as shown in Figure 1, the sheath 16 is 35 attached to the vessel by a second elastic ring 20 JSU 67 236 8 0 -li- disposed over the lip 22 about opening 24 of vessel 14. Though the vessel shown is cylindrical, the vessel may comprise any three dimensional container preferably of semi-rigid material, having an opening therein. The 5 vessel may be made of, e.g., polyethylene, polypropylene, glass or any other-material which is nonreactive to the antimicrobial solution of vapor. The sheath.may also be formed of polyethylene, polypropylene or other material which is relatively nonreactive to the antimicrobial 10 vapor. The elastic rings may be formed of natural latex or butyl rubber which are relatively resistant to the sterilant vapors; however, resistivity is less critical when the device is constructed for one time use. Disposed within the vessel may be a substrate 26 comprising a woven 15 or nonwoven fabric or sponge for containing the liquid antimicrobial solution. The vessel preferably has a means 28 associated with the opening for attaching a closure cap over the opening prior to use in order to maintain the antimicrobial solution therein. As shown in Figure 1, 20 means 28 comprises threads for a screw cap fitting about the lip of the vessel. Another embodiment of the device of the present invention is depicted in Figure 2 where the device is indicated 25 generally at 30. The means for connecting the vessel 34 to the end of a tubular instrument comprises a bushing 36 disposed within the open end of the vessel. In the particular embodiment shown in Figure 2, the bushing comprises a series of rings 38 and 40 of inwardly 30 extending plastic flaps defining a flexible aperture 32 to receive the tubular instrument. The flaps can be made of any flexible material which is non reactive to the antimicrobial solution or vapor, such as polyethylene, and of sufficient thickness that the flaps provide resistance 35 to withdrawal of a tube inserted through the aperture. JSU 67 23 6 8 0 9 -12- Disposed within the vessel is a substrate 42 containing the antimicrobial solution. Preferably, the vessel 34 is provided with means 44 for attaching a closure cap thereto prior to use. As shown in Figure 2, means 44. comprise 5 threads for attaching a screw cap (not shown) within the opening of the vessel. Figure 2A illustrates a variation in the design of the device of Fig. 2 which utilizes the same basic vessel and 10 means for attachment to a tubular device. In the device shown in Fig. 2A, end 45 of the vessel opposite the open end is provided with aperture 46 for attaching a disposable cartridge 47 containing a supply of antimicrobial on a substrate, such as a woven or nonwoven 15 fabric or sponge 48 as illustrated. The aperture 46 of the vessel is designed in conjunction with neck 49 of the cartridge to provide quick and easy attachment and release of the cartridge and the vessel. In the embodiment shown in Fig. 2A, aperture 46 is provided with reverse threads 20 for engaging the threads of the neck 49 of the cartridge. In this variation of the device it is not necessary for a substrate contain the antimicrobial solution to be disposed within the vessel since the antimicrobial solution is provided in premeasured aliquots in the 25 cartridges. With the device of Fig. 2A one achieves the convenience and accuracy of disposable, premeasured aliquots of antimicrobial solution without the expense associated with the device of Fig. 2. 30 The following table sets forth the effectiveness of the devices depicted in Figures 1 and 2 in a sterilization procedure described below. \ 236809 -13-Table II Effect of Devices on Efficacy of Sterilization Inside Tubes Efficacy (S/So) No Device Device 10 Material I.D. Lencrth Fio.l Fia (cm) (cm) Surgical Tygon 0.64 10 0 0. 64 20 4.4 X 10~5 -■ ' .' - 0.64 30 1-1 X 10~2 - 15 0. 64 45 8.8 X 10"1 • 0 0 Rubber tubing 0. 64 25 1.7 X 10"1 - . , - 0.64 45 7.9 X M O 1 H 0 0 The efficacy as recorded in terms of the ratio of the 20 number of microorganisms surviving the test, S, to the number of challenge organisms, SQ (approx. 1 x 106), on a paper strip disposed within the tube equidistant from the ends. In the sterilization procedure, 100 microliters of 30% aqueous H2°2 so-*-uti°n was supplied in each of 25 the devices. The devices were attached to the ends of tubes of the indicated length and 0.64 cm in internal diameter. All of the tube samples were placed within TYVEKm/MYLAR'" packaging prior to sterilization. The packaged tubes were placed within the sterilizing chamber 30 and the pressure therein was reduced to about 0.1 torr in about 10 minutes. Additional 30% H202 solution was injected into the chamber to achieve a concentration of 2.0 milligrams K2°2 ^er chamber volume. Following injection of the ^2^2' t^ie tubes were 35 retained in the chamber an additional 50 minutes. JSU 67 \ 236 &()b -14- Injection of the H202 solution raised the pressure in the chamber to about 6 torr and the pressure was again reduced to about 0.1 torr. During the last-10 minutes of exposure, low temperature gas plasma was generated in the 5 chamber at 300 watts. The challenge micro organisms used in the test were Bacillus subtilis (var. globigii) spores. As shown in Table II above, when the tube length was only 10 centimeters, sterilization was achieved without the use 10 of the device according to the present invention. However, for tubing of 20 and 30 centimeters in length, a device of the present invention would be needed in order to achieve sterility within the exposure time of the test. For tubes of 45 centimeters in length, total kill 15 was achieved during the 1 hour exposure time of the test, using either of the devices depicted in Figure 1 and Figure 2. A further experiment utilizing 1 ram medical grade Teflon 20 tubing 183 cm in length. The tubing was cut into three pieces to obtain a 5 cm long center section which was joined to the end sections by external tubing connectors. 4 In the experiment, approximately 1.0 x 10 Bacillus subtilis (var. globigii) spores were deposited in the 25 center section of the Teflon tubing, and the tubing assembled and subjected to sterilization with hydrogen peroxide vapor as described above at a concentration of 2.0 mg/liter of chamber volume. The chamber was evacuated to a pressure of 0.1 torr before the peroxide was injected 30 as a 30% aqueous solution and allowed to vaporize. After 20 minutes, a continuous gas plasma was generated in the chamber at 300 watts 13.5 MgH2 and the sterilization continued for an additional 5 minutes after which the vacuum was released with sterile, filtered air, and the 35 number of surviving spores determined. JSU 67 % 236 8 09 10 -15- The experiment was first conducted without a device of the present invention attached to the tubing, then repeated with a device of Figure 3 as described below containing 100 ml of 30% hydrogen peroxide attached to one end of the tubing. The experimental results of the tests are presented in Table. Ill below. Table III Sterilization of 1 mm Tubing Efficacy (S/So) 15 Material I ,dt. Eenqth No Pevi.ce pigt i Device Teflon 1 mm 183 cm 1.9 x 10_1 0 The data of Table III demonstrate the efficacy of the method of the present invention in sterilizing the lumen of very long tubes having very small diameters as often used in certain endoscopic procedures. 20 Additional embodiments of the device of the present invention are depicted in Figures 3 and 3A. The device shown in Figure 3 indicated generally at 50, comprises a vessel 52 in the form of a pouch constructed of a flexible 25 material. The means for connecting the vessel or pouch 52 to the end of an instrument tube comprises a first drawstring 54, and preferably a second drawstring 62. These drawstrings are preferably arranged in the configuration as shown in Figure 2 to be drawn from 30 opposite sides of the pouch. The pouch is preferably provided with an airtight seal to maintain the antimicrobial solution therein prior to use, and includes a means for creating an opening in the sealed pouch so that it may be disposed over the end of a tube. The seal 35 may be created by sealing the ends 66 of the pouch, and JSU 67 \ 236809 -16- the means for opening the sealed pouch may comprise, for example, a line of weakening at 68, preferably in combination with a notch also shown generally at 68, to permit the pouch to be opened by tearing off one end. 5 Figure 3A shows a device indicated generally at 50A, similar to device 50, but wherein the airtight seal and the means for creating and opening the sealed pouch is a line of fastening 64 similar to a "zip-lock" closure. 10 Optionally, opening flaps 70 may be provided on either side of the pouch adjacent closure 64 of Figure 3A, or the line of weakening 68 of Figure 3. These flaps are firmly secured to the pouch. In use, after the sealed end 66 of the pouch of Fig. 3 has been removed along the line of 15~ weakening 68, the flaps when pulled oppositely from each other will distend the opening of the pouch for disposal around the end of an instrument tube. The flaps of Fig. 3A, when pulled in opposite directions, can be used to open the zip-lock fastening,' or if the fastening is 20 already opened, to distend the opening for disposal around the end of an instrument tube. A substrate 72 such as a woven or nonwoven fabric or sponge may be disposed within the pouch for containing the antimicrobial solution. 25 In a preferred construction, the drawstrings are provided with a locking means as illustrated. Though many means for locking or catching a drawstring are known in the art and may be used in conjunction with the present invention, , the locking means depicted at 56 at Figure 3 comprise a 30 catch 60 for a serrated edge 58 provided on the drawstring. As shown in Figure 3, the catch, comprising an opening for disposing one end of the drawstring therethrough, is located at the opposite end of the drawstring. The catch, however, may be provided by a 35 flap, with opening therein, attached to the edge of the rsu 67 •• 20 25 236 -17- pouch, provided the other end of the drawstring must also be attached to the pouch. When two drawstrings are used, one or both drawstrings may be provided with a locking means. By pulling the end 73 of the drawstring, the 5 flexible pouch is gathered and a firm fastening may be made to a tube inserted within the pouch. Although the present invention has been described in terms of specific devices for use in a preferred method of vapor 10 sterilization, it will be understood that various modifications in the device will be apparent to those skilled in the art and are within the scope of this invention. 15 30 35 JSU 67 </div>

Claims

<div class="application article clearfix printTableText" id="claims"> 236 - 18 - WHAT WE CLAIM IS: 5 1. A vapor sterilization device, comprising a vessel formed to contain a vaporisable antimicrobial solution, said vessel including an opening and connection means to connect the opening to the lumen of s. medical article to be sterilised, the construction and arrangement being that subsequent to an antimicrobial solution being placed within the device and the device being connected to the medical article, the 10 device and the article may be placed inside a chamber and vacuum drawn on the chamber, and the antimicrobial solution will vaporise and bp drawn into the lumen of the article.
2. The device of claim 1, wherein said connection means comprises an 15 expandable tubular sheath, one end of which is securely attached about the opening of the vessel and the other end of which comprises an elastic ring for releasable attachment about the end of the article.
3. The device of claim 2, wherein the sheath is securely attached to the vessel 20 by means of a second elastic ring at said one end of the sheath disposed over a lip about the opening of the vessel.
4. The device of claim 1, wherein said connection means comprises a flexible bushing disposed within the opening of the vessel for receiving one end of said article. 25
5. The device of claim 4, wherein the bushing comprises a plurality of inwardly extending plastics flaps.
6. The device of claim 1, wherein the vessel comprises a flexible pouch and the 30 connection means comprises at least one drawstring disposed about the opening of said pouch.
7. The device of claim 1, wherein the vessel includes a second opening for releasably attaching a cartridge containing a measured aliquot of said antimicrobial 35 solution. 10 NOV 1997 l:\RM\VWDOCS\WPSHARE\FNW\C 1081 (3.002 I - - ""*;236809;■ 19 -;8. The device of claim 1, wherein the vessel contains a porous absorbejit substrate for containing said antimicrobial solution.;9. The device of claim 1, wherein the vessel has means for attaching a; removable closure cap to the opening thereof.;10. A vapor sterilization device for delivering antimicrobial vapor to the lumen 10 of an article during vapor sterilization substantially as herein described with reference to any of the drawings. ,;RUSSELL McVi;FOR THE APPLICANT;END OF CLAIMS;w;10 NOV 1997;I:\RMWWDOCS\WPSHARE\FNWC 15816.002* </div>