US3819106A

US3819106A - Sample bag

Info

Publication number: US3819106A
Application number: US00243347A
Authority: US
Inventors: S Schuster
Original assignee: Individual
Current assignee: Individual
Priority date: 1972-04-12
Filing date: 1972-04-12
Publication date: 1974-06-25
Anticipated expiration: 1991-06-25

Abstract

A pre-sterilizable sample bag is disclosed for receiving and storing a sample for analysis at a location remote from the situs of sample collection. The bag is fabricated of material essentially completely impermeable to bacteria and other foreign matter and includes an access opening covered by a removable closure membrane essentially completely impermeable to bacteria and other foreign matter but highly permeable, in comparison to said bag material, to sterilizing vapor. The outer surface of the bag includes an adhesive coating adapted to be engaged in sealing contact with the area of the bag material about the access opening to completely seal the opening after removal of the closure membrane and insertion of the sample into the bag.

Description

United States Patent [191 Schuster SAMPLE BAG 22 Filed: Apr. 12, 1972 211 App1.No.:243,347

[76] Inventor:

[52] U.S. Cl. 229/62, 206/632 R, 229/80 [51] Int. Cl. 365d 33/20 [58] Field of Search 229/62, 80; 206/632 R; 150/3 [56] References Cited UNITED STATES PATENTS 2,793,743 5/1957 Lefebvre 229/62 X 3,070,280 12/1962 Richmond 229/62 X 3,194,124 7/1965 Warp t 229/69 X 3,338,019 8/1967 Trewella et al. 229/62 3,472,369 10/1969 Schuster 229/66 X g 5.6 E E 34 June 25, 1974 Primary Examiner-William 1. Price Assistant Examiner-Stephen P. Garbe Attorney, Agent, or FirmFraser and Bogucki [5 7] ABSTRACT The outer surface of the bag includes an adhesive coating adapted to be engaged in sealing contact with the area of the bag material about the access opening to completely seal the opening after removal of the closure membrane and insertion of thesample into the bag.

15 Claims, 7 Drawing; Figures l///////////////////fl/////////fl///l//7/ SAMPLE BAG FIELD'OF THE INVENTION The present invention relates generally to sample receptacles and particularly to pre-sterilizable, readily openable sample bags resealable to completely prevent the entry of foreign matter so as to maintain the condition of said sample for subsequent analysis.

BACKGROUND OF THE INVENTION There are presently available various kinds of receptacles for collecting biological, marine, agricultural and other samples for analysis at a location remote from the situs of sample collection. Such sampling, collection and analysis have always been of substantial importance to a number of industries and government agencies for monitoring water resources, crops, and so forth, and is assuming even greater importance today in light of the increasing emphasis of the study and preservation of environmental and ecological parameters.

The sample that is obtained in the field must, of course, be retained in a state in which introduction of extraneous factors at the time of collection or during retention are completely avoided or at least minimized. One way to accomplish this is to insert the sample in a container or receptacle that has been previously sterilized and to immediately reseal the receptacle in a manner to preclude the entry of foreign matter which would introduce unknown qualitative and quantitative variables into the subsequent analysis. The object is to preserve the sample in a condition in which its subsequent laboratory analysis will be meaningful insofar as ascertaining accurately its state at the time of collection.

SUMMARY OF THE INVENTION According to the present invention there is provided a sample receptacle in the form of a flexible bag whose interior may be readily 'pre-sterilized. The sample bag of the invention is further characterized by the ability to maintain a sterilized condition over a long period of time and by the ease with which it may be opened, loaded and sealed.

In accordance with the broad structural aspects of the invention, a bag is provided that is fabricated of a material essentially completely impermeable to bac teria and which includes an access opening covered by a removable closure membrane essentially completely impermeable to bacteria but highly permeable, in comparison to the bag material, to sterilizing vapor such as steam or ethylene oxide. The outer surface of the bag includes sealing means shaped and positioned to be engaged in sealing contact with the portions of the bag material about the access opening so that the bag may be completely sealed after removal of the closure membrane and insertion of the sample.

In accordance with other, more specific aspects of the invention, the bag is foldable along a portion thereof between the sealing means and the access opening so that the parts of the bag about the access opening may be brought into sealing contact with the sealing means. Indicia, such as a pair of spaced lines printed on the bag, may be provided to facilitate sealing of the bag. Upon folding of the bag, such indicia are brought into registry to assist in the positioning of the access slit relative to the sealing means so that complete sealing of the access opening is assured.

The bag is preferably constructed of transparent, heat sealable plastic such as polyethylene or polypropylene or the like and the closure membrane typically comprises a paper tear strip removably attached to the outer surface of the bag about the access opening.

According to a more specific form of the invention, the bag may be constructed along the lines disclosed in U. S. Pat. No. 3,472,369 issued Oct. 14, 1969 to the inventor of the present invention, and entitled Readily Opened Package For Storing Items In Bacteria-Free Condition. Pursuant to that construction, certain features of which are incorporated herein, the bag is fabricated of a heat sealable plastic sheet essentially completely impermeable to bacteria. The sheet has longitudinal andtransverse edgesand is folded along longitudinal fold lines so that the longitudinal edges define a longitudinally extending access opening. A removable closure membrane of paper, for example, essentially completely impermeable to bacteria but highly permeable, in comparison to the plastic sheet, to sterilizing vapor, extends the length of the bag and closes the access opening, the membrane being secured to the exterior of the bag by longitudinal, continuous, pressure heat seal joinder lines adjacent the access opening on each side thereof. Continuous pressure heat seal joinder lines extend along the transverse edges closing the bag and further uniting the membrane to the plastic sheet along the transverse edges.

Pursuant to specific aspects of the present invention, a pressure-sensitive adhesive is applied to a longitudinally extending rectangular area of the exterior surface of the bag, the area lying parallel to the access opening. The adhesive area is overlaid with a protective paper strip pending use of the bag. The interior of the bag is sterilized by any of the well-known processes involving the exposure of the bag interior to a sterilizing vapor passing through the strip. In use, the closure membrane is removed permitting insertion of the sample into the bag through the access opening, following which the bag is sealed by removing the protective strip and fold ing the bag to bring the area of the bag about the access opening into sealing contact with the pressure-sensitive adhesive area.

BRIEF DESCRIPTION OF THE DRAWINGS Further objects, advantages and feature of the pres ent invention will become readily apparent from a reading of the detailed description in conjunction with the accompanying drawings, in which:

FIG. 1 is a perspective view of a sample bag constructed pursuant to the teachings of the present invention;

FIG. 2 is a cross-section view of the bag of FIG. 1 as seen along 2-2;

FIGS. 3, 4, 5 and 6 are perspective views of a sample bag according to the present invention illustrating, in sequence, the manner in which the bag is used; and

FIG. 7 is an enlarged cross-section view of the upper portion of sample bag in the sealed configuration, the section being taken along 7-7 in FIG. 6.

DETAILED DESCRIPTION For purposes of illustrating the background of the invention and the state of the art, the aforementioned U. S. Pat. No. 3,472,369 issued to the present inventor on Oct. 14, 1969 is incorporated herein byreference.

At the outset, it is to be noted that in the accompanying drawings the thicknesses of the plastic and paper sheet material and that of the adhesive coating have been greatly exaggerated to clearly show their interrelationship. Further, in the description that follows, the terms longitudinal and length denote directions and dimensions parallel with the access opening and closure membrane directions and the terms transverse and width denote directions and dimensions perpendicular to the longitudinal direction.

Referring now to the drawings, sample bags according to the present invention comprise mainly a flexible container 10, a closure membrane 12 and an adhesive coating 14 covered by a protective strip 16. The container portion of the bag comprises a rectangular sheet of plastic such as polyethylene having a thickness sufficient for purposes of strength and durability and for rendering the container essentially completely impermeable to bacteria and other foreign matter. Heat sealable materials other than polyethylene, may, of course, be used, such materials including polypropylene, nylon, polybutylene, and so forth, but polyethylene has the added desirable properties of being low in cost and easily processed for purposes of fabrication of the sample bag.

The container is preferably made of transparent stock to facilitate identification of the contents of the bag once the sample is enclosed but it will be appreciated that translucent or even opaque plastic can be utilized if desired for particular applications. Tinted plastics to selectively filter light or other electromagnetic radiation may also be employed. Further, the plastic sheet stock may be treated by embossing in accordance with techniques well known in the art and further may be a composite structure fabricated of two every thin sheets cohered together mechanically. Such coherence can be enhanced by subjecting the sheet stock to corona discharge as is well known in the art.

Containers according to the present invention may be readily formed from a continuous sheet of material, the

longitudinal edges

18 and 20 thereof being folded inwardly along spaced, parallel

longitudinal fold lines

22 and 24.

Portions

26 and 28 of the sheet adjacent the

longitudinal edges

18 and 20 are brought into overlapping relation, with the upwardly extending portion 28 overlying the downwardly extending portion 26. The overlapping

portions

26 and 28 of the container 10 define a longitudinal access slit or opening 30 which for purposes ofthe present invention is preferably disposed near the upper longitudinal fold line 22 of the con tainer.

The closure membrane 12 comprises a longitudinal strip bonded to the container by parallel heat

seal joinder lines

32 and 34. The functions of the membrane 12 are to close the access opening 30 and form a barrier to bacteria and other foreign matter while simultaneously being highly permeable to sterilizing vapor, such as steam or ethylene oxide, in comparison to the plastic container 10. The longitudinal heat

seal joinder lines

32 and 34 bracket the overlapping

portions

26 and 28 of the container 10. Although these bonds are preferably and most easily obtained by heat sealing, using spaced-apart heat seal sealer bars elevated to the required heat sealing temperature, they may also be provided by adhesive or other forms of chemical or mechanical bonding.

The closure membrane 12 may be made of conventional paper 3 to 7 mils thick. Paper is characterized by several important properties for purposes of this invention. Unlike plastic, increasing the thickness of paper does not substantially affect its permeability to sterilizing vapors. On the other hand, the labyrinth, fibrous structure of paper is such that it effectively prevents bacteria from penetrating into the container 10.

The closure membrane 12 may be provided with a thin polyethylene coating (not shown), such coating being in contact with the outer surface of the container 10. The thickness of the polyethylene coating would preferably be of the order of H2 mil which is insufficnet to impede the passage of sterilizing vapor but nevertheless provides a sufiicient thickness to facilitate the heat seal joinder of the closure membrane 12 and the container 10. Preferably, however, the container 10 is treated by corona discharge along the longitudinal heat seal areas so as to render the described thin polyethylene coating unnecessary, the membrane 12 being thereby directly heat sealable to the container 10.

Many kinds of inexpensive paper may be employed for the closure membrane but depending upon particular needs other materials, both woven and nonwoven, that are impermeable to bacteria yet are comparatively highly permeable to sterilizing vapors may be used. These alternatives would include various paper-like materials such as glass fiber products and Tyvac, a spun polyolefin of the Dupont Company, all of which are impermeable to bacteria but in comparison to the plastic container 10 highly permeable to sterlizing vapor.

As shown in FIG. 1, the

longitudinal joinder lines

32 and 34 may be terminated short of the end of the closure membrane 12 to define a pull tab 36 which serves as a manual gripping edge and thereby facilitates re moval of the closure membrane. The membrane 12 may also have

transverse extensions

38 and 40 beyond the

longitudinal joinder lines

32 and 34 of sufficient width to provide a lateral pull tab along each longitudinal side in addition to, or instead of, the end tab 36. It is generally sufficient to provide a pull tab of only so much width that it can be grasped with the tips of the fingers. Where greater tearing forces are involved more area may be provided for more secure gripping.

The transverse end edges of the bag are joined to each other and to the closure membrane 12 by

transverse joinder lines

42 and 44 each of which is adjacent one of the ends of the bag. The joinder lines 42 and 44 are also preferably and most conveniently produced by heat seals. Thus, it will be apparent from FIG. 1 that the longitudinal access opening 30 is completely bounded by a continuous bond or heat seal which is completely impervious to the passage of bacteria and foreign matter; likewise, the interior of the bag is completely isolated against the entry of bacteria and foreign matter. The transverse heat seal 42 along the end of the bag having the pull tab 36 may be spaced somewhat further from the corresponding edge of the bag than the seal 44 so that a sufficient pull tab area is exposed.

The adhesive coating 14 is applied to the outer surface of the container along a longitudinally extending rectangular area adjacent the lower edge of the closure membrane 12. The adhesive coating 14 is covered by te protective strip 16 of wax-impregnated paper or the like. The adhesive coating 14 may comprise any pressure sensitive bonding material such as a latex type adhesive or the like.

indicia, which maybe in the form of parallel broken lines 46 and 48printed on the container 10, insure that the access opening 30 is in proper relationship with the adhesive coating 14 when the bag is folded for sealing after the sample has been inserted. In the example under consideration, the upper broken line 46 is positioned parallel with and just below the longitudinal edge 20 and the lower broken line 48 is placed parallel with and below the upper boundary of the adhesive coating 14. It will be evident that the placement of the indicia may vary according to the particular design but in any event, when the bag is folded for sealing, the longitudinal edge 20 should lie approximately along the longitudinal center line of the adhesive coating 14.

The bag may have appropriate printed matter including blanks to be filled in with the identification of the sample collected, and other information. The closure membrane 12 may likewise include printed matter and also have marginal indicia showing the points at which the membrane may be most readily gripped for removal and the preferred direction of removal.

The bags may be fabricated individually on suitable bag-making apparatus such as the Simplex machine manufactured by FMC Corp. of San Jose, Calif. In these machines, plastic sheet stock is fed intermittently in successive steps, heat sealed across the ends and cut into separate bags. Such standard bag-making machines require certain modifications the nature of which are unimportant to the disclosure of the present invention but which facilitate the production of the bags of the present invention at an extremely high rate with a great deal of reliability, accuracy and repeatability.

Generally, the sheet stock forming the container is fed from asupply roll, folded over along the

longitudinal fold lines

22 and 24 as explained andjoined to the closure membrane 12 to form a composite tube stock. The closure membrane 12 is fed concurrently with the plastic sheet stock and is fed along the longitudinal access opening 30 and into contact with the outer surface of the container 10. The adhesive coating 14 may be simultaneouslyand continuously applied along with the overlying protective strip 16. The

longitudinal joinder lines

32 and 34 are added by a heat seal mechanism using longitudinal parallel spaced heater bars and actuated intermittently in timed relation with the feeding of the stock material. The transverse heat sealing operations and the cutting operation may take place in conventional fashion using, for example, either roller elements or heat seal bars to apply the transverse heat seals and either a mechanical or thermal cutter to separate the tube stock adjacent the transverse heat seals 42 and 44 thereby forming individual bags.

Following fabrication of the bag, the interior thereof is sterilized by any of the wellknown sterilizing vapor techniques such as the ethylene oxide process. The interior of the bag will remain in sterile condition over an extended period of time, typically in excess of one year and may thus be stored until ready for use.

ln accordance with one practical example of a sample bag embodying the invention, the bag has an overall length of I] 1/4 inches and an overall width of 18 inches. The closure membrane 12 and protective strip 16 are in abutment and have widths of 3 inches and l l/2 inches respectively. The width of the adhesive coating 14 is also 1 U2 inches. The upper edge of the'closure membrane 12 lies about 5/8 inch from the upper longitudinal fold line 22. The

portions

26 and 28 of the container have an overlap of 1 inch, the longitudinal edge 20 lying about 1 3/4 inches from the fold line 22. The length of the pull tab 36 is about l/2 inch and the

broken line indicia

46 and 48 are spaced 2 inches apart, the upper line 46 being positioned about US inch below the longitudinal edge 20.

Turning now specifically to FIGS. 3-7, the utilization of the sample bag of the present invention will be de scribed. First, the closure membrane 12 is removed by graspingthe tab 36 and pulling the membrane toward the right, as viewed in FIG. 3. Next (FIGS. 3 and 4), the protective strip 16 is pulled away from the adhesive coating 14. If there are two persons handling the sample collection operation, as is usually the case, the sample loading technique shown in FIG. 5 may be employed. One person holds the sample bag with one hand along the upper margin thereof. lBy lightly contacting the adhesive coating 14 with the thumb of the other hand, and applying a gentle pull, the overlapping

portions

26 and 28 of the bag are separated to open the access opening 30. The other person then drops the sample 50 into the bag which is then sealed (FIGS. 6 and 7) by folding the upper part of the bag along a longitudinal line about mid-way between the indicia lines 46 and 48 to bring the lines into registry and firmly pressing the portion of the bag about the access opening into engagement with the adhesive coating 14. The access opening 30 is thus completely sealed by the adhesive coating 14 against the entry of bacteria or other foreign matter. Although it appears from FIG. 7 that bacteria may enter through an opening below the edge 20, because of the thinness and flexibility of the plastic sheet and the flowability of commercially available pressure sensitive adhesives which may be used for the adhesive coating 14, said opening, below edge 20, does not exist in actual practice. If only one person is available to both manipulate the sample bag and insert the sample, a small area of the adhesive coating 14 may be pressed lightly into engagement with a stationary object. With one hand the rest of the bag is pulled away to open the access opening 30 and the sample 50 is then inserted with the other hand.

What is claimed is:

l. A pre-sterilizable bag for receiving and storing a sample for analysis at a location remote from the situs of sample collection, said bag being fabricated of a material essentially completely impermeable to bacteria and including an access opening covered by a removable closure membrane essentially completely impermeable to bacteria, but highly penneable, incomparison to said bag material, to sterilizing vapor, the outer surface of said bag including sealing means shaped and positioned to be engaged in sealing contact with the area of said bag material about said access opening to completely seal said opening after removal of said clo sure membrane and insertion of said sample into said bag.

2. A bag, as defined in claim l, in which saidbag material is transparent plastic and said closure membrane comprises a paper strip removably attached to the outer surface of said bag about said access opening.

3. A bag, as defined in claim 1, in which said sealing means and access opening are in spaced relation, said bag being foldable along a portion of said bag between said sealing means and said access opening for bringing the portion s of said bag about said access opening into sealing contact with said sealing means.

4. A bag, as defined in claim 3, in which said access opening comprises an elongated, generally linear slit and said sealing means includes a pressure-sensitive adhesive coating applied to said bag as a strip substantially parallel to said access opening.

5. A bag, as defined in claim 4, which includes indicia adapted to be brought into registry upon folding of said bag to assist in the positioning of said access opening relative to said adhesive coating.

6. A bag, as defined in claim 5, in which said indicia includes a pair of spaced, linear marks parallel to each other and said access opening.

7. A pre-sterilizable bag for receiving and storing biological samples for subsequent analysis, said bag being fabricated of a material essentially completely impermeable to bacteria and including an access opening covered by a closure membrane, said membrane being essentially completely impermeable to bacteria but highly permeable, in comparison to said bag material, to sterilizing vapor, said bag further including an adhesive coating, said closure membrane being removable and said bag being foldable to bring the region about said access opening into sealing engagement with said adhesive coating to seal said opening against the entry into said bag of bacteria, foreign matter or the like.

8. A bag, as defined in claim 7, in which said bag material is transparent plastic and said closure membrane comprises a paper strip removably attached to the outer surface said bag about said access opening.

9. A bag, as defined in claim 7, in which said adhesive coating and access opening are in spaced, parallel relation, said bag being foldable along a portion thereof between said adhesive coating and said access opening for bringing the portions of said bag about said access opening into sealing contact with said adhesive coating.

l0. A bag, as defined in claim 9, in which said access opening is defined by overlapping longitudinal edge portions of said bag and said adhesive coating comprises a pressure-sensitive adhesive applied to the outer surface of said bag as a strip substantially parallel to said access opening.

ll. A bag, as defined in claim 10, which includes indicia adapted to be brought into registry upon folding of said bag to assist in the positioning of said access opening relative to said adhesive coating and insure complete sealing of said opening.

12. A bag, as defined in claim 11, in which said indicia comprises a pair of spaced, parallel lines.

13. A flexible sample bag, capable of having its interior sterilized by sterilizing vapor, comprising:

a heat sealable plastic sheet essentially completely impermeable to bacteria, said sheet having longitudinal and transverse edges and being folded along longitudinal fold lines, said longitudinal edges defining a longitudinally extending access opening;

a removable closure membrane of a material essentially completely impermeable to bacteria and highly permeable, in comparison to said plastic sheet material, to sterilizing vapor, said membrane extending the length of said bag and closing said access opening, said membrane being secured to the exterior of said bag by a longitudinally extending, continuous, pressure heat seal joinder line on each side of said opening;

continuous, pressure heat seal joinder lines extending along said transverse edges closing said bag and further uniting said strip to said plastic sheet along transverse edges; and

a pressure-sensitive adhesive coating applied to a longitudinally extending area of the exterior surface of said bag, said area lying in spaced, parallel relation to said access opening, said region being overlayed by a protective strip ending use of said bag whereby the interior of said bag is sterilizable by a process involving the exposure of said bag interior to a sterilizing vapor passed through said membrane, said membrane being removable to permit insertion of said sample into said bag through said access opening, said bag being sealable by removing said protective strip and folding said bag to bring the area of said bag about said access opening into sealing contact with said pressure-sensitive adhesive area.

14. A sample bag, as defined in claim 13, in which at least one of said transverse heat seal joinder lines is spaced from the corresponding transverse edge to define a pull tab on said removable membrane.

15. A sample bag, as defined in claim 13, which includes spaced indicia registrable upon folding of said bag to assist in the positioning of said access opening relative to said pressure-sensitive adhesive coating to insure complete sealing of said access opening.

Claims

1. A pre-sterilizable bag for receiving and storing a sample for analysis at a location remote from the situs of sample collection, said bag being fabricated of a material essentially completely impermeable to bacteria and including an access opening covered by a removable closure membrane essentially completely impermeable to bacteria, but highly permeable, in comparison to said bag material, to sterilizing vapor, the outer surface of said bag including sealing means shaped and positioned to be engaged in sealing contact with the area of said bag material about said access opening to completely seal said opening after removal of said closure membrane and insertion of said sample into said bag.

2. A bag, as defined in claim 1, in which said bag material is transparent plastic and said closure membrane comprises a paper strip removably attached to the outer surface of said bag about said access opening.

10. A bag, as defined in claim 9, in which said access opening is defined by overlappIng longitudinal edge portions of said bag and said adhesive coating comprises a pressure-sensitive adhesive applied to the outer surface of said bag as a strip substantially parallel to said access opening.

11. A bag, as defined in claim 10, which includes indicia adapted to be brought into registry upon folding of said bag to assist in the positioning of said access opening relative to said adhesive coating and insure complete sealing of said opening.

13. A flexible sample bag, capable of having its interior sterilized by sterilizing vapor, comprising: a heat sealable plastic sheet essentially completely impermeable to bacteria, said sheet having longitudinal and transverse edges and being folded along longitudinal fold lines, said longitudinal edges defining a longitudinally extending access opening; a removable closure membrane of a material essentially completely impermeable to bacteria and highly permeable, in comparison to said plastic sheet material, to sterilizing vapor, said membrane extending the length of said bag and closing said access opening, said membrane being secured to the exterior of said bag by a longitudinally extending, continuous, pressure heat seal joinder line on each side of said opening; continuous, pressure heat seal joinder lines extending along said transverse edges closing said bag and further uniting said strip to said plastic sheet along transverse edges; and a pressure-sensitive adhesive coating applied to a longitudinally extending area of the exterior surface of said bag, said area lying in spaced, parallel relation to said access opening, said region being overlayed by a protective strip ending use of said bag whereby the interior of said bag is sterilizable by a process involving the exposure of said bag interior to a sterilizing vapor passed through said membrane, said membrane being removable to permit insertion of said sample into said bag through said access opening, said bag being sealable by removing said protective strip and folding said bag to bring the area of said bag about said access opening into sealing contact with said pressure-sensitive adhesive area.