MEDICAL GAUZE
20220040005 · 2022-02-10
Assignee
Inventors
- Koichi Sato (Tokyo, JP)
- Hiroshi OGURA (Tokyo, JP)
- Kenji ITO (Fukui, JP)
- Yusuke HOSHIDA (Fukui, JP)
- Hisaharu TAKEUCHI (Osaka, JP)
Cpc classification
A61F13/44
HUMAN NECESSITIES
C08L67/02
CHEMISTRY; METALLURGY
A61F13/36
HUMAN NECESSITIES
C08L67/02
CHEMISTRY; METALLURGY
A61F2013/00238
HUMAN NECESSITIES
D10B2331/04
TEXTILES; PAPER
A61F13/00063
HUMAN NECESSITIES
D04B21/20
TEXTILES; PAPER
International classification
Abstract
Medical gauze includes a warp knitted fabric having a warp and weft direction and composed of loops continued in the warp direction. The warp knitted fabric is made of 100% long fiber containing 70% by weight or more of regenerated cellulose-based long fiber. The warp knitted fabric is preferably configured in a marquisette construction. The regenerated cellulose-based long fiber is preferably cuprammonium rayon. Preferably having a width of equal to or greater than 5 mm and equal to or less than 600 mm, and a weight of equal to or greater than 28 g and equal to or less than 290 g per square meter. As the warp knitted fabric is composed of the loops continued in the warp direction and made of 100% long fiber containing 70% by weight or more of the regenerated cellulose-based long fiber, the occurrence of lint can be reduced to improve lint-free performance.
Claims
1. A medical gauze comprising a warp knitted fabric having a warp direction and a weft direction and composed of loops continued in the warp direction, wherein the warp knitted fabric comprises a 100% long fiber containing 70% by weight or more of regenerated cellulose-based long fiber.
2. The medical gauze according to claim 1, wherein the warp knitted fabric is configured in a marquisette construction.
3. The medical gauze according to claim 1, wherein the regenerated cellulose-based long fiber is cuprammonium rayon.
4. The medical gauze according to claim 1, wherein the medical gauze has a width of equal to or greater than 5 mm and equal to or less than 600 mm, and a weight of equal to or greater than 28 g and equal to or less than 290 g per square meter.
5. The medical gauze according to claim 1, comprising: x-ray contrast yarn arranged in the warp knitted fabric.
6. The medical gauze according to claim 5, wherein the x-ray contrast yarn is welded to the warp knitted fabric.
7. The medical gauze according to claim 5, wherein the x-ray contrast yarn is interlaced in the warp knitted fabric.
8. The medical gauze according to claim 7, wherein at least one chemical fiber is intertwined with the x-ray contrast yarn in the warp direction, and similar chemical fiber is arranged in the warp direction in the vicinity of the at least one chemical fiber.
9. The medical gauze according to claim 8, wherein the total number of the chemical fibers is between four and eight.
10. The medical gauze according to claim 8, wherein the chemical fiber is polyethylene terephthalate fiber.
Description
BRIEF DESCRIPTION OF DRAWINGS
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DETAILED DESCRIPTION
[0047] The configuration of one embodiment of the present invention will be described below in detail by referring to the drawings.
[0048] Referring to
[0049] The medical gauze 1 includes a warp knitted fabric 3 of a warp knitted construction composed of loops 2 continued in a warp direction formed by a warp knitting method.
[0050] The warp knitted fabric 3 is configured in a marquisette construction. The marquisette construction is prepared by forming chain stitches (loops) using a front reed, making a combination of inlaid knitting with two or more needles and one-needle interval inlaid knitting using one or two back reeds for connecting the chain stitches formed using the front reed, and making such combinations along several courses. That is, the marquisette construction is prepared by knitting yarn in the warp direction into a chain, connecting adjacent chain stitches to each other with inlaid yarn extending further in the weft direction, and forming the warp knitted fabric 3 as a whole into a square mesh-like shape.
[0051] The marquisette construction will be described in more detail. As shown in
[0052] Yarn from a second guide bar 6 forms a construction (inlaid construction) by repeating movements of moving for three needles in the weft direction without being used for interlacing, then moving for one needle in the opposite direction, then moving further for one needle in the opposite direction, and thereafter moving for three needles in the opposite direction.
[0053] Yarn is aligned in all guides in both of the first guide bar 5 and the second guide bar 6.
[0054] Using only the first guide bar 5 does not provide connection between yarns adjacent to each other, so that a resultant construction does not fulfill a function as a fabric. Using only the second guide bar 6 does not achieve interlacing, so that a resultant construction does not fulfill a function as a fabric. However, combining these two constructions provides connection in the weft direction and achieves interlacing to fix an inlaid part, thereby fulfilling formation as a fabric.
[0055] For reference, with the first guide bar 5 defined as GB1 and the second guide bar 6 as GB2, the marquisette construction is expressed in a numerical form as follows: GB1: 01-10 and GB2: 33-00-11-00.
[0056] The warp knitted fabric 3 is made of 100% long fiber containing 70% by weight or more of regenerated cellulose-based long fiber.
[0057] The long fiber is one continuous long yarn (filament yarn) with no cut. The warp knitted fabric 3 is formed by a warp knitting method using such long fiber.
[0058] Regarding the warp knitted fabric 3, the percentage by weight of regenerated cellulose-based long fiber of being less than 70% by weight reduces fluid absorbing property, causing a probability of failing to absorb body fluids or blood sufficiently in medical use or a probability of softness reduction during fluid absorption. In this regard, the percentage of the regenerated cellulose-based long fiber in the long fiber is set at equal to or greater than 70% by weight.
[0059] To absorb blood or body fluids efficiently, the conventional medical gauze is generally required to be made of a material with high water absorbing property. However, a material for a surgical operation and the like is not always required to have high water absorbing property. In such cases, for use for blood stanching purpose, a material to absorb a small quantity of body fluid such as blood may be required. For this reason, in addition to the water-absorbing regenerated cellulose-based long fiber, synthetic fiber with no water absorbing property such as nylon, polyester, or polypropylene may also be used to control fluid absorbing property appropriately according to an expected purpose of use.
[0060] As the regenerated cellulose-based long fiber is one continuous long fiber with no cut, it does not cause short fiber trash. By contrast, as cotton yarn is spun yarn prepared by tying and twisting short fibers together, it is likely to cause fiber trash.
[0061] The regenerated cellulose-based long fiber is highly-pure chemical fiber prepared by dissolving a natural product such as pulp or cotton linter in a chemical agent, extracting plant cellulose chemically, and regenerating the extracted plant cellulose into fiber. Conventional cotton gauze requires scouring process by means of degreasing process and bleaching process after weaving. By contrast, as the warp knitted fabric 3 is made of the regenerated cellulose-based long fiber having high cellulose purity and high water absorbing property, it does not require degreasing process intended for washing away impurity and applying water absorbing property.
[0062] The degreasing process is performed by boiling gauze in a high-concentration alkaline liquid under high temperature and high pressure. Thus spun cotton yarn (short fiber) may be loosen and this can inadvertently cause fiber trash on the verge of coming off during cutting of the gauze to drop during use of the gauze.
[0063] More specifically, the regenerated cellulose-based long fiber is preferably viscose rayon (rayon), cuprammonium rayon (cupra), or solvent spun fiber (Lyocell), for example, having more favorable absorbing property than other types of cellulose fiber, fulfilling excellent softness during fluid absorption, and containing a small amount of mixed impurity other than cellulose.
[0064] Also, the total size of the regenerated cellulose-based long fiber to be used can be selected appropriately from a range of equal to or greater than 30 dtex and equal to or less than 200 dtex. For manufacturing the medical gauze 1 with the warp knitted fabric 3 having an appearance and mechanical strength quite similar to those of conventional cotton gauze (a weight of 36 g/m.sup.2), a preferable range is equal to or greater than 50 dtex and equal to or less than 100 dtex.
[0065] Further, the single yarn size (filament size) of the regenerated cellulose-based long fiber is not particularly limited and in a range from 0.5 to 5 dtex. From a viewpoint of knitting performance and grade during implementation of warp knitting and the softness of warp knitted gauze, a preferable range is from 1 to 3 dtex.
[0066] In addition, the regenerated cellulose-based long fiber is available, either it is untwisted or twisted. To use the twisted regenerated cellulose-based long fiber, the number of twisted yarns is selected appropriately in response to the total size of fiber to be used.
[0067] Further, the regenerated cellulose-based long fiber may be bulky textured yarn. Examples of available yarn include false-twisted textured yarn, force textured yarn, textured yarn with loop pile prepared by intertwining long-fiber single yarns with each other using compressed air, and chenille yarn.
[0068] These types of bulky textured yarn to be used can also be yarn having a composite structure of the regenerated cellulose-based long fiber and synthetic resin such as polyester or nylon, for example.
[0069] The medical gauze 1 configured using the warp knitted fabric 3 described above is required to be sterilized for use in a case such as an operation. Thus, the medical gauze is preferably given guaranteed sterilization by formation into the shape of the medical gauze 1 and then implementation of scouring process and sterilizing process.
[0070] The scouring process is preferably performed by scouring the warp knitted fabric 3 at about 70° C. using a bleaching agent such as hydrogen peroxide water. Implementation of this scouring process makes it possible to reduce the number of living bacteria in the warp knitted fabric 3, compared to that at the time of finish of the warp knitting.
[0071] It is noted that the bleaching process using the bleaching agent is not an absolute necessity in the scouring process. For the purpose of smoothing and softening a fabric only, the scouring process to be applied may also be performed only through dipping into warm water.
[0072] The sterilizing process after the scouring process is preferably performed through sterilization using ethylene oxide gas (EOG sterilization) or through sterilization using high-pressure steam (AC sterilization). A product to be formed is preferably guaranteed sufficiently in terms of sterilization by the implementation of the sterilizing process.
[0073] Also, in consideration of use in a surgical operation, the medical gauze 1 preferably has a width of equal to or greater than 5 mm and equal to or less than 600 mm.
[0074] Further, the weight of the warp knitted fabric 3 of less than 28 g per square meter causes a probability of failing to ensure water absorbing property sufficiently in the medical gauze 1. On the other hand, conventional plain woven gauze normally has a weight of 36 g per square meter. In some causes, eight pieces of such gauze are stacked and sewed together to manufacture thick gauze having a weight of 288 g per square meter. Hence, use of the medical gauze 1 having a similar weight is also expected. For this reason, in the medical gauze 1, the warp knitted fabric 3 preferably has a weight of equal to or greater than 28 g and equal to or less than 290 g per square meter.
[0075] The action and effect of the foregoing one embodiment will be described next.
[0076] In the foregoing medical gauze 1, the warp knitted fabric 3 is composed of the loops 2 continued in the warp direction and is formed only of long fiber that is continuous yarn with no cut. This makes fiber unlikely to drop not only in use in a normal state but also in use in a cut state, making it possible to improve lint-free performance effectively.
[0077] Also, the long fiber contains 70% by weight or more of the regenerated cellulose-based long fiber. This makes it possible to ensure water absorbing property and softness for medical use as well as to improve lint-free performance.
[0078] Here, comparison is made between the medical gauze 1 shown in
[0079] The warp knitted fabric 3 is configured in the marquisette construction. By doing so, a stable shape is easily retained using a chain construction continued in the warp direction and inlaid yarn stretching in the weft direction.
[0080] The marquisette construction is also unlikely to cause defective stitches, even if it is thin or low-weight. This allows improvement of dimensional stability.
[0081] Formation using the warp knitting method further allows interlacing in a thickness direction while such interlacing is infeasible by the plain weaving method. This allows the weight of gauze to be changed freely by increasing the fiber diameter of yarn or increasing a swing range of an inlaid construction, thereby facilitating formation into a configuration responsive to a purpose of use.
[0082] Using viscose rayon, cuprammonium rayon, or solvent spun fiber, particularly using cuprammonium rayon as the regenerated cellulose-based long fiber makes it possible to ensure proper water absorbing property and improve softness, thereby achieving improvement of the feel of use and usability.
[0083] The medical gauze 1 is made available for use in a surgical operation by setting the width dimension of the medical gauze 1 at equal to or greater than 5 mm and equal to or less than 600 mm, and setting the weight thereof at equal to or greater than 28 g and equal to or less than 290 g per square meter.
[0084] It is noted that the present invention is not limited to the foregoing configuration of the one embodiment described above but can be changeable, if appropriate, as long as the configuration includes a warp knitted fabric composed of loops continued in the warp direction, the warp knitted fabric is made of 100% long fiber containing 70% by weight or more of regenerated cellulose-based long fiber.
[0085] Namely, as shown in
[0086] During warp knitting, the x-ray contrast yarn 4 is preferably aligned between the regenerated cellulose-based long fibers in the warp knitted fabric 3.
[0087] The x-ray contrast yarn 4 is prepared by adding barium sulfate, for example, having x-ray contrast effect into plastic resin such as polyvinyl chloride, polypropylene, polystyrene, or silicon, or regenerated cellulose-based long fiber such as cuprammonium rayon, for example.
[0088] Also, the x-ray contrast yarn 4 to be used may either be monofilament yarn formed of a single filament, or a multifilament formed by mixing an x-ray contrast agent into fibrous resin.
[0089] The x-ray contrast yarn 4 may further be composite yarn prepared by twisting the x-ray contrast yarn 4 with other synthetic resin or regenerated cellulose fiber with no x-ray contrast property, or by covering the x-ray contrast yarn 4 with such resin or fiber.
[0090] After being used in a surgical operation and the like, the medical gauze 1 is removed from a body after the operation. As the medical gauze 1 is frequently stained with blood during the operation, it becomes difficult to distinguish the medical gauze 1 from an organ, and the like. This causes a risk of proceeding to suture and finishing the operation while the medical gauze 1 is left in the body.
[0091] In this regard, arranging the x-ray contrast yarn 4 in the warp knitted fabric 3 makes it possible to check the retention of the medical gauze 1 easily in an x-ray photograph taken after the operation.
[0092] It is noted that, while medical gauze with x-ray contrast yarn has conventionally been known, the x-ray contrast yarn 4 is generally prepared by weaving yarn thicker than cotton yarn (generally, 40-cotton yarn) in order to facilitate check to see the presence or absence of the retention in the body.
[0093] Such thick x-ray contrast yarn causes a probability that weaving performance will be deteriorated or the x-ray contrast yarn will drop easily. However, in the medical gauze according to the present invention, interlacing the x-ray contrast yarn into the warp knitted fabric 3 can prevent deterioration of knitting performance or dropping of the x-ray contrast yarn 4.
[0094] The x-ray contrast yarn 4 can also be attached by welding as described later. However, forming the x-ray contrast yarn 4 as a part of the warp knitted fabric 3 achieves a higher level of x-ray contrast in an x-ray photograph than the attachment by welding.
[0095] If forming the x-ray contrast yarn 4 as a part of the warp knitted fabric 3 is impossible, the x-ray contrast yarn 4 can be attached easily by welding.
[0096] The x-ray contrast yarn 4 can be attached by welding by melting plastic resin (polyvinyl chloride, polypropylene, polystyrene, or silicon, for example) forming the x-ray contrast yarn 4 using a heat or ultrasonic welding machine, and pressing the resin under pressure against the warp knitted fabric 3.
[0097] In addition, the medical gauze 1 is not limited to the configuration shown in
[0098] In the configuration shown in
[0099] In the configuration shown in
[0100] The medical gauze 1 having the configuration described above shown in
[0101] It is noted that the number of the foregoing chemical fibers is not always required to be an even number (four, six, or eight, for example), and these chemical fibers are not always required to be arranged bilaterally symmetrically. In consideration of right and left balance, however, the same number of chemical fibers are preferably arranged on the right and left sides of the x-ray contrast yarn 4.
[0102] In addition, yarn breakage can be prevented by making change to chemical fiber having higher fiber strength than long fiber. The chemical fiber to be used as replacement for the long fiber is preferably PET fiber having high heat resistance in consideration of the scouring process. It is noted that, not using PET fiber is not preferable, as it causes a risk of dropping of the x-ray contrast yarn 4 from the warp knitted yarn 3 if the long fiber is cut in a place adjacent to the x-ray contrast yarn 4 to break the warp knitted fabric 3.
[0103] On the other hand, as shown in
[0104] For the reason given above, the total number of chemical fibers is preferably between four and eight. However, the number of chemical fibers to be intertwined with x-ray contrast yarn may be at least one or more. In consideration of the point that the minimum number of chemical fibers settable at a knitting machine (marquisette construction) is two, the minimum number of chemical fibers to be intertwined with the x-ray contrast yarn is preferably two. It is noted that, in addition to being the two needle swing yarn shown in
EXAMPLES
[0105] Examples and Comparative Examples will be described below.
[0106] Medical gauze was formed into a configuration shown in Table 1, and then performance evaluation was conducted.
[0107] According to the JIS L 1096A method, the weight of the gauze was calculated as a mass per unit area (g/m.sup.2).
[0108] Lint-free performance was evaluated as follows.
[0109] Cellophane adhesive tape having a width of 10 mm was cut into about 30 mm and affixed to a surface of the medical gauze. After 60 seconds, the cellophane adhesive tape was removed from the medical gauze and affixed to slide glass. The affixed cellophane adhesive tape was given marks of a length of 10 mm and the number of lints within a range of 10 mm 10 mm square was counted using an optical microscope of a magnification of 40. This measurement was conducted six times and an average thereof was employed as a numerical value showing the lint-free performance.
[0110] Water absorbing property was evaluated by the following method.
[0111] The medical gauze was cut into a size of 200 mm 200 mm, a weight (W1) in a normal state (20° C. 65% RH) and a weight (W2) in a wet state were measured, the amount of water absorption (M1) was determined using the formula of M1(%)=(W2−W1)/W1*100, and an average thereof was calculated.
[0112] It is noted that the weight in the wet state (W2) is a weight determined after the medical gauze was dipped in water for 10 minutes, then taken out of the water, and left unattended for 10 minutes while being stretched on a wire mesh to remove excessive moisture from the medical gauze.
[0113] According to Example 1, a warp knitted fabric (without x-ray contrast yarn) was formed under the following conditions using a 28 GG warp knitting machine.
[0114] Yarn used for forming the warp knitted fabric was Bemberg fiber 56 dtex/30f as cupra (available from Asahi Kasei Kabushiki Kaisha, Bemberg is a registered trademark).
[0115] Then, with the number of reeds of 2, the number of courses on the machine of 45, and the number of wales on the machine of 28, a marquisette construction was formed as shown in
[0116] The warp knitted fabric formed in this way was subjected to scouring process at 70° C. for 60 minutes in a solution containing 0.2% by weight of hydrogen peroxide water (a content from 30 to 30.5% by weight).
[0117] Then, the warp knitted fabric after the scouring was cut into 30 cm 30 cm, and then the foregoing performance evaluation was conducted.
[0118] According to Example 2, a warp knitted fabric (without x-ray contrast yarn) was formed under the following conditions using a 28 GG warp knitting machine.
[0119] Yarn used for forming the warp knitted fabric includes Bemberg fiber 56 dtex/30f available from Asahi Kasei Kabushiki Kaisha, and polyester fiber 56 dtex/24f (available from KB SEIREN LTD.). The Bemberg fiber was mixed to a ratio of 70% by weight.
[0120] Then, with the number of reeds of 2, the number of courses on the machine of 45, and the number of wales on the machine of 28, a marquisette construction was formed.
[0121] According to Example 2, a weight was set at 28 g/m.sup.2, which is a lower limit of a preferable range.
[0122] The warp knitted fabric formed in this way was subjected to process in the same way as Example 1, and then performance evaluation was conducted.
[0123] According to Example 3, except for using viscose rayon fiber 56 dtex/24f instead of the Bemberg fiber used in Example 1, process was performed in completely the same way as in Example 1 and performance evaluation thereof was conducted.
[0124] According to Example 4, one polystyrene-based contrast yarn as a 0.85 mmφ monofilament (with a content of barium sulfate of 50 percent by weight) was bonded by thermal compression using an ultrasonic welding machine to the prototype of the medical gauze of 30 cm 30 cm formed in Example 1, and then performance evaluation was conducted.
[0125] According to Example 5, a warp knitted fabric (with x-ray contrast yarn) was formed under the following conditions using a 28 GG warp knitting machine.
[0126] The warp knitted fabric was configured in a marquisette construction as shown in
[0127] The warp knitted fabric formed in this way was subjected to process in the same way as Example 1 and then performance evaluation was conducted.
[0128] According to Example 6, except for using Bemberg fiber 84 dtex/45f as cupra (available from Asahi Kasei Kabushiki Kaisha) instead of the Bemberg fiber 56 dtex/30f used in Example 5, process was performed in completely the same way as in Example 5 and then performance evaluation was conducted.
[0129] According to Example 7, except for using yarn formed by twisting five Bemberg x-ray contrast yarns 300 dtex/60f together (sheath-core fiber with a content of barium sulfate of 60 percent by weight) at Z100t/m instead of the polystyrene-based x-ray contrast yarn used in Example 6, process was performed in the same way as in Example 6 to obtain performance evaluation result.
[0130] According to Comparative Example 1, plain woven gauze was formed using Bemberg fiber 167 dtex/70f available from Asahi Kasei Kabushiki Kaisha as warp yarn and weft yarn to a warp yarn density and a weft yarn density of 12/cm. Then, process was performed in the same way as in Example 1 and performance evaluation was conducted.
[0131] It is noted that the resultant gauze was determined to be incapable of retaining a shape as a woven fabric as at least one of the warp yarn and the weft yarn was moved easily only with touch by a hand to cause slippage phenomena frequently.
[0132] According to Comparative Example 2, by using 40-cotton yarn as warp yarn and weft yarn to a warp yarn density and a weft yarn density of 12/cm, plain woven gauze was formed as cotton gauze as an ordinary item.
[0133] This plain woven gauze was also subjected to degreasing process and bleaching process continuously under conditions same as scouring conditions for ordinary cotton gauze. Then, the gauze was cut into 30 cm 30 cm and performance evaluation was conducted.
[0134] Table 1 shows result of the performance study conducted on each of Examples and each of Comparative Examples described above. In Table 1, PS shows polystyrene-based x-ray contrast yarn and BB shows Bemberg x-ray contrast yarn.
TABLE-US-00001 TABLE 1 REGENERATED PRESENCE/ CELLULOSE ABSENCE REGENERATED WEIGHT OF X-RAY FABRIC CELLULOSE OTHER PERCENT CONTRAST CONSTRUCTION FIBER FIBER (%) YARN EXAMPLE 1 WARP KNITTING CUPRA 56 NO 100 NO 2 CUPRA 56 POLYESTER 56 70 NO 3 RAYON 56 NO 100 NO 4 CUPRA 56 NO 100 YES (PS WELDED) 5 CUPRA 56 NO 100 YES (PS) 6 CUPRA 84 NO 100 YES (PS) 7 CUPRA 84 NO 100 YES (BB) COMPARATIVE 1 PLAIN WEAVING CUPRA 167 NO 100 NO EXAMPLE 2 NATURAL FIBER (COTTON) — YES (PS) GAUZE PROPERTY AMOUNT OF GAUZE GAUZE WATER X-RAY SIZE WEIGHT LINT FREE ABSORPTION CONTRAST (mm) (g/m.sup.2) PERFORMANCE (%) PERFORMANCE EXAMPLE 1 300 * 300 30 <1 320 — 2 28 <1 230 — 3 30 6 310 — 4 30 <1 320 ◯ 5 30 <1 320 ⊚ 6 90 <1 280 ⊚ 7 30 <1 280 ◯ COMPARATIVE 1 300 * 300 40 <1 360 — EXAMPLE 2 36 23 340 ⊚
[0135] As shown in Table 1 and each photograph, according to each of Examples, the construction was retained successively with favorable lint-free performance and without the occurrence of slippage, and the like. By contrast, Comparative Example 1 corresponding to the weaving using cupra failed to retain the construction due to the occurrence of slippage while favorable lint-free performance was achieved. Comparative Example 2 corresponding to the plain weaving using natural fiber resulted in considerably bad lint-free performance.
[0136] Strength Test
[0137] Described next is a strength test conducted using the warp knitted gauze (medical gauze) according to Examples.
[0138] (1) Specimen
[0139] Specimens used include a specimen prepared by interlacing x-ray contrast yarn in a warp knitted fabric made of cupra 84 shown in
[0140] (2) Scouring Condition
[0141] Scouring process was performed on the specimens using hydrogen peroxide water of 0.2% as a processing solution at a processing temperature from 65 to 70° C. and for a processing duration of 60 minutes.
[0142] (3) Test Result
[0143]
[0144] A specimen wet with water (wet gauze) was reduced in strength in long fiber intertwined with the x-ray contrast yarn and was broken easily at this part (see
[0145] As shown in the photograph of
[0146] As shown in the table in
[0147] Thus, in order to reinforce an area around the x-ray contrast yarn and prevent dropping of the x-ray contrast yarn, PET fiber higher in fiber strength than other long fiber is necessary and an appropriate number of PET fibers according to Examples is considered to be four.
[0148] Surface Resistance Check Test
[0149] Described next is a surface resistance check test conducted using the warp knitted gauze (medical gauze) according to Examples and the plain woven cotton gauze according to Comparative Examples.
[0150] (1) Specimen
[0151] Specimens used include a warp knitted gauze low-weight item (weight of 56 g/m.sup.2), a warp knitted gauze large-weight item (weight of 84 g/m.sup.2), and plain woven cotton gauze (weight of 38 g/m.sup.2). It is noted that the warp knitted gauze is gauze with a warp knitted fabric made of cupra 84.
[0152] (2) Test Method
[0153] Petri dishes having glass petri dish bottom surfaces with affixed PP plates (a plate with a smooth surface and a plate with an uneven surface) were placed over the specimens (gauze), and moved at a constant speed by a tensile testing machine. Tensile test strength (testing force) was determined to be a resistance value at a gauze surface. The petri dishes with the affixed PP plates have a weight of 200 g, were installed in an area of 60 cm.sup.2, and were pulled at a speed of 30 cm/min.
[0154] (3) Test Result
[0155]
[0156] Accordingly, in the warp knitted gauze of either case, a surface resistance value is lower than that of the plain woven cotton gauze, showing that the surface of the warp knitted gauze is more slippery than the surface of the plain woven cotton gauze. In a scene of using a port in an endoscopic operation, for example, gauze is preferably easy to slip inside a cylindrical port. In this regard, the warp knitted gauze can be loaded and unloaded more easily than the plain woven cotton gauze, so that the warp knitted gauze according to Examples is considered to be more superior to the plain woven cotton gauze according to Comparative Examples.
[0157] Fabric Detachability Check Test
[0158] Described next is a fabric detachability check test conducted using the warp knitted gauze (medical gauze) according to Examples and the plain woven cotton gauze according to Comparative Examples.
[0159] (1) Specimen
[0160] Specimens used include a warp knitted gauze low-weight item (weight of 56 g/m.sup.2) and plain woven cotton gauze (weight of 36 g/m.sup.2). The warp knitted gauze is gauze with a warp knitted fabric made of cupra 84.
[0161] (2) Test Method
[0162] A plate used is a test metallic plate used in the clinging measurement according to JIS L 1094. This metallic plate is a stainless steel plate having a size of about 100 mm 450 mm and a thickness of about 1.3 mm, and with a 70-degree bend at a position of about 150 mm from one end thereof.
[0163] Two pieces (about 75 mm 230 mm) were taken from each specimen, the upper and lower ends of one of the specimen pieces were fixed with adhesive tape to the metallic plate, the other specimen piece was superimposed on the fixed specimen piece, and then the upper ends of the two specimen pieces were attached together to the metallic plate with a clamp.
[0164] Two specimen pieces attached in this way to the metallic plate were rubbed three times in the palms of hands at a speed of once in one second, then the metallic plate was erected to an upright position, and the angle of the metallic plate was read when the two specimen pieces were detached from each other by tilting the metallic plate gradually.
[0165] (3) Test Result
[0166]
[0167] The foregoing shows that warp knitted gauze has favorable fabric detachability compared to plain woven cotton gauze and thus achieves more excellent ease of handling during actual use. Thus, in a scene of using gauze pieces superimposed on each other in a bundle, for example, the warp knitted gauze is more detachable than the plain woven cotton gauze. As a result, the warp knitted gauze according to Examples is considered to be more superior (in terms of improvement of workability, and the like) to the plain woven cotton gauze according to Comparative Examples.
[0168] Performance Check Test
[0169] Described next is a performance check test conducted using the warp knitted gauze (medical gauze) according to Examples and the plain woven cotton gauze according to Comparative Examples.
[0170] (1) Specimen
[0171] Specimens used include a warp knitted gauze low-weight item, a warp knitted gauze large-weight item, and plain woven cotton gauze. It is noted that the warp knitted gauze is gauze with a warp knitted fabric made of cupra 84.
[0172] (2) Test Method
[0173] A. Basic Performance Check (Weight, Air Permeability, Open Area Ratio)
[0174] For an air permeability test, an airflow quantity (cc/cm.sup.2/sec) was measured under pressure loss of 12.5 mm H.sub.2O according to the JIS L 1096A method (fragile method). As a textile in a sparse construction provides a large airflow quantity, four pieces were stacked for the measurement. In addition, for an open area ratio check test, image analysis was performed using a microscope available from KEYENCE CORPORATION.
[0175] B. Mechanical Characteristic Check
[0176] Kawabata evaluation system (KES) tensile characteristic, KES bending characteristic, and bending resistance (JIS 1096) were measured. It is noted that a WET state was created by dipping gauze into water, then measuring a weight after dewatering for 30 seconds using a dryer of a twin-tub washing machine, and making adjustment to achieve a water content of about 80 wt %.
[0177] (3) Test Result
[0178]
[0179] The present invention is applied as medical gauze capable of absorbing blood or body fluids, for example.