WO2017110717A1

WO2017110717A1 - Absorbent article

Info

Publication number: WO2017110717A1
Application number: PCT/JP2016/087723
Authority: WO
Inventors: 木村　真由美; 剛大石川; 佑佳鈴木; 繁宏松原
Original assignee: 花王株式会社
Priority date: 2015-12-22
Filing date: 2016-12-19
Publication date: 2017-06-29

Abstract

An absorbent article (1) is provided with: an absorbent (4) having a super-absorbent polymer (41), pulp (42), and a blood coagulant (43); and a top sheet (2) and a back sheet (3) for holding the absorbent therebetween. The absorbent (4) has, as viewed in a cross-section, a polymer-rich area (PT) having a relatively high mass ratio of the super-absorbent polymer in relation to the total mass of the pulp (42) and the mass of the super-absorbent polymer (41), and a pulp-rich area (FT) having a relatively lower mass ratio than the polymer-rich area (PT). The blood coagulant (43) is present in at least the pulp-rich area (FT) in the portion where the pulp-rich area (FT) is placed and used on the skin-facing surface side.

Description

Absorbent articles

The present invention relates to an absorbent article.

A technique for improving various performances of an absorbent article by applying an agent that acts on the blood itself to change the state of the blood to the absorbent article is known. Patent Document 1 discloses a menstrual band including an absorbent pad containing a salt of multivalent ions. Patent Document 2 discloses a napkin containing a partially hydrated dicarboxylic anhydride copolymer or polycation as a blood gelling agent. Patent Document 3 proposes a personal care absorbent article containing a triblock polymer or polycation containing polypropylene oxide and polyethylene oxide as a fluid treatment material.

The applicant previously proposed an absorbent article containing a blood coagulant containing a water-soluble metal compound in an absorbent core (see Patent Document 4).

Japanese Patent Publication No. 38-17449 JP-A-57-153648 Special table 2002-528232 gazette Japanese Patent Laying-Open No. 2005-287997

The present invention is an absorbent article comprising an absorber containing a superabsorbent polymer, hydrophilic fibers and a blood coagulant, and a top sheet and a back sheet sandwiching the absorber. The absorbent body has a polymer-rich region in which the mass ratio of the superabsorbent polymer to the total amount of the mass of the hydrophilic fiber and the mass of the superabsorbent polymer in a cross-sectional view is relatively high, and the polymer-rich region. And a hydrophilic fiber rich region relatively lower than the region. In the portion where the hydrophilic fiber-rich region is used on the skin facing surface side, the blood coagulant is present at least in the hydrophilic fiber-rich region.

FIG. 1 is a plan view of a sanitary napkin which is a preferred embodiment of the absorbent article for menstrual absorption of the present invention. FIG. 2 is a plan view showing the skin facing surface side (surface sheet side) of the absorbent body of the sanitary napkin shown in FIG. 3 is a cross-sectional view schematically showing a cross section taken along line III-III in FIG. FIG. 4 is an enlarged cross-sectional view of an absorbent body included in the sanitary napkin shown in FIG. FIG. 5 is an enlarged schematic cross-sectional view of a main part of one absorbent sheet constituting the absorbent body shown in FIG. Drawing 6 is an expanded sectional view of an absorber of other embodiments with which an absorptive article of the present invention is provided. FIG. 7 is an enlarged cross-sectional view of an absorbent body according to still another embodiment provided in the absorbent article of the present invention.

Detailed Description of the Invention

Patent Documents

1 and 4 do not describe any structure for improving the blood absorption rate except that a water-soluble metal compound is used as a blood coagulant. On the other hand, although the absorbent articles described in Patent Literature 2 and Patent Literature 3 describe that a fluid treatment agent containing a polycation can be used, only data on nonionic treatment materials is actually disclosed. Not. In addition, in the techniques disclosed in these, it takes time to absorb blood, and menstrual blood leaks easily.

Therefore, an object of the present invention is to provide an absorbent article that can eliminate the above-mentioned drawbacks of the prior art.

Hereinafter, the absorbent article of the present invention will be described with reference to the drawings based on a sanitary napkin 1 (hereinafter also referred to as “napkin 1”) which is a preferred embodiment thereof. The napkin 1 includes an absorbent body 4 made of an absorbent sheet containing a superabsorbent polymer 41, hydrophilic fibers, and a blood coagulant 43, and a top sheet 2 and a back sheet 3 that sandwich the absorbent body 4. . Moreover, in the napkin 1 of this embodiment, the absorber 4 is comprised from the absorptive sheet, and, specifically, it has the structure where the absorptive sheet overlapped in the multiple layer thickness direction. Preferably, FIG. 1 shows a plan view of a napkin which is a preferred embodiment of the absorbent article for menstrual absorption of the present invention, and FIG. 2 shows the skin of the absorbent body shown in FIG. The top view which shows an opposing surface side (surface sheet side) is shown. FIG. 3 shows a cross-sectional view of the napkin 1 of the present embodiment. The absorbent article of the present invention is preferable for menstrual blood absorption.

In the present embodiment, as shown in FIGS. 1 to 3, the napkin 1 includes a liquid-permeable surface sheet 2 that forms a skin facing surface, a back sheet 3 that forms a non-skin facing surface, and both of these

sheets

2 and 3. It has an absorbent main body 10 having an absorbent body 4 interposed between them and made of an absorbent sheet containing pulp 42 and blood coagulant 43.

As shown in FIG. 1, the absorbent main body 10 of the napkin 1 is a wearer than the excretion part facing part B, which is disposed opposite to the excretion part (vagina mouth or the like) of the wearer when worn, and the wearer facing part B. The front part A is arranged closer to the stomach side (front side) and the rear part C is arranged closer to the wearer's back side (rear side) than the excretory part facing part B. The napkin 1 and the absorbent main body 10 have a longitudinal direction X corresponding to the wearer's front-rear direction and a transverse direction Y orthogonal to the longitudinal direction X. That is, the absorbent main body 10 is divided in the order of the front part A, the excretory part opposing part B, and the rear part C in the vertical direction X.

Moreover, in this specification, a skin opposing surface is a surface in the napkin 1 or its component (for example, surface sheet 2) orient | assigned to a wearer's skin side at the time of wear of the napkin 1, and a non-skin opposing surface is a napkin. 1 or a component thereof, which is a surface directed to the side opposite to the skin side (clothing side) when the napkin 1 is worn. Further, the longitudinal direction X coincides with the longitudinal direction of the napkin 1 and the absorbent main body 10, and the lateral direction Y coincides with the width direction (direction orthogonal to the longitudinal direction) of the napkin 1 and the absorbent main body 10.

In this embodiment, as shown in FIGS. 1 and 3, the napkin 1 is further laterally extended from both side portions along the longitudinal direction X of the excretory part-facing portion B of the absorbent main body 10 in addition to the absorbent main body 10. It has a pair of

wing parts

10W and 10W extending outward of Y.

In the absorbent article of the present invention, when the excretory part facing part B has the wing part 10W like the napkin 1 of the present embodiment, the longitudinal direction of the absorbent article (the longitudinal direction of the absorbent article, FIG. (X direction in the middle) means a region having a wing portion 10W (a region sandwiched between a root along the vertical direction X of one wing portion 10W and a root along the vertical direction X of the other wing portion 10W). The excretion part opposing part B in the absorbent article which does not have a wing part is produced when the absorbent article is folded into a three-fold individual packaging form. With respect to two folding curves (not shown) crossing in the Y direction in the middle, it means a region surrounded by the first folding curve and the second folding curve counted from the front end in the longitudinal direction X of the absorbent article. To do.

In the napkin 1 of the present embodiment, the top sheet 2 covers the entire area of the skin facing surface of the absorbent body 4 as shown in FIG. 1, and the outer side in the lateral direction Y from both side edges along the longitudinal direction X of the absorbent body 4. It extends to the direction. On the other hand, the back sheet 3 covers the entire area of the non-skin facing surface of the absorbent body 4 and further extends outward in the lateral direction Y from both side edges along the longitudinal direction X of the absorbent body 4 to be described later. In addition, a side flap portion 10S is formed. The top sheet 2 and the back sheet 3 are joined to each other by known joining means such as an adhesive, heat seal, ultrasonic seal, and the like, at portions extending from both end edges in the longitudinal direction X of the absorber 4. In addition, between each of the top sheet 2 and the back sheet 3 and the absorbent body 4 may be joined by an adhesive.

In the napkin 1, as shown in FIGS. 1 and 3, the side sheets 7 are disposed on both sides along the longitudinal direction X of the skin facing surface of the absorbent main body 10 (skin facing surface of the top sheet 2). Preferably, the side sheet 7 is arranged over the entire length in the longitudinal direction X of the absorbent main body 10 so as to overlap the left and right side portions along the longitudinal direction X of the absorbent body 4 in plan view.

In the napkin 1, as shown in FIG. 1, the pair of

side sheets

7 and 7 each have a linear first joining line 61 located in the excretory part facing part B and the longitudinal direction X of the first joining line 61. Are joined to the topsheet 2 by linear second joining lines 62 located in the front and rear (front part A and rear part C). The first joint line 61 is a curved line convex outward in the lateral direction Y in plan view, and the second joint line 62 is a line (zigzag) extending so as to alternately intersect the vertical direction in plan view. Linear). Thus, when the side sheet 7 is joined to the surface sheet 2 by the first joining line 61 and the second joining line 62 and fixed to the skin facing surface of the absorbent main body 10, as shown in FIG. A space P defined by the side sheet 7 and the top sheet 2 is formed inward in the lateral direction Y with respect to the first joint line 61 and the second joint line 62. Since the space P is opened toward the center in the lateral direction Y of the absorbent main body 10, body fluid such as menstrual blood flowing outward from the center in the lateral Y is accommodated in the space P. As a result, leakage of body fluid can be effectively prevented. It should be noted that a pair of leak-proof cuffs along the vertical direction X may be arranged by disposing an elastic member extending in the vertical direction X at the free ends of the pair of

side sheets

7, 7. The leak-proof cuff has an upright property and can prevent the side leakage of menstrual blood disposed on the skin facing surface.

In the napkin 1, as shown in FIG. 1, the side flap part 10S protrudes greatly outward in the lateral direction Y at the excretory part facing part B, and thereby the left and right along the longitudinal direction X of the absorbent main body 10 A pair of

wing portions

10W and 10W are extended on both sides. Further, as shown in FIG. 1, the top sheet 2 and the back sheet 3 extend outward in the longitudinal direction X from the front end and the rear end in the longitudinal direction X of the absorbent body 4. The end seal portion is formed by bonding to each other by a known bonding means such as an agent, heat sealing, ultrasonic sealing or the like.

The wing part 10W is used by being folded back to the non-skin facing surface side of the crotch part of clothes such as shorts. In the napkin 1, the wing portion 10 </ b> W has a substantially trapezoidal shape in which a lower base (a side longer than the upper base) is located on a side portion along the longitudinal direction X of the absorbent main body 10 in a plan view, as shown in FIG. 1. It has a shape. A wing portion adhesive portion (not shown) for fixing the wing portion 10W (napkin 1) to clothes (not shown) such as shorts is formed on the non-skin facing surface of the wing portion 10W. The wing portion 10W folded back to the non-skin facing surface (outer surface) side of the crotch portion of the clothes can be adhesively fixed to the crotch portion by the adhesive portion during use. Moreover, the main body adhesion part (not shown) for fixing the absorptive main body 10 to clothes, such as shorts, is also formed in the non-skin opposing surface of the absorptive main body 10.

In the present embodiment, as shown in FIG. 3, the napkin 1 is provided with a second sheet 5 made of a nonwoven fabric between the top sheet 2 and the absorbent body 4. In the napkin 1, the second sheet 5 covers substantially the entire area of the skin-facing surface of the absorbent body 4, as shown in FIG. The second sheet 5 is a sheet called a sublayer sheet in the technical field, which is a separate body from the top sheet 2 and the absorber 4. The second sheet 5 is a sheet that plays a role of improving the liquid permeability from the top sheet 2 to the absorber 4 or reducing the return of the liquid absorbed by the absorber 4 to the top sheet 2. . In the napkin 1, the second sheet 5 is a sheet that does not contain a blood coagulant 43 described later.

FIG. 4 shows an enlarged cross-sectional view of the absorber 4 in the cross-sectional view shown in FIG. Moreover, the principal part expanded sectional view of one absorbent sheet which comprises the absorber 4 shown in FIG. 4 is shown by FIG. As shown in FIG. 5, the absorbent body 4 made of an absorbent sheet has a superabsorbent polymer 41 that is three-dimensionally distributed, pulp 42 as hydrophilic fibers, and a blood coagulant 43. . The absorbent sheet 4 has a polymer-rich region PT in which the mass ratio of the superabsorbent polymer 41 to the total amount of the mass of the pulp 42 and the mass of the superabsorbent polymer 41 is relatively high in a cross-sectional view, And a pulp rich region FT as a hydrophilic fiber rich region that is relatively lower than the polymer rich region PT. In the napkin 1, the polymer rich region PT and the pulp rich region FT are divided in the thickness direction of the absorbent sheet 4. The absorbent body 4 made of an absorbent sheet includes pulp 42 and has an integral structure in which a superabsorbent polymer 41 and a blood coagulant 43 are contained. As the absorbent body 4 made of an absorbent sheet, between the pulps 42 and the superabsorbent polymer via the adhesive force generated in the wet superabsorbent polymer 41 and a binder such as an adhesive or an adhesive fiber added separately. A sheet or the like obtained by bonding between 41 and pulp 42 can be preferably used. In addition, an absorptive sheet | seat is an absorber currently shape | molded by the sheet form, and generally distinguishes it from the absorber of the structure where the absorptive material was piled up. Typical examples of the absorbent sheet include those described in Japanese Patent No. 2963647 and those described in Japanese Patent No. 2955223.

As the superabsorbent polymer 41 possessed by the absorbent body 4, particles are generally used, but fibers may be used. When the particulate superabsorbent polymer is used, the shape thereof may be any of a spherical shape, a block shape, a bowl shape, and an amorphous shape. As the superabsorbent polymer, generally, a polymer or copolymer of acrylic acid or an alkali metal acrylate can be used. Examples thereof include polyacrylic acid and salts thereof and polymethacrylic acid and salts thereof. As the polyacrylate and polymethacrylate, sodium salts can be preferably used. In addition, acrylic acid or methacrylic acid, maleic acid, itaconic acid, acrylamide, 2-acrylamido-2-methylpropanesulfonic acid, 2- (meth) acryloylethanesulfonic acid, 2-hydroxyethyl (meth) acrylate, styrenesulfonic acid, etc. It is also possible to use a copolymer obtained by copolymerizing the above-mentioned comonomer within a range that does not deteriorate the performance of the superabsorbent polymer.

Examples of the hydrophilic fiber possessed by the absorbent body 4 include those obtained by hydrophilizing hydrophobic fibers and those that are hydrophilic per se. Particularly preferred are those which are themselves hydrophilic and have water retention. Preferred examples of the latter hydrophilic fibers include natural fibers, cellulosic regenerated fibers, and semi-synthetic fibers. As the hydrophilic fiber, pulp and rayon are particularly preferable, and pulp is more preferable. In the napkin 1, pulp is used as the hydrophilic fiber. Furthermore, a bulky cellulose fiber obtained by mercerizing a crosslinked cellulose fiber or wood pulp in which cellulose fibers are intermolecularly and / or intermolecularly crosslinked may be used. Examples of the pulp 42 include, but are not limited to, wood pulp such as coniferous kraft pulp or hardwood kraft pulp, natural cellulose fibers such as cotton pulp or straw pulp, and the like. These pulps can be used alone or in combination of two or more.

The absorbent article of the present invention includes a blood aggregating agent 43 in the absorbent body 4. Hereinafter, the blood coagulant used in the present invention will be described. The blood aggregating agent used in the present invention is an agent that aggregates erythrocytes in blood to form erythrocyte aggregates and can be separated from plasma components, and preferably has the following properties.
That is, when 1000 ppm of the measurement sample agent is added to the simulated blood, at least two or more red blood cells aggregate to form an aggregate while maintaining the fluidity of the blood.
The simulated blood has a viscosity of 8 mPa · s measured using a B-type viscometer (manufactured by Toki Sangyo Co., Ltd., model number TVB-10M, measurement conditions: rotor No. 19, 30 rpm, 25 ° C., 60 seconds). The blood cell / plasma ratio of defibrinated horse blood (manufactured by Japan Biotest Laboratories, Inc.) was prepared.

Here, “the state in which the fluidity of blood is maintained” means that 10 g of the simulated blood to which 1000 ppm of the measurement sample agent is added is a screw tube (product number “Screw tube No. 4” manufactured by Marum Co., Ltd.). 5 mm, body diameter 27 mm, total length 55 mm), and when the screw tube bottle containing the simulated blood is inverted 180 degrees, the simulated menstrual blood of a volume of 60% or more flows down within 20 seconds.
Further, whether or not “two or more red blood cells aggregate to form an aggregate” is determined as follows. That is, the simulated blood to which the measurement sample agent was added at 1000 ppm was diluted 4000 times with physiological saline, and a laser diffraction / scattering type particle size distribution measuring device (manufactured by HORIBA, Inc., model number: LA-950V2, measurement condition: flow type cell). The average median diameter of the volume particle diameter measured at a temperature of 25 ° C. by a laser diffraction scattering method using a measurement, a circulation speed of 1 and no ultrasonic wave corresponds to the size of an aggregate in which two or more red blood cells are aggregated. When it is 10 μm or more, it is determined that “two or more red blood cells aggregate to form an aggregate”.

In the napkin 1, the blood aggregating agent 43 included in the absorber 4 includes a cationic polymer. Examples of the cationic polymer include cationized cellulose and cationized starch such as hydroxypropyltrimonium chloride. The blood coagulant 43 can also contain a quaternary ammonium salt homopolymer, a quaternary ammonium salt copolymer or a quaternary ammonium salt polycondensate as a cationic polymer. In the present invention, the “quaternary ammonium salt” includes a compound having a plus monovalent charge at the nitrogen atom position, or a compound that generates a plus monovalent charge at the nitrogen atom position by neutralization. Specific examples thereof include a salt of a quaternary ammonium cation, a neutralized salt of a tertiary amine, and a tertiary amine having a cation in an aqueous solution. The “quaternary ammonium moiety” described below is also used in the same meaning and is a moiety that is positively charged in water. Further, in the present invention, the “copolymer” is a polymer obtained by copolymerization of two or more kinds of polymerizable monomers, and is a binary copolymer or a ternary copolymer or more. Includes both things. In the present invention, the “polycondensate” is a polycondensate obtained by polymerizing a condensate composed of two or more monomers. When the blood agglutinating agent 43 includes a quaternary ammonium salt homopolymer and / or a quaternary ammonium salt copolymer and / or a quaternary ammonium salt polycondensate as the cationic polymer, the blood aggregating agent 43 is , Quaternary ammonium salt homopolymer, quaternary ammonium salt copolymer and quaternary ammonium salt polycondensate may be included, or any combination of two or more may be included. You may go out. Moreover, a quaternary ammonium salt homopolymer can be used individually by 1 type or in combination of 2 or more types. Similarly, the quaternary ammonium salt copolymer can be used alone or in combination of two or more. Furthermore, similarly, a quaternary ammonium salt polycondensate can be used individually by 1 type or in combination of 2 or more types. In the present specification, the “blood aggregating agent” is a compound capable of aggregating blood erythrocytes or a combination thereof, and further an agent that expresses erythrocyte aggregation by a combination of compounds. That is, the blood aggregating agent is an agent limited to those having a hemagglutinating action. Therefore, when the blood coagulant contains the third component, it is expressed as a blood coagulant composition and is distinguished from the blood coagulant.

Among the various cationic polymers described above, in particular, the use of a quaternary ammonium salt homopolymer, a quaternary ammonium salt copolymer or a quaternary ammonium salt polycondensate is advantageous from the viewpoint of adsorptivity to erythrocytes. preferable. In the following description, for convenience, the quaternary ammonium salt homopolymer, the quaternary ammonium salt copolymer and the quaternary ammonium salt polycondensate are collectively referred to as “quaternary ammonium salt polymer”.

The quaternary ammonium salt homopolymer is obtained by polymerizing one type of polymerizable monomer having a quaternary ammonium moiety. On the other hand, the quaternary ammonium salt copolymer uses at least one polymerizable monomer having a quaternary ammonium moiety and, if necessary, at least one polymerizable monomer having no quaternary ammonium moiety. It was obtained by using seeds and copolymerizing them. That is, the quaternary ammonium salt copolymer is obtained by using two or more polymerizable monomers having a quaternary ammonium moiety and copolymerizing them, or having a quaternary ammonium moiety. It is obtained by copolymerizing one or more polymerizable monomers having one or more polymerizable monomers having no quaternary ammonium moiety. The quaternary ammonium salt copolymer may be a random copolymer, an alternating copolymer, a block copolymer, or a graft copolymer. The quaternary ammonium salt polycondensate is obtained by polymerizing these condensates using a condensate composed of one or more monomers having a quaternary ammonium moiety. That is, the quaternary ammonium salt polycondensate is obtained by polymerizing two or more condensates having two or more monomers having a quaternary ammonium moiety, or the quaternary ammonium moiety. And a condensate comprising one or more monomers having quaternary ammonium moieties and one or more monomers having no quaternary ammonium moiety, and obtained by condensation polymerization.

The quaternary ammonium salt polymer is a cationic polymer having a quaternary ammonium moiety. A quaternary ammonium moiety can be generated by quaternary ammoniumation of a tertiary amine using an alkylating agent. Alternatively, the tertiary amine can be dissolved in acid or water and generated by neutralization. Or it can produce | generate by the quaternary ammonium formation by the nucleophilic reaction containing a condensation reaction. Examples of the alkylating agent include alkyl halides and dialkyl sulfates such as dimethyl sulfate and dimethyl sulfate. Of these alkylating agents, the use of dialkyl sulfate is preferable because the problem of corrosion that may occur when an alkyl halide is used does not occur. Examples of the acid include hydrochloric acid, sulfuric acid, nitric acid, acetic acid, citric acid, phosphoric acid, fluorosulfonic acid, boric acid, chromic acid, lactic acid, oxalic acid, tartaric acid, gluconic acid, formic acid, ascorbic acid, and hyaluronic acid. . In particular, it is preferable to use a quaternary ammonium salt polymer in which a tertiary amine moiety is quaternized with an alkylating agent, because the electric double layer of erythrocytes can be reliably neutralized. Quaternary ammoniumation by a nucleophilic reaction including a condensation reaction can be caused by a ring-opening polycondensation reaction of dimethylamine and epichlorohydrin or a cyclization reaction of dicyandiamide and diethylenetriamine.

As a result of the inventor's examination, it has been found that it is particularly effective to use a cationic polymer in order to generate an aggregate of red blood cells during menstrual blood. The reason for this is as follows. Red blood cells have a red blood cell membrane on their surface. The erythrocyte membrane has a two-layer structure. This two-layer structure is composed of a red blood cell membrane skeleton as a lower layer and a lipid membrane as an upper layer. The lipid film exposed on the surface of erythrocytes contains a protein called glycophorin. Glycophorin has a sugar chain to which a sugar having an anionic charge called sialic acid is bonded at its end. As a result, erythrocytes can be treated as colloidal particles having an anionic charge. In general, an aggregating agent is used for aggregating the colloidal particles. Considering that erythrocytes are anionic colloidal particles, it is advantageous to use a cationic substance as an aggregating agent from the viewpoint of neutralizing the electric double layer of erythrocytes. Further, if the aggregating agent has a polymer chain, the polymer chains of the aggregating agent adsorbed on the surface of the erythrocyte tend to be entangled with each other, thereby promoting the aggregation of erythrocytes. Further, when the aggregating agent has a functional group, it is preferable because the aggregation of erythrocytes is promoted by the interaction between the functional groups.

From the viewpoint of effectively generating red blood cell aggregates, the cationic polymer preferably has a molecular weight of 2000 or more, more preferably 10,000 or more, and even more preferably 30,000 or more. When the molecular weight of the cationic polymer is not less than these values, the entanglement of the cationic polymers between the erythrocytes and the crosslinking of the cationic polymer between the erythrocytes are sufficiently caused. The upper limit of the molecular weight is preferably 10 million or less, more preferably 5 million or less, and even more preferably 3 million or less. When the molecular weight of the cationic polymer is not more than these values, the cationic polymer dissolves well into menstrual blood. The molecular weight of the cationic polymer is preferably 2000 or more and 10 million or less, more preferably 2000 or more and 5 million or less, still more preferably 2000 or more and 3 million or less, and 10,000 or more and 3 million or less. It is even more preferable, and it is particularly preferably 30,000 to 3,000,000. The molecular weight referred to in the present invention is a weight average molecular weight. The molecular weight of the cationic polymer can be controlled by appropriately selecting the polymerization conditions. The molecular weight of the cationic polymer can be measured using HLC-8320GPC manufactured by Tosoh Corporation. Specific measurement conditions are as follows. As the column, a column in which a guard column α and an analytical column α-M manufactured by Tosoh Corporation are connected in series is used at a column temperature of 40 ° C. The detector uses RI (refractive index). As a measurement sample, 1 mg of the treatment agent (quaternary ammonium salt polymer) to be measured is dissolved in 1 mL of the eluent. A copolymer containing a water-soluble polymerizable monomer such as hydroxyethyl methacrylate uses an eluent in which 150 mmol / L sodium sulfate and 1% by mass acetic acid are dissolved in water. A copolymer containing a water-soluble polymerizable monomer such as hydroxyethyl methacrylate has a molecular weight of 5900, a pullulan with a molecular weight of 47300, a pullulan with a molecular weight of 212,000, and a molecular weight of 788,000 with respect to 10 mL of the eluent. Pullulan, a pullulan mixture with 2.5 mg each dissolved, is used as the molecular weight standard. A copolymer containing a water-soluble polymerizable monomer such as hydroxyethyl methacrylate is measured at a flow rate of 1.0 mL / min and an injection amount of 100 μL. Except for a copolymer containing a water-soluble polymerizable monomer such as hydroxyethyl methacrylate, elution with 50 mmol / L lithium bromide and 1% by mass acetic acid dissolved in ethanol: water = 3: 7 (volume ratio) Use liquid. Except for a copolymer containing a water-soluble polymerizable monomer such as hydroxyethyl methacrylate, a polyethylene glycol (PEG) having a molecular weight of 106, a PEG having a molecular weight of 400, a PEG having a molecular weight of 1470, and a PEG having a molecular weight of 6450 with respect to 20 mL of the eluent. Polyethylene oxide (PEO) having a molecular weight of 50,000, PEO having a molecular weight of 235,000, PEO having a molecular weight of 875,000, and a PEG-PEO mixture in which 10 mg of each is dissolved is used as a molecular weight standard. Except for a copolymer containing a water-soluble polymerizable monomer such as hydroxyethyl methacrylate, the flow rate is 0.6 mL / min and the injection amount is 100 μL.

In the case of using a quaternary ammonium salt polymer as the cationic polymer, it is preferable that the quaternary ammonium salt polymer has a flow potential of 1500 μeq / L or more from the viewpoint of more effectively generating red blood cell aggregates. , More preferably 2000 μeq / L or more, still more preferably 3000 μeq / L or more, still more preferably 4000 μeq / L or more. When the flow potential of the quaternary ammonium salt polymer is not less than these values, the electric double layer of erythrocytes can be sufficiently neutralized. The upper limit of the streaming potential is preferably 13000 μeq / L or less, more preferably 8000 μeq / L or less, and even more preferably 6000 μeq / L or less. When the flow potential of the quaternary ammonium salt polymer is below these values, the electrical repulsion between the quaternary ammonium salt polymers adsorbed on the erythrocytes can be effectively prevented. The streaming potential of the quaternary ammonium salt polymer is preferably 1500 μeq / L or more and 13000 μeq / L, more preferably 2000 μeq / L or more and 13000 μeq / L or less, and 3000 μeq / L or more and 8000 μeq / L or less. Is more preferably 4000 μeq / L or more and 6000 μeq / L or less. The flow potential of the quaternary ammonium salt polymer adjusts, for example, the molecular weight of the constituting cationic monomer itself, and the copolymerization molar ratio of the cationic monomer and the anionic monomer or nonionic monomer constituting the copolymer. Can be controlled. The streaming potential of the quaternary ammonium salt polymer can be measured using a streaming potential measuring device (PCD04) manufactured by Spectris Co., Ltd. Specific measurement conditions are as follows. First, hot melt bonding each member to a commercially available napkin is invalidated using a dryer or the like, and decomposed into members such as a top sheet, an absorber, and a back sheet. For each decomposed member, a multi-stage solvent extraction method from a nonpolar solvent to a polar solvent is performed to separate the treating agent used in each member to obtain a solution containing a single composition. The obtained solution was dried and solidified, and 1H-NMR (nuclear magnetic resonance method), IR (infrared spectroscopy), LC (liquid chromatography), GC (gas chromatography), MS (mass spectrometry), GPC (gel) Permeation chromatography) and fluorescent X-rays are combined to identify the structure of the treatment agent. With respect to a measurement sample in which 0.001 g of a treatment agent (quaternary ammonium salt polymer) to be measured is dissolved in 10 g of physiological saline, a 0.001N sodium polyethylene sulfonate aqueous solution (if the measurement sample has a negative charge) , 0.001N polydiallyldimethylammonium chloride aqueous solution) is titrated, and the titer XmL required until the potential difference between the electrodes disappears is measured. Thereafter, the streaming potential of the quaternary ammonium salt polymer is calculated by Equation 1.
Streaming potential = (X + 0.190 *) × 1000 Equation 1
(* Titration required for the physiological saline solution)

In order for the cationic polymer to be successfully adsorbed on the surface of red blood cells, it is advantageous that the cationic polymer easily interacts with sialic acid present on the surface of red blood cells. From this point of view, the present inventors proceeded with studies, and as a result, inorganic value / organic value (hereinafter referred to as “IOB (Inorganic Organic Balance) value”), which is the ratio between the inorganic value and the organic value of the substance. It was found that the degree of interaction between the sialic acid conjugate and the cationic polymer can be evaluated on the basis of. Specifically, it has been found advantageous to use a cationic polymer having an IOB value that is the same as or close to that of the sialic acid conjugate. The sialic acid conjugate is a compound in which sialic acid can exist in a living body, and examples thereof include a compound in which sialic acid is bound to the end of a glycolipid such as galactolipid.

Generally, the properties of a substance are largely controlled by various intermolecular forces between molecules, and this intermolecular force mainly consists of Van Der Wals force due to molecular mass and electric affinity due to the polarity of the molecule. If the Van Der Waals force, which has a great influence on changes in the properties of substances, and the electrical affinity can be grasped individually, the properties of unknown substances or their mixtures can be predicted from the combination. be able to. This idea is a theory well known as “organic conceptual diagram”. Conceptual diagram of organic materials is, for example, “Organic analysis” written by Kei Fujita (Kanya Shoten, Showa 5), “Organic qualitative analysis: Systematic. Pure products” by Kyoda Fujita (Kyoritsu Shuppan, 1953), Jun Fujita “Revised Chemistry Experiments—Organic Chemistry” by Kawasaki Shobo (1971), “Systematic Organic Qualitative Analysis (mixture)” by Kaoru Fujita and Masami Akatsuka (Kasama Shobo, 1974), and Yoshio Koda It is described in detail in Shiro Sato and Yoshio Honma's “New Basic Concept of Organic Conception and Application” (Sankyo Publishing, 2008). In organic conceptual diagram, regarding the physicochemical properties of substances, the degree of physical properties due to Van Der Waals force is called `` organic '', and the degree of physical properties mainly due to electrical affinity is called `` inorganic ''. The physical properties of substances are considered as a combination of “organic” and “inorganic”. Then, one carbon (C) is defined as organic 20, and the inorganic and organic values of various polar groups are defined as shown in Table 1 below. The sum of the values is obtained, and the ratio between the two is defined as the IOB value. In the present invention, the IOB value of the sialic acid conjugate described above is determined based on these organic and inorganic values, and the IOB value of the cationic polymer is determined based on the value.

Specifically, when the cationic polymer is a homopolymer, the inorganic value and the organic value are determined based on the repeating unit of the homopolymer, and the IOB value is calculated. For example, in the case of polydiallyldimethylammonium chloride, which is a cationic polymer used in Example 1 described later, an organic value of -C-x8 = 160, an inorganic value of AmmoAand NH4 salt × 1 = 400, Since it has an inorganic value of Ring (non-aromatic single ring) × 1 = 10, an organic value of −Cl × 1 = 40, and an inorganic value of 10, the total inorganic value is 400 + 10 + 10 = 420 The sum of the organic values is 160 + 40 = 200. Therefore, the IOB value is 420/200 = 2.10.

On the other hand, when the cationic polymer is a copolymer, the IOB value is calculated according to the following procedure according to the molar ratio of the monomers used for the copolymerization. That is, a copolymer is obtained from monomer A and monomer B, the organic value of monomer A is ORA, the inorganic value is INA, the organic value of monomer B is ORB, and the inorganic value is INB. Yes, when the molar ratio of monomer A / monomer B is MA / MB, the IOB value of the copolymer is calculated from the following equation.

The IOB value of the cationic polymer thus determined is preferably 0.6 or more, more preferably 1.8 or more, further preferably 2.1 or more, 2.2 It is still more preferable that it is above. Further, the IOB value of the cationic polymer is preferably 4.6 or less, more preferably 3.6 or less, and even more preferably 3.0 or less. Specifically, the IOB value of the cationic polymer is preferably 0.6 or more and 4.6 or less, more preferably 1.8 or more and 3.6 or less, and 2.1 or more and 3.6 or less. More preferably, it is 2.2 or more and 3.0 or less. The IOB value of sialic acid is 4.25 for sialic acid alone and 3.89 for sialic acid conjugate. The sialic acid conjugate is a glycolipid in which a sugar chain in a glycolipid and sialic acid are bound, and the sialic acid conjugate has a higher organic value ratio and a lower IOB value than sialic acid alone.

Where the IOB value of the cationic polymer is as described above, the organic value itself is preferably 40 or more, more preferably 100 or more, and even more preferably 130 or more. Further, it is preferably 310 or less, more preferably 250 or less, still more preferably 240 or less, and even more preferably 190 or less. For example, the organic value is preferably 40 or more and 310 or less, more preferably 40 or more and 250 or less, still more preferably 100 or more and 240 or less, and still more preferably 130 or more and 190 or less. By setting the organic value of the cationic polymer within this range, the cationic polymer is more successfully adsorbed to erythrocytes.

On the other hand, the inorganic value of the cationic polymer is preferably 70 or more, more preferably 90 or more, still more preferably 100 or more, still more preferably 120 or more, and 250 or more. It is particularly preferred that Further, it is preferably 790 or less, more preferably 750 or less, still more preferably 700 or less, still more preferably 680 or less, and particularly preferably 490 or less. For example, the inorganic value is preferably from 70 to 790, more preferably from 90 to 750, even more preferably from 90 to 680, still more preferably from 120 to 680, It is especially preferable that it is 250 or more and 490 or less. By setting the inorganic value of the cationic polymer within this range, the cationic polymer can be more effectively adsorbed to erythrocytes.

From the viewpoint of further successfully adsorbing the cationic polymer to erythrocytes, it is preferable that x and y satisfy the following formula A when the organic value of the cationic polymer is x and the inorganic value is y.
y = ax (A)
In the formula, a is preferably 0.66 or more, more preferably 0.93 or more, and even more preferably 1.96 or more. Further, a is preferably 4.56 or less, more preferably 4.19 or less, and even more preferably 3.5 or less. For example, a is preferably a number from 0.66 to 4.56, more preferably from 0.93 to 4.19, and a number from 1.96 to 3.5. Is more preferable. In particular, when the organic value and the inorganic value of the cationic polymer satisfy the above formula A, provided that the organic value and the inorganic value of the cationic polymer are within the above-mentioned ranges, the cation The functional polymer is likely to interact with the sialic acid conjugate, and the cationic polymer is more easily adsorbed to erythrocytes.

From the viewpoint of effectively producing red blood cell aggregates, the cationic polymer is preferably water-soluble. In the present invention, “water-soluble” means that 0.05 g of a 1 mm or less powdery or 0.5 mm or less film-like cationic polymer is added to a 100 mL glass beaker (5 mmΦ) and mixed with 50 mL ion-exchanged water at 25 ° C. In this case, a stirrer chip having a length of 20 mm and a width of 7 mm is inserted, and the whole amount is dissolved in water within 24 hours under stirring at 600 rpm using a magnetic stirrer HPS-100 manufactured by ASONE Co., Ltd. In the present invention, as a more preferable solubility, the total amount is preferably dissolved in water within 3 hours, and the total amount is more preferably dissolved in water within 30 minutes.

The cationic polymer preferably has a structure having a main chain and a plurality of side chains bonded thereto. In particular, the quaternary ammonium salt polymer preferably has a structure having a main chain and a plurality of side chains bonded thereto. The quaternary ammonium moiety is preferably present in the side chain. In this case, when the main chain and the side chain are bonded at one point, the flexibility of the side chain is difficult to be hindered, and the quaternary ammonium moiety present in the side chain is smoothly formed on the surface of the erythrocyte. Adsorbs. However, in the present invention, it is not hindered that the main chain and the side chain of the cationic polymer are bonded at two points or more. In the present invention, “bonded at one point” means that one of the carbon atoms constituting the main chain is single-bonded with one carbon atom located at the end of the side chain. . “Connected at two or more points” means that two or more of the carbon atoms constituting the main chain are each single-bonded with two or more carbon atoms located at the end of the side chain. Say.

When the cationic polymer has a structure having a main chain and a plurality of side chains bonded thereto, for example, a quaternary ammonium salt polymer has a structure having a main chain and a plurality of side chains bonded thereto. In this case, the number of carbon atoms in each side chain is preferably 4 or more, more preferably 5 or more, and even more preferably 6 or more. The upper limit of the carbon number is preferably 10 or less, more preferably 9 or less, and even more preferably 8 or less. For example, the number of carbon atoms in the side chain is preferably 4 or more and 10 or less, more preferably 5 or more and 9 or less, and still more preferably 6 or more and 8 or less. The carbon number of the side chain is the carbon number of the quaternary ammonium moiety (cation moiety) in the side chain, and even if carbon is contained in the anion that is the counter ion, the carbon is counted. Not included. In particular, among the carbon atoms in the side chain, the number of carbon atoms from the carbon atom bonded to the main chain to the carbon atom bonded to the quaternary nitrogen is in the above range, so that the quaternary ammonium salt. This is preferable because the steric hindrance when the polymer is adsorbed on the surface of the erythrocyte is reduced.

When the quaternary ammonium salt polymer is a quaternary ammonium salt homopolymer, examples of the homopolymer include a polymer of a vinyl monomer having a quaternary ammonium moiety or a tertiary amine moiety. . In the case of polymerizing a vinyl monomer having a tertiary amine moiety, a quaternary ammonium salt homopolymer in which the tertiary amine moiety is quaternized with an alkylating agent before and / or after polymerization. Becomes a polymer, becomes a tertiary amine neutralized salt obtained by neutralizing a tertiary amine site with an acid before and / or after polymerization, or becomes a tertiary amine having a cation in an aqueous solution after polymerization. . Examples of the alkylating agent and the acid are as described above.

In particular, the quaternary ammonium salt homopolymer preferably has a repeating unit represented by the following formula 1.

Specific examples of the quaternary ammonium salt homopolymer include polyethyleneimine. In addition, poly (2-methacryloxyethyldimethylamine quaternary salt), poly (2-methacryloxyethyltrimethylammonium salt) in which the side chain having a quaternary ammonium moiety is bonded to the main chain at one point. ), Poly (2-methacryloxyethyldimethylethylammonium methylsulfate), poly (2-acryloxyethyldimethylamine quaternary salt), poly (2-acryloxyethyltrimethylamine quaternary salt), poly (2-acryloxy) Ethyldimethylethylammonium ethyl sulfate), poly (3-dimethylaminopropylacrylamide quaternary salt), dimethylaminoethyl polymethacrylate, polyallylamine hydrochloride, cationized cellulose, polyethyleneimine, polydimethylaminopropylacrylamide, polyamidine, etc. And the like. On the other hand, examples of the homopolymer in which the side chain having a quaternary ammonium moiety is bonded to the main chain at two or more points include polydiallyldimethylammonium chloride and polydiallylamine hydrochloride.

When the quaternary ammonium salt polymer is a quaternary ammonium salt copolymer, two kinds of polymerizable monomers used for the polymerization of the quaternary ammonium salt homopolymer described above are used as the copolymer. A copolymer obtained by the above copolymerization can be used. Alternatively, as the quaternary ammonium salt copolymer, one or more polymerizable monomers used for the polymerization of the quaternary ammonium salt homopolymer described above and a polymerizable monomer having no quaternary ammonium moiety The copolymer obtained by copolymerizing using 1 or more types of bodies can be used. Further, in addition to or instead of the vinyl polymerizable monomer, other polymerizable monomers such as —SO 2 — can be used. As described above, the quaternary ammonium salt copolymer may be a binary copolymer or a ternary or higher copolymer.

In particular, the quaternary ammonium salt copolymer has a repeating unit represented by the above-described formula 1 and a repeating unit represented by the following formula 2 to effectively produce an agglomerate of erythrocytes. It is preferable from the viewpoint.

Also, as the polymerizable monomer having no quaternary ammonium moiety, a cationic polymerizable monomer, an anionic polymerizable monomer, or a nonionic polymerizable monomer can be used. Among these polymerizable monomers, in particular, by using a cationic polymerizable monomer or a nonionic polymerizable monomer, charge cancellation with a quaternary ammonium moiety in a quaternary ammonium salt copolymer is achieved. Therefore, erythrocyte aggregation can be effectively generated. Examples of cationic polymerizable monomers include linear compounds having a cation-carrying nitrogen atom in the main chain, such as vinylpyridine as a cyclic compound having a cation-carrying nitrogen atom under a particular condition And a condensed compound of dicyandiamide and diethylenetriamine. Examples of the anionic polymerizable monomer include 2-acrylamido-2-methylpropane sulfonic acid, methacrylic acid, acrylic acid, styrene sulfonic acid, and salts of these compounds. On the other hand, examples of nonionic polymerizable monomers include vinyl alcohol, acrylamide, dimethylacrylamide, ethylene glycol monomethacrylate, ethylene glycol monoacrylate, hydroxyethyl methacrylate, hydroxyethyl acrylate, methyl methacrylate, methyl acrylate, ethyl methacrylate, ethyl Examples include acrylate, propyl methacrylate, propyl acrylate, butyl methacrylate, and butyl acrylate. One of these cationic polymerizable monomers, anionic polymerizable monomers, or nonionic polymerizable monomers can be used, or any two or more of them can be used in combination. Can do. Also, two or more cationic polymerizable monomers can be used in combination, two or more anionic polymerizable monomers can be used in combination, or two or more nonionic polymerizable monomers can be used in combination. Can also be used. A quaternary ammonium salt copolymer copolymerized using a cationic polymerizable monomer, an anionic polymerizable monomer and / or a nonionic polymerizable monomer as a polymerizable monomer has a molecular weight of However, as described above, it is preferably 10 million or less, particularly preferably 5 million or less, and particularly preferably 3 million or less (the same applies to the quaternary ammonium salt copolymer exemplified below).

As the polymerizable monomer having no quaternary ammonium moiety, a polymerizable monomer having a functional group capable of hydrogen bonding can also be used. When such a polymerizable monomer is used for copolymerization, and when erythrocytes are aggregated using a quaternary ammonium salt copolymer obtained therefrom, a hard aggregate is likely to be formed. Absorption performance is less likely to be disturbed. Examples of the functional group capable of hydrogen bonding include —OH, —NH 2, —CHO, —COOH, —HF, —SH and the like. Examples of polymerizable monomers having functional groups capable of hydrogen bonding include hydroxyethyl methacrylate, vinyl alcohol, acrylamide, dimethylacrylamide, ethylene glycol, propylene glycol, ethylene glycol monomethacrylate, ethylene glycol monoacrylate, Examples thereof include hydroxyethyl methacrylate and hydroxyethyl acrylate. In particular, hydroxyethyl methacrylate, 2-hydroxyethyl methacrylate, hydroxyethyl acrylate, dimethylacrylamide, and the like, in which hydrogen bonds work strongly, are preferable because the adsorption state of quaternary ammonium salt polymers on erythrocytes is stabilized. These polymerizable monomers can be used individually by 1 type or in combination of 2 or more types.

As the polymerizable monomer having no quaternary ammonium moiety, a polymerizable monomer having a functional group capable of hydrophobic interaction can also be used. By using such a polymerizable monomer for copolymerization, the same advantageous effect as that in the case of using the polymerizable monomer having a functional group capable of hydrogen bonding described above, that is, the hardness of erythrocytes The effect that it becomes easy to produce an agglomerate is produced. Examples of functional groups capable of hydrophobic interaction include alkyl groups such as methyl, ethyl, and butyl groups, phenyl groups, alkylnaphthalene groups, and fluorinated alkyl groups. Examples of polymerizable monomers having functional groups capable of hydrophobic interaction include methyl methacrylate, methyl acrylate, ethyl methacrylate, ethyl acrylate, propyl methacrylate, propyl acrylate, butyl methacrylate, butyl acrylate, styrene, etc. Is mentioned. In particular, methyl methacrylate, methyl acrylate, butyl methacrylate, butyl acrylate, etc., which have a strong hydrophobic interaction and do not significantly reduce the solubility of the quaternary ammonium salt polymer, are adsorbed to erythrocytes by the quaternary ammonium salt polymer. Is preferable because of stabilization. These polymerizable monomers can be used individually by 1 type or in combination of 2 or more types.

The molar ratio of the polymerizable monomer having a quaternary ammonium moiety and the polymerizable monomer having no quaternary ammonium moiety in the quaternary ammonium salt copolymer is the quaternary ammonium salt. It is preferable that the red blood cells are appropriately adjusted so as to be sufficiently aggregated by the ammonium salt copolymer. Or it is preferable to adjust so that the streaming potential of a quaternary ammonium salt copolymer may become the value mentioned above. Or it is preferable to adjust so that IOB of a quaternary ammonium salt copolymer may become the value mentioned above. In particular, the molar ratio of the polymerizable monomer having a quaternary ammonium moiety in the quaternary ammonium salt copolymer is preferably 10 mol% or more, more preferably 22 mol% or more, and 32 mol. % Or more, more preferably 38 mol% or more. Further, it is preferably 100 mol% or less, more preferably 80 mol% or less, still more preferably 65 mol% or less, and even more preferably 56 mol% or less. Specifically, the molar ratio of the polymerizable monomer having a quaternary ammonium moiety is preferably 10 mol% or more and 100 mol% or less, more preferably 22 mol% or more and 80 mol% or less, More preferably, it is 32 mol% or more and 65 mol% or less, and more preferably 38 mol% or more and 56 mol% or less.

When the quaternary ammonium salt polymer is a quaternary ammonium salt polycondensate, as the polycondensate, a condensate composed of one or more monomers having the quaternary ammonium moiety described above is used. Polycondensates obtained by polymerizing these condensates can be used. Specific examples include dicyandiamide / diethylenetriamine polycondensate, dimethylamine / epichlorohydrin polycondensate, and the like.

The above-described quaternary ammonium salt homopolymer and quaternary ammonium salt copolymer can be obtained by a homopolymerization method or copolymerization method of a vinyl polymerizable monomer. As the polymerization method, for example, radical polymerization, living radical polymerization, living cation polymerization, living anion polymerization, coordination polymerization, ring-opening polymerization, polycondensation and the like can be used. There are no particular limitations on the polymerization conditions, and the conditions under which a quaternary ammonium salt polymer having the desired molecular weight, streaming potential, and / or IOB value can be obtained may be appropriately selected.

The cationic polymer described in detail above is an example of the above-mentioned “preferable blood coagulant 43”, and the effect thereof can be referred to in Examples 1 to 45 of Japanese Patent Application No. 2015-239286.

In addition to the polycation (cationic polymer), as described above, the blood aggregating agent 43 of the absorbent body 4 is a third component such as a solvent, a plasticizer, a fragrance, an antibacterial / deodorant, and a skin care agent. And the like (blood aggregating agent composition). In addition, components other than the cationic polymer that can be included in the blood aggregating agent 43 can be used alone or in combination. As the solvent, water, a water-soluble organic solvent such as a saturated aliphatic monohydric alcohol having 1 to 4 carbon atoms, or a mixed solvent of the water-soluble organic solvent and water can be used. As the plasticizer, glycerin, polyethylene glycol, propylene glycol, ethylene glycol, 1,3-butanediol and the like can be used. As a fragrance | flavor, the fragrance | flavor which has the green herbal-like fragrance described in patent 4776407, the extract of a plant, the extract of citrus fruits, etc. can be used. As an antibacterial / deodorant, it is polymerized from a cancrinite-like mineral containing a metal having antibacterial properties described in Japanese Patent No. 4526271, and a polymerizable monomer having a phenyl group described in Japanese Patent No. 4587928. Porous polymers, quaternary ammonium salts, activated carbon, clay minerals and the like described in Japanese Patent No. 4651392 can be used. As the skin care agent, plant extracts, collagen, natural moisturizing ingredients, moisturizing agents, keratin softening agents, anti-inflammatory agents and the like described in Japanese Patent No. 4084278 can be used.

The proportion of the cationic polymer in the blood aggregating agent composition is preferably 1% by mass or more, more preferably 3% by mass or more, and further preferably 5% by mass or more. Further, it is preferably 50% by mass or less, more preferably 30% by mass or less, and still more preferably 10% by mass or less. For example, the proportion of the cationic polymer is preferably 1% by mass to 50% by mass, more preferably 3% by mass to 30% by mass, and even more preferably 5% by mass to 10% by mass. preferable. By setting the proportion of the cationic polymer in the blood coagulant composition within this range, an effective amount of the cationic polymer can be imparted to the absorbent article.

The amount of the blood aggregating agent 43 contained in the absorbent sheet constituting the absorbent body 4 is preferably 0.1 g / m ² or more, more preferably 0.5 g / m ² or more. More preferably, it is 5 g / m ² or more. Further, it is preferably 25 g / m ² or less, more preferably 15 g / m ² or less, and even more preferably 10 g / m ² or less. For example, the amount of the blood coagulant 43 is preferably 0.1 g / m ² or more and 25 g / m ² or less, more preferably 0.5 g / m ² or more and 15 g / m ² or less, and more preferably 1.5 g / m ^2. it is more preferred m ² or more and 10 g / m ² or less. By applying the blood aggregating agent 43 in an amount within this range, the excreted menstrual red blood cells can be effectively aggregated. In addition, when the blood aggregating agent 43 is applied to two or more parts, for example, when applied to both the main body absorbent sheet 401 and the central absorbent sheet 402 described later, the amount is It is the sum total of the blood coagulant 43 applied to the site. It is particularly preferable that the blood coagulant 43 is a cationic polymer and the amount of the cationic polymer contained in the absorbent sheet is in the above range.

In the napkin 1, the absorbent body 4 has a multilayer structure formed of an absorbent sheet as shown in FIGS. Here, the formed multilayer structure may be formed by overlapping a plurality of absorbent sheets, or may be formed by folding a single absorbent sheet. However, it may be formed by combining these. In the napkin 1, the absorbent body 4 includes, as shown in FIGS. 3 and 4, a central absorbent sheet 402 formed of an absorbent sheet on the excretory part facing part B that is disposed to face the excretion part of the wearer when worn. The main body absorbent sheet 401 covers the central absorbent sheet 402. That is, the absorbent body 4 of the napkin 1 has a multilayer structure formed of the main body absorbent sheet 401 and the central absorbent sheet 402, and forms a middle-high part 403 in the excretory part facing part B. The multilayer structure of the absorbent body 4 of the napkin 1 has a structure in which a central absorbent sheet 402 is included in the folded structure of one main body absorbent sheet 401, and the central absorbent sheet 402 is formed in the middle and high portions 403. It is arranged.

Preferably, in the napkin 1, as shown in FIG. 3 and FIG. 4, the main body absorbent sheet 401 is composed of one sheet having a length (width) in the lateral direction Y longer than that of the napkin 1, and the main body absorbent sheet 401 Of the absorbent sheet 401 is folded back to the back sheet 3 side to form a two-layer structure, and both side edges along the vertical direction X are overlapped at the center in the horizontal direction Y, The outer shape is formed. Thus, the main body absorbent sheet 401 which forms a two-layer structure has the surface side absorbent sheet 401a by the side of the surface sheet 2, and the back surface side absorbent sheet 401b by the side of the back sheet 3. The central absorbent sheet 402 is composed of a single sheet having a rectangular shape in plan view, and has a three-layer structure in which the central absorbent sheet 402 is folded in three in the lateral direction Y. When the central absorbent sheet 402 has a three-layer structure, in the two fold lines crossing the central absorbent sheet 402 in the longitudinal direction X, the second fold line counted from the free end in the lateral direction Y is used. Bend to the back sheet 3 side, and then bend to the top sheet 2 side at the first fold line counted from the free end in the lateral direction Y so that the free end in the lateral direction Y is arranged inside the three-layer structure Fold it in a spiral. Thus, the central absorbent sheet 402 that forms a three-layer structure folded in a spiral shape includes an upper absorbent sheet 402a on the front surface side absorbent sheet 401a side and a lower absorbent sheet on the back surface side absorbent sheet 401b side. 402b and an intermediate absorbent sheet 402c between the

sheets

402a and 402b. The middle-high portion 403 is formed by sandwiching a sheet having a three-layer structure including an upper absorbent sheet 402a, an intermediate absorbent sheet 402c, and a lower absorbent sheet 402b between the front side absorbent sheet 401a and the rear side absorbent sheet 401b. Has been. The middle-high part 403 is formed only in the excretion part facing part B, and is not formed in the front part A and the rear part C. As shown in FIG. 4, the number of laminated absorbent sheets constituting the absorber 4 around the middle-high portion 403 is two, whereas the number of laminated absorbent sheets constituting the absorber 4 in the middle-high portion 403. However, the number of laminated sheets is large and the thickness is large. For this reason, the middle-high part 403 is a raised part that protrudes from the excretory part facing part B to the topsheet 2 side (skin facing side of the napkin 1).

The thickness per absorbent sheet is preferably 0.1 mm or more, particularly 0.3 mm or more, and preferably 2 mm or less, particularly 1.5 mm or less. More specifically, it is 0.1 mm or more and 2 mm or less, particularly 0.3 mm or more and 1.5 mm or less to obtain an absorbent article having sufficient liquid diffusibility and liquid retention and having a good wearing feeling. It is preferable from the point.

The absorber 4 has a thickness at the middle-high portion 403 of preferably 0.7 mm or more, more preferably 1 mm or more, preferably 5 mm or less, more preferably 4 mm or less, more specifically preferably It is 0.7 mm or more and 5 mm or less, More preferably, it is 1 mm or more and 4 mm or less. By setting the thickness of the mid-high portion 403 in such a range, it becomes easy to achieve both a good wearing feeling and high absorption performance in the excretory portion facing portion B where the mid-high portion 403 is formed. Moreover, when the absorbent article is provided with a wing part like the napkin 1 of this embodiment, it becomes easy to suppress the twist of the absorber in an excretion part opposing part at the time of mounting | wearing. The thickness of the absorber other than the middle-high portion 403 is preferably 0.3 mm or more, more preferably 0.5 mm or more, and preferably 3 mm or less, more preferably 2.5 mm or less, More specifically, it is preferably 0.3 mm or more and 3 mm or less, more preferably 0.5 mm or more and 2.5 mm or less. This range is preferable from the viewpoint of enhancing the high absorption performance and the ability to follow the wearer's movement. In addition, the thickness of an absorber and an absorptive sheet is measured by the following method.

<Measurement method of thickness of absorbent sheet and absorber>
The absorbent sheet or absorbent body, which is the measurement object, is placed in a horizontal place so as not to be wrinkled or bent, and the thickness under a load of 5 cN / cm ² is measured. A thickness meter PEACOCK DIAL UPRIGHT GAUGES R5-C (manufactured by OZAKI MFG.CO.LTD.) Was used for measuring the thickness in the present invention. At this time, a circular plate or a square plate (acrylic plate having a thickness of about 5 mm) in plan view is disposed between the tip of the thickness meter and the measurement portion of the measurement object, and the load is 5 cN / cm ² . Adjust the size of the plate so that

And in the napkin 1, the blood coagulant 43 is present at least in the pulp rich region FT in the portion used by arranging the pulp rich region FT on the skin facing surface side. Here, when the absorbent body 4 has a multilayer structure formed of an absorbent sheet like the napkin 1, even if the blood aggregating agent 43 is not disposed on all the absorbent sheets forming the multilayer structure. Good. In the napkin 1, as shown in FIG. 4, a blood coagulant 43 is disposed on a main body absorbent sheet 401 that forms a two-layer structure including a front-side absorbent sheet 401a and a back-side absorbent sheet 401b. As described above, since it has a two-layer structure in which both side portions along the longitudinal direction X of the main body absorbent sheet 401 are folded back, the front side absorbent sheet 401a places the pulp rich region FT on the skin facing surface side. The back side absorbent sheet 401b is used with the pulp rich region FT disposed on the non-skin facing surface side. Accordingly, in the middle-high portion 403, the surface side absorbent sheet 401a, the upper side absorbent sheet 402a, and the intermediate absorbent sheet 402c are all in the order of the pulp rich region FT and the polymer rich region PT when viewed from the skin contact surface side. As for the lower side absorbent sheet 402b and the back side absorbent sheet 401b, the polymer rich region PT and the pulp rich region FT are arranged in this order as viewed from the skin contact surface. And in the surface side absorbent sheet 401a used by arranging the pulp rich region FT on the skin facing surface side, the blood coagulant 43 is present in the polymer rich region PT and the pulp rich region FT, and the polymer rich region It exists more in the pulp rich region FT than in PT. Here, “existingly” means that the mass of the blood coagulant 43 present per area of each region FT, PT, that is, the basis weight of the blood coagulant 43 in each region FT, PT is compared. This means that the basis weight of the blood coagulant 43 in one region is relatively large. Further, in the back side absorbent sheet 401b in which the pulp rich region FT is used on the non-skin facing surface side, in other words, in the back side absorbent sheet 401b used in which the polymer rich region PT is placed on the skin facing surface side, a blood coagulant 43 exists in the polymer rich region PT and the pulp rich region FT, and is present more in the pulp rich region FT than in the polymer rich region PT. The blood aggregating agent 43 is not disposed on the central absorbent sheet 402 that forms a three-layer structure including the upper absorbent sheet 402a, the intermediate absorbent sheet 402c, and the lower absorbent sheet 402b.

Whether or not the blood coagulant 43 is disposed is determined as follows.
Using an energy dispersive X-ray analyzer (EDX) attached to a scanning electron microscope (SEM), the superabsorbent polymer 41 that the absorber 4 has, the pulp 42 that the absorber 4 has, and the absorber 4 Each elemental analysis of the blood agglutinating agent 43 is performed. Next, a sample piece to be judged as to whether or not the blood agglutinating agent 43 is disposed is attached to an aluminum sample table using a double-sided carbon tape, and after performing platinum / vanadium coating as necessary, SEM observation is performed. The presence or absence of an element in the blood coagulant 43 is checked using EDX (element analysis device) while expanding. The measurement is performed at an acceleration voltage of 15 kV to 40 kV.

Whether blood coagulant 43 is present in the pulp rich region FT more than the polymer rich region PT is determined semi-quantitatively as follows.
A sample piece comprising an absorbent sheet having a polymer-rich region PT and a pulp-rich region FT and containing a blood aggregating agent 43 is attached to an aluminum sample table using a double-sided carbon tape, and platinum is added if necessary. / After performing vanadium coating, using EDX (element analysis device) while enlarging with SEM observation, mapping of element of superabsorbent polymer 41, mapping of element of pulp 42, mapping of element of blood coagulant 43 Do. The measurement is performed at an acceleration voltage of 15 kV to 40 kV. Then, comparing the obtained elemental distribution mapping, when the elemental mapping of blood coagulant 43 is more similar to the elemental mapping of pulp 42 than the elemental mapping of superabsorbent polymer 41, blood It is determined that the flocculant 43 is present more in the pulp rich region FT than in the polymer rich region PT.

Further, the absorbent sheet in which the blood coagulant 43 is present in the pulp rich region FT more than the polymer rich region PT is selectively used with respect to the pulp rich region FT in the manufacturing process of the absorbent sheet. It can be created if it contains. For example, when the absorbent sheet has a structure in which a pulp rich layer that is a pulp rich region FT and a polymer rich layer that is a polymer rich region PT are overlapped on each of the upper and lower sides, each other layer is created separately, A blood aggregating agent 43 may be included in the pulp-rich layer before overlapping with the polymer-rich layer.

For example, the case of the absorbent sheet described in Japanese Patent No. 2963647 will be described. The superabsorbent polymer is dispersed between the fibers by spraying the superabsorbent polymer on a wet fiber web made by wet papermaking with water slurry containing at least hydrophilic fiber and hot melt adhesive fiber or paper strength reinforcing agent. A superabsorbent polymer-rich layer (corresponding to polymer-rich region PT) is formed, and a fiber assembly containing hydrophilic fibers and hot-melt adhesive fibers or paper strength reinforcing agents is layered on top of each other and dried. Thus, by manufacturing the absorbent sheet, the fiber aggregate to be overlapped becomes a pulp rich layer (corresponding to the pulp rich region FT). By incorporating a flocculant in the fiber assembly to be overlapped in advance, or by manufacturing an absorbent sheet while spraying or coating the flocculant on the fiber aggregate to be overlapped, More flocculant can be present in the pulp rich layer than in the polymer rich layer.
The layer to which the superabsorbent polymer is dispersed is not limited to a wet web, and may be a piled pulp, papermaking, paper produced by drying, or a nonwoven fabric. From the viewpoint that the superabsorbent polymer can easily enter between fibers, bulky paper such as creped or air-through non-woven fabric is preferable, the fibers of the superabsorbent polymer and the superabsorbent polymer rich layer, and the superabsorbent A hot melt, a water-soluble adhesive, or the like may be used as an adhesion means between the polymer-rich layer and the pulp-rich layer. Furthermore, the pulp rich layer may be formed by stacking or spraying hydrophilic fibers on the superabsorbent polymer rich layer. In addition, as a method for applying the flocculant, the flocculant may be sprayed or applied to the pulp rich layer side after the production of the absorbent sheet.

Further, in the napkin 1, the absorbent body 4 is provided with the vertical slit 44 extending in the vertical direction X as shown in FIGS. The longitudinal slit 44 makes it easy for menstrual blood that has reached the absorber 4 to be diffused in the longitudinal direction X and also to penetrate in the thickness direction of the absorber 4. In the napkin 1, the vertical slits 44 extending in the vertical direction X have slit regions 44 </ b> S formed so as to be dispersed in both the vertical direction X and the horizontal direction Y. As shown in FIG. 2, the slit region 44 </ b> S in which the plurality of vertical slits 44 are arranged extends not only to the excretory part facing part B but also to a part of the front part A and a part of the rear part C. That is, the vertical slit 44 exists at least in the excretory part facing part B, and a region including the slit 44 located in the excretion part facing part B is referred to as a slit region 44S.

In the napkin 1, it is preferable that the vertical slit 44 penetrates the absorbent sheet on the most skin-facing surface side including the blood coagulant 43. In the napkin 1, the most skin-facing surface-side absorbent sheet containing the blood coagulant 43 is the surface-side absorbent sheet 401a. As shown in FIG. 3 and FIG. 4, when the absorbent body 4 is viewed in cross-section along the lateral direction Y, the longitudinal slit 44 only needs to penetrate only the surface-side absorbent sheet 401 a. Is penetrated through the entire thickness direction. Preferably, in the napkin 1, the vertical slit 44 has five laminated sheets constituting the middle-high portion 403 in the excretory part facing part B, that is, the surface side absorbent sheet 401 a, the upper absorbent sheet 402 a, and the intermediate absorbent part. The sheet 402c, the lower side absorbent sheet 402b, and the back side absorbent sheet 401b are all penetrated. In the napkin 1, the vertical slit 44 penetrates the front side absorbent sheet 401a and the rear side absorbent sheet 401b in a part of the front part A and a part of the rear part C.

In the napkin 1, the arrangement of the vertical slits 44 in the slit area 44S is not particularly limited as long as the vertical slits 44 are distributed in both the vertical direction X and the horizontal direction Y, but the central slit area 44S1 It is preferable that four or more slits are dispersedly arranged. The central slit region 44S1 is a region overlapping with the central absorbent sheet 402 in the slit region 44S.
In the central slit region 44S1, it is preferable that three or more slit rows are formed in the longitudinal direction X, more preferably four rows or more, and still more preferably five rows or more. Moreover, the number of the vertical slits 44 spaced apart in the horizontal direction Y included in each slit row is preferably 2 or more, more preferably 3 or more.
In the longitudinal direction X of the slit region 44S, in addition to the slit rows included in the central slit region 44S1, it is preferable to have one row or two or more slit rows before and after the longitudinal direction X of the central slit region 44S1.

The width W44 (see FIG. 2) when each vertical slit 44 is viewed in plan is preferably 0.1 mm or more, more preferably 0.2 mm or more, more preferably 1 mm or less, still more preferably 0.8 mm or less, 0.1 mm or more and 1 mm or less is preferable, and 0.2 mm or more and 0.8 mm or less is more preferable.
The length (longitudinal length) L44 when the vertical slit 44 in the slit region 44S is viewed in plan is preferably 10 mm or more, more preferably 15 mm or more, and preferably 35 mm or less, more preferably 25 mm or less. And preferably 10 mm or more and 35 mm or less, more preferably 15 mm or more and 25 mm or less.
The interval (width direction interval) D44 between the vertical slits 44 in the same slit row in the slit region 44S is preferably 3 mm or more, more preferably 7 mm or more, preferably 20 mm or less, more preferably 15 mm or less. Preferably they are 3 mm or more and 20 mm or less, More preferably, they are 7 mm or more and 15 mm or less.

The formation material of each structural member of the napkin 1 of this embodiment mentioned above is demonstrated.
As the top sheet 2 and the back sheet 3, various kinds of materials conventionally used for absorbent articles such as sanitary napkins can be used without particular limitation. For example, as the surface sheet 2, a single layer or multilayer nonwoven fabric, an apertured film, or the like can be used. As the back sheet 3, a moisture-permeable resin film or the like can be used.

The second sheet 5 is preferably made of a hydrophilic nonwoven fabric or a hydrophilic fiber assembly. Examples of the nonwoven fabric include air-through nonwoven fabric, point bond nonwoven fabric, resin bond nonwoven fabric, spunlace nonwoven fabric, and airlaid nonwoven fabric. The basis weight of the second sheet 5 is preferably 10 g / m ² or more and 50 g / m ² or less, and more preferably 15 g / m ² or more and 40 g / m ² or less. The thickness of the second sheet 5 is preferably 0.1 mm or more and 5 mm or less.

In the napkin 1, an adhesive is applied and fixed between the top sheet 2 and the second sheet 5, between the second sheet 5 and the absorber 4, and between the absorber 4 and the back sheet 3. Is preferred. The adhesive can be applied using a known means such as a slot coat gun, a spiral spray gun, a spray gun, or a dot gun. In the napkin 1, the adhesive can be applied in a spiral shape using a spiral spray gun. preferable. As the adhesive to be applied, for example, a hot melt adhesive is preferably used. The application amount of the hot melt adhesive is preferably 1.5 g / m ² or more and 10 g / m ² or less.

Moreover, like the napkin 1, in order to form the vertical slit 44 in the absorber 4, the laminated body of an absorbent sheet should just be partially cut | disconnected by a well-known cutting means, for example, on the surrounding surface of a roll, A cutting device including a cutter roll in which a large number of cutting blades extending in the circumferential direction are dispersed in the circumferential direction and the axial length direction of the roll and an anvil roll that receives the blade of the cutter roll can be used.

The operational effect and estimation mechanism of the napkin 1 described above will be described.
In the napkin 1, as shown in FIG. 5, the absorbent body 4 made of an absorbent sheet includes a polymer-rich region PT having a relatively high amount of the superabsorbent polymer 41 and a relatively superabsorbent polymer 41. In the portion where the pulp rich region FT is used on the skin facing surface side, the blood coagulant 43 is present at least in the pulp rich region FT. Therefore, during the use of the napkin 1, the menstrual blood is separated into red blood cells and plasma by the blood aggregating agent 43 in the pulp rich region FT on the skin facing surface side, and can be absorbed by the superabsorbent polymer 41. , Can effectively absorb menstrual blood. Also, menstrual blood erythrocytes and plasma are separated before menstrual blood is absorbed by the superabsorbent polymer 41, so that plasma having a viscosity lower than that of blood is diffused by the pulp 42, and further, the aggregated red blood cells are as much as plasma. However, by diffusing together, it is possible to prevent blood cell aggregates from collecting locally, the absorption rate for repeatedly absorbing blood is increased, and the side leakage of menstrual blood can be prevented. In particular, in the napkin 1, the blood coagulant 43 is present in the polymer rich region PT and the pulp rich region FT, and more in the pulp rich region FT than in the polymer rich region PT. Therefore, it is easy to disperse many blood cell aggregates in the pulp-rich region FT on the skin-opposing surface side, and it is possible to efficiently absorb blood plasma and absorb the blood in the polymer-rich region PT. The speed can be further increased, and the side leakage of menstrual blood can be further prevented.

Moreover, in the napkin 1, as shown in FIG.3 and FIG.4, it has the multilayer structure in which the absorber 4 was formed with the absorbent sheet. Therefore, a space is formed between the respective sheets, the space becomes resistance, and the blood cell aggregate formed in the front-side absorbent sheet 401a is difficult to move to a lower layer sheet from 401a. The more it moves to the side, the easier it is for blood plasma to increase and to diffuse. In addition, plasma can easily diffuse even in a small space between sheets, rather than permeate and diffuse into the next sheet, and the absorption rate for absorbing blood can be further increased, thereby further reducing the side leakage of menstrual blood. Can be prevented.

Further, in the napkin 1, as shown in FIGS. 1 to 3, the absorbent body 4 has a vertical slit 44 in the excretory part facing part B. Therefore, menstrual blood can be easily transferred in the vertical direction X, and the side leakage of menstrual blood can be further prevented. Further, a space is formed in the portion of the absorbent body 4 where the vertical slits 44 are provided so that menstrual blood from the surface sheet 2 can be easily taken in, and menstrual blood can easily enter the thickness direction of the absorbent body 4. Further, menstrual blood easily enters the surface of the absorbent body 4 in the cross section of the vertical slit 44. For this reason, even if blood cell aggregates exist in one place on the skin contact surface side of the absorbent body 4, the menstrual blood easily enters the back sheet side of the absorbent body 4 and is absorbed and leaked. Is less likely to occur. Further, when a blood aggregating agent is present on the non-skin facing surface side of the absorbent body 4, efficient absorption of menstrual blood can be performed in the region, so that there is an advantage that the absorption speed is dramatically increased.

Also, since the cut portion of the vertical slit 44 is often slightly compressed when cutting, the density is higher than that of the portion where the vertical slit 44 is not provided, and the absorption speed is further increased. In addition, since the vertical slit 44 completely penetrates the absorber 4, the liquid that has reached the absorber 4 easily reaches the non-skin facing surface side of the absorber 4, and the absorption using the absorber 4 efficiently. This is advantageous from the viewpoint of improving the absorption capacity and suppressing the liquid return. These effects due to the slits provided in the absorbent body 4 are obtained when the blood coagulant 43 is present only in the pulp rich region FT, or in both regions when the blood aggregating agent 43 is present in the polymer rich region PT and the pulp rich region FT. Expression is expected in either the case where the blood coagulant 43 is present in an equivalent amount or the case where the pulp rich region FT contains more blood coagulant 43 than the polymer rich region PT.

Moreover, in the napkin 1, as shown in FIG.1 and FIG.3, the 2nd sheet | seat 5 comprised by the nonwoven fabric is distribute | arranged between the surface sheet 2 and the absorber 4. As shown in FIG. Therefore, the blood cell aggregate formed in the absorbent body 4 is covered with the second sheet 5 to prevent the blood cell agglomeration from returning to the surface and making it feel sticky. Can be prevented.

As mentioned above, although this invention was demonstrated based on the preferable embodiment, the absorbent article of this invention is not restrict | limited to the napkin 1 of the said embodiment at all, and can be changed suitably.
For example, in the napkin 1 described above, the absorbent body 4 has a structure made of an absorbent sheet. Instead, the absorbent body structure has a structure in which hydrophilic fibers and / or superabsorbent polymers are stacked. In addition, the structure may include a polymer rich region and a hydrophilic fiber rich region in which the blending ratio of the hydrophilic fiber and the superabsorbent polymer is different on the skin facing surface side and the non-skin facing surface side. Furthermore, it is good also as a structure which covers the whole absorber structure of the above-mentioned pile type with a hydrophilic core wrap material. However, in the case of an absorbent body having a structure in which the pile-type absorbent structure is covered with a hydrophilic core wrap material, it is necessary that the hydrophilic fiber-rich region excluding the core wrap contains a blood coagulant.

Moreover, in the napkin 1, as shown in FIG. 4, the blood aggregating agent 43 is arranged on the main body absorbent sheet 401 forming a two-layer structure composed of the front side absorbent sheet 401a and the back side absorbent sheet 401b. However, as shown in FIG. 6, blood coagulant 43 is not arranged on the main body absorbent sheet 401, and a three-layer structure comprising an upper absorbent sheet 402a, an intermediate absorbent sheet 402c, and a lower absorbent sheet 402b. The blood aggregating agent 43 may be disposed on the central absorbent sheet 402 to be formed. In the absorbent body 4 shown in FIG. 6, as described above, the central absorbent sheet 402 has a three-layer structure in which the central absorbent sheet 402 is folded in three, so that the upper absorbent sheet 402a and the intermediate absorbent sheet 402c are respectively The pulp rich region FT is used on the skin facing surface side, and the lower absorbent sheet 402b is used with the pulp rich region FT arranged on the non-skin facing surface side. In the upper absorbent sheet 402a and the intermediate absorbent sheet 402c that are used with the pulp rich region FT disposed on the skin facing surface side, the blood aggregating agent 43 is present in the polymer rich region PT and the pulp rich region FT. More in the pulp rich region FT than in the polymer rich region PT. Further, in the lower absorbent sheet 402b in which the pulp-rich region FT is used on the non-skin facing surface side, in other words, in the lower absorbent sheet 402b that is used by placing the polymer-rich region PT on the skin facing surface side, a blood coagulant 43 exists in the polymer rich region PT and the pulp rich region FT, and is present more in the pulp rich region FT than in the polymer rich region PT. In addition, although the surface side absorbent sheet 401a is used with the pulp rich region FT disposed on the skin facing surface side, the blood aggregating agent 43 is not disposed. Further, the back side absorbent sheet 401b is used with the pulp rich region FT disposed on the non-skin facing surface side, but the blood coagulant 43 is not disposed. According to the absorbent body 4 shown in FIG. 6, in the central absorbent sheet 402 arranged inside the folded structure of the single main body absorbent sheet 401, the blood aggregating agent 43 is in the pulp rich region FT rather than the polymer rich region PT. Therefore, even if excretion is repeated at the same absorption site, absorption inhibition due to blood cell aggregates on the absorption surface hardly occurs, and the absorption rate is increased.

In addition, as shown in FIG. 7, the blood aggregating agent 43 is disposed on the central absorbent sheet 402 that forms a three-layer structure including the upper absorbent sheet 402a, the intermediate absorbent sheet 402c, and the lower absorbent sheet 402b. A blood aggregating agent 43 may also be disposed on the main body absorbent sheet 401. In the absorbent body 4 shown in FIG. 7, the front surface side absorbent sheet 401 a formed by the main body absorbent sheet 401 is used with the pulp rich region FT disposed on the skin facing surface side, and the back surface formed by the main body absorbent sheet 401. The side absorbent sheet 401b is used with the pulp rich region FT disposed on the non-skin facing surface side. And in the surface side absorbent sheet 401a used by arranging the pulp rich region FT on the skin facing surface side, the blood coagulant 43 is present in the polymer rich region PT and the pulp rich region FT, and the polymer rich region It exists more in the pulp rich region FT than in PT. Further, in the back-side absorbent sheet 401b that is used with the pulp-rich region FT disposed on the non-skin facing surface side, in other words, with the polymer-rich region PT disposed on the skin facing surface side, blood aggregation The agent 43 is present in the polymer rich region PT and the pulp rich region FT, and is present more in the pulp rich region FT than in the polymer rich region PT. Further, the upper absorbent sheet 402a and the intermediate absorbent sheet 402c are respectively used with the pulp rich region FT disposed on the skin facing surface side, and the lower absorbent sheet 402b is used for the non-skinned pulp rich region FT. Used on the opposite side. In the upper absorbent sheet 402a and the intermediate absorbent sheet 402c that are used with the pulp rich region FT disposed on the skin facing surface side, the blood aggregating agent 43 is present in the polymer rich region PT and the pulp rich region FT. More in the pulp rich region FT than in the polymer rich region PT. Further, in the lower absorbent sheet 402b in which the pulp-rich region FT is disposed on the non-skin facing surface side, in other words, in the lower absorbent sheet 402b in which the polymer-rich region PT is disposed on the skin facing surface side, The flocculant 43 is present in the polymer rich region PT and the pulp rich region FT, and more in the pulp rich region FT than in the polymer rich region PT. According to the absorbent body 4 shown in FIG. 7, since any of the

absorbent sheets

401a, 401b, 402a, 402b, and 402c has the blood aggregating agent 43, the absorption rate for absorbing blood is likely to be further increased. Lateral leakage of blood can be further prevented.

In addition, as shown in FIGS. 4, 6 and 7, when the absorber 4 has a multilayer structure formed of an absorbent sheet, the contained blood aggregating agent 43 contains any absorbent sheet 401a. 401b, 402a, 402b, 402c may be the same blood aggregating agent 43 or different blood aggregating agents 43.

Further, as shown in FIGS. 4, 6 and 7, the absorbent sheet constituting the absorbent body 4 is formed of a two-layer region of a polymer rich region PT and a pulp rich region FT. And if it has the pulp rich area | region FT, you may form in the area | region of 3 or more layers.

Moreover, in the napkin 1, the diffusing means for diffusing menstrual blood in the longitudinal direction X is provided in the excretory part facing part B, but the diffusing means may be omitted. Further, the diffusion means of the napkin 1 is the vertical slit 44 extending in the vertical direction X as shown in FIGS. 1 to 4, but may be a diffusion means other than the vertical slit 44.

Moreover, although the some slit 44 which the absorber 4 of the napkin 1 has is a slit along the vertical direction X as shown in FIG.1 and FIG.2, it makes an angle with respect to both the vertical direction X and the horizontal direction Y. It may be a slit extending in an oblique direction.

Further, the absorbent article for absorbing menstrual blood of the present invention may be a panty liner (cage sheet) or the like in addition to a sanitary napkin.

The following absorbent article is further disclosed regarding the embodiment of the present invention described above.

<1>
An absorbent article comprising an absorbent having a superabsorbent polymer, a hydrophilic fiber, and a blood coagulant, and a front sheet and a back sheet sandwiching the absorbent, wherein the absorbent is viewed in cross section A polymer-rich region in which the mass ratio of the superabsorbent polymer to the total mass of the pulp and the mass of the superabsorbent polymer is relatively high, and a hydrophilic fiber rich that is relatively lower than the polymer-rich region. The absorbent article in which the blood coagulant is present in at least the hydrophilic fiber-rich region in a portion used by arranging the hydrophilic fiber-rich region on the skin facing surface side. .
<2>
The absorbent article according to <1>, wherein the absorbent body is made of an absorbent sheet.
<3>
Either <1> or <2>, wherein the absorbent body has diffusion means for diffusing blood in a longitudinal direction in an excretion portion facing portion that is disposed to face the excretion portion of the wearer when worn. Absorbent article as described in 1.
<4>
The absorbent article according to any one of <1> to <3>, wherein the blood coagulant is a cationic polymer.
<5>
The absorbent article according to <4>, wherein the cationic polymer is a quaternary ammonium salt homopolymer, a quaternary ammonium salt copolymer, or a quaternary ammonium salt polycondensate.
<6>
The absorbent article according to any one of <1> to <5>, wherein the absorbent body is made of an absorbent sheet and has a multilayer structure in which a plurality of the absorbent sheets are stacked in the thickness direction.
<7>
The absorbent body is made of an absorbent sheet, and has a diffusing means for diffusing blood in the longitudinal direction in the excretory part-facing portion that is disposed facing the excretory part of the wearer when worn,
The diffusing means is a longitudinal slit extending in the longitudinal direction, and the longitudinal slit penetrates the absorbent sheet closest to the skin-facing surface containing the blood aggregating agent, according to the items <1> to <6> The absorbent article of any one.
<8>
The absorbent body has a diffusing means for diffusing blood in the longitudinal direction in the excretory part facing part disposed opposite to the excretion part of the wearer when worn,
The diffusion means is a vertical slit extending in the vertical direction,
The absorbent article according to any one of <1> to <7>, wherein the vertical slit has a width of 0.1 mm to 1 mm, preferably 0.3 mm to 0.8 mm.
<9>
The absorbent body has a diffusing means for diffusing blood in the longitudinal direction in the excretory part facing part disposed opposite to the excretion part of the wearer when worn,
The diffusion means is a vertical slit extending in the vertical direction,
The absorbent article according to any one of <1> to <8>, wherein a length of the vertical slit when viewed in plan is 10 mm or more and 35 mm or less, preferably 15 mm or more and 25 mm or less.
<10>
The absorbent body has a diffusing means for diffusing blood in the longitudinal direction in the excretory part facing part disposed opposite to the excretion part of the wearer when worn,
The diffusion means is a vertical slit extending in the vertical direction,
The vertical slit has a plurality of rows arranged in the horizontal direction in the vertical direction, and the interval between the vertical slits in the same row is 3 mm or more and 20 mm or less, preferably 7 mm or more and 15 mm or less, <1 The absorbent article according to any one of> to <9>.

<11>
The absorbent body has a diffusing means for diffusing blood in the longitudinal direction in the excretory part facing part disposed opposite to the excretion part of the wearer when worn,
The diffusion means is a vertical slit extending in the vertical direction,
The vertical slit has a plurality of rows arranged in the horizontal direction in the vertical direction,
The absorbent article according to any one of <1> to <10>, wherein a plurality of the vertical slits are dispersed in the same row.
<12>
The absorbent body is made of an absorbent sheet, and the absorbent sheet is formed in a central absorbent sheet formed in an excretory part facing part that is disposed to face the excretion part of the wearer when worn, and a main body that covers the central absorbent sheet <1> to <2>, wherein the basis weight of the blood aggregating agent in the excretory part facing part is greater than the basis weight of the blood aggregating agent in the peripheral part of the excretion part facing part. The absorbent article according to any one of <11>.
<13>
The absorbent article according to <12>, wherein the central absorbent sheet has a multilayer structure in which a plurality of the absorbent sheets are overlapped.
<14>
The absorbent body is made of an absorbent sheet, and the absorbent sheet is formed in a central absorbent sheet formed in an excretory part facing part that is disposed to face the excretion part of the wearer when worn, and a main body that covers the central absorbent sheet It consists of an absorbent sheet,
The central absorbent sheet has a portion in which the polymer-rich region of the absorbent sheet and the arrangement in the thickness direction of the hydrophilic fiber are reversed between adjacent absorbent sheets as seen in the thickness direction. The absorbent article according to any one of <1> to <13>.
<15>
The absorbent body is made of an absorbent sheet, and the absorbent sheet is formed in a central absorbent sheet formed in an excretory part facing part that is disposed to face the excretion part of the wearer when worn, and a main body that covers the central absorbent sheet It consists of an absorbent sheet,
The central absorbent sheet has a structure in which one absorbent sheet is bent so as to have at least a three-layer structure, of which the uppermost layer located closest to the skin contact surface side and the thickness direction The second layer adjacent to the uppermost layer as viewed, according to any one of <1> to <14>, wherein the hydrophilic fiber-rich region and the polymer-rich region have the same arrangement in the thickness direction. Absorbent article.
<16>
The absorbent body is made of an absorbent sheet, and the absorbent sheet is formed in a central absorbent sheet formed in an excretory part facing part that is disposed to face the excretion part of the wearer when worn, and a main body that covers the central absorbent sheet It consists of an absorbent sheet,
The absorbent article according to any one of <1> to <15>, wherein the blood aggregating agent is contained only in the central absorbent sheet.
<17>
The absorbent body is made of an absorbent sheet, and the absorbent sheet is formed in a central absorbent sheet formed in an excretory part facing part that is disposed to face the excretion part of the wearer when worn, and a main body that covers the central absorbent sheet It consists of an absorbent sheet,
The absorbent article according to any one of <1> to <15>, wherein the blood aggregating agent is contained only in the main body absorbent sheet.
<18>
The absorbent body is made of an absorbent sheet, and the absorbent sheet is formed in a central absorbent sheet formed in an excretory part facing part that is disposed to face the excretion part of the wearer when worn, and a main body that covers the central absorbent sheet It consists of an absorbent sheet,
The absorbent article according to any one of <1> to <17>, wherein the blood aggregating agent is contained in the central absorbent sheet and the main body absorbent sheet.
<19>
The absorbent body is made of an absorbent sheet, and the absorbent sheet located closest to the skin contact surface side is viewed in the thickness direction, the hydrophilic fiber rich region is the skin contact surface side, and the polymer rich region is not. The absorbent article according to any one of <6> to <18>, which is located on the skin contact surface side.
<20>
Any one of the items <1> to <19>, wherein a second sheet made of a nonwoven fabric is disposed between the top sheet and the absorbent body, and the second sheet does not contain the blood aggregating agent. Or an absorbent article according to claim 1.

<21>
The blood coagulant is a cationic polymer;
The molecular weight of the cationic polymer is 2,000 to 10,000,000, preferably 2,000 to 5,000,000, more preferably 2,000 to 3,000,000, and more preferably 10,000 to 3,000,000. The absorbent article according to any one of> to <20>.
<22>
The amount of the blood coagulation agent is preferably 0.1 g / m ² or more 25 g / m ² or less, more preferably 0.5 g / m ² or more 15 g / m ² or less, more preferably 1.5 g / m ² or more 10g The absorbent article according to any one of <1> to <21>, which is / m ² or less.
<23>
The blood coagulant is a water-soluble cationic polymer, the water-soluble cationic polymer has a structure having a main chain and a side chain bonded thereto, and has a molecular weight of 2000 or more, and the water-soluble cationic polymer Is a quaternary ammonium salt homopolymer having a repeating unit represented by the following formula 1, or a repeating unit represented by the following formula 1 and a repeating unit represented by the following formula 2: A quaternary ammonium salt copolymer having the main chain of the water-soluble cationic polymer and the side chain bonded at one point, and the side chain having a quaternary ammonium moiety. The absorbent article according to any one of <1> to <22>, wherein a certain water-soluble cationic polymer is applied.

<24>
As the blood coagulant, 1 g / m of a water-soluble cationic polymer made of a quaternary ammonium salt homopolymer or a quaternary ammonium salt copolymer having a streaming potential of 1500 μeq / L or more and a molecular weight of 2000 or more. The absorbent article according to any one of <1> to <23>, having ^{2 to} 20 g / m ² .
<25>
The water-soluble cationic polymer has a structure in which a quaternary ammonium salt homopolymer or a quaternary ammonium salt copolymer has a main chain and a side chain bonded thereto, and the main chain and the side chain are The absorbent article according to <24>, which is bonded at one point.
<26>
The blood coagulant includes a water-soluble cationic polymer having a molecular weight of 2000 or more, and the water-soluble cationic polymer has an inorganic value / organic value that is a ratio of an inorganic value to an organic value. <1, wherein the water-soluble cationic polymer is a quaternary ammonium salt homopolymer, a quaternary ammonium salt copolymer or a quaternary ammonium salt polycondensate. Any one of> to <25> is an absorbent article.
<27>
The absorbent article according to any one of <1> to <26>, wherein the absorbent article is a sanitary napkin.

Hereinafter, the absorbent article of the present invention will be described in more detail with reference to examples. However, the scope of the present invention is not limited by the examples.

<Example 1>
A sanitary napkin having the same basic structure as the sanitary napkin 1 shown in FIGS. 1 to 3 having the absorbent body shown in FIGS. 4 and 5 was produced, and this was used as a sample of Example 1. As the surface sheet, an air-through nonwoven fabric sheet having a single layer structure with a basis weight of 25 g / m ² was used. A moisture-permeable resin film was used as the back sheet. As the second sheet, a point bond air-through nonwoven fabric having a basis weight of 25 g / m ² was used.
As an absorptive sheet which comprises an absorber, it created according to Example 2 of patent 2963647. However, High Bulk Additive HBA manufactured by Weyerhauser Paper was used as the crosslinked pulp, and Aqualic CA manufactured by Nippon Shokubai Co., Ltd. was used as the highly absorbent polymer. In this absorber preparation step, a blood coagulant was previously contained in the absorbent paper to be overlaid with the fiber web sprinkled with the superabsorbent polymer. As a result, the blood coagulant was present more in the absorbent paper in the pulp rich region FT than in the fiber web sprinkled with the superabsorbent polymer in the polymer rich region PT. As the cationic polymer contained in the blood aggregating agent, trade name Marcoat 106 (weight average molecular weight: 15,000, IOB value 2.10, flow potential 7345 μeq / L) manufactured by Nippon Lubrizol Co., Ltd. was used. The basis weight of the cationic polymer applied to the absorbent sheet was 1.5 g / m ² for each of the front-side absorbent sheet 401a and the back-side absorbent sheet 401b. And the blood coagulant | flocculant 43 is distribute | arranged only to the main body absorbent sheet 401 which forms the 2 layer structure which consists of the surface side absorbent sheet 401a and the back surface side absorbent sheet 401b like the absorber shown in FIG. . In other words, the blood aggregating agent 43 is not arranged on the central absorbent sheet 402 forming the three-layer structure. Further, a longitudinal slit was arranged in the absorber as shown in FIG.

<Example 2>
A sanitary napkin was prepared in the same manner as in Example 1 except that the absorbent shown in FIG. 6 was used. As in the case of the absorber shown in FIG. 6, the absorbent is only a central absorbent sheet 402 that forms a three-layer structure including an upper absorbent sheet 402a, an intermediate absorbent sheet 402c, and a lower absorbent sheet 402b. Agent 43 is arranged. That is, the blood aggregating agent 43 is not disposed on the main body absorbent sheet 401 that forms a two-layer structure including the front surface side absorbent sheet 401a and the back surface side absorbent sheet 401b. The basis weight of the cationic polymer applied to the absorbent sheet was 1.5 g / m ² for each of the upper absorbent sheet 402a, the intermediate absorbent sheet 402c, and the lower absorbent sheet 402b.

<Example 3>
A sanitary napkin was prepared in the same manner as in Example 1 except that the absorbent shown in FIG. 7 was used. As in the absorbent body shown in FIG. 7, the absorbent body has a blood aggregating agent 43 disposed on a main body absorbent sheet 401 that forms a two-layer structure composed of a front surface side absorbent sheet 401a and a back surface side absorbent sheet 401b. Yes. A blood aggregating agent 43 is disposed on a central absorbent sheet 402 that forms a three-layer structure including an upper absorbent sheet 402a, an intermediate absorbent sheet 402c, and a lower absorbent sheet 402b. The basis weight of the cationic polymer applied to the absorbent sheet was 1.5 g / m ² , respectively.

<Comparative Example 1>
In the sample of Example 1, the absorber was changed to an absorber not provided with the blood coagulant 43, and the sample of Comparative Example 1 was prepared in the same manner as in Example 1 except that.

[Evaluation]
For the sample of Example 1 to Example 3 (Sanitary napkin) and the sample of Comparative Example 1 (Sanitary napkin), the static maximum absorption amount, the dynamic diffusion area, the static absorption time, and the static diffusion area, respectively, Evaluation was made by the following method. The results are shown in Table 1 below.

<Static maximum absorption>
Each sample of the example and comparative example was spread and placed on a test bench, and an elliptical cylinder with an acrylic cylinder having a major axis of 50 mm, a minor axis of 22.5 mm, and a cylinder height of 30 mm was integrally formed on each sample. The acrylic injection plate was placed so that the injection hole was positioned at the center of the excretory part facing part on the skin facing surface (surface sheet side) of the sample, and 3 g of simulated blood was injected from the injection port. After injection, the state was held for 3 minutes. Next, the acrylic plate with an ellipse is removed, and the above acrylic plate is again placed on the surface of the top sheet on a sample with a pressure of 50 g / cm ² , and 3 g of pseudo blood is again injected from the injection port 4 minutes after the first injection. And injected. The injection position of the simulated blood into each sample of the example and the comparative example was the same as the position where the first 3 g was injected. From the second time onward, the same operation as the first time was repeated, and when the liquid oozed out from the wing part of each sample of Examples and Comparative Examples, the operation was finished and the static maximum absorption amount was obtained.
The simulated blood was measured using a B-type viscometer (model number TVB-10M manufactured by Toki Sangyo Co., Ltd., measurement conditions: rotor No. 19, 30 rpm, 25 ° C., 60 seconds) as described in this specification. The blood cell / plasma ratio of defibrinated horse blood (manufactured by Japan Biotest Laboratories Co., Ltd.) was prepared so that the viscosity obtained was 8 mPa · s.

<Dynamic diffusion area in absorber>
Each sample of the example and the comparative example was evaluated using the movable female waist model described in paragraphs [0082] and [0083] of JP-A-9-187476. After putting each sample on a movable female waist model and putting on shorts, while walking at a speed of 100 steps / minute, 2 g of simulated blood was injected up to 8 g at intervals of 3 minutes (the simulated blood injection speed was 15 The napkin was removed from the movable female waist model (1 g per second) and the area of the adhering pseudo blood on the absorber was measured. Measurement of the diffusion area was performed by using a NEWQUE (manufactured by NEXTUS) (ver. 4.20) as an image analysis apparatus (through a CCD camera or a scanner) to capture an image.

<Static absorption time>
Each sample of Example and Comparative Example was spread and placed on a laboratory table, and an acrylic injection plate in which an acrylic injection cylindrical portion having a cylinder height of 50 mm having an injection hole with a diameter of 1 cm was integrally formed on the sample. The liquid injection hole is placed so as to be positioned at the center of the excretory part facing part on the skin facing surface (surface sheet side) of the sample, and a suitable weight plate (including the liquid injection plate itself) is placed on the load. It adjusted so that it might be set to 0.85 g / cm < ² >. 3 g of simulated blood is injected into the cylinder of the liquid injection plate up to 9 g at intervals of 3 minutes, and the time (seconds) from the moment when injection is completed to 9 g until there is no pseudo blood in the cylinder and the surface sheet of the sample is exposed. ) Was measured. Each sample was measured three times, and the average value was taken as the static absorption time of the sample.

<Static diffusion area>
The area where the pseudo blood on the surface sheet in each sample after the measurement of the static absorption time was attached was measured. Measurement of the diffusion area was performed by using a NEWQUE (manufactured by NEXTUS) (ver. 4.20) as an image analysis apparatus (through a CCD camera or a scanner) to capture an image.

According to the results in Table 2, it was found that the sanitary napkins of Examples 1 to 3 had a shorter static absorption time and a smaller static diffusion area than the sanitary napkins of Comparative Example 1. Further, it was found that the sanitary napkins of Examples 1 to 3 had a larger dynamic diffusion area on the absorbent body than the sanitary napkin of Comparative Example 1. Therefore, the sanitary napkins of Examples 1 to 3 can absorb blood more effectively than the sanitary napkin of Comparative Example 1, and the absorption rate of blood is faster, resulting in the side leakage of menstrual blood. Can be expected to prevent.

According to the absorbent article of the present invention, blood can be effectively absorbed into the superabsorbent polymer, and the absorption rate for absorbing blood is high, so that side leakage of menstrual blood can be prevented.

Claims

An absorbent article comprising an absorbent containing a superabsorbent polymer, hydrophilic fibers and a blood coagulant, and a top sheet and a back sheet sandwiching the absorbent,
The absorbent body has a polymer-rich region in which a mass ratio of the superabsorbent polymer to a total amount of a mass of the hydrophilic fiber and a mass of the superabsorbent polymer is relatively high in a cross-sectional view, and the polymer Having a hydrophilic fiber rich region relatively lower than the rich region,
The absorbent article in which the blood coagulant is present at least in the hydrophilic fiber-rich region in the portion used by arranging the hydrophilic fiber-rich region on the skin facing surface side.
The absorbent article according to claim 1, wherein the absorbent body is made of an absorbent sheet.
The absorbent article according to claim 1 or 2, wherein the absorbent body has a diffusing means for diffusing blood in the longitudinal direction in a portion of the excretory part facing the excretion part of the wearer when worn.
The absorbent article according to any one of claims 1 to 3, wherein the blood coagulant is a cationic polymer.
The absorbent article according to claim 4, wherein the cationic polymer is a quaternary ammonium salt homopolymer, a quaternary ammonium salt copolymer or a quaternary ammonium salt polycondensate.
The absorbent article according to any one of claims 1 to 5, wherein the absorbent body is made of an absorbent sheet and has a multilayer structure in which a plurality of the absorbent sheets are stacked in the thickness direction.
The absorbent body is made of an absorbent sheet, and has a diffusing means for diffusing blood in the longitudinal direction in the excretory part-facing portion that is disposed facing the excretory part of the wearer when worn,
The diffusion means is a vertical slit extending in the vertical direction, and the vertical slit penetrates the absorbent sheet on the most skin-facing surface side containing the blood aggregating agent. Absorbent article according to item.
The absorbent body has a diffusing means for diffusing blood in the longitudinal direction in the excretory part facing part disposed opposite to the excretion part of the wearer when worn,
The diffusion means is a vertical slit extending in the vertical direction,
The absorbent article according to any one of claims 1 to 7, wherein a width of the vertical slit is 0.1 mm or more and 1 mm or less.
The absorbent body has a diffusing means for diffusing blood in the longitudinal direction in the excretory part facing part disposed opposite to the excretion part of the wearer when worn,
The diffusion means is a vertical slit extending in the vertical direction,
The absorbent article according to any one of claims 1 to 8, wherein the longitudinal slit has a length in a plan view of 10 mm or more and 35 mm or less.
The absorbent body has a diffusing means for diffusing blood in the longitudinal direction in the excretory part facing part disposed opposite to the excretion part of the wearer when worn,
The diffusion means is a vertical slit extending in the vertical direction,
The vertical slit has a plurality of rows arranged in the horizontal direction in the vertical direction,
The absorbent article according to any one of claims 1 to 9, wherein an interval between vertical slits in the same row is 3 mm or more and 20 mm or less.
The absorbent body has a diffusing means for diffusing blood in the longitudinal direction in the excretory part facing part disposed opposite to the excretion part of the wearer when worn,
The diffusion means is a vertical slit extending in the vertical direction,
The vertical slit has a plurality of rows arranged in the horizontal direction in the vertical direction,
The absorbent article according to any one of claims 1 to 10, wherein a plurality of the longitudinal slits are dispersed in the same row.
The absorber comprises an absorbent sheet,
The absorbent sheet is composed of a central absorbent sheet formed in the excretory part facing part disposed opposite to the excretion part of the wearer when worn, and a main body absorbent sheet covering the central absorbent sheet,
The absorptivity according to any one of claims 1 to 11, wherein a basis weight of the blood aggregating agent in the excretory part facing part is larger than a basis weight of the blood aggregating agent in a peripheral part of the excretion part facing part. Goods.
The absorbent article according to claim 12, wherein the central absorbent sheet has a multilayer structure in which a plurality of the absorbent sheets are overlapped.
The absorber comprises an absorbent sheet,
The absorbent sheet is composed of a central absorbent sheet formed in the excretory part facing part disposed opposite to the excretion part of the wearer when worn, and a main body absorbent sheet covering the central absorbent sheet,
The central absorbent sheet has a portion in which the polymer-rich region of the absorbent sheet and the arrangement in the thickness direction of the hydrophilic fiber are reversed between adjacent absorbent sheets as seen in the thickness direction. The absorbent article according to any one of claims 1 to 13.
The absorber comprises an absorbent sheet,
The absorbent sheet is composed of a central absorbent sheet formed in the excretory part facing part disposed opposite to the excretion part of the wearer when worn, and a main body absorbent sheet covering the central absorbent sheet,
The central absorbent sheet has a structure in which one absorbent sheet is bent so as to have at least a three-layer structure, of which the uppermost layer located closest to the skin contact surface side and the thickness direction The absorptivity according to any one of claims 1 to 14, wherein the second layer adjacent to the uppermost layer as viewed has the same arrangement in the thickness direction of the hydrophilic fiber rich region and the polymer rich region. Goods.
The absorber comprises an absorbent sheet,
The absorbent sheet is composed of a central absorbent sheet formed in the excretory part facing part disposed opposite to the excretion part of the wearer when worn, and a main body absorbent sheet covering the central absorbent sheet,
The absorbent article according to any one of claims 1 to 15, wherein the blood coagulant is contained only in the central absorbent sheet.
The absorber comprises an absorbent sheet,
The absorbent sheet is composed of a central absorbent sheet formed in the excretory part facing part disposed opposite to the excretion part of the wearer when worn, and a main body absorbent sheet covering the central absorbent sheet,
The absorbent article according to any one of claims 1 to 15, wherein the blood aggregating agent is contained only in the main body absorbent sheet.
The absorber comprises an absorbent sheet,
The absorbent sheet is composed of a central absorbent sheet formed in the excretory part facing part disposed opposite to the excretion part of the wearer when worn, and a main body absorbent sheet covering the central absorbent sheet,
The absorbent article according to any one of claims 1 to 17, wherein the blood aggregating agent is contained in the central absorbent sheet and the main body absorbent sheet.
The absorber comprises an absorbent sheet,
When the absorbent sheet located closest to the skin contact surface is viewed in the thickness direction, the hydrophilic fiber rich region is positioned on the skin contact surface side, and the polymer rich region is positioned on the non-skin contact surface side. The absorbent article according to any one of claims 6 to 18.
The second sheet made of a nonwoven fabric is disposed between the top sheet and the absorber, and the second sheet does not contain the blood aggregating agent. Absorbent article as described in 1.
The blood coagulant is a cationic polymer;
The absorbent article according to any one of claims 1 to 20, wherein the molecular weight of the cationic polymer is 2000 or more and 10 million or less.
The absorbent article according to any one of claims 1 to 21, wherein an amount of the blood aggregating agent is 0.1 g / m 2 or more and 25 g / m 2 or less.
The blood coagulant is a water-soluble cationic polymer, the water-soluble cationic polymer has a structure having a main chain and a side chain bonded thereto, and has a molecular weight of 2000 or more, and the water-soluble cationic polymer Is a quaternary ammonium salt homopolymer having a repeating unit represented by the following formula 1, or a repeating unit represented by the following formula 1 and a repeating unit represented by the following formula 2: A quaternary ammonium salt copolymer having the main chain of the water-soluble cationic polymer and the side chain bonded at one point, and the side chain having a quaternary ammonium moiety. The absorbent article according to any one of claims 1 to 22, to which a certain water-soluble cationic polymer is applied.
As the blood coagulant, 1 g / m of a water-soluble cationic polymer made of a quaternary ammonium salt homopolymer or a quaternary ammonium salt copolymer having a streaming potential of 1500 μeq / L or more and a molecular weight of 2000 or more. The absorbent article according to any one of claims 1 to 23, wherein the absorbent article has 2 or more and 20 g / m 2 .
The water-soluble cationic polymer has a structure in which a quaternary ammonium salt homopolymer or a quaternary ammonium salt copolymer has a main chain and a side chain bonded thereto, and the main chain and the side chain are The absorbent article according to claim 24, which is bonded at one point.
The blood coagulant includes a water-soluble cationic polymer having a molecular weight of 2000 or more, and the water-soluble cationic polymer has an inorganic value / organic value that is a ratio of an inorganic value to an organic value. The water-soluble cationic polymer is 0.6 or more and 4.6 or less, and the water-soluble cationic polymer is a quaternary ammonium salt homopolymer, a quaternary ammonium salt copolymer or a quaternary ammonium salt polycondensate. The absorbent article according to any one of 1 to 25.
The absorbent article according to any one of claims 1 to 26, wherein the absorbent article is a sanitary napkin.