Abstract: An apparatus for releasably holding a surgical tool having a body, the body having a longitudinal axis, a monolithic construction, and a shape apportioned to be grasped by a human hand, with body further having a tool engaging portion, a hand receiving portion, and a button pressing portion. A longitudinal bore is disposed along the longitudinal axis of the body, and on one end. A transverse bore is disposed through the body into the longitudinal bore, with the transverse bore disposed such that the longitudinal axis of the transverse bore intersects the longitudinal axis of the longitudinal bore. A button disposed on and pivotably attached at a resilient member to the button pressing portion of the exterior of the body, with the button being proximal to the tool engaging portion. The button has a button bore and a boss extending from the button bore into the transverse bore which is alignable with the longitudinal bore.

Abstract: This disclosure relates to a graft preparation station and methods for repairing bone defects. The station described herein may be utilized for dimensioning a graft prior to positioning the shaped graft at a surgical site.

Abstract: An orthopedic measurement system is disclosed to measure leg alignment. The measurement system includes a tri-axial gyroscope configured to measure movement of a leg. The gyroscope is coupled to a tibia of the leg. For example, the gyroscope can be placed in an insert or tibial prosthetic component that couples to the tibia. The gyroscope is used to measure alignment relative to the mechanical axis of the leg. The leg alignment measurement is performed by putting the leg through a first leg movement and a second leg movement. The gyroscope outputs angular velocities on the axes the sensor is rotated about. The gyroscope is coupled to a computer that calculates the alignment of the leg relative to the mechanical axis from the gyroscope measurement data.

Abstract: An endovascularly deployed prosthetic includes a portion for being positioned within an ascending aorta. The prosthesis includes a replacement aortic valve on a proximal end thereof. The prosthesis includes an increased diameter portion that seals against the aorta at a more distal portion, and a pair of conduits extend from the increased diameter portion to the coronaries for fluidly coupling the coronaries to the prosthesis.

Abstract: Deflection devices, systems, and methods for the prevention of stroke. Devices hereof comprise an extension portion and an anchor portion, both of which are configured to prevent the device from advancing into the artery extending from the aortic arch in which the device may be positioned. Additionally, a retrieval system is provided, the system comprising a sleeve catheter and a retrieval device slidably disposed therein. The distal end of the retrieval device comprises one or more attachment portions configured to engage at least a portion of the anchor portion of a device positioned within an artery extending from the aortic arch.

Abstract: A biodegradable stent prosthesis formed from a degradable material, having a plurality of luminal, abluminal, and side surface regions, wherein a surface portion extending between the abluminal and luminal surface region of at least some structural elements is convex.

Abstract: A vascular remodeling device has a plurality of sections, sized for deployment in a blood vessel, that is radially expandable from a collapsed state to an expanded state. Each section has a plurality of interconnected struts that define a waist, a proximal face, and a distal face. Each face comprises (i) a plurality of distal strut portions extending proximally from a distal side of the face, (ii) a plurality of proximal strut portions extending distally from a proximal side of the face, and (iii) a plurality of sub-struts, wherein, from each proximal strut portion, two of the sub-struts each extend to a different one of the distal strut portions.

Abstract: The present disclosure relates generally to stents and methods for managing passage of material through a body lumen. In some embodiments, a medical stent may include a stent body defined by a hollow tubular elongate structure extending along a central axis, the stent body including a first portion and a second portion. The medical stent may further include a control region between the first and second portions, wherein in a first configuration the hollow tubular elongate structure of the control region is in a closed, twisted configuration, and wherein in a second configuration the hollow tubular elongate structure of the control region is in an open, expanded configuration.

Abstract: A convertible nephroureteral catheter is used in the treatment of urinary system complications, particularly on the need for a single surgically delivered device to treat patients who must be seen by an interventional radiologist (IR). In many current procedures, patients need to return to the operating room to remove a previously delivered nephroureteral catheter to exchange this catheter with a fully implanted ureteral stent delivered though the same access site at the flank. The present convertible nephroureteral catheter reduces the need to return for a second surgical procedure. Two weeks after initial implantation, the proximal portion of the convertible nephroureteral catheter extending out from the body may simply be removed. A simple action at the catheter hub allows this proximal portion to be removed, leaving behind the implanted ureteral stent within the patient's urinary system. Other medical procedures, devices, and technologies may benefit from the described convertible catheter.

Abstract: A device for enclosing a finger includes a protective shell having an opening for receiving the finger. The protective shell defines an interior cavity that is sized and shaped to allow extension and flexion of the finger within the shell.

Abstract: A sports tape for placement at a user's knee or elbow includes a first stabilizer portion and a second stabilizer portion configured for placement on opposite sides of the user's knee or elbow. A central portion comprising a bar or circle connects the first stabilizer portion and the second stabilizer portion and is configured to wrap around the user's knee or elbow. A first stabilizer is embedded in the first stabilizer portion, and a second stabilizer is embedded in the second stabilizer portion, disposed inside the sports tape, sandwiched between sports tape layers to provide strength and resiliency to the sports tape.

Abstract: A thumb brace comprising a glove having a thumb portion disposed between a palm side and a back side and comprising a first attachment region positioned adjacent a base of the thumb portion and a second attachment region positioned on the back side of the glove; a first elastic strap whereby the first strap extends a distal end of a thumb metacarpal bone of a user of the brace; a second elastic strap having a first end attached to the palm side of the glove and the second end releasably attached to the second attachment region, whereby the second strap reduces a proximal end of a thumb metacarpal bone of a user of the brace; and a pad attached to the glove such that the pad cushions a CMC joint of the user of the brace from impact.

Abstract: Wearable devices protect against musculoskeletal injuries and enhance performance. Systems and methods provide wearable devices to assist with human motion during physical activities, such as performing movements (e.g., lifting) and holding static poses (e.g., crouching, or holding a tool while working overhead). Materials, constructions, and system architectures allow the wearable devices to be worn over, under, or integrated into clothing for extended periods of time to improve performance or reduce risk of injury. Sensors may be included in the wearable devices to detect various activities, motions, and postures of the wearer, and various active and semi-active controls approaches may leverage sensor information to provide tailored assistance to individual users. Various controls optimization techniques ensure the wearable devices operate at peak efficiency.

Abstract: An exoskeleton includes two torque generators, two thigh links, and a supporting trunk rotatably coupled to the thigh links. When a wearer bends forward in the sagittal plane such that the supporting trunk extends beyond a predetermined angle A with respect to vertical, at least one of the torque generators imposes a resisting torque between the supporting trunk and a corresponding thigh link, thus imposing a force onto a wearer's trunk and thighs to aid in supporting the wearer in a bent position. The exoskeleton may include an active or passive means for actuating the generators. When the supporting trunk does not extend beyond the predetermined angle A, the torque generators do not impose resisting torques between the supporting trunk and the thigh links during the entire range of motion of the thigh links, thus enabling a wearer to walk, run and sit without constraint while in an upright position.

Abstract: There is provided a neck collar including: a ring-shaped lower support being open forward from a user and surrounding the user's neck; a vertical support protruding upward from two open ends of the lower support; and a jaw support protruding in two side directions from the upper end of the vertical support and supporting the user's jaw.

Abstract: Systems and methods are provided for mitigating and/or preventing a hernia using a wearable device worn by a user such that an output device is positioned at a predetermined location corresponding to a target hernia mitigation site on the user's body. One or more physical parameters of the user are monitored to identify when the user is about to perform a predetermined physical activity, and the output device is activated to provide an output to mitigate a hernia or prevent a hernia from occurring at the mitigation site when the predetermined activity is performed.

Abstract: An anti-fatigue foot pad manufacturing method. According to the anti-fatigue foot pad manufacturing method, a protective layer is formed in a cavity of a mold firstly, and then massage blocks and a foamed elastic body are fixed by the protective layer, so that the massage blocks are mounted and supported independently, and the technical defect that in the prior art, all massage blocks/protrusions have to be fixed to a hard support plate is overcome.

Abstract: An absorbent article can have a topsheet layer, a liquid impermeable layer, and an absorbent core positioned between the topsheet layer and the liquid impermeable layer. The absorbent article can further include an exudate management layer in fluid communication with the topsheet layer. In various embodiments, the exudate management layer can be positioned on a body facing surface of the topsheet layer. In various embodiments, the exudate management layer can be positioned between the topsheet layer and the absorbent core. The exudate management layer has a first component which defines an opening for direct passage of body exudates into the absorbent core. The exudate management layer has a second component which at least partially overlaps the first component of the exudate management layer and further extends in the longitudinal direction of the absorbent article in a direction towards the posterior region of the absorbent article.

Abstract: In general, the present invention is directed to systems and methods for providing ostomy faceplates in proximity to negative pressure wound devices. This may be achieved, for example through the use of an ostomy appliance or faceplate with a non-circular flange for attachment of a bag or pouch. In accordance with some embodiments, this non-circular flange may be substantially “D”-shaped, and/or have at least one substantially straight edge. In some embodiments, the ostomy faceplate may itself be noncircular and/or “D”-shaped; may include a cutting guide for cutting materials used with an NPWD; may contain an asymmetrically located aperture; and/or may comprise one or more tapered edges.

Abstract: The present disclosure provides a method, performed by an accessory device (i.e. an accessory device of an ostomy system disclosed herein), for monitoring an ostomy system. The accessory device comprises an interface configured to communicate with one or more devices of the ostomy system, the interface comprising a display. The accessory device is configured to communicate with an ostomy system as disclosed herein. The ostomy system comprises a monitor device, and/or an ostomy appliance configured to be placed on a skin surface of a user. The ostomy appliance comprises a base plate. The method comprises: obtaining monitor data from the one or more devices, obtaining context data, determining one or more future operating states of the ostomy appliance based on the monitor data and the context data, wherein a future operating state is indicative of future adhesive performance of the ostomy appliance, and communicating the one or more future operating states.

Abstract: This application relates to a hand-held cooling device for supplying a cryogen to a target region for cryotherapy. The device can include a cryogen container configured to contain a first cryogen having a first temperature and a nozzle configured to spray a first modified cryogen to the target region, the first modified cryogen having a second temperature higher than the first temperature. The device can also include a cryogen temperature regulator configured to receive the first cryogen and output the first modified cryogen to the nozzle, the cryogen temperature regulator disposed closer to the nozzle than the cryogen container. The cryogen temperature regulator can include a holder tube, a porous structure disposed inside a holder tube and a heater disposed around the holder tube and heating the holder tube so as to increase the first temperature to the second temperature while the first cryogen passes through the porous structure.

Abstract: This application relates to a hand-held cooling device for supplying a cryogen to a target region for cryotherapy. The device can include a cryogen transfer unit configured to receive a first cryogen from an external cryogen reservoir, the first cryogen including i) a first amount of a liquid phase cryogen and ii) at least one of a first solid phase cryogen and a first gas phase cryogen. The device can also include a nozzle configured to spray a first modified cryogen to the target region. The device can further include a cryogen liquefier disposed between the cryogen container and the nozzle and configured to cool the first cryogen received from the cryogen transfer unit and output the first modified cryogen to the nozzle, the first modified cryogen including at least a second amount of the liquid phase cryogen more than the first amount of the liquid phase cryogen.

Abstract: A therapeutic hyperthermia device and method for using the same includes a cooling blanket dimensioned to at least partially cover a human, a conduit coupled to the cooling blanket, and cooling liquid. Each of the cooling blanket, conduit, and cooling liquid have a negligible effect on a magnetic resonance (MR) image taken by an MRI device. The cooling liquid may have a spin-lattice relaxation time (T1) and a spin-spin relaxation time (T2), where either or both of T1 and T2 are less than 2 milliseconds in duration. The cooling liquid may be one of water with manganite chloride, and water with sodium chloride.

Abstract: The present invention relates to thin polymeric films containing nanoparticles with tunable absorption in the visible and near infrared (NIR) region. When these films are irradiated with NIR sources, they show a pronounced photo-thermal effect. Said effect allows a localized temperature increase, which can be controlled both spatially and temporally. Once the irradiation source has been turned off, the temperature returns within a few seconds to the initial value and then raises again as soon as the film is irradiated again. These films can be used as reusable medical devices, with a controllable and reproducible heating profile, in particular thermal or heating patches.

Abstract: A facial cold compress assembly for reducing facial swelling includes a strip that has a pair of pouches each being integrated into the strip. The strip is wearable on a user's face having the strip extending across the user's nose and beneath each of the user's eyes. In this way the strip is aligned with the user's nasal pathways. The strip is comprised of a thermally conductive material such that the strip is in thermal communication with the user's face when the strip is worn. An adhesive layer is bonded to the strip to retain the strip on the user's face. A pair of thermal packs is each removably positionable into a respective one of the pouches. Each of the thermal packs is positionable in a refrigerator for chilling and subsequently reducing swelling on the user's face and reduce congestion in the user's nasal pathways when the strip is worn.

Abstract: A heating implement includes a sheet-shaped main body sheet having an exothermic element, and a projection part sheet provided on a surface on one side of the main body sheet; the projection part sheet has a projection part projecting toward the one side, where a profile of a relationship between a load and an amount of crush includes a first region in which the amount of crush increases as the load increases, and a second region located on a side in which a value on a first axis is larger than that in the first region and having a larger increase rate of the amount of crush associated with increase in the load than the first region; and a range of the second region is wider than that of the first region in a direction of the first axis.

Abstract: A wearable rehabilitation and relaxation sleeve aid is described that provides support and therapeutic benefits to an injured area. The wearable sleeve aid includes a first inner protective layer and an outer protective layer that form a pocket area between them. A removable pack may be inserted in the pocket area. The removable pack may be cooled or heated to bring the removable pack to the desired temperature. The wearable sleeve aid further provides compression to the targeted recovery area of a user's body to reduce swelling and pain.

Abstract: A device for delivering a treatment medium to an eye includes a first body portion configured to be removably inserted and secured in an opening of the eye, and a second body portion supported by the first body portion. At least the second body portion includes a treatment medium, and a coating having an opening through which the treatment medium elutes out of the device.

Abstract: An apparatus includes a body, a needle, a catheter, and an actuator assembly. The needle extends distally from the body. The needle has an inner wall defining a needle lumen. The needle lumen is in fluid communication with a fluid port of the body. The catheter is slidably disposed in the needle lumen. The catheter has a catheter lumen. The first actuator assembly is configured to translate the catheter within and relative to the needle. The apparatus may also include an actuator assembly that is configured to rotate the needle relative to the body. The apparatus may be used to first deliver a leading bleb of fluid to the subretinal space in a patient's eye via the needle. The apparatus may then be used to deliver a therapeutic agent to the subretinal space in the patient's eye via the catheter.

Abstract: An apparatus, system and method for a phacoemulsification handpiece. The phacoemulsification handpiece may include: a proximal portion having a longitudinal axis, and a first end and a second end, wherein at least aspiration, irrigation and power connectors couple with the first end; a distal portion along the longitudinal axis and comprising a coupling configured to couple a needle with the distal portion; and a lever connectively associated with the coupling extending outwardly from the coupling through the distal portion, wherein actuation of the outwardly extending aspect of the lever provides a rotation of the coupling independent of rotation of the distal portion.

Abstract: A device for isolating a lenticle in the cornea of an eye. The device includes: a laser beam source to emit pulsed laser radiation having a pulse frequency of 1.2 MHz to 10 MHz, a pulse energy of 1 nJ to 200 nJ and a wavelength penetrating the cornea; a beam-forming unit having beam optics with an image field and that bundles pulsed laser radiation into a focus located inside the image field, and which has a maximum diameter of less than 3 ?m; a beam-deflection unit shifting the focus in the cornea and inside the image field, the focus moving along a path when the image field is resting; and a control unit to control the source and the beam-forming unit to isolate the lenticle by specifying the path. The lenticle is delimited by a cut surface which is curved with regard to a front surface of the cornea.

Abstract: An incisional instrument and method of use for creating accurate, reproducible surgical incisions. An exemplary embodiment includes an incisional instrument configured for attachment to a patient's eye and for use performing arcuate limbal relaxing incisions (LRIs). The incisional instrument is made up of two coaxial, interconnecting pieces: a docking piece and a cutting piece. The docking piece includes a suction mechanism and is configured for being secured to a patient's eye just outside the corneal limbus. The cutting piece is configured to fit flush within the docking piece and includes cutting blades and one or more handles for rotating the cutting piece relative to the docking piece. When assembled, the cutting blades extend beyond the proximal end of the docking piece by a length equal to the desired depth of LRIs to be cut. The incisional instrument further includes measurement markings for properly positioning and measuring incisions.

Abstract: Ski goggles convenient to replace comprise a ski goggles body, a mounting pad and a face sponge; a groove is formed in the inner side of the ski goggles body, the mounting pad is mounted on the groove, the groove is provided with two or more through holes, the mounting pad is provided with columns with the same number as the through holes, a limiting device in limiting fit with the corresponding through hole is formed on each column, each limiting device is positioned on one side of the corresponding column and protrudes out of the side wall of the column, the limiting devices protrude away from the center of the ski goggles body, the limiting device positioned on the nose part protrudes towards the center of the ski goggles body, and the characteristic of facilitating mounting and replacing of the face sponge is realized.

Abstract: A film roll for use in a film advance system for eye protective goggles comprises a transparent film wound on the spindle. The film has an inner trailing end, a leading end, and a total film length. In use, the transparent film extends across a lens of the goggles. The transparent film presents a transparent main film part, which extends in the longitudinal direction from the trailing end to the leading end, and which presents optically uniform characteristics at least in the longitudinal direction. The transparent film is provided with at least one visual indication, which is located above the main film part and extends along an upper film edge of the transparent film, said at least one visual indication being limited to a trailing part of said total film length.

Abstract: A method of preparing a crosslinked, collagen-based wound care dressing is provided, comprising: (a) immersing a sample of fibrous and/or non-fibrous collagen in a buffered acidic, aqueous solution comprising an alcohol; (b) contacting the collagen in solution with a catalytic component comprising 1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride for a time at least sufficient to effect reaction between amino and carboxyl groups present on the collagen and to yield crosslinked collagen that is resistant to pronase degradation; and (c) drying the crosslinked collagen to yield a porous, crosslinked collagen article wherein the porous, crosslinked collagen article demonstrates a pore size of 10-500 microns. Also provided are bioactive collagen medical scaffolds for hernia repair prosthetics and surgical incision closure members, prepared using the method above.

Abstract: Embodiments disclosed within herein relate to a wound dressing, suitable for use in negative pressure wound therapy, comprising a body of porous material, the body of porous material comprising a plurality of cuts which provide regions of flexibility within the body. Further embodiments relate to methods of manufacturing and method of use of such wound dressings. In addition, the wound dressing can comprise a retaining mechanism removably coupled to the material and configured to retain the material in the expanded conformation.

Abstract: There is provided improved therapy methods and apparatus for treating a patient's brain and spinal cord. The apparatus further relates to a flexible surgical balloon or cap-like device comprising one or more material layers that may have an antimicrobial element. The therapy apparatus may include portals for introducing diagnostic monitoring and/or therapeutic devices, and delivery of therapeutic drug delivery systems. Certain embodiments of the invention have an output emission area positioned to irradiate a portion of the brain with an efficacious power density and wavelength of light for diagnostic and/or therapeutic purposes.

Abstract: This invention provides compositions and methods of treating subjects with wounds. Compositions include dressings comprising a sheet and an adhesive, wherein the adhesive is adhered to the sheet, and wherein the sheet has channels. In some embodiments, the channels comprise two different classes of channels (e.g. liquid channels and air channels). These dressing can be applied to various kinds of skin injuries and remain affixed, protecting the injury from contaminants and at the same time, allowing exchange of exudates on the proximal (injury) side to the distal side and exchange of topical agents applied from the distal side of the dressing to the wound while also allowing exchange of gasses from the injury to the air and air to the wound.

Abstract: This is a device that will make it easy for seniors and for the general public to use compression stocking to deal with medical problems of the lower legs. It will be produced in several sizes to fit men and woman and the various leg configurations.

Abstract: A device for cutting a web of material comprises movement means for moving a web of material to be cut, defining a feed path for the web at least partly rotatable about a central axis and equipped with at least one conveyor mounted around the central axis, at least one cutting head equipped with a laser source and an optical system configured to direct the laser beam towards a cutting zone, where the optical system of the cutting head comprises at least one directing member located inside the conveyor to direct the laser beam away from the central axis towards the cutting zone.

Abstract: An absorbent article can have a topsheet layer, a liquid impermeable layer, and an absorbent core positioned between the topsheet layer and the liquid impermeable layer. The absorbent article can further include an exudate management layer in fluid communication with the topsheet layer. In various embodiments, the exudate management layer can be positioned on a body facing surface of the topsheet layer. In various embodiments, the exudate management layer can be positioned between the topsheet layer and the absorbent core. The exudate management layer has a first component which defines an opening for direct passage of body exudates into the absorbent core. The exudate management layer has a second component which at least partially overlaps the first component of the exudate management layer and further extends in the longitudinal direction of the absorbent article in a direction towards the posterior region of the absorbent article.

Abstract: Disclosed is a deformable analgesic nose plug, comprising a deformable core material and an outer coating provided on said deformable core material, wherein said outer coating comprises one or more analgesic compounds. The nose plug has a tapered distal end for insertion into a nostril and a proximal end whereby the nose plug is inserted into the nostril. The deformable core material may comprise a multi-phasic core material wherein a first phase of the multi-phasic core material is a solid or a semi-solid structure at a temperature of 35° C. or less and a second phase of the multi-phasic core material is characterized by liquefaction at a temperature of 37° C. or greater. The deformable core material may also comprise a porous resiliently compressible substrate. The deformable porous resiliently compressible core material may be one of polymeric sponges, naturally occurring sponges, fluffy cellulosic materials, cotton, rolled gauze, and mixtures thereof.

Abstract: An apparatus for manufacturing an intravaginal tampon for feminine hygiene includes a tampon press having a plurality of elongate press dies disposed about central press axis to form a press cavity and a cylindrical carrier having a diameter less than that of the predetermined finished diameter. The elongate press dies include a plurality of longitudinal penetrating dies, each having a pressing face notch disposed proximate a first end thereof and an end notch disposed on an edge perpendicular to the pressing face at the opposite second end thereof that cooperate with corresponding notches in an adjacent penetrating die.

Abstract: A polymer composition comprising an organic polymer and a mica containing effect pigment, e.g., a pearlescent pigment comprising mica, well suited for producing molded articles, in particular, for molding articles comprising thin sections and or delicate features, such as a hollow interior defined by a thin wall or structural features susceptible to tear or other damage and the like, is provided as are a method for preparing molded articles comprising the polymer composition and articles comprising the polymer composition, including, for example, an article used to deliver a medical or personal care component such as a tampon applicator, and a method for preparing molded articles comprising the polymer composition. Optionally, articles of the present disclosure have a varying translucency or opacity about a dimension of the article.

Abstract: A low bulk, high capacity disposable absorbent pant is disclosed. The pant may have a variety of combinations of features that contribute to imparting the pant with a more close-fitting, discreet appearance, particularly under outer clothing, more resembling that of an ordinary undergarment. The features may include an arrangement of relatively closely-spaced elastomeric strands in a belt structure; elastomeric strands in the belt structure having active portions that traverse forward and rearward portions of an absorbent pad assembly; an arrangement of elastomeric strands in the belt structure below the side seams; an arrangement of longitudinal elastic strands in the absorbent pad assembly that are closer to the longitudinal axis of the pant than to the side seams; and/or an absorbent core structure having portions that are tapered and/or channeled.

Abstract: A laminate web having a polymer film layer and a nonwoven layer is disclosed. The polymer film layer makes up a first side of the laminate web and the nonwoven layer makes up a second side of the laminate web. The laminate web has a plurality of first elements extending from the polymer film. The web also has a plurality of second elements formed outwardly from the first side of the laminate web.

Abstract: Fabrics having a desirable softness and exhibiting a low lint level are provided. The fabrics include an embossed bonding pattern, in which the embossed bonding pattern includes a plurality of icons (e.g., geometric shapes, caricatures, etc.). The plurality of icons may be defined by a plurality of perimeter bonding points. Additionally, from 1 to about 10 internal bonding points may be located within at least one of the plurality of icons.

Abstract: An absorbent article comprising a top-surface sheet, a second sheet, and an absorber interposed between the top-surface sheet and the second sheet. The absorbent article allows a body fluid absorbed by the top-surface sheet to move to a non-skin side without deteriorating a soft touch feeling of cotton. The top-surface sheet 3 has a multi-layer structure including a non-heat fusible layer 10 made of a cellulose fiber and arranged on a skin side and a heat-fusible layer 11 made of a heat-fusible fiber and arranged on the non-skin side. The second sheet 6 made of a heat-fusible fiber is arranged on the non-skin side of the top-surface sheet 3. A large number of compressed parts 15 are formed on the non-skin side of the second sheet 6 by integrally recessing the second sheet 6 and the top-surface sheet 3 toward the skin side.

Abstract: An absorbent article that improves contact efficiency between a deodorant substance and an odor. The problem is solved by an absorbent article including an absorber and a liquid impervious resin film covering an outside of the absorber, in which a cellulose nanofiber layer is attached directly to a member outside the liquid impervious resin film, and the cellulose nanofiber layer can come into contact with an odor in an atmosphere outside the absorbent article.

Abstract: An absorbent article having a fluid-handling system includes a fluid permeable bodyside liner; a fluid impermeable outer cover; an absorbent core disposed between the liner and the outer cover, wherein the absorbent core includes superabsorbent material and optionally fluff pulp; and a core wrap at least partially encircling the absorbent core, wherein the core wrap includes a three-dimensionally patterned, wetlaid, cellulosic tissue nonwoven material. Fibers of the nonwoven material are entirely cellulose fibers, and the core wrap includes opposing core wrap surfaces each having a textured surface. Each surface includes an average material plane, a plurality of ridges extending in a z-direction from the average material plane, and a plurality of grooves alternating with the plurality of ridges, wherein the grooves depth extend in the opposite z-direction from the average material plane.