Abstract: A disposable absorbent article having a topsheet, a backsheet, and an absorbent core disposed therebetween is described. The topsheet includes a plurality of apertures arranged in a first zone and a first plurality of structures which are disposed adjacent to the first plurality of apertures. The plurality of apertures have an Effective Aperture Area of from between 0.5 mm2 to about 8 mm2 as measured by the Aperture/Feret Angle test as described herein, and the topsheet has a top layer and a lower layer, wherein the top layer is more hydrophobic than the lower layer.

Abstract: An absorbent article includes a first waist region, a second waist region, and a crotch region, wherein the first waist region and second waist region are joined with each other such that a pair of side seams are formed and the absorbent article has two leg openings and a waist opening. At least one of the first waist region and the second waist region include graphics disposed in a first graphic zone, a second graphic zone, and/or a third graphic zone, wherein the first graphic zone, the second graphic zone.

Abstract: A disposable diaper has an absorber including. The absorber includes a first region including a center of the absorber, a pair of second regions between the first folding lines and the second folding lines inward of the first folding lines, and a pair of third regions outward of the second folding lines and on the skin contact surface side of the second regions. Outer side edges of the third regions are outward of the first folding lines. The absorbent article includes a first bonded portion in which the first and second regions are bonded, a third bonded portion in which the third regions are bonded with the non-skin surface sheet, and a third non-bonded portion inward of the third bonded portion and outward of the first folding lines. The third non-bonded portion are across the center of the absorbent article in the crotch region.

Abstract: Provided is an ultrasmall-sized fixing tape suitable for a disposal tape for an absorbent article, such as a disposable diaper, a sanitary napkin, or an incontinence pad. The ultrasmall fixing tape of the present invention includes: an extending portion; and a non-extending portion that is substantially free from extending, in which: the non-extending portion includes securing means in at least part thereof; the ultrasmall fixing tape has a base material layer B; the base material layer B has a thickness of 50 ?m or more; and the base material layer B has an upper yield strength in a longitudinal direction thereof at a temperature of 23° C. and a humidity of 50% of from 5 N/25 mm to 15 N/25 mm.

Abstract: A wheelchair includes a pivotable mechanism. The pivotable mechanism allows for a pivoting movement about an axis defined by an interface between adjacent components. These components may be (a) a seat member and a back member, (b) a seat member and a footrest, (c) a foot rest and a footplate support, (d) a baseplate and a footplate, or (e) a back member and a headrest.

Abstract: A bed base frame assembly of a bed generally comprises a base frame, a plurality of steerable and lockable casters, a lateral support assembly at the first and second sides of the base frame assembly, and an in-line support assembly at the foot end of the base frame assembly. The lateral support assembly may further include: a base frame; a first leg and a second leg rotatably connected to the base frame; a first actuator connected to the first leg and the second leg, wherein the first leg and the second leg rotate from the retracted position to the extended position; a third leg and a fourth leg rotatably connected to the base frame; and a second actuator connected to the third leg and the fourth leg, wherein the third leg and the fourth leg rotate from the retracted position to the extended position.

Abstract: A siderail assembly for a person support apparatus comprises a siderail body, a grip portion, and a power communication device. The siderail body includes a front surface, a back surface, and a side surface extending between the front surface and the back surface. The side surface defines a perimeter of the siderail body. The grip portion includes a siderail opening through a portion of the siderail body. The grip opening has an upper grip opening portion that cooperates with the side surface to define a grip. The power communication device is configured to communicate power wirelessly to a device in communication therewith.

Abstract: A rail cover assembly includes first and second cover portions coupled to one another. The first and second cover portions have surface regions made from an antimicrobial material. The first cover portion has opposing and longitudinally-extending L-shaped lips. The second cover portion has opposing longitudinal edges for nesting with the first cover portion's lips.

Abstract: Modular chair systems and methods of transporting a subject using a modular chair system are described. A modular chair system includes a seat component, a chair component, and a wheelchair component. The seat component includes a seat having a planar lower surface with one or more recesses and one or more attachment bars disposed in each of the recesses. The chair component includes one or more chair latch mechanisms and the wheelchair component includes one or more wheelchair latch mechanisms. Each attachment bar corresponds to one of the chair latch mechanisms and one of the wheelchair latch mechanisms such that the seat component is configured to be placed upon the chair component or the wheelchair component and releasably held in place by the chair latch mechanisms or the wheelchair latch mechanisms.

Abstract: Patient transfer chairs are disclosed, with the transfer chairs comprising; a rigid frame supporting a seating surface, with the seating surface being deployable under a patient in a plurality of incremental configurations between a first configuration where the seating surface supports a patient only underneath the bend of their knee and a second configuration where the seating surface supports the majority of a patient's femur.

Abstract: The inventive device and methods disclosed herein allow an individual to create and sustain a differential stretch to the anterior muscles and ligaments of the torso, hips and legs. The device is comprised of a base frame, a vertical member secured to the base frame, a rotational lift lever secured to the vertical member at a vertical pivot member, a lower extremity elevation member secured to the rotational lift member, and at least one lower extremity attachment device secured to the lower extremity elevation member. In methods of use, the device is used to lift an individual's legs off of the ground, while the person is lying face down, so as to create a stretch in the anterior muscles, fascia, or ligaments. The device has various planes of rotation, which allows for differential stretching in the various quadrants of the person's torso. In addition, the device is adjustable in height as well as displacement along a track within the base to accommodate different body types.

Abstract: A rehabilitation apparatus for facilitating joint movement in a patient having a limb with a joint, the apparatus including an actuation member and an actuation strap extending from the actuation member, the actuation member selectively retracting the actuation strap, the actuation strap having a strap end engageable with the limb of the patient. A security strap is connected to the actuation member. When the limb of the patient is engaged with the strap end of the actuation strap and the actuation member retracts the actuation strap, the actuation strap produces a force on the limb. The security strap can be a harness receivable about a patient's upper torso. The apparatus can further include a brace, the joint of the patient's limb receivable in the brace, the actuation strap engageable with the brace, the actuation strap producing a force on the limb via the brace.

Abstract: High Grade Aluminum Alloy Tuning Fork—Anodized with a Pointed Stem that gives precise directional type treatment on clients is disclosed. Each Tuning fork is precisely and uniformly made by a CNC and Turning machine to maintain consistency. This is operated by a medical equipment and aerospace designer & machinist. The stem and tines are created separately and fused together during production. The weights are also custom made making the entire product a smooth surface that is color coded and anodized to each Tuning Fork in the set. Each fork in this production is then calibrated to a specific frequency within 0.1 to 0.5 Hz.

Abstract: A handheld multi-tip scraping and moxibustion device, including: pushing and scraping air-guiding tips distributed on a panel each having a through-cavity;—and a moxa burning chamber communicating with the through-cavity to enable heat and air in the moxa burning chamber to be discharged gradually for use through the pushing and scraping heat-conducting and air-guiding tips. The pushing and scraping air-guiding tips including a first set of pushing and scraping heat-conducting and air-guiding tips located in a middle portion of the panel and a second set of pushing and scraping heat-conducting and air-guiding tips located around the first set of pushing and scraping air-guiding tips, wherein the height of the first set of pushing and scraping heat-conducting and air-guiding tips is less than the height of the second set of pushing and scraping heat-conducting and air-guiding tips in order to form a multi-layered stepped air discharge.

Abstract: A puncture needle connector (1) includes an outer cylinder (11), an inner cavity (1a) formed within the outer cylinder (11), an arm (15) provided at the outer cylinder (11), the arm (15) being elastically deformable by bending, and a claw (16) provided on the arm (15). The inner cavity (1a) is in communication with the outside via a first opening (21) and a second opening (22). When a puncture needle (210) is inserted into the inner cavity (1a) via a first opening (21), the claw (16) engages with an engagement structure (217) provided integrally with the puncture needle (210), a liquid-tight seal (25) is formed between an outer circumferential surface of the puncture needle (210) and an inner circumferential surface of the inner cavity (1a), and the puncture needle (210) and the second opening (22) are in communication with the each other.

Abstract: The present invention relates, in some embodiments thereof, to systems, devices and methods for decontaminating a surface of one or more vessels. In some embodiments, the systems and devices of the invention include a housing, and a wiping member disposed within the housing being configured to wipe off the surface of one or more vessels, thereby establishing a contaminant-free fluid passageway between vessels.

Abstract: The present invention relates, in some embodiments thereof, to systems, devices and methods allowing for an engagement of two or more vessels or devices in a decontaminated manner. In some embodiments of the invention, the systems and devices of the invention include a first connection interface attached to a first vessel and a second connection interface attached to a second vessel, wherein the first connection interface and the second connection interface are configured to allow for an engagement between the first vessel and the second vessel, and wherein the first and second connection interfaces are further configured to externally displace from the engagement between the first vessel and the second vessel while a hermetically sealed connection is maintained between the first vessel and the second vessel.

Abstract: The present invention relates, in some embodiments thereof, to systems, devices and methods allowing for an engagement of two or more vessels or devices in a decontaminated manner. In some embodiments of the invention, the systems and devices of the invention include a first connection interface attached to a first vessel and a second connection interface attached to a second vessel, wherein the first connection interface and the second connection interface are configured to allow for an engagement between the first vessel and the second vessel, and wherein the first and second connection interfaces are further configured to externally displace from the engagement between the first vessel and the second vessel while a hermetically sealed connection is maintained between the first vessel and the second vessel.

Abstract: The present invention relates, in some embodiments thereof, to systems, devices and methods allowing for an engagement of two or more vessels or devices in a decontaminated manner. In some embodiments of the invention, the systems and devices of the invention include a first connection interface attached to a first vessel and a second connection interface attached to a second vessel, wherein the first connection interface and the second connection interface are configured to allow for an engagement between the first vessel and the second vessel, and wherein the first and second connection interfaces are further configured to externally displace from the engagement between the first vessel and the second vessel while a hermetically sealed connection is maintained between the first vessel and the second vessel.

Abstract: The present invention relates, in some embodiments thereof, to systems, devices and methods allowing for an engagement of two or more vessels or devices in a decontaminated manner. In some embodiments of the invention, the systems and devices of the invention include a first connection interface attached to a first vessel and a second connection interface attached to a second vessel, wherein the first connection interface and the second connection interface are configured to allow for an engagement between the first vessel and the second vessel, and wherein the first and second connection interfaces are further configured to externally displace from the engagement between the first vessel and the second vessel while a hermetically sealed connection is maintained between the first vessel and the second vessel.

Abstract: The present invention relates, in some embodiments thereof, to systems, device and methods for establishing a contaminant-free fluid passageway between vessels. In some embodiments of the invention, the systems and devices of the invention include a first connection interface configured to be coupled to a first vessel, and a second connection interface configured to be coupled to a second vessel, the first and second connection interfaces configured to engage with each other and entrap contaminants, the first connection interface and the second connection interface, following the engagement, are configured to internally displace within the first vessel or the second vessel, while allowing for a contaminant-free fluid passageway and hermetically sealed engagement of the vessels.

Abstract: The present invention relates, in some embodiments thereof, to systems, device and methods for establishing a contaminant-free fluid passageway between vessels. In some embodiments of the invention, the systems and devices of the invention include a first connection interface configured to be coupled to a first vessel, and a second connection interface configured to be coupled to a second vessel, the first and second connection interfaces configured to engage with each other and entrap contaminants, the first connection interface and the second connection interface, following the engagement, are configured to internally displace within the first vessel or the second vessel, while allowing for a contaminant-free fluid passageway and hermetically sealed engagement of the vessels.

Abstract: The present invention relates, in some embodiments thereof, to systems, device and methods for establishing a contaminant-free fluid passageway between vessels. In some embodiments of the invention, the systems and devices of the invention include a first connection interface configured to be coupled to a first vessel, and a second connection interface configured to be coupled to a second vessel, the first and second connection interfaces configured to engage with each other and entrap contaminants, the first connection interface and the second connection interface, following the engagement, are configured to internally displace within the first vessel or the second vessel, while allowing for a contaminant-free fluid passageway and hermetically sealed engagement of the vessels.

Abstract: The present invention relates, in some embodiments thereof, to systems, device and methods for establishing a contaminant-free fluid passageway between vessels. In some embodiments of the invention, the systems and devices of the invention include a first connection interface configured to be coupled to a first vessel, and a second connection interface configured to be coupled to a second vessel, the first and second connection interfaces configured to engage with each other and entrap contaminants, the first connection interface and the second connection interface, following the engagement, are configured to internally displace within the first vessel or the second vessel, while allowing for a contaminant-free fluid passageway and hermetically sealed engagement of the vessels.

Abstract: The present invention relates, in some embodiments thereof, to systems, devices and methods for decontaminating a surface of one or more vessels. In some embodiments, the systems and devices of the invention include a housing, and a wiping member disposed within the housing being configured to wipe off the surface of one or more vessels, thereby establishing a contaminant-free fluid passageway between vessels.

Abstract: The present invention relates, in some embodiments thereof, to systems, devices and methods for decontaminating a surface of one or more vessels. In some embodiments, the systems and devices of the invention include a housing, and a wiping member disposed within the housing being configured to wipe off the surface of one or more vessels, thereby establishing a contaminant-free fluid passageway between vessels.

Abstract: Coated glass pharmaceutical packages are disclosed. According to embodiments, a coated glass pharmaceutical package may include a glass container formed from one of a borosilicate glass composition that meets Type 1 criteria according to USP <660> or an alkali aluminosilicate glass having a Class HGA 1 hydrolytic resistance when tested according to the ISO 720-1985 testing standard. A low-friction coating may be bonded to the exterior surface of the glass container. The low-friction coating may include a polymer. The exterior surface of the glass container with the low-friction coating may have a coefficient of friction of less than or equal to 0.7. The coated glass pharmaceutical package may be thermally stable after depyrogenation in air at a temperature of at least about 260° C. for 30 minutes.

Abstract: A cartridge for dispensing a pre-measured buffering agent together with a medical fluid such as dental anesthetic. The cartridge includes a sharp piercing element at one end, a frangible barrier proximate the piercing element, and a traveling closure. The buffering solution is in a chamber between the barrier and the closure. When loaded into a syringe and subjected to operating pressures, the barrier is pierced, enabling the buffering solution to mix with the medical fluid. Continued pressure propels a desired, controlled mixture into a tissue of a patient. A dye may be included for visual confirmation of mixing.

Abstract: A portable pill/tablet/capsule dispensing device. The device's purpose is to enhance the doctor/patient relationship by providing patient doses of medication as prescribed by physician. Since medications are consumed outside of the supervision of the prescribing entity, this device helps to affirm to the prescriber that medications are taken by the patient as prescribed, thus minimizing the potential for medical abuse. The device's body has 2 clam shell halves, ultrasonically welded together and therefore the contents inside the device are not accessible by the patient without proper authorization. The device uses a variety of disposable magazines, prefilled with medications to load into the device by an authorized medication provider. Medications within the device are regulated by a computer program which allows for variable time dosing of medication types according to the patient's needs.

Abstract: An orthodontic adhesive includes components capable of allowing easy debonding of an orthodontic device from a patient's tooth. The adhesive includes an engineered marine mussel protein. The adhesive may include at least one photocleavable moiety. The adhesive is applied in one or more individual layers. One of the components of the adhesive is capable of binding to a tooth and the other component may be capable of binding to an orthodontic device. A method of adhering an orthodontic device to a tooth includes applying a layer of an orthodontic adhesive to either the tooth or the orthodontic device or the tooth and the orthodontic device and affixing the orthodontic device to the tooth with the orthodontic adhesive situated between the tooth and the orthodontic device. The engineered marine mussel protein includes one or more catechol moieties or one or more derivatives of a catechol moiety.

Abstract: The invention includes a toothpaste or other orally applied product to be used at least once daily to help prevent or inhibit the acquisition of a number of infections by oral or pharyngeal tissues, including the “common” cold. These compositions possess a combination of ingredients not found in other toothpastes or other orally applied products, and these ingredients work together to synergistically interfere with the acquisition of a number of pathogens. The toothpastes will have the usual dentifrice ingredients known to prevent tooth decay, as well as those that reduce halitosis (i.e., bad breath), and prevent gingivitis. In addition, the toothpastes will include one or more of: 1) starch impregnated with a zinc salt, preferably zinc gluconate; 2) corilagin as an individual compound, and not as an extract component; 3) zinc protoporphyrin IX; and 4) one or more other colorless or low-color tannin each as an individual compound, and not as an extract component.

Abstract: According to an aspect of the present invention, a dental alginate impression material includes an alginate, calcium sulfate, and an aminocarboxylic acid compound.

Abstract: The present invention provides a method for preparing porous organic/inorganic composite powder which includes attaching inorganic oxide nanoparticles in a multi-layer form by repeating steps of attaching polyphenol to porous polymethyl methacrylate (PMMA) microspheres and attaching inorganic oxide nanoparticles to the porous polymethyl methacrylate (PMMA) microspheres to which polyphenol is attached, and a cosmetic composition including the porous organic/inorganic composite powder.

Abstract: The invention includes saponin-containing compositions, wipes impregnated with these compositions, and related methods. Specifically, the invention includes a cleansing and deodorizing composition that includes a saponin; a deodorizer; cyclodextrin and a solvent. The saponin may be derived from botanical sources, such as, for example, Sapindus mukorossi or trifoliatus. Also included are textiles that are impregnated with the composition of the invention. Such textiles may be, for example, made of biodegradable materials. The invention also includes related methods of use and treatment.

Abstract: The present invention relates to a foamable vehicle or cosmetic or pharmaceutical composition, comprising: (1) an organic carrier, at a concentration of 10% to 70% by weight, wherein said organic carrier concurrently comprises: (i) at least one hydrophobic organic carrier, and (ii) at least one polar solvent; (2) at least one surface-active agent; (3) water; and (4) at least one liquefied or compressed gas propellant at a concentration of 3% to 25% by weight of the total composition. The present invention further provides a method of treating, alleviating or preventing a disorder of mammalian subject, comprising administering the above-mentioned compositions to an afflicted target site.

Abstract: A cosmetic composition that fluoresces when irradiated with electromagnetic energy is disclosed. The cosmetic composition may comprise a cosmetically accept medium comprising at least one inorganic compound, wherein the inorganic compound is doped with an inorganic fluorescence activator to cause the composition to emit a fluorescent response when irradiated with light, such as UV light. Related products that include such a composition are also disclosed, including a lip stick, an eyeliner, foundation, blush, body paint, a hair gel, or nail polish. There is also a method for imparting a fluorescent response to at least once keratinous surface of a person that comprises applying to the keratinous surface an effective amount of the composition described herein.

Abstract: The present inventions relates to a composition for treating hair, especially human hair, the use of the composition, a process to treat human hair and a kit of parts comprising the composition. The inventors surprisingly found that a composition comprising a silicone vinyl dendrimer, a homopolymeric olefin, monomeric alkanes and/or cyclic silicones, and copolymers comprising olefinic and aromatic monomers mends hair split ends whose effect sustains several washes.

Abstract: An aqueous cosmetic composition provides a proper amount of a hydrophobic spherical powder blended in an aqueous phase stably even though an aqueous base material having a fresh sensation upon use is used, and which corrects the appearance of skin. The present invention provides a cosmetic composition characterized by comprising (A) at least one higher alcohol having a saturated straight alkyl chain, (B) hydrophilic surfactants including a nonionic surfactant, (C) a powder having an average particle diameter of 1 to 30 ?m in an amount of 4 to 30% by mass and (D) water, wherein the ratio of the number of moles of a hydrophilic nonionic surfactant to the total number of moles of the hydrophilic surfactants (B) is 0.5 or more, the percentage of the amount of a hydrophobic spherical powder in the total amount of the powder having an average particle diameter of 1 to 30 ?m (C) is 50% by mass or more, and the hydrophobic spherical powder is added to an aqueous phase.

Abstract: An oral care product comprising at least one of phytomenadione (vitamin K1), menaquinone (vitamin K2), vitamin C, selenium, ubiquinone (Coenzyme Q10), Astragalus, Ginseng, Schisandra, adaptogenic herbs, cannabidiol, or the like. An oral care product directed toward rebalancing micro-bacterial homeostasis in the mouth, or establishing and maintaining a healthy oral microbiome.

Abstract: N-methyl-N-acylglucamines are suitable as thickening agents in aqueous surfactant solutions containing one or more anionic surfactants of the group including alkyl ether sulfates and alkyl sulfates, the N-methyl-N-acylglucamines containing at least 60 wt.-% of N-methyl-N-acylglucamines that have a C12-, C14-acyl group or an unsaturated C18-acyl group and at the same time less than 5 wt.-% of N-methyl-N-acylglucamines that contain an acyl group <C12. The surfactant solutions are particularly used in cosmetic compositions.

Abstract: Compositions comprising one or more chelating agents and optionally zinc ion salts are used to inhibit the growth or biofilm formation in bacteria associated with personal care products such as ophthalmic, pedicure, manicure or podiatric solutions. The compositions of the present application can also comprise gelling agents, antimicrobials, antibiotic or a pH adjuster. The compositions may be in the form of a solution, a gel, a cream, a jelly, a powder, a paste, a lotion, soap and a cleaner.

Abstract: The present invention relates to sunscreen compositions. More specifically, the present invention relates to sunscreen compositions that, when applied to the skin, prevent sun damage while allowing the passage of sufficient UVB in the range of 290 nm-298 nm to produce vitamin D, while also inhibiting melanogenesis.

Abstract: Provided herein are long lasting hair compositions, color enhancers, and markers for selecting the same.

Abstract: Provided herein are color protectant compositions for dyed human hair, and methods for determining the same.

Abstract: This application discloses oral care compositions comprising cannabinoids, preferably cannabidiol and/or cannabigerol. The oral care composition disclosed in this application may be a tooth paste, a tooth powder, or a mouthwash solution. The oral care composition may be used to treat oral infectious disease, including periimplantitis, periodontitis, oral mucositis, and dental pain.

Abstract: A coconut shell extract characterized by a particular level of trans-piceatanol and cosmetic and/or dermatological compositions comprising the coconut shell extract. Methods comprising a cosmetic application of at least one of compositions.

Abstract: The present invention provides an oral care composition comprising: (a) a dipeptide of the formula Xaa1-Xaa2 or Xaa2-Xaa1; wherein Xaa1 is an amino acid with a polar uncharged side chain; and Xaa2 is selected from an amino acid with a hydrophobic side chain, an amino acid with a polar uncharged side chain, and proline; or (b) a dipeptide of the formula Xaa3-Xaa4 or Xaa4-Xaa3; wherein Xaa3 is an amino acid with a hydrophobic side chain; and Xaa4 is selected from an amino acid with a hydrophobic side chain and an amino acid with a charged side chain.

Abstract: The disclosure is directed to medroxyprogesterone compositions suitable for subcutaneous injection comprising about 360 mg/ml to 440 mg/ml medroxyprogesterone acetate, 1.35 mg/ml to 1.65 mg/ml docusate sodium, polyethylene glycol, and water. Methods of using these compositions are also described.

Abstract: A multi-step method of making a mammalian subcutaneous medical implant or non-implant for releasing self-contained drugs on a controlled basis over at least a 3 day period includes depositing at least portions of one or more individual layers of the implant by at least one computer controlled 3-D printer. The 3-D printing method may be accomplished via an array of 3-D nozzles that deposit materials (such as plastics, thermoplastics, coating materials, drug-containing matrix materials, non-drug containing matrix materials, bonding materials, biodegradable materials and/or the like) in very small, precise portions. The materials may be deposited in liquid, powder, sheet or other forms. Non-implant forms may also be provided by the techniques disclosed herein.

Abstract: The present invention provides ophthalmic formulations containing cyclosporine, methods for preparing the formulation, and methods for using the formulation.