Abstract: A pad wetness detection method and a pad wetness detection device are provided. The pad wetness detection method includes the following steps. A plurality of initial electrical records of a medical pad are obtained via two detecting areas after a pad wetness detection device is coupled to the two detecting areas of the medical pad. A threshold value is obtained via a learning algorithm according to the initial electrical records. At least one measured electrical record of the medical pad is obtained via the two detecting areas. Whether the at least one measured electrical record reaches the threshold value is determined and a warning signal is outputted accordingly.

Abstract: An absorbent article comprising a topsheet, a backsheet, and an absorbent core disposed between the topsheet and the backsheet. The absorbent article comprises a first fluid handling zone having a first Transverse Fluid Travel Distance and a second fluid handling zone having a second Transverse Fluid Travel Distance. The first Transverse Fluid Travel Distance is at least about 50% greater than said second Transverse Fluid Travel Distance, which results in an absorbent article that is better able to handle bodily fluids and reduce the risk of accidental leakage of bodily fluids onto a consumer's undergarments.

Abstract: A retrofitable drive assembly attaches and detaches quickly, easily, and reversibly from a conventional, manually powered wheelchair and is employed to convert the manually powered wheelchair into an electrically powered wheelchair. The drive assembly includes a plurality of wheel troughs, each adjustably sizeable to receive therein a rear push wheel of the manually powered wheelchair, regardless of the wheelchair's size and its rear push wheels' dimensions. In addition, the drive assembly includes two drive wheels positioned towards a front end of the drive assembly and a single caster-wheel assembly positioned towards a rear end of the drive assembly.

Abstract: A trolley (1), for a beam-mounted supply unit, for fastening medical devices to a ceiling. The trolley has a chassis (2) which can be meshed with a rail track of the beam-mounted supply unit for moving the trolley (1) along the rail track. A medical device can be fastened to the trolley (1). The trolley has a brake unit (3) with at least one braking element (7), which exerts a braking force on the rail track and/or on the chassis in the activated state of the brake unit (3), so that a movement of the chassis along the rail track is at least made difficult compared to an operating state with the brake unit (3) deactivated. In the activated state of the brake unit (3), the braking force exerted by the braking element (7) on the rail track and/or on the chassis is generated without the aid of electric energy.

Abstract: A novel technique for the fabrication of a casket dome lid from, for example, Smooth-One-Side (“S1S”) hardboard is disclosed. The invention is also directed to the fabrication of a casket lid which has a domed configuration both in the lateral and longitudinal directions of the lid. The method comprises the steps of providing a lid blank having a first end, second end, and a central region; providing a pair of diagonal voids oriented at corners of the first end of said blank and extending inward toward the central region; placing the lid blank in a vacuum fixture; and flexing the lid blank into a domed configuration via the vacuum fixture, such that the blank is domed in both a longitudinal and a transverse direction.

Abstract: In an assistance apparatus, when assisting a user in walking with an object, a motor generates, in a gait phase of a left leg, a tension less than a second threshold value in a first wire during a fifth period other than a first period during which a tension greater than or equal to a first threshold value is generated in the first wire, and a tension greater than or equal to the second threshold value in a second wire during a sixth period other than a second period during which a tension greater than or equal to the first threshold value is generated in the second wire, and generates, in a gait phase of a right leg, a tension less than the second threshold value in a third wire during a seventh period other than a third period during which a tension greater than or equal to the first threshold value is generated in the third wire, and a tension greater than or equal to the second threshold value in a fourth wire during an eighth period other than a fourth period during which a tension greater than or equal

Abstract: A crutch handle is positionably adjustable to crutch at an offset angle to provide an ergonomic position of a user's hand. The crutch handle has a curved adjustment adapter on both a first and second end of a handle-grip portion of the crutch handle. A fastener slot extends through the first and second adjustment adapters to allow a fastener to extend though and secure the handle to the crutch at an offset angle. The handle-grip has a fastener opening on at least one of the first or second ends to allow the fastener to be positioned along the handle-grip portion of the handle. A conventional crutch may be adapted with this angle adjustable crutch handle with the fasteners being in apertures that are aligned across the crutch support.

Abstract: A massage mechanism includes a portion, which, in a muscle hardness measurement mode, drives an advancing/retreating motor to rotate in a predetermined direction by constant-speed control to press a massage element into a body of a person to be treated, a portion monitoring a change rate of a motor current flowing through the advancing/retreating motor during driving of the advancing/retreating motor and stopping the driving of the advancing/retreating motor when the change rate of the motor current becomes not less than a predetermined threshold, a portion, which, after stoppage of the driving of the advancing/retreating motor, drives a tapping motor to rotate by constant-speed control to make the massage element perform a tapping operation, a current detection portion, detecting a motor current flowing through the tapping motor during driving of the tapping motor, and a portion measuring a muscle hardness of the person to be treated based on the motor current detected by the current detection portion.

Abstract: Systems, apparatuses, and methods for providing a negative-pressure therapy system are described. The system includes a first dressing, a second dressing, and a negative-pressure source. The negative-pressure source includes a first pump and a second pump. A first valve is fluidly coupled to the first dressing and the first pump to selectively permit fluid communication to the first dressing. A second valve is fluidly coupled to the second dressing and the second pump to selectively permit fluid communication to the second dressing. A cross-over valve is fluidly coupled to the first pump, the first valve, the second pump, and the second valve. The cross-over valve permits fluid communication between the first pump and the second valve and/or the second pump and the first valve. A controller is communicatively coupled to the first pump, the second pump, the first valve, the second valve, and the cross-over valve for operating the same.

Abstract: An improved therapeutic roller device comprising a cylindrical core and roller members originating from said cylindrical core. The roller members are separated, from each other, by a distance that is intended to generate lateral stretch on a muscle or other soft tissue. The amount of lateral stretch placed on a muscle, or other soft tissue, is proportional to the distance between roller elements up to a maximum distance at which lateral stretch can no longer be achieved. The diameter of the roller members determines the amount of longitudinal stretch placed on a muscle or other soft tissue. Additional longitudinal stretch is attained by ribbing of the roller members so that the roller members have projections. The length of the projections and distance between subsequent projections determine the extent of additional longitudinal stretch that can be placed on a muscle or other soft tissue.

Abstract: An ankle-mounted sexual stimulation device and method of use enhances human sexual pleasure. The device includes a bar having a center region and a pair of terminal regions. A pair of ankle cuffs attach to the terminal regions in a freely rotating, swiveling relationship. A strap extends between the terminal regions of bar. A plate slides across length of the bar, and carries a protruding member. A pin passes through apertures in the bar and plate to fixedly fasten the protruding member at the bar. The ankle cuffs detachably attach to the ankles. A leg force applied to the ankle cuffs manipulates the bar and the protruding member in axial, rotational, and lateral directions relative to the vagina or anus. The hands grip the strap and apply a hand force to manipulate the bar and attached protruding member in axial, rotational, and lateral directions relative to the vagina or anus.

Abstract: A hand-attached controlled pulsed vibration device, allowing for transmission of an enhanced massage, allowing full skin-to-skin contact between the hand of the person giving a massage and the skin of the person receiving the massage, by mounting on the back of the hand, with no glove, partial glove, or straps on the palm-side of the hand, and providing for vibration of controllable intensities and cycle times not normally achievable from a small vibrating motor, by controlling the electric power provided to one or more small vibrating motors, such that the operation of one motor or the interactions between two or more motors result in desirable intensities and cycle times of overall vibration.

Abstract: Methods of operating a haptic actuator to apply physical and/or thermal sensations to a user to provide subjective symptom relief to a user are described. In some embodiments, a haptic actuator may be automatically activated when one or more detected user states are compared to one or more predetermined activation parameters to determine the user is experiencing an episode related to a condition of the user. In another embodiment, one or more operating parameters of a haptic actuator may be updated if the haptic actuator did not provided a desired amount of subjective symptom relief to a user during use. In yet another embodiment, a haptic actuator may create an event log based on activation events when the haptic actuator is used to provide symptom relief for a condition of the user.

Abstract: Methods and apparatus for washing systems, both industrial and residential. Some embodiments pertain to face washing systems that provide a gentle upward flow of water for washing a person's face, but which can be easily reconfigured to provide a downward flow of aerated water for washing of the user's hands. Other embodiments pertain to visual indicators to help a user in a dark environment in the use of an emergency eyewash system. Yet other embodiments pertain to eyewashing systems incorporating filters that are automatically flushed of debris. Still further embodiments pertain to emergency eyewashing systems in which a mixing chamber is located downstream of a thermostatically controlled valve to reduce the possibility of a hot temperature spike being provided to the eyewashing outlet apertures, which could be harmful to users.

Abstract: A lockbox to store medication therein and to be secured within a medicine cabinet, the lockbox including a main body to fit into the medicine cabinet, a door disposed at a front portion of the main body, a plurality of anchor holes disposed within the main body to allow the main body to be secured to at least one wall or shelf within the medicine cabinet, and a lock to disposed at a top portion of the door to prevent the door from opening when the lock is locked.

Abstract: A filling aid for self-filling a cartridge from a storage vessel is disclosed. The filling aid has a housing that receives a fillable cartridge. A stopper is provided that interacts with the housing and is configured to enter the cartridge and a cannula is provided that is configured to pierce a septum of the cartridge. The housing is movable from an initial position in which the stopper is maintained outside the cartridge to an activated position in which the stopper is inserted in the cartridge and the septum is pierced by the cannula. Methods of manufacturing and using the filling aid are also disclosed.

Abstract: A handheld Multi-chamber dispensing system comprising a connecting body configured for accepting multiple liquid compound vials/cartridges for attachment. A triple location within the connecting body with at least three separate reservoirs. The modules/vials containing at least one dose of a liquid compound and configured for fluid communication with a delivery spout. A microprocessor controlled circuit that serves as a controller for the multiple reservoirs of liquid compounds.

Abstract: An apparatus for aseptic sealing a capsule having coaxial parts that at least partly overlap when telescopically joined, certain embodiments of the apparatus comprising: a capsule carrier assembly provided with at least one cavity for accommodating a respective capsule therein; a clamping member comprising a first half and a second half disposed on either side of the cavity at a capsule processing station, and each half arranged to linearly displace towards the cavity containing the capsule to a clamped position over and/or around at least a portion of the capsule; wherein the clamping member comprises a sealing means adapted to apply a sealing fluid uniformly to a circumferential gap around the capsule to be sealed when in the clamped position, and wherein the clamping member further comprises a suction means adapted to provide an area of low pressure around the capsule after application of the sealing fluid so as to remove any excess sealing fluid from the capsule when in the same clamped position.

Abstract: A container assembly includes a container body, a container capable of being received within the container body, and a collar. The container body includes an upper end having a first compression surface. The container includes a first flange configured to engage the first compression surface. The collar is capable of being releasably secured to the container body. The collar includes a second compression surface. A dispensing portion includes a second flange configured to engage the second compression surface. When securing the collar to the container body, the first compression surface engages the first flange and the second compression surface engages the second flange to cause the first flange to sealingly engage the second flange.

Abstract: Systems, methods, and apparatus for gastric pressure relief, flow regulation, location, gastric residual volume, a placement reminder, bidirectional fluid flow markings, reintroducing gastric material, collection reservoir raising, collection reservoir hanging, a drain port, setting tube length, and vent membranes. A gastric pressure relief system is used in connection with an enteral feeding system, which includes a feeding container, administration tubing and a delivery tube, where the gastric pressure relief system is interposed between the administration tubing and the delivery tube. The gastric pressure relief system includes a collection reservoir with a gas vent to ambient atmosphere, relief tubing secured to both the collection reservoir and a multi-way connector. The multi-way connector joins the administration tubing to the relief tubing and a delivery tube at a point below a patient's stomach, which is designated on a placement reminder apparatus.

Abstract: A pacifier having a nipple portion and a handle portion separated by a collar. One or more sensors are disposed within the pacifier. The one or more sensors are configured to receive data from a user, wherein the user engages the nipple portion.

Abstract: The present invention comprises a new material used to form semi-rigid shapes. The new material comprises a specific blend of materials and a method of making the blend pertaining to temperatures and conditions. Items made of or comprising the new material in accordance with the invention will exhibit both suitable rigidity and durability along with long-lasting flavor to be used in the construction of a number of items, including teething devices, drinking cups, drinking straws and other utensils. The material itself and the inventive devices may be used to flavor other foods. For example, a teething device made from the flavor infused material encourages the child to use the device for longer periods, thereby providing better relief than prior art teethers. Flavored straws may be employed to add, or provided to blend, the flavor of the straw with the flavor of the liquid pulled through the straw. The flavor character is expected to last a minimum of 6 months and typically at least to 2 years or more.

Abstract: The present invention relates to a hardenable dental composition comprising (A) a curable component comprising curable moieties (AC), (B) a crosslinker component as component (B) capable of crosslinking said component (A), (C) a catalyst as component (C) capable of catalyzing a crosslinking reaction of component (A) and component (B), (D) polymeric particles as filler component (D), the polymeric particles having a maximum particle size of 150 ?m or below and being composed of organic polymers, silicone elastomers or a combination or mixture thereof and preferably (E1) an inorganic filler component having a BET surface from 50 to 400 m2/g. The invention also relates to the use of a polymeric particulate filler component (D) for producing a hardenable dental composition, the hardenable dental composition being in particular useful as dental impression or dental retraction material or for dental impression or dental retraction purposes.

Abstract: The present invention relates to a nonwoven sheet for a mask pack, which has the improved adhesion and attachment to the skin due to the good flexibility of a material, which has improved wettability with respect to cosmetics, and which secures self-supporting force and good strength. Specifically, the present invention relates to a nonwoven sheet for a mask pack, which includes split yarns formed from two or more types of thermoplastic resin.

Abstract: A wipe includes a cleansing composition disposed on a cloth. The cleansing composition can include an antiseptic, a humectant, an emollient, a surfactant, and a monohydric alcohol. A wipe can be made by preparing a cleansing composition and disposing the cleansing composition on a cloth. Two or more wipes may be included in a sealed package to maintain the sterile state of the wipes. A method of disinfecting skin can include applying a wipe to skin.

Abstract: Cosmetic compositions, including hair coloring compositions, comprising graphene oxide (GO), reduced graphene oxide (r-GO), or both, and water are provided.

Abstract: The present disclosure relates to the use of kaolin as an opacifier in cosmetic compositions, cosmetic compositions comprising kaolin and methods of making said cosmetic compositions.

Abstract: An oral care composition comprising zinc phosphate, sodium fluoride, stannous pyrophosphate, and an organic acid buffer system, as well as methods of using the same.

Abstract: The present disclosure relates to a product for care of keratinic fibers, in particular human hair, comprising a bag (pouch) comprising at least one sealed chamber, wherein the sealed chamber comprises at least one wall of one water-soluble film, and a conditioner composition which is in the sealed chamber of the bag (pouch) wherein the conditioner composition contains, based on its total weight (iia) from about 0 to about 20 wt % water and (iib) at least one fatty ingredient from the group of C8-C30 fatty alcohols and C8-C30 fatty acid triglycerides.

Abstract: The disclosure relates to an aqueous cosmetic composition that includes at least one effect pigment is present up to about 0.02 wt %, an emulsion of at least one oil and at least one surfactant, and at least one active selected to provide one or more benefits, including, but not limited to brightening/whitening, improvement of skin tone, blemish control or reduction, reduction of redness, anti-aging, and hydration, in an aqueous solvent. The composition may include a thickener and a preservative. Methods include forming the composition and applying the composition to the skin to provide an instant “glowing” or “brightening” effect.

Abstract: Disclosed herein are compositions of synephrine and a penetration enhancer and methods of reducing hair loss from pulling by applying the compositions. In one embodiment, the composition is a prewash composition comprising water, synephrine, and PEG-6 caprylic/capric glycerides.

Abstract: The present technology provides compositions that include a coenzyme, an epigenetic modifier, a blood circulator, a 5-alpha reductase modulator, and a cosmetically acceptable carrier, as well as methods of preparing and using such compositions. The present technology also provides methods of growing hair and/or stimulating hair growth where the method includes administering a cosmetically effective amount of a coenzyme and a cosmetically effective amount of an epigenetic modifier.

Abstract: The present disclosure relates to a cosmetic product cleaning and care of the keratinous, fibres, in particular human hair, comprising (i) a pouch, comprising at least one sealed chamber, wherein the sealed chamber has at least one wall made from a water-soluble foil, and (ii) a shampoo composition, which is present in the sealed chamber of the pouch, wherein the shampoo composition contains—relative to its total weight (iia) from about 0 to about 20 wt % water (iib) at least one anionic tenside and (iic) at least one cationic tenside.

Abstract: Orthodontic brackets promote the formation of bacterial biofilms in the human oral cavity, which lead to a variety of oral health problems, including plaque, gingivitis, and white spot lesions. Disclosed herein are methods and compositions for the preventing or inhibiting biofilm formation and associated diseases.

Abstract: The present invention relates to a composition that acts prior to the action of a tooth whitening composition or tooth whitening patch, the composition containing an oral cavity stimulation alleviating component able to reduce stimulation by the tooth whitening composition or patch. The present invention also relates to a tooth whitening kit whereby oral cavity stimulation is alleviated. The composition that acts prior to the action of a tooth whitening composition or patch of the present invention provides an outstanding tooth whitening effect while alleviating pain by mitigating intra-oral stimulation brought about by the rapid action of a tooth whitening component due to a tooth whitening component active agent.

Abstract: A novel anti-dandruff agent being a fumagillin derivative according to formula (I), and use of said agent as an anti-dandruff actives in anti-dandruff compositions, particularly shampoos and conditioners. The active is particularly effective against Malassezia yeasts and Malassezia furfur which may cause dandruff. A method of obtaining the fumagillin derivative from culturing of Peyronellaea sp. strain RKDO347 is also described.

Abstract: Embodiments of the present invention are directed to kits, compositions and methods for modifying and altering polysaccharide fillers and drug delivery systems with the application of an ascorbate.

Abstract: An object of the present invention is to provide a copolymer which is capable of forming a viscous aqueous solution having a desired viscosity in the presence of an electrolyte, in particular, a polyvalent electrolyte, a thickening agent comprising the copolymer, and a cosmetic preparation comprising the copolymer. The present invention relates to an acrylic acid ester (A)/compound (B) copolymer, comprising, as constitutional components, an acrylic acid ester (A) and a compound (B), wherein the acrylic acid ester (A) is represented by the general formula [1], and the compound (B) has, in each molecule, a polymerizable unsaturated group and any functional group selected from the group consisting of a carboxyl group, a sulfo group, and a phosphate group, and a weight ratio of the acrylic acid ester (A) and the compound (B), which is (A)/(B), is 9.0/91.0 to 28.5/71.

Abstract: The invention relates to a composition, especially a cosmetic composition, comprising at least one acrylic thickener and at least one oil, as well as to methods of using such compositions.

Abstract: Kit for formulation of a cosmetic product in emulsion form containing a composition A containing oil and a gelling agent which is in dispersed form, composition A containing less than 10% by weight of water, and an aqueous composition B, compositions A and B being packed separately. Compositions A and B are intended to be mixed on the spot to form a product in emulsion form which can be a make-up product, or for removing make-up or cleaning the skin or for care of the skin, mucous membranes, integuments or hair. Process of using product.

Abstract: An organic liquid soap composition; and a foam producing soap product comprising: a) a foamable organic liquid soap composition comprising the anti-microbial active ingredients of: organic shea butter; organic spearmint oil; USDA approved lime oil; organic thyme oil; and organic rosemary extract; and, b) a foam soap dispenser for dispensing the organic liquid soap composition as a premeasured amount of foaming soap, wherein the foam dispenser comprises: a recyclable plastic; a bottom front tab comprising a green color and a label indicating the composition is an organic soap. The organic soap composition may further comprise: glycerin; saponified organic coconut oil; organic olive oil; organic sunflower oil; organic jojoba oil; and organic aloe vera. And the organic soap composition has a shelf-life of about three years, and able to eradicate about 74.6% through 77.6% of the bacterial strain Staphylococcus aureus after at least one minute of direct contact with the composition.

Abstract: The present invention relates to a cosmetic cleansing composition comprising at least: a) one or more vegetable oil(s), in an amount of at least 0.3 pbw relative to the total weight of the composition, b) from about 2 pbw to about 40 pbw, relative to the total weight of the composition, of a surfactant system comprising at least one sultaine surfactant and one taurate surfactant, and c) at least 0.1 pbw, relative to the total weight of the composition, of a non-ionic solubilizer which is a mono- or poly- alkyl or alkenyl ester of an alkoxylated fatty acid.

Abstract: The present invention relates to a cosmetic composition for wrinkle reduction comprising, as an active ingredient, a Gynostemma pentaphyllum gypenoside fraction and, more specifically, to a cosmetic composition for wrinkle reduction, wherein the Gynostemma pentaphyllum gypenoside fraction includes at least one gypenoside selected from the group consisting of gypenoside UL1, gypenoside UL2, gypenoside UL3, gypenoside UL4, gypenoside UL5, gypenoside UL6, and gypenoside UL7.

Abstract: The disclosure provides pharmaceuticals, cannabinoids, and nutraceuticals and dermal patches, as well as chemicals that enhance delivery of pharmaceuticals from a buccal patch or from a dermal patch, where the patch may include a film, adhesive, emulsifier, tackifier, or hydrogel.

Abstract: Effective treatments of pain and/or inflammation are provided. Through the administration of a porous biodegradable drug depot film, patch, strip or sponge being implantable within a nasal or sinus cavity and having pores sized to prevent the depot from functioning as a scaffold for tissue growth, one can reduce, prevent or treat pain and/or inflammation and prevent cells from infiltrating the drug depot and laying down scaffolding cells.

Abstract: The present invention relates to a pharmaceutical formulation for vaginal administration, wherein the formulation comprises a pharmaceutical acceptable excipient and glucono ?-lactone, wherein the glucono ?-lactone is present in an amount of 5 to 99 wt % of the formulation. The invention also relates to a pharmaceutical formulation according to the invention for use in the prevention or treatment of a urogenital fungal infection. Furthermore, the invention relates to glucono ?-lactone (formula (III)), for use in the in the prevention or treatment of a fungal infection.

Abstract: Compositions and methods for inducing pterygium regression from visual axis/central cornea, stabilizing pterygium, treating hyperemia and symptoms in pterygium patients, and treating pterygium recurrence following pterygiectomy are disclosed. The methods include administration of a multikinase inhibitor, an antimetabolite or a combination thereof to patients in need thereof.

Abstract: The present invention relates to a process for preparing shaped articles for administration to animals, to the shaped articles obtainable according to the process and to their use.

Abstract: The present invention provides an O/W type emulsion having a volume median diameter of not more than 100 nm and containing a compound represented by the formula (1) wherein Xa and Xb are each independently X1, X2 or a 1,4-piperazinediyl group; s is 1 or 2, R4 is an alkyl group having 1-6 carbon atoms, na and nb are each independently 0 or 1, R1a, R1b, R2a and R2b are each independently an alkylene group having 1-6 carbon atoms, Ya and Yb are each independently an ester bond, or the like, and R3a and R3b are each independently a liposoluble vitamin residue or the like.

Abstract: Hybrid amphiphilic star copolymer nano micelles are prepared in the invention. Cage shaped octa(?-aminopropyl) silsesquioxanes is selected as the inorganic part, and L-glutamic benzyl ester-five membered ring anhydride is ring-opening polymerized by the initiation of amino groups on the surface of cage shaped octa(?-aminopropyl) silsesquioxanes, producing copolymers with cage shaped octa(?-aminopropyl) silsesquioxanes as nucleus and poly (L-glutamic-benzyl ester) as arms. The copolymers reacts with monomethoxy poly (ethylene glycol) carboxylic acid by condensation. Finally, the benzyl groups in the side chains of poly (L-glutamic acid-benzyl ester) are converted into hydrazine groups by acylhydrazination to obtain hybrid amphiphilic star copolymer nano micelles. The micelles can load doxorubicin, they are safe to human body and have good application prospects.