Abstract: Techniques for a patient support apparatus are provided to assist in transferring power/data to an external electronic device, such as a smartphone. The patient support apparatus comprises a support structure, a power supply and a portable charging device. The charging device comprises an energy storage unit and a receiving element coupled to the energy storage unit. The receiving element is configured to wirelessly receive power. A receptacle is coupled to the support structure and comprises a surface including a sending element being coupled to the power supply. The surface is configured to receive the charging device. The charging device is removable from the surface. The sending element is configured to wirelessly transfer power to the receiving element of the charging device such that the energy storage unit of the charging device stores the transferred power for charging an external electronic device.

Abstract: A transfer device is used to help a person move from one seated position at a first location to another seated position at a second location. The device is particularly useful for persons who cannot use their legs because the device is structurally supported to allow the person using the device to support himself by his arms and upper body muscles. The device is supported by the floor joists disposed below the floor. The person can have multiple support frames installed at different locations in his house so that the device can be moved from place to place as needed. Each location only requires a small hole to be cut in the floor with the unused holes being closed by plugs. The device allows the person to place his feet on a pivot disc while bracing his knees or shins against a knee board. The person then grasps handgrips and secures his forearms in an arm support assembly and lifts his lower body out of the first location.

Abstract: A device for supporting a patient's arm includes a rail clamp configured to be secured to a rail or other structure on a table such as an operating table. The rail clamp includes a clamp body and a socket configured to receive a base on an attachment such as a lateral brace. The base may be inserted longitudinally in the longitudinal socket on the rail clamp. The base may comprise an arm brace. The base is moveable in the longitudinal socket such that the arm brace may be raised or lowered relative to the rail clamp. The arm brace may be used when a patient is lying prone or laterally on a table.

Abstract: A surgical table includes a sagittal adjustment device for manipulating the position of a patient. The surgical table includes a base portion including an upper surface for spacing the sagittal adjustment device from the ground. The sagittal adjustment device includes a first support portion and a second support portion. The first and second support portions are supported by and moveable over the upper surface of the base portion. The first and second support portions each include an upper surface configured to support portions of the body of the patient thereon. One of the first and second support portions is pivotally attached to the base portion, and moveable between a first position and a second position. The pivotal movement between the first and second positions of the one of the first and second portions serves in repositioning the body of patient to manipulate the spine of the patient.

Abstract: The invention provides a wearable hand rehabilitation apparatus equipped on the back of users' hand. The wearable hand rehabilitation device could help the users to do their hand or finger rehabilitation. The wearable hand rehabilitation apparatus includes a thumb mechanism, three finger mechanisms and a pinky finger mechanism. These mechanisms could make the user's fingers bent or straightened. And the wearable hand rehabilitation apparatus could reduce the physical damage of the users during the period of doing rehabilitation with the present invention.

Abstract: An apparatus providing heat for treatment of an eyelid includes a heater unit configured to apply heat directly to an outer surface of the eyelid when an electrical signal is applied to the heater unit. The heater unit is affixed directly to the outer surface of the eyelid using an adhesive. A temperature regulator applies the electrical signal to the heater unit in order to achieve heating of the outer surface of the eyelid to a specified temperature range. A method is also disclosed that comprises affixing a heater unit directly into contact with the outer surface of the eyelid using an the adhesive. A control signal is applied to the heater unit to generate heat to the outer surface of the eyelid and is maintained for a period of time until the outer surface of the eyelid is heated to a specified temperature range.

Abstract: A pressure therapy device includes a pressure chamber, an inflatable padding, a seal, and a positioning mechanism. The pressure chamber has an opening arranged for admitting the inflatable padding and a limb of a user. The inflatable padding is inflatable to enclose and fix the limb in position. The seal covers the opening, including the inflatable padding and the limb to seal the pressure chamber from ambient atmospheric pressure. A pump unit is provided to generate a non-atmospheric pressure within the pressure chamber and includes a first valve system and a piston with safety release features for preventing unsafe pressure levels.

Abstract: Disclosed embodiments provide an improved personal massager device. The massager device includes a stimulator, which is G-spot stimulator or a prostate stimulator. The stimulator includes an enclosure having an opening. A threaded post is disposed within the enclosure. The threaded post has a plurality of pitched threads. A roller is disposed within the plurality of pitched threads. The roller protrudes outside the opening of the enclosure. The threaded post is rotated back and forth by a motor, and as it does so, the roller traverses a path. A sheath is disposed tightly over the enclosure. The roller presses the sheath against the G-spot or prostate of the user, providing stimulation. In some embodiments, one or more of a start position of the roller and an end position of the roller are defined by user input.

Abstract: Methods and systems are disclosed for capturing sensor data collected by a personal massaging device with associated sensors, analyzing the data, determining biofeedback data based on the sensor data, and according to some embodiments generating a sexual response profile based on the biofeedback data and a model of human sexual response. Data may be collected and analyzed for a number of uses, including but not limited to: (1) studying human sexual response, (2) adjusting outputs of the personal massaging device based on preset conditions, (3) treating sexual dysfunction conditions, and (4) improving sexual experiences.

Abstract: The invention provides a vibration massage apparatus wherein one or more vibrators which can be housed in rigid elongate capsules are supported by respective pairs of flexible members relative to a main body that can serve as a handle and/or a relatively non vibrational flesh-contacting surface, thus having a wide range of application and significantly optimizing user experience.

Abstract: Described herein are interactive devices that mimic a portion of a human male and a female genitalia. The male device includes a unique bead drive assembly for providing an extending and retracting motion. Also included on the male device is a massager sub-assembly able to inflate and deflate while being able to slide along a shaft of the male device. The female device includes a clamshell constrictor having an inflation mechanism that is able to provide a squeezing motion as well as being able to slide back and forth within the body of the female device. Also disclosed herein are method of communication and interaction between a pair of interactive devices or multiple interactive devices. Finally, methods of managing interactive sessions between multiple interactive devices are also described.

Abstract: A sexual stimulation method which may comprise a plurality of light sources for photostimulation of the vagina; one or more vibrators for mechanical stimulation of an area of the vagina; a handle; a controller and programmable memory for containing non-transitory instructions for modes of operation and driving the light sources and vibrators of the invention; a vaginal finger; a handle for ease of use; a keypad for user entry of commands; and a charging or programming port. The invention may also comprise sensors that sense physiologic parameters of a user and adjust sexual stimulation parameters to achieve a desired sexual stimulation effect. Blood oxygen level, temperature, pulse rate and muscle electrical activity may be sensed. The invention also may comprise a flexible covering that provides smooth sliding engagement with an area of the vagina of a user.

Abstract: A percussive massage device with a force meter that includes a housing, an electrical source, a motor positioned in the housing, a switch for activating the motor, and a controller configured to obtain a voltage of the motor, generate a lookup table correlating voltage to force applied by the percussive massage device, and display a force magnitude corresponding to the obtained voltage using the lookup table.

Abstract: A person's sleep disorders are resolved by applying low frequency vibration. Mechanical vibrators (1) present on a first side of a plate type base member (9) set the plate type base member (9) in vibration in such a way that its second surface transmits mechanical vibration. A plurality of first low frequency pulse trains (100; 101, 102, 103 . . . ) of mechanical vibration are conducted to a part of the person's body, at successive time periods (T; T1, T2, T3 . . . ). A frequency (f) of vibration in each individual pulse train (100) is maintained constant (f; fa, fb, fc . . . ) within the range of 20-50 Hz. The pressure pulses (400) of said pulse train (100) have a contact power (I) with said part of the body within the range of 40-70 dB. The constant frequencies (fa, fb, fc . . . ) of the successive pulse trains (100; 101, 102, 103 . . . ) are mutually different and change monotonously and mostly linearly. At least one second pulse train (100) is transmitted to said part of the body.

Abstract: An adjustable respirator shell, suitable for being worn on a human body trunk, includes a body, a belt and a buffer. The body includes a protrusive portion and a contact portion. The protrusive portion has an opening connecting a fluid pressure controller, and the contact portion is to contact the human body trunk. The belt, connecting the body, is to surround the human body trunk so as to fasten the adjustable respirator shell on the human body trunk. The buffer covers a circumference of the contact portion, and the contact portion contacts the human body trunk via the buffer. In addition, the buffer includes at least one cushion.

Abstract: A bathtub (1) which comprises: —a main body (2) having side walls (22, 22a, 22b), at least one of which presents an inner surface provided with guide means (3); —supporting means (4) engaged with guide means (3) and configured for supporting at least a portion of user's body in order to allow, in use, simulating user flotation.

Abstract: A cartridge, which may be suitable for use as a portion of a transdermal drug delivery apparatus, may include a body at least partially defining an interior for containing fluid for being delivered by the transdermal drug delivery apparatus. The body may also at least partially define first and second openings to the interior of the body, wherein the first and second openings are respectively proximate opposite first and second ends of the body. The cartridge may also include a self-sealing member at least partially closing the first opening, and a movable member at least partially closing the second opening, wherein at least a portion of the movable member is for being urged into the interior of the body for increasing pressure within the interior of the body.

Abstract: A mount for supporting a cylindrical bottle includes an annular core having an inner side surface defining a hollow opening, an outer side surface, a top surface and a base surface. A plurality of pliable ribs each at least partially encircles the annular core so as to overlap the outer side surface, the top surface and the base surface such that at least an upper end of each rib where it overlaps the top surface extends into the hollow opening. The mount may be used in conjunction with a collar having a body portion for surrounding the bottleneck and defining along at least a portion of an axis thereof a substantially quadrilateral cross-section having in each corner thereof a respective arcuate recess.

Abstract: Methods and apparatus for preparing autologous blood serum eye drops within a potentially contaminating environment are disclosed. Key convenience kit apparatus providing novel methodology includes a plastic bag in which an innovative tray securely holds a plurality of empty eye drop bottles and associated caps disposed and sealed therein. Providing the only access pathway into the bag is a sterilizing filter appliance which filters all fluid entering the bag and provides a nozzle for dispensing into bottles disposed in the tray. The key convenience kit apparatus is sterilized prior to use, assuring all components disposed within the bag are within a desired sterility assurance level. The sterilized state of items associated with the key apparatus is maintained by the single pathway for fluid. Capping and sealing the bottles before opening the bag permits delivery of sterile product for use outside the bag.

Abstract: Low dose pharmaceutical formulations may be prepared to deliver consistent low doses of a variety of pharmaceuticals with minimal additives. In particular, the low dose pharmaceutical formulations are solid unit dosage forms of low dose drug substances which may be prepared by a method that provides content uniformity across prepared solid unit dosage forms.

Abstract: Described herein is a medication crushing, grinding, and administering device generally adapted to transform a solid pharmaceutical into a powered form for dissolving into a fluid within a syringe body. The device includes a plunger portion including the working portion of the device in the form of a blade generally extending from the plunger portion and configured for rotation. The rotating blade manipulated within an interior of the syringe body for generally breaking apart a pill within the syringe body for dispersal into a solution for administering.

Abstract: A syringe assembly (2) comprises a syringe barrel (4) comprising an inner chamber (14) filled or adapted to be filled with medicament, and a channel (18) in fluid communication with the chamber and through which medicament is dispensed. The assembly further comprises an outer sheath (6) configured to be removably attached to the syringe barrel, and comprising a projection (40) which is received by the channel when the outer sheath is attached to the barrel, thereby creating a seal, which prevents medicament from flowing therethrough.

Abstract: A liquid dispensing system for oral administration comprises a dispenser (16,18,20) and cartridges (14) from which medicine is dispensed. Each cartridge (14) includes a hollow shell (22,24) with a septum (26) at one end, a piston (28) at the other end, and the medicine in a cavity (23) between the septum and the piston. The dispenser includes receiver (20) in which a cartridge (14) is received, a plunger (18) that can slide relative to the receiver and that has a plunging head (52) that can drive the piston (28), and a barrel (16) in which the cartridge (14), receiver (20) and plunger (18) can be received, at least partly. Once a cartridge (14) has been inserted into the receiver (20), the receiver and cartridge are inserted into the barrel (16) and a piercing head (44) ruptures the septum (26). The plunger (18) is pushed to drive the piston (28) and the medicine is dispensed by the piston, through a discharge passage (42) of the barrel (16).

Abstract: In an apparatus for dispensing, a dispenser includes a housing, a reservoir housed within the housing, a chute in fluid communication with the reservoir, wherein the chute is adjacent to the reservoir, a user input device, a power source housed within the housing, a logic housed within the housing, wherein the power source powers the logic, a motor housed within the housing, wherein the power source powers the motor, wherein the logic controls the motor, a gear train housed within the housing, wherein the motor drives the gear train, a first platform defining an opening, wherein a portion of the first platform abuts a bottom portion of the chute when the dispenser is in a non-dispensing state, and a second platform including a well, wherein the gear train is configured to rotate the second platform relative to the housing, and wherein when the logic sets the dispenser to a dispensing state a position of the well is adjustable relative to the housing via the user input device, such that the well substantially

Abstract: A medication dispensing apparatus includes a housing for at storing at least one medication in bulk, a dispenser and a verification sensor. The at least one medication including a plurality of doses of the at least one medication. The dispenser separates a single dose from the at least one medication in bulk. The dispenser moves the single dose of the at least one medication from a position within the housing to a position outside the housing. The verification sensor verifies that the at least one medication is a correct medication.

Abstract: A pill dispensing assembly comprises a pill bottle that is securely locked between a base and an attachable sleeve. The pill bottle and base form an enclosure in which pills are stored above a top portion of a dosing mechanism of the base. The top portion of the dosing mechanism comprises a ramp and a rotating arm that carries a pill from a base of the ramp to a position in which the pill will drop through an aperture in a bottom portion of the dosing mechanism into a channel that connects the aperture to a dispensing slot in a housing of the base. The base includes a microcontroller that interacts with a servomotor to control rotation of the arm and thereby the dispensing of a pill. The base also includes a wireless communication interface that enables the dispensing of the pill to be controlled by a remote entity.

Abstract: In one aspect of the invention features nursing bottle. The nursing bottle includes a container for holding a liquid and having a rim defining an open end and a nipple assembly secured to the container at the open end. The nipple assembly includes a flexible nipple extending away from the container and defining an interior nipple volume, a vent bulb disposed within the interior nipple volume and defining an interior bulb volume, a tube extending into the container to a distal end disposed in a closed end of the container, and a vent manifold. The vent manifold defines a first aperture providing fluid communication between the container and the interior nipple volume, a second aperture providing fluid communication between the tube and the interior bulb volume, and a vent conduit providing fluid communication between the interior bulb volume and atmosphere.

Abstract: A system for purging air from a feeding line is set forth. The system includes a charging device configured to selectively provide an air charge in the system. A restricting tubing can be located between the charging device and a delivery tube. The restricting tubing can be configured to tunably limit the air charge delivered from the charging device to the feeding line through the delivery tube.

Abstract: A glass based fibrous filler having bioactive particles such as hydroxyapatite deposited on a surface of glass fibers. Methods of preparing the fibrous filler are specified. A resin composite containing a polymerizable system reinforced with the fibrous filler, as well as a biomedical restoration based on the cured resin composite are also provided.

Abstract: A method of manufacturing a series of capsules (1A) comprising a core (3), and a gelled envelope (5) completely encapsulating the core and comprising at least two external phases (5A, 5B), wherein the gelled envelope has a external surface comprising at least two distinct portions (7A, 7B) formed respectively by the two external phases, and comprising the following steps: conveying a first flow (F1) that is intended to form the core, and a second flow (F2) of at least the two external phases that are intended to form the gelled envelope, wherein each external phase contains a liquid polyelectrolyte that is able to gel, at least one of the two external phases comprising a coloring agent, while the second flow surrounds the first flux about an axis (D2); successive formation of a plurality of liquid bodies (57) comprising a drop (107), and a film coating (109) coating the drop and having the two external phases, wherein the film has on its external surface at least two portions (109A, 109B) formed by the two

Abstract: The present invention provides methods for preparing emulsions of silicone fluids having pituitous rheological properties. The present invention also provides emulsions of a silicone fluid having pituitous rheological properties and composition comprising the emulsions. The compositions include, but are not limited to, personal care compositions and compositions for hair shampoo, hair conditioner, hair treatment composition, or skin care product.

Abstract: Disclosed is a long wearing cosmetic product with elegant glide and feel with cooling sensation and impactful color intensity with high coverage. The disclosed combination of a silicone resin, an ethylenic polymer including a monomer having a bicyclic group, and a taurate copolymer provides a flexible/soft film on eye lids which is not brittle and wears longer for hours.

Abstract: Zinc oxide compositions and methods for applying anti-reflective coating on oxide particles for sunscreen applications are provided herein. A composition includes multiple zinc oxide particles suspended within a medium forming sunscreen composition, and two or more coating materials applied to each of the multiple zinc oxide particles in distinct layers via a gradation based on refractive index, wherein each of the coating materials has a refractive index that is between the refractive index of air and the refractive index of zinc oxide, and wherein the two or more coating materials comprise zinc sulfide and titanium dioxide.

Abstract: The invention relates to i) a process for treating keratin fibres, in particular human keratin fibres such as the hair, employing a) at least one oxidized polysaccharide, in particular oxidized inulin, and b) at least one (poly)saccharide with amine group(s); ii) a composition comprising the ingredients a) and b); iii) the use of a) and b) to treat keratin fibres, in particular human keratin fibres such as the hair, and iv) a multi-compartment kit or device comprising a) and b). The invention makes it possible to obtain good hair-conditioning cosmetic properties, with a long-lasting effect.

Abstract: The instant disclosure relates to masks, methods for making masks, methods for improving film elasticity of masks, and to methods of treating skin with masks. The masks are formed by applying a mask base composition onto a surface, the mask base composition comprising: (i) alginic acid and/or a salt thereof; (ii) hectorite (lithium magnesium sodium silicate); (iii) one or more water-soluble solvents; and (iv) water; and exposing the mask base composition to a crosslinking composition for a time sufficient to crosslink the alginic acid and/or a salt thereof and form a final mask, the crosslinking composition being an aqueous liquid comprising (i) one or more polyvalent cations of one or more metals; and (ii) water. The instant disclosure further relates to masks formed by the disclosed methods and to kits comprising the compositions for making and/or using the masks.

Abstract: To provide an oil in water type solid cosmetic composition which can be solidified into a stable solid shape, has a desired sensation of elasticity, has favorable take up properties when taken up with a finger, and imparts a superior sensation of freshness when utilized, as an oil in water type preparation. An oil in water type solid cosmetic includes: (a) 0.1 to 5% by mass of a hydrophobically modified polyether urethane; (b) 0.01 to 5% by mass of a hydrophilic plate shaped powder; (c) a hydrophobic powder; (d) an oil component; and (e) water.

Abstract: Provided is a resin-linear organopolysiloxane block copolymer which has a high degree of freedom in formulation due to excellent compatibility with other materials, in addition to exhibiting excellent film forming properties and followability of a film, while the stickiness of a film is suppressed. The resin-linear organopolysiloxane block copolymer has: a resin structure (A1) block that has siloxane units represented by R1SiO3/2 (wherein R1 represents a monovalent organic group, a hydroxyl group, or an alkoxy group having 1 to 6 carbon atoms) and SiO4/2; and a linear structure (A2) block represented by (R2SiO2/2)n (wherein n represents a number of 5 or more while R represents an alkyl group, a fluoroalkyl group, or an aryl group) in each molecule. The resin structure (A1) and the linear structure (A2) are linked to each other by an Si—O—Si bond, and an Si atom bonded to the resin structure (A1) constitutes an RSiO3/2 unit.

Abstract: Biodegradable copolymers for cosmetic use are described, obtained by reaction between lactide and a silicone initiator. Said copolymers are used for the preparation of cosmetic products such as lipsticks, facial cosmetic powders, creams, eyeliners, eye shadows.

Abstract: The present disclosure provides a non-autologous product that is a mixture of two or more cells or tissue cultures of fibroblast, or extracts from cultures, or media cultures, isolated from separate individuals, either homogeneous or heterogeneous. The cells or factors are blended together in a product that imparts desired characteristics to the skin of a recipient who is not a source of the mixture. The present disclosure also relates to methods of making and using and/or culturing the fibroblasts including to optimize the potency of the mixture to impart one or more the desired characteristics to the skin of a recipient.

Abstract: Particles, compositions, and methods that aid particle transport in mucus are provided. The particles, compositions, and methods may be used, in some instances, for ophthalmic and/or other applications. In some embodiments, the compositions and methods may involve modifying the surface coatings of particles, such as particles of pharmaceutical agents that have a low aqueous solubility. Such compositions and methods can be used to achieve efficient transport of particles of pharmaceutical agents though mucus barriers in the body for a wide spectrum of applications, including drug delivery, imaging, and diagnostic applications. In certain embodiments, a pharmaceutical composition including such particles is well-suited for ophthalmic applications, and may be used for delivering pharmaceutical agents to the front of the eye and/or the back of the eye.

Abstract: The disclosure relates to multilayer polymeric matrix based medical devices. In one example, a device comprises an inner first polymeric matrix and an outer second polymeric matrix. The addition of second polymeric matrix modifies bulk properties of each matrix thus resulting in a device where specific bulk properties are incorporated. The disclosure also relates to methods of manufacturing various embodiments of medical devices and their uses.

Abstract: A method is provided for improving lung function in COPD by administering a muscarinic antagonist with a high efficiency nebulizer.

Abstract: A method of reducing a friction coefficient of a surface is disclosed herein, comprising attaching a water-soluble polymer to the surface, and contacting the water-soluble polymer with liposomes, thereby coating the surface with an amphiphilic lipid. Further disclosed herein are solutions comprising a water-soluble polymer attachable to the surface, liposomes, and an aqueous carrier, for reducing a friction coefficient of a surface, and methods utilizing same. Articles of manufacture comprising a substrate coated by a water-soluble polymer which is coated by an amphiphilic lipid are also described, as are uses and methods for treating a synovial joint disorder associated with increased articular friction.

Abstract: This disclosure relates to a targeted PEGylated liposomal gemcitabine (PLG) composition comprising a PEGylated liposome encapsulating one or more agents comprising gemcitabine and a targeting moiety; pharmaceutical composition and methods comprising PLG or producing PLG; and manufacturing equipment for performing the methods.

Abstract: A pharmaceutical composition for colon targeting, a method for treating a colon-related disease using the same and a preparation method thereof are disclosed. The pharmaceutical composition of the present disclosure comprises: a core matrix comprising a cross-linked hydrogel and an active ingredient, wherein the active ingredient is dispersed in the cross-linked hydrogel, and a content of the active ingredient is 65 wt % to 95 wt % based on a total weight of the core matrix.

Abstract: The invention discloses a double-layer tablet, wherein one layer has hole in which the ingredients of the other layer are filled; the number of said hole is 1-3, the diameters of the holes are 1-10 mm. Each layer of the double-layer tablet includes the active ingredients and the adjuvant materials and can be the rapid-release layer or sustained-release layer respectively. The preparation method: Preparing respectively a component I and a component II, both of them containing the active ingredients and the pharmaceutical excipients, and preparing the tablet having holes from component I; Forming the double-layer tablet composed of the component I layer and the component II layer after pressing said tablet having holes with the component II together; and filling the component II into the holes during compressing.

Abstract: The invention is directed to pharmaceutical compositions such as tablets that exhibit delayed release properties when administered as either whole or half tablets. The invention is also directed to delayed release tablets comprising deferiprone for oral administration, for which twice daily administration is bioequivalent to the same daily dose of an immediate release tablet administered thrice daily. The invention is also directed to methods of making and using the same.

Abstract: The invention is directed to pharmaceutical compositions such as tablets that exhibit delayed release properties when administered as either whole or half tablets. The invention is also directed to delayed release tablets comprising deferiprone for oral administration, for which twice daily administration is bioequivalent to the same daily dose of an immediate release tablet administered thrice daily. The invention is also directed to methods of making and using the same.

Abstract: Improved oral dosage forms of methyl hydrogen fumarate and prodrugs thereof are disclosed. Methods of treating diseases such as multiple sclerosis and psoriasis using such dosage forms are also disclose.

Abstract: The present disclosure provides methods and compositions related to nanoparticles comprising an encapsulated hydrophobic drug. The methods described herein provide nanoparticles having a small size and a narrow size distribution.