Abstract: In some embodiments, the present disclosure provides an exemplary method that may include steps of accessing a set of data records; receiving an instruction to perform an action; determining input data associated with the instruction; verifying the input data; identifying a pattern of behavior associated with each type of data; converting verified input data of a particular data type into a uniform secure data state; dynamically enabling a communication session between at least two security modules; orchestrating a delay within the communication session; and automatically programming a plurality of controls to modify the communication session.

Abstract: In some embodiments, the present disclosure provides an exemplary method that may include steps of accessing a set of data records; receiving an instruction to perform an action; determining input data associated with the instruction; verifying the input data; identifying a pattern of behavior associated with each type of data; converting verified input data of a particular data type into a uniform secure data state; dynamically enabling a communication session between at least two security modules; orchestrating a delay within the communication session; and automatically programming a plurality of controls to modify the communication session.

Abstract: In some embodiments, the present disclosure provides an exemplary method that may include steps of identifying a plurality of entities seeking to interact with each other; determining a set of artifacts associated with each entity of the plurality of entities; Utilizing a cloud-based functionality to dynamically connect at least two entities based on a determination of the set of artifacts shared between the at least two entities; dynamically integrating a plurality of protocols into an interaction session associated with the at least two entities; verifying the plurality of protocols associated with the interaction session; initiating the interaction session between at least two entities based on the plurality of protocols and the set of artifacts; and automatically modifying the interaction session to orchestrate a transfer of at least one artifact of the set of artifacts between the at least two entities.

Abstract: A water sorption device includes a catalytic combustor configured to, in a desorption state, combust a hydrocarbon fuel mixture to generate heat; a thermoelectric generator configured to, in the desorption state, generate electricity from a first portion of the heat from the catalytic combustor; and an adsorber configured to in an adsorption state, adsorb water from ambient air from an environment and in the desorption state, desorb the adsorbed water as vapor using a second portion of the heat from the catalytic combustor.

Abstract: A water sorption device includes a catalytic combustor configured to, in a desorption state, combust a hydrocarbon fuel mixture to generate heat; a thermoelectric generator configured to, in the desorption state, generate electricity from a first portion of the heat from the catalytic combustor; and an adsorber configured to in an adsorption state, adsorb water from ambient air from an environment and in the desorption state, desorb the adsorbed water as vapor using a second portion of the heat from the catalytic combustor.

Abstract: An air inflatable and thus collapsible when air is removed, safety helmet preferably comprised of multiple inflatable lobes with a head conforming and surrounding inflatable ring and separate or integrated skull cap, for wear by the user, for placement on top of the lobes and/or for location within the chamber(s) formed of the lobes, or worn by the wearer directly upon the head, made of flexible, force absorbing and dissipating material. The lobes and ring are provided with quick release air inflation and deflation valves. The safety helmet can simply alternatively comprise air inflatable lobes with a minimally elastic outer covering to encase and minimize the movement or air within the chambers during a collision.

Abstract: An air inflatable and thus collapsible when air is removed, safety helmet preferably comprised of multiple inflatable lobes with a head conforming and surrounding inflatable ring and separate or integrated skull cap, for wear by the user, for placement on top of the lobes and/or for location within the chamber(s) formed of the lobes, or worn by the wearer directly upon the head, made of flexible, force absorbing and dissipating material. The lobes and ring are provided with quick release air inflation and deflation valves. The safety helmet can simply alternatively comprise air inflatable lobes with a minimally elastic outer covering to encase and minimize the movement or air within the chambers during a collision.

Abstract: Described are transdermal and transmucosal pharmaceutical compositions exhibiting reduced skin or mucosa irritation potential comprising a phytoestrogen and an antioxidant, useful for reducing the skin or mucosa irritation associated with the use of transdermal or transmucosal drug delivery compositions. Methods of making and using the compositions also are described.

Abstract: The invention provides a system for characterizing a patient undergoing hemodialysis, featuring: 1) a body-worn biometric sensor, worn on a single location of the patient, and featuring: i) sensing elements for measuring electrocardiogram (ECG), thoracic bio-impedance (TBI), photoplethysmogram (PPG), and phonocardiogram (PCG) waveforms; ii) a processor for collectively analyzing the ECG, TBI, PPG, and PCG waveforms to determine a set of physiological parameters; and iii) a first wireless transceiver configured to transmit the set of physiological parameters; 2) a gateway system comprising a second wireless transceiver configured to receive the set of physiological parameters; and 3) a data-analytics system configured to analyze the set of physiological parameters to determine the patient's status.

Abstract: Described are methods for oral administration of therapeutic proteins and peptides, more specifically to the oral administration of therapeutic proteins and peptides with gastric acid modulators, and compositions of comprising a gastric acid modulator and a protein or peptide.

Abstract: Described are transdermal pharmaceutical compositions exhibiting reduced skin irritation potential comprising a steroid and an antioxidant, useful for reducing the skin irritation associated with the use of transdermal drug delivery compositions. Methods of making and using the compositions also are described.

Abstract: A system is described for breast imaging that includes spatially registering sequential mammographic images of the same breast. The system includes a first compression member configured to contact a first side of a breast, a second compression member configured to contact a second side of a breast that is substantially opposite the first side. The system further includes a first image sensor, coupled to the first compression member and configured to detect a position of a first fiducial marker located at the first side of the breast, and a second image sensor, coupled to the second compression member and configured to detect a position of a second fiducial marker located at the second side of the breast.

Abstract: A system is described for breast imaging that includes spatially registering sequential mammographic images of the same breast. The system includes a first compression member configured to contact a first side of a breast, a second compression member configured to contact a second side of a breast that is substantially opposite the first side. The system further includes a first image sensor, coupled to the first compression member and configured to detect a position of a first fiducial marker located at the first side of the breast, and a second image sensor, coupled to the second compression member and configured to detect a position of a second fiducial marker located at the second side of the breast.

Abstract: A system is described for breast imaging that includes spatially registering sequential mammographic images of the same breast. The system includes a first compression member configured to contact a first side of a breast, a second compression member configured to contact a second side of a breast that is substantially opposite the first side. The system further includes a first image sensor, coupled to the first compression member and configured to detect a position of a first fiducial marker located at the first side of the breast, and a second image sensor, coupled to the second compression member and configured to detect a position of a second fiducial marker located at the second side of the breast.

Abstract: A system is described for breast imaging that includes spatially registering sequential mammographic images of the same breast. The system includes a first compression member configured to contact a first side of a breast, a second compression member configured to contact a second side of a breast that is substantially opposite the first side. The system further includes a first image sensor, coupled to the first compression member and configured to detect a position of a first fiducial marker located at the first side of the breast, and a second image sensor, coupled to the second compression member and configured to detect a position of a second fiducial marker located at the second side of the breast.

Abstract: An infiltration cannula and method of using the infiltration cannula during an infiltration procedure are disclosed herein. The infiltration cannula has a flexible cannula and a hub. The cannula has a proximal end and a distal end. The cannula also has a plurality of apertures disposed in a pattern about the distal end. The apertures are configured to infiltrate fluid into the subcutaneous or muscle tissue of a patient. The hub is configured to be held by a person performing the infiltration procedure. The hub has a first end and an opposing second end. The first end is attached to the proximal end of the flexible cannula and the second end includes a connector configured to connect to an input source for receiving the fluid to be infiltrated into the subcutaneous tissue of the patient. The fluid flows from the connector, through the hub and into the cannula.

Abstract: An infiltration cannula and method of using the infiltration cannula during a tumescent infiltration procedure are disclosed herein. The infiltration cannula may have an outwardly flaring hub which may be wedged into an adit of a patient to minimize leakage of fluid being infiltrated into the patient. Also, the infiltration cannula may be utilized to hydrate a dehydrated patient by a medically untrained person. The infiltration cannula may also be used to deliver an antibiotic/vasoconstrictive drug solution to minimize surgical site infections.

Abstract: The present invention provides waterproof, breathable non-textile seamed articles which exhibit high levels of durability and allow wearers a high level of flexibility and article strength. This invention is of particular interest for use in dexterous hand coverings and conformable foot coverings.

Abstract: An infiltration apparatus, having a cannula, a flexible tubing connecting to one end of the cannula, a peristaltic pump comprising a pathway for the flexible tubing to extend through and a plurality of non-conductive rollers installed along the pathway to exerting force on the flexible tubing, a reservoir in fluid communication with the cannula via the flexible tubing extending through the peristaltic pump, a foot pedal pneumatically connected to the peristaltic pump to control operation thereof. The response of the foot pedal can be programmed into various modes. Under one of the modes, when the foot pedal is depressed, the peristaltic pump is switched on and remains as long as the foot pedal is depressed. Once the foot pedal is released, the peristaltic pump is switched off. Under another mode, one depression event, regardless how long the depression event lasts, the peristaltic pump is switched from on to off, or from off to on, and remains off/on before a next depression event occurs.

Abstract: A new and distinct strain of Trifolium repens (white clover) named ‘Coretta Clover’ is disclosed, characterized by its consistent ability to produce a higher percentage of compound leaves with four and five leaflets, in combination with its leaf shape. This unique strain exhibits a propensity for approximately 0.5% to 5% of its compound leaves to be four-leaf clovers and 0.075% to 0.75% to be five-leaf clovers, a significant deviation from the typical three-leaflet morphology common to the species. The distinctive traits are stable and reproducible in asexual propagation, providing a novel variety of Trifolium repens that combines aesthetic appeal with rarity, while maintaining the general hardiness and adaptability of the species. The strain's unique phenotypic traits are of particular interest for ornamental, agricultural, artistic, cultural, and commercial applications.