Abstract: A topical temperature therapy device that imparts known temperatures as a function of time to the therapy skin surface of a user during the course of therapy. The skin surface can be intact or breached through injury or surgery. The therapy temperature and time profile can be varied by varying the selections of, among several parameters, the formulation of the heat exchange material and the material and dimensions of the heat exchange material container, thus meeting the needs of a wide range of injuries and demographics. The therapy device contains a temperature indicator indicating the temperature of the heat exchange material in real time. The therapy device further provides visibility to the therapy skin surface during the course of the therapy to allow visual inspection of the therapy area as means to improve therapeutic outcomes. The therapy device is flexible and conforms to the anatomy of the therapy area.

Abstract: A topical cooling compressive hemostasis wound healing device and methods thereof for affecting a percutaneous access site wound or an acute surgical wound. The device delivers and transports cooling to affect and control vasculature and musculoskeletal motions surrounding the injury site during the blood coagulation, hemostasis, and wound healing phases. The device has a viscoelastic and thermally conductive surface to deliver and transport an adjustable compressive pressure to resist outward blood flow, thus improving patient safety and clinical outcomes. The device is anatomically conforming and treats not only the specific injury site, but also its surrounding anatomical structures together as means to prevent unpredictable delayed hemostasis breach. The device provides comfort to the patient by allowing mobility upon wound healing, thus reducing back pain and strain resulting from being in a constrained position for a prolonged period of time which is known to cause additional medical events.

Abstract: This invention discloses a topical cooling compressive hemostasis and wound healing device and methods thereof for affecting a percutaneous access wound or an acute surgical wound where the device is compatible with physiological, circulatory and cellular microenvironments of the injury and conforming to the injury site anatomy. The device promotes hemostasis, sustains hemostasis and improves wound healing quality by controlling and affecting vasculature motions of the injury site during various wound healing phases. The device incorporates an elastic material compatible with the elastic nature of the injured vessel to promote comfort and safety. The elastic material is further thermally conductive to deliver and transport cooling and a therapeutic agent to the wound site. The device further incorporates an anatomically conforming lateral stabilization component to stabilize the injury sits and its surroundings.

Abstract: A topical cooling compressive hemostasis wound healing device and methods thereof for affecting a percutaneous access site wound or an acute surgical wound. The device delivers and transports cooling to affect and control vasculature and musculoskeletal motions surrounding the injury site during the blood coagulation, hemostasis, and wound healing phases. The device comprises a viscoelastic and thermally conductive surface to deliver and transport an adjustable compressive pressure to resist outward blood flow, thus improving patient safety and clinical outcomes. The device is anatomically conforming and treats not only the specific injury site, but also its surrounding anatomical structures together as means to prevent unpredictable delayed hemostasis breach. The device provides comfort to the patient by allowing mobility upon wound healing, thus reducing back pain and strain resulting from being in constrained position for a prolonged period of time which is known to cause additional medical events.

Abstract: The present invention relates to a catheter with an expandable distal end for delivering one or more medicaments. The catheter is manufactured with materials of construction that allow the transfer of electrical energy from the proximal end of the catheter to the distal expandable end. The catheter also has a means for controlling or manipulating the expandable distal end to expand and contract into various configurations. The distal end of the catheter is processed by a specific method of manufacturing whereby the expandable distal end is coated with one or more layers of a hydrogel copolymer wherein at least one layer of which coating encapsulates one or more medicaments and zero or more charged carriers to facilitate the electrophoretic and electro-osmostic mobilities of the medicaments.

Abstract: The present invention relates to a catheter with an expandable distal end for delivering one or more medicaments. The catheter is manufactured with materials of construction that allow the transfer of electrical energy from the proximal end of the catheter to the distal expandable end. The catheter also has a means for controlling or manipulating the expandable distal end to expand and contract into various configurations. The distal end of the catheter is processed by a specific method of manufacturing whereby the expandable distal end is coated with one or more layers of a hydrogel copolymer wherein at least one layer of which coating encapsulates one or more medicaments and zero or more charged carriers to facilitate the electrophoretic and electro-osmostic mobilities of the medicaments.

Abstract: The present invention comprises method of detecting biomolecules in situ in gel separation medium following electrophoresis that provides sensitivity similar to blotting. This method is applicable to in situ detection of a wide range of biomolecules including proteins and nucleic acids. After electrophoretic separation of a sample in gel separation media comprising a gellable polymeric material other than cross-linked polyacrylamide, the gel is contacted with a solution comprising at least one detectably labeled reagent directed to a biomolecule under conditions suitable for binding of the reagent to the biomolecule. Alternatively, the gel is contacted with a solution comprising at least one non-detectably labeled reagent directed to a biomolecule and a solution comprising at least on detectably labeled reagent directed to a biomolecule. In either case, binding of the detectably labeled reagent is assessed and indicates detection of biomolecules in the gel.

Abstract: The present invention provides various electrophoretic apparatuses for discontinuous gel electrophoresis. One apparatus comprises a vessel and a removable gel cassette for holding the gel, the cassette divided into two separate compartments, each in fluid communication with a buffer reservoir. Access holes provided on the top of the cassette allow sample to be added to the gel inside the cassette. The cassette also optionally includes a gel viewing window and sample loading window. Another apparatus comprises a vessel with a raised platform in the middle on which the gel is placed and over which a gel restraining frame, generally rectangular in shape, is secured close to the gel surface. The frame when in place acts as a barrier to movement of electrode buffer between reservoirs. The frame and an open interior for buffer or fluid, which assists in gel cooling during electrophoresis.

Abstract: In accordance with the present invention, there are provided methods for the separation of biological materials employing a variety of polymeric materials with defined chemical, physical and mechanical properties. Thus, a wide range of biological materials (i.e., from very low to very high molecular weight) can be separated according to the present invention. Polymeric materials contemplated for use in the practice of the present invention are block copolymers of partially hydrolyzed acrylonitrile which have excellent storage stability, are chemically inert, contain minimal residual concentration of monomeric species, and can be prepared in large scale.

Abstract: Disclosed is a free-radical addition polymer containing from 55 mole percent to about 95 mole percent of units derived from maleic anhydride and from about 5 mole percent to about less than 45 mole percent of units derived from 1-alkenes having at least 4 carbon atoms wherein the polymer has an average of at least one unit derived from a 1-alkene per polymer chain making up the polymer based on the number average molecular weight of the polymer and thus contains excess units derived from maleic anhydride randomly dispersed throughout the polymer. The polymers are useful in detergents as stabilizers, additives to floor polishes and, especially when esterified with alcohols, as surfactants.