Abstract: A system for converting an existing hand push wheelbarrow to a powered wheelbarrow by way of a single unit kit that comprises a motorized wheel, a battery, and all other necessary electrical components. The system includes wheel brackets with mounting holes sized to fit most standard wheelbarrows, so that the original passive wheel can be easily removed, and the Kit installed using the same mounting hardware. The larger of the two mounting brackets supports the component case with the battery and the motor controller, and acts as the heat sink for all the heat generating electronics within the case. This enables the entire system to be sealed and waterproof. The Kit is intended to be used in situations where heavy loads need to be transported by wheelbarrow over bumpy ground or up inclines, and motorized assistance to propel the wheelbarrow may be needed.

Abstract: Apparatus and methods for repairing a cardiac valve, e.g., a tricuspid valve, are provided. The apparatus may include a prosthetic device coupled to an elongated support to suspend and maintain the prosthetic device within the cardiac valve. The support may include a proximal elongated shaft detachably coupled, in a delivery state, to a distal elongated shaft coupled to the prosthetic device. The proximal elongated shaft may detach from the distal elongated shaft at a detachment area within the patient responsive to actuation and components of the distal elongated shaft may lock to implant the prosthetic device and the distal elongated shaft within the patient. The prosthetic device may be formed of biocompatible material coupled to a frame, and may have prosthetic leaflets that allows blood to flow through in one direction during a phase of the cardiac cycle (e.g., diastole) but prevent blood regurgitation during the other phase (e.g., systole).

Abstract: Apparatus and methods for repairing a cardiac valve, e.g., a tricuspid valve, are provided. The apparatus may include a prosthetic device coupled to an elongated support to suspend and maintain the prosthetic device within the cardiac valve. The support may include a proximal elongated shaft detachably coupled, in a delivery state, to a distal elongated shaft coupled to the prosthetic device. The proximal elongated shaft may detach from the distal elongated shaft at a detachment area within the patient responsive to actuation and components of the distal elongated shaft may lock to implant the prosthetic device and the distal elongated shaft within the patient. The prosthetic device may be formed of biocompatible material coupled to a frame, and may have prosthetic leaflets that allows blood to flow through in one direction during a phase of the cardiac cycle (e.g., diastole) but prevent blood regurgitation during the other phase (e.g., systole).

Abstract: Apparatus and methods for repairing a cardiac valve, e.g., a tricuspid valve, are provided. The apparatus may include a prosthetic device coupled to an elongated support to suspend and maintain the prosthetic device within the cardiac valve. The support may include a proximal elongated shaft detachably coupled, in a delivery state, to a distal elongated shaft coupled to the prosthetic device. The proximal elongated shaft may detach from the distal elongated shaft at a detachment area within the patient responsive to actuation and components of the distal elongated shaft may lock to implant the prosthetic device and the distal elongated shaft within the patient. The prosthetic device may be formed of biocompatible material coupled to a frame, and may have prosthetic leaflets that allows blood to flow through in one direction during a phase of the cardiac cycle (e.g., diastole) but prevent blood regurgitation during the other phase (e.g., systole).

Abstract: A sling with multiple openings may be installed in a mitral valve annulus. Within each opening, individual valves may be placed. The sling and valves may be delivered via catheter, and in some cases, the catheter size may be 18 French or smaller. The sling may have a cuff that may block otherwise open areas of the opening. The sling may be installed using commissural attachments that engage a mitral valve near the commissural point. The sling, valves, and cuff may be installed without stopping the heart, and because multiple valves are used, much smaller valves can be used, thereby reducing the catheter size.

Abstract: A system includes a first chamber configured to receive a hydrogel and a scaffold comprising a cell, wherein the hydrogel is in fluid communication with the scaffold, and wherein the hydrogel includes a plurality of unidirectional pores. The system also includes a second chamber configured to receive a first fluid and a second fluid, wherein the second chamber includes a wall that separates the first fluid from the second fluid. The system further includes a porous membrane configured to separate the first chamber from the second chamber. The wall is configured to move along the porous membrane as cellular extensions are projected into at least a portion of the plurality of unidirectional pores of the hydrogel.

Abstract: A valve assembly with an exchangeable valve member and a docking station, and a tool set that facilitates the exchange of a valve member. The tool set includes a stabilizer or holding tool for holding the docking station during an exchange procedure, a valve extraction or removal tool for removing an existing valve member from an installed docking station, and an insertion tool for installing a replacement valve member.

Abstract: A process for the synthesis and purification of F-series prostaglandin compounds and synthetic intermediates used to prepare them. The synthetic intermediates are solid and may be purified by precipitation and therefore may form the representative F-series prostaglandin compounds such as latanoprost, bimatoprost, fluprostenol, cloprostenol, and substituted analogs therefrom in highly pure forms.

Abstract: A system for generating a tissue construct includes a mixing chamber, a piston chamber, a reaction chamber, and a pump. The mixing chamber is configured to receive a hydrogel solution and a cell suspension solution. The piston chamber includes a first piston and is configured to receive a mixture of the hydrogel solution and the cell suspension solution from the mixing chamber. The first piston is configured to push the mixture through one or more capillaries into the reaction chamber. The reaction is configured to receive the mixture and a cross-linking initiator. The pump is configured to move the mixture through the reaction chamber such that the mixture and the cross-linking initiator combine to form an encapsulated cell material.

Abstract: A resizable valve base for a cardiovascular valve assembly that is comprised of the resizable valve base and a valve member that is detachably coupled thereto. The resizable valve base has adjustable dimensions to allow use with both small and large size valve members. The valve base comprises a frame comprised of a plurality of frame sections, and each frame section includes a mounting portion and a pair of arcuate portions extending from opposite sides of the mounting portion. The valve base also includes a plurality of joining elements for joining together the frame sections to define a generally cylindrical opening having a diameter, wherein said plurality of joining elements allow adjacent frame sections to move towards or away from each other in order to modify the diameter of the opening, thereby moving the valve base between a collapsed position and an expanded position.

Abstract: A method and apparatus for facilitating transapical removal of a prosthetic heart valve, i.e., percutaneously implantable valve (PIV), without open-heart surgery. The apparatus includes a holding tool for holding the PIV, a cutting tool for separating the PrV from fibrotic tissue accumulating around the PIV, and a removal tool for extracting the PIV from the heart.

Abstract: Tools for the removal and installation of exchangeable cardiovascular valves. The tools facilitate rapid exchange of a cardiovascular valve member mounted in the aortic position (retrograde exchange) or the mitral position (transapical exchange).

Abstract: A system for generating a tissue construct includes a mixing chamber, a piston chamber, a reaction chamber, and a pump. The mixing chamber is configured to receive a hydrogel solution and a cell suspension solution. The piston chamber includes a first piston and is configured to receive a mixture of the hydrogel solution and the cell suspension solution from the mixing chamber. The first piston is configured to push the mixture through one or more capillaries into the reaction chamber. The reaction is configured to receive the mixture and a cross-linking initiator. The pump is configured to move the mixture through the reaction chamber such that the mixture and the cross-linking initiator combine to form an encapsulated cell material.

Abstract: A system includes a first chamber configured to receive a hydrogel and a scaffold comprising a cell, wherein the hydrogel is in fluid communication with the scaffold, and wherein the hydrogel includes a plurality of unidirectional pores. The system also includes a second chamber configured to receive a first fluid and a second fluid, wherein the second chamber includes a wall that separates the first fluid from the second fluid. The system further includes a porous membrane configured to separate the first chamber from the second chamber. The wall is configured to move along the porous membrane as cellular extensions are projected into at least a portion of the plurality of unidirectional pores of the hydrogel.

Abstract: A process for the synthesis and purification of F-series prostaglandin compounds and synthetic intermediates used to prepare them. The synthetic intermediates are solid and may be purified by precipitation and therefore may form the representative F-series prostaglandin compounds such as latanoprost, bimatoprost, fluprostenol, cloprostenol, and substituted analogs therefrom in highly pure forms.

Abstract: Technologies are generally described for an adjustable display screen such as for a notebook computer or other portable device. In some examples, at least one display screen rail may be rotatably coupled to a back edge of a notebook computer base unit at a hinge rod. The display screen of the notebook computer may slide along and/or pivot on the at least one display screen rail in a direction to bring the display screen toward a user of the notebook computer while leaving room for the user to access a keyboard located on a top surface of the base unit. Mechanisms may be coupled to the notebook computer to transmit motion of the display screen along a first display screen rail to motion of the display screen along a second display screen rail, thereby mitigating binding of the display screen as it slides along the display screen rails.

Abstract: A collapsible docking station for a valve assembly that includes the collapsible docking station and an exchangeable valve member detachably coupled thereto. The collapsible docking station includes a band that is moveable between a collapsed position where the band forms a wound coil, and a fully expanded position where the band forms a circular ring.

Abstract: A multi-function valve exchange apparatus including an alignment tool for locating tools of the multi-function valve exchange apparatus proximate to an installed cardiovascular valve assembly comprised of a base member and an exchangeable valve member detachably coupled thereto; a stabilizer tool for grabbing the base member and preventing the base member from moving during a procedure for exchanging the existing valve member with a new valve member; removal and collapsing tools for uncoupling and removing the existing valve member; and an installation tool for installing a new exchangeable valve member having a new leaflet set. A method for exchanging a valve member uses the multi-function valve exchange apparatus to facilitate removal of the existing exchangeable valve member and installation of the new exchangeable valve member.

Abstract: A temporary subvalvular check valve has a collar and an expandable seal structure connected by pivotable struts that together support flexible leaflets. The check valve can be introduced along a tool shaft and positioned in a chamber or vasculature by expanding the seal structure against an adjacent wall. Cardiac function is augmented during valve procedures, such as valve excision, valve implantation, or valve leaflet replacement, by placing the temporary check valve just upstream of the valve being treated. The temporary check valve is collapsible so that it can be inserted through a small incision or port in the apex of the heart or through the aorta, into the ventricular cavity. Such a system thus does not require arrest or pacing of the heart and will allow such valve repair or replacement procedures to be done without concern for time or compromise to the patients' physiology.

Abstract: A method and apparatus for facilitating transapical removal of a prosthetic heart valve, i.e., percutaneously implantable valve (PIV), with-out open-heart surgery. The apparatus includes a holding tool for holding the PIV, a cutting tool for separating the PrV from fibrotic tissue accumulating around the PIV, and a removal tool for extracting the PIV from the heart.