Abstract: The present invention provides a method for isolating RNA from a biological material comprising RNA and contaminants, wherein: the biological material is disrupted in the presence of a chaotropic agent, the resulting lysate is diluted to precipitate out contaminants, and the precipitate is removed from the lysate. RNA is preferably isolated from the resulting cleared lysate, using a silica matrix to bind and then release RNA bound thereto under particular conditions. The present invention also provides a method for isolating RNA from a solution comprising RNA and DNA, wherein: the RNA and DNA are bound to a silica matrix in the presence of at least one binding enhancer, the DNA is digested with DNase, and the RNA fluted therefrom.

Abstract: A guidewire extension system including a guidewire and an extension wire is disclosed. The system includes female and male connector segments located on the proximal end of the guidewire or the distal end of the extension wire. The hollow female connector segment, in one embodiment, includes a radial lip which intersects with at least one, i.e., one or more, lateral slots. The male connector segment includes an external groove. When the male connector is inserted into the female connector segment, the slots are expanded and the lip snaps into the groove providing a tactile indication that connection is completed. No restriction or frictional fit is created. The guidewire and extension wire are freely rotatable with respect to each other and can be multiply connected and disconnected. Methods of catheter exchange with tactile indication of guidewire extension wire connection are disclosed.

Abstract: The present invention presents a novel method for removing endotoxins from nucleic acids, such as DNA, RNA, or hybrids thereof, contaminated therewith. Nucleic acid solutions which can be treated using the method of this invention include, but are not limited to, lysates of gram-negative bacteria and nucleic acid solutions contaminated with endotoxins from external sources. The present method removes endotoxins from such solutions using silica-based materials, such as silica gel particles, magnetic silica particles, or diatomaceous earth. In a preferred aspect of the method of this invention, magnetic silica particles are used to isolate plasmid DNA from a lysate of gram-negative bacteria transformed with the plasmid DNA. Application of the disclosed method produces nucleic acids which are sufficiently free of endotoxin contamination to be useful for a variety of different practical applications.

Abstract: Provided are a magnetic particle separation assembly and method for separating a magnetically responsive complex from a non-magnetic test media in which the magnetically responsive complex is suspended. The assembly comprises an invertible rack for holding specimen containers and a magnetic support member for supporting the rack. The magnetic support member has a base and a planar member bisecting the base and extending upwardly therefrom. The planar vertical member has a plurality of magnets embedded therein. The magnets are disposed in a substantially horizontal orientation parallel to the base and spaced from the base. The invertible rack has a slot therethrough dimensioned to accept the planar vertical member of the magnetic support member. In one position, at least one container of a particular size is positioned within the rack so as to be adjacent to the magnetic support member in final assembly such that the magnetically responsive complex is separated from the non-magnetic media.

Abstract: The present invention provides novel phosphonic acid-based cationic lipids of the general structure: or a salt, or solvate, or enantiomers thereof wherein; (a) R1 is a lipophilic moiety; (b) R2 is a positively charged moiety; (c) R3 is a lipophilic moiety of 1 to about 24 carbon atoms, a positively charged moiety, or a negatively charged moiety; (d) n is an integer from 0 to 8; (e) X− is an anion or polyanion; (f) Y is N or 0, and (g) m is an integer from 0 to a number equivalent to the positive charge(s) present on the lipid. The present invention further provides compositions of these lipids with polyanionic macromolecules, methods for interfering with protein expression in a cell utilizing these compositions and a kit for preparing the same.

Abstract: An iontophoretic delivery device (10) is provided. Device (10) has an electronic circuit (32) having electronic components such as batteries (30) mounted thereon. Device (10) also includes a pair of electrode assemblies (18, 19). The electronic circuit (32) is electrically connected to the electrode assemblies (18, 19) using an electrically conductive adhesive (34). The adhesive can also be used to electrically connect two or more electronic components within circuit (32) or to connect an electronic component to the electronic circuit (32). In one practice of the invention, the electrically conductive adhesive (44) functions as an electrode and electrically connects the circuit (32) to an agent-containing reservoir (24, 25). In a further practice of the invention, the electrically conductive adhesive (93) functions as an agent reservoir and contains the agent to be iontophoretically delivered.

Abstract: A process for producing and purifying peptides and for producing peptide/protein antigens for antibody production is described. The process utilizes fusion proteins and specifically fusion proteins in which the fusion protein carrier segment includes an amino acid sequence at least about 65 amino acids long and in which the amino acid sequence does not contain negative or positive charged side chains of amino acids.

Abstract: A method for 1.alpha.-hydroxylation of vitamin D compounds using the appropriate vitamin D as the starting material. The method requires no separatory procedures prior to the actual hydroxylation step.

Abstract: A wire containing or dispensing article and method are disclosed. The invention is used to dispense wire from a tubular wire carrier. The invention is particularly useful for containing/dispensing a guidewire, especially a coated guidewire. The article is an elongate dispensing sleeve or collar having an axial hole or bore through which a wire may pass. The sleeve has a cylindrical sleeve body with lateral projections on its outside and a plurality of transverse slits passing through its wall. The lateral projections and slits cooperate to permit wire to be restrictively engaged at the bore and to be controllably dispensed from the carrier by the partial insertion and removal of the sleeve into and out of the carrier. The method is controllable dispensing of the wire from the carrier by utilization of the article.

Abstract: A guide wire having a solid core wire which runs its entire length. The core wire has a proximal portion which constitutes the majority of its length and which tapers to a distal portion. The distal portion terminates in an atraumatic tip at the extreme distal end of the guide wire. In one embodiment a portion of the distal segment of the core wire adjacent the tip is flattened. The guide wire further includes an integral, flexible, flat wire coil attached to the core wire at its taper and to the core wire distal tip and running the entire distance therebetween. Lastly, the flattened wire coil has a non-metallic lubricous or hydrophilic coating on at least a portion of its exterior. In a preferred embodiment the proximal portion of the core wire tapers to a second diameter medial portion or segment which itself tapers to a third diameter distal segment.

Abstract: Methods for delivering therapeutic agents by iontophoresis with reduced or mitigated sensation are disclosed. The methods generally involve the step of delivering therapeutic agent by iontophoresis in the presence of an intentionally added sensation reducing amount of a multivalent ion. Preferred multivalent ions useful to mitigate sensation are calcium, magnesium, phosphate and zinc.

Abstract: A guide wire having state-of-the-art handling characteristics for ease in positioning a variety of catheters and other devices within the cardiovascular or other body system wherein the guide wire is also suitable for infusion of small volumes of fluid. The exceedingly small diameter guide wire has unique infusion properties. The guide wire body has at least one helical coil having a flexible nonporous sheath within the lumen. The helical coil is close wound along the majority of its length. The distal end of the helical coil has spaced windings to permit infusion of the fluid. The flexible nonporous sheath terminates proximal to the space wound portion. The solid core wire, which runs the entire length of the guide wire, is located within the same lumen used for infusion. This provides a greatly increased surface area in relation to the cross sectional area of the infusion lumen ensuring a slow but extremely constant infusion rate over a wide range of infusion pressures.

Abstract: A hollow lumen cable is formed by helically winding inner and outer coils with the helices of each coil being in an abutting relationship and the outer coil inner diameter being less than the outer, peripheral, diameter of the inner coil. Preferably, each coil is multifilar. After the coils are wound, an unwinding force is applied to the outer coil and the inner coil is inserted into the outer coil to have its winding inclined opposite to that of the outer coil; and thence, the outer coil is allowed to contract to form an interference fit with the inner coil. The cable may be incorporated as part of various medical systems e.g., implantable pumps or other rotatable medical apparatuses. The cable is bendable about the tight radii, has a high torque transfer, a small outer diameter, and a hollow lumen through which fluid, wires or medical devices may pass.

Abstract: An apparatus for and method of selectively occluding a lumen of a multilumen catheter during a medical procedure. The catheter may have any variety of functions of either diagnostic and/or therapeutic nature. A first open lumen to be occluded may have one or more orifices at the distal tip and/or in the side wall of the catheter for infusion of a liquid, injection of a dye, or operation of a guide wire or other control device. A small balloon adjacent the lumen to be occluded is inflated with fluid from a second, closed lumen. Whenever the small balloon is completely inflated, the first, open lumen is occluded. Whenever the small balloon is deflated, the lumen is open to the orifices distal to the small balloon.

Abstract: An iontophoretic agent delivery device having a simplified structure and ease of manufacture. The device utilizes an electrical pathway comprising a source of electrical energy and an output means. The electrical pathway is disposed upon one of the two sides of a flexible, non-conductive substrate (e.g., a film). The output means of the pathway are connected directly or indirectly, e.g., by means of an electrically conductive adhesive tape, to the remaining components of the device such as current distribution members, lead wires, or electrodes. In this arrangement, the circuit is inverted from that of conventional devices. Economical, reel-to-reel methods of manufacturing a one-sided iontophoretic circuit apparatus of the invention are disclosed.

Abstract: Liquid metal electrical contact compositions are disclosed. Compositions of this invention consist of a metal mixture of first and second Periodic Table Group III metals and a lubricant. A gallium/indium metal mixture is preferred. Preferred lubricants are metal-based, most preferably molybdenum-based. The liquid metal electrical contact compositions are particularly useful for high current density applications.

Abstract: A wire containing or dispensing article and method are disclosed. The invention is used to dispense wire from a tubular wire carrier. The invention is particularly useful for containing/dispensing a guidewire, especially a coated guidewire. The article is an elongate dispensing sleeve or collar having an axial hole or bore through which a wire may pass. The sleeve has a cylindrical sleeve body with lateral projections on its outside and a plurality of transverse slits passing through its wall. The lateral projections and slits cooperate to permit wire to be restrictively engaged at the bore and to be controllably dispensed from the carrier by the partial insertion and removal of the sleeve into and out of the carrier. The method is controllable dispensing of the wire from the carrier by utilization of the article.

Abstract: A catheter for removing vascular obstruction(s) is disclosed. The catheter employs a configuration comprising generally coaxial, rapidly rotatable drive cable, fluid output lumens or channels, and fluid input lumens or channels. The drive cable is fixedly coupled to an elongate head so as to permit the head to be rapidly rotated by the drive cable. The head includes flats or impellers which, when rapidly rotated, generate a zone of turbulence or a vortex adjacent the vascular obstruction. The turbulence generated by the device tends to break up or dismantle the obstruction. The fluid input and output mechanisms permit fluid to be delivered to the vicinity of the obstruction and debris from the obstruction to be removed.In a preferred practice, a catheter of the invention is hollow, permitting it to be slid over a guide wire which has been steered to the site of the vascular obstruction.

Abstract: An apparatus for removing obstructions within a blood vessel of a patient using mechanical motion. The device has a catheter which is inserted into the vascular system at a convenient point, such as the femoral artery. The distal end of the catheter is advanced until it reaches the occlusion. A central lumen within the catheter contains a coil spring which functions as a flexible shaft to couple rotational motion provided by an electric motor or other source of rotational motion at the proximal end of the catheter to a cutting head at the distal end of the catheter. As the cutting head is rotated, the occlusion is milled away by the internal cutting edges of the cutting head. The particles cut from the occlusion are forced by the rotational motion of the cutting head into one of a number of outer lumens of the catheter. A vacuum is applied to the proximal end of some of the outer lumens to remove the particles from the patient's body.

Abstract: Methods for delivering therapeutic agents by iontophoresis with reduced or mitigated sensation are disclosed. The methods generally involve the step of delivering therapeutic agent by iontophoresis in the presence of an intentionally added sensation reducing amount of a multivalent ion. Preferred multivalent ions useful to mitigate sensation are calcium, magnesium, phosphate and zinc.