Abstract:
An automated analyzer for performing multiple diagnostic assays simultaneously includes multiple stations, or modules, in which discrete aspects of the assay are performed on fluid samples contained in reaction receptacles. The analyzer includes stations for automatically preparing a specimen sample, incubating the sample at prescribed temperatures for prescribed periods, performing an analyte isolation procedure, and ascertaining the presence of a target analyte. An automated receptacle transporting system moves the reaction receptacles from one station to the next. The analyzer further includes devices for carrying a plurality of specimen tubes and disposable pipette tips in a machine-accessible manner, a device for agitating containers of target capture reagents comprising suspensions of solid support material and for presenting the containers for machine access thereto, and a device for holding containers of reagents in a temperature controlled environment and presenting the containers for machine access thereto. A method for performing an automated diagnostic assay includes an automated process for isolating and amplifying a target analyte. The process is performed by automatically moving each of a plurality of reaction receptacles containing a solid support material and a fluid sample between stations for incubating the contents of the reaction receptacle and for separating the target analyte bound to the solid support from the fluid sample. An amplification reagent is added to the separated analyte after the analyte separation step and before a final incubation step.
Abstract:
Antimicrobial electret material are described. In some embodiments, the materials comprise a unitary web comprising an antimicrobial surface treatment and having certain properties. In other embodiments, an antimicrobial electret material is described comprising an electret web comprising an antimicrobial surface treatment wherein the surface treatment comprises a sparingly soluble silver-containing compound, a photosensitive antimicrobial agent that forms reactive oxygen species, a biguanide compound, or a combination thereof.
Abstract:
A magnetic separation plate for use in methods employing magnetic particles, said magnetic separation plate comprising a support plate and magnetic pins in a predetermined geometrical arrangement, said magnetic pins having a fastening portion, an intermediate portion and a separation portion and being fastened to said support plate at their fastening portion, wherein said magnetic pins are individually displaceable at their separation portion. The invention further provides a method for the separation of magnetic particles using the separation plate.
Abstract:
An effective technique for balancing mask breathability and mask trapping capability at higher levels is provided in a mask to be worn on a wearer's face. A mask 1 has a mask body 10 that covers at least wearer's mouth and nose and a pair of ear straps 20 that extend from both sides of the mask body 10 and are designed to be hooked around wearer's ears. The mask body 10 includes a first fiber sheet and a second fiber sheet which are electret nonwoven fabric sheets formed of polyolefin fiber. The first fiber sheet is a nonwoven fabric sheet having an average fiber diameter of 0.5 to 3 μm and a basis weight of 1.5 to 5 g/m2, and the second fiber sheet is a nonwoven fabric sheet having a larger average fiber diameter and a heavier basis weight than the first fiber sheet.
Abstract translation:在面罩上设置有用于平衡面罩透气性和较高水平的面膜捕获能力的有效技术,以佩戴在佩戴者的脸部上。 面具1具有覆盖至少佩戴者的嘴和鼻的面罩主体10和从面罩主体10的两侧延伸并被设计成钩在佩戴者的耳朵周围的一对耳带20。 面罩主体10包括由聚烯烃纤维形成的驻极体无纺布片的第一纤维片和第二纤维片。 第一纤维片是平均纤维直径为0.5〜3μm,单位面积重量为1.5〜5g / m 2的无纺布片,第二纤维片为平均纤维直径较大的无纺布片 基重比第一纤维片材。
Abstract:
A method of trapping a charged particle. The method includes providing a planar substrate having a conductive surface thereon, the conductive surface having at least one non-conductive region. The method also includes applying a solution to the conductive surface, the solution comprising at least one charged particle. The method further includes applying a voltage of a threshold level to the conductive surface. The method also includes, in response to the voltage, generating an electrostatic field in the solution adjacent to a boundary between the conductive surface and the non-conductive region. The method also includes setting the threshold level of voltage to result in a strength of the electrostatic field sufficient to prevent the particle from crossing the electrostatic field.
Abstract:
An apparatus for magnetically separating constituents of blood includes: a first portion having a solid support haying fixedly attached thereon a plurality of ring magnets, each ring magnet defining an interior perimeter enclosing an aperture; and a second portion removably attached to the first portion, wherein the second portion includes a solid substrate having surfaces defining a plurality of second apertures, each second aperture configured to removably hold a vial.
Abstract:
Arrays of spin-valve elements that can be selectively activated to trap, hold, manipulate and release magnetically tagged biological and chemical particles, including molecules and polymers. The spin-valve elements that can be selectively activated and deactivated by applying a momentary applied magnetic field thereto. The spin valve element array can be used for selectively sorting and transporting magnetic particles one particle at a time within the array. As the magnetically tagged particles are held by the spin-valve elements, application of an auxiliary magnetic field can be used to apply tension or torsion to the held particles or to move, e.g. rotate, the trapped particles. The arrays of spin-valve elements can be used in a variety of applications including drug screening, nucleic acid sequencing, structural control and analysis of RNA/DNA and protiens, medical diagnosis, and magnetic particle susceptibility and size homogenization for other medical applications.
Abstract:
A magnetic separation device is provided, including a first magnetic field unit and a first separation unit disposed at a side of the first magnetic field unit. The first magnetic field unit includes a first magnetic yoke having opposite first and second surfaces, and a plurality of first magnets respectively disposed over the first and second surfaces, wherein the same magnetic poles of the plurality of first magnets face the first magnetic yoke. The first separation unit includes a body made of non-magnetic materials and a continuous piping disposed in the body, including at least one first section and at least one second section, wherein at least one second section is perpendicular to at least one first section, and at least one second section is adjacent to, and in parallel to a side of the first magnetic yoke not in contact with the plurality of first magnets.
Abstract:
A reconfigurable modular microfluidic system for preparation of a biological sample including a series of reconfigurable modules for automated sample preparation adapted to selectively include a) a microfluidic acoustic focusing filter module, b) a dielectrophoresis bacteria filter module, c) a dielectrophoresis virus filter module, d) an isotachophoresis nucleic acid filter module, e) a lyses module, and f) an isotachophoresis-based nucleic acid filter.
Abstract:
The present invention provides a method for detecting easily and efficiently a chemical substance contained in a gas sample at an ultralow amount.The present invention is directed to detecting method of a chemical substance contained in a gas sample, using an analyzing device with electrostatic atomizer. The analyzing device comprises a vessel, a inlet, a cooling part, an atomizing electrode, a counter electrode, an intermediate electrode, a liquid detecting part, and a detecting electrode. According to a detecting method of the present invention, the gas sample is condensed as a first condensate liquid at the surface of the atomizing electrode. The first condensate liquid is configured to be electric-charged fine particles to obtain a second condensate liquid at the surface of the counter electrode. The resulted second condensate liquid is brought in contact with the detecting electrode and a current voltage is applied between the counter electrode and the detecting electrode. The chemical substance is detected on the basis of the generated current value.