Abstract:
A cold stable liquid reagent system suitable for use in a Jaffe method for the determination of creatinine comprises: a) a homogeneous liquid picric acid component comprising picric acid in an amount of no more than about 35 mM, such that the picric acid component remains visibly homogeneous at a temperature between about 2 to about 8°C for 30 days or more; b) a homogeneous liquid alkaline buffer component comprising: i) an alkaline material in sufficient amount to maintain the pH of the alkaline buffer component at more than about 13, for controlling the pH of the assay ready reagent formed by combining the picric acid and alkaline buffer components; ii) at least one pH buffer material; iii) a detergent for reducing interference by proteins in the Jaffe method; and iv) borate for reducing interference by carbohydrates in the Jaffe method; wherein the alkaline buffer components contains substantially no metallic cations such that the component remains visibly homogeneous at a temperature between about 2 to about 8°C for 30 days or more. Preferably the alkaline material is tetramethylammonium hydroxide, and the detergent is diethanolamine dodecyl sulfate.
Abstract:
This invention relates to a diluting and mixing device which is capable of diluting a first solution to produce a second solution which is mixed with an undiluted third solution, to reproducibly produce a unique series of combined solutions. Each solution in said series of combined solutions may vary only in the concentration of a single (selected) reactant, and typically, each successive solution becomes increasingly more concentrated in the selected reactant. By employing a modification in procedure, each successive solution in said series may become decreasingly less concentrated in the selected reactant. This invention further relates to an automated system comprising the device connected to a stepping motor so as to rapidly and reproducibly produce said series of solutions, said device being further connected to an analyzer means for obtaining chemical, biochemical, or physical chemical data on said series of solutions. This invention especially relates to an embodiment of the device for obtaining kinetic data on enzyme reactions in solutions. The device is useful because it provides a means for rapidly obtaining chemical, biochemical, or physical chemical data on reactions in solution.
Abstract:
A temperature control apparatus for controlling the temperature of a plurality of cuvettes (32) consisting of an annular sealed chamber (20) containing a refrigerant (120), means (18) fixed to the sealed chamber (20) for receiving the sample cuvettes (32), a heater (44, 76) in thermal contact with the sealed chamber, and a temperature sensor (52, 78) in thermal contact with the sealed chamber (20). The sealed chamber (20) may include a plurality of thermally conductive posts (28) fixed to the chamber (20), the spacing between adjacent ones of the posts (28) being adapted to receive the sample cuvettes (32).
Abstract:
A method of operating a clinical analyzer wherein the analyzer includes a plurality of reaction locations (30) divided into two groups. Predetermined operations are performed on the first and second groups during corresponding processing cycles. A process that is common to both cycles is performed simultaneously for reaction locations (30) in the first and second groups during only one of the cycles. The other of the cycles can thus accommodate operations unique to particular tests that would not otherwise be available on the analyzer. The common process may be washing of adjacent reaction locations included in the first and second groups.
Abstract:
A system and method of immunoassay, both including the use of a reaction capsule (14) having a hydrophobic membrane (22) which may be repeatedly wetted and rendered hydrophobic. A pressure differential across the membrane causes liquid flow therethrough to be initiated and the hydrophobic state is then achieved by flowing gas through the membrane. The system includes a turntable (12) supporting a plurality of reaction capsules (14) and eccentric (66) means for agitating the turntable and capsules. The turntable is rotated to position the capsules at various processing stations, including sample introduction (86), reagent introduction (98), wash (100), substrate introduction (130) and read stations (132). A single cylinder two-inlet valve (178) may be used, one inlet (190) connected to liquid (196) and a second inlet (192) connected to a gas source (202), to provide both liquid and gas flow through the membrane.
Abstract:
A centrifuge rotor (18) is presented having a pivotal mount (26) for a sample container (10) upwardly offset from the radial plane (A-A') of maximal strength of the rotor (18) permitting a smaller diameter rotor (18) container (10) assembly and reducing exposed surface area of the rotor (18) container assembly.
Abstract:
A thermoelectric temperature control assembly (10) for transferring heat to or from a heat sink (30). A nonconducting substrate (40) is provided with a plurality of mounting openings (44) for receiving the mounting features of a plurality of respective thermoelectric devices (50), (52) and (54). Each mounting openings (44) is internally partitioned so as to form a pair of flexible tongues (48) by which the thermoelectric devices may be clamped to a heat sink (30) to assure a good thermal contact therewith.
Abstract:
A improved immunoassay for assaying an antigenic substance (Ag) in a fluid. The immunoassay is the type which comprises contacting the fluid with at least one first entity selected from a group consisting of an antibody (Ab) to the Ag, a soluble, labeled antibody (L-Aba) to the Ag, and an antibody (Abb) to the Ag bound to a solid support (SC). The immunoassay is characterized in that the fluid is contacted with at least one additional entity selected from a group consisting of at least one different type of soluble, labeled antibody (L-Abc) to the Ag, at least one different type of antibody (Abd) bound to a solid carrier (SC1), and at least one different type of antibody (Abe) to the Ag. The SC1 is selected from a group consisting of SC, at least one different solid carrier (SC2), and mixtures thereof (SC and SC2). Each type of L-Abc, Abd-SC1, and Abe has a lower average affinity constant (K) for Ag than each respective K of L-Aba, Abb-SC and Abe; and the additional entity is present in an amount sufficient to avoid a hook effect. Also, an improved reagent of the type comprising at least one first entity selected from a group consisting of L-Aba, Abb-SC, and Ab. The reagent is characterized in that it further comprises at least one additional entity selected from a group consisting of at least one different type of L-Abc and at least one different type Abd-SC1, and at least one different type of Abe. Ab, L-Aba, Abb-SC, L-Abc, Abd-SC1, and Abe are as defined above.
Abstract:
A multicomponent quantitative analytical method and apparatus wherein the method includes the steps of and the apparatus is capable of performing steps of obtaining a plurality of calibration spectra, transforming the calibration spectra using a transform with orthogonal basis vectors, obtaining a calibration matrix relating the transform spectra to concentrations of analytes in the calibration samples, obtaining a spectrum for an unknown sample, transforming the unknown sample spectrum, and relating the transformed unknown sample spectrum to the calibration matrix to thereby determine the concentration of analytes in the unknown sample.
Abstract:
The method includes varying the width of the high level drive impulses of a bi-level drive system based on the desired speed to be achieved by the stepper motor. A microprocessor is used to vary the pulse width.