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    • 2. 发明专利
    • METHOD FOR SAMPLING MINUTE AMOUNT OF SPECIMEN FOR AUTOMATIC ANALYZER
    • JPH0560769A
    • 1993-03-12
    • JP22394691
    • 1991-09-04
    • HITACHI LTDHITACHI INSTRUMENTS ENG
    • YOKOSE TAIZOUSUI SHINOBUOTAKI TOMOMASA
    • G01N1/00G01N21/31G01N31/20G01N31/22G01N35/10
    • PURPOSE:To sample a minute amount of specimen efficiently and highly accurately by detecting the level of a sample-shortage detecting region with a sample probe, which also serves the role of a liquid-level sensor, and controlling the depth of the tip of the probe and the driving of a syringe. CONSTITUTION:A sampling arm 5 is driven 6. A sampling probe 4, which also serves the roles of a liquid level sensor and a sampling nozzle, is brought into contact with the liquid surface of a specimen in a sample cup 10b, and the specimen is sampled. When the amount of the specimen is as minute as about, e.g. 20-30mul, the tip of the probe 4 is inserted down to the bottom of the cup 10b. Therefore, there is no dummy amount of the specimen, which is caused by the difference between the heights of both tips of the sensor and the nozzles, at all. The tip of the probe 4 is inserted beneath the liquid surface by the amount of the level after the tip of the probe 4 comes into contact with the liquid surface based on the level information in a sample-shortage detecting region from the bottom of the cup 10b. Therefore, the specimen is not attached. When the total amount of the specimen becomes lower than the maximum amount of the apparatus, the driving of a specimen sampling syringe 1 is controlled, and the sucking of air is prevented. Therefore, the sampling accuracy can be maintained.
    • 3. 发明专利
    • BIOCHEMICAL AUTOMATIC ANALYZER
    • JP2000105239A
    • 2000-04-11
    • JP27459598
    • 1998-09-29
    • HITACHI LTDHITACHI INSTRUMENTS ENG
    • OTAKI TOMOMASASAITO KIYOTAKAYOKOSE TAIZOIMAI KYOKO
    • G01N33/52G01N21/27G01N35/00
    • PROBLEM TO BE SOLVED: To simply and surely detect abnormality, and to predict a life of a replacing component, by measuring an absorbance using a colored substance after absorbance measurement using pure water to determine that a data trouble exists in any side out of a photometric system and a dispensing system. SOLUTION: Washing for reaction vessels is started, a fixed amount of water are dispensed into one specified vessel and a plurality of reaction vessels, respectively, to measure absorbances, and measured results are determined as a check (1) and a check (2) respectively. The check (1) is compared with the check (2) to judge whether a cause exists in the reaction vessel or a light source based on an allowance value. Pure water is thereafter dispensed after a fixed amount of colored substance are dispenced from a sample probe into the plural reaction vessels (group A) after washing. The fixed amounts of the colored substance and pure water are delivered at the same time into another reaction vessels (group B) with no sample dispensed, using a reagent probe. Absorbance- measured values of the groups A, B are determined as checks (4), (5), and the checks (4), (5) are compared each other to judge whether a cause exists in deterioration of sampling precision or in a reagent pipetting mechanism.