会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 1. 发明专利
    • AUTOMATIC CHEMICAL ANALYZER
    • JPH09274045A
    • 1997-10-21
    • JP8120696
    • 1996-04-03
    • HITACHI LTDHITACHI INSTRUMENTS ENG
    • KAMIMURA YASUKOYOKOSE TAIZOSHICHIJI MASARUSUGAWARA KENJIHATTORI MITSUO
    • G01N21/75G01N21/27G01N35/00G01N35/02
    • PROBLEM TO BE SOLVED: To obtain an automatic chemical analyzer in which a photometric accuracy during an analysis is diagnosed accurately, by which measures are taken quickly and precisely against the trouble of a photometric system and which prevents a delay in a measured result by a method wherein the absorbance of purified water is measured photometrically in a multiple manner at a specific wavelength which remarkably reflects the photometric accuracy. SOLUTION: The absorbance (water blank value) of purified water which is dispensed automatically into a reaction container 12 is measured photometarically in a multiple manner at two proper wavelength which reflect a photometaric accuracy remarkably. A central processing unit 11 accumulates the water clank value at every analysis which is measured in the same reaction container 12 so as to perform a statistical processing operation (to obtain an SD value). The SD value is compared with a tolerance which is set in advance as a parameter so as to be judged, and whether a photometric accuracy is good or not is judged. When the SD value is outside the tolerance, an alarm is issued immediately so as to be reported to an operator. When the SD value is within the tolerance, a sampling operation is started, and an ordinary analysis is performed. Thereby, since a photometric accuracy during an analysis can be controlled accurately, the defect of the photometric accuracy due to the reaction container 12 can be diagnosed quickly, and the efficiency of an inspection can be enhanced.
    • 4. 发明专利
    • ENZYME ACTIVITY MEASUREMENT
    • JPH10282000A
    • 1998-10-23
    • JP9341097
    • 1997-04-11
    • HITACHI LTDHITACHI INSTRUMENTS ENG
    • SHICHIJI MASARUYOKOSE TAIZO
    • G01N21/75G01N35/00
    • PROBLEM TO BE SOLVED: To detect and reject an abnormal value for attaining accurate measured results by sequentially-calculating an gradient between respective photometry points in reacting process to obtain respective relative values, and comparing them with preset permissible values for confirmation of the linearity of a change in an absorption value. SOLUTION: In this enzyme activity measurement, such as GOT, which permits enzyme to react in a container disposed on a rotating disc and obtains the enzyme activity by the change of absorbancy, absorbancy measuring is conducted at a prescribed number of photometry points of a reaction time course. Gradient (absorbancy variance per unit-hour) is computed sequentially from the photometry point lm where calculation preset as analysis parameter is started, through points lm+1 , lm+2 ,..., the point ln where the calculation is completed. A relative value is calculated by a prescribed method for respective calculated gradients, and comparative discrimination with permissible value preset arbitrarily is conducted. By rejecting the absorbancy at the point which is discriminated to be abnormal compared with the permissible value, and obtaining absorbancy changing speed by the method of least squares from remaining data, it is possible to calculate the enzyme activity.
    • 9. 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.
    • 10. 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.