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    • 11. 发明专利
    • 細胞培養装置及び細胞培養方法
    • 细胞培养装置和细胞培养方法
    • JP2015050983A
    • 2015-03-19
    • JP2013186430
    • 2013-09-09
    • 株式会社日立製作所Hitachi Ltd
    • NANBA MASARUHAGA RYOICHIMURAKAMI SEISUZUKI HARUO
    • C12M1/00
    • C12M41/30C12M23/14C12M23/22C12M23/26C12M37/00C12M41/36
    • 【課題】外部から無菌バッグ内に濁度センサを挿入することなしに細胞培養液の濁度を連続的且つ正確に測定し、細胞を培養することのできる細胞培養装置を提供する。【解決手段】細胞培養装置1は、装置内の所定の位置にセットされ、光透過性と可撓性を有し、内部で細胞培養液4を培養する無菌バッグ2と、前記無菌バッグ2の一部2aを介して前記無菌バッグ2内の細胞培養液4に光を照射する光照射部31、及び、前記無菌バッグ2の他の一部2bを介して前記無菌バッグ2内の細胞培養液4を透過した光を受光する光受光部32を有し、前記光照射部31、前記無菌バッグ2の一部2a、前記無菌バッグ2の他の一部2b及び前記光受光部32を光学的に一直線に配置した濁度センサ部3と、を備えることを特徴とする。【選択図】図1
    • 要解决的问题:提供一种连续精确地测量细胞培养液浊度的细胞培养装置,而不将浊度传感器从外部插入无菌袋中,并可培养细胞。解决方案:细胞培养装置1包括 :设置在设备中规定位置的无菌袋2具有透光性和柔韧性,并在其中培养细胞培养液4; 以及具有通过无菌袋2的部分2a将无菌袋2中的细胞培养液4照射到无菌袋2中的光照射部31的浊度传感器部分3和接收通过细胞培养液的光的受光部32 4的无菌袋2通过无菌袋2的另一部分2b,并将光照射部31,无菌袋2的部分2a,无菌袋2的另一部分2b和光接收部32配置在 光学直线。
    • 12. 发明专利
    • WASHING METHOD AND WASHER
    • JPH08299923A
    • 1996-11-19
    • JP11282395
    • 1995-05-11
    • HITACHI LTD
    • HAGA RYOICHINITSUTA MICHIYOMURAKAMI SEI
    • B08B3/10
    • PURPOSE: To prevent defective washing when the composition, the temperature, the flow rate and the washing time of a washing liquid is set in advance to wash a material to be washed by preparing change pattern with time in which various conditions in a case when washing had suitably been performed in advance are fetched and performing washing while comparing the actually measured value with the change pattern. CONSTITUTION: Washing work of a pipe line 53 partitioned by valves 42, 45, 46, 47, 48 is carried out in compliance with work procedures prepared based on the results of a washing test made in advance. That is, first, a washing liquid is prepared in a washing liquid preparing tank 1 based on the work procedures and is heated to a prescribed temp. Next, the washing liquid is forcibly fed by a pump 5 with the opening degree of a valve 19 being controlled so that the flow rate in the pipe line 53 becomes a prescribed value. During washing,by a flow meter 9, a temperature gage 10, a pH meter 11, conductometric devices 12, 13, flow meters 21, 22 and temperature gages 24, 26, information on washing is collected with time to monitor the washing conditions. From a point of time when all the monitors satisfy the prescribed washing conditions, washing is continued for a set time.
    • 17. 发明专利
    • METHOD AND APPARATUS FOR PREPARATION OF MEDICINE, ETC.
    • JPH07190883A
    • 1995-07-28
    • JP33060293
    • 1993-12-27
    • HITACHI LTD
    • MATSUOKA TATSUHIKOMURAKAMI SEINAKANO TAKAMORI
    • G01M3/04A61J3/00G01M3/28
    • PURPOSE:To provide the preparation method and the preparation apparatus, of a medicine or the like, in which the validation of a valve assembled in an apparatus or a plant is performed in the preparation operation of the medicine or the like and which prepares a normal medicine or the like. CONSTITUTION:Valves 6, 7 which are installed in a preparation line 1 and a cleaning line 2 are closed, and a space A which has been sealed airtightly by the valves is formed. Then, a valve 8 is closed, and the air is supplied to an air supply line 5 via a valve 9 which has been opened. Then, the valve 9 is closed, and a space B which is formed by means of the valves 6, 8, 9 is formed as a space whose pressure is higher than that of the space A. For a prescribed time, the pressure of the spaces A, B is measured by a pressure gage 10, and a change in the pressure is recorded by a recorder 12 via a cable 11. An inspection process which is described above is incorporated into an apparatus having a line, the change in the pressure is recorded, the validation materials of the valve 6 as an object are obtained by using a sheet of recording paper in which the pressure of the spaces A, B is not changed.
    • 19. 发明专利
    • CULTURE APPARATUS
    • JPH06181737A
    • 1994-07-05
    • JP33836492
    • 1992-12-18
    • HITACHI LTD
    • YAMAGUCHI SHUJIMURAKAMI SEINAKANO TAKAMORI
    • C12M1/00C12M1/12
    • PURPOSE:To determine the sterilization effect at various parts of a culture apparatus by filling a suspension of indicator microorganism in the apparatus, sterilizing with high-pressure steam, recovering the proliferation medium of the indicator microorganism from each part and determining the growth of bacteria after cultivation. CONSTITUTION:A bacterial strain having strong resistance to high-pressure steam sterilization treatment and free from pathogenicity (e.g. thermostable sporangium) is used as an indicator microorganism and filled together with a culture liquid into a culture apparatus through indicator microorganism filling pipes 14-17. The indicator microorganism is distributed throughout the apparatus by extracting the culture liquid through indicator microorganism recovery pipes 18-21 connected to drain exhaustion ports 10-13. High-pressure steam is blown into the apparatus through steam inlet pipes 6-9 to sterilize the apparatus. The culture liquid is filled into the apparatus through the pipes 14-17, the system is maintained to the state for a prescribed period, the culture liquid is recovered from the system through the pipes 18-21 and the growth of bacteria (or clouding of the medium) is determined by culturing the liquid.