• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    Calibration apparatus is described for use in a calibratable analytical system wherein a continuously flowing liquid sample, either alone or in admixture with other liquids, is normally caused to contact a sensor. The novel calibration apparatus enables diversion of said continuously flowing sample out of contact with the sensor and alternate contact of a calibration reference liquid or other calibration sample with the sensor. The calibration apparatus of the present invention is particularly useful in a system for analytical monitoring of a continuously flowing liquid blood sample obtained through a double lumen cannula inserted into a blood vessel of a human or animal subject. This apparatus permits the analytical system to be calibrated without the necessity of removing any portion of the cannula from the subject thereby avoiding the risk of loss of sterility inherent in such removal.
    公开号:SU999954A3
    申请号:SU772477159
    申请日:1977-05-04
    公开日:1983-02-23
    发明作者:Хуберт Клеменс Антон
    申请人:Майлз Лабораториз Инк (Фирма)；
    IPC主号:
    专利说明:

    one
    The invention relates to medical technology and can be used for diagnostic purposes.
    A device for blood analysis is known, which contains a para-5 meter measuring unit of blood with several channels, connected to a recorder, a pump with sleeves, a drain, an anticoagulant source and a collector containing a series-connected mixer and an anti-, () vesicle chamber tl j.
    However, the known device does not allow for the calibration of a cat in the process of withdrawing a sample of flowing blood.
    The aim of the invention is to calibrate the device during removal of a sample of flowing blood.
    To achieve this goal, a blood analysis device containing a blood pressure measurement unit with input and output channels, connected to a recorder, a pump with sleeves, a drain, a source of water and a collector containing a series-connected mixer and
    the antibubble chamber additionally has a catheter, a source of buffer solution, a source of gas and sources of reference fluid, the anticoagulant source through the pump is connected to one of the catheter cavities, the sources of the reference fluid are connected through corresponding pump sleeves to one of the channels of the blood parameters measuring unit, the source of buffer the solution, the source of gas and the other cavity of the catheter are connected through a series-connected pump, mixer and anti-bubble chamber with the input channel of the measuring unit Parameters blood, measuring the output of the channel parameters of the blood through the respective pump hose connected to the drain, which is also connected to a debubbler.
    The drawing shows a device for blood analysis, a general view.
    权利要求:
    Claims (1)
    [1]
    The device contains a catheter 1, a source of anticoagulant 2, a source of buffer 3, a source of gas, sources 5 and 6 of the reference fluid, a pump 7 with arms O, a collector 9 with series-connected mixer 10 and a bladder 11, channels 12 and 13 and 14 of measurement blood parameters, recorder 15 and drain 16. Two options are possible for connecting sources 5 and 6 of the reference liquid through pump 7 with sleeves 8 to the measuring unit for parameters of blood: through channel 12 and through channel 13 (not displayed). In the catheter 1, an anticoagulant nt post-swallowing from the source 2 anticoagulant is mixed with blood. The resulting mixture through the pumps 7 with sleeves 8 enters the mixer 10 of the collector 9. The latter also receives the buffer solution and gas from the source 3 of the buffer solution and the gas source. Gas from gas source A, for example, air does not react with blood, anticoagulant or buffer solution, but helps to mix the buffer solution with the mixture entering the mixer 10 from the catheter 1. The passage of the mixture separated by gas bubbles through the spiral section of the mixer 10 helps to obtain required homogeneity of the mixture of liquid. When this mixture enters the anti-chambers chamber 11, the gas flows upwards and is thus separated from the liquid mixture. Next, the gas is emitted into the drain 1b, and the mixture of the test liquid through channel 12 enters the blood parameters measurement unit. A pump 7 with sleeves 8 ensures that the mixture of the test liquid is pumped out of the unit 1 for measuring blood parameters. The results of the study are recorded on the recorder 15. In the process of the study, it becomes necessary to calibrate the device. In the first variant of connecting the sources 5 and 6 of the reference fluid, through the pump 7 with sleeves 8 to the measurement unit H, clamps are removed from one of the sleeves 8 through which the calibration gauge of the proposed device is sent, through which the reference fluid is supplied with a small amount of the test substance 5 reference fluid. The flow rate and pressure of the reference fluid coming from the source L of the reference fluid is greater than the flow rate and pressure of the test mixture. A sample of the mixture of the test liquid coming from the exit of the collector 9 cannot pass through the channel 12 to the blood parameters measurement unit 1 and therefore, together with the excess part of the reference liquid, is discharged through the counterflow into the drain 1b, and the blood parameters measurement block 1A enters the drain chamber 11 reference fluid. Next, an adjustment is made to the blood parameter measurement unit 14. After calibrating the proposed device in accordance with the reference liquid with a small / l amount of the test substance, the Bjno sleeve to which the reference liquid comes from the source 5 of the reference liquid from the source 5 of the reference liquid is blocked, fitting the clamp on it. In order to calibrate the blood parameter measurement unit 14 in accordance with the reference liquid with a high level of the test substance, remove the clamp from the sleeve, through which the standard liquid with a high level of the test substance from the source b of the reference substance flows; liquidity The flow rate and pressure of the second reference fluid exceeds the flow rate and pressure of the mixture of the test fluid, thereby diverting the flow of the mixture of the test fluid from the blood measurement unit 14 to the flow side 1b. An excess of reference fluid from the source 6, the reference fluid to the blood measurement unit 14 is also diverted to drain 1b through the antibubble chamber 11. Next, the blood parameter measurement unit 14 is calibrated in accordance with the level of the test substance dissolved in the reference fluid. After installing the clamp on the sleeve B, through which the reference enters: {liquid from the source 6 of the reference fluid, the flow of the reference fluid to the blood measurement unit 14 is stopped and the flow of the test mixture from the collector 9 to the blood measurement parameter 14 is restored. the device can be carried out without affecting the catheter 1, therefore, without violating its sterility. The reference solutions may not be sterilized, since they never come into contact with the elements for which it is necessary to maintain sterility, for example, a catheter 1. In the second variant of connecting sources 5 and 6 of the reference liquid k to the unit T measuring blood parameters when the device is operating Calibration The reference liquid passes through the unit for measuring blood parameters in the opposite direction to the movement of the mixture of the test liquid. To calibrate the device in this case, it is necessary to remove the clamps from one of the sleeves 8 of the pump 7, through which the reference fluid passes from the source 5 or 6-20 of the reference fluid, and install the clamps on the channel 13 of the blood parameters measurement unit 1A. After that, the flow of fluid through the channel to drain 1b and, consequently, any movement of the mixture under study is stopped. In this case, this liquid from the source 6 or 5 of the reference liquid enters through a series-connected pump with a sleeve 8, a canpan 13, a unit for measuring blood parameters and a channel 12 into the anti-bubble chamber. The test mixture has a lower pressure than the reference fluid, which prevents the first to pass to the blood parameters measurement unit. After setting up the blood pressure measurement unit 1 and complying with the reference fluids of sources 5 and 6 of the reference fluid to the sleeves 8 that pass through reference liquids, clamps are installed, and they are removed from channel 13. At the same time, the flow of the tested mixture: the fluid is restored through the blood parameter measurement unit. The second way to connect the sources 5 and 6 of the reference liquid requires less reference liquid for the 99995 calibration of the proposed device than the first option. The proposed device allows the calibration to be performed during the continuous removal of a sample of flowing blood, which eliminates the need to rinse the catheter or replace it during the examination process associated with inconveniences for the patient. Claims An apparatus for blood analysis, comprising a blood measurement unit with inlet and outlet chambers, connected to a recorder, with sleeves, drain, anticoagulant source and a collector containing a series-connected mixer and anti-bubble chamber, characterized in that for the purpose of calibration devices in the process of withdrawing a sample of flowing blood, it additionally has a catheter, a source of buffer solution, a source of gas and sources of reference fluid, and the source of anticoagulum through the pump connected to one of the cavities of the catheter, the sources of the reference fluid are connected through an appropriate pump head to one of the channels of the blood parameter measurement unit, the source of the buffer solution, the gas source and the other cavity of the catheter are connected through a serially connected pump, mixer and protraction chamber to the parameter measurement channel Blood supply, flow through the channel for measuring the blood flow through the corresponding pump sleeve is connected to the drain, which is also connected to the anti-bubble chamber. Sources of information taken into account in the examination 1. US Patent Vf nnOG CL. 23-253, published. 1966.
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    同族专利:
    公开号 | 公开日
    GB1545014A|1979-05-02|
    NL7704948A|1977-11-08|
    DE2720210C3|1980-08-07|
    FR2350584B1|1980-05-09|
    US4119406A|1978-10-10|
    NL172699B|1983-05-02|
    CA1063379A|1979-10-02|
    DE2720210B2|1979-11-29|
    AU2394877A|1978-10-12|
    FR2350584A1|1977-12-02|
    JPS52135795A|1977-11-14|
    NL172699C|1983-10-03|
    AU498647B2|1979-03-22|
    IT1079631B|1985-05-13|
    JPS5811018B2|1983-03-01|
    SE7705083L|1977-11-07|
    HU175801B|1980-10-28|
    DE2720210A1|1977-11-10|
    SE426266B|1982-12-20|
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    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    US05/683,806|US4119406A|1976-05-06|1976-05-06|Calibration apparatus|
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