JPH055735A - Method for continuous quantitative analysis of component in urine by flow injection system - Google Patents

Method for continuous quantitative analysis of component in urine by flow injection system

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Publication number
JPH055735A
JPH055735A JP18322191A JP18322191A JPH055735A JP H055735 A JPH055735 A JP H055735A JP 18322191 A JP18322191 A JP 18322191A JP 18322191 A JP18322191 A JP 18322191A JP H055735 A JPH055735 A JP H055735A
Authority
JP
Japan
Prior art keywords
passage
urine
cell
liquid
urine sample
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP18322191A
Other languages
Japanese (ja)
Other versions
JP2555002B2 (en
Inventor
Shigeo Imai
茂雄 今井
Haruyuki Mizuno
治幸 水野
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Inax Corp
Original Assignee
Inax Corp
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Filing date
Publication date
Application filed by Inax Corp filed Critical Inax Corp
Priority to JP3183221A priority Critical patent/JP2555002B2/en
Publication of JPH055735A publication Critical patent/JPH055735A/en
Application granted granted Critical
Publication of JP2555002B2 publication Critical patent/JP2555002B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Investigating Or Analysing Biological Materials (AREA)
  • Automatic Analysis And Handling Materials Therefor (AREA)

Abstract

PURPOSE:To obtain a method for analysis which enables easy analysis of a component in urine and automation of measurement and makes it possible to construct an apparatus to be small in size. CONSTITUTION:A urine sample liquid is made to flow into an inflow passage 12 through an introduction passage 16, while a prescribed precipitant is injected into the inflow passage 12 or a measuring cell 10 through an introduction passage 18 or 32. The liquid is made to flow in one direction through a route including the measuring cell 10, a reaction precipitate of the urine sample liquid and the precipitant is precipitated on the surface of a quartz oscillator inside the measuring cell 10 in the above process, a change in an oscillation frequency of the quartz oscillator before and after the precipitation is determined and thereby a component in urine is analyzed quantitatively.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】この発明は尿中成分の定量分析方
法に係り、詳しくは水晶振動子を用いて尿中成分を測定
する方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for quantitatively analyzing urinary components, and more particularly to a method for measuring urine components using a crystal oscillator.

【0002】[0002]

【従来の技術】尿中の蛋白の量を知ることは、生体の状
態に関する情報を得る方法として有用な方法である。そ
こで近時、図9に示しているように各家庭等のトイレ
(便器)100に尿中成分の測定装置を設け、これを電
話回線102で医療機関104と結んで、各家庭等で得
られたデータをオンラインで医療機関104に送り、医
療機関104において患者の健康状態をチェックできる
ようにすることが構想されている。
2. Description of the Related Art Knowing the amount of protein in urine is a useful method for obtaining information on the condition of a living body. Therefore, recently, as shown in FIG. 9, a urine component measuring device is provided in a toilet (toilet bowl) 100 of each home, etc., and this is connected to a medical institution 104 by a telephone line 102 to obtain at each home. It is envisaged to send such data to the medical institution 104 online so that the medical institution 104 can check the health condition of the patient.

【0003】このシステムは、早朝起床尿の成分を測定
出来るという点で大きなメリットがある。尿中成分は日
差変動が大きく、食事内容と運動負荷状態,環境等によ
って影響を受け易い。従って検尿の日時によって尿中成
分は大きく変動する。このような影響を受けにくいのが
臨床的に早朝起床尿(早朝第一尿)とされており、而し
て上記構想によれば、この早朝起床尿を容易に採尿で
き、尿中成分を測定できるメリットがあるのである。
This system has a great advantage in that it can measure the components of urine that wakes up early in the morning. The urinary components have large daily fluctuations and are easily affected by the content of meals, exercise load status, environment, etc. Therefore, urinary components greatly vary depending on the date and time of urinalysis. It is clinically said that early morning wake-up urine (early morning first urine) is less likely to be affected by this. Therefore, according to the above concept, this early morning wake-up urine can be easily collected and the urinary components can be measured. There is a merit that can be done.

【0004】従来、尿中の蛋白の測定方法として主に臨
床的に用いられている方法は、採取した尿を含む液を酸
性として蛋白を正に帯電させ、そしてこれにスルホサリ
チル酸等の沈澱剤を加えて蛋白とスリホサリチル酸等と
の反応による塩を沈澱せしめ、その沈澱により液に濁り
が出ることを利用したものである。
[0004] Conventionally, the method mainly clinically used as a method for measuring protein in urine is to make the collected urine-containing liquid acidic to positively charge the protein, and to add a precipitating agent such as sulfosalicylic acid to this. Is used to precipitate a salt due to the reaction of protein with sulphosalicylic acid and the like, and the fact that the solution causes turbidity is utilized.

【0005】詳述すると、まず蛋白量が既知の、且つそ
の含量が種々異なった尿中にスルホサリチル酸等の沈澱
剤を加えて沈澱生成せしめる。一方蛋白量の未知の尿に
ついても同様の操作を施して濁りを生ぜしめる。そして
蛋白量未知の試料の濁度を蛋白量が既知のものの濁度と
目視で比較することにより、蛋白量を知るといったもの
である。
More specifically, first, a precipitating agent such as sulfosalicylic acid is added to urine of which the amount of protein is known and the contents thereof are different from each other to form a precipitate. On the other hand, urine with an unknown protein content is also subjected to the same operation to cause turbidity. Then, the amount of protein is known by visually comparing the turbidity of a sample with an unknown amount of protein with the turbidity of a sample with a known amount of protein.

【0006】尿中蛋白の測定方法としては、この外、試
料の濁度を吸光度計により測定する方法も行われてい
る。即ち濁りを与えた試料に特定波長の光を当てて、試
料の吸光度を測定するといったものである。
As a method for measuring urinary protein, a method of measuring the turbidity of a sample with an absorptiometer is also used. That is, a sample having turbidity is irradiated with light having a specific wavelength, and the absorbance of the sample is measured.

【0007】しかしながら、これらの方法は操作が煩雑
であり、測定のために多大な手間と時間とを要してしま
う外、測定精度の点でも充分に満足のいくものでなかっ
た。また吸光度計を用いた方法ではセルの汚れが問題と
なり、これが測定誤差を生ぜしめるといった問題が存在
していた。
However, these methods are complicated in operation and require a great deal of labor and time for measurement, and they are not sufficiently satisfactory in terms of measurement accuracy. In addition, in the method using an absorptiometer, there is a problem that cell contamination becomes a problem, which causes a measurement error.

【0008】そこで後者の方法にあっては、セルの汚れ
が影響しないように測定に当っては注意を払い、またセ
ルを清浄に保つように充分なメンテナンスを行うように
しており、こうした作業が面倒且つ煩雑な作業となって
いた。
Therefore, in the latter method, care is taken in the measurement so as to prevent the contamination of the cell from affecting, and sufficient maintenance is performed to keep the cell clean. It was a troublesome and complicated task.

【0009】またこれらの方法は、医療機関において行
う場合はよいが、上述のように家庭内のトイレにおいて
行う尿中成分の測定方法としては採用困難であり、前述
した構想を現実化する上においても簡便且つ容易,正確
に尿中成分を測定し得る方法の実現が望まれるところで
あった。
Although these methods are suitable for use in medical institutions, they are difficult to use as methods for measuring urinary components in domestic toilets as described above, and in realizing the concept described above. It was desired to realize a method that can measure urinary components simply, easily and accurately.

【0010】そこで本出願人は、先の特許願(特願平2
−417139号)において、採取した尿中に沈澱剤を
加えて尿中の蛋白等を水晶振動子表面上に沈澱させ、そ
して水晶振動子の発振周波数の変化を測定することによ
り尿中蛋白等の成分の量を求める方法を提案した。
[0010] Therefore, the applicant of the present invention is
No. 417139), a precipitating agent is added to the collected urine to precipitate proteins and the like in the urine on the surface of the crystal oscillator, and by measuring the change in the oscillation frequency of the crystal oscillator, A method for determining the amounts of components was proposed.

【0011】この方法は、水晶振動子表面に沈澱物があ
るとその発振周波数が変化することを利用したものであ
って、本法によると尿中の蛋白等を正確に測定すること
ができる。
This method makes use of the fact that the oscillation frequency changes when a precipitate is present on the surface of the crystal oscillator, and according to this method, proteins and the like in urine can be accurately measured.

【0012】ところで前述したように家庭等のトイレに
おいて尿中蛋白等を測定する場合、用を足したときに自
動的に測定できることが望ましく、またその測定装置は
小型であって、便器等に容易に内蔵でき或いは組み付け
られるものであることが望ましい。
By the way, as described above, when measuring urinary proteins and the like in household toilets, it is desirable to be able to automatically measure when urine is used, and the measuring device is compact and easy to use in toilet bowls and the like. It is desirable that it can be built in or assembled to the.

【0013】[0013]

【課題を解決するための手段】本発明の方法はこのよう
な課題を解決すべく案出されたもので、その要旨は、
(イ)容器内部に水晶振動子が設けられるとともに、液の
流入口と排出口とが設けられた測定セルと、(ロ)該測定
セル内部に測定対象としての液を流入させる流入通路
と、(ハ)該測定セル内部の測定済みの液を排出する排出
通路と、(ニ)尿サンプル液を該流入通路に導く尿サンプ
ル液導入通路と、(ホ)該導入通路を通じて尿サンプル液
を流入通路に注入する尿サンプル液注入手段と、(ヘ)尿
中成分を沈澱せしめる所定の沈澱剤を該流入通路に又は
前記測定セル内部に導くための沈澱剤導入通路と、(ト)
該沈澱剤導入通路を通じて該沈澱剤を注入する沈澱剤注
入手段とを設け、尿サンプル液を前記測定セルを含む経
路を一方向に流通させてセル内部の水晶振動子表面上に
前記沈澱剤との反応による沈澱物を沈澱せしめ、該水晶
振動子の沈澱前後の周波数変化を測定することにより尿
中成分を測定することにある。
The method of the present invention has been devised to solve such a problem, and its gist is as follows.
(A) a crystal oscillator provided inside the container, a measurement cell provided with a liquid inlet and a liquid outlet, and (b) an inflow passage through which a liquid to be measured flows into the measurement cell, (C) A discharge passage for discharging the measured liquid in the measurement cell, (d) a urine sample liquid introducing passage for guiding the urine sample liquid to the inflow passage, and (e) a urine sample liquid for flowing in through the introducing passage. A urine sample liquid injecting means for injecting into the passage, (f) a precipitating agent introducing passage for introducing a predetermined precipitating agent for precipitating urinary components into the inflow passage or into the measurement cell, and (g)
A precipitant injecting means for injecting the precipitant through the precipitant introducing passage is provided, and the urine sample liquid is unidirectionally circulated through a path including the measurement cell so that the precipitant and The precipitation in the reaction is caused to precipitate, and the urinary component is measured by measuring the frequency change before and after the precipitation of the crystal oscillator.

【0014】[作用及び発明の効果]本発明の方法にお
いては、尿サンプル液がその導入通路を通じて流入通路
内に注入されるとともに、所定の沈澱剤が沈澱剤導入通
路を通じて流入通路内に注入され、そしてそれらの混合
液が流入通路を通じて測定セル内部に流入させられる。
[Operation and Effect of the Invention] In the method of the present invention, the urine sample liquid is injected into the inflow passage through the introduction passage, and a predetermined precipitant is injected into the inflow passage through the precipitant introduction passage. , And their mixed liquid is caused to flow into the measuring cell through the inflow passage.

【0015】あるいはまた尿サンプル液が流入通路を通
じて測定セル内部に流入させられるとともに沈澱剤がセ
ル内部に直接注入される。そしてそれらの反応による沈
澱物が測定セル内部の水晶振動子表面に沈澱させられ
る。そしてその沈澱前後の水晶振動子の発振周波数変化
が測定され、その周波数変化によって尿中成分の量が求
められる。
Alternatively, the urine sample liquid is caused to flow into the measurement cell through the inflow passage and the precipitant is directly injected into the cell. Then, the precipitate due to these reactions is deposited on the surface of the quartz oscillator inside the measuring cell. Then, the oscillation frequency change of the crystal oscillator before and after the precipitation is measured, and the amount of the urinary component is obtained from the frequency change.

【0016】一方測定セル内部に導かれ、測定の行われ
た液は排出通路を通じてセル外部に流出せしめられる。
即ち本発明では液が一方向に流通させられ、その過程に
おいて尿中成分が定量分析される。
On the other hand, the liquid that has been introduced into the measuring cell and has been measured is allowed to flow out of the cell through the discharge passage.
That is, in the present invention, the liquid is circulated in one direction, and in the process, urine components are quantitatively analyzed.

【0017】このように本方法は流れの中に尿サンプル
液を注入して成分分析を行うものであり、分析装置を小
型に構成することができ、従ってこれを容易に便器内部
に内蔵させることができる。或いはまた所定の測定ユニ
ットとして便器に付設することができる。
As described above, this method is for injecting a urine sample solution into a flow for component analysis, and the analyzer can be constructed in a small size. Therefore, it can be easily incorporated in the toilet bowl. You can Alternatively, it can be attached to the toilet bowl as a predetermined measuring unit.

【0018】更にバッチ方式で尿中成分を測定する方法
と異なって自動化が容易であり、これにより便器使用者
は用を足すことで自動的に尿中成分を知ることができる
ようになり、健康管理を行い易くなるとともに前述した
図9に示す構想も実現可能となる。
Further, unlike the method of measuring the urinary components by the batch method, it is easy to automate, so that the toilet user can automatically know the urinary components by adding the urine. The management is facilitated and the concept shown in FIG. 9 described above can be realized.

【0019】[0019]

【実施例】次に本発明を尿中蛋白の定量分析に適用した
場合の実施例を図面に基づいて詳しく説明する。図1
(A)は尿中成分としての蛋白を分析するためのフロ−
インジェクションシステムを示したものである。図中1
0は測定セルで、容器内部に水晶振動子が設けられてい
る。
EXAMPLES Examples of the present invention applied to quantitative analysis of protein in urine will be described in detail with reference to the drawings. Figure 1
(A) is a flow chart for analyzing protein as a urinary component.
It shows an injection system. 1 in the figure
Reference numeral 0 is a measuring cell, and a crystal oscillator is provided inside the container.

【0020】測定セル10には流入通路12と排出通路
14とが接続されており、測定対象としての液が流入通
路12を通じて測定セル10内部に流入し、さらに測定
後において排出通路14を通じて外部に排出されるよう
になっている。
An inflow passage 12 and a discharge passage 14 are connected to the measuring cell 10, a liquid to be measured flows into the measuring cell 10 through the inflow passage 12, and after measurement, is discharged to the outside through the discharging passage 14. It is supposed to be discharged.

【0021】流入通路12には尿サンプル液の導入通路
16と尿中蛋白の沈澱剤(スルホサリチル酸,トリクロ
ール酢酸等)の導入通路18とが同一の個所で接続され
ている。尿サンプル液導入通路16は尿サンプル液を流
入通路12に導くためのもので、途中に混合コイル20
と尿サンプルを導入通路16に注入するための弁22と
が設けられている。
The inflow passage 12 is connected with an introduction passage 16 for introducing a urine sample liquid and an introduction passage 18 for introducing a precipitation agent for protein in urine (sulfosalicylic acid, trichloracetic acid, etc.) at the same position. The urine sample liquid introducing passage 16 is for guiding the urine sample liquid to the inflow passage 12, and the mixing coil 20 is provided on the way.
And a valve 22 for injecting a urine sample into the introduction passage 16.

【0022】尚30は洗浄液の導入通路であり、電磁弁
28を介して流入通路12に接続されている。
A cleaning liquid introduction passage 30 is connected to the inflow passage 12 via a solenoid valve 28.

【0023】このフロ−インジェクションシステムの場
合、まず緩衝溶液がポンプ24により送られて導入通路
16から流入通路12へと流入した上、測定セル10内
に流入せしめられる。そして一旦ポンプ24が停止され
て送液が中断され、その状態で測定セル10内の水晶振
動子の発振周波数F1が測定される。
In the case of this flow injection system, first, the buffer solution is sent by the pump 24 to flow from the introduction passage 16 into the inflow passage 12 and then into the measuring cell 10. Then, the pump 24 is once stopped and the liquid supply is interrupted, and in that state, the oscillation frequency F 1 of the crystal oscillator in the measurement cell 10 is measured.

【0024】次に尿サンプル液が導入通路16に注入さ
れて混合コイル20で緩衝溶液と混合された上、流入通
路12へと流入せしめられる。同時に沈澱剤が導入通路
18を通じて流入通路12に導かれ、そして合流した液
が反応コイル26を通過した後電磁弁28を経て測定セ
ル10内に流入する。
Next, the urine sample solution is injected into the introduction passage 16 and mixed with the buffer solution in the mixing coil 20, and then flown into the inflow passage 12. At the same time, the precipitant is introduced into the inflow passage 12 through the introduction passage 18, and the combined liquid passes through the reaction coil 26 and then flows into the measuring cell 10 via the solenoid valve 28.

【0025】この段階でポンプ24が停止され、測定セ
ル10内の水晶振動子の発振周波数F2が測定される。
そして発振周波数変化ΔF=F1−F2に基づいて沈澱物
の量、即ち尿中蛋白の総量が求められる。
At this stage, the pump 24 is stopped and the oscillation frequency F 2 of the crystal oscillator in the measuring cell 10 is measured.
Then, based on the oscillation frequency change ΔF = F 1 −F 2 , the amount of precipitate, that is, the total amount of urinary protein is obtained.

【0026】さて水晶振動子の周波数変化の測定が終わ
ったら、次に電磁弁28の流路を切り替えて洗浄溶液を
導入通路30を通じてポンプ24により流入通路12に
流入させ、更に測定セル10内部を流通させて水晶振動
子表面を含む測定セル10内部を洗浄する。
When the measurement of the frequency change of the crystal unit is completed, the flow path of the solenoid valve 28 is next switched to cause the cleaning solution to flow into the inflow passage 12 by the pump 24 through the introduction passage 30, and the inside of the measurement cell 10 is further changed. The inside of the measurement cell 10 including the surface of the crystal resonator is washed by flowing the crystal.

【0027】図1(B)は別のフローインジェクション
システムの例を示したもので、この例では沈澱剤導入通
路32が直接測定セル10に接続されている。
FIG. 1 (B) shows another example of the flow injection system, in which the precipitant introducing passage 32 is directly connected to the measuring cell 10.

【0028】このシステムにおいては、まず緩衝溶液と
尿サンプル液とが混合された上測定セル10内部に導か
れ、そして一旦ポンプ24が停止された状態で水晶振動
子の発振周波数F1が測定される
In this system, first, a buffer solution and a urine sample solution are mixed and introduced into the upper measuring cell 10. Then, the oscillation frequency F 1 of the crystal oscillator is measured with the pump 24 temporarily stopped. Ru

【0029】次に沈澱剤が導入通路32を通じて測定セ
ル10内部に注入され、セル10内部の尿サンプル液と
沈澱剤とが反応せしめられて沈澱物が水晶振動子表面上
に沈澱せしめられる。そして一定時間経過後の水晶振動
子の発振周波数F2が読み取られる。この時のF2とF1
との差ΔF=F1−F2から尿中の蛋白の総量が求められ
る。
Next, a precipitating agent is injected into the measuring cell 10 through the introduction passage 32, and the urine sample solution in the cell 10 is reacted with the precipitating agent to deposit the precipitate on the surface of the quartz oscillator. Then, the oscillating frequency F 2 of the crystal unit after a lapse of a certain time is read. F 2 and F 1 at this time
The total amount of protein in urine can be calculated from the difference ΔF = F 1 −F 2 .

【0030】測定終了後、緩衝溶液及び沈澱剤を送液し
ていたポンプ24が停止され、これとともに電磁弁28
の流路の切り替え,洗浄溶液の送液が行われて測定セル
10内部が洗浄溶液にて洗浄される。これにより一連の
測定操作が終了し、以後同様の操作の繰り返しによって
次の尿サンプル中の蛋白の分析が行われる。
After the measurement was completed, the pump 24, which was sending the buffer solution and the precipitant, was stopped, and at the same time, the solenoid valve 28 was stopped.
The flow paths are switched and the cleaning solution is sent to clean the inside of the measurement cell 10 with the cleaning solution. As a result, a series of measurement operations are completed, and thereafter, the same operation is repeated to analyze the protein in the next urine sample.

【0031】図2は図1(A)のフローインジェクショ
ンシステムにおいて用いられる測定セル構造の例を示し
たもので、内部に水晶振動子38が収容されている。水
晶振動子38は一面側のみが容器内部に露出する状態で
設けられている。
FIG. 2 shows an example of a measuring cell structure used in the flow injection system of FIG. 1A, in which a crystal oscillator 38 is housed. The crystal oscillator 38 is provided such that only one surface side is exposed inside the container.

【0032】測定セル36には、容器底部で開口する流
入用パイプ40と容器上部で開口する排出用パイプ41
とが設けられている。
In the measuring cell 36, an inflow pipe 40 opened at the bottom of the container and an exhaust pipe 41 opened at the top of the container.
And are provided.

【0033】この測定セル36においては、尿サンプル
液と沈澱剤との混合液が流入用パイプ40より測定セル
36内部に流入し、セル36内部に充満せしめられる。
そして反応による沈澱物が水晶振動子38表面に沈澱し
て水晶振動子の発振周波数が測定された後、セル36内
部の液が排出用パイプ41を通じて外部に排出される。
In the measuring cell 36, the mixed liquid of the urine sample liquid and the precipitant flows into the measuring cell 36 through the inflow pipe 40 and fills the inside of the cell 36.
Then, the precipitate due to the reaction is deposited on the surface of the crystal oscillator 38, the oscillation frequency of the crystal oscillator is measured, and then the liquid inside the cell 36 is discharged to the outside through the discharge pipe 41.

【0034】この測定セル36の場合、内部にエアが残
存せしめられず、排出用パイプ41を通じて十分に抜き
出される。
In the case of this measuring cell 36, air is not allowed to remain inside and is sufficiently extracted through the discharge pipe 41.

【0035】図3は同じフローインジェクションシステ
ムにおいて用いられる測定セルの別の構造例を示したも
ので、この例では流入用及び流出用のパイプ42,44
が測定セル43上面から内部に突入している。
FIG. 3 shows another structural example of the measuring cell used in the same flow injection system. In this example, inflow and outflow pipes 42 and 44 are shown.
Rushes in from the upper surface of the measuring cell 43.

【0036】一方のパイプ42は測定セル43の底部ま
で延び出しており、液が底部において測定セル43内部
に流入させられるようになっている。また他方のパイプ
44は測定セル43内の上部で開口しており、測定セル
43内部の液が上部より外部に排出されるようになって
いる。
One of the pipes 42 extends to the bottom of the measuring cell 43 so that the liquid can flow into the inside of the measuring cell 43 at the bottom. The other pipe 44 is open at the upper part inside the measuring cell 43, and the liquid inside the measuring cell 43 is discharged from the upper part to the outside.

【0037】図4は図1(B)に示すフローインジェク
ションシステムにおいて用いられる測定セルの構造例を
示したものである。この例では、沈澱剤を測定セル46
内部に導くための沈澱剤注入用パイプ48が流入用パイ
プ40,流出用パイプ41と別途に設けられている。
FIG. 4 shows an example of the structure of a measuring cell used in the flow injection system shown in FIG. 1 (B). In this example, the precipitating agent is added to the measuring cell 46.
A precipitant injection pipe 48 for guiding the inside is provided separately from the inflow pipe 40 and the outflow pipe 41.

【0038】図5は同様のフローインジェクションシス
テムにおいて用いられるセル構造の他の例を示したもの
で、図中52は沈澱剤注入用パイプである。
FIG. 5 shows another example of the cell structure used in the same flow injection system. In the figure, reference numeral 52 is a precipitant injection pipe.

【0039】図6は別のセル構造例を示したもので、測
定セル内部の天井面が傾斜面58とされている。このよ
うにすると、測定セル内部のエアを傾斜面58により排
出用パイプ56まで導いてエア抜きを十分に行い得る利
点がある。
FIG. 6 shows another example of the cell structure in which the ceiling surface inside the measuring cell is an inclined surface 58. This has the advantage that the air inside the measuring cell can be guided to the discharge pipe 56 by the inclined surface 58 and the air can be sufficiently evacuated.

【0040】次に図7,図8は図1(A)に示すフロー
インジェクションシステムに従って装置を構成し、これ
を便器に組み付けた場合の例を示したものである。まず
図7において60は洋風便器で、62は便器60に組み
付けられた尿中蛋白分析装置ユニットである。
Next, FIGS. 7 and 8 show an example in which an apparatus is constructed according to the flow injection system shown in FIG. 1A and is assembled in a toilet bowl. First, in FIG. 7, 60 is a Western-style toilet bowl, and 62 is a urine protein analyzer unit assembled in the toilet bowl 60.

【0041】この分析装置ユニット62の具体的構成が
図8に示してある。図8において64は測定セルで、内
部に水晶振動子65が組み込まれている。この測定セル
64には流入通路66及び排出通路67が接続されてお
り、その流入通路66に反応コイル70が設けられてい
る。
The concrete structure of the analyzer unit 62 is shown in FIG. In FIG. 8, reference numeral 64 is a measurement cell, in which a crystal oscillator 65 is incorporated. An inflow passage 66 and an exhaust passage 67 are connected to the measuring cell 64, and a reaction coil 70 is provided in the inflow passage 66.

【0042】72は尿サンプル液を緩衝溶液とともに流
入通路66に導入するための導入通路で、途中に混合コ
イル74が設けられている。そしてこの導入通路72と
流入通路66との接続部に電磁弁76が設けられてい
る。
Reference numeral 72 denotes an introduction passage for introducing the urine sample solution into the inflow passage 66 together with the buffer solution, and a mixing coil 74 is provided on the way. An electromagnetic valve 76 is provided at the connecting portion between the introduction passage 72 and the inflow passage 66.

【0043】82,84はそれぞれ緩衝溶液,沈澱剤
で、各々容器78,80内部に収容され、ポンプ86,
88にて送液される。
Reference numerals 82 and 84 respectively denote a buffer solution and a precipitating agent, which are accommodated in the containers 78 and 80, respectively, and are pump 86 and
The solution is delivered at 88.

【0044】尚図7に示しているように尿は便器60に
設けた採尿シリンダ83において一部が採取され、そし
て採取された尿サンプル液がポンプ90により所定の経
路内に送液される。
As shown in FIG. 7, part of the urine is collected by the urine collection cylinder 83 provided in the toilet bowl 60, and the collected urine sample solution is sent by the pump 90 into a predetermined path.

【0045】前記水晶振動子65には発振回路92が接
続され、更にこの発振回路92に周波数カウンタ94
が、更に周波数カウンタ94にコンピュータ96が接続
され、その演算結果即ち測定結果が表示器98に表示さ
れるようになっている。
An oscillator circuit 92 is connected to the crystal oscillator 65, and a frequency counter 94 is connected to the oscillator circuit 92.
Further, a computer 96 is further connected to the frequency counter 94, and the calculation result, that is, the measurement result is displayed on the display 98.

【0046】以上本発明の実施例を詳述したがこれはあ
くまで一例示であり、本発明はその主旨を逸脱しない範
囲において、当業者の知識に基づき様々な変更を加えた
態様で実施可能である。
Although the embodiment of the present invention has been described in detail above, this is merely an example, and the present invention can be carried out in a mode in which various modifications are made based on the knowledge of those skilled in the art without departing from the spirit of the invention. is there.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明のフローインジェクション式尿中成分の
分析方法の例を示す説明図である。
FIG. 1 is an explanatory diagram showing an example of a flow injection type urinary component analysis method of the present invention.

【図2】図1に示す方法において用いられる測定セルの
例を示す図である。
FIG. 2 is a diagram showing an example of a measuring cell used in the method shown in FIG.

【図3】その測定セルの他の例を示す図である。FIG. 3 is a diagram showing another example of the measurement cell.

【図4】その測定セルの更に他の例を示す図である。FIG. 4 is a diagram showing still another example of the measurement cell.

【図5】その測定セルの更に他の例を示す図である。FIG. 5 is a diagram showing still another example of the measurement cell.

【図6】その測定セルの更に他の例を示す図である。FIG. 6 is a diagram showing still another example of the measurement cell.

【図7】図1(A)に従って構成した分析装置ユニット
を便器に取り付けた例を示す図である。
FIG. 7 is a diagram showing an example in which an analyzer unit configured according to FIG. 1 (A) is attached to a toilet bowl.

【図8】その分析装置ユニットの具体的構成図である。FIG. 8 is a specific configuration diagram of the analyzer unit.

【図9】本発明の背景説明のための説明図である。FIG. 9 is an explanatory diagram for explaining the background of the present invention.

【符号の説明】[Explanation of symbols]

10,36,43,46,50,54,64 測定セル 12,66 流入通路 14,67 排出通路 16,72 尿サンプル液導入通路 18,32 沈澱剤導入通路 24,86,88,90 ポンプ 38,65 水晶振動子 40,42 流入用パイプ 41,44,56 排出用パイプ 10, 36, 43, 46, 50, 54, 64 Measuring cell 12, 66 Inflow passage 14, 67 Discharge passage 16, 72 Urine sample liquid introduction passage 18, 32 Precipitant introduction passage 24, 86, 88, 90 Pump 38, 65 Quartz crystal unit 40,42 Inflow pipe 41,44,56 Discharge pipe

Claims (1)

【特許請求の範囲】 【請求項1】 (イ)容器内部に水晶振動子が設けられる
とともに、液の流入口と排出口とが設けられた測定セル
と、(ロ)該測定セル内部に測定対象としての液を流入さ
せる流入通路と、(ハ)該測定セル内部の測定済みの液を
排出する排出通路と、(ニ)尿サンプル液を該流入通路に
導く尿サンプル液導入通路と、(ホ)該導入通路を通じて
尿サンプル液を流入通路に注入する尿サンプル液注入手
段と、(ヘ)尿中成分を沈澱せしめる所定の沈澱剤を該流
入通路に又は前記測定セル内部に導くための沈澱剤導入
通路と、(ト)該沈澱剤導入通路を通じて該沈澱剤を注入
する沈澱剤注入手段とを設け、尿サンプル液を前記測定
セルを含む経路を一方向に流通させてセル内部の水晶振
動子表面上に前記沈澱剤との反応による沈澱物を沈澱せ
しめ、該水晶振動子の沈澱前後の周波数変化を測定する
ことにより尿中成分を測定することを特徴とするフロ−
インジェクション方式による尿中成分の連続定量分析方
法。
Claims: (a) A measuring cell provided with a crystal resonator inside the container, and a liquid inlet and outlet, and (b) measurement inside the measuring cell. An inflow passage for inflowing a liquid as a target, (c) an exhaust passage for exhausting the measured liquid inside the measurement cell, and (d) a urine sample liquid introduction passage for guiding the urine sample liquid to the inflow passage, (E) Urine sample liquid injecting means for injecting the urine sample liquid into the inflow passage through the introduction passage, and (f) Precipitation for introducing a predetermined precipitating agent for precipitating components in urine into the inflow passage or inside the measurement cell. A reagent introducing passage and (g) a precipitating agent injecting means for injecting the precipitating agent through the precipitating agent introducing passage are provided, and the urine sample liquid is circulated in one direction through the passage including the measurement cell to cause crystal vibration in the cell. Precipitate the precipitate from the reaction with the precipitant on the surface of the child. And a urinary component by measuring the frequency change before and after the precipitation of the crystal oscillator.
Continuous quantitative analysis of urinary components by injection method.
JP3183221A 1991-06-27 1991-06-27 Continuous quantitative analysis method of urinary components by flow injection method Expired - Fee Related JP2555002B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3183221A JP2555002B2 (en) 1991-06-27 1991-06-27 Continuous quantitative analysis method of urinary components by flow injection method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3183221A JP2555002B2 (en) 1991-06-27 1991-06-27 Continuous quantitative analysis method of urinary components by flow injection method

Publications (2)

Publication Number Publication Date
JPH055735A true JPH055735A (en) 1993-01-14
JP2555002B2 JP2555002B2 (en) 1996-11-20

Family

ID=16131913

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3183221A Expired - Fee Related JP2555002B2 (en) 1991-06-27 1991-06-27 Continuous quantitative analysis method of urinary components by flow injection method

Country Status (1)

Country Link
JP (1) JP2555002B2 (en)

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WO2006064954A1 (en) * 2004-12-15 2006-06-22 Nihon Dempa Kogyo Co., Ltd Quartz sensor and sensing device
US7552639B2 (en) 2004-12-15 2009-06-30 Nihon Dempa Kogyo Co., Ltd. Quartz sensor and sensing device
US7554247B2 (en) 2004-12-15 2009-06-30 Nihon Dempa Kogyo Co., Ltd Component measuring device
US7555952B2 (en) 2004-12-28 2009-07-07 Nihon Dempa Kogyo Co., Ltd. Sensing device
US7845230B2 (en) 2005-08-03 2010-12-07 Nihon Dempa Kogyo Co., Ltd. Concentration sensor and concentration detector
JP2022065194A (en) * 2016-06-17 2022-04-26 シーメンス・ヘルスケア・ダイアグノスティックス・インコーポレイテッド Devices, methods and kits for multiplexing fluid sample via fluid sample reuse

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004245613A (en) * 2003-02-12 2004-09-02 Japan Science & Technology Agency Flow cell type qcm device and specimen measuring method
WO2006064954A1 (en) * 2004-12-15 2006-06-22 Nihon Dempa Kogyo Co., Ltd Quartz sensor and sensing device
US7552639B2 (en) 2004-12-15 2009-06-30 Nihon Dempa Kogyo Co., Ltd. Quartz sensor and sensing device
US7554247B2 (en) 2004-12-15 2009-06-30 Nihon Dempa Kogyo Co., Ltd Component measuring device
US7677087B2 (en) 2004-12-15 2010-03-16 Nihon Dempa Kogyo Co., Ltd. Quartz sensor and sensing device
US7555952B2 (en) 2004-12-28 2009-07-07 Nihon Dempa Kogyo Co., Ltd. Sensing device
US7845230B2 (en) 2005-08-03 2010-12-07 Nihon Dempa Kogyo Co., Ltd. Concentration sensor and concentration detector
JP2022065194A (en) * 2016-06-17 2022-04-26 シーメンス・ヘルスケア・ダイアグノスティックス・インコーポレイテッド Devices, methods and kits for multiplexing fluid sample via fluid sample reuse

Also Published As

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