JPS6011135A - Method for extracting vital sample - Google Patents
Method for extracting vital sampleInfo
- Publication number
- JPS6011135A JPS6011135A JP58119824A JP11982483A JPS6011135A JP S6011135 A JPS6011135 A JP S6011135A JP 58119824 A JP58119824 A JP 58119824A JP 11982483 A JP11982483 A JP 11982483A JP S6011135 A JPS6011135 A JP S6011135A
- Authority
- JP
- Japan
- Prior art keywords
- sample
- organic solvent
- cap
- beads
- stopper
- 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.)
- Pending
Links
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/483—Physical analysis of biological material
- G01N33/487—Physical analysis of biological material of liquid biological material
- G01N33/49—Blood
- G01N33/491—Blood by separating the blood components
Abstract
Description
【発明の詳細な説明】 イ 技術分野の利用分野 本発明は、生体試料の抽出方法に関する。[Detailed description of the invention] B Fields of application in the technical field The present invention relates to a biological sample extraction method.
口 従来技術
血液等の生体試料からコレステリンや薬物を抽出する場
合には、一定量の生体試料を分液ロートに採って有機溶
媒を加えて激しく振盪し、有機溶媒を分離した後、さら
に新しい有機溶媒を加え、同様の過程を数回繰り換えし
、得られた有機溶媒を濃縮して目的成分を抽出するよう
にしていた。Conventional technology When extracting cholesterin or drugs from biological samples such as blood, a certain amount of the biological sample is taken into a separating funnel, an organic solvent is added and shaken vigorously, and the organic solvent is separated. An organic solvent was added, the same process was repeated several times, and the resulting organic solvent was concentrated to extract the target component.
しかし、試料を大量の有機溶媒により抽出する関係」二
、危険な濃縮作業を必要とするのみならず、加振器や分
液σ−トを必要とし、作業が繁雑で分析装置の側で作業
を行なうことができないという問題があった。However, since the sample is extracted with a large amount of organic solvent, it not only requires dangerous concentration work, but also requires a vibrator and liquid separation plate, making the work complicated and having to be done on the side of the analyzer. The problem was that it was not possible to do so.
ハ、目的
本発明は、このような問題に鑑み、簡単な作業により直
ちに分析可能な試料を得ることができる新規な試料抽出
方法を提案することを目的とする。C. Objective: In view of the above-mentioned problems, it is an object of the present invention to propose a novel sample extraction method that can obtain a sample that can be immediately analyzed with simple operations.
こ 発明の構成
すなわち、本発明の特徴とするところは、生体試料の有
用成分を固体の表面に一旦コーティングせしめたのち、
このコーティング層を有機溶媒により溶出するようにし
た点にある。The structure of the present invention, that is, the feature of the present invention is that once the useful components of a biological sample are coated on the surface of a solid,
This coating layer is made to be eluted with an organic solvent.
ホ、実施例
そこで、以下に本発明の詳細を実施例に基づいて説明す
る。E. EXAMPLES The details of the present invention will now be explained based on examples.
第11Δは、本発明に使用する抽出器具の一例を示す外
観図であって5図中将号1は、試料抽出管をなす合成樹
脂やガラス製の容器で、その上端には試料注入口2が、
下端には排出口3が形成され、それぞれ共栓4と可撓性
キャップ5により密栓され、その内部にガラス製ビーズ
等の固体球状体6.6・・・・を封入して構成されてい
る。なお、図中符号7は、球状体6の流出を防止するフ
ィルタを示している。No. 11Δ is an external view showing an example of an extraction device used in the present invention, and No. 1 in Figure 5 is a container made of synthetic resin or glass that forms a sample extraction tube, with a sample injection port 2 at the upper end. but,
A discharge port 3 is formed at the lower end, each of which is hermetically sealed with a common stopper 4 and a flexible cap 5, and solid spherical bodies 6, 6, such as glass beads, etc. are sealed inside. . Note that the reference numeral 7 in the figure indicates a filter that prevents the spherical body 6 from flowing out.
このように構成した器具において、共栓4を外し、採取
した血液Sを注入口2から滴下すると(第2図工)、ガ
ラス製ビーズ6.6・・・・の表面が試料中の有用成分
により薄層状にコーティング′される(第2図H)。こ
の段階で可撓性キャップ5を外し、排出口3にから清浄
な空気Aを吹き込んで余った液体を放散させて乾燥する
(第2図工)。乾燥が終了した時点で再ひキャップ5を
閉め、注入口2かも一定量の有機溶媒Oを注入して共栓
4をして容器1を軽く振ると、ビーズ6.6・・・・の
表面に付着している目的成分が溶媒中に溶出する(第2
1図IT )。溶出後、キャップ5を外して内部の有機
溶媒を試料カンプC等に移すと、所定の濃度の目的成分
を得ることができる(第2図V)。In the device configured in this way, when the stopper 4 is removed and the collected blood S is dripped from the injection port 2 (see Figure 2), the surface of the glass beads 6. It is coated in a thin layer (Fig. 2H). At this stage, the flexible cap 5 is removed, and clean air A is blown into the discharge port 3 to disperse the excess liquid and dry it (second figure). When the drying is completed, close the cap 5 again, inject a certain amount of organic solvent O into the injection port 2, close the stopper 4, and shake the container 1 lightly. The target component attached to the solvent is eluted into the solvent (second
Figure 1 IT). After elution, by removing the cap 5 and transferring the organic solvent inside to a sample comp C or the like, the target component at a predetermined concentration can be obtained (FIG. 2 V).
なお、この実施例では、固体球状体としてカラス製ビー
ズを使用しているが、シリカゲル等の吸着剤を球形状に
成形したものを使用してもよい。In this example, glass beads are used as the solid spherical bodies, but spherical adsorbents such as silica gel may also be used.
[実施例]
1:、述した抽出方法によって得た血液中のコレステロ
ールとコレステリルエステルに内部標準物質としてコレ
ステけ一ルベンゾエートを混入してなるものを試料にし
、キャピラリーカラム及び充填カラムを備えたガスクロ
マトグラフにより分析したところ、それぞれ第31J(
A)、(B)に示したようにコレステロール(I)、コ
レステロールベンンエート(II)、コレステリルCI
5:+又は2エステル(■)、コレステリルc +b:
oエステル(IV )、コレステリルCIl?l、2又
は3エステル(V)、及びコレステリルC180エステ
ル(V7)を検出することができ、分析結果に悪影響を
及ぼすような夾雑物を含まないことが解った。[Example] 1: A gas chromatograph equipped with a capillary column and a packed column was prepared by using a sample obtained by mixing cholesterol and cholesteryl ester in blood obtained by the above extraction method with cholesteryl benzoate as an internal standard substance. When analyzed by
As shown in A) and (B), cholesterol (I), cholesterol bennate (II), cholesteryl CI
5: + or 2 ester (■), cholesteryl c +b:
o ester (IV), cholesteryl CIl? 1, 2, or 3 ester (V), and cholesteryl C180 ester (V7) could be detected, and it was found that the sample did not contain any impurities that would adversely affect the analysis results.
へ、効果
以上、説明したように本発明によれば、生体試料中の有
用成分を一旦、固体の表面に薄層状に付着せしめた後、
有機溶媒により抽出するようにしたので、分液ロートや
加振器等を用いることなく、簡単な作業により分析装置
の側で目的成分を抽出することができ、生体試料を迅速
かつ簡便に分析することができる。B. Effects As explained above, according to the present invention, after the useful components in the biological sample are once attached to the surface of the solid in a thin layer,
Since extraction is performed using an organic solvent, the target component can be easily extracted on the analyzer side without using a separating funnel or a shaker, allowing biological samples to be analyzed quickly and easily. be able to.
第1図は、本発明に使用する抽出器具の一例を示す外観
図、第2[多(I)乃至(V)は、それぞれ本発明の抽
出作業を示す説明図、第3図(A)(B)は、それぞれ
本発明により得られた試料の分析結果を示すクロマトグ
ラムである。
1・・・・試料抽出管 2・・・・試料注入1」3・・
・・排出口 4・・・・共栓
5・・・・キャップ 6・・・・ガラス製ビーズ出願人
株式会社 島津製作所
代理人 弁理士 四 川 慶 治
同 木 村 勝 彦
第7図
第2図
m (x)(It)(y>
第3図
(A>
(B)Fig. 1 is an external view showing an example of the extraction device used in the present invention, Fig. 2 (I) to (V) are explanatory drawings showing the extraction work of the present invention, and Fig. B) is a chromatogram showing the analysis results of samples obtained according to the present invention. 1... Sample extraction tube 2... Sample injection 1" 3...
...Discharge port 4...Plug 5...Cap 6...Glass beads Applicant: Shimadzu Corporation Representative Patent attorney: Harutoshi Yotsukawa Katsuhiko Kimura Figure 7 Figure 2 m (x) (It) (y> Figure 3 (A> (B)
Claims (1)
て該試料中の有用成分により前記球状体の表面をコーテ
ィングする工程、余剰の液体を放Qiさせる工程、前記
球状体を有機溶媒に浸漬して表面に付着している目的成
分を溶出する工程とからなる生体試料抽出方法。A step of injecting a biological sample into a container containing a large number of solid spherical bodies and coating the surface of the spherical bodies with useful components in the sample, a step of releasing excess liquid Qi, and a step of dissolving the spherical bodies in an organic solvent. A biological sample extraction method consisting of a step of immersing the sample and eluting the target component attached to the surface.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58119824A JPS6011135A (en) | 1983-06-30 | 1983-06-30 | Method for extracting vital sample |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58119824A JPS6011135A (en) | 1983-06-30 | 1983-06-30 | Method for extracting vital sample |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6011135A true JPS6011135A (en) | 1985-01-21 |
Family
ID=14771156
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58119824A Pending JPS6011135A (en) | 1983-06-30 | 1983-06-30 | Method for extracting vital sample |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6011135A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0241441A (en) * | 1988-07-29 | 1990-02-09 | Tsudakoma Corp | Method for controlling feed of fluid in textile machine |
US5695989A (en) * | 1990-10-18 | 1997-12-09 | Cellpro, Inc. | Apparatus and method for separating particles using a pliable vessel |
-
1983
- 1983-06-30 JP JP58119824A patent/JPS6011135A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0241441A (en) * | 1988-07-29 | 1990-02-09 | Tsudakoma Corp | Method for controlling feed of fluid in textile machine |
US5695989A (en) * | 1990-10-18 | 1997-12-09 | Cellpro, Inc. | Apparatus and method for separating particles using a pliable vessel |
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