JP4403568B2 - Sweat collection method - Google Patents
Sweat collection method Download PDFInfo
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- JP4403568B2 JP4403568B2 JP09820999A JP9820999A JP4403568B2 JP 4403568 B2 JP4403568 B2 JP 4403568B2 JP 09820999 A JP09820999 A JP 09820999A JP 9820999 A JP9820999 A JP 9820999A JP 4403568 B2 JP4403568 B2 JP 4403568B2
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- sweat
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- solvent
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- 210000004243 sweat Anatomy 0.000 title claims description 93
- 238000000034 method Methods 0.000 title claims description 33
- 239000002904 solvent Substances 0.000 claims description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 230000035900 sweating Effects 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 5
- 238000003825 pressing Methods 0.000 claims description 2
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 description 19
- 229960001948 caffeine Drugs 0.000 description 10
- LPHGQDQBBGAPDZ-UHFFFAOYSA-N Isocaffeine Natural products CN1C(=O)N(C)C(=O)C2=C1N(C)C=N2 LPHGQDQBBGAPDZ-UHFFFAOYSA-N 0.000 description 9
- VJEONQKOZGKCAK-UHFFFAOYSA-N caffeine Natural products CN1C(=O)N(C)C(=O)C2=C1C=CN2C VJEONQKOZGKCAK-UHFFFAOYSA-N 0.000 description 9
- 238000012544 monitoring process Methods 0.000 description 5
- 239000008280 blood Substances 0.000 description 4
- 210000004369 blood Anatomy 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 239000012153 distilled water Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 210000003813 thumb Anatomy 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 238000005070 sampling Methods 0.000 description 2
- 230000028327 secretion Effects 0.000 description 2
- 206010040880 Skin irritation Diseases 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000002306 biochemical method Methods 0.000 description 1
- 238000010241 blood sampling Methods 0.000 description 1
- 229940124827 caffeine tablet Drugs 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 210000004247 hand Anatomy 0.000 description 1
- 230000001900 immune effect Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
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- Measuring And Recording Apparatus For Diagnosis (AREA)
Description
【0001】
【発明の属する技術分野】
本発明は被験者が発汗する汗を採取する方法で、特に採取した汗に含まれる生体成分を測定する非侵襲測定に用いるのに好適な汗採取方法に関する。
【0002】
【従来の技術】
ひとの血液や血清を試料として生化学的手法や免疫学的手法で各種の生体成分測定する方法が臨床検査等で広く行われている。しかし、その測定をするためには被験者より血液を採血しなくてはならず被験者の負担が大きく、又その採血は医師など血液採血資格者によって行われなくてはならないため、いつでもどこででも行なえるような検査ではない。
【0003】
そこで、被験者に負担のかからない非侵襲検査にて生体成分を測定する方法が各種試みられている。そのなかでも、汗は体表面に発汗される液体で非侵襲的に採取することが可能であり、人の代謝に基づいて分泌された各種の生体成分が含まれているため、非侵襲検査の対象のひとつとして注目されている。そこで被験者の汗を採取する方法が幾つか検討されている。
【0004】
汗の採取方法としては、皮膚表面に装着するパッチ式のものが簡便なものとして用いられている。この方法は吸湿素材を皮膚表面に貼り付ける方法で、吸湿素材に含まれる汗中生体成分を測定することができる。又、アームパック法として、肘から先をビニール袋で覆いゴムバンド等で袋を塞いで、腕から滴下する汗を採取する方法が知られている。
【0005】
【発明が解決しようとする課題】
しかし、パッチ法では吸湿素材に吸収された状態で汗を採取するため、汗成分を測定する測定方法にどうしても制限があるという問題があり、ビニールパック法で汗を必要量滴下させるまで発汗させるのは大変でなかなか採取できないという問題がある。そして、吸湿素材に吸収されたり、ビニール袋に滴下した汗だけが採取されるので、皮膚表面で乾燥した汗に含まれていた生体成分は皮膚についたままで採取はされない。さらに、パッチ法では採取された汗の量がわからないため、測定にて成分が検出できなかった際も、汗自体の採取が不充分であったのか、汗に含まれていなかったのかが分らないという問題がある。
【0006】
これらの問題を解決するため、本発明の発明者らから、皮膚表面にカプセルを密着させその中に除湿空気を供給して、その水分量を測定してコンプレッサーで採取部に移送して分泌物を測定する装置が出願されている(特開平10―239309号)。しかしこの装置には冷却採取部が必要で大がかりになるという問題が残されている。
【0007】
本発明は、被験者に負担を与えないような簡単かつ短時間で被験者の汗を効率的に採取することができる方法を提供するものである。さらに、対応する別の部位の発汗量を測定することで、発汗採取のモニタリングをすることができる汗採取方法を提供するものである。
【0008】
【課題を解決するための手段】
本発明の汗採取方法は、溶媒としてアルコールを含む水をいれた小型容器を片方の手の所定部位へ押し当てて皮膚に溶媒を浸たし、皮膚から発汗される汗を溶媒に溶かすことで汗を採取する汗採取方法である。
さらに第二の発明として、汗を採取する際に、もう片方の手の採取する部位と対応する部位の発汗量を測定し、測定された発汗量を採取された汗の量とみなして、採取される汗の量をモニタリングすることを特徴とする汗採取方法である。
【0009】
本発明で採取される汗には、皮膚表面より分泌される生体成分も含まれる。本発明の汗の採取に用いる採取容器は、容器中の溶媒が皮膚を浸すようにすることで汗を溶媒に溶かし込むためのものである。この採取容器の開口面積が一定にすれば皮膚単位面積あたりの発汗を反映する。採取容器としてサンプルチューブ(500μl容)を用いると採取した後、蓋をして保管することができ、遠心機にそのままかけることもできる。平べったい容器を用いれば皮膚表面に貼付けやすい。
【0010】
本発明に用いる溶媒は、汗を汗中生体成分とともに溶かす溶媒が測定する生体成分の種類や測定方法に応じて適宜選択される。アルコールを含む蒸留水が汗と汗中生体成分とを溶かすのに好適である。
【0011】
被験者の皮膚表面には通常、他への接触等による様々な成分がついているので、汗を採取する前に採取する皮膚表面部を清浄にする必要がある。この清浄方法については、アルコール消毒では皮膚に対する刺激が強すぎるのか発汗が制限されるため好ましくない。常温の蒸留水を汗採取部位に短時間(5から15秒間位が好適)流すことで、皮膚表面の不純物は落とされ、汗の発汗も制限されないので汗採取前の清浄方法として好適である。
【0012】
又、汗の発汗量については外部環境や個人差さらにその日の体調などで大きく変化するため、採取条件を一定にしてもどの程度の汗が採取されたのかが分らない。しかし、本法では汗を直接溶媒に溶かし込むため、汗の採取量を測定することは困難である。そこで、特定部位の発汗量を調べる装置を用いて、右手と左手との掌側の同じ部位の発汗量をしらべたところ、驚くことにほぼ同じ量の汗が発汗されているという結果が図2のように得られた。それで、片方の手で汗採取を行ない、同時に逆の手の同じ部位における発汗量を発汗量測定装置を用いて測定することで、採取された汗の量を推定することが可能となった。すなわち汗を採取する部位と体の左右で対称となる部位の発汗量をこの発汗量測定装置で測定し、測定された発汗量を採取された汗の量とみなして、汗採取量をモニタリングすることである。この方法では汗採取条件をモニタリングによって任意に設定することが可能となり、測定した生体成分の汗中の濃度を演算することも可能となった。
【0013】
【実施例】
以下、本発明の一実施例を図面を参照しながら説明する。本実施例では被験者の汗中のカフェイン濃度の測定を以下のように行なった。
(1)被験者にはカフェイン錠剤(Kafe soft 無水カフェイン93mg含有)を飲用させる。
(2)被験者の両手を常温の蒸留水にて10秒間流し、清浄にする。
(3)それから5分間待った後、1%アルコール水溶液70μlを入れた500μl容サンプルチューブを拇指掌側中心部に図1のようにひっくり返して押し当て、押し当てたままひっくり返す転倒を3分間行ない、皮膚表面を溶媒に浸す。
(4)それと同時にもう片方の手の拇指の同じ部位に局所発汗計測装置(スズケン製Kenz Perspiro OSS−100)を取り付け、汗の発汗量をモニタリングする。
(5)このようにして汗採取したサンプルチューブ中の溶媒をガスクロマトグラフィー/質量分析計にて、カフェイン濃度を測定した。
【0014】
以上の操作により、溶媒中のカフェイン濃度(図3の■)と汗発汗量(図3の▲)と汗中のカフェイン濃度(図4)が得られた。汗中のカフェイン量は、採取後25分ですでに分泌され、1時間あたりに最大値を持ち、5時間でかなり低下してしまうというカフェイン摂取後のモニタリング結果が得られた。
【0015】
【発明の効果】
この方法によって、血液を採血することもなく容易にモニタリングするための汗採取することができる。汗の発汗量も測定しているので汗採取の実質的な監視をすることもできる。本発明が提供する汗採取方法は簡便な方法でモニタリングも容易であるので、汗の非侵襲検査に役立てることができるものである。又、汗に分泌される生体成分についてはまだまだ調べられていないものが多い。熱や刺激をくわえることで汗の量が増えることが知られているが、その際単に水分のみが増えるのか生体成分の分泌量も増えるのかなど本発明で様々な汗に関する研究も可能となる。
【0016】
【図面の簡単な説明】
【図1】拇指に容器を押し当て、皮膚表面を溶媒に浸した状態のブロック図である。
【図2】左右拇掌側の発汗量の相関を調べた相関図である。
【図3】本実施例の採取された汗を含む溶媒のカフェイン濃度と発汗量の経時変化図である。
【図4】本実施例の採取された汗を含む溶媒のカフェイン濃度と発汗量より求められた汗中のカフェイン濃度の経時変化図である。[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a method for collecting sweat perspired by a subject, and particularly to a method for collecting sweat suitable for use in non-invasive measurement for measuring biological components contained in the collected sweat.
[0002]
[Prior art]
A method of measuring various biological components using human blood or serum as a sample by a biochemical technique or an immunological technique is widely used in clinical examinations and the like. However, in order to perform the measurement, blood must be collected from the subject, and the burden on the subject is heavy. In addition, blood collection must be performed by a blood sampling qualified person such as a doctor, so it can be performed anytime and anywhere. It is not such an inspection.
[0003]
Therefore, various methods have been attempted for measuring biological components in a non-invasive test that does not burden the subject. Among them, sweat is a liquid that is perspired on the body surface and can be collected non-invasively and contains various biological components secreted based on human metabolism. It is attracting attention as one of the objects. Thus, several methods for collecting the subject's sweat have been studied.
[0004]
As a method for collecting sweat, a patch type attached to the skin surface is used as a simple method. This method is a method of sticking a hygroscopic material to the skin surface, and can measure biological components in sweat contained in the hygroscopic material. As an arm pack method, a method is known in which the tip of the elbow is covered with a plastic bag, the bag is closed with a rubber band or the like, and the sweat dripped from the arm is collected.
[0005]
[Problems to be solved by the invention]
However, since the patch method collects sweat in a state absorbed by the moisture-absorbing material, there is a problem that there is a limit to the measurement method for measuring the sweat component, and the vinyl pack method causes sweat until the required amount of sweat is dripped. Has a problem that it is difficult to collect. Since only the sweat absorbed by the hygroscopic material or dripped onto the plastic bag is collected, the biological components contained in the sweat dried on the skin surface remain on the skin and are not collected. In addition, since the amount of sweat collected by the patch method is unknown, even if the component cannot be detected by measurement, it is not known whether the sweat itself was insufficiently collected or not contained in the sweat. There is a problem.
[0006]
In order to solve these problems, the inventors of the present invention have closely attached a capsule to the skin surface, supplied dehumidified air therein, measured the amount of water, and transferred it to a sampling section with a compressor to be a secretion. Has been filed (Japanese Patent Laid-Open No. 10-239309). However, this apparatus has a problem that a cooling sampling part is required and becomes large-scale.
[0007]
The present invention provides a method capable of efficiently collecting a subject's sweat in a simple and short time without burdening the subject. Furthermore, the present invention provides a sweat collection method capable of monitoring the collection of sweat by measuring the amount of sweat at another corresponding site.
[0008]
[Means for Solving the Problems]
The method for collecting sweat of the present invention involves pressing a small container containing alcohol as a solvent against a predetermined part of one hand to immerse the solvent in the skin, and dissolve the sweat sweated from the skin in the solvent. This is a sweat collection method for collecting sweat.
Further, as a second invention, when collecting sweat, measure the amount of sweat in the part corresponding to the part to be collected in the other hand, and consider the measured amount of sweat as the amount of collected sweat. This is a sweat collection method characterized by monitoring the amount of sweat produced.
[0009]
The sweat collected in the present invention includes biological components secreted from the skin surface. The collection container used for collecting sweat of the present invention is for dissolving sweat in a solvent by allowing the solvent in the container to soak the skin. If the opening area of the collection container is made constant, the perspiration per unit skin area is reflected. When a sample tube (500 μl) is used as a collection container, it can be stored after being collected, and can be directly applied to a centrifuge. If you use a flat container, it can be easily applied to the skin surface.
[0010]
The solvent used in the present invention is appropriately selected according to the type and measuring method of the biological component measured by the solvent that dissolves sweat together with the biological component in sweat. Distilled water containing alcohol is suitable for dissolving sweat and sweat biological components.
[0011]
Since the skin surface of the subject usually has various components due to contact with others, it is necessary to clean the skin surface portion collected before collecting the sweat. As for this cleaning method, alcohol disinfection is not preferable because the skin irritation is too strong or sweating is limited. By flowing distilled water at room temperature through the sweat collection site for a short time (preferably about 5 to 15 seconds), impurities on the skin surface are removed and sweat perspiration is not limited, which is suitable as a cleaning method before sweat collection.
[0012]
In addition, since the amount of sweat perspiration varies greatly depending on the external environment, individual differences, and physical condition of the day, it is not possible to know how much sweat has been collected even if the collection conditions are constant. However, in this method, since sweat is directly dissolved in a solvent, it is difficult to measure the amount of collected sweat. Thus, using a device for examining the sweating amount of a specific part, the amount of sweating of the same part on the palm side of the right hand and the left hand was examined. As a result, surprisingly the same amount of sweat was sweated. Was obtained as follows. Therefore, it was possible to estimate the amount of collected sweat by collecting sweat with one hand and simultaneously measuring the amount of sweat in the same part of the opposite hand using a sweat amount measuring device. That is, the amount of sweat collected at the site where the sweat is collected and the part which is symmetrical on the left and right of the body are measured by this sweat amount measuring device, and the measured amount of sweat is regarded as the amount of the collected sweat and the amount of sweat collected is monitored That is. In this method, it is possible to arbitrarily set the sweat collection condition by monitoring, and it is also possible to calculate the concentration of the measured biological component in the sweat.
[0013]
【Example】
Hereinafter, an embodiment of the present invention will be described with reference to the drawings. In this example, the caffeine concentration in the sweat of the subject was measured as follows.
(1) Have subjects drink caffeine tablets (containing 93 mg of Kafe soft anhydrous caffeine).
(2) Clean both hands of the subject with normal temperature distilled water for 10 seconds.
(3) After waiting for 5 minutes, a 500 μl sample tube containing 70 μl of 1% alcohol aqueous solution was turned over and pressed against the center of the thumb palm as shown in FIG. Soak the skin surface in a solvent.
(4) At the same time, a local sweat measurement device (Kenz Perspiro OSS-100 manufactured by Suzuken) is attached to the same part of the thumb of the other hand, and the amount of sweat perspiration is monitored.
(5) The caffeine concentration of the solvent in the sample tube collected as described above was measured with a gas chromatography / mass spectrometer.
[0014]
By the above operation, the caffeine concentration in the solvent (■ in FIG. 3), the sweat perspiration (▲ in FIG. 3), and the caffeine concentration in sweat (FIG. 4) were obtained. The monitoring result after caffeine intake was obtained that the amount of caffeine in sweat was already secreted 25 minutes after collection and had a maximum value per hour and decreased considerably in 5 hours.
[0015]
【The invention's effect】
By this method, it is possible to collect sweat for easy monitoring without collecting blood. Since the amount of sweat perspiration is also measured, it is possible to substantially monitor sweat collection. Since the sweat collection method provided by the present invention is a simple method and easy to monitor, it can be used for a noninvasive examination of sweat. Many biological components secreted by sweat have not been investigated yet. It is known that the amount of sweat increases by adding heat and stimuli, but in this case, various studies on sweat such as whether only the amount of water increases or the amount of secretion of biological components also increases are possible.
[0016]
[Brief description of the drawings]
FIG. 1 is a block diagram of a state where a container is pressed against a thumb and the skin surface is immersed in a solvent.
FIG. 2 is a correlation diagram in which the correlation between sweating amounts on the left and right palm sides is examined.
FIG. 3 is a graph showing changes over time in the concentration of caffeine and the amount of perspiration of a solvent containing sweat collected in this example.
FIG. 4 is a graph showing a change over time of the caffeine concentration in sweat obtained from the caffeine concentration of the solvent containing sweat collected in this example and the amount of perspiration.
Claims (4)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP09820999A JP4403568B2 (en) | 1999-04-05 | 1999-04-05 | Sweat collection method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP09820999A JP4403568B2 (en) | 1999-04-05 | 1999-04-05 | Sweat collection method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2000287942A JP2000287942A (en) | 2000-10-17 |
| JP4403568B2 true JP4403568B2 (en) | 2010-01-27 |
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| Application Number | Title | Priority Date | Filing Date |
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| JP09820999A Expired - Fee Related JP4403568B2 (en) | 1999-04-05 | 1999-04-05 | Sweat collection method |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4827032B2 (en) * | 2005-06-10 | 2011-11-30 | クラシエフーズ株式会社 | Skin release component measurement method |
| JP2010266203A (en) * | 2008-05-20 | 2010-11-25 | Sony Corp | Biological information acquisition method, biological information acquisition device, physiologically active substance measuring method, and physiologically active substance measuring device |
| US9918671B2 (en) * | 2012-05-29 | 2018-03-20 | Stellenbosch University | Sweat measurement device |
| JP6383920B2 (en) * | 2013-09-11 | 2018-09-05 | 有限会社ピコデバイス | Methods used as criteria for Parkinson's disease |
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