JP4576222B2 - In vivo characteristic sensor and biological information monitoring system - Google Patents

In vivo characteristic sensor and biological information monitoring system Download PDF

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JP4576222B2
JP4576222B2 JP2004366599A JP2004366599A JP4576222B2 JP 4576222 B2 JP4576222 B2 JP 4576222B2 JP 2004366599 A JP2004366599 A JP 2004366599A JP 2004366599 A JP2004366599 A JP 2004366599A JP 4576222 B2 JP4576222 B2 JP 4576222B2
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幸宏 赤堀
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Nikkiso Co Ltd
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Description

本発明は、体内特性センサ及び生体情報モニタリングシステムに関する。 The present invention relates to an in-vivo characteristic sensor and a biological information monitoring system .

従来、医療現場において薬物を体内に投与する場合、使用する薬物が決まると、その薬物について得られている一般的データと、患者の臨床データに基づき動力学的モデルが立てられる。前記モデルに基づき薬剤の血中濃度が治療範囲に入るような投与計画が設定され、実際に薬剤が投与される。   Conventionally, when a drug is administered into the body at a medical site, when a drug to be used is determined, a kinetic model is established based on general data obtained for the drug and clinical data of the patient. Based on the model, a dosage plan is set so that the blood concentration of the drug falls within the therapeutic range, and the drug is actually administered.

投与後の血中濃度の測定からモデルが補正され、再び適正な投与計画が設定される。設定された投与計画に基づき薬剤を投与し、投与後の血中濃度を測定して再び投与計画にフィードバックし、薬剤の投与量をコントロールする。このようなシステムは、すでに糖尿病治療システムにおいて実用化の研究が行われている。   The model is corrected from the measurement of blood concentration after administration, and an appropriate administration plan is set again. The drug is administered based on the set administration plan, the blood concentration after the administration is measured, and fed back to the administration plan again to control the dose of the drug. Such a system has already been studied for practical use in a diabetes treatment system.

例えば、この糖尿病治療システムにおいては、インシュリン投与による血糖値の変化をグルコースセンサーでモニターする仕組になっており、インシュリン濃度は直接測定されることなく、インシュリン投与量を制御できる。   For example, in this diabetes treatment system, changes in blood glucose level due to insulin administration are monitored by a glucose sensor, and the insulin dose can be controlled without directly measuring the insulin concentration.

ここで、例えば、薬剤の適切な注入量を知るために、連続的な生体情報をモニタリングする場合は、生体情報をモニタするモニタリング用のセンサーと、生体内へ薬剤を注入する薬剤注入用ポートとを備えた装置が必要であった(非特許文献1参照)。   Here, for example, when monitoring continuous biological information in order to know an appropriate injection amount of the drug, a monitoring sensor for monitoring the biological information, a drug injection port for injecting the drug into the living body, (See Non-Patent Document 1).

榊田 典治、外4名,「携帯型人工膵島の開発」,化学工業,平成14年12月,p.60−64Noriharu Hamada, 4 others, “Development of portable artificial islets”, Chemical Industry, December 2002, p. 60-64

しかしながら、非特許文献1記載の技術によれば、このモニタリング用のセンサー部分が大きいので、該センサー部分と薬剤注入用ポートは別個の装置からなり、穿刺が2回必要であった。このため、患者に身体的負担を強いていた。   However, according to the technique described in Non-Patent Document 1, since the sensor part for monitoring is large, the sensor part and the drug injection port are composed of separate devices, and two punctures are required. For this reason, the physical burden was imposed on the patient.

さらに、生体の接触部分が2箇所であるということは感染症を引き起こす可能性も大きくしていた。したがって、患者のQOLという点からも、穿刺を1回にすることが望ましかったが、そのためにはモニタリング用のセンサー部材と、薬剤注入用ポートを一体化する必要があった。   Furthermore, the fact that there are two contact portions of the living body has increased the possibility of causing infection. Therefore, from the viewpoint of the patient's QOL, it was desired to puncture once, but in order to do so, it was necessary to integrate the monitoring sensor member and the drug injection port.

本発明は、このような従来の問題点を解消し、人体への液体の注入と、人体内の所定の特性の測定を1度に行うことができる体内特性センサ及び生体情報モニタリングシステムを提供することをその課題とする。 The present invention provides an in-vivo characteristic sensor and a biological information monitoring system capable of solving such a conventional problem and injecting a liquid into the human body and measuring a predetermined characteristic in the human body at a time. That is the issue.

前記課題を解決するための請求項1に記載の発明は、人体に注入される液体が内部を流通可能に形成されてなる筒部材と、前記筒部材の外周部分に設けられ、人体内の所定の特性を感知可能に形成されてなるセンサ部材と、前記筒部材の外周部分に設けられ、前記センサ部材からの信号を伝達可能な導電体とを備え、前記センサ部材が、前記筒部材と前記センサ部材と前記導電体とにより形成される部材表面から露出し、前記部材表面がなだらかな曲面を有し、人体への液体の注入と人体内の所定の特性の測定とを同時に実施可能であることを特徴とする体内特性センサであり、
請求項2に記載の発明は、前記筒部材が、穿刺可能に形成されてなることを特徴とする前記請求項1に記載の体内特性センサであり、
請求項3に記載の発明は、前記筒部材が、多孔質性材料で形成されてなることを特徴とする前記請求項1または請求項2に記載の体内特性センサであり、
前記課題を解決するための請求項4に記載の発明は、前記請求項1〜3のいずれか1項に記載の体内特性センサと、前記体内センサに接続され、前記センサ部材から前記導電体を介して送られてくる信号を増幅する増幅器と、前記増幅器で増幅された信号を受信し記録する記録計と、前記記録計から伝達された信号に基づいて薬剤の注入量を算出する薬剤注入量制御装置とを備えてなることを特徴とする生体情報モニタリングシステムである。
The invention according to claim 1 for solving the above problems, a cylindrical member which is liquid to be injected into the human body formed by fluidly form an internal, set at the periphery of the tubular member vignetting, in the human body A sensor member formed so as to be capable of sensing a predetermined characteristic; and a conductor provided on an outer peripheral portion of the cylindrical member and capable of transmitting a signal from the sensor member , wherein the sensor member includes the cylindrical member and It is exposed from the surface of the member formed by the sensor member and the conductor, the surface of the member has a gentle curved surface, and it is possible to simultaneously inject liquid into the human body and measure a predetermined characteristic in the human body. It is an internal characteristic sensor characterized by being,
The invention according to claim 2 is the in-vivo characteristic sensor according to claim 1, wherein the cylindrical member is formed to be puncturable.
The invention according to claim 3 is the in-vivo characteristic sensor according to claim 1 or 2, wherein the cylindrical member is formed of a porous material.
The invention according to claim 4 for solving the above-mentioned problem is characterized in that the in-vivo characteristic sensor according to any one of claims 1 to 3 is connected to the in-vivo sensor, and the conductor is transferred from the sensor member. An amplifier for amplifying a signal sent through the amplifier, a recorder for receiving and recording the signal amplified by the amplifier, and a medicine injection amount for calculating a medicine injection amount based on the signal transmitted from the recorder A biological information monitoring system comprising a control device.

本発明によれば、前記筒部材と、前記センサ部材と、前記導電体とを備えてなることにより、筒部材を人体内へ挿入することで、筒部材内部を通って、液体が人体内に注入される。そして、同時に、筒部材に設けられたセンサ部材によって、人体内の所定の特性が測定される。ここで、測定された所定の特性は、導電体によって、信号として外部に伝達される。したがって、人体への液体の注入と、人体内の所定の特性の測定を1度に行うことができる。   According to the present invention, since the cylindrical member, the sensor member, and the conductor are provided, the cylindrical member is inserted into the human body, so that the liquid passes through the cylindrical member and enters the human body. Injected. At the same time, predetermined characteristics in the human body are measured by the sensor member provided on the cylindrical member. Here, the measured predetermined characteristic is transmitted to the outside as a signal by the conductor. Therefore, it is possible to inject liquid into the human body and measure predetermined characteristics in the human body at one time.

また、本発明によれば、前記筒部材が、穿刺可能に形成されてなることにより、特に測定対象物が生体、特に人体である場合に好適である。   In addition, according to the present invention, the cylindrical member is formed so as to be puncturable, which is particularly suitable when the measurement target is a living body, particularly a human body.

さらに、本発明によれば、前記筒部材が、多孔質性材料で形成されてなることにより、筒部材内部を流通する液体を筒部材の外周方向からも浸透させるので、液体を人体内に、偏りなく注入することができる。なお、前記筒部材のセンサ部材が設けられた部分付近においては、多孔質に形成されている必要はない。前記筒部材のセンサ部材が設けられた部分付近も多孔質に形成されていると、筒部材内部を流通する液体によって、測定対象に影響を与え、人体の所定の特性の測定を精度良く行うことができない場合がある。   Furthermore, according to the present invention, since the cylindrical member is formed of a porous material, the liquid flowing through the cylindrical member is also permeated from the outer peripheral direction of the cylindrical member. It can be injected evenly. In the vicinity of the portion where the sensor member of the cylindrical member is provided, it is not necessary to be formed porous. If the vicinity of the portion of the cylindrical member where the sensor member is provided is also porous, the liquid flowing inside the cylindrical member will affect the measurement target and accurately measure the predetermined characteristics of the human body. May not be possible.

以下、本発明の実施の形態を図面に基づいて説明する。なお、本発明は、この図面に記載された形態に限定されるものではない。   Hereinafter, embodiments of the present invention will be described with reference to the drawings. In addition, this invention is not limited to the form described in this drawing.

[体内特性センサ]
なお、図1は、本発明における体内特性センサを示す概略図である。また、図2は、本発明における体内特性センサの断面を示す斜視図である。
[Body characteristics sensor]
FIG. 1 is a schematic view showing an in-vivo characteristic sensor according to the present invention. FIG. 2 is a perspective view showing a cross section of the in-vivo characteristic sensor according to the present invention.

なお、本発明に係る体内特性センサは、本発明の目的を達成できるものであれば、すなわち、人体内の所定の特性を測定できるものであれば制限はなく、例えば、体内の所定の物質の濃度を測定可能な濃度センサ、体内の所定の部位の温度を測定可能な温度センサ、体内の酵素の種類、濃度等を測定可能な酵素センサ、体内の所定の物質を検出可能な化学センサ等を挙げることができる。   The in-vivo characteristic sensor according to the present invention is not limited as long as the object of the present invention can be achieved, that is, a predetermined characteristic in the human body can be measured. A concentration sensor that can measure the concentration, a temperature sensor that can measure the temperature of a predetermined part in the body, an enzyme sensor that can measure the type and concentration of enzymes in the body, a chemical sensor that can detect predetermined substances in the body, etc. Can be mentioned.

本実施形態に係る体内特性センサ1は、筒部材2と、センサ部材3と、導電体4とを備えてなる。   The in-vivo characteristic sensor 1 according to this embodiment includes a cylindrical member 2, a sensor member 3, and a conductor 4.

[筒部材]
筒部材2は、液体が内部を流通可能に形成されていればよい。筒部材2を構成する材質としては、例えば、SUS等を挙げることができ、多孔質セラミック等の多孔質性材料であることが好ましい。なお、筒部材2のセンサ部材3が設けられた部分付近においては、多孔質に形成されている必要はない。筒部材2のセンサ部材3が設けられた部分付近も多孔質に形成されていると、筒部材2内部を流通する液体、例えば、薬剤によって、測定対象に影響を与え、測定を精度良く行うことができない場合がある。
[Cylinder member]
The cylindrical member 2 should just be formed so that a liquid can distribute | circulate the inside. Examples of the material constituting the cylindrical member 2 include SUS, and a porous material such as porous ceramic is preferable. In the vicinity of the portion of the cylindrical member 2 where the sensor member 3 is provided, it need not be formed porous. If the vicinity of the portion of the cylindrical member 2 where the sensor member 3 is provided is also porous, the liquid that flows through the cylindrical member 2, for example, a drug, affects the measurement target and performs measurement accurately. May not be possible.

筒部材2は、穿刺可能に形成されてなることが好ましい。穿刺可能に形成する例としては、筒部材2の先端が、はす形状に形成する例等を挙げることができる。なお、筒部材2の断面形状としては、特に制限はなく、人体に挿入する際に、妨げることのない断面形状であればよい。筒部材2の断面形状として、具体的には、円形、楕円形、多角形等を挙げることができる。   The cylindrical member 2 is preferably formed so as to be puncturable. As an example which forms so that puncture is possible, the example etc. in which the front-end | tip of the cylinder member 2 forms in a helical shape can be mentioned. In addition, there is no restriction | limiting in particular as a cross-sectional shape of the cylinder member 2, What is necessary is just a cross-sectional shape which does not prevent when inserting in a human body. Specific examples of the cross-sectional shape of the cylindrical member 2 include a circle, an ellipse, and a polygon.

[センサ部材]
センサ部材3は、筒部材2の外周部分に設けられ、人体内の所定の特性を感知可能に形成されてなるものであればよい。なお、当然のことながら、少なくとも、センサ部材3外側表面が、人体内の所定の特性を感知可能に形成されてなるものであればよい。ここで、センサ部材3は、体内特性センサ1全体としてみた場合に、体内特性センサ1表面から実質的に突出していないように形成されていることが好ましい。
[Sensor member]
The sensor member 3 may be any member provided on the outer peripheral portion of the cylindrical member 2 and formed so as to be able to sense predetermined characteristics in the human body. As a matter of course, it is sufficient that at least the outer surface of the sensor member 3 is formed so as to be able to sense a predetermined characteristic in the human body. Here, the sensor member 3 is preferably formed so as not to substantially protrude from the surface of the in-vivo characteristic sensor 1 when viewed as the entire in-vivo characteristic sensor 1.

このように形成する例としては、例えば、筒部材2の外周部分にセンサ部材3を埋め込むようにして形成し、筒部材2の表面と、センサ部材3の表面とを面一にする例等を挙げることができる。また、体内特性センサ1表面から鋭角に突出しないように、例えば、なだらかな曲面を有するようにセンサ部材3および筒部材2の表面が加工されていてもよい。   As an example of forming in this way, for example, the sensor member 3 is embedded in the outer peripheral portion of the cylindrical member 2 so that the surface of the cylindrical member 2 and the surface of the sensor member 3 are flush with each other. Can be mentioned. Further, for example, the surfaces of the sensor member 3 and the cylindrical member 2 may be processed so as to have a gentle curved surface so as not to protrude from the surface of the in-vivo characteristic sensor 1 at an acute angle.

このようにセンサ部材3を形成すれば、体内特性センサ1を人体内に挿入する際に、センサ部材3が人体の体組織にひっかかることがないので、人体に傷みを与えることなく挿入することができる。   If the sensor member 3 is formed in this way, when the in-vivo characteristic sensor 1 is inserted into the human body, the sensor member 3 does not get caught in the body tissue of the human body, so that it can be inserted without damaging the human body. it can.

前記センサ部材3は、測定する対象物により異なる。例えば、人体の血液中のグルコースを測定する場合には、センサ部材3は、酵素電極である。また、血液中の薬物量を測定する場合には、センサ部材3は、イオン選択性電極などを用いることができる。さらに、例えば、テオフィリン(気管支拡張薬)を測定する場合には、センサ部材3は、エンザイムイムノセンサーである。   The sensor member 3 differs depending on the object to be measured. For example, when measuring glucose in the blood of a human body, the sensor member 3 is an enzyme electrode. When measuring the amount of drug in blood, the sensor member 3 can use an ion selective electrode or the like. Furthermore, for example, when measuring theophylline (bronchodilator), the sensor member 3 is an enzyme immunosensor.

そして、例えば、セファロスポリン(抗生物質)を測定する場合には、センサ部材3は、微生物センサーである。なお、その他、各人体の所定の特性の測定に適したFET(電界効果トランジスター)センサーや光学センサ等を使用することもできる。   For example, when measuring cephalosporins (antibiotics), the sensor member 3 is a microorganism sensor. In addition, an FET (field effect transistor) sensor or an optical sensor suitable for measuring predetermined characteristics of each human body can be used.

[導電体]
導電体4は、センサ部材3からの信号を伝達可能であればよい。導電体4としては、金属等の公知の信号伝達物質を材質とするものであればよい。導電体4としては、例えば、フィルム状のものを使用することができる。導電体4は、図2に示されるように、筒部材2の外周部分であり、かつほぼ中央部分に設けられたセンサ部材3を筒部材2とで、挟み込むようにして装着されている。前記導電体4の装着時の形状は、体内特性センサ1自体が、例えば、人体内に挿入されることを妨げない形状であればよい。
[conductor]
The conductor 4 only needs to be able to transmit a signal from the sensor member 3. The conductor 4 may be made of a known signal transmission material such as metal. For example, a film-like material can be used as the conductor 4. As shown in FIG. 2, the conductor 4 is mounted so as to sandwich the sensor member 3 provided on the outer peripheral portion of the cylindrical member 2 and substantially at the center portion with the cylindrical member 2. The shape when the conductor 4 is mounted may be a shape that does not prevent the in-vivo characteristic sensor 1 itself from being inserted into the human body, for example.

[体内特性センサの使用方法および作用]
体内特性センサ1の使用する際に、図1に示されるように、体内特性センサ1は、増幅器5、記録計6、および薬剤注入量制御装置7に接続されている。
[Usage characteristic sensor usage and action]
When the in-vivo characteristic sensor 1 is used, as shown in FIG. 1, the in-vivo characteristic sensor 1 is connected to an amplifier 5, a recorder 6, and a medicine injection amount control device 7.

なお、増幅器5は、センサ部材3から導電体4を介して送られてくる信号を増幅するものであり、増幅された信号は記録計6へと送られる。   The amplifier 5 amplifies a signal sent from the sensor member 3 via the conductor 4, and the amplified signal is sent to the recorder 6.

記録計6は、増幅器5より増幅された信号を記録するものであり、その信号は薬剤注入量制御装置7へと送られる。   The recorder 6 records the signal amplified by the amplifier 5, and the signal is sent to the medicine injection amount control device 7.

薬剤注入量制御装置7は、記録計6より伝達された信号により、薬剤の最適注入量を算出し、体内特性センサ1の筒部材2に注入される薬剤の量を調整するものである。   The medicine injection amount control device 7 calculates the optimum medicine injection amount based on the signal transmitted from the recorder 6 and adjusts the amount of medicine injected into the cylindrical member 2 of the in-vivo characteristic sensor 1.

まず、体内特性センサ1を人体の所定の部位へ挿入する。人体の生体内に挿入された体内特性センサ1のセンサ部材3により、人体の所定の特性、例えば、血液中のグルコースが測定される。   First, the in-vivo characteristic sensor 1 is inserted into a predetermined part of the human body. A predetermined characteristic of the human body, for example, glucose in the blood, is measured by the sensor member 3 of the in-vivo characteristic sensor 1 inserted into the living body of the human body.

センサ部材3から導電体4を介して、信号が増幅器5に送られる。増幅器5に送られた信号は、増幅器5により増幅される。増幅された信号は、記録計6へと送られる。記録計6に送られた信号は、記録計6に記録される。   A signal is sent from the sensor member 3 to the amplifier 5 through the conductor 4. The signal sent to the amplifier 5 is amplified by the amplifier 5. The amplified signal is sent to the recorder 6. The signal sent to the recorder 6 is recorded in the recorder 6.

また、記録計6に送られた信号は、薬剤注入量制御装置7へ送られる。薬剤注入量制御装置7へ送られた信号に基づいて、薬剤注入量制御装置7は、人体の所定の特性、例えば、血液中のグルコース量を算出する。   Further, the signal sent to the recorder 6 is sent to the medicine injection amount control device 7. Based on the signal sent to the drug injection amount control device 7, the drug injection amount control device 7 calculates a predetermined characteristic of the human body, for example, the amount of glucose in the blood.

算出された人体の所定の特性、例えば、血液中のグルコース量に基づいて、薬剤注入量制御装置7は、薬剤の最適注入量を算出する。   Based on the calculated predetermined characteristics of the human body, for example, the amount of glucose in the blood, the drug injection amount control device 7 calculates the optimal injection amount of the drug.

最適注入量の薬剤が、筒部材2に送られる。筒部材2に送られた薬剤は、筒部材2を通って、人体内に注入される。   The optimal amount of medicine is sent to the tubular member 2. The medicine sent to the cylinder member 2 is injected into the human body through the cylinder member 2.

上述のような本実施形態によれば、次のような効果がある。
(1)筒部材2と、センサ部材3と、導電体4とを備えてなることにより、筒部材2を人体の生体内へ挿入することで、筒部材2内部を通って、薬剤が注入される。そして、同時に、筒部材2に設けられたセンサ部材3によって、人体の所定の特性、例えば、血液中のグルコースが測定される。ここで、注入された薬剤による人体の所定の特性の変化が、測定する人体の部位によって、差が生じる可能性があり、そして、この人体の所定の特性値が安定するまでの時間差が測定部位により生じることがある。この筒部材2に設けられたセンサ部材3によって、体内特性センサ1が挿入された状態のままで、血液中のグルコースが測定される。そして、測定された血液中のグルコースは、導電体4によって、信号として外部に伝達される。したがって、上記したように、人体への薬剤の注入と、人体における血液中のグルコースの測定を1度の穿刺で行うことができる。
According to this embodiment as described above, the following effects are obtained.
(1) By including the cylindrical member 2, the sensor member 3, and the conductor 4, the drug is injected through the cylindrical member 2 by inserting the cylindrical member 2 into the living body of the human body. The At the same time, a predetermined characteristic of the human body, for example, glucose in the blood, is measured by the sensor member 3 provided on the cylindrical member 2. Here, there is a possibility that a change in the predetermined characteristic of the human body due to the injected medicine varies depending on the part of the human body to be measured, and the time difference until the predetermined characteristic value of the human body becomes stable is a measurement part May occur. The glucose in the blood is measured by the sensor member 3 provided on the cylindrical member 2 while the in-vivo characteristic sensor 1 is inserted. The measured glucose in the blood is transmitted to the outside as a signal by the conductor 4. Therefore, as described above, injection of a drug into the human body and measurement of glucose in the blood in the human body can be performed with a single puncture.

(2)筒部材2が、穿刺可能に形成されてなることにより、特に、測定対象物が人体である場合に好適である。 (2) Since the cylindrical member 2 is formed so as to be puncturable, it is particularly suitable when the measurement object is a human body.

(3)筒部材2が、多孔質性材料で形成されてなることにより、筒部材2内部を流通する薬剤を筒部材2の外周方向からも浸透させるので、薬剤を人体内に、偏りなく注入することができる。なお、筒部材2のセンサ部材3が設けられた部分付近においては、多孔質に形成されている必要はない。筒部材2のセンサ部材3が設けられた部分付近も多孔質に形成されていると、筒部材2内部を流通する液体、例えば、薬剤によって、測定対象に影響を与え、例えば、人体における血液中のグルコースの測定を精度良く行うことができない場合がある。 (3) Since the cylindrical member 2 is formed of a porous material, the drug circulating inside the cylindrical member 2 is also permeated from the outer peripheral direction of the cylindrical member 2, so that the drug is injected into the human body without any deviation. can do. In the vicinity of the portion of the cylindrical member 2 where the sensor member 3 is provided, it need not be formed porous. If the vicinity of the portion of the cylindrical member 2 where the sensor member 3 is provided is also porous, the liquid to be circulated inside the cylindrical member 2, for example, a drug affects the measurement target, for example, in blood in the human body In some cases, it is not possible to accurately measure glucose.

なお、本発明は、前記実施形態に限定されるものではなく、本発明の目的を達成できる範囲での変形、改良は、本発明に含まれるものである。   It should be noted that the present invention is not limited to the above-described embodiment, and modifications and improvements within the scope that can achieve the object of the present invention are included in the present invention.

第1の変形例として、例えば、図3に示されるように、体内特性センサ1Aにおいては、筒部材2の外周部分の先端部分にセンサ部材3Aが設けられている。また、筒部材2は、形状記憶合金で形成され、かつ未使用時には、先端に向かって、鋭角を成す形状に形成されてなる。   As a first modification, for example, as shown in FIG. 3, in the in-vivo characteristic sensor 1 </ b> A, a sensor member 3 </ b> A is provided at the distal end portion of the outer peripheral portion of the cylindrical member 2. Moreover, the cylindrical member 2 is formed of a shape memory alloy, and is formed in a shape that forms an acute angle toward the tip when not in use.

このようにすれば、上記の効果に加えて、例えば、人体内に体内特性センサ1Aを挿入した後は、体内の温度が、センサ部材3Aおよび筒部材2の温度を上昇させる。その結果、筒部材2が鋭角を成す形状から、人体内中に開放する形状へと変化する。このように、筒部材2が人体内中に開放されることによって、センサ部材3Aが人体内中に露出され、即ち人体内の測定対象物に接触しやすくなるという利点がある。   If it does in this way, in addition to said effect, for example, after inserting in-body characteristic sensor 1A in a human body, the temperature in a body will raise the temperature of sensor member 3A and cylinder member 2. As a result, the shape of the cylindrical member 2 changes from an acute angle to a shape that opens into the human body. As described above, when the cylindrical member 2 is opened in the human body, the sensor member 3A is exposed in the human body, that is, there is an advantage that the measuring member in the human body is easily contacted.

第2の変形例として、例えば、図4に示されるように、体内特性センサ1Bにおいては、筒部材2Bの先端部分および基端部分が中央部分に対して縮径した形状に形成されてなる。   As a second modification, for example, as shown in FIG. 4, in the in-vivo characteristic sensor 1 </ b> B, the distal end portion and the proximal end portion of the cylindrical member 2 </ b> B are formed in a shape whose diameter is reduced with respect to the central portion.

このようにすれば、上記の効果に加えて、筒部材2Bの基端部分も縮径していることで、例えば、人体内に体内特性センサ1Bを挿入した後は、筒部材2Bの基端部分で、係止され、人体内で、固定をすることができる。その結果、ある一定の部位を測定する際に、測定対象物の変動を少なくするため、より正確な測定を行うことができる。   In this way, in addition to the above effect, the proximal end portion of the cylindrical member 2B is also reduced in diameter, so that, for example, after the in-vivo characteristic sensor 1B is inserted into the human body, the proximal end of the cylindrical member 2B It is locked at the part and can be fixed inside the human body. As a result, more accurate measurement can be performed in order to reduce the fluctuation of the measurement object when measuring a certain part.

図1は、本発明における体内特性センサを示す概略図である。FIG. 1 is a schematic view showing an in-vivo characteristic sensor according to the present invention. 図2は、本発明における体内特性センサの断面を示す斜視図である。FIG. 2 is a perspective view showing a cross section of the in-vivo characteristic sensor according to the present invention. 図3は、本発明における体内特性センサの第1の変形例を示す概略図である。FIG. 3 is a schematic diagram showing a first modification of the in-vivo characteristic sensor according to the present invention. 図4は、本発明における体内特性センサの第2の変形例を示す概略図である。FIG. 4 is a schematic diagram showing a second modification of the in-vivo characteristic sensor according to the present invention.

符号の説明Explanation of symbols

1 体内特性センサ
2 筒部材
3 センサ部材
4 導電体
5 増幅器
6 記録計
7 薬剤注入量制御装置
1A 体内特性センサ
3A センサ部材
1B 体内特性センサ
2B 筒部材

DESCRIPTION OF SYMBOLS 1 Body characteristic sensor 2 Cylinder member 3 Sensor member 4 Electric conductor 5 Amplifier 6 Recorder 7 Drug injection amount control apparatus 1A Body characteristic sensor 3A Sensor member 1B Body characteristic sensor 2B Tube member

Claims (4)

人体に注入される液体が内部を流通可能に形成されてなる筒部材と、
前記筒部材の外周部分に設けられ、人体内の所定の特性を感知可能に形成されてなるセンサ部材と、
前記筒部材の外周部分に設けられ、前記センサ部材からの信号を伝達可能な導電体とを備え、
前記センサ部材が、前記筒部材と前記センサ部材と前記導電体とにより形成される部材表面から露出し、前記部材表面がなだらかな曲面を有し、
人体への液体の注入と人体内の所定の特性の測定とを同時に実施可能であることを特徴とする体内特性センサ。
A cylindrical member formed so that the liquid injected into the human body can circulate inside;
Setting vignetting at the periphery of the tubular member, a sensor member formed by appreciably forming a predetermined characteristic of the human body,
A conductor provided on an outer peripheral portion of the cylindrical member and capable of transmitting a signal from the sensor member;
The sensor member is exposed from a member surface formed by the cylindrical member, the sensor member, and the conductor, and the member surface has a gentle curved surface,
An in-vivo characteristic sensor capable of simultaneously injecting a liquid into a human body and measuring a predetermined characteristic in the human body.
前記筒部材が、穿刺可能に形成されてなることを特徴とする前記請求項1に記載の体内特性センサ。   The in-vivo characteristic sensor according to claim 1, wherein the cylindrical member is formed to be puncturable. 前記筒部材が、多孔質性材料で形成されてなることを特徴とする前記請求項1または前記請求項2に記載の体内特性センサ。   The in-vivo characteristic sensor according to claim 1 or 2, wherein the cylindrical member is made of a porous material. 前記請求項1〜3のいずれか1項に記載の体内特性センサと、
前記体内センサに接続され、前記センサ部材から前記導電体を介して送られてくる信号を増幅する増幅器と、
前記増幅器で増幅された信号を受信し記録する記録計と、
前記記録計から伝達された信号に基づいて薬剤の注入量を算出する薬剤注入量制御装置とを備えてなることを特徴とする生体情報モニタリングシステム。
The in-vivo characteristic sensor according to any one of claims 1 to 3,
An amplifier connected to the in-vivo sensor and amplifying a signal sent from the sensor member via the conductor;
A recorder for receiving and recording the signal amplified by the amplifier;
A biological information monitoring system comprising: a medicine injection amount control device that calculates a medicine injection amount based on a signal transmitted from the recorder.
JP2004366599A 2004-12-17 2004-12-17 In vivo characteristic sensor and biological information monitoring system Expired - Fee Related JP4576222B2 (en)

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JPH0251564U (en) * 1988-10-07 1990-04-11
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