Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JP4875315B2 - Intra-subject introduction device - Google Patents
[go: Go Back, main page]

JP4875315B2 - Intra-subject introduction device - Google Patents

Intra-subject introduction device Download PDF

Info

Publication number
JP4875315B2
JP4875315B2 JP2005108713A JP2005108713A JP4875315B2 JP 4875315 B2 JP4875315 B2 JP 4875315B2 JP 2005108713 A JP2005108713 A JP 2005108713A JP 2005108713 A JP2005108713 A JP 2005108713A JP 4875315 B2 JP4875315 B2 JP 4875315B2
Authority
JP
Japan
Prior art keywords
subject
capsule
width
extending
extending member
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.)
Expired - Fee Related
Application number
JP2005108713A
Other languages
Japanese (ja)
Other versions
JP2006280858A5 (en
JP2006280858A (en
Inventor
利正 赤木
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.)
Olympus Medical Systems Corp
Original Assignee
Olympus Medical Systems Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Olympus Medical Systems Corp filed Critical Olympus Medical Systems Corp
Priority to JP2005108713A priority Critical patent/JP4875315B2/en
Publication of JP2006280858A publication Critical patent/JP2006280858A/en
Publication of JP2006280858A5 publication Critical patent/JP2006280858A5/ja
Application granted granted Critical
Publication of JP4875315B2 publication Critical patent/JP4875315B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/00147Holding or positioning arrangements
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/04Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor combined with photographic or television appliances
    • A61B1/041Capsule endoscopes for imaging

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Surgery (AREA)
  • Biomedical Technology (AREA)
  • Medical Informatics (AREA)
  • Optics & Photonics (AREA)
  • Pathology (AREA)
  • Radiology & Medical Imaging (AREA)
  • Biophysics (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Molecular Biology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)
  • Endoscopes (AREA)

Description

本発明は、所定の機能を実行する機能実行手段を内蔵し、使用の際に口腔を経由して被検体内に導入される先端部を備えた被検体内導入装置に関するものである。   The present invention relates to an in-subject introduction apparatus that includes a function execution means for executing a predetermined function and includes a distal end portion that is introduced into the subject via the oral cavity during use.

近年、内視鏡の分野においては、飲込み型のカプセル型内視鏡が提案されている。このカプセル型内視鏡には、撮像機能と無線通信機能とが設けられている。カプセル型内視鏡は、観察(検査)のために被検体の口から飲込まれた後、自然排出されるまでの間、体腔内、例えば胃、小腸などの臓器の内部をその蠕動運動に従って移動し、移動に伴い、例えば0.5秒間隔で被検体内画像の撮像を行う機能を有する。   In recent years, in the field of endoscopes, swallowable capsule endoscopes have been proposed. This capsule endoscope is provided with an imaging function and a wireless communication function. The capsule endoscope is swallowed from the mouth of the subject for observation (examination) until it is spontaneously discharged until it is spontaneously discharged. It has a function of moving and taking images of the in-subject image at intervals of 0.5 seconds, for example.

体腔内を移動する間、カプセル型内視鏡によって体内で撮像された画像データは、順次無線通信により外部に送信され、外部に設けられたメモリに蓄積される。無線通信機能とメモリ機能とを備えた受信機を携帯することにより、被検体は、カプセル型内視鏡を飲み込んだ後、排出されるまでの間に渡って、自由に行動できる。カプセル型内視鏡が排出された後、医師もしくは看護士においては、メモリに蓄積された画像データに基づいて臓器の画像をディスプレイに表示させて診断を行うことができる(例えば、特許文献1参照。)。   While moving inside the body cavity, image data captured inside the body by the capsule endoscope is sequentially transmitted to the outside by wireless communication and stored in a memory provided outside. By carrying a receiver having a wireless communication function and a memory function, the subject can freely act after swallowing the capsule endoscope and before being discharged. After the capsule endoscope is ejected, the doctor or nurse can make a diagnosis by displaying an organ image on the display based on the image data stored in the memory (see, for example, Patent Document 1). .)

ところで、カプセル型内視鏡の外装部分に牽引用の紐状部材を付したものが提案されている。図12は、かかる紐状部材を付したカプセル型内視鏡の構造を示す模式図である。具体的には、図12に示すカプセル型内視鏡は、撮像機構等を内蔵したカプセル101と、一端がカプセル101に対して固定された紐状部材102と、紐状部材102の他端と接続された把持部103とによって構成される。   By the way, the thing which attached the string-like member for a pull to the exterior part of a capsule type endoscope is proposed. FIG. 12 is a schematic diagram showing the structure of a capsule endoscope provided with such a string-like member. Specifically, the capsule endoscope shown in FIG. 12 includes a capsule 101 incorporating an imaging mechanism, a string-like member 102 having one end fixed to the capsule 101, and the other end of the string-like member 102. It is comprised by the connected holding part 103. FIG.

紐状部材102は、被検体内に導入されたカプセル101を外部から牽引するためのものである。具体的には、例えば食道部分における被検体内画像を撮像する場合には、一般的なカプセル型内視鏡は食道内にて高速に移動するために充分な撮像動作を行うことが困難であるという問題が存在する。従って、図12に示すようにカプセル101に対して紐状部材102の一端を接続すると共に他端に接続された把持部103を医師等が牽引することによって、カプセル101の被検体内における位置または移動速度を調整することが可能である。かかる構成を採用することによって、食道等のような領域であってもカプセル型内視鏡の移動速度を低下させて多数の被検体内画像を撮像することや、既に通過した領域に関して再度被検体内画像を撮像することなどが可能となる。   The string-like member 102 is for pulling the capsule 101 introduced into the subject from the outside. Specifically, for example, when imaging an in-subject image in the esophagus, it is difficult to perform a sufficient imaging operation because a general capsule endoscope moves at high speed in the esophagus. There is a problem. Therefore, as shown in FIG. 12, the position of the capsule 101 in the subject or the position of the capsule 101 can be obtained by connecting one end of the string-like member 102 to the capsule 101 and pulling the grip portion 103 connected to the other end. It is possible to adjust the moving speed. By adopting such a configuration, even in an area such as the esophagus, the moving speed of the capsule endoscope can be reduced to capture a large number of in-subject images, and the subject can be re-examined with respect to the already passed area. An internal image can be taken.

特開2003−19111号公報Japanese Patent Laid-Open No. 2003-19111

しかしながら、上述した従来のカプセル型内視鏡は、紐状部材102を備えたことにより、飲み込み時またはカプセル101の位置調整を行う際に患者(被検体)の負担が大きいという課題を有する。以下、かかる課題について詳細に説明する。   However, the above-described conventional capsule endoscope has the problem that the burden on the patient (subject) is heavy when swallowed or when the position of the capsule 101 is adjusted because the string-like member 102 is provided. Hereinafter, this problem will be described in detail.

導入する際の被検体の負担を軽減する観点からは、紐状部材102は細い糸状に形成されていることが好ましい。すなわち、従来のカプセル型内視鏡100は口腔を経由して被検体内に導入される構成を有することから、口腔を通過する際に被検体に与える異物感を軽減し、飲みやすくする観点からは紐状部材102を糸状に形成することが必要となる。   From the viewpoint of reducing the burden on the subject at the time of introduction, the string-like member 102 is preferably formed in a thin thread shape. That is, since the conventional capsule endoscope 100 is configured to be introduced into the subject via the oral cavity, from the viewpoint of reducing the feeling of foreign matter given to the subject when passing through the oral cavity and making it easier to drink. It is necessary to form the string-like member 102 in a thread shape.

これに対して、位置調整を行う場合には紐状部材102が糸状に形成されることは好ましくない。すなわち、紐状部材102を用いてカプセル101の位置調整を行う場合には、紐状部材102のうち被検体外に位置する端部(カプセル101と接続する側と反対側の端部)を使用者が牽引すること等によって位置調整が行われることとなり、紐状部材102には張力が生じることとなる。そして、人体の消化器官の構造に鑑みれば明らかなように、カプセル型内視鏡が導入される口腔から食道に至る経路は途中でほぼ直角に湾曲した構造を有することから、カプセル101を食道、胃等まで導入させた場合には、かかる湾曲構造近傍にて紐状部材102と被検体の体内組織(例えば喉頭蓋)とが接触することとなる。所定の張力を生じた紐状部材102が湾曲構造近傍の体内組織と接触した場合には、体内組織に対して紐状部材102から押圧力が印加されることとなり、かかる押圧力の印加に伴い被検体は強い違和感を覚えることとなり、カプセル型内視鏡の使用に伴う被検体の負担が増大することとなる。   On the other hand, when position adjustment is performed, it is not preferable that the string-like member 102 is formed in a thread shape. That is, when the position of the capsule 101 is adjusted using the string-like member 102, the end portion of the string-like member 102 located outside the subject (the end opposite to the side connected to the capsule 101) is used. The position adjustment is performed by the person pulling or the like, and the string-like member 102 is tensioned. And, as is clear in view of the structure of the digestive organs of the human body, since the path from the oral cavity where the capsule endoscope is introduced to the esophagus has a structure that is curved at a substantially right angle, the capsule 101 is esophagus, When it is introduced to the stomach or the like, the string-like member 102 comes into contact with the body tissue of the subject (for example, the epiglottis) in the vicinity of the curved structure. When the string-like member 102 having a predetermined tension comes into contact with the body tissue in the vicinity of the curved structure, a pressing force is applied from the string-like member 102 to the body tissue. The subject will feel a strong sense of incongruity, and the burden on the subject associated with the use of the capsule endoscope will increase.

特に、カプセル型内視鏡を用いた検査終了後にカプセル101を口腔を経由して被検体外に取り出す際には、かかる被検体の負担はより顕著なものとなる。上述したように紐状部材102はカプセル101と一端が接続されるとともに被検体外にて他端を牽引等することによって位置調整を行うものであり、カプセル101の取り出しもかかる位置調整の一態様として同様の操作によって行われることとなる。従って、被検体は、カプセル101が再び被検体外に取り出されるまでの所定時間に渡って喉頭蓋等の体内組織において押圧力を受け続けることとなり、強い違和感を長時間に渡って我慢する必要が生じる。   In particular, when the capsule 101 is taken out of the subject through the oral cavity after the examination using the capsule endoscope, the burden on the subject becomes more conspicuous. As described above, one end of the string-like member 102 is connected to the capsule 101 and the position is adjusted by pulling the other end outside the subject. It will be performed by the same operation. Therefore, the subject continues to receive a pressing force in the body tissue such as the epiglottis for a predetermined time until the capsule 101 is taken out of the subject again, and it is necessary to endure a strong sense of incongruity for a long time. .

本発明は、上記に鑑みてなされたものであって、撮像機構等の所定の機能実行手段を内蔵したカプセルに対して紐状部材等の位置調整部材が備えられたカプセル型内視鏡等の被検体内導入装置において、被検体に対するカプセルの導入および導入後の位置調整の際に被検体に及ぼす負担を軽減した被検体内導入装置を実現することを目的とする。   The present invention has been made in view of the above, and is a capsule endoscope or the like in which a position adjustment member such as a string-like member is provided with respect to a capsule incorporating a predetermined function execution unit such as an imaging mechanism. It is an object of the present invention to provide an intra-subject introduction device that reduces the burden on the subject when introducing a capsule into the subject and adjusting the position after introduction.

上述した課題を解決し、目的を達成するために、本発明にかかる被検体内導入装置は、所定の機能を実行する機能実行手段を内蔵し、使用の際に口腔を経由して被検体の内部に導入される先端部を備えた被検体内導入装置であって、前記先端部に対して一部が接続され、可撓性を備えると共に前記先端部から離隔する方向に所定長だけ延伸し、少なくとも前記被検体の咽頭部の体内組織と接触した部分にて、前記体内組織に対する接触面の幅が接触面の法線方向の幅よりも大きくなるよう形成された延伸部材を備えたことを特徴とする。 In order to solve the above-described problems and achieve the object, the in-subject introduction apparatus according to the present invention has a function execution means for executing a predetermined function, and uses the subject via the oral cavity at the time of use. An intra-subject introduction apparatus provided with a tip portion to be introduced therein, which is partially connected to the tip portion, has flexibility, and extends by a predetermined length in a direction away from the tip portion. A stretching member formed so that a width of a contact surface with respect to the body tissue is larger than a width in a normal direction of the contact surface at least in a portion of the subject in contact with the body tissue of the pharynx. Features.

発明によれば、使用の際に咽頭部の体内組織と接触した部分にて、接触面の幅が接触面と垂直な方向の幅よりも大きくなる延伸部材を備えたこととしたため、延伸部材は、咽頭部の体内組織に対して最も面積の広い面にて接触することとなり、体内組織に対する単位面積あたりの押圧力を低減することが可能となる。 According to the present invention, the stretch member is provided with the stretch member whose width of the contact surface is larger than the width in the direction perpendicular to the contact surface at the portion of the pharynx that is in contact with the body tissue during use. Is in contact with the body tissue of the pharynx at the surface having the largest area, and the pressing force per unit area against the body tissue can be reduced.

また、本発明にかかる被検体内導入装置は、上記の発明において、前記延伸部材は、断面における第1方向の幅が前記第1方向と垂直な第2方向の幅よりも大きな値を有し、前記第2方向の曲げ抵抗が前記第1方向の曲げ抵抗よりも小さくなるよう形成された特徴とする。 In the in-vivo introduction device according to the present invention as set forth in the invention described above, the extending member has a value in which the width in the first direction in the cross section is larger than the width in the second direction perpendicular to the first direction. The bending resistance in the second direction is smaller than the bending resistance in the first direction.

また、本発明にかかる被検体内導入装置は、上記の発明において、前記延伸部材は、帯状の部材によって形成されたことを特徴とする。 The in-subject introduction device according to the present invention is characterized in that, in the above invention, the extending member is formed of a band-shaped member.

また、本発明にかかる被検体内導入装置は、上記の発明において、前記先端部は、前記延伸部材との接続部分に挿通孔を有し、前記延伸部材は、一部が前記挿通孔に挿通した状態にて前記カプセルに対して接続されたことを特徴とする。 In the in-subject introduction device according to the present invention , in the above invention, the distal end portion has an insertion hole in a connection portion with the extension member, and the extension member is partially inserted into the insertion hole. In this state, the capsule is connected.

また、本発明にかかる被検体内導入装置は、上記の発明において、前記延伸部材は、前記先端部の外表面と連続性を維持しつつ前記先端部に対して接続されたことを特徴とする。 The in-subject introduction device according to the present invention is characterized in that, in the above invention, the extending member is connected to the distal end portion while maintaining continuity with the outer surface of the distal end portion. .

また、本発明にかかる被検体内導入装置は、上記の発明において、前記延伸部材は、前記体内組織と接触した際に前記体内組織から受ける垂直抗力によって、前記第1方向の幅が前記第2方向の幅よりも大きな値となるよう断面形状が変化することを特徴とする。 In the in-vivo introduction device according to the present invention , in the above-described invention, the extending member has a width in the first direction due to a normal force received from the body tissue when contacting the body tissue. The cross-sectional shape is changed so as to have a value larger than the width in the direction.

本発明にかかる被検体内導入装置は、使用の際に咽頭部の体内組織と接触した部分にて、接触面の幅が接触面と垂直な方向の幅よりも大きくなる延伸部材を備えたこととしたため、延伸部材は、咽頭部の体内組織に対して最も面積の広い面にて接触することとなり、体内組織に対する単位接触面積あたりの押圧力を低減することが可能であり、押圧力を低減することによって被検体が感ずる違和感を低減または解消できるという効果を奏する。   The in-subject introduction apparatus according to the present invention includes an extending member in which the width of the contact surface is larger than the width in the direction perpendicular to the contact surface at the portion of the pharynx that is in contact with the body tissue during use. Therefore, the extending member comes into contact with the body tissue of the pharynx at the surface having the largest area, and the pressing force per unit contact area with the body tissue can be reduced, and the pressing force is reduced. By doing so, the sense of incongruity felt by the subject can be reduced or eliminated.

以下、この発明を実施するための最良の形態(以下では、単に「実施の形態」と称する)である被検体内導入装置について説明する。なお、図面は模式的なものであり、各部分の厚みと幅との関係、それぞれの部分の厚みの比率などは現実のものとは異なることに留意すべきであり、図面の相互間においても互いの寸法の関係や比率が異なる部分が含まれていることはもちろんである。   Hereinafter, an in-subject introduction apparatus which is the best mode for carrying out the present invention (hereinafter simply referred to as “embodiment”) will be described. Note that the drawings are schematic, and it should be noted that the relationship between the thickness and width of each part, the ratio of the thickness of each part, and the like are different from the actual ones. Of course, the part from which the relationship and ratio of a mutual dimension differ is contained.

(実施の形態1)
まず、実施の形態1にかかる被検体内導入装置について説明する。図1は、本実施の形態1にかかる被検体内導入装置の全体構成を示す模式図である。図1に示すように、本実施の形態1にかかる被検体内導入装置は、機能実行部2を内蔵し、特許請求の範囲における先端部の一例として機能するカプセル1と、カプセル1に対して一部が接続し、カプセル1から離隔する方向に所定距離だけ延伸した延伸部材3とを備える。
(Embodiment 1)
First, the in-subject introduction device according to the first embodiment will be described. FIG. 1 is a schematic diagram illustrating an overall configuration of the intra-subject introduction device according to the first embodiment. As shown in FIG. 1, the in-subject introduction apparatus according to the first embodiment includes a function execution unit 2, and functions as an example of a distal end portion in the scope of claims. A stretching member 3 that is partially connected and stretched by a predetermined distance in a direction away from the capsule 1 is provided.

カプセル1は、所定の形状を有する筐体中に機能実行部2を内蔵した構造を有する。具体的には、プラスチック等の材料によって形成された外装ケース内に機能実行部2が配置され、機能実行部2は、例えば所定の対物光学系およびCCD等の撮像素子を備えることによって被検体内部の画像を撮像する機能等を有する。なお、機能実行部2によって実行される機能としては撮像機能に限定して解釈する必要はない。   The capsule 1 has a structure in which a function execution unit 2 is built in a casing having a predetermined shape. Specifically, the function execution unit 2 is arranged in an outer case formed of a material such as plastic, and the function execution unit 2 includes, for example, a predetermined objective optical system and an imaging element such as a CCD, so that the inside of the subject is And the like. The function executed by the function execution unit 2 need not be interpreted as being limited to the imaging function.

延伸部材3は、一部がカプセル1と接続する一方で、カプセル1を被検体内に導入した際に他の一部が被検体外に残置する程度の長さを有し、かかる被検体外の部分を使用者が把持しつつ牽引等することによってカプセル1の位置調整を行うためのものである。かかる位置調整を可能とする観点から、延伸部材3は、所定長だけ延伸した構造を有すると共に、カプセル1が通過する被検体内の経路にあわせて湾曲するよう可撓性を備えた部材によって形成される。   The extending member 3 is connected to the capsule 1 in part, and has a length that allows another part to remain outside the subject when the capsule 1 is introduced into the subject. This is for adjusting the position of the capsule 1 by pulling the portion of the capsule 1 while holding it. From the viewpoint of enabling such position adjustment, the extending member 3 has a structure extended by a predetermined length and is formed by a member having flexibility so as to bend in accordance with a path in the subject through which the capsule 1 passes. Is done.

図2は、延伸部材3の断面形状を示す模式図である。図1にも示したように延伸部材3は帯状の構造を有しており、具体的には、図2に示すような断面形状を有する。すなわち、延伸部材3は、断面がほぼ矩形状に形成されており、第1方向(図2における横方向)の幅d1が、第1方向と垂直な第2方向(図2における縦方向)の幅d2よりも大きな値となる形状を有する。なお、第1方向の幅と第2方向の幅の大小関係が上述の条件を満たしていれば本実施の形態1における延伸部材3として機能することが可能であるが、第2方向の幅は、第1方向の幅と比較して無視しうる程度の小さな値(d1>>d2)となることが好ましい。かかる観点から、本実施の形態1の延伸部材3は、より好ましい構造として帯状の部材によって形成されることとしている。 FIG. 2 is a schematic diagram showing a cross-sectional shape of the extending member 3. As shown also in FIG. 1, the extending | stretching member 3 has a strip | belt-shaped structure, and specifically has a cross-sectional shape as shown in FIG. That is, the extending member 3 has a substantially rectangular cross section, and the width d 1 in the first direction (lateral direction in FIG. 2) is the second direction (vertical direction in FIG. 2) perpendicular to the first direction. It has a shape having a value larger than the width d 2 . In addition, if the magnitude relationship between the width in the first direction and the width in the second direction satisfies the above-described conditions, it can function as the extending member 3 in the first embodiment, but the width in the second direction is In addition, it is preferable to have a small value (d 1 >> d 2 ) that is negligible compared to the width in the first direction. From this viewpoint, the extending member 3 of the first embodiment is formed by a band-shaped member as a more preferable structure.

また、本実施の形態1では、延伸部材3は、外部から印加される曲げ応力に対する抵抗力(以下、単に「曲げ抵抗」と称する。)に関して異方性を備えるよう形成される。具体的には、延伸部材3は、上述の第1方向の曲げ抵抗が第2方向の曲げ抵抗よりも大きくなるよう形成される。すなわち、延伸部材3は、第2方向に外部から曲げ応力が与えられた場合には容易に湾曲する一方で、第1方向に外部から曲げ応力が与えられた場合は、第2方向の場合よりも湾曲しづらい構造を有する。なお、単一の材料にて均質に形成された部材の場合、一般に曲げ抵抗の大きさは曲げ応力が印加される方向の幅(厚み)が増加するに従って増大することから、本実施の形態1でも、図2に示す構造を実現することによって曲げ抵抗の異方性を容易に実現している。   In the first embodiment, the extending member 3 is formed to have anisotropy with respect to a resistance force (hereinafter simply referred to as “bending resistance”) against a bending stress applied from the outside. Specifically, the extending member 3 is formed such that the bending resistance in the first direction is greater than the bending resistance in the second direction. That is, the extending member 3 is easily bent when a bending stress is applied from the outside in the second direction, whereas when the bending stress is applied from the outside in the first direction, the extending member 3 is more than the case of the second direction. Has a structure that is difficult to bend. In the case of a member formed uniformly from a single material, generally, the magnitude of bending resistance increases as the width (thickness) in the direction in which bending stress is applied increases. However, the anisotropy of the bending resistance is easily realized by realizing the structure shown in FIG.

次に、本実施の形態1にかかる被検体内導入装置の使用態様について説明する。本実施の形態1にかかる被検体内導入装置では、撮像等の所定の機能を実行する機能実行部2がカプセル1に内蔵されており、使用の際には、延伸部材3を牽引等することによってカプセル1を被検体内の所望の位置に移動させて所望の部位の被検体内画像の取得等が行われる。   Next, a usage mode of the intra-subject introduction device according to the first embodiment will be described. In the in-subject introduction apparatus according to the first embodiment, a function execution unit 2 that executes a predetermined function such as imaging is built in the capsule 1, and the stretching member 3 is pulled when used. As a result, the capsule 1 is moved to a desired position in the subject, and an in-subject image of a desired portion is acquired.

図3は、カプセル1が被検体内に導入された状態における被検体内導入装置の状態を示す模式図である。カプセル1を被検体13内に導入した場合には、カプセル1と接続した延伸部材3がカプセル1から離隔する方向、すなわち口腔に向かう方向に延伸した状態となる。一般に、カプセル1に内蔵された機能実行部2を用いた所定機能の実行は、食道、胃等にて行われることから、一部がカプセル1と接続し、他の部分が被検体13の外に残置された延伸部材3は、図3にも示したように途中でほぼ必ず咽頭部を経由した状態で使用されることとなる。また、図3に示すように被検体13の内部のうちカプセル1が通過する経路たる消化管の延伸方向は、咽頭部にてほぼ垂直に湾曲した構造を有することから、延伸部材3は、咽頭部近辺の消化管の形状に合わせて湾曲した状態にて使用される。そして、図3に示すようにカプセル1が被検体内に導入された状態において、延伸部材3は、咽頭部の体内組織に対して第2方向を法線とした面、すなわち延伸方向と垂直な方向の幅がd1となる面が接触するようあらかじめ形成されている。以下、咽頭部の体内組織に対する延伸部材3の湾曲作用について詳細に説明する。 FIG. 3 is a schematic diagram showing a state of the intra-subject introduction apparatus in a state where the capsule 1 is introduced into the subject. When the capsule 1 is introduced into the subject 13, the extending member 3 connected to the capsule 1 is extended in the direction away from the capsule 1, that is, in the direction toward the oral cavity. In general, execution of a predetermined function using the function execution unit 2 incorporated in the capsule 1 is performed in the esophagus, stomach, etc., so that a part is connected to the capsule 1 and the other part is outside the subject 13. As shown in FIG. 3, the extending member 3 left in is almost always used in the state of passing through the pharynx on the way. Further, as shown in FIG. 3, the extending direction of the digestive tract, which is the path through which the capsule 1 passes, inside the subject 13 has a structure that is curved substantially perpendicularly at the pharynx. Used in a curved state according to the shape of the gastrointestinal tract in the vicinity. In the state where the capsule 1 is introduced into the subject as shown in FIG. 3, the extending member 3 is a surface normal to the second direction with respect to the body tissue of the pharynx, that is, perpendicular to the extending direction. It is formed in advance so that the surfaces whose direction width is d 1 are in contact with each other. Hereinafter, the bending action of the extending member 3 on the body tissue of the pharynx will be described in detail.

図4−1〜図4−3は、咽頭部における延伸部材3の湾曲作用について説明するための模式図である。図4−1は、延伸部材3に対して曲げ応力の印加が開始された時点における延伸部材3の形状を模式的に示し、図4−2は、印加された応力に起因したねじれによる延伸部材3の回転の様子を模式的に示し、図4−3は、曲げ応力に対して、力学的に安定な状態で湾曲した延伸部材3の形状を示す。   4A to 4C are schematic diagrams for explaining the bending action of the extending member 3 in the pharynx. 4A schematically illustrates the shape of the stretching member 3 at the time when the application of the bending stress to the stretching member 3 is started, and FIG. 4B illustrates the stretching member due to torsion caused by the applied stress. FIG. 4-3 schematically illustrates the shape of the extending member 3 that is curved in a mechanically stable state against bending stress.

延伸部材3は、カプセル1と接続した構造を有し、カプセル1が咽頭部を通過した後に進行方向がほぼ垂直に変化することによって、図4−1に矢印にて模式的に示すように延伸部材3に対しては曲げ応力が印加される。ここで、通常の部材、例えば紐状の部材であれば、曲げ応力の印加方向にそのまま曲がるが、本実施の形態1における延伸部材3は、紐状の部材等と異なり、曲げ抵抗に関して異方性を備えた構造を有する。すなわち、上述したように延伸部材3は、第1方向に関する曲げ抵抗が第2方向に関する曲げ抵抗よりも大きな値となるよう形成されており、第1方向よりも第2方向に曲がりやすいという特性を有する。   The extending member 3 has a structure connected to the capsule 1, and the extending direction changes substantially perpendicularly after the capsule 1 passes through the pharynx, thereby extending as schematically shown by an arrow in FIG. 4-1. A bending stress is applied to the member 3. Here, if it is a normal member, for example, a string-like member, it bends in the direction in which the bending stress is applied, but the stretching member 3 in the first embodiment is anisotropic with respect to the bending resistance unlike the string-like member. It has a structure with characteristics. That is, as described above, the extending member 3 is formed such that the bending resistance in the first direction is larger than the bending resistance in the second direction, and has a characteristic that it is easier to bend in the second direction than in the first direction. Have.

このような特性を有するため、延伸部材3は、第1方向に湾曲するよりも曲げ抵抗の小さい第2方向に湾曲する方が力学的に安定する。従って、延伸部材3は、曲げ応力に応じて曲げ抵抗の小さい第2方向に曲がろうとして、図4−2に示すように延伸方向を軸としてねじれが生じ、延伸方向(図4−1、図4−2における破線矢印)を軸として、曲げ応力の印加方向と第2方向とが一致するように所定角だけ回転する。   Since it has such a characteristic, the extending | stretching member 3 is more stable mechanically in the direction bent in the 2nd direction with small bending resistance than it curves in a 1st direction. Therefore, the extending member 3 tries to bend in the second direction having a small bending resistance in accordance with the bending stress, and twists occur around the extending direction as shown in FIG. The axis is rotated by a predetermined angle so that the direction in which the bending stress is applied and the second direction coincide with each other with the broken line arrow in FIG.

図4−2に示すように回転した結果、延伸部材3は、曲げ抵抗が小さい第2方向と曲げ応力の印加方向とがほぼ一致するため、力学的に安定した状態で湾曲する。具体的には、延伸部材3は、図4−3に示すように、曲げ応力の方向に従って湾曲し、図4−3に示す状態にて力学的に安定化する。この結果、延伸部材3のうち咽頭部の体内組織と接触する部分は、広い幅d1を有する面となり、かかる面が体内組織と接触した状態を維持しつつ、カプセル1の位置調整が行われる。すなわち、カプセル1の移動に伴い咽頭部の体内組織と接触する延伸部材3の部分は変化するが、接触部分が変化した場合であっても、延伸方向と垂直な方向の幅がd2の面が体内組織と接触することはなく、図4−3に示すように幅がd1の面が体内組織と接触した状態が維持される。 As a result of the rotation as shown in FIG. 4B, the extending member 3 bends in a mechanically stable state because the second direction having a low bending resistance and the direction in which the bending stress is applied substantially coincide. Specifically, as shown in FIG. 4-3, the extending member 3 is bent according to the direction of the bending stress and is mechanically stabilized in the state shown in FIG. 4-3. As a result, the portion of the extending member 3 that contacts the body tissue of the pharynx becomes a surface having a wide width d 1 , and the position of the capsule 1 is adjusted while maintaining the state where the surface is in contact with the body tissue. . That is, as the capsule 1 moves, the portion of the stretching member 3 that contacts the body tissue of the pharynx changes, but even if the contact portion changes, the width of the direction perpendicular to the stretching direction is d 2 . Does not contact the body tissue, and the state where the surface having the width d 1 is in contact with the body tissue as shown in FIG. 4-3 is maintained.

なお、図4−1では、曲げ応力の印加開始時における延伸部材3に対する曲げ応力の印加方向と延伸部材3の第1方向とが一致する場合について説明したが、他の位置関係であった場合でも図4−3に示すよう延伸部材3が第2方向に湾曲した形状に変化する。例えば、曲げ応力の印加開始時に応力印加方向と延伸部材3の第2方向とが平行となる場合には、曲げ方向と曲げ抵抗が弱い方向とが既に一致していることから、延伸部材3は延伸方向を軸として回転することなくそのまま第2方向に湾曲し、図4−3と同様な湾曲形状にて力学的に安定化する。また、曲げ応力の印加方向が第1、第2方向のいずれとも非平行となる場合には、曲げ応力の分力は第1、第2方向のいずれに対しても作用するが、より曲がりやすい第2方向に延伸部材3は湾曲すると共に、曲げ応力の印加方向と湾曲方向とが一致するよう延伸方向を軸として回転することによって、図4−3の例と同様の湾曲形状にて安定化する。   In addition, in FIG. 4-1, although the case where the application direction of the bending stress with respect to the extending | stretching member 3 at the time of the start of application of a bending stress and the 1st direction of the extending | stretching member 3 corresponded was demonstrated, it was another positional relationship However, as shown in FIG. 4-3, the extending member 3 changes to a shape curved in the second direction. For example, when the stress application direction and the second direction of the extending member 3 are parallel at the start of applying the bending stress, the extending direction of the extending member 3 is the same because the bending direction and the direction in which the bending resistance is weak are already matched. It curves in the second direction as it is without rotating about the stretching direction as an axis, and is mechanically stabilized with the same curved shape as in FIG. 4-3. Further, when the direction in which the bending stress is applied is non-parallel to both the first and second directions, the bending stress component acts in both the first and second directions, but is more easily bent. The stretching member 3 is curved in the second direction, and is stabilized in a curved shape similar to the example of FIG. 4-3 by rotating around the stretching direction so that the bending stress application direction and the bending direction coincide with each other. To do.

次に、本実施の形態1にかかる被検体内導入装置の利点について説明する。まず、本実施の形態1にかかる被検体内導入装置は、カプセル1を被検体13の内部に導入した後、カプセル1の位置調整を行う際に被検体13に与える違和感を緩和または解消することが可能であるという利点を有する。   Next, advantages of the in-subject introduction device according to the first embodiment will be described. First, the in-subject introduction apparatus according to the first embodiment alleviates or eliminates the uncomfortable feeling given to the subject 13 when the position of the capsule 1 is adjusted after the capsule 1 is introduced into the subject 13. Has the advantage of being possible.

上述したように、延伸部材3は、断面形状に関して第1方向に幅d1、第1方向と垂直な第2方向に幅d2(<d1)となるよう形成されると共に、第1方向の曲げ抵抗が第2方向の曲げ抵抗よりも大きな値となるよう形成される。従って、延伸部材3は、被検体13内の咽頭部近傍にて湾曲する際に曲げ応力の方向と曲げ抵抗の弱い第2方向とが平行となるよう必要に応じて回転した状態で曲げ応力の印加方向に湾曲し、より広い幅d1を有する面が咽頭部の体内組織の表面と接した状態にて力学的に安定化する。換言すれば、本実施の形態1では、延伸部材3は、カプセル1の位置調整を行う際には、咽頭部の体内組織に対する接触面積が最も大きくなる状態にて力学的に安定化することとなる。従って、延伸部材3から体内組織に対して印加される単位接触面積あたりの押圧力の値が低減され、被検体13がカプセル1の位置調整を行う際に感ずる違和感を緩和または解消することが可能である。 As described above, the extending member 3 is formed to have the width d 1 in the first direction and the width d 2 (<d 1 ) in the second direction perpendicular to the first direction with respect to the cross-sectional shape, and the first direction. The bending resistance is greater than the bending resistance in the second direction. Therefore, when the extending member 3 is bent in the vicinity of the pharynx in the subject 13, the bending stress is in a state of being rotated as necessary so that the direction of the bending stress and the second direction having a low bending resistance are parallel to each other. The surface is curved in the application direction, and is mechanically stabilized in a state where the surface having a wider width d 1 is in contact with the surface of the body tissue of the pharynx. In other words, in the first embodiment, when the position of the capsule 1 is adjusted, the extending member 3 is mechanically stabilized in a state where the contact area with the body tissue of the pharynx is maximized. Become. Accordingly, the value of the pressing force per unit contact area applied from the stretching member 3 to the body tissue is reduced, and the uncomfortable feeling that the subject 13 feels when adjusting the position of the capsule 1 can be alleviated or eliminated. It is.

また、本実施の形態1にかかる被検体内導入装置は、体内組織と接触する面積を増加させつつ延伸部材3の体積を従来の紐状部材と同程度に抑制し、カプセル1を被検体13に導入する際に被検体13が感ずる違和感の増加を回避できるという利点を有する。体内組織との接触面積を増加させる構造としては、例えば延伸部材の外径を増加させた構造が考えられるが、かかる構造を採用した場合には、外径の増加に応じて延伸部材の体積が増加することとなる。従って、延伸部材の外径を増加した場合には、カプセル1を被検体13内に導入する際に、無視し得ない体積を有する延伸部材に起因した異物感を被検体13が強く感ずるという問題が新たに生ずることとなる。   Further, the in-subject introduction apparatus according to the first embodiment suppresses the volume of the extending member 3 to the same level as that of the conventional string-like member while increasing the area in contact with the body tissue, and the capsule 1 is placed on the subject 13. This has the advantage that an increase in the sense of incongruity felt by the subject 13 can be avoided. As a structure that increases the contact area with the body tissue, for example, a structure in which the outer diameter of the extending member is increased is conceivable, but when such a structure is adopted, the volume of the extending member increases with the increase in the outer diameter. Will increase. Therefore, when the outer diameter of the extending member is increased, the subject 13 strongly feels a foreign object caused by the extending member having a volume that cannot be ignored when the capsule 1 is introduced into the object 13. Will be newly generated.

これに対して、本実施の形態1にかかる被検体内導入装置では、延伸部材3は、断面形状に関して第1方向に広い幅を有する一方で、第2方向は小さくなるよう形成されている。周知のように、延伸部材3の体積は断面積に延伸方向長さを乗算することによって導出され、断面積の値は、第1方向の幅と第2方向の幅との積に応じた値となる。そして、本実施の形態1にかかる被検体内導入装置では、延伸部材3の第2方向の幅d2の値を大きくする理由はなく、むしろ第2方向の曲げ抵抗を低減する観点からは、可能な限りd2を小さな値とすることが好ましい。 On the other hand, in the intra-subject introduction apparatus according to the first embodiment, the extending member 3 is formed so as to have a wide width in the first direction with respect to the cross-sectional shape, while being small in the second direction. As is well known, the volume of the extending member 3 is derived by multiplying the cross-sectional area by the length in the extending direction, and the value of the cross-sectional area is a value corresponding to the product of the width in the first direction and the width in the second direction. It becomes. In the intra-subject introduction apparatus according to the first embodiment, there is no reason to increase the value of the width d 2 of the extending member 3 in the second direction. Rather, from the viewpoint of reducing the bending resistance in the second direction, It is preferable to make d 2 as small as possible.

このため、本実施の形態1では、延伸部材3に関して第1方向の幅d1と第2方向の幅d2の積は、幅d1の値の増加に関わらずある程度の値に抑制することが可能であり、本実施の形態1にかかる被検体内導入装置では、延伸部材3の断面積の増加を抑制することが可能である。この結果、カプセル1を導入する際に被検体13の口腔内における延伸部材3の占有領域が増加することはなく、体内組織に対する接触面積を増加させたにもかかわらず被検体13が感じる違和感の増加を回避できるという利点を有する。 Therefore, in the first embodiment, the product of the width d 2 of the first width d 1 and second directions with respect to the stretching members 3, to suppress to a certain value irrespective of the increase in the value of the width d 1 In the in-subject introduction device according to the first embodiment, it is possible to suppress an increase in the cross-sectional area of the extending member 3. As a result, the area occupied by the extending member 3 in the oral cavity of the subject 13 does not increase when the capsule 1 is introduced, and the subject 13 feels uncomfortable even though the contact area with the body tissue is increased. It has the advantage that an increase can be avoided.

さらに、本実施の形態1にかかる被検体内導入装置は、延伸部材3の作製が容易であるという利点を有する。延伸部材3を構成する部材の条件としては、断面形状に関して第1方向の幅が、第1方向と垂直な第2方向よりも大きな値を有すると共に第1方向の曲げ抵抗が第2方向の曲げ抵抗よりも小さな値となることが挙げられる。かかる条件を満たす構造としては、所定の長さを有するシート状の既存の部材によって容易に実現することが可能であり、例えば、包装の装飾等に用いられるリボン等によって延伸部材3を実現することが可能である。従って、本実施の形態1にかかる被検体内導入装置は、延伸部材3を実現するにあたり既存の部材等を用いることが可能であり、容易に作製できるという利点を有することとなる。   Furthermore, the in-subject introduction device according to the first embodiment has an advantage that the stretching member 3 can be easily manufactured. The conditions of the members constituting the stretching member 3 include that the cross-sectional shape has a width in the first direction larger than that in the second direction perpendicular to the first direction, and the bending resistance in the first direction is the bending in the second direction. It is mentioned that it becomes a value smaller than resistance. As a structure satisfying such a condition, it can be easily realized by a sheet-like existing member having a predetermined length. For example, the extending member 3 is realized by a ribbon or the like used for packaging decoration or the like. Is possible. Therefore, the in-subject introduction apparatus according to the first embodiment has an advantage that an existing member or the like can be used to realize the stretching member 3 and can be easily manufactured.

(実施の形態2)
次に、実施の形態2にかかる被検体内導入装置について説明する。本実施の形態2にかかる被検体内導入装置は、カプセルが所定の挿通孔を有し、かかる挿通孔に延伸部材を挿通すると共に延伸部材の両端を被検体外部にて保持することによって、カプセルに対して延伸部材を接続した構造を有する。
(Embodiment 2)
Next, the intra-subject introduction device according to the second embodiment will be described. The in-subject introduction apparatus according to the second embodiment has a capsule having a predetermined insertion hole, and by inserting an extending member into the insertion hole and holding both ends of the extending member outside the object. It has the structure which connected the extending | stretching member with respect to.

図5は、本実施の形態2にかかる被検体内導入装置の構成を示す模式図である。図5に示すように、本実施の形態2にかかる被検体内導入装置は、挿通孔15aが形成されたカプセル15と、カプセル15に形成された挿通孔15aに挿通した延伸部材16と、延伸部材16の両端部と接続した把持部17とを備える。   FIG. 5 is a schematic diagram illustrating a configuration of the intra-subject introduction device according to the second embodiment. As shown in FIG. 5, the in-subject introduction apparatus according to the second embodiment includes a capsule 15 in which an insertion hole 15 a is formed, a stretching member 16 that is inserted into the insertion hole 15 a that is formed in the capsule 15, and stretching. A gripping portion 17 connected to both ends of the member 16 is provided.

挿通孔15aは、延伸部材16を挿通するために形成されており、延伸部材16が挿通孔15aを貫通するよう配置されることによって、カプセル15と延伸部材16とを接続する機能を有する。なお、カプセル15は、挿通孔15aが形成されたこと以外の点に関しては実施の形態1におけるカプセル1と同様の構成を有し、所定の機能を実行する機能実行部2を内蔵するものとする。   The insertion hole 15 a is formed to insert the extending member 16, and has a function of connecting the capsule 15 and the extending member 16 by arranging the extending member 16 so as to pass through the inserting hole 15 a. The capsule 15 has the same configuration as that of the capsule 1 in the first embodiment except for the insertion hole 15a, and incorporates a function execution unit 2 that executes a predetermined function. .

延伸部材16は、実施の形態1における延伸部材3と同様に、断面形状に関して第1方向に所定の幅を有すると共に、第1方向と垂直な方向である第2方向に第1方向の幅よりも小さな幅を有し、第1方向の曲げ抵抗よりも第2方向の曲げ抵抗が小さくなるよう形成された構造を有する。また、延伸部材16は、カプセル15に形成された挿通孔15aに摺動自在に挿通され、カプセル1が被検体内に導入された際にも両端部が被検体の外に残置するに充分な延伸長を有し、両端部を保持しつつ牽引等がなされることによってカプセル15の位置調整を行う機能を有する。   Similar to the extending member 3 in the first embodiment, the extending member 16 has a predetermined width in the first direction with respect to the cross-sectional shape, and in the second direction, which is a direction perpendicular to the first direction, from the width in the first direction. Has a small width, and has a structure formed such that the bending resistance in the second direction is smaller than the bending resistance in the first direction. Further, the extending member 16 is slidably inserted into an insertion hole 15a formed in the capsule 15, and even when the capsule 1 is introduced into the subject, both ends are sufficient to remain outside the subject. It has a stretched length and has a function of adjusting the position of the capsule 15 by being pulled while holding both ends.

把持部17は、延伸部材16の両端部と接続することによって両端部間の位置関係を固定するためのものである。本実施の形態2では、延伸部材16は、カプセル15に形成された挿通孔15aを挿通することによってカプセル15に対して接続する構成を有する。このため、カプセル15の位置調整を行う際に延伸部材16の挿通孔15aに対する移動を回避する必要があり、かかる観点より把持部17が延伸部材16の両端部と接続した構成を採用する。なお、把持部17と延伸部材16の間の接続態様としては、例えば固着することとしても良いが、好ましくは、一方の端部については把持部17に対して固定する一方で、他方の端部に関しては着脱自在な状態にて接続することとする。かかる構成を採用することによって、後述するようにカプセル15の使用が完了した後の処置を容易に行うことが可能となるためである。   The gripping part 17 is for fixing the positional relationship between both ends by connecting to both ends of the extending member 16. In the second embodiment, the extending member 16 has a configuration in which the extending member 16 is connected to the capsule 15 by being inserted through the insertion hole 15 a formed in the capsule 15. For this reason, when the position of the capsule 15 is adjusted, it is necessary to avoid the movement of the extending member 16 with respect to the insertion hole 15a. From this point of view, a configuration in which the gripping portion 17 is connected to both ends of the extending member 16 is adopted. In addition, as a connection aspect between the holding part 17 and the extending | stretching member 16, it is good also as adhering, for example, Preferably, while fixing with respect to the holding part 17 about one edge part, it is the other edge part As for, it shall be connected in a detachable state. By adopting such a configuration, it is possible to easily perform treatment after the use of the capsule 15 is completed, as will be described later.

本実施の形態2にかかる被検体内導入装置の使用態様について説明する。図6は、カプセル15を被検体内に導入した後に行われるカプセル15の位置調整の状態を示す模式図である。図6に示すように、カプセル15の位置調整を行う際には、把持部17によって延伸部材16の両端部の間の位置関係を固定しつつ使用者が把持部17を牽引する等によってカプセル15の位置調整を行う。延伸部材16の両端部間の位置関係を固定しておくことによって、実施の形態1の場合と同様に、延伸部材16を牽引した際には接触部分を介してカプセル15に対して引っ張り方向の力が与えられ、カプセル15の位置の調整が行われることとなる。なお、位置調整を行う際には、実施の形態1と同様に延伸方向と垂直な方向の幅が大きい面が体内組織と接触することとなり、延伸部材16から体内組織に対して与えられる単位接触面積あたりの押圧力を低減することはもちろんである。   A usage mode of the intra-subject introduction device according to the second embodiment will be described. FIG. 6 is a schematic diagram showing a state of position adjustment of the capsule 15 performed after the capsule 15 is introduced into the subject. As shown in FIG. 6, when the position of the capsule 15 is adjusted, the capsule 15 is pulled by the user pulling the gripping portion 17 while fixing the positional relationship between both ends of the extending member 16 by the gripping portion 17. Adjust the position of. By fixing the positional relationship between the both ends of the stretching member 16, as in the case of the first embodiment, when the stretching member 16 is pulled, the capsule 15 is pulled in the pulling direction via the contact portion. A force is applied, and the position of the capsule 15 is adjusted. When the position adjustment is performed, the surface having a large width in the direction perpendicular to the stretching direction is in contact with the body tissue as in the first embodiment, and unit contact given from the stretching member 16 to the body tissue. Of course, the pressing force per area is reduced.

次に、カプセル15を被検体13から排出する際の動作について説明する。カプセル1の使用が完了した後にはカプセル15を被検体13の外部に取り出す必要があるが、本実施の形態2では、カプセル15と延伸部材16とを分離し、延伸部材16を口腔部を介して回収する一方、カプセル15に関しては消化管を通過させることによって被検体13の外部に排出することとしている。   Next, an operation when the capsule 15 is discharged from the subject 13 will be described. After the use of the capsule 1 is completed, it is necessary to take out the capsule 15 to the outside of the subject 13, but in the second embodiment, the capsule 15 and the stretching member 16 are separated, and the stretching member 16 is passed through the oral cavity. On the other hand, the capsule 15 is discharged outside the subject 13 by passing through the digestive tract.

図7は、カプセル15の使用が完了した状態における被検体内導入装置の使用態様を示す模式図である。図7に示すように、カプセル15の使用が完了した後には、延伸部材16の一方の端部を把持部17から取り外し、延伸部材16の両端部間の位置関係の固定状態を解除する。かかる状態にて把持部17を牽引することによって、延伸部材16は挿通孔15aから抜き取られることとなり、延伸部材16とカプセル15とが分離する。その後、延伸部材16は口腔部を経由して被検体13の外部に取り出され、カプセル15は食道、胃、小腸等を順次通過し、最終的に体外に排出される。   FIG. 7 is a schematic diagram illustrating a usage mode of the intra-subject introduction device in a state where the use of the capsule 15 is completed. As shown in FIG. 7, after the use of the capsule 15 is completed, one end portion of the stretching member 16 is removed from the gripping portion 17, and the fixed state of the positional relationship between the both end portions of the stretching member 16 is released. By pulling the gripping part 17 in such a state, the extending member 16 is extracted from the insertion hole 15a, and the extending member 16 and the capsule 15 are separated. Thereafter, the extending member 16 is taken out of the subject 13 via the oral cavity, and the capsule 15 sequentially passes through the esophagus, stomach, small intestine, etc., and is finally discharged out of the body.

次に、本実施の形態2にかかる被検体内導入装置の利点について説明する。まず、本実施の形態2にかかる被検体内導入装置は、延伸部材16が実施の形態1における延伸部材3と同様の断面形状を有することから、実施の形態1と同様に、咽頭部の体内組織に対する接触面積を増加させ、単位接触面積あたりの押圧力を低減できる等の利点を有する。   Next, advantages of the in-subject introduction device according to the second embodiment will be described. First, in the intra-subject introduction apparatus according to the second embodiment, since the extending member 16 has the same cross-sectional shape as the extending member 3 in the first embodiment, the body of the pharynx is similar to the first embodiment. There are advantages such as increasing the contact area with the tissue and reducing the pressing force per unit contact area.

また、本実施の形態2にかかる被検体内導入装置は、カプセル使用後の処理の際に被検体13の負担を軽減できるという利点を有する。すなわち、本実施の形態2にかかる被検体内導入装置は、上述したようにカプセル15と延伸部材16とを分離することが可能であるため、カプセル15は体内の排泄物等と一緒に排出する一方で、延伸部材16については口腔部を介して回収することが可能である。このため、本実施の形態3にかかる被検体内導入装置では、カプセル15を被検体13の外部に取り出す際に口腔部を経由する必要が無く、被検体13の負担を軽減できるという利点を有する。   Further, the in-subject introduction device according to the second embodiment has an advantage that the burden on the subject 13 can be reduced during the processing after the capsule is used. That is, since the in-subject introduction apparatus according to the second embodiment can separate the capsule 15 and the extending member 16 as described above, the capsule 15 is discharged together with excrement and the like in the body. On the other hand, the stretching member 16 can be collected through the oral cavity. For this reason, the in-subject introduction device according to the third embodiment has an advantage that the burden on the subject 13 can be reduced without having to go through the oral cavity when the capsule 15 is taken out of the subject 13. .

(実施の形態3)
次に、実施の形態3にかかる被検体内導入装置について説明する。本実施の形態3にかかる被検体内導入装置は、延伸部材がカプセルの外表面との間で連続性を維持するようカプセルに対して接続した構造を有する。
(Embodiment 3)
Next, the in-subject introduction device according to the third embodiment will be described. The in-subject introduction device according to the third embodiment has a structure in which the extending member is connected to the capsule so as to maintain continuity with the outer surface of the capsule.

図8は、本実施の形態3にかかる被検体内導入装置の全体構成を示す模式図である。図8に示すように、本実施の形態3にかかる被検体内導入装置は、実施の形態1と同様に機能実行部2を内蔵したカプセル1を備えた一方、カプセル1に対する接続態様が異なる延伸部材3a、3bを備えた構成を有する。   FIG. 8 is a schematic diagram illustrating an overall configuration of the intra-subject introduction device according to the third embodiment. As shown in FIG. 8, the in-subject introduction apparatus according to the third embodiment includes the capsule 1 including the function execution unit 2 as in the first embodiment, but has a different connection mode with respect to the capsule 1. It has the structure provided with member 3a, 3b.

すなわち、延伸部材3a、3bは、それぞれの構造としては実施の形態1における延伸部材3と同様(すなわち、第1方向の幅d1が第2方向の幅d2よりも大きくなるよう、例えば帯状に形成される)の構成を有する。その一方で、延伸部材3a、3bは、それぞれ接続部分にてカプセル1の外表面と連続性を維持するよう形成されており、カプセル1から延伸部材3a、3bに至る外表面はなだらかに変化している。 That is, the extending members 3a and 3b have the same structure as that of the extending member 3 in the first embodiment (that is, for example, a band shape so that the width d 1 in the first direction is larger than the width d 2 in the second direction). Formed). On the other hand, the extending members 3a and 3b are formed so as to maintain continuity with the outer surface of the capsule 1 at the connection portions, respectively, and the outer surface from the capsule 1 to the extending members 3a and 3b changes gently. ing.

本実施の形態3にかかる被検体内導入装置の利点について説明する。本実施の形態3にかかる被検体内導入装置は、実施の形態1における利点に加え、延伸部材3a、3bとカプセル1との接続部分が被検体13の体内組織と接触した際に被検体13に生ずる違和感を低減または解消できるという利点を有する。   The advantages of the intra-subject introduction device according to the third embodiment will be described. In addition to the advantages of the first embodiment, the in-subject introduction apparatus according to the third embodiment has the subject 13 when the connecting portion between the extending members 3a and 3b and the capsule 1 comes into contact with the body tissue of the subject 13. It is possible to reduce or eliminate the uncomfortable feeling that occurs.

例えば、カプセル1を用いた被検体内画像の撮像等が完了した後には、延伸部材3a、3bを被検体外部から牽引することによって、口腔を経由してカプセル1を被検体13外部に取り出すこととなる。図3等を参照すれば明らかなように、かかる場合にはまず延伸部材3a、3bのいずれか一方が咽頭部の体内組織と接触するが、カプセル1が口腔に近づくにつれて咽頭部の体内組織と接触する部材が延伸部材3a、3bからカプセル1に変化する。   For example, after the imaging of the in-subject image using the capsule 1 is completed, the capsule 1 is taken out of the subject 13 via the oral cavity by pulling the extending members 3a and 3b from the outside of the subject. It becomes. As apparent from FIG. 3 and the like, in such a case, one of the extending members 3a and 3b first comes into contact with the internal tissue of the pharynx, but as the capsule 1 approaches the oral cavity, The contacting member changes from the stretching members 3 a and 3 b to the capsule 1.

ここで、体内組織に対する接触部材が変化する際に、体内組織に対する接触面の面積が不連続に変化した場合、接触面積に応じた値となる単位接触面積あたりの押圧力の値も不連続に変化し、単位接触面積あたりの押圧力の絶対値が大きい場合と同様に被検体13に強い違和感を与えることとなる。従って、本実施の形態3にかかる被検体内導入装置では、外表面の連続性を維持するように延伸部材3a、3bをカプセル1に対して接続することとし、かかる接続態様を実現することによって単位接触面積あたりの押圧力の不連続変化の発生を抑制または防止し、被検体13に与える違和感を低減または解消することとしている。   Here, when the area of the contact surface with respect to the body tissue changes discontinuously when the contact member for the body tissue changes, the value of the pressing force per unit contact area that becomes a value according to the contact area also becomes discontinuous. As a result, the subject 13 is strongly discomforted as in the case where the absolute value of the pressing force per unit contact area is large. Therefore, in the intra-subject introduction apparatus according to the third embodiment, the extending members 3a and 3b are connected to the capsule 1 so as to maintain the continuity of the outer surface, and by realizing such a connection mode, The generation of discontinuous changes in the pressing force per unit contact area is suppressed or prevented, and the uncomfortable feeling given to the subject 13 is reduced or eliminated.

(実施の形態4)
次に、実施の形態4にかかる被検体内導入装置について説明する。本実施の形態4にかかる被検体内導入装置は、延伸部材が、外力印加の際に第1方向の幅が第1方向と垂直な第2方向の幅よりも大きくなるよう断面形状が変化するよう形成される。
(Embodiment 4)
Next, the in-subject introduction device according to the fourth embodiment will be described. In the intra-subject introduction apparatus according to the fourth embodiment, the cross-sectional shape of the extending member changes so that the width in the first direction becomes larger than the width in the second direction perpendicular to the first direction when external force is applied. Formed.

図9は、本実施の形態4にかかる被検体内導入装置の全体構成を示す模式図である。図9に示すように、本実施の形態4では、延伸部材21は、自然状態(外力が与えられない状態)では、ほぼ一定の外径を有する部材によって形成される一方で、外力に対して容易に変形可能な、柔軟な材料によって形成されるものである。   FIG. 9 is a schematic diagram illustrating an overall configuration of the intra-subject introduction device according to the fourth embodiment. As shown in FIG. 9, in the fourth embodiment, the extending member 21 is formed by a member having a substantially constant outer diameter in a natural state (a state where no external force is applied), whereas It is formed of a flexible material that can be easily deformed.

図10は、外力が印加された際における延伸部材21の断面構造を示す模式図である。延伸部材21は柔軟な材料によって形成されることから、図10に示すように、ほぼ一定の外径を有していた状態(図10にて破線で示す部分)から、外力が与えられることによって実線にて示されるように外力印加方向に圧縮され、断面形状が変化する。すなわち、図10に示すように外力印加方向を第2方向とし、第2方向と垂直な方向を第1方向とした場合には、外力が印加されることによって、実施の形態1〜3と同様に第2方向の幅d2よりも第1方向の幅d1が大きな値となる。 FIG. 10 is a schematic diagram showing a cross-sectional structure of the extending member 21 when an external force is applied. Since the extending member 21 is formed of a flexible material, as shown in FIG. 10, an external force is applied from a state having a substantially constant outer diameter (part indicated by a broken line in FIG. 10). As indicated by the solid line, the cross-sectional shape changes due to compression in the external force application direction. That is, when the external force application direction is the second direction and the direction perpendicular to the second direction is the first direction as shown in FIG. In addition, the width d 1 in the first direction is larger than the width d 2 in the second direction.

次に、本実施の形態4にかかる被検体内導入装置に備わる延伸部材21が、実施の形態1における延伸部材3等と同様に被検体に与える違和感を低減できる点につき説明する。延伸部材21は、咽頭部の体内組織と接触して体内組織に印加する押圧力の反作用として、体内組織から垂直抗力を受けることとなる。かかる垂直抗力が外力として作用することにより、図10の第2方向に対して垂直抗力が印加され、延伸部材21の断面形状が変化し、第1方向の幅が第2方向の幅よりも大きくなる。   Next, the point that the stretching member 21 provided in the intra-subject introduction apparatus according to the fourth embodiment can reduce the uncomfortable feeling given to the subject as in the stretching member 3 and the like in the first embodiment will be described. The extending member 21 receives vertical drag from the body tissue as a reaction of the pressing force applied to the body tissue in contact with the body tissue of the pharynx. When the normal force acts as an external force, the normal force is applied to the second direction in FIG. 10, the cross-sectional shape of the extending member 21 is changed, and the width in the first direction is larger than the width in the second direction. Become.

ここで、垂直抗力は延伸部材21が接触する体内組織の表面の法線方向に印加されることから、図10の例では、体内組織の表面は第2方向を法線方向とすることとなる。従って、垂直抗力によって変形した延伸部材21は、体内組織の表面に対して、第2方向を法線とする面、すなわち幅d1を有する面が接触する。かかる接触態様は、実施の形態1等と同様であり、本実施の形態4でも、延伸部材21は、幅の広い面が体内組織と接触することとなり、単位接触面積あたりの押圧力の値を低減し、被検体に与える違和感を低減または解消することが可能である。このように、延伸部材は、図2に示す断面形状を常に保持する必要は必ずしもなく、図10に示すように、外力に応じて変形する構造であっても実施の形態1と同様の利点を享受することが可能である。 Here, since the normal force is applied in the normal direction of the surface of the body tissue with which the extending member 21 contacts, in the example of FIG. 10, the surface of the body tissue has the second direction as the normal direction. . Therefore, the extending member 21 deformed by the normal force is in contact with the surface of the body tissue, the surface having the second direction as the normal line, that is, the surface having the width d 1 . This contact mode is the same as in Embodiment 1 and the like, and in Embodiment 4 as well, the extending member 21 has a wide surface in contact with the body tissue, and the value of the pressing force per unit contact area is set. It is possible to reduce or eliminate the uncomfortable feeling given to the subject. As described above, the extending member does not always need to maintain the cross-sectional shape shown in FIG. 2, and as shown in FIG. 10, even if the extending member is deformed according to an external force, the same advantages as in the first embodiment are obtained. It is possible to enjoy.

以上、実施の形態1〜4に亘って本発明を説明したが、本発明は上記の実施の形態に限定して解釈するべきではなく、当業者であれば様々な実施例、変形例に想到することが可能である。例えば、実施の形態1〜4では、先端部としてカプセル1等を用いることとしたが、被検体内導入装置の構造を、カプセルを用いたものに限定する必要はない。   As mentioned above, although this invention was demonstrated over Embodiment 1-4, this invention should not be limited to said embodiment and should be interpreted by those skilled in the art to various Examples and modifications. Is possible. For example, in Embodiments 1 to 4, the capsule 1 or the like is used as the tip, but the structure of the intra-subject introduction device need not be limited to that using a capsule.

図11は、カプセルを用いない被検体内導入装置の一例たる内視鏡装置を示す模式図である。図11に示すように、内視鏡装置22は、CCD、照明光源等の機能実行部が内蔵された先端部23と、先端部23と連接され、内部に所定の管路等が形成された挿入部24と、挿入部24の基端側と接続され、使用者が把持しつつ所定の操作を行うための操作部25とを備える。ここで、挿入部24は、先端部23と接続し、先端部23から離隔する方向に所定距離だけ延伸した構造を有することから、本発明における延伸部材の一例として機能しうることとなる。このため、挿入部24を実施の形態1〜4における延伸部材3、16、21のいずれかと同様の構造とすることにより、実施の形態1〜4と同様の利点を享受できることとなる。このように、被検体内導入装置を構成するにあたってカプセル型内視鏡に限定して解釈するべきではなく、内視鏡装置等のように、先端部および先端部と接続された延伸部材を備えた装置であれば本発明における被検体内導入装置として機能することが可能である。   FIG. 11 is a schematic diagram showing an endoscope apparatus as an example of an in-subject introduction apparatus that does not use a capsule. As shown in FIG. 11, the endoscope device 22 is connected to a distal end portion 23 having a function execution unit such as a CCD and an illumination light source built therein, and the distal end portion 23, and a predetermined pipe line and the like are formed therein. The insertion portion 24 includes an operation portion 25 that is connected to the proximal end side of the insertion portion 24 and that allows a user to perform a predetermined operation while holding the insertion portion 24. Here, since the insertion portion 24 has a structure that is connected to the distal end portion 23 and is extended by a predetermined distance in a direction away from the distal end portion 23, the insertion portion 24 can function as an example of the extending member in the present invention. For this reason, the same advantage as in the first to fourth embodiments can be obtained by making the insertion portion 24 the same structure as that of any of the extending members 3, 16, and 21 in the first to fourth embodiments. As described above, the configuration of the in-subject introduction apparatus should not be interpreted as being limited to the capsule endoscope, and includes a distal end portion and an extending member connected to the distal end portion, such as an endoscope apparatus. Any device can function as the intra-subject introduction device in the present invention.

実施の形態1にかかる被検体内導入装置の全体構成を示す模式図である。1 is a schematic diagram illustrating an overall configuration of an intra-subject introduction device according to a first embodiment. 被検体内導入装置を構成する延伸部材の断面形状を示す模式図である。It is a schematic diagram which shows the cross-sectional shape of the extending | stretching member which comprises the in-subject introduction apparatus. 被検体内導入装置を被検体に導入した状態を示す模式図である。It is a schematic diagram which shows the state which introduce | transduced the in-subject introduction apparatus into the subject. 延伸部材の湾曲作用を説明するための模式図である。It is a schematic diagram for demonstrating the bending effect | action of an extending | stretching member. 延伸部材の湾曲作用を説明するための模式図である。It is a schematic diagram for demonstrating the bending effect | action of an extending | stretching member. 延伸部材の湾曲作用を説明するための模式図である。It is a schematic diagram for demonstrating the bending effect | action of an extending | stretching member. 実施の形態2にかかる被検体内導入装置の全体構成を示す模式図である。FIG. 6 is a schematic diagram illustrating an overall configuration of an intra-subject introduction device according to a second embodiment. 被検体内導入装置を被検体に導入した状態を示す模式図である。It is a schematic diagram which shows the state which introduce | transduced the in-subject introduction apparatus into the subject. カプセルおよび延伸部材を被検体外部に取り出す態様を説明するための模式図である。It is a schematic diagram for demonstrating the aspect which takes out a capsule and an extending | stretching member outside a subject. 実施の形態3にかかる被検体内導入装置の全体構成を示す模式図である。FIG. 6 is a schematic diagram illustrating an overall configuration of an intra-subject introduction device according to a third embodiment. 実施の形態4にかかる被検体内導入装置の全体構成を示す模式図である。FIG. 9 is a schematic diagram illustrating an overall configuration of an in-subject introduction device according to a fourth embodiment. 外力が与えられた際の延伸部材の断面形状変化を説明するための模式図である。It is a schematic diagram for demonstrating the cross-sectional shape change of the extending | stretching member when external force is given. 被検体内導入装置の変形例たる内視鏡装置の構成を示す模式図である。It is a schematic diagram which shows the structure of the endoscope apparatus which is a modification of the in-subject introduction apparatus. 従来の被検体内導入装置の構成を示す模式図である。It is a schematic diagram which shows the structure of the conventional intra-subject introduction apparatus.

符号の説明Explanation of symbols

1 カプセル
2 機能実行部
3、3a、3b 延伸部材
13 被検体
15 カプセル
15a 挿通孔
16 延伸部材
17 把持部
21 延伸部材
22 内視鏡装置
23 先端部
24 挿入部
25 操作部
100 カプセル型内視鏡
101 カプセル
102 紐状部材
103 把持部
DESCRIPTION OF SYMBOLS 1 Capsule 2 Function execution part 3, 3a, 3b Stretching member 13 Subject 15 Capsule 15a Insertion hole 16 Stretching member 17 Holding part 21 Stretching member 22 Endoscope 23 End part 24 Insertion part 25 Operation part 100 Capsule type endoscope 101 Capsule 102 String member 103 Grasping part

Claims (4)

被検体の内部に導入される先端部と、可撓性を備えると共に前記先端部から離隔する方向に延伸する延伸部材とを備えた被検体内導入装置において、
前記先端部は、前記延伸部材を挿通可能な挿通孔を有し、
前記延伸部材は、一部が前記挿通孔に挿通された状態にて前記先端部に対して接続され、断面が略矩形状であって、該略矩形状の断面の第1方向の幅が該第1方向と垂直な第2方向の幅よりも大きく、且つ、前記第2方向の曲げ抵抗が前記第1方向の曲げ抵抗よりも小さくなるように形成されることを特徴とする被検体内導入装置。
In the in-subject introduction apparatus comprising a tip portion introduced into the subject and a stretching member that is flexible and extends in a direction away from the tip portion.
The tip has an insertion hole through which the extending member can be inserted,
The extending member is connected to the tip in a state where a part thereof is inserted through the insertion hole, and has a substantially rectangular cross section, and the width of the substantially rectangular cross section in the first direction is Introduction into a subject characterized by being formed so as to be larger than a width in a second direction perpendicular to the first direction and having a bending resistance in the second direction smaller than a bending resistance in the first direction. apparatus.
所定の機能を実行する機能実行手段を内蔵し、使用の際に口腔を経由して被検体の内部に導入される先端部を備えた被検体内導入装置であって、
前記先端部は、挿通孔を有し、
一部が前記挿通孔に挿通された状態にて前記先端部に対して接続され、可撓性を備えると共に前記先端部から離隔する方向に所定長だけ延伸し、少なくとも前記被検体の咽頭部の体内組織と接触した部分にて、前記体内組織に対する接触面の幅が接触面の法線方向の幅よりも大きくなるよう形成された延伸部材を備えたことを特徴とする被検体内導入装置。
Incorporating a function execution means for executing a predetermined function, and an in-subject introduction apparatus provided with a tip portion that is introduced into the subject via the oral cavity during use,
The tip has an insertion hole,
A portion is connected to the distal end portion in a state of being inserted through the insertion hole , is flexible and extends a predetermined length in a direction away from the distal end portion, and at least of the pharynx of the subject An in-subject introduction apparatus comprising an extending member formed so that a width of a contact surface with respect to a body tissue is larger than a width in a normal direction of the contact surface at a portion in contact with the body tissue.
前記延伸部材は、断面における第1方向の幅が前記第1方向と垂直な第2方向の幅よりも大きな値を有し、前記第2方向の曲げ抵抗が前記第1方向の曲げ抵抗よりも小さくなるよう形成されたことを特徴とする請求項に記載の被検体内導入装置。 The extending member has a width in the first direction in the cross section that is greater than the width in the second direction perpendicular to the first direction, and the bending resistance in the second direction is greater than the bending resistance in the first direction. The in-subject introduction device according to claim 2 , wherein the introduction device is formed to be small. 前記延伸部材は、帯状の部材によって形成されたことを特徴とする請求項またはに記載の被検体内導入装置。 The stretching member is the body-insertable apparatus according to claim 2 or 3, characterized in that it is formed by a strip-shaped member.
JP2005108713A 2005-04-05 2005-04-05 Intra-subject introduction device Expired - Fee Related JP4875315B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2005108713A JP4875315B2 (en) 2005-04-05 2005-04-05 Intra-subject introduction device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2005108713A JP4875315B2 (en) 2005-04-05 2005-04-05 Intra-subject introduction device

Publications (3)

Publication Number Publication Date
JP2006280858A JP2006280858A (en) 2006-10-19
JP2006280858A5 JP2006280858A5 (en) 2008-05-01
JP4875315B2 true JP4875315B2 (en) 2012-02-15

Family

ID=37403359

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2005108713A Expired - Fee Related JP4875315B2 (en) 2005-04-05 2005-04-05 Intra-subject introduction device

Country Status (1)

Country Link
JP (1) JP4875315B2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7530948B2 (en) 2005-02-28 2009-05-12 University Of Washington Tethered capsule endoscope for Barrett's Esophagus screening
JP2010537771A (en) * 2007-09-07 2010-12-09 ユニヴァーシティ オブ ワシントン Monitoring the placement of tethered capsule endoscopes in the esophagus
CN103222844B (en) * 2013-04-25 2016-01-27 中国人民解放军成都军区总医院 Controllable capsule endoscopy
WO2021198717A1 (en) * 2020-04-01 2021-10-07 Artedrone A medical device, a method for controlling a device, and a system comprising a device
CN111588413B (en) * 2020-05-19 2021-08-03 郴州市第一人民医院 Convenient oropharyngeal swab

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4910149Y1 (en) * 1969-09-03 1974-03-11
JPS6476822A (en) * 1987-09-17 1989-03-22 Toshiba Corp Endoscopic apparatus for observing total digestive tract
CN1765429B (en) * 1999-04-09 2010-12-08 喉症治疗防护罩有限公司 Disposable laryngeal mask airway device
JP4472069B2 (en) * 1999-11-10 2010-06-02 オリンパス株式会社 Medical capsule endoscope
JP4754743B2 (en) * 2001-09-18 2011-08-24 オリンパス株式会社 Endoscope device
JP3993550B2 (en) * 2003-09-30 2007-10-17 オリンパス株式会社 Gastrointestinal inspection device

Also Published As

Publication number Publication date
JP2006280858A (en) 2006-10-19

Similar Documents

Publication Publication Date Title
US7288074B2 (en) Guide wire structure for insertion into an internal space
US8465419B2 (en) Endoscope insertion unit, endoscope and endoscope system
US8092374B2 (en) Variably flexible insertion device and method for variably flexing an insertion device
ES2873206T3 (en) Cover for medical examination device
US20060189844A1 (en) Endoscopic devide
JP3623894B2 (en) In-vivo endoscope
CN102448364A (en) Device for delivering capsules inside the body
EP2953518A1 (en) Endoscopic sleeve
JP2009285004A (en) Guide device for transnasal endoscope
JP4875315B2 (en) Intra-subject introduction device
JP2009291372A (en) Transnasal endoscope guide device
KR100597616B1 (en) Endoscope Mouthpieces
EP1608424B1 (en) Guide wire structure for insertion into an internal space
JP3772085B2 (en) Endoscope device
CN215191386U (en) Endoscope and endoscope system
JP5052105B2 (en) Transnasal endoscope guide tube
JP5161420B2 (en) Endoscope insertion part
CN115067858A (en) Endoscope and endoscope system
JP2006280859A (en) Intra-subject introduction device
JP4611053B2 (en) Intra-subject introduction device
US12201275B2 (en) Endoscopy device having a flexible shaft
KR102389453B1 (en) Mouthpiece for endoscope
JP2005046279A (en) Endoscope
JPS5820243Y2 (en) Guide device for inserting an endoscope into a body cavity
JP5577537B2 (en) Nasal piece for transnasal endoscope

Legal Events

Date Code Title Description
A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20080317

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20080317

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20101014

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20101124

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20110124

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20111115

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20111125

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20141202

Year of fee payment: 3

R151 Written notification of patent or utility model registration

Ref document number: 4875315

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R151

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20141202

Year of fee payment: 3

S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313111

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

LAPS Cancellation because of no payment of annual fees