JPH0541707Y2 - - Google Patents
Info
- Publication number
- JPH0541707Y2 JPH0541707Y2 JP2169191U JP2169191U JPH0541707Y2 JP H0541707 Y2 JPH0541707 Y2 JP H0541707Y2 JP 2169191 U JP2169191 U JP 2169191U JP 2169191 U JP2169191 U JP 2169191U JP H0541707 Y2 JPH0541707 Y2 JP H0541707Y2
- Authority
- JP
- Japan
- Prior art keywords
- tube
- drug
- present
- powdered
- ulcer
- 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 - Lifetime
Links
- 239000003814 drug Substances 0.000 claims description 53
- 229940079593 drug Drugs 0.000 claims description 37
- 238000002347 injection Methods 0.000 claims description 11
- 239000007924 injection Substances 0.000 claims description 11
- 239000000843 powder Substances 0.000 claims description 11
- 208000025865 Ulcer Diseases 0.000 description 12
- 231100000397 ulcer Toxicity 0.000 description 12
- 230000003902 lesion Effects 0.000 description 9
- 239000007789 gas Substances 0.000 description 8
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 235000010413 sodium alginate Nutrition 0.000 description 7
- 229940005550 sodium alginate Drugs 0.000 description 7
- 239000000661 sodium alginate Substances 0.000 description 7
- 230000000740 bleeding effect Effects 0.000 description 5
- 238000010586 diagram Methods 0.000 description 4
- 210000001035 gastrointestinal tract Anatomy 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000012530 fluid Substances 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 208000008469 Peptic Ulcer Diseases 0.000 description 2
- 208000007107 Stomach Ulcer Diseases 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- 239000003699 antiulcer agent Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 208000000718 duodenal ulcer Diseases 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 210000004798 organs belonging to the digestive system Anatomy 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 210000002784 stomach Anatomy 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- IVVHAAOJLULJLK-YDXSIYMFSA-E Aceglutamide aluminum Chemical compound [OH-].[OH-].[OH-].[OH-].[Al+3].[Al+3].[Al+3].CC(=O)N[C@H](C([O-])=O)CCC(N)=O.CC(=O)N[C@H](C([O-])=O)CCC(N)=O.CC(=O)N[C@H](C([O-])=O)CCC(N)=O.CC(=O)N[C@H](C([O-])=O)CCC(N)=O.CC(=O)N[C@H](C([O-])=O)CCC(N)=O IVVHAAOJLULJLK-YDXSIYMFSA-E 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 206010027146 Melanoderma Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 229930192392 Mitomycin Natural products 0.000 description 1
- NWIBSHFKIJFRCO-WUDYKRTCSA-N Mytomycin Chemical compound C1N2C(C(C(C)=C(N)C3=O)=O)=C3[C@@H](COC(N)=O)[C@@]2(OC)[C@@H]2[C@H]1N2 NWIBSHFKIJFRCO-WUDYKRTCSA-N 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 208000005718 Stomach Neoplasms Diseases 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229960002627 aceglutamide aluminum Drugs 0.000 description 1
- 239000002246 antineoplastic agent Substances 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 238000009534 blood test Methods 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- FHRSHSOEWXUORL-HDJSIYSDSA-N cetraxate Chemical compound C1C[C@@H](C[NH3+])CC[C@@H]1C(=O)OC1=CC=C(CCC([O-])=O)C=C1 FHRSHSOEWXUORL-HDJSIYSDSA-N 0.000 description 1
- 229950009533 cetraxate Drugs 0.000 description 1
- 238000002512 chemotherapy Methods 0.000 description 1
- CCGSUNCLSOWKJO-UHFFFAOYSA-N cimetidine Chemical compound N#CNC(=N/C)\NCCSCC1=NC=N[C]1C CCGSUNCLSOWKJO-UHFFFAOYSA-N 0.000 description 1
- 229960002908 cimetidine hydrochloride Drugs 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 230000002183 duodenal effect Effects 0.000 description 1
- 210000001198 duodenum Anatomy 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002550 fecal effect Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 206010017758 gastric cancer Diseases 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 201000005917 gastric ulcer Diseases 0.000 description 1
- 230000007721 medicinal effect Effects 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 229960004857 mitomycin Drugs 0.000 description 1
- 210000004877 mucosa Anatomy 0.000 description 1
- 231100000957 no side effect Toxicity 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 231100000241 scar Toxicity 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 201000011549 stomach cancer Diseases 0.000 description 1
- -1 suralfate Chemical compound 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- WFWLQNSHRPWKFK-ZCFIWIBFSA-N tegafur Chemical compound O=C1NC(=O)C(F)=CN1[C@@H]1OCCC1 WFWLQNSHRPWKFK-ZCFIWIBFSA-N 0.000 description 1
- 229960001674 tegafur Drugs 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 210000003813 thumb Anatomy 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 238000001665 trituration Methods 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
Landscapes
- Infusion, Injection, And Reservoir Apparatuses (AREA)
Description
【考案の詳細な説明】
本考案は粉末薬剤の局所投与装置、詳しくは消
化器官等の体腔内に体外よりチユーブを挿入し、
該チユーブを通して直接体腔内壁に粉末薬剤を投
与する装置に関する。[Detailed description of the invention] The present invention is a local administration device for powdered drugs, specifically, a tube is inserted into a body cavity such as the digestive tract from outside the body.
The present invention relates to a device for administering a powdered drug directly to the inner wall of a body cavity through the tube.
胃潰瘍、十二指腸潰瘍等の所謂消化性潰瘍を始め
とする体腔内粘膜欠損や癌、ポリーブ等の之等粘
膜・組織の病変状態の治療には、現在種々の化学
療法が実施されている。また近年フアイバースコ
ープ(内視鏡)を利用した上記病症、病変状態の
診断技術の進歩発展と共に、該内視鏡下での医薬
品の局所投与(経内視鏡的注入)療法が注目され
つつある。例えば近年新たに研究開発されたアル
ギン酸ナトリウム水溶液は、経口的投与と共に経
内視鏡的注入より、消化管粘膜保護及び消化管止
血作用を奏し得、消化性潰瘍の止血及び治癒に用
い得ることが確認されている(特願昭55−122565
号)。しかるに上記経内視鏡的注入は、通常内視
鏡の鉗子孔よりチユーブを挿入し、該チユーブを
通じて薬剤を注入するものであるため、用いられ
る薬剤が水溶液等の液剤に限定される。粉末薬剤
に上記注入操作を適用する場合、チユーブ内での
閉塞(特にチユーブ先端は、消化器官内等の液流
と接触しているため容易に粉末薬剤が湿潤凝集す
る)の危険があり、また該薬剤の注入量、注入速
度等を調整し難い欠点がある。更に粉末薬剤に限
らず、液剤の場合においても、その経内視鏡的投
与では、これが消化器官等の内壁に付着する前
に、之等器官内液によつて流動乃至拡散されて、
目的とする病変部位に均一に高濃度でもしくは高
濃度となる量で使用薬剤を局所投与できず、従つ
て所望の投与効果(治療効果)を発揮し難い難点
がある。Various chemotherapy methods are currently being used to treat mucosal and tissue lesions such as so-called peptic ulcers such as gastric ulcers and duodenal ulcers, as well as mucosal defects in body cavities, cancers, and polyps. In addition, in recent years, with the progress and development of diagnostic technology for the above-mentioned diseases and lesion states using fiberscopes (endoscopes), local administration of pharmaceuticals (transendoscopic injection) therapy using fiberscopes has been attracting attention. . For example, an aqueous sodium alginate solution, which has been newly researched and developed in recent years, can protect the gastrointestinal mucosa and stop bleeding in the gastrointestinal tract by oral administration and endoscopic injection, and can be used to stop bleeding and heal peptic ulcers. Confirmed (Patent application 1987-122565)
issue). However, in the above-mentioned transendoscopic injection, a tube is usually inserted through the forceps hole of an endoscope and the drug is injected through the tube, so the drugs used are limited to liquid drugs such as aqueous solutions. When applying the above injection operation to powdered drugs, there is a risk of blockage within the tube (in particular, the tip of the tube is in contact with the liquid flow in the digestive tract, so powdered drugs easily become wet and aggregate), and There is a drawback that it is difficult to adjust the injection amount, injection speed, etc. of the drug. Furthermore, in the case of not only powder medicines but also liquid medicines, when administering them endoscopically, before they adhere to the inner walls of the digestive organs, etc., they are fluidized or diffused by the internal fluids of these organs.
There is a drawback that the drug cannot be locally administered uniformly to the target lesion site at a high concentration or in a high concentration amount, and therefore it is difficult to exert the desired administration effect (therapeutic effect).
本考案は、上記従来技術の難点を解消して、必要
量の粉末薬剤を常に安定して経内視鏡的に局所投
与でき、しかもこれによつて目的とする医療効果
を充分に発揮し得る装置を提供するものである。The present invention solves the above-mentioned drawbacks of the conventional technology, and enables stable local administration of the required amount of powdered medicine at all times through an endoscopic method, and thereby fully exerts the intended medical effect. It provides equipment.
即ち本考案は、体外より内視鏡鉗子口を通じ体腔
内に挿入可能なチユーブ、該チユーブの途中に設
けられた薬剤充填部、薬剤充填部に充填された粉
末薬剤をチユーブ先端より体腔内壁に吹き付ける
ためのガス圧入手段とを備えていることを特徴と
する粉末薬剤局所投与装置に係る。That is, the present invention includes a tube that can be inserted into a body cavity from outside the body through an endoscope forceps port, a drug filling section provided in the middle of the tube, and a powder drug filled in the drug filling section being sprayed onto the inner wall of the body cavity from the tip of the tube. The present invention relates to a powder drug local administration device characterized in that it is equipped with a gas pressure injection means.
本考案によれば胃、十二指腸等の消化器官を始め
とする各種の体腔内壁の所定箇所(病変部)に、
常に安定して一定量の粉末薬剤を瞬時に且つ極め
て容易に直接散布投与することができる。しかも
本考案によれば上記粉末薬剤の散布がガス圧を利
用して行われるため体腔内液の動きに影響される
ことなく、目的とする病変部位に確実に所定量の
粉末薬剤を均一且つ多量に付着させることができ
る。本考案はこのように局所的に多量の薬剤を投
与できるものであるため、殊に潰瘍等の病変が深
部におよぶ場合等に極めて有効に適用でき、従来
の液剤の経内視鏡的注入や通常の医薬品の経口乃
至局所投与等では到底達成できない優れた治療効
果を奏し得る。According to the present invention, at specified locations (lesioned areas) on the inner walls of various body cavities, including digestive organs such as the stomach and duodenum,
It is possible to always stably and directly spray and administer a constant amount of powdered medicine instantaneously and extremely easily. Furthermore, according to the present invention, the powdered drug is dispersed using gas pressure, which ensures that a predetermined amount of the powdered drug is uniformly and in large quantities applied to the target lesion site without being affected by the movement of fluid in the body cavity. can be attached to. Since the present invention allows for the local administration of a large amount of drug, it can be applied extremely effectively, especially when lesions such as ulcers extend deep into the body, and can be applied to conventional transendoscopic injection of liquid drugs Excellent therapeutic effects that cannot be achieved by oral or local administration of ordinary pharmaceuticals can be achieved.
本考案に適用される粉末薬剤は、粉末形態を有す
る限り特に限定はなく、従来より知られている各
種の医薬品のいずれであつてもよい。特に本考案
は粉末薬剤を病変部位に直接局所投与できるので
あるため、従来その代謝吸収性の面等より経口投
与等によつては効果を発揮し得なかつた薬剤をも
極めて有効に投与することを可能としたものであ
り、その有用性は非常に高い。代表的粉末薬剤と
してはアルギン酸ナトリウムを例示できる。その
他の抗潰瘍剤例えばアルザオキサ、アセグルタミ
ドアルミニウム、スクラルフアート、シメチジ
ン、塩酸セトラキサート等もまた夫々単独でまた
はアルギン酸ナトリウムと混合して使用でき、更
に胃癌等に適用される5−フルオロウラシン、フ
トラフール、マイトマイシン等の抗癌剤もまた
夫々単独で又は上記アルギン酸ナトリウム等の抗
潰瘍剤と混合して使用することができる。The powdered medicine applied to the present invention is not particularly limited as long as it is in powder form, and may be any of various conventionally known pharmaceuticals. In particular, the present invention allows for the local administration of powdered drugs directly to the lesion site, making it extremely effective to administer drugs that have conventionally been ineffective through oral administration due to their metabolic and absorption properties. , and its usefulness is extremely high. An example of a typical powdered drug is sodium alginate. Other anti-ulcer agents such as alzaoxa, aceglutamide aluminum, suralfate, cimetidine, and cetraxate hydrochloride can also be used alone or in combination with sodium alginate, as well as 5-fluorouracine, which is applied to gastric cancer, etc. Anticancer agents such as ftorafur and mitomycin can also be used alone or in combination with the above-mentioned antiulcer agents such as sodium alginate.
以下本考案を添付図面により説明する。The present invention will be explained below with reference to the accompanying drawings.
図1は本考案の一実施例を示す図である。図にお
いて1は注射器、2は注射針、3はチユーブ、4
は粉末薬剤、5は栓、6は薬剤充填部を示す。FIG. 1 is a diagram showing an embodiment of the present invention. In the figure, 1 is a syringe, 2 is a needle, 3 is a tube, and 4
5 indicates a powder medicine, 5 a stopper, and 6 a medicine filling part.
本考案装置は以下の如くして使用される。即ちま
ず注射器1の注射筒に粉末薬剤を入れ、これに注
射針2及び先端を適宜の手段により閉栓されたチ
ユーブ3に連結し、注射器の吸子(注射内筒)を
押して、注射筒内粉末薬剤を注射針2を経てチユ
ーブ先端部の薬剤充填部6まで圧送する。又は予
め粉末薬剤をチユーブ3内に適当な装置でもつて
入れ更に振動機等を利用して薬剤充填部6に充填
する。上記において栓5としては通気性を有し且
つ粉末薬剤の漏れを防止できる限り特に制限はな
いが、体腔内液で湿潤し密封栓となり且つ人体に
無害で、使用後はそのまま排泄されるもの、具体
的には繊維、綿、スポンジ、植物性、動物性もし
くは合成樹脂のものが好ましい。次いで上記によ
り先端部の薬剤充填部6に粉末薬剤4を充填され
たチユーブ3を例えば内視鏡鉗子孔より消化管等
の薬剤散布を要望される病変部近くまで挿入し、
注射器の吸子をやや強く押す。この操作によりチ
ユーブ内は加圧状態となり、チユーブ先端の栓5
がはずれると共に、該先端より粉末薬剤4が体腔
内に散布され、体腔内壁(病変部)に付着され
る。The device of the present invention is used as follows. That is, first, a powdered drug is put into the syringe barrel of the syringe 1, the syringe needle 2 and the tip are connected to the closed tube 3 by an appropriate means, and the sucker (inner barrel) of the syringe is pushed to release the powder in the syringe barrel. The medicine is force-fed through the injection needle 2 to the medicine filling part 6 at the tip of the tube. Alternatively, a powdered medicine is placed in the tube 3 in advance using an appropriate device and then filled into the medicine filling part 6 using a vibrator or the like. In the above, the plug 5 is not particularly limited as long as it has air permeability and can prevent leakage of the powder medicine, but it can be moistened with body cavity fluid, forms a sealing plug, is harmless to the human body, and is excreted as is after use; Specifically, fibers, cotton, sponge, vegetable, animal or synthetic resins are preferred. Next, the tube 3 filled with the powdered drug 4 is inserted into the drug filling part 6 at the tip as described above, for example, through the endoscope forceps hole to the gastrointestinal tract or the like, near the lesion where the drug is desired to be sprayed.
Press the syringe sucker a little harder. With this operation, the inside of the tube becomes pressurized, and the plug 5 at the tip of the tube
As the needle is removed, the powdered medicine 4 is dispersed into the body cavity from the tip and adheres to the inner wall (lesioned area) of the body cavity.
また本考案装置におけるガス圧入手段としては、
第1図に示す空気を利用する注射器1に限らず、
エアゾール缶やその他のガスボンベ、二連球等を
例示できる。上記ガスボンベやエアゾール缶等に
充填され、粉末薬剤の吹き付けに用いられるガス
は、特に空気に限定されず、通常医療機関に常備
されている窒素ガス、酸素ガス、炭酸ガス等であ
つてよく、更に噴射によつてガス状となるフロン
等や他の液化ガス等であつてもよい。之等は単に
粉末薬剤をチユーブを通じて病変部に吹き付ける
ために用いられるものであり、通常その使用量は
非常に少量であるため特に人体に危険を及ぼすお
それはない。In addition, the gas pressurization means in the device of the present invention is as follows:
Not limited to the syringe 1 using air shown in FIG.
Examples include aerosol cans, other gas cylinders, and double balls. The gas filled in the gas cylinder, aerosol can, etc. and used for spraying the powdered medicine is not particularly limited to air, and may be nitrogen gas, oxygen gas, carbon dioxide gas, etc., which are normally kept in medical institutions, and It may also be fluorocarbon or other liquefied gas that becomes gaseous by injection. These are simply used to spray powdered medicine onto the affected area through a tube, and the amount used is usually very small, so there is no danger of it posing any particular danger to the human body.
上記本考案装置に利用されるチユーブ3、注射器
1等の各器具自体は、従来より医療器具として知
られる通常のものでよい。また粉末薬剤の1回当
りの使用量は、該薬剤の種類、これを投与すべき
患者やその疾病状態等に応じて適宜に決定すれは
よいが通常約0.1〜5g前後、好ましくは約0.3〜
3gとされるのが一般的である。薬剤を0.1g以
下で投与したい場合、これは好ましくは適当な倍
散の形態で本考案に利用される。The tube 3, syringe 1, and other instruments used in the device of the present invention may be conventionally known medical instruments. The amount of powdered drug to be used per time may be determined appropriately depending on the type of drug, the patient to whom it is administered, the disease state, etc., but it is usually about 0.1 to 5 g, preferably about 0.3 to 5 g.
It is generally set at 3g. If it is desired to administer the drug in less than 0.1 g, it is preferably utilized in the present invention in the form of a suitable trituration.
以下本考案装置の使用方法の実施例を挙げる。Examples of how to use the device of the present invention will be given below.
実施例1 本症例は難治性漬瘍で、内視鏡検査
で、胃角部に大きな潰瘍が認められ、潰瘍底から
出血が認められる。上記胃潰瘍患者に、本使用方
法を実施した。即ち先端に紙栓を5mm程度軽くつ
めたチユーブに適当な振動を与えながらアルギン
酸ナトリウム1.5gを充填した。次いで上記チユ
ーブをフアイバースコープの鉗子孔より挿入し、
先端を病変部まで到達させた後、注射内筒を強く
押した。末端紙栓がはずれ、アルギン酸ナトリウ
ム粉末が潰瘍部位全般に亘つて散布され、該病変
部を被覆したことが観察された。Example 1 This case was an intractable ulcer, and endoscopic examination revealed a large ulcer at the angle of the stomach and bleeding from the bottom of the ulcer. This usage method was applied to the above gastric ulcer patient. That is, 1.5 g of sodium alginate was filled into a tube whose tip was lightly stuffed with a paper stopper of about 5 mm, while applying appropriate vibrations. Next, insert the tube through the forceps hole of the fiberscope,
After the tip reached the lesion, the syringe barrel was pressed firmly. It was observed that the terminal paper stopper was removed and the sodium alginate powder was spread over the ulcer site and coated the lesion.
上記方法を3週間に9回繰返し実施したところ、
7日後に潰瘍がかなり小さくなつたことが確認さ
れ、潰瘍底には黒点が見られたが、潜血はマイナ
スとなつた。また21日後に潰瘍は直径5mm前後に
縮少した。本法実施による副作用は全く認められ
なかつた。尚上記患者については、患者の苦痛を
避けるため上記内視鏡下での投与と、通常の投与
(アルギン酸ナトリウム5%水溶液50〜100mlを1
日2回(昼間1回及び就寝前1回)投与した)と
を併用した。When the above method was repeated 9 times in 3 weeks,
Seven days later, it was confirmed that the ulcer had become considerably smaller, and a black spot was seen at the bottom of the ulcer, but the occult blood was negative. Moreover, after 21 days, the ulcer had shrunk to around 5 mm in diameter. No side effects were observed due to implementation of this method. For the above patient, in order to avoid pain to the patient, the above-mentioned endoscopic administration and normal administration (1 dose of 50 to 100 ml of 5% sodium alginate aqueous solution)
The drug was administered twice a day (once during the day and once before bedtime).
実施例2 十二指腸球部前壁に親指大の大きな深
い潰瘍が観察され、出血を伴う十二指腸潰瘍患者
に、上記実施例1と同様の本法を3日に1回繰返
し実施した。Example 2 The same method as in Example 1 above was repeated once every 3 days on a patient with a duodenal ulcer in which a large, deep ulcer the size of a thumb was observed on the anterior wall of the duodenal bulb, accompanied by bleeding.
本法実施の5日後に潰瘍はやや浅くなり、便潜血
陰性となつた。また12日後には潰瘍が縮少し、出
血がマイナスとなつた。更に24日後には潰瘍は線
状の白い瘢痕となり治療された。Five days after implementing this method, the ulcer became slightly shallower, and the fecal occult blood test became negative. After 12 days, the ulcer had shrunk and the bleeding became negative. After another 24 days, the ulcer turned into a linear white scar and was treated.
【図1】本考案装置の一具体例を示す図である。FIG. 1 is a diagram showing a specific example of the device of the present invention.
【図2】本考案装置の他の一具体例を示す図であ
る。FIG. 2 is a diagram showing another specific example of the device of the present invention.
【図3】薬剤充填部の一態様を示す図である。FIG. 3 is a diagram showing one embodiment of a drug filling part.
1……注射器 2……注射針 3……チユーブ 4……粉末薬剤 5……栓 6……薬剤充填部。 1...Syringe 2……syringe needle 3...Tube 4...Powder drug 5...stopper 6...Drug filling section.
Claims (1)
内に挿入可能なチユーブ、該チユーブの途中に設
けられた薬剤充填部、薬剤充填部に充填された粉
末薬剤をチユーブ先端より体腔内壁に吹き付ける
ためのガス圧入手段とを備えていることを特徴と
する粉末薬剤局所投与装置。Claims 1: A tube that can be inserted into a body cavity from outside the body through an endoscope forceps port, a drug filling section provided in the middle of the tube, and a powder drug filled in the drug filling section being sprayed onto the inner wall of the body cavity from the tip of the tube. A powder drug local administration device characterized in that it is equipped with a gas pressure injection means.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2169191U JPH0541707Y2 (en) | 1991-04-04 | 1991-04-04 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2169191U JPH0541707Y2 (en) | 1991-04-04 | 1991-04-04 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0488953U JPH0488953U (en) | 1992-08-03 |
JPH0541707Y2 true JPH0541707Y2 (en) | 1993-10-21 |
Family
ID=31756631
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2169191U Expired - Lifetime JPH0541707Y2 (en) | 1991-04-04 | 1991-04-04 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0541707Y2 (en) |
-
1991
- 1991-04-04 JP JP2169191U patent/JPH0541707Y2/ja not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH0488953U (en) | 1992-08-03 |
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