JPS58222020A - Purgative for pretreatment - Google Patents

Purgative for pretreatment

Info

Publication number
JPS58222020A
JPS58222020A JP10378282A JP10378282A JPS58222020A JP S58222020 A JPS58222020 A JP S58222020A JP 10378282 A JP10378282 A JP 10378282A JP 10378282 A JP10378282 A JP 10378282A JP S58222020 A JPS58222020 A JP S58222020A
Authority
JP
Japan
Prior art keywords
colon
pretreatment
magnesium citrate
purgative
laxative
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.)
Granted
Application number
JP10378282A
Other languages
Japanese (ja)
Other versions
JPH0121811B2 (en
Inventor
Tsutomu Sasagawa
笹川 力
Akira Kimura
明 木村
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.)
Teijin Ltd
Original Assignee
Teijin Ltd
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 Teijin Ltd filed Critical Teijin Ltd
Priority to JP10378282A priority Critical patent/JPS58222020A/en
Publication of JPS58222020A publication Critical patent/JPS58222020A/en
Publication of JPH0121811B2 publication Critical patent/JPH0121811B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:The titled purgative, containing picosulfate sodium in combination with magnesium citrate, easily administered, and capable of completely excreting and cleaning the contents in the colon in tests of the colon or abdominal surgical operation, etc. with almost no side effect. CONSTITUTION:A purgative for pretreatment containing (A) magneisum citrate and (B) picosulfate sodium: 4,4'-(2-pyridylmethylen)diphenolbis(sodium sulfate) monohydrate which is a laxative as active constituents. The dose thereof a time is 14-20g component (A) and 37-80mg component (B). Preferably the purgative is formulated in the form of a mixture (a solution). Thus, the dose of the magnesium citrate can be reduced, and side effects, e.g. nausea, vomiting or adbominal pain, are reduced to make the administration of the total dose possible. Thus, sufficient tests can be made.

Description

【発明の詳細な説明】 本発明は、大腸検査や腹部外科手術時等における前処置
用下剤に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a laxative for pretreatment during colon examinations, abdominal surgery, and the like.

近年、我1での大% yi、、 、@ 、例えば、大腸
がん。
In recent years, a large percentage of patients have been diagnosed with colon cancer, for example, colon cancer.

大腸ポリープ、潰瘍性大腸炎、大腸クローン−等の増加
に【著しく、大腸疾患に対する診断が、上部i内化管同
様に微細診断まで求められるようになっており、その意
味で大腸内視鏡やX線造影検査@−による正確な診断の
重要性が高まっている。そして、か\る大腸検査におい
て正確な検査テークを得るためになよ、検査に際しての
適切で、かつ患者に対する負担の少な(^前処置が必要
であり、この前処置の如伺が大腸内の微細構造の描出の
良・不良に非常な影響を与えることが知られている。壕
だ、腹部外科手術に際しても腸管内容物を十分に排除す
る前処置が必要である。
Due to the increase in colon polyps, ulcerative colitis, colon clones, etc., the diagnosis of colon diseases is now required to be as detailed as the upper i.p. The importance of accurate diagnosis by X-ray contrast examination@- is increasing. In order to obtain an accurate test take in such a colon examination, it is necessary to perform a pretreatment that is appropriate for the examination and that places less of a burden on the patient. It is known that it has a great effect on the quality of fine structure visualization.Even during abdominal surgery, pretreatment to thoroughly remove intestinal contents is necessary.

従来、大腸検査や腹部4科手術時の前処置のためには、
クエン酸マグ坏シウム液250−とビサコジル錠9℃ン
ノサイド錠等の緩下剤を併用する方法が頻用さhている
が、クエン酸マグネシウム液は異味であり、かつ余りに
大量である)tめ、服用後の悪心、嘔吐や腹痛等の副作
用があり、あるいは全音服用が不能で十分な検査ができ
ないといった問題点があった。
Conventionally, for pretreatment for colon examinations and abdominal surgery,
A method of using laxatives such as Magnesium Citrate Solution 250- and Bisacodyl Tablets 9℃ Nnoside Tablets is often used, but the Magnesium Citrate Solution has an unpleasant taste and is in too large a quantity. There were problems such as side effects such as nausea, vomiting, and abdominal pain, as well as the inability to take full doses and not be able to perform adequate tests.

本発明者らは、前記欠点を有しない前処置用下剤′fr
開発すべく鋭意研究の結果、クエン酸ママグネシウムと
緩下剤のピコスルファートナトリウムを組み合せたもの
が非常に好ましい前処置用下剤となることを知見し本発
明に到達した。
The inventors have proposed a pretreatment laxative 'fr which does not have the above-mentioned drawbacks.
As a result of intensive research for development, it was discovered that a combination of magnesium citrate and sodium picosulfate, a laxative, is a very preferred pretreatment laxative, and the present invention was achieved.

Fillち、本発明は、クエン酸マグネシウムとピコフ
ルファードブトリウムを有効成分とする前処置用下剤で
ある。
The present invention is a pretreatment laxative containing magnesium citrate and picofulfuride butrium as active ingredients.

本発明におけるクエン酸マグネシウムの主体れ【、?−
ヒトr7キンー1.2.3−プロノくントリカルボン酸
マグネシワム塩MgHC,H60)・5)40  で6
 リ、通常、水性液として用いられる。そして通常、ク
エン酸マグネシウム液と呼ばれるものは、10〇−中に
、MgOVC換算して1.55〜1.9PK相当する量
の前記クエン酸マグネシウムを含有する水性液をいう。
The main component of the present invention is magnesium citrate. −
Human r7kin-1.2.3-pronoquinone tricarboxylic acid magnesium salt MgHC, H60) 5) 40 in 6
It is usually used as an aqueous liquid. Generally, what is called a magnesium citrate solution is an aqueous solution containing the above-mentioned magnesium citrate in an amount equivalent to 1.55 to 1.9 PK in terms of MgOVC.

これは、例えば、以下の組成のものを混合し加熱するこ
とによって得られる。
This can be obtained, for example, by mixing and heating the following compositions.

、市販品としては、例えば、250+n7!中にクエン
酸マグネシウムを34を含有するマダコロール(堀井薬
品工業■製)が知られている。
For example, 250+n7! is a commercially available product. Madacolor (manufactured by Horii Pharmaceutical Co., Ltd.) containing 34% of magnesium citrate is known.

本発明によれば、クエン酸マグネシウムの一回当りの服
用量を、従来の約309前後から約14〜20t(液と
して約100〜150 d )K減少きせることができ
る。
According to the present invention, the daily dose of magnesium citrate can be reduced by about 14 to 20 t (about 100 to 150 d as a liquid) from the conventional dose of about 309 d.

本発明におけるピコスルファートナトリウム(化学名:
 4,4’−(2−ビリジルーメチレン)ジフェノール
ビス(ソジウムスルンアート)七ツバイドノート)は、
通常、水f#’llkとし7て緩下剤に用いられている
。市販品としては、例えば1ml中にピコスルファート
ナトリウムを7.5〜含有するラキソペロン液(帝人医
薬■製)が知られている。
Sodium picosulfate (chemical name:
4,4'-(2-pyridyl-methylene) diphenol bis(sodium srunate) heptubide note) is
It is usually used in laxatives as water f#'llk7. As a commercially available product, for example, Laxoperone solution (manufactured by Teijin Pharmaceutical Co., Ltd.) containing 7.5 to 7.5 ml of sodium picosulfate per ml is known.

本発明においては、ピコスルファ−) −11−) I
)    ’11ウムの一回当りの服用量は、約37〜
80■(液として約5〜10−)が適当で、あり、これ
は前記クエン酸ママグネシウムの約14〜20tと、液
状の合剤(水剤)としてNil製した方が↓ 好しい。
In the present invention, picosulfur-)-11-) I
) '11 um per dose is approximately 37 ~
80 (as a liquid, about 5 to 10) is appropriate, and it is preferable to use about 14 to 20 tons of the above-mentioned magnesium citrate and Nil as a liquid mixture (water solution).

本発明の前処置用下剤は、少量の無味無臭のピコスルフ
ァートナトリウムと、従来よりも少ない量のクエン酸マ
グネシウムからなっているので、しかも水剤として調製
できるので、服用が簡単であり、副作用もほとんどなく
、大腸検査や腹部外科手術時等に際し、大腸の内容物を
十分に排泄させ、大l15+を清浄化子ることかできき
The pretreatment laxative of the present invention consists of a small amount of tasteless and odorless sodium picosulfate and a smaller amount of magnesium citrate than conventional ones, and can be prepared as a liquid solution, so it is easy to take and has no side effects. During colon examinations, abdominal surgery, etc., the contents of the large intestine can be fully excreted and the large 115+ can be used as a purifier.

以下、実施例により本発明を詳述する。Hereinafter, the present invention will be explained in detail with reference to Examples.

実施例1 38才の女性の大腸ポリープのポリペクトミーの前処f
uとし、て、検査前日は、Brown法の変法による低
残洒食として、午後3時にコツプ1杯(I P Ome
 ) bl−ヒの水11せ、5時〜6時に実のないスー
プ、くず湯、ジュース、3分粥などの夕食をとらせた。
Example 1 Preparation f for polypectomy of a colon polyp in a 38-year-old woman
The day before the test, I consumed one cup of ice cream (I P Ome) at 3pm as a low-residue diet using a modified Brown method.
) I gave them 11 servings of water, and from 5:00 to 6:00, I had them eat a dinner of fruitless soup, kudzu soup, juice, and 3-minute porridge.

7時半に再度コツプ1杯以上の水を飲ませた。そして9
時半に本発明の前処置用下剤、即ちクエン酸マグネシウ
ム液125 ml (クエン酸マグネシウムを17?含
む)と、ピコスルファートナトリウム水溶液10ηi(
ピコスルファートナトリウムを75’II! 含む)を
、同時に服用させた。
At 7:30, I gave him another glass of water to drink. And 9
At half an hour, I added 125 ml of the pretreatment laxative of the present invention, namely a magnesium citrate solution (containing 17 ml of magnesium citrate) and 10 ηi of a sodium picosulfate aqueous solution (
Sodium picosulfate 75'II! ) were administered at the same time.

検査当日は、午前7時にコツプ1杯以−ヒの水。On the day of the test, drink a glass of water at 7am.

8時には、コーヒー、紅茶、ジュース等を朝食とし、こ
れ」ソ後、検光終了1で飲づξさぜkかった。午前1.
0時に、大腸ファイバースコープにより、寵腸を最深検
査部位とし、て観察しまたところ、直腸、S状結腸、下
行結腸、1ノ4行結腸では糞便及び粘液状残存物は全く
みられず、十分な検査がb[能の状態が確保された。」
−行結腸、盲腸では少にの粘11に状残存物がみらnた
が、吸引。
At 8 o'clock, I had a breakfast of coffee, tea, juice, etc. After that, I couldn't drink it until the end of the light analysis. AM 1.
At 0 o'clock, the intestine was examined using a fiberoptic colonoscope, and no fecal matter or mucous residue was observed in the rectum, sigmoid colon, descending colon, and 1st and 4th colon. A state of competence was ensured when the test was completed. ”
- A small amount of sticky residue was found in the colon and cecum, but it was aspirated.

洗浄により簡単に清浄化され、観察が充分+11能であ
った。
It was easily cleaned by washing and the observation was satisfactory.

実施例2 20才、男性のクローン病の患者、で、これによる回腸
終末部位に狭窄がみられていたが、便通は軟便であるが
、規則的に1日1回みられていた。病変の観察のため、
大腸ファイバースコープを宗脈したが、その前処置とし
て、検査前日tよ実施例1の場合と同様にBrownの
変法による低残渣食を供し、その後も実施例1の場合と
同様に本発明の前処置用下剤(クエン酸マグネシウム液
125+ne十ピコスルファートナトリウム水溶液1o
 ad )を投与し、検査当日の状況も同様にしfC6
そして、患者の検査に臨み、大腸ファイバースコープに
よ()、終末1i5I腸を最探検青部位として観察した
ところ、直腸からS状結腸、下行結腸、横行結腸、上行
結腸、盲腸、終末同腸に紋るまでlt便及び粘液状残存
物は全くみられず、病変の充分な観察が可能であった。
Example 2 A 20-year-old male patient with Crohn's disease was found to have stricture at the terminal ileum, but had soft bowel movements once a day regularly. For observation of lesions,
A fiberoptic colonoscope was used, and as a pretreatment, a low-residue diet according to Brown's modified method was provided on the day before the examination, as in Example 1, and thereafter, the same method as in Example 1 was used. Pretreatment laxative (125 ml of magnesium citrate solution + 1 ml of sodium picosulfate aqueous solution)
ad ), and the same conditions were used on the day of the test.
Then, when examining the patient, we observed the terminal 1i5I intestine as the bluest part to explore using a fiberoptic colonoscope (), and found that from the rectum, the sigmoid colon, descending colon, transverse colon, ascending colon, cecum, and terminal intestine. No stool or mucous residue was observed until the lesions appeared, allowing sufficient observation of the lesions.

゛  実施例3 33才、男性のクローン病の患者で、これによる回盲部
腸管の狭窄がみられていた。また、便通は、下痢状態が
つづいていた。病変の観察のため大腸ファイバースコー
プを実施したが、その前処置として、検査前日は、実施
例1の場合と同様1cBrownの変法による低残渣食
を供し、そして、9時半に、本発明の前処置用下剤(ク
エン酸マグネシウム液125−十ピコスルファートナト
リウム水溶液5−)を服用させた。検査当日は実施例1
の場合と同様にして、午前10時に、大腸ファイバース
コープにより、終末回腸を最深検査部位として観察した
ところ、直腸、S状結腸、下行結腸、4%行結腸、上行
結腸、盲腸には糞便及び粘液状残存物はみられず、病変
部の充分な観察が可能であった。終末回腸に少量の粘液
状残存物がみられたが、吸引、洗浄することにより簡琳
に清浄化され、観察が可能となった。
Example 3 A 33-year-old male patient with Crohn's disease had ileocecal intestinal stenosis. In addition, his bowel movements continued to be diarrhea. A fiberoptic colonoscopy was performed to observe the lesions.As a pretreatment, the day before the examination, a low-residue diet of 1 c Brown was provided as in Example 1, and at 9:30 a.m. A pretreatment laxative (magnesium citrate solution 125-deca-sodium picosulfate aqueous solution 5-) was administered. Example 1 on the day of the test
At 10:00 a.m., we observed the terminal ileum using a fiberoptic colonoscope as the deepest part of the examination, and found that feces and mucus were found in the rectum, sigmoid colon, descending colon, 4% colon, ascending colon, and cecum. No residual material was observed, and the lesion could be sufficiently observed. A small amount of mucus-like residue was observed in the terminal ileum, but it was easily cleaned by suctioning and washing, making it possible to observe it.

実施例4 53才の女性で、2年前より下痢と便秘を訴   □え
る過敏性大腸症候群の患者で、腸管狭窄は見られなかっ
た。検査前日は、実施例1の場合と同様にBr0Wnの
変法による低残渣食を供し、9時半に、本発明の前処置
用下剤(クエン酸マグネシウム液125 rl+ピコス
ルファートナトリウムtom/)を投与した。検査当日
は午前7時にコツプ1杯以上の水、8時忙はコーヒー、
紅茶、ジュース等を朝食とし、これ以後検査終了まで飲
食させなかった。更に検査30分前K、レジカルボン坐
剤2個を投毒し、直腸の残留側を排泄させた後、X線造
影剤(67%W/V )200−を、用いて注腸法によ
る大腸X線検査を実施した。終末回腸、盲腸を最深検査
部として撮影を行なったが、直腸、S′状結腸、下行結
腸、横行結腸、上行結腸、盲腸、終末回、腸において、
残存便もなく、造影剤ののりもよく、網目像を含めて良
い画像が得られた。
Example 4 A 53-year-old female patient with irritable bowel syndrome had been complaining of diarrhea and constipation for the past 2 years, and no intestinal stricture was observed. On the day before the test, a low-residue diet using a modified Br0Wn diet was provided as in Example 1, and at 9:30 a. administered. On the day of the test, have at least one glass of water at 7am, coffee at 8am,
The subjects had tea, juice, etc. for breakfast, and were not allowed to eat or drink anything after this until the end of the test. Furthermore, 30 minutes before the examination, two Resicarbon suppositories were administered and the remaining side of the rectum was excreted, and then an X-ray contrast agent (67% W/V) 200- was used to remove the large intestine by enema. An X-ray examination was performed. The terminal ileum and cecum were the deepest parts of the examination, but the rectum, sigmoid colon, descending colon, transverse colon, ascending colon, cecum, terminal gyrus, and intestines were
There was no residual stool, the contrast agent applied well, and good images, including mesh images, were obtained.

実施例5 63才の女性で、上行結腸癌で、摘発生部において完全
に近い腸管狭窄をきたしていた。大腸注腸検査の前処置
として、検査前日は、実施例1の場合と同様にBrow
nの変法による低残渣食を供し、そして、9時牛に本発
明の前処置用下剤(クエン酸マ、グネシウム液100−
十ピコスルファートナトリウム水溶液10d)を投与し
た。その後は実施例4の場合と全く同様にして、大腸X
線検査を実施した。この患者は、上行結腸部の完全狭窄
のため、口側への硫酸バリウム注入は不能であったが、
直腸、S状結腸。
Example 5 A 63-year-old woman had ascending colon cancer and had nearly complete intestinal stenosis at the site of resection. As a pretreatment for the colon enema test, the day before the test, perform the Brow procedure as in Example 1.
At 9 o'clock, the cows were fed with a pretreatment laxative of the present invention (citrate, magnesium solution 100%).
Ten picosulfate sodium aqueous solution 10d) was administered. Thereafter, in exactly the same manner as in Example 4, the large intestine
Conducted line inspection. In this patient, oral barium sulfate injection was not possible due to complete stenosis of the ascending colon.
Rectum, sigmoid colon.

下行結腸、槙行結膓、上行結腸には残便が全くなく、満
足すべき画像を有ることができた。
There was no residual feces in the descending colon, tuberosity, and ascending colon, and we were able to obtain satisfactory images.

Claims (1)

【特許請求の範囲】 1、 ピコスルファートナトリウムとクエン酸マグネシ
ウムを有効成分とする前処置用下剤。 21回の投与分としてピコスルファートナトリウム約3
7〜80 +19とクエン酸マグネシウム約14〜20
9を特徴する特許請求の範囲第1項記載の前処置用下剤
。 a、 剤型が水剤である特許請求の範囲第1項又は2項
記載の前処置用下剤。
[Claims] 1. A pretreatment laxative containing sodium picosulfate and magnesium citrate as active ingredients. Approximately 3 sodium picosulfate for 21 doses
7-80 +19 and magnesium citrate approximately 14-20
9. The laxative for pretreatment according to claim 1, characterized in that: a. The pretreatment laxative according to claim 1 or 2, which is in the form of a liquid solution.
JP10378282A 1982-06-18 1982-06-18 Purgative for pretreatment Granted JPS58222020A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10378282A JPS58222020A (en) 1982-06-18 1982-06-18 Purgative for pretreatment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10378282A JPS58222020A (en) 1982-06-18 1982-06-18 Purgative for pretreatment

Publications (2)

Publication Number Publication Date
JPS58222020A true JPS58222020A (en) 1983-12-23
JPH0121811B2 JPH0121811B2 (en) 1989-04-24

Family

ID=14362979

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10378282A Granted JPS58222020A (en) 1982-06-18 1982-06-18 Purgative for pretreatment

Country Status (1)

Country Link
JP (1) JPS58222020A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014502598A (en) * 2010-12-13 2014-02-03 トーマス・ジュリアス・ボロディ Gastric and colon preparations and methods for making and using them

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014502598A (en) * 2010-12-13 2014-02-03 トーマス・ジュリアス・ボロディ Gastric and colon preparations and methods for making and using them
US10092573B2 (en) 2010-12-13 2018-10-09 Salix Pharmaceuticals, Inc. Gastric and colonic formulations and methods for making and using them

Also Published As

Publication number Publication date
JPH0121811B2 (en) 1989-04-24

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