JPS61240970A - Suppression of malignant tumor - Google Patents

Suppression of malignant tumor

Info

Publication number
JPS61240970A
JPS61240970A JP60081297A JP8129785A JPS61240970A JP S61240970 A JPS61240970 A JP S61240970A JP 60081297 A JP60081297 A JP 60081297A JP 8129785 A JP8129785 A JP 8129785A JP S61240970 A JPS61240970 A JP S61240970A
Authority
JP
Japan
Prior art keywords
tumor
eosin yellow
malignant tumor
suppression
laser beam
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.)
Pending
Application number
JP60081297A
Other languages
Japanese (ja)
Inventor
高瀬 靖広
吉野 清高
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.)
Mitsui Pharmaceuticals Inc
Original Assignee
Mitsui Pharmaceuticals Inc
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 Mitsui Pharmaceuticals Inc filed Critical Mitsui Pharmaceuticals Inc
Priority to JP60081297A priority Critical patent/JPS61240970A/en
Publication of JPS61240970A publication Critical patent/JPS61240970A/en
Pending legal-status Critical Current

Links

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 産業上の利用分野 この発明は医療の分野においてヒトを含む動物の悪性腫
瘍を抑制する方法に関する。詳しくは悪性腫瘍を有する
動物の体内にエオシンイエローを投与した後、悪性腫瘍
にレーザー光線を照射し腫瘍を抑制または縮退せしめる
腫瘍の処理方法に関する。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application This invention relates to a method for suppressing malignant tumors in animals including humans in the medical field. Specifically, the present invention relates to a method for treating a tumor in which eosin yellow is administered into the body of an animal having a malignant tumor, and then the malignant tumor is irradiated with a laser beam to suppress or shrink the tumor.

従来の技術 ヒトを含む動物に発生した悪性腫瘍の治療方法として手
術による腫瘍の除去などの外科的処置と抗ガン剤を使用
する内科的治療が行われている。
BACKGROUND OF THE INVENTION Methods for treating malignant tumors occurring in animals including humans include surgical procedures such as surgical removal of the tumor and medical treatments using anti-cancer drugs.

外科的方法として、近時レーザー光線照射と光感受性薬
剤とを併用する処理により悪性腫瘍の抑制または縮退を
はかる方法が研究されている。光感受性薬剤としてヘマ
トポルフィリン誘導体(以下HpDと略記する)が良く
用いられている。例えば肺ガンの治療について次の文献
がある。「早田養博、日本臨床、第42巻、第1号、1
84〜195ページ、1984年」 発明が解決しようとする問題点 腫瘍のレーザー光線処理に用いる光感受性薬剤に要求さ
れる条件は、薬剤が1Iffi瘍に高い親和性を有する
ことと薬剤が生体に安全に使用できることである。)I
 p Dは腫瘍に高い親和性を有しているが、日焼けな
どの副作用が認められている。またアクリジンオレンジ
も高い親和性を有しているが、発ガン性の疑いがあり安
全性の点で問題がある。
As a surgical method, research has recently been conducted on a method of suppressing or degenerating malignant tumors through treatment using a combination of laser beam irradiation and photosensitizing drugs. Hematoporphyrin derivatives (hereinafter abbreviated as HpD) are often used as photosensitizing drugs. For example, there is the following literature regarding the treatment of lung cancer. “Yoshihiro Hayata, Japanese Clinical Journal, Volume 42, No. 1, 1
Pages 84-195, 1984. Problems to be Solved by the Invention The conditions required for a photosensitizing drug used in laser beam treatment of tumors are that the drug has a high affinity for tumors and that the drug is safe for living organisms. It can be used. )I
Although pD has a high affinity for tumors, side effects such as sunburn have been observed. Acridine orange also has a high affinity, but it is suspected of being carcinogenic and poses a safety problem.

レーザー光線による腫瘍処理にはさらに有用な光感受性
薬剤の開発が望まれている。
The development of more useful photosensitizing drugs for tumor treatment with laser beams is desired.

問題点を解決するための手段 本発明者は光感受性薬剤について研究を進めた結果、エ
オシンイエローが腫瘍に対して高い親和性を有すること
を見出した。エオシンイエローは螢光性物質であり、腫
瘍細胞や腫瘍組織に強く親和したエオシンイエローの発
する螢光を観察することにより悪性腫瘍を他の組織と区
別して観察でき、診断上極めて有用である。これについ
ては癌診断用試薬として特許出願を行った(特願昭59
−27224)。本発明者はさらに研究を進めた結果、
エオシンイエローが腫瘍のレーザー光線処理に用いる光
感受性薬剤としても有用であることを見出した。エオシ
ンイエローを動物の静脈内に投与し、適当な時間の経過
後、特定の波長のレーザー光線をI!瘍内に照射するこ
とにより、腫瘍の抑制ないし縮退が認められ悪性腫瘍の
治療に効果があった。
Means for Solving the Problems As a result of conducting research on photosensitizing drugs, the present inventor discovered that eosin yellow has a high affinity for tumors. Eosin yellow is a fluorescent substance, and by observing the fluorescence emitted by eosin yellow, which has a strong affinity for tumor cells and tumor tissues, malignant tumors can be distinguished from other tissues and can be observed, making it extremely useful for diagnosis. A patent application was filed for this as a cancer diagnostic reagent (patent application filed in 1983).
-27224). As a result of further research, the inventor found that
We have found that eosin yellow is also useful as a photosensitizing agent for laser treatment of tumors. Eosin yellow is administered intravenously to an animal, and after an appropriate period of time, a laser beam of a specific wavelength is applied to the animal. By irradiating the tumor into the tumor, tumor suppression or regression was observed, and it was effective in treating malignant tumors.

エオシンイエローは食用色素第103号として食品に使
用されたこともあり、安全性も高く、光感受性薬剤とし
て好適である。
Eosin yellow has been used in foods as food coloring No. 103, is highly safe, and is suitable as a photosensitizer.

以下実施例により本発明の主題と作用l、7ついて詳細
を述べる。
Hereinafter, the subject matter and effects 1 and 7 of the present invention will be described in detail with reference to Examples.

実施例 7週齢のトンリュー系雌ラットを用い、1匹当たり腹水
型肝癌(AH−130)細胞を6X10’個背側部皮下
に移植し、皮下にAI(−130が20〜30mmに増
殖したラットを試験に用いた。
Example 7 Using 7-week-old Tonryu female rats, 6 x 10' ascites-type hepatoma (AH-130) cells were subcutaneously transplanted into the dorsal region of each rat, and AI (-130) cells were subcutaneously transplanted to a size of 20 to 30 mm. Rats were used in the study.

エオシンイエロー(東京化成製特級試薬)500mgを
10o+1の生理的食塩水に溶解し、上記ラットに1匹
当たり100mg/kgの割合で経尾静脈的に投与した
500 mg of Eosin Yellow (special grade reagent manufactured by Tokyo Kasei) was dissolved in 10o+1 physiological saline and administered to the above rats via the tail vein at a rate of 100 mg/kg per rat.

エオシンイエロー投与後6時間目に、波長514.5 
ns、出力200mWのアルゴンレーザー(機種、NE
CGLG3300)を誘導した針1mmφを腫瘍塊に刺
して3分間照射し、経口的に腫瘍塊の長径および短径を
計測した。
Six hours after administration of eosin yellow, wavelength 514.5
ns, argon laser with output 200mW (model, NE
A 1 mmφ needle guided with CGLG3300) was inserted into the tumor mass, irradiated for 3 minutes, and the major and minor axes of the tumor mass were orally measured.

対照例として、上記ラットを用い、エオシンイエロー投
与もレーザー光線照射も行わなかった群、さらにレーザ
ー光線照射のみを行った群についても実施した。
As a control example, using the above-mentioned rats, experiments were conducted on a group in which neither eosin yellow administration nor laser beam irradiation was performed, and a group in which only laser beam irradiation was performed.

式(長径×(短径)2 )÷2により腫瘍塊の重量(g
)を算出した。この式は、本邦でも抗腫瘍剤の効果判定
のために用いられている(例えば飯郷正明、J、Pha
rm、Dyn、、第1巻、49〜54ページ、1978
年)。効果判定を容易にするために、エオシンイエロー
投与およびレーザー光線照射前の腫瘍塊の重量を100
として腫瘍の増殖率を算出した。
The weight of the tumor mass (g
) was calculated. This formula is also used in Japan to determine the effectiveness of antitumor drugs (for example, Masaaki Iigo, J. Pha
rm, Dyn, Volume 1, Pages 49-54, 1978
Year). To facilitate efficacy evaluation, the weight of the tumor mass before eosin yellow administration and laser beam irradiation was
The tumor growth rate was calculated as follows.

このようにして得られた結果を表1にまとめた。The results thus obtained are summarized in Table 1.

また、効果のt検定の結果を表2に記載した。In addition, the results of the t-test of effectiveness are listed in Table 2.

検定結果から明らかなように、レーザー単独でも抗1l
ffi瘍効果は見られるが、エオシンイエローとの併用
でさらに有意(p < 0.05)に腫瘍の増殖を抑え
ることがわかる。
As is clear from the assay results, the laser alone has anti-1L
ffi tumor effect was observed, but it was found that combined use with eosin yellow suppressed tumor growth even more significantly (p < 0.05).

さらには、エオシンイエローの投与量、レーザー光線照
射量および両者併用のタイミングを工夫することにより
一層効果を増強させることができる。
Furthermore, the effect can be further enhanced by adjusting the dose of eosin yellow, the amount of laser beam irradiation, and the timing of the combined use of both.

発明の効果 安全性の高いエオシンイエローとレーザー光線を併用す
る腫瘍抑制方法は、実施例で明らかなように有意に腫瘍
の増殖を抑制し、本発明の医療分野への利用価値も非常
に高いものである。
Effects of the Invention The tumor suppression method using a combination of highly safe eosin yellow and laser beams significantly suppresses tumor growth as shown in the examples, and the present invention has very high utility value in the medical field. be.

Claims (1)

【特許請求の範囲】[Claims] 悪性腫瘍を有する動物の体内にエオシンイエローを投与
した後、腫瘍部位にレーザー光線を照射することを特徴
とする悪性腫瘍抑制方法。
A method for suppressing a malignant tumor, which comprises administering eosin yellow into the body of an animal having a malignant tumor, and then irradiating the tumor site with a laser beam.
JP60081297A 1985-04-18 1985-04-18 Suppression of malignant tumor Pending JPS61240970A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60081297A JPS61240970A (en) 1985-04-18 1985-04-18 Suppression of malignant tumor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60081297A JPS61240970A (en) 1985-04-18 1985-04-18 Suppression of malignant tumor

Publications (1)

Publication Number Publication Date
JPS61240970A true JPS61240970A (en) 1986-10-27

Family

ID=13742454

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60081297A Pending JPS61240970A (en) 1985-04-18 1985-04-18 Suppression of malignant tumor

Country Status (1)

Country Link
JP (1) JPS61240970A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6291215B1 (en) * 1996-07-24 2001-09-18 Govind J. Kapadia Inhibitory effects on synthetic and natural colorants on carcinogenes

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6291215B1 (en) * 1996-07-24 2001-09-18 Govind J. Kapadia Inhibitory effects on synthetic and natural colorants on carcinogenes

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