JPH1149673A - Cancer specific medicine - Google Patents
Cancer specific medicineInfo
- Publication number
- JPH1149673A JPH1149673A JP22744997A JP22744997A JPH1149673A JP H1149673 A JPH1149673 A JP H1149673A JP 22744997 A JP22744997 A JP 22744997A JP 22744997 A JP22744997 A JP 22744997A JP H1149673 A JPH1149673 A JP H1149673A
- Authority
- JP
- Japan
- Prior art keywords
- hydroxybenzaldehyde
- medicine
- cancer specific
- specific medicine
- drug
- 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
Links
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、副作用なく使用できる
ガン特効薬に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a specific cancer drug which can be used without side effects.
【0002】[0002]
【従来の技術】従来、抗ガン剤としてベンズアルデヒド
の誘導体について、種々の検討がなされてきている。こ
れは、刺激性の強い有機溶媒であるベンズアルデヒド
は、薬剤として使用できないが、水溶性固体の誘導体に
することで、使用可能となり、その薬効を期待できるか
らである。しかし、このような誘導体は、患者体内で結
合部位が分解されなければ、薬効が発揮されない。従っ
て、非経済的なだけでなく、使用法及び投与量に限度が
あり、従って薬効にも限度があった。2. Description of the Related Art Various studies have been made on derivatives of benzaldehyde as anticancer agents. This is because benzaldehyde, which is a highly irritating organic solvent, cannot be used as a drug, but can be used by making it a water-soluble solid derivative, and its drug efficacy can be expected. However, such derivatives do not exhibit their efficacy unless the binding site is degraded in the patient. Therefore, it is not only uneconomical, but also has a limited use and dosage, and thus a limited efficacy.
【0003】[0003]
【発明が解決しようとする課題】そこで、本発明者は、
安息香酸の抗ガン性を種々研究してきたが、所望の薬効
を得るためには、投与量を非常に多く要するものであっ
た。本発明は、かかる安息香酸よりも少量の投与量で、
副作用なく、より効率のよい薬効を得ることができる、
新規なガン特効薬を提供することを課題とする。Therefore, the present inventor has proposed:
Various studies have been made on the anticancer properties of benzoic acid, but in order to obtain a desired drug effect, a very large dose was required. The present invention provides a smaller dose than such benzoic acid,
You can get more efficient medicinal effects without side effects,
It is an object to provide a new cancer specific medicine.
【0004】[0004]
【課題を解決するための手段】本発明者は、ベンズアル
デヒド化合物で、常温で固体で、比較的親水性かつ低分
子のp−ヒドロキシベンズアルデヒドに着目し、本発明
を完成した。Means for Solving the Problems The present inventors have focused on a relatively hydrophilic and low molecular weight p-hydroxybenzaldehyde which is a benzaldehyde compound which is solid at ordinary temperature and completed the present invention.
【0005】本発明のガン特効薬は、p−ヒドロキシベ
ンズアルデヒドを有効成分として含有するものであり、
経口投与及び注射いずれの場合も、p−ヒドロキシベン
ズアルデヒドを1g/日以下、例えば5〜500mg/日
程度、投与することで顕著な薬効が認められる。[0005] The cancer specific medicine of the present invention contains p-hydroxybenzaldehyde as an active ingredient.
In both cases of oral administration and injection, remarkable efficacy is observed when p-hydroxybenzaldehyde is administered at 1 g / day or less, for example, about 5 to 500 mg / day.
【0006】本発明のガン特効薬は、p−ヒドロキシベ
ンズアルデヒド単独を水溶液とした水剤又はそれをシロ
ップ剤と混和した水剤、あるいは粉末状担体を使用した
錠剤に形成されてもよいし、また、生理食塩水に溶解す
るなどして、注射液に形成されてもよい。The cancer specific drug of the present invention may be formed into a solution using p-hydroxybenzaldehyde alone as an aqueous solution, a solution prepared by mixing it with a syrup, or a tablet using a powdery carrier. It may be formed into an injection solution by, for example, dissolving in physiological saline.
【0007】[0007]
実施例1 悪性腫瘍細胞増殖に対する、安息香酸、p−ヒドロキシ
安息香酸及びp−ヒドロキシベンズアルデヒドの影響を
下記の通り試験した。 使用細胞: ×63(マウス ミエローマ細胞) 培養条件 1.1×104 cells/well/200マイクロ
リットル培地で24時間培養する(培地には、安息香
酸、p−ヒドロキシ安息香酸及びp−ヒドロキシベンズ
アルデヒドをそれぞれ25.000mM、12.500m
M、6.250mM、3.125mM、1.562mM、0.7
81mM、0.391mM及び0.195mM添加した)。
各添加物1濃度当たり3本の培養管を使用した。 2.0.5μCi/wellの 3H−チミジンを添加、更
に18時間培養し、DNA合成中の細胞に 3H−チミジ
ンを取り込ませる。 3. 3H−チミジンを取り込んだ細胞を、放射活性とし
て、液体シンチレーションカウンターで計測し、その数
をcounts per minute で表す。 得られた結果を (3本の培養管で得られた結果の平均値
と標準偏差)、表1及び図1に示す。Example 1 The effects of benzoic acid, p-hydroxybenzoic acid and p-hydroxybenzaldehyde on malignant tumor cell growth were tested as follows. Cells used: × 63 (mouse myeloma cells) Culture conditions 1.1 × 10 4 cells / well / cultured in 200 microliter medium for 24 hours (in the medium, benzoic acid, p-hydroxybenzoic acid and p-hydroxybenzaldehyde were used). 25.000 mM, 12.500 m respectively
M, 6.250 mM, 3.125 mM, 1.562 mM, 0.7
81 mM, 0.391 mM and 0.195 mM were added).
Three culture tubes were used per concentration of each additive. 2. Add 0.5 μCi / well of 3 H-thymidine, and further culture for 18 hours to incorporate 3 H-thymidine into the cells during DNA synthesis. 3. Cells that have taken up 3 H-thymidine are counted as radioactivity with a liquid scintillation counter, and the number is expressed as counts per minute. The results obtained are shown in Table 1 and FIG. 1 (average and standard deviation of the results obtained in three culture tubes).
【0008】[0008]
【表1】 [Table 1]
【0009】表1及び図1から明らかなように、p−ヒ
ドロキシベンズアルデヒドだけは、12.5mM以上で顕
著な腫瘍細胞増殖抑制が認められる。この場合、顕微鏡
で見ると細胞が死んでいることが確認できる。これに対
して、安息香酸は、25mM以下では、効果が認められ
ない。As is apparent from Table 1 and FIG. 1, only p-hydroxybenzaldehyde shows a remarkable inhibition of tumor cell proliferation at 12.5 mM or more. In this case, it can be confirmed by microscopic observation that the cells are dead. In contrast, benzoic acid has no effect at 25 mM or less.
【0010】実施例2 下記の症例により、本発明の効果を確認した。症例1 61才の男性で、55才の時に肺癌の診断を受け、安息
香酸ナトリウムの内服(2g/日より暫増して最終30
g/日)にて治療し、経過良好であったが、約6年を経
過した本年4月に、同薬内服後、嘔気を来したため、同
内服を中止したところ、6月に右胸部に違和感を生じ、
食欲不振、咳嗽、血痰の症状を発現したため、同月下
旬、p−ヒドロキシベンズアルデヒドの内服を開始し
た。薬剤の投与量は、70mg/日より暫増して最終30
0mg/日としたが、その内服を開始した2週間後には、
血痰が停止し、4週間後には、胸部違和感が改善される
など、著効が認められた。Example 2 The effects of the present invention were confirmed by the following cases. Case 1 A 61-year-old man was diagnosed with lung cancer at the age of 55, and was treated with sodium benzoate (30 g after 2 g / day).
g / day), and the course was good. However, in April of this year, about 6 years later, the patient had nausea after taking the drug. Cause discomfort,
Due to anorexia, cough, and bloody sputum, she started taking p-hydroxybenzaldehyde later in the month. The dose of the drug was increased from 70 mg / day to 30
0 mg / day, but 2 weeks after starting the oral administration,
Blood sputum stopped, and 4 weeks later, remarkable effects were observed, such as improvement in chest discomfort.
【0011】症例2 38才の女性で、32才の時に右季肋下部痛を発症し、
胆嚢超音波検査で胆嚢新生物が確認され、自覚症状と併
せて、胆嚢癌と診断されたため、安息香酸ナトリウムの
内服(1g/日より暫増して最終15g/日)にて治療
し、1年後には超音波検査所見は正常化したが、自覚症
状は軽度ながら持続したため、本年4月に、内服薬をp
−ヒドロキシベンズアルデヒドに変更したところ(薬剤
投与量:70mg/日より暫増して最終300mg/日)、
1カ月後には、右季肋下部痛は軽快し、3カ月後に消失
した。 Case 2 A 38-year-old woman who developed right subcostal pain at the age of 32,
A gallbladder ultrasonography confirmed a gallbladder neoplasm, and the patient was diagnosed with gallbladder cancer in addition to the subjective symptoms. Later, ultrasonographic findings were normalized, but subjective symptoms persisted, albeit mildly.
-Changed to hydroxybenzaldehyde (drug dose: 70 mg / day, increased to 300 mg / day)
One month later, right subcostal pain subsided and disappeared three months later.
【0012】[0012]
【発明の効果】本発明の薬剤の投与により、副作用な
く、悪性腫瘍の増殖を防止でき、癌性疾患が軽快するの
みならず、最終的には完治する。By the administration of the drug of the present invention, the growth of malignant tumors can be prevented without side effects, and not only the cancerous disease is relieved, but also it is finally cured.
【図1】図1は、悪性腫瘍細胞増殖に対する、安息香
酸、p−ヒドロキシ安息香酸及びp−ヒドロキシベンズ
アルデヒドの影響を試験した結果を示すグラフである。FIG. 1 is a graph showing the results of testing the effects of benzoic acid, p-hydroxybenzoic acid and p-hydroxybenzaldehyde on malignant tumor cell growth.
Claims (1)
成分として含有するガン特効薬。1. A cancer specific medicine comprising p-hydroxybenzaldehyde as an active ingredient.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22744997A JPH1149673A (en) | 1997-08-08 | 1997-08-08 | Cancer specific medicine |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22744997A JPH1149673A (en) | 1997-08-08 | 1997-08-08 | Cancer specific medicine |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH1149673A true JPH1149673A (en) | 1999-02-23 |
Family
ID=16861054
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP22744997A Pending JPH1149673A (en) | 1997-08-08 | 1997-08-08 | Cancer specific medicine |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH1149673A (en) |
-
1997
- 1997-08-08 JP JP22744997A patent/JPH1149673A/en active Pending
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