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高倬,姜平,熊惠周,熊辛,陈光祥.斑蝥素衍生物与铂络合物抗癌活性的实验研究[J].中国中西医结合杂志,1999,(1):37-39,38
斑蝥素衍生物与铂络合物抗癌活性的实验研究
Experimental Study on Anti Cancer Effect of Cantharidine Derivatives and Platinum Complex
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DOI:
中文关键词:  斑蝥素衍生物  顺铂  抗癌活性  小鼠  S180肉瘤  H22肝癌
英文关键词:Cantharidine derivatives  cisplatinum  anti tumor effect  mice  S 180 sarcoma  H 22 hepatocarcinoma
基金项目:国家自然科学基金
作者单位
高倬 Gao Zhuo, Jiang Ping, Xiong Huizhou, et al Institute of Oncology, First Affiliated Hospital, Kunming Medical College, Kunming (650032 
姜平 Gao Zhuo, Jiang Ping, Xiong Huizhou, et al Institute of Oncology, First Affiliated Hospital, Kunming Medical College, Kunming (650032 
熊惠周 Gao Zhuo, Jiang Ping, Xiong Huizhou, et al Institute of Oncology, First Affiliated Hospital, Kunming Medical College, Kunming (650032 
熊辛 Gao Zhuo, Jiang Ping, Xiong Huizhou, et al Institute of Oncology, First Affiliated Hospital, Kunming Medical College, Kunming (650032 
陈光祥 Gao Zhuo, Jiang Ping, Xiong Huizhou, et al Institute of Oncology, First Affiliated Hospital, Kunming Medical College, Kunming (650032 
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中文摘要:
      目的:研究4种斑蝥素衍生物与铂络合物(斑铂,Dpt)对实验动物的抗癌作用,力图开发一种新型的铂族金属抗癌药。方法:以S180肉瘤、H22肝癌实体瘤及其腹水瘤小鼠为实验动物,通过腹腔或静脉给予不同剂量的4种化合物Dpt1-15、Dpt5-10、Dpt12-3、Dpt6-2,分别观察药物对小鼠瘤重及存活天数的影响,以顺铂为阳性对照,生理盐水为阴性对照。所有数据进行t检验。结果:4种斑铂(Dpt1-15、Dpt5-10、Dpt12-3、Dpt6-2)均有抗癌活性。其中Dpt5-10、Dpt1-15对小鼠S180肉瘤及H22实体瘤的抑制率与顺铂相似;Dpt5-10对H22腹水瘤小鼠生命延长率与顺铂相似;Dpt1-15的有效剂量毒性较大。结论:斑铂是有效的新型抗癌化合物,其中Dpt5-10抗癌作用较好,应进一步改进药物溶解性,并从与顺铂抗药性不同方面开发利用。
英文摘要:
      Objective: To certify the anti tumor effects of the four Cantharidine derivatives and platinum complex on transplanted tumor in mice to search for new anti tumor drugs. Methods: Complex of four Cantharidine derivatives (Dpt 1-15, Dpt 5-10, Dpt 12-3 and Dpt6-2) and platinum were given to tumor beating mice of transplanted S 180 sarcoma, H 22 solid hepatocarcinoma and ascites hepatocarcinoma through intraperitoneal or intravenous injection, and the effect of treatment on tumor weight and survival of animal were observed. Cisplatin was used as positive control and 0.9% normal saline used as negative control. All data were treated with t test. Results: All the four complex had anti tumor effect. The inhibition rate of Dpt5-10 and Dpt1-15 on S 180 sarcoma and H 22 solid hepatocarcinoma and the survival prolongation rate of Dpt5-10 on H 22 ascites hepatocarcinoma were similar to those of cisplatin. The toxicity of effective dose of Dpt1-15 was rather high. Conclusions: Cantharidine derivatives and platinum complex is new effective anti tumor drug, among them the Dpt5-10 is the most effective one. Further study for improving the solubility of drug is necessary and study the difference of cross resistance between the new complex and cisplatinum.
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