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酒石酸长春瑞滨长循环热敏脂质体的荷瘤小鼠药效学研究
引用本文:王幸平,王志媛,龚伟,梅兴国.酒石酸长春瑞滨长循环热敏脂质体的荷瘤小鼠药效学研究[J].军事医学科学院院刊,2012,36(5):362-364.
作者姓名:王幸平  王志媛  龚伟  梅兴国
作者单位:1. 武汉工程大学化工与制药学院,武汉,430073;军事医学科学院毒物药物研究所,北京,100850
2. 军事医学科学院毒物药物研究所,北京,100850
基金项目:国家“十二五”重大专项资助项目(2012ZX09301003-001)
摘    要:目的评价酒石酸长春瑞滨长循环热敏脂质体(V-LCTL)对荷瘤小鼠的药效和不良反应。方法建立荷Lewis肺癌小鼠皮下肿瘤模型,静脉注射药品,比较V-LCTL与酒石酸长春瑞滨注射液(V-I)、酒石酸长春瑞滨长循环脂质体(V-LCL)的抗肿瘤作用,包括肿瘤生长曲线,抑瘤率,考察给药频率及量效关系。结果各治疗组均有抑瘤作用。相同剂量下V-LCTL的抑瘤效果明显强于V-LCL和V-I。单次给药和多次给药对V-LCTL和V-I的抑瘤率无显著影响。单次给药时不良反应明显。V-LCTL的抑瘤效果呈剂量依赖性(低、中、高剂量组抑瘤率分别为54.6%,72.1%,81.5%)。结论 V-LCTL具有比V-I和V-LCL更好的抑瘤效果,多次给药不良反应小,且V-LCTL的抑瘤效果具有剂量依赖关系。

关 键 词:酒石酸长春瑞滨  长循环热敏脂质体  药效学  抗肿瘤药

Pharmacodynamics of vinorelbine tartrate long-circulating thermosensitive liposomes in mice bearing Lewis lung carcinoma cells
WANG Xing-ping , WANG Zhi-yuan , GONG Wei , MEI Xing-guo.Pharmacodynamics of vinorelbine tartrate long-circulating thermosensitive liposomes in mice bearing Lewis lung carcinoma cells[J].Bulletin of the Academy of Military Medical Sciences,2012,36(5):362-364.
Authors:WANG Xing-ping  WANG Zhi-yuan  GONG Wei  MEI Xing-guo
Affiliation:WANG Xing-ping , WANG Zhi-yuan GONG Wei , MEI Xmg-guo ( 1. School of Chemical Engineering and Pharmacy, Wuhan Institute of Technology, Wuhan 430073, China; 2 Pharmacology and Toxicology, Academy of Military Medical Sciences, Beijing 100850, China)
Abstract:Objective To investigate the tumor inhibition effect and toxicity of vinorelbine tartrate long-circulating ther- mosensitive liposome (V-LCTL) in mice bearing Lewis lung carcinoma cells. Methods A model of tumor-bearing mice was established by subcutaneous injection of Lewis lung cancer cells. The drag solution was intravenously administered to compare the anti-tumor effect of V-LCTL ,vinorelbine tartrate long-circulating liposome (V-LCL) and vinorelbine tartrate injection (V-I). The tumor growth curve was obtained and the tumor inhibitory rate was calculated. The frequency of ad- ministration and dose-effect relat:~onship of V-LCTL were systematically investigated. Results Each administered group showed inhibition effect on the growth of tumor. The inhibition effect of V-LCTL was better than that of V-LCL group and V- I group, respectively. Two methods of administration showed no significant difference in the inhibition rate of V-LCTL and V-I, but the toxicity and side effect of mice treated by single administration of 30 mg/kg were increased. There was a dose- effect relationship in the treatment of V-LCTL(54.6%, 72. 1%, and 81.5% in its low, medium and higher dose sub- groups). Conclusion The inhibitory efficiency of V-LCTL is better than that of V-I and V-LCL. Three-time administration of V-LCTL decreases the toxicity and side effect. Th~ tumor inhibitory effect of V-LCTL is positively correlated with the dose.
Keywords:vinorelbine tartrate  long-circulating thermosensitive liposome  pharmacodynamics  antineoplastic agents
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