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机构地区:[1]华中科技大学同济医学院附属同济医院药学部,武汉430030
出 处:《医药导报》2008年第6期623-624,共2页Herald of Medicine
摘 要:目的研究STEM-X的急性毒性和体内对肿瘤的抑制作用。方法采用急性毒性实验:选取昆明种小鼠30只,随机分为3组,每组10只。禁食24h后一次性给药。给药后连续观察14d,详细记录小鼠的死亡数目、死亡时间及主要毒性反应。抗肿瘤实验:建立S180荷瘤小鼠模型40只,随机分为4组,每组10只,即低剂量药物组(浓缩液10mL.kg-1),高剂量药物组浓缩液(20mL.kg-1),氟尿嘧啶(5-Fu)阳性对照组(20mg·kg-1),空白对照组。连续灌胃给药10d,处死动物,称重,完整剥离瘤块并称瘤重。计算肿瘤抑制率。结果急性毒性实验的3个剂量组均未出现小鼠死亡,无明显异常。STEM-X浓缩液的半数致死量(LD50)>50mL.kg-1。抗肿瘤活性实验中,高、低剂量组、阳性对照组的瘤重和空白组比较,差异有显著性。高剂量组的肿瘤抑制率和阳性对照组比较,差异无显著性。低剂量组和阳性对照组比较,差异有显著性。结论STEM-X在正常剂量下,安全、毒副作用极低。对S180肉瘤有明显抑制作用。Objective To study the acute toxicities and anti-tumor activity of STEM-X in vivo. Methods The acute toxicity of STEM-X was assayed as followed : thirty mice were averagely divided into three groups. After 24 hours fasting, STEM- X was given to the mice. The numbers and time of death mice, and primary toxic symptom were observed. The anti-tumor activity of STEM-X was research as followed: forty mice were randomly divided to four groups ( each group with 10 mice) : low dose group ( concentrated STEM-X 10 mL·kg^-1 ), high dose group ( concentrated STEM-X 20 mL·kg^-1 ), 5-Fu control group (20 mg·kg^-1) and blank control group and transplanted with the sarcocarcinoma 180 according to a standard method. The STEM-X solution was given to mice for 10 days by i. g route. Results No dead mouse was observed in three STEM-X groups in acute toxicity assay. The LD50 of concentrated STEM-X was over than 50 mL·kg^-1. For the anti-tumor activity of STEM-X, the tumor weight in high dose group and 5-Fu control group is obviously different from that in control group. The inhibitory rate has no marked difference between high dose group and 5-Fu control group, but is higher than that in low dose group. Conclusion In the normal dose, STEM-X is a safe agent with lowly toxicity and shows an obvious anti-tumor activity to sarcocarcinoma 180.
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