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作 者:王士勇[1] 杨振君[2] 于环[1] 杜微丽[1] 刘飒[1] 张哲[1] 张远[1] 邓英杰[3]
机构地区:[1]中国医科大学附属第四医院生物治疗科,辽宁省沈阳市110032 [2]中国医科大学附属第二医院信息科,辽宁省沈阳市110004 [3]沈阳药科大学药学院,辽宁省沈阳市110016
出 处:《世界华人消化杂志》2008年第10期1059-1063,共5页World Chinese Journal of Digestology
基 金:教育部归国博士启动课题资助项目;No.2004-527~~
摘 要:目的:评价β-榄香烯脂质体注射剂实验性治疗消化系肿瘤的作用.方法:用细胞培养方法测定β-榄香烯脂质体及其乳剂对5株人消化系癌细胞株和1株人胚肺成纤维细胞的半数抑制浓度(IC50);建立肝癌H22昆明鼠实体瘤和腹水模型,尾静脉注射高(80mg/kg)、中(40mg/kg)、低(20mg/kg)剂量β-榄香烯脂质体,测定其在动物体内的抑瘤率和生命延长率,注射葡萄糖和40mg/kgβ-榄香烯乳剂注射液作为阴性和阳性对照.结果:β-榄香烯脂质体及乳剂对5株人消化系癌细胞株的IC50分别为34.1±4.5mg/L-51.4±4.2mg/L和41.5±4.7mg/L-82.3±8.8mg/L,前者约为后者的1/2.在实体瘤鼠,高、中、低剂量β-榄香烯脂质体和乳剂的抑瘤率分别为47.4%-50.8%、38.2%-45.0%、23.2%-28.2%和21.8%-43.0%,平均瘤质量明显低于葡萄糖组(t>4.09,P<0.05).在腹水瘤鼠,脂质体和乳剂较葡萄糖组生存期延长51.3%-153.0%(t>7.92,P<0.05),中、高剂量脂质体组较乳剂组明显延长(t>4.64,P<0.05).β-榄香烯脂质体的刺激症状、尾静脉炎明显低于乳剂组.结论:β-榄香烯脂质体较乳剂有明显抗肿瘤作用和较低的副作用.AIM: To investigate the inhibitory effects of β-elemene liposome on digestive tumors in vitro and in vivo.METHODS: Five digestive tumor cell lines and one human lung embryonic fibroblast cell line were used to test the IC50 values of β-elemene liposome in vitro by cell culture. H22-bearing Kunming mice were treated with injection of β-elemene liposome through the tail vein at 20, 40 or 80 mg/kg to establish solid and ascites tumor models. Mice treated with glucose or elemene emulsion served as negative or positive controls, respectively. The anti-tumor effects, sur- vival and side effects of β-elemene liposome observed and compared between different groups. RESULTS: IC50 values of β-elemene liposome and elemene emulsion for the five digestive tumor cell lines were from 34.1 ± 4.5 to 51.4 ± 4.2 mg/L and 41.5 ± 4.7 mg/L to 82.3 ± 8.8 mg/L, respectively, and IC50 of the former was half of the later. In solid tumor models, the inhibitory rates of 80-, 40- or 20-mg/kg β-elemene liposome and elemene emulsion were 47.4%-50.8%, 38.2%45.0%, 23.2%-28.2% and 21.8%-43.0%, respectively, and the average tumor weights were lower than those in the glucose control group (t 〉 4.09, P 〈 0.05). In ascites tumor models, the survival time was 51.3%-153.0% longer in β-elemene liposome or emulsion group than that in the glucose control group (t 〉 7.92, P 〈 0.05). Furthermore, the survival time in 80- or 40-rag/ kg β-elemene liposome group was longer than that in elemene emulsion group (t 〉 4.64, P 〈 0.05). The stimulating symptoms and phlebitis of tail vein generated by injection of β-elemene liposome were slighter than those by elemene emulsion. CONCLUSION: β-elemene liposome has greater ability to inhibit tumor growth and relieve side effects than elemene emulsion.
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