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出 处:《中国现代医药杂志》2009年第2期10-12,共3页Modern Medicine Journal of China
基 金:辽宁省教育厅资助项目(项目编号:2004F068)
摘 要:目的采用薏米仁油研制紫杉醇微乳,评价其抗肿瘤作用。方法采用聚乙二醇-二硬脂酰基磷脂酰乙醇胺(PEG-DSPE)和薏米仁油,制备紫杉醇微乳,并测定其Zeta电位和粒度分布。评价紫杉醇微乳对小鼠的急性毒性及其抗肿瘤作用。结果紫杉醇微乳粒径为112.6±2.5nm,Zeta电位为-32.4±3.5mV。在本实验条件下,紫杉醇微乳显著降低了紫杉醇的急性毒性,紫杉醇和薏米仁油具有显著的协同抗肿瘤作用(P<0.01)。结论我们制备的紫杉醇微乳有可能成为一种较好的抗肿瘤药物。Objective To prepare coix seed oil microemulsion to carry paclitaxel and evaluate its acute toxicity and anticaneer effect. Methods The paclitaxel microemulsion was a semi-transparent solution containing paclitaxel, coxi seed oil and PEG-DSPE (polylene glycol derivative of distearoyl phosphatidyl ethanolamine, mean molecular weight of PEG: 2000). The Zeta potential and particle size distribution were determined using a laser light scattering instrument. The acute toxicity of the pacli- taxel microemulsion was studied using mice and its anticancer effect was evaluated using Lewis lung and M5076 tumor models. Results The average diameter of the paclitaxel microemulsion was 112.6±2.5nm and its Zeta potential was -32.4±3.5mV while its paclitaxel concentration was 0.29mg/mL. Compared with paclitaxe and coxi seed oill, the paclitaxel microemulsions showed lower acute toxicity and synergysitic anticancer effect. Conclusion The paclitaxel microemulsion may become a better anti- cancer drug than paclitaxel and coxi seed oil.
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