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- daunorubicin liposome 柔红霉素脂质体<抗肿瘤药>
- This structure is termed a liposome. 这种结构被称为微脂粒。
- Objective:To prepare oxaprozin liposome. 目的:制备恶丙嗪脂质体。
- Objective To establish preparation of matrine liposome. 目的建立苦参碱脂质体的制备工艺。
- The top encapsulation percentage of Evans blue liposome is 25 30%. 伊文思蓝脂质体的包封率最高为 2 5 30%25。
- The application of new liposome in DDS was explored. 探讨了新型脂质体在药物传递过程中的应用。
- AIM: To study preparation of strychnine solid liposome. 目的:探讨番木鳖碱固体脂质体的最佳制备方法。
- Ganciclovir liposome was prepared by reverse evaporating method. 方法采用逆相蒸发法制备脂质体。
- Methods The cytotoxicity of daunorubicin(DNR) was assayed by MTT method. 方法 采用甲基四唑蓝法 (MTT)测定柔红霉素 (DNR)的细胞毒性 ;
- Method Silybin liposome was prepared by ethanol injection method. 方法 采用乙醇注入法制备水飞蓟宾脂质体；
- Method The cytotoxicities of daunorubicin(DNR) were assayed by MTT method. 方法以甲基四唑蓝法测定柔红霉素（DNR）的细胞毒性；
- Study on the improvement of affinity of the liposome carried medicine. 提高载药脂质体亲和性的探讨。
- Conclusions As a new drug delivery system,liposome entrapped cyclodextri. 目的介绍环糊精包合物脂质体给药系统的研究进展。
- Physical stability of dipalmitoyl cyclocytidine(DPCC) liposome was evaluated. 对环胞苷二棕榈酸酯脂质体的物理稳定性进行了评价。
- Ingredients: Pea peptide, allantoin, compound vitamin liposome, HA, etc. 主要成份：碗豆肽、尿囊素、复合维他命脂质体、透明质酸等。
- Objective: Daunorubicin (DNR) is the main remedy in chemotherapytreating acute leukemia ,but DNR has the high toxic side-effect on normalcells . 目的：柔红霉素（DNR）是急性白血病化疗的主要药物，但对正常细胞也有较高的毒副作用。
- Objective To prepare Coenzyme Q10 (CoQ10) liposome, and study its stability. 目的 制备辅酶Q10脂质体，并考察其稳定性。
- Objective To explore the effect of VEGF antisense on sensitivity of AML and CML cells to Daunorubicin (DNR). 目的 探讨血管内皮生长因子VEGF(VascularEndothelialGrowthFactor)反义核酸与柔红霉素联用 ,对AML、CML细胞药物敏感性的影响。
- The pharmacokinetics of the liposome after intravenous injection was studied. 同时考察包合物脂质体的体内药物动力学性质。
- The modified semisynthetic process development of idarubicin was achieved in eight steps starting from daunorubicin. 以柔红霉素为原料;经八步反应制得盐酸伊达比星;总收率为24.;2%25。
