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- METHODS: The study was performed by a randomized multicenter way. The trial group was administered with paclitaxel liposome (at a dose of 135mg/m+2) and cisplatin for 2 cycles (1 cycle=every 3 weeks). 方法:采用多中心随机入组的方法进行研究,试验组给紫杉醇脂质体每次剂量135mg/m2,联合使用顺铂,每3周为1周期,共2周期。
- Paclitaxel liposome 紫杉醇脂质体
- 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。
- 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；
- Paclitaxel is considered one of the most promising antitumor druggery. 摘要紫杉醇是当今最有效的抗癌药物之一。
- Objective To investigate the antiangiogenesis ability of Paclitaxel. 目的探讨紫杉醇的抗血管生成作用。
- Conclusion: Paclitaxel and mitoxantone may be first-selected chemotherapeutics. 结论:推荐紫杉醇与米托蒽醌作为有效的化疗药物。
- AIM: To develop and characterize lyophilized paclitaxel nanoemulsions. 目的:制备紫杉醇冻干纳米乳,研究其体外理化性质。
- 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 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。
- 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。
