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目的探讨长循环(BR38)微泡和血管内皮生长因子2(VEGFR2)靶向(BR55)微泡临床运用的可行性并评价这两种微泡对不同侵袭性乳腺癌小鼠模型的鉴别能力。方法研究BR38和BR55在健康小鼠体内的循环特性。实验通过
Objective To investigate the feasibility of clinical application of BR38 microvesicles and vascular endothelial growth factor 2 (VEGFR2) targeting (BR55) microbubbles and to evaluate their ability to differentiate into different invasive breast cancer mouse models. Methods Cyclic properties of BR38 and BR55 in healthy mice were studied. Experiment passed