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作 者:杨健[1] 康娟[2] 曾妍[3] 吴小翎[1] 梅浙川[1] 王志刚[4]
机构地区:[1]重庆医科大学附属第二医院消化内科,重庆400010 [2]重庆医科大学附属第二医院肝病中心,重庆400010 [3]重庆医科大学附属第二医院精神心理科,重庆400010 [4]重庆医科大学超声影像学研究所,重庆400010
出 处:《中国生物制品学杂志》2012年第7期873-876,共4页Chinese Journal of Biologicals
基 金:国家自然科学基金委员会科学部主任基金(81041064);国家自然科学基金重点项目(81130025)
摘 要:目的制备一种携带肝癌DR5单克隆抗体(DR5mAb)的载多烯紫杉醇靶向脂质超声微泡(Docetaxel-loaded lipidmicrobubbles,DLLM),并检测其体外寻靶能力。方法采用机械振荡法制备载多烯紫杉醇的DLLM,并制备生物素化的肝癌DR5mAb,通过生物素-亲和素连接方法,将DR5mAb连接于载多烯紫杉醇的DLLM表面,制备DR5-DLLM。检测DR5-DLLM的粒径、浓度、Zeta电位、包封率、载药量、稳定性及其体外寻靶能力。结果 DR5-DLLM的平均粒径为1 232 nm,Zeta电位为-9.86 mV,平均浓度为3.1×109个/ml,微泡的包封率为73.5%,平均载药量为25.3%。60Co射线灭菌前后以及4℃、-20℃保存14 d,微泡的形态、包封率、载药量未见明显改变。靶向微泡组的HepG2细胞周围可见DR5-DLLM微泡紧密结合,而非靶向微泡DLLM组未见特异性微泡结合。结论成功制备了携带肝癌DR5mAb的载多烯紫杉醇靶向脂质超声微泡,该微泡能够与HepG2细胞牢固结合,有望成为一种新型、高效、可用于超声分子显像的肝癌靶向药物载体。Objective To prepare the docetaxel-loaded lipid microbubbles (DLLM) coupled with DR5mAb against liver cancer, and determine its targeting ability in vitro. Methods DLLM were prepared by mechanical oscillation, based on which DR5- targeted docetaxel-loaded lipid microbubbles (DR5-DLLM) were prepared by attaching biotinylated DR5mAb to the surface of DLLM via avidin-biotin interaction, and determined for size, concentration, Zeta potential, entrapment efficiency, drug-load, stability and targeting ability in vitro. Results The mean size, Zeta potential, mean concentration, entrapment efficiency and mean drug-load of DR5,DLLM were 1 232 rim, -9. 86 mV, 3. 1 ×109 microbubbles/ml, 73. 5% and 25. 3%, respectively. No obvious change was observed in appearance, entrapment efficiency or drug-load of DRS-DLLM before and after sterilization with ℃o and after storage at 4 and -20℃ for 14 d. DR5-DLLM were tightly conjugated with HepG2 cells, while DLLM showed no specific conjugation with the cells. Conclusion DR5-DLLM was successfully prepared, which were conjugated with HepG2 cells tightly, and might be used as a novel and highly effective liver cancer-targeted drug carrier for uhrasonund molecular imaging.
分 类 号:R318[医药卫生—生物医学工程]
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