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作 者:周洋[1] 郑元义[1] 沈红霞[1] 余进洪[1] 孙阳[1] 王志刚[1]
机构地区:[1]重庆医科大学附属第二医院超声影像学研究所,重庆市400010
出 处:《中国超声医学杂志》2012年第3期193-196,共4页Chinese Journal of Ultrasound in Medicine
基 金:国家重点基础研究发展计划(973计划)(No.2011CB707900);国家自然科学基金(No.81071158,No.81130025)
摘 要:目的观察经静脉注射脂质包裹液态氟碳纳米粒对高强度聚焦超声(HIFU)治疗肿瘤的增效作用,并探讨其增效机制。方法首先制备脂质包裹的液态氟碳纳米粒。然后选取建模成功后3周的荷VX2肝癌移植瘤的新西兰大白兔36只,随机等分为3组,用HIFU对兔肝肿瘤进行辐照。A组为对照组,即辐照前经兔耳缘静脉注射生理盐水,B组在辐照前注射液态氟碳纳米粒,30 s后用HIFU辐照,C组在辐照前24 h注射液态氟碳纳米粒。观察各组辐照区域视频灰度变化及肿瘤凝固性坏死情况。结果 B组和C组均见到辐照区域明显灰度变化,A组仅部分见到灰度变化,B、C组辐照前后灰度变化面积和变化值与A组有显著差异(P<0.05);3组兔肝肿瘤内均观察到明显的凝固性坏死,B、C组坏死的范围明显大于A组(P<0.05)。结论经静脉注射脂质包裹的液态氟碳纳米粒能够增强HIFU的疗效,此效应可能与纳米粒改变组织声环境、增加聚焦超声的空化作用有关,但具体作用机制有待进一步探讨。Objective To observe the increased efficacy of HIFU treating tumors using lipids encapsulated liquid fluorocarbon nanoparticles by intravenous injection and explore the synergistic mechanism. Methods Firstly, the lip- ids coated liquid fluorocarbon nanoparticles were prepared. Thirty-six New Zealand white rabbits borne VX2 tumors in liver for 3 weeks were randomly divided into three groups and underwent focused ultrasound irradiation. A group (the control group), was irradiated 30 s after the injection of saline by the rabbit ear vein, B group was irradiated 30 s after the injection of liquid fluorocarbon nanoparticles, C group was irradiated 24 hours after the injection of liquid fluoro- carbon nanoparticles. The gray changes of irradiation areas and coagulation necrosis in tumors were observed. Results Obvious gray change can be seen in all of group B and C, but partly in group A. There were significant differences in gray change values and squares among group B, C and A(P~ 0.05). Coagulative necrosis with round shape and clear boundary was observed in every group immediately after irradiation, and the range of necrosis in group B and C was much larger than that in group A (P^0.05). Conclusions The lipids encapsulated liquid fluorocarbon nanoparticles by intravenous injection can increase the therapeutic efficacy of HIFU. The effect may be due to the nan- oparticles changed the sound environment of tissue, and increased the cavitation of focused ultrasound, but the exact mechanism needs further investigation.
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