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低强度聚焦超声靶向爆破微泡 被引量:2

Targeted microbubbles destruction with low intensity focused ultrasound
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摘要 目的探讨自制低强度聚焦超声(LIFU)体外靶向爆破微泡范围、空间分布,及在兔肝脏组织中应用LIFU辐照载紫杉醇脂质微泡(PLM)的定位控释情况。方法①采用4种不同声强(0.3、0.6、0.9、1.2 W/cm2)LIFU(频率1MHz,焦距160mm,占空比50%)分别辐照含脂质微泡的水囊,同时从不同切面观察并记录水囊内微泡爆破范围及空间分布形态;②选取新西兰大白兔10只,随机平均分为聚焦超声组(A组)和非聚焦超声组(B组);对实验兔静脉注射PLM后,对A、B组分别采用LIFU和非聚焦超声定位辐照肝脏2min;辐照后1h处死实验兔,取焦域中心及距离中心1cm、2cm、3cm处的肝脏组织,采用反相高效液相色谱法测定各肝脏组织内的紫杉醇含量。结果①LIFU体外定位爆破微泡范围局限、形状规则,爆破范围随声强增高而增大;②A组辐照中心处紫杉醇浓度最大,距离中心处越远,紫杉醇浓度越低(F=201.81,P<0.05);B组中各位置紫杉醇浓度的差异无统计学意义(F=1.36,P>0.05);辐照中心处,A组紫杉醇浓度高于B组(t=5.28,P<0.05)。结论 LIFU能够实现体内外靶向爆破微泡,其聚焦部位和微泡爆破范围可调。 Objective To explore the destruction range and space distribution of microbubbles using low power focused ultrasound (LIFU), and to observe the targeted destruction using paclitaxel-carrying liposome microbubbles (PLM) and LIFU in the liver of rabbits. Methods ①The bladder containing lipid microbubbles was irradiated with 4 different intensities of LIFU (0.3, 0.6, 0.9, 1.2 W/cm2), and the destruction ranges and spatial distribution shapes of the microbubbles in the bladder were observed and recorded from different facets. ②Ten rabbits were randomly divided into focused ultrasound group (group A, n=5) and focused ultrasound group (group B, n=5). After injection of PLM, rabbits in group A and B were irradiated respectively with LIFU and non-focused ultrasound at the liver for 2 min. The rabbits were sacrificed after 1 h, and the liver tissue at the center of the focal region and 1 cm, 2 cm, 3 cm from the center were harvested. The paclitaxel concentration was measured with reversed-phase high-performance liquid chromatography. Results ①LIFU could destruct microbubbles in a specific position, and the ranges were limited and increased with the increase of intensities. ②In group A, paclitaxel concentration at the center was the highest, and drug concentration decreased with the increase of distance from the center (F=201.81, P〈0.05). There was no significant difference of drug concentration at different distances in group B (F=1.36, P〉0.05). The paclitaxel concentration at the center in group A was higher than that in group B (t=5.28, P〈0.05). Conclusion LIFU can target microbubbles destruction, and its focused sites and microbubbles destruction ranges are adjustable.
出处 《中国介入影像与治疗学》 CSCD 2013年第3期171-174,共4页 Chinese Journal of Interventional Imaging and Therapy
基金 重庆市科技攻关项目(CSTC 2009AB5216) 国家自然科学基金面上项目(81071157)
关键词 低强度聚焦超声 靶向 爆破 定位 Low intensity focused ultrasound Targeted Destruction Located
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  • 1杨钰楠,高云华.靶向超声造影剂制备的方法学研究[J].中华超声影像学杂志,2006,15(1):65-67. 被引量:12
  • 2贺宇路,黄康强,姜飞,等.基于CdTe和CdSe量子点体外PDT灭活白血病HL60细胞实验研究.生物医学,2012,2(1): 1-5.
  • 3Klarreich E. Biologists join the dots. Nature, 2001, 413(6855): 450-452.
  • 4Carron G, Stuchinskaya T, Edwards DR, et al. Insights into the mechanism of quantum dot-sensitized singlet oxygen production for photodynamic therapy. J Phys Chem C, 2012, 116(16): 9334-9342.
  • 5Chen N, He Y, Su Y, et al. The cytotoxicity of cadmium-based quantum dots. Biomaterials, 2012, 33(5): 1238-1244.
  • 6Agarwal ML, Clay ME, Harvey EJ, et al. Photodynamic therapy induces rapid cell death by apoptosis in L5178Y mouse lymphoma cells. Cancer Res, 1991, 51(21): 5993-5996.
  • 7Maruvada SK, Hynynen K. Optical monitoring of ultrasound- induced bioeffects in glass catfish. Ultrasound Med Biol, 2004, 30( 1 ): 67-74.
  • 8Wyld L, Reed MW, Brown NJ. Differential cell death response to photodynamic therapy is dependent on dose and cell type. Br J Cancer, 2001, 8400): 1384-1386.
  • 9沈圆圆,高钟镐,Natalya Rapoport.超声微泡作为基因或药物载体的研究进展[J].药学学报,2009,44(9):961-966. 被引量:12
  • 10郑海荣,钱明.超声造影微泡:敏锐成像、定点给药与治疗[J].中国医疗器械信息,2011,17(7):1-5. 被引量:5

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