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载尿激酶阴离子脂质微泡联合低频超声体外溶栓的效率研究

Thrombolysis efficiency of urokinase plasminogen activator-loaded anionic lipid microbubbles com bined with low-frequency ultrasound in vitro
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摘要 目的制备载尿激酶(uPA)阴离子脂质微泡,探讨其联合低频超声的体外溶栓效果。方法利用二硬脂酸磷酯酰胆碱(DSPC)、二棕榈酰磷酯酰甘油(DPPG)、PEG2000修饰二硬脂酸磷酯酰乙醇胺(DSPE-PEG2000)3种磷脂,通过机械振荡法制备阴离子微泡,再将微泡与uPA混合孵育,两者结合即得载药微泡,用粒径分析仪测定其粒径及分布。用FITC标记uPA,制得荧光标记的载药微泡,在荧光显微镜下观察微泡的形态及uPA与微泡的黏附情况。用Zeta电位仪分别测定载药微泡与未载药微泡的表面电荷;用十二烷基磺酸钠-聚丙烯酰胺凝胶电泳(SDS—PAGE)对载药微泡进行验证;测量加入10000、50000和100000UuPA时微泡的包封率。抽取大鼠血液制作体外血栓模型,测定载药微泡联合低频超声的体外溶栓效果。采用两样本t检验、单因素方差分析及Bonferroni法进行数据比较。结果载药微泡的平均粒径为(1.76±0.29)μm,在荧光显微镜下可以观察到FITC标记的uPA成功结合到阴离子微泡表面。载药微泡的表面电荷明显低于未载药微泡的表面电荷:(-36.64±0.21)mV与(-66.33±2.38)mV,t=21.538,P〈0.05;SDS—PAGE显示载药微泡的泳道有明显的蛋白质条带,而未载药微泡没有;当uPA加入量分别为10000、50000和100000U时,药物包封率分别为(42.01±2.02)%、(33.24±1.95)%和(33.10±1.65)%(F=22.340,P〈0.05)。生理盐水组、生理盐水±超声组、未载药微泡±超声组、载药微泡±超声组、单纯uPA组的体外溶栓效率分别为(4.09±0.80)%、(8.50±1.48)%、(14.27±1.59)%、(35.72±6.31)%、(16.87±0.46)%,载药微泡超声组最高(F=48.783,t=-8.613、-7.273、-5.942及-6.908,均P〈0.05)。结论阴离子微泡能成功搭载uPA,该微泡联合低频超声的溶栓效果良好。 Objective To prepare urokinase plasminogen activator (uPA)-loaded anionic lipid mi- crobubbles (uPA-MBs) for thrombolysis with low-frequency ultrasound in vitro. Methods Anionic micro bubbles composing of 1,2-distearoyl-sn-glycero-3-phosphocholine ( DSPC ), 1,2-dipalmitoyl-sn-glycero-3- phospho-( l'-rac-glycerol ) ( DPPG ), 1, 2-distearoyl-sn-glycero-3-phosphoethanol amine-N ( succinyl PEG2000) (DSPE-PEG2000) and perfluoropropane ( C3Fs ) were prepared by the mechanical vibration method. Then, the resulting anionic microbubbles were incubated with uPA. uPA-MBs were obtained via e lectrostatic adsorption. Bubble size and distribution were measured by particle size analyzer. FITC-labeled uPA-MBs were obtained and observed under fluorescence microscope. The surface potential of uPA-MBs and plain microbubbles (P-MBs) were detected by Zeta potential analyzer. Sodium dodecyl sulfonate-polyacryl amide gel electrophoresis (SDS-PAGE) was used for confirming the binding of uPA protein and anionic mi crobubbles. The encapsulation efficiency of uPA-MBs was determined by bicinchoninic acid (BCA) proteinassay kit under three different dosages of uPA ( 10 000, 50 000 and 100 000 U). The thrombolysis efficiency of uPA-MBs combined with low-frequency ultrasound was examined in vitro. Two-sample t test, one-way anal ysis of variance and Bonferroni test were performed to analyze the data. Results UPA-MBs were successfully obtained with the mean particle size of (1.76±0.29) μm. The surface potential of these bubbles was signifi cantly higher than that of P-MBs : (-36.64±0.21) mV vs (-66.33±2.38) mV (t = 21.538, P〈0.05). FIu orescence microscope showed a green shell of FITC-labeled uPA-MBs. The encapsulation efficiency of uPA MBs with the added dosage of 10 000 U was (42.01_±2.02)% ,which was significantly higher than those of 50 000 and 100 000 U ((33.24±1.95)% and (33.10±1.65)% respectively, F=22.340,P〈0.05). The thrombolysis efficiency b
出处 《中华核医学与分子影像杂志》 CSCD 北大核心 2014年第2期121-124,共4页 Chinese Journal of Nuclear Medicine and Molecular Imaging
基金 国家自然科学基金(81000191,81101063,61020106008) 广东省自然科学基金(S2012010008115)
关键词 血栓溶解疗法 微气泡 尿激酶 超声检查 Thrombolytic therapy Microbubbles Urokinase Ultrasonography
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参考文献10

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