Ma Yunn-Hwa, Wu Siao-Yun, Wu Tony, Chang Yeu-Jhy, Hua Mu-Yi, Chen Jyh-Ping
Department of Physiology and Pharmacology, College of Medicine, Chang Gung University, 259 Wen-Hwa 1st Road, Kuei-Shan, Tao-Yuan 33302, Taiwan, ROC.
Biomaterials. 2009 Jul;30(19):3343-51. doi: 10.1016/j.biomaterials.2009.02.034. Epub 2009 Mar 18.
We investigated the feasibility and efficacy of target thrombolysis with recombinant tissue plasminogen activator (rtPA) covalently bound to magnetic nanoparticle (MNP) and retained to the target site in vivo by an external magnet. Polyacrylic acid-coated magnetite (PAA-MNP, 246 nm) was synthesized and characterized; rtPA was immobilized to PAA-MNP through carbodiimide-mediated amide bond formation. The enzyme activities of the bound rtPA, as measured by a chromogenic substrate assay and (125)I-fibrinolysis assay, were 87+/-1% and 86+/-3% of that of free rtPA. Under guidance with the magnet moving back and forth along the iliac artery, the thrombolytic activity of PAA-MNP-rtPA with rtPA equivalent to 0.2mg/kg was determined by flowmetry in a rat embolic model. Intra-arterial administration of PAA-MNP-rtPA restored the iliac blood flow within 75 min to 82% of that before the clot lodging, whereas equivalent amount of PAA-MNP or free rtPA exerted no improvement on hemodynamics. At the end of 2-h period, PAA-MNP-rtPA did not alter levels of hemoglobin, hematocrit, or blood cell count. In conclusion, immobilization of rtPA to PAA-MNP with covalent binding resulted in a stable rtPA preparation and predictable amount of rtPA around the target site under magnetic guidance; this approach may achieve reproducible and effective target thrombolysis with <20% of a regular dose of rtPA.
我们研究了将重组组织型纤溶酶原激活剂(rtPA)与磁性纳米颗粒(MNP)共价结合,并通过外部磁体在体内将其保留在靶位点进行靶向溶栓的可行性和疗效。合成并表征了聚丙烯酸包覆的磁铁矿(PAA-MNP,246 nm);通过碳二亚胺介导的酰胺键形成将rtPA固定在PAA-MNP上。通过发色底物测定法和(125)I纤维蛋白溶解测定法测量,结合的rtPA的酶活性分别为游离rtPA的87±1%和86±3%。在磁体沿髂动脉来回移动的引导下,在大鼠栓塞模型中通过血流测定法测定了rtPA等效于0.2mg/kg的PAA-MNP-rtPA的溶栓活性。动脉内给予PAA-MNP-rtPA可在75分钟内将髂血流量恢复至血栓形成前的82%,而等量的PAA-MNP或游离rtPA对血流动力学无改善作用。在2小时结束时,PAA-MNP-rtPA未改变血红蛋白、血细胞比容或血细胞计数水平。总之,通过共价结合将rtPA固定在PAA-MNP上可得到稳定的rtPA制剂,并在磁引导下在靶位点周围获得可预测量的rtPA;这种方法可以用常规剂量rtPA的不到20%实现可重复且有效的靶向溶栓。