Thrombolysis with tissue-plasminogen activator: Results with a high-dose transthrombus technique

1994 ◽  
Vol 19 (3) ◽  
pp. 503-508 ◽  
Author(s):  
Anthony S. Ward ◽  
Shahriyour K. Andaz ◽  
Sean Bygrave
2012 ◽  
Vol 17 (3) ◽  
pp. 434-440 ◽  
Author(s):  
Obead Yaseen ◽  
Maher M. El‐Masri ◽  
Wasim S. El Nekidy ◽  
Derrick Soong ◽  
Mohammed Ibrahim ◽  
...  

2007 ◽  
Vol 5 ◽  
pp. P-T-386-P-T-386
Author(s):  
J.D.A. Carneiro ◽  
E.A. D'Amico ◽  
L.A. Matsumoto ◽  
M.P. Garanito ◽  
M.V. Santos ◽  
...  

2020 ◽  
Vol 21 (8) ◽  
pp. 2690 ◽  
Author(s):  
Huai-An Chen ◽  
Yunn-Hwa Ma ◽  
Tzu-Yuan Hsu ◽  
Jyh-Ping Chen

Recombinant tissue plasminogen activator (rtPA) is the only thrombolytic agent that has been approved by the FDA for treatment of ischemic stroke. However, a high dose intravenous infusion is required to maintain effective drug concentration, owing to the short half-life of the thrombolytic drug, whereas a momentous limitation is the risk of bleeding. We envision a dual targeted strategy for rtPA delivery will be feasible to minimize the required dose of rtPA for treatment. For this purpose, rtPA and fibrin-avid peptide were co-immobilized to poly(lactic-co-glycolic acid) (PLGA) magnetic nanoparticles (PMNP) to prepare peptide/rtPA conjugated PMNPs (pPMNP-rtPA). During preparation, PMNP was first surface modified with avidin, which could interact with biotin. This is followed by binding PMNP-avidin with biotin-PEG-rtPA (or biotin-PEG-peptide), which was prepared beforehand by binding rtPA (or peptide) to biotin-PEG-maleimide while using click chemistry between maleimide and the single –SH group in rtPA (or peptide). The physicochemical property characterization indicated the successful preparation of the magnetic nanoparticles with full retention of rtPA fibrinolysis activity, while biological response studies underlined the high biocompatibility of all magnetic nanoparticles from cytotoxicity and hemolysis assays in vitro. The magnetic guidance and fibrin binding effects were also confirmed, which led to a higher thrombolysis rate in vitro using PMNP-rtPA or pPMNP-rtPA when compared to free rtPA after static or dynamic incubation with blood clots. Using pressure-dependent clot lysis model in a flow system, dual targeted pPMNP-rtPA could reduce the clot lysis time for reperfusion by 40% when compared to free rtPA at the same drug dosage. From in vivo targeted thrombolysis in a rat embolic model, pPMNP-rtPA was used at 20% of free rtPA dosage to restore the iliac blood flow in vascular thrombus that was created by injecting a blood clot to the hind limb area.


2001 ◽  
Vol 7 (3) ◽  
pp. 214-218 ◽  
Author(s):  
Michio Sakai ◽  
Kohtaro Asayama ◽  
Hiroyuki Otabe ◽  
Takeo Kohri ◽  
Akira Shirahata

To determine whether the fibrinolytic system is related to the occurrence of cardiac complication in Kawasaki disease, we measured tissue plasminogen activator, plasminogen activator inhibitor-1, and related factors in the plasma of children with Kawasaki disease. Patients (mean age, 1.8 years) were classified into patients with cardiac complication (n = 9) and no complication (n = 14) groups echocardiographically. They underwent single, high-dose, intravenous γ-globulin infusion therapy. Blood was drawn just before and the day after the single high-dose intravenous γ-globulin infusion therapy (acute phase), and at early and late convalescent phases. Leukocytosis was normalized immediately after the single, high-dose, intravenous γ-globulin infusion therapy. C-reactive protein and fibrinogen were increased in the acute phase and normalized by convalescent phases. D-dimer fraction of fibrin degradation products changed in a similar manner. Tissue plasminogen activator and plasminogen activator inhibitor-1 were increased in acute phase. The tissue plasminogen activator/plasminogen activator inhibitor-1 ratio was lower in the complication group than in the no complication group throughout the observation period (0.095 versus 0.208 after single, high-dose, intravenous γ-globulin infusion therapy, p = 0.006; 0.094 versus 0.183 at late convalescent phase, p = 0.024). A low tissue plasminogen activator/plasminogen activator inhibitor-1 ratio can predict the propensity for cardiac complication, and can help the physician to decide whether additional therapies are necessary in acute phase Kawasaki disease.


2002 ◽  
Vol 25 (1) ◽  
pp. 36-41 ◽  
Author(s):  
Dimitrios K. Tsetis ◽  
George E. Kochiadakis ◽  
Adam A. Hatzidakis ◽  
Emannuel I. Skalidis ◽  
Evangelia G. Chryssou ◽  
...  

2011 ◽  
Vol 51 (11) ◽  
pp. 1095-1098 ◽  
Author(s):  
Olugbenga Akingbola ◽  
Dinesh Singh ◽  
Rodney Steiner ◽  
Edwin Frieberg ◽  
Matei Petrescu

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