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dc.creatorKatsimpoulas, M.en
dc.creatorZacharoulis, D.en
dc.creatorRountas, C.en
dc.creatorDimitriou, C.en
dc.creatorMantziaras, G.en
dc.creatorKostomitsopoulos, N.en
dc.creatorHabib, N.en
dc.creatorKostakis, A.en
dc.date.accessioned2015-11-23T10:34:14Z
dc.date.available2015-11-23T10:34:14Z
dc.date.issued2011
dc.identifier10.3109/08941939.2010.519815
dc.identifier.issn8941939
dc.identifier.urihttp://hdl.handle.net/11615/29261
dc.description.abstractIntroduction: The feasibility and outcome of large volume injection of gene solution in a segment of a liver lobe, without backflow, were studied in a porcine model, using a custom-designed balloon catheter. Method: Eight anesthetized pigs underwent successful injection of 200 ml of gene solution at a rate of 20 ml/s via a minimally invasive technique without backflow. A custom-made balloon catheter was introduced under fluoroscopy guidance into the right lateral liver lobe via the right external jugular vein. The vein of the liver lobe was occluded with the balloon catheter and contrast material was injected to check if total occlusion was achieved. Since there was no backflow an angiographic pump injected the solution. The catheter was left in place for 10 min. Then contrast material was injected to check whether the vein remained occluded. Results: All animals tolerated the procedure without obvious adverse effects. Ultrasound scan showed no gross changes within liver three days following the infusion. A transient rise in platelet count was observed which returned to normal after 13 days and remained stable; all other biochemistry values were normal. Conclusions: Injecting large volume of gene solution in a liver lobe segment using this minimally invasive technique in a porcine model is possible, making the development of a successful gene transfer protocol in humans feasible. © 2011 Informa Healthcare USA, Inc.en
dc.source.urihttp://www.scopus.com/inward/record.url?eid=2-s2.0-79551522263&partnerID=40&md5=4044a20f3c9fc962d31524ffeda7f212
dc.subjectfluoroscopyen
dc.subjectHydrodynamic gene therapyen
dc.subjectinfusionen
dc.subjectliveren
dc.subjectminimal invasive techniqueen
dc.subjectporcine modelen
dc.subjectalanine aminotransferaseen
dc.subjectalbuminen
dc.subjectalkaline phosphataseen
dc.subjectamylaseen
dc.subjectaspartate aminotransferaseen
dc.subjectcontrast mediumen
dc.subjectcreatine kinaseen
dc.subjectcreatinineen
dc.subjectgamma glutamyltransferaseen
dc.subjecthigh density lipoproteinen
dc.subjectlactate dehydrogenaseen
dc.subjectlow density lipoproteinen
dc.subjectrecombinant thrombopoietinen
dc.subjecttriacylglycerolen
dc.subjecturic aciden
dc.subjectalanine aminotransferase blood levelen
dc.subjectalbumin blood levelen
dc.subjectalkaline phosphatase blood levelen
dc.subjectamylase blood levelen
dc.subjectanimal experimenten
dc.subjectanimal modelen
dc.subjectanimal tissueen
dc.subjectarticleen
dc.subjectaspartate aminotransferase blood levelen
dc.subjectballoon catheteren
dc.subjectblood samplingen
dc.subjectcontrolled studyen
dc.subjectcreatine kinase blood levelen
dc.subjectcreatinine blood levelen
dc.subjectexternal jugular veinen
dc.subjectgamma glutamyl transferase blood levelen
dc.subjecthistopathologyen
dc.subjecthydrodynamics based transfectionen
dc.subjectlactate dehydrogenase blood levelen
dc.subjectlipoprotein blood levelen
dc.subjectliver biopsyen
dc.subjectliver sinusoiden
dc.subjectliver vein obstructionen
dc.subjectminimally invasive procedureen
dc.subjectnonhumanen
dc.subjectpriority journalen
dc.subjectswineen
dc.subjectthrombocyte counten
dc.subjecttriacylglycerol blood levelen
dc.subjecturic acid blood levelen
dc.subjectvein dilatationen
dc.subjectAnimalsen
dc.subjectCathetersen
dc.subjectGene Transfer Techniquesen
dc.subjectInjectionsen
dc.subjectModels, Animalen
dc.titleMinimal invasive technique for gene delivery in porcine liver lobe segmenten
dc.typejournalArticleen


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