Pigs treated with ultrasound and intravenous perfluorocarbon microbubbles (PESDA) had significantly

greater improvements in ST segments over a 30-minute treatment period when compared with pigs treated with ultrasound alone or with control animals. Moreover, there was a significantly smaller myocardial contrast defect size after treatment with ultrasound and PESDA [15]. Recently, nano-CT was used to demonstrate complete reversal of microcirculatory impairment in a rodent reperfusion model following treatment with rt-PA, ultrasound and microbubbles [16]. The mechanism of the microcirculatory selleck kinase inhibitor effect of ultrasound and microbubbles may involve improvement of blood flow to risk tissue via collaterals and changes in the microenvironment of damaged tissue, like decreased cell damaging factors, e.g. glutamate or enhanced enzyme activity of endothelial nitric oxide [17]. Further work is necessary to elucidate the exact mechanisms of salvaging of tissue-at-risk by ultrasound-mediated microbubble thrombolysis. The blood–brain barrier is a significant obstacle for delivery of both small molecules and macromolecular agents. Indeed, potential therapeutic substances, which cannot be applied in the presence

of an intact BBB are neuropeptides, proteins and chemotherapeutic agents. Likewise, large-molecules such as monoclonal antibodies, recombinant proteins, antisense, or gene therapeutics do not cross the BBB. There is a good deal of evidence showing that ultrasound can be used to permeate blood-tissue barriers. Large molecules

and genes can cross ABT-199 solubility dmso the plasma membrane of cultured cells after application of acoustic energy [18]. Indeed, electron microscopy has revealed ultrasound-induced membrane porosity in both in vitro and in vivo experiments [19]. High-intensity focused ultrasound has been shown to allow selective and non-destructive disruption Silibinin of the BBB in rats [20]. If microbubbles are introduced to the blood stream prior to focused US exposure, the BBB can be transiently opened at the ultrasound focus without acute neuronal damage [21]. Thus, the introduction of cavitation nuclei into the blood stream can confine the ultrasound effects to the vasculature and reduce the intensity needed to produce BBB opening ( Fig. 4). This can diminish the risk of tissue damage and make the technique more easily applied through the intact skull. In most studies, the confirmation of BBB disruption has been obtained with MR contrast imaging at targeted locations [21], [22] and [23] or with post mortem histology [20] and [24]. Targeted delivery of antibodies to the brain has been accomplished with focused ultrasound. Dopamine D(4) receptor-targeting antibody was injected intravenously and shown to recognize antigen in the murine brain following disruption of the BBB with ultrasound [22].