Abstract

Targeted drug delivery by magnetic resonance (MR)-guided ultrasound (US)-induced blood-brain barrier (BBB) disruption has been developed using focused US in combination with encapsulated gas-filled microbubbles (MBs). However, the occurrence of intracerebral hemorrhage may hamper the usefulness of US-induced BBB opening, which is effectively indicated by gadolinium (Gd)-based contrast enhancement in T 1 -weighted MR scans. This paper reports the dual function of paramagnetic particles of perfluorocarbon-filled albumin-gadolinium-diethylene-triamine penta-acetic acid (Gd-DTPA) MBs for BBB opening and for distinguishing between focused-US-induced BBB opening and intracerebral hemorrhage in MR contrast images. Perfluorocarbon-filled albumin-(Gd-DTPA) MBs were prepared with a mean diameter of 2320 nm and concentration of 2.903×109 MBs/ml using albumin-(Gd-DTPA) and by sonication with perfluorocarbon (C 3 F 8 ) gas. The albumin-(Gd-DTPA) MBs were then centrifuged and the procedure was repeated until the free Gd3+ ions were eliminated (which were detected by xylenol orange sodium salt solution). In vitro US imaging experiments showed that albumin-(Gd-DTPA) MBs can significantly enhance the US contrast in T 1 -, T 2 -, and T 2 ∗-weighted MR images. The r 1 and r 2 relaxivities for Gd-DTPA were 7.69 and 21.35 s−1 mM−1, respectively, indicating that the MBs represent a positive contrast agent in T 1 -weighted images. In vivo MR imaging experiments on 18 rats showed that focused US combined with albumin-(Gd-DTPA) MBs can be used to both induce and detect disruption of the BBB. After disrupting the BBB, the leakage of albumin-(Gd-DTPA) MBs shells can be detected for distinguishing between focused-US-induced disruption of the BBB and intracerebral hemorrhage in T 1 -weighted images. The results indicate that albumin-(Gd-DTPA) MBs have potential as a US/MR dual-modality contrast agent for BBB opening and differentiating focused-US-induced BBB opening from intracerebral hemorrhage.

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