Study of a novel ultrasonically triggered drug vehicle with magnetic resonance properties

• Published in: Acta biomaterialia 2011-02, Vol.7 (2), p.578-584
• Main Authors: Liu, Tse-Ying, Huang, Hsin-Hui, Chen, Yen-Ju, Chen, Yu-Jen
• Format: Article
• Language: English
• Subjects: coatings; Drug Carriers - chemistry; drugs; Durapatite - chemistry; encapsulation; Hydroxyapatite; iron oxides; Liposome; Liposomes - ultrastructure; Magnetic Resonance Spectroscopy; MR-guided drug vehicle; nanoparticles; Sonication; SPIO; Ultrasonically triggered release; ultrasonics; Ultrasonics - methods; X-Ray Diffraction
• ISSN: 1742-7061; 1878-7568
• DOI: 10.1016/j.actbio.2010.09.018

We developed a novel ultrasonically triggered drug vehicle with magnetic resonance (MR) properties by encapsulating superparamagnetic iron oxide (SPIO) nanoparticles in hydroxyapatite (HA)-coated liposomes. The effects of HA coating on the background leakage, ultrasound response and MR signal were investigated. HA coating of liposomes significantly reduced the background leakage of liposome. It also enhanced their sensitivity to ultrasound regardless of HA thickness or ultrasound frequency, even under sonication conditions of high frequency (1 and 3 MHz) and low power density (0.2–0.4 W cm −2) used for diagnosis. However, it was found that the ultrasonically triggered vehicle could exhibit T 2 contrast in MR images by encapsulating SPIO. However, HA coating reduced the r 2 value of SPIO encapsulated in liposomes, but had no significant effect on the r 2 ∗ value, implying that MR images of HA-coated liposomes encapsulating SPIO could be probed by the T 2 ∗ signal. Most importantly, the r 2 ∗ – r 2 value of HA-coated liposomes encapsulating SPIO decreased after sonication, suggesting that the proposed vehicle could be used not only as a MR-guided drug vehicle capable of ultrasonically triggered release but also as a MR reporter to probe ultrasonic triggering.