A liposomal Gd contrast agent does not cross the mouse placental barrier

• Published in: Scientific reports 2016-06, Vol.6 (1), p.27863-27863, Article 27863
• Main Authors: Shetty, Anil N., Pautler, Robia, Ghaghada, Ketan, Rendon, David, Gao, Haijun, Starosolski, Zbigniew, Bhavane, Rohan, Patel, Chandreshkumar, Annapragada, Ananth, Yallampalli, Chandrasekhar, Lee, Wesley
• Format: Article
• Language: English
• Subjects: 631/61/350/354; 692/308/575; Animals; Contrast agents; Contrast Media - administration & dosage; Echo-Planar Imaging - methods; Female; Fetus - diagnostic imaging; Fetuses; Gadolinium; Gadolinium - administration & dosage; Humanities and Social Sciences; Male; Mass spectrometry; Maternal-Fetal Exchange; Meglumine - administration & dosage; Meglumine - analogs & derivatives; Mice; Mice, Inbred BALB C; multidisciplinary; Nanoparticles; Organometallic Compounds - administration & dosage; Permeability; Placenta; Placenta - diagnostic imaging; Pregnancy; Science; Toxicity; Ultrasonic imaging; Uterus - diagnostic imaging
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/srep27863

The trans-placental permeability of liposomal Gadolinium (Gd) nanoparticle contrast agents was evaluated in a pregnant mouse model. Pregnant Balb/c mice at 16.5 (±1) days of gestation were imaged using a 3D Spoiled Gradient Echo method at 9.4 T using two contrast agents: a clinically approved Gd chelate, Multihance ® (gadobenate dimeglumine), and a novel experimental liposomal Gd agent. A Dynamic Contrast Enhancement (DCE) protocol was used to capture the dynamics of contrast entry and distribution in the placenta, and clearance from circulation. A blinded clinical radiologist evaluated both sets of images. A reference region model was used to measure the placental flow and physiological parameters; volume transfer constant (K trans ), efflux rate constant (K ep ). The Gd content of excised placentae and fetuses was measured, using inductively coupled plasma mass spectrometry (ICP-MS). MRI images of pregnant mice and ICP-MS analyses of placental and fetal tissue demonstrated undetectably low transplacental permeation of the liposomal Gd agent, while the clinical agent (Multihance) avidly permeated the placental barrier. Image interpretation and diagnostic quality was equivalent between the two contrast agents. Additional testing to determine both maternal and fetal safety of liposomal Gd is suggested.