Safety and Efficacy of A High Performance Graphene-Based Magnetic Resonance Imaging Contrast Agent for Renal Abnormalities
| Autor: | Shruti Kanakia, Slah Khan, William Moore, Balaji Sitharaman, Stephen Lee, Jimmy Toussaint, Sayan Mullick Chowdhury, Sandeep K. Mallipattu, Praveen Kukarni, Kenneth R. Shroyer |
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| Jazyk: | angličtina |
| Rok vydání: | 2016 |
| Předmět: |
medicine.medical_specialty
Gadolinium chemistry.chemical_element 02 engineering and technology Article 030218 nuclear medicine & medical imaging 03 medical and health sciences 0302 clinical medicine medicine.artery medicine Polycystic kidney disease Renal artery Kidney medicine.diagnostic_test business.industry Gadofosveset Magnetic resonance imaging General Medicine 021001 nanoscience & nanotechnology medicine.disease medicine.anatomical_structure chemistry Nephrogenic systemic fibrosis Radiology 0210 nano-technology Nuclear medicine business medicine.drug Kidney disease |
| Popis: | The etiology of renal insufficiency includes primary (e.g polycystic kidney disease) or secondary (e.g. contrast media, diabetes) causes. The regulatory restrictions placed on the use of contrast agents (CAs) for non-invasive imaging modalities such as X-ray computed tomography (CT) and magnetic resonance imaging (MRI) affects the clinical management of these patients. With the goal to develop a next-generation CA for unfettered use for renal MRI, here we report, in a rodent model of chronic kidney disease, the preclinical safety and efficacy of a novel nanoparticle CA comprising of manganese (Mn2+) ions intercalated graphene coated with dextran (hereafter called Mangradex). Nephrectomized rats received single or 5 times/week repeat (2 or 4 weeks) intravenous (IV) injections of Mangradex at two potential (low = 5 mg/kg, and high = 50 mg/kg) therapeutic doses. Histopathology results indicate that Mangradex does not elicit nephrogenic systemic fibrosis (NSF)-like indicators or questionable effects on vital organs of rodents. MRI at 7 Tesla magnetic field was performed on these rats immediately after IV injections of Mangradex at one potential therapeutic dose (25 mg/kg, [Mn2+] = 60 nmoles/kg) for 90 minutes. The results indicated significant (>100%) and sustained contrast enhancement in the kidney and renal artery at these low paramagnetic ion (Mn2+) concentration; 2 orders of magnitude lower than the paramagnetic ion concentration in a typical clinical dose of long circulating Gd3+-based MRI CA gadofosveset trisodium. The results open avenues for further development of Mangradex as a MRI CA to diagnose and monitor abnormalities in renal anatomy and vasculature. |
| Databáze: | OpenAIRE |
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