TY - JOUR
T1 - Biocompatibility of ferritin-based nanoparticles as targeted MRI contrast agents
AU - Charlton, Jennifer R.
AU - Pearl, Valeria M.
AU - Denotti, Anna R.
AU - Lee, Jonathan B.
AU - Swaminathan, Sundararaman
AU - Scindia, Yogesh M.
AU - Charlton, Nathan P.
AU - Baldelomar, Edwin J.
AU - Beeman, Scott C.
AU - Bennett, Kevin M.
N1 - Publisher Copyright:
© 2015 Elsevier Inc.
PY - 2016/8/1
Y1 - 2016/8/1
N2 - Ferritin is a naturally occurring iron storage protein, proposed as a clinically relevant nanoparticle with applications as a diagnostic and therapeutic agent. Cationic ferritin is a targeted, injectable contrast agent to measure kidney microstructure with MRI. Here, the toxicity of horse spleen ferritin is assessed as a step to clinical translation. Adult male mice received cationic, native and high dose cationic ferritin (CF, NF, or HDCF) or saline and were monitored for 3 weeks. Transient weight loss occurred in the ferritin groups with no difference in renal function parameters. Ferritin-injected mice demonstrated a lower serum iron 3 weeks after administration. In ferritin-injected animals pre-treated with hydrocortisone, there were no structural or weight differences in the kidneys, liver, lung, heart, or spleen. This study demonstrates a lack of significant detrimental effects of horse-derived ferritin-based nanoparticles at MRI-detectable doses, allowing further exploration of these agents in basic research and clinical diagnostics.
AB - Ferritin is a naturally occurring iron storage protein, proposed as a clinically relevant nanoparticle with applications as a diagnostic and therapeutic agent. Cationic ferritin is a targeted, injectable contrast agent to measure kidney microstructure with MRI. Here, the toxicity of horse spleen ferritin is assessed as a step to clinical translation. Adult male mice received cationic, native and high dose cationic ferritin (CF, NF, or HDCF) or saline and were monitored for 3 weeks. Transient weight loss occurred in the ferritin groups with no difference in renal function parameters. Ferritin-injected mice demonstrated a lower serum iron 3 weeks after administration. In ferritin-injected animals pre-treated with hydrocortisone, there were no structural or weight differences in the kidneys, liver, lung, heart, or spleen. This study demonstrates a lack of significant detrimental effects of horse-derived ferritin-based nanoparticles at MRI-detectable doses, allowing further exploration of these agents in basic research and clinical diagnostics.
KW - Cationic ferritin
KW - Ferritin
KW - Kidney
KW - Magnetic resonance imaging
KW - Nephron number
KW - Toxicity
UR - http://www.scopus.com/inward/record.url?scp=84966711057&partnerID=8YFLogxK
U2 - 10.1016/j.nano.2016.03.007
DO - 10.1016/j.nano.2016.03.007
M3 - Article
C2 - 27071333
AN - SCOPUS:84966711057
SN - 1549-9634
VL - 12
SP - 1735
EP - 1745
JO - Nanomedicine: Nanotechnology, Biology, and Medicine
JF - Nanomedicine: Nanotechnology, Biology, and Medicine
IS - 6
ER -