Abstract
A uridine-quantum dot conjugate, a contrast agent for multimodal imaging, was synthesized. Its T(1) relaxivity was 655 and 571.2 mM(-1) s(-1) per particle at 36 °C in phosphate buffered saline at 60 and 200 MHz, respectively. In vitro multimodal images confirmed its uptake by RAW 264.7 cells.
This journal is © The Royal Society of Chemistry 2012
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Cell Line, Tumor
-
Contrast Media* / chemical synthesis
-
Contrast Media* / chemistry
-
Flow Cytometry
-
Gadolinium / chemistry
-
Magnetic Resonance Imaging
-
Mice
-
Microscopy, Fluorescence
-
Molecular Structure
-
Neoplasms / diagnosis*
-
Organometallic Compounds* / chemical synthesis
-
Organometallic Compounds* / chemistry
-
Quantum Dots*
-
Uridine / chemistry*
Substances
-
Contrast Media
-
Organometallic Compounds
-
Gadolinium
-
Uridine