Premium
Multifunctional Nanoprobe for MRI/Optical Dual‐Modality Imaging and Radical Scavenging
Author(s) -
Zhen Mingming,
Zheng Junpeng,
Wang Yifan,
Shu Chunying,
Gao Fabao,
Zou Jing,
Pyykkö Ilmari,
Wang Chunru
Publication year - 2013
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201301601
Subject(s) - in vivo , nanoprobe , mri contrast agent , magnetic resonance imaging , gadolinium , chemistry , nuclear magnetic resonance , inner ear , hydroxyl radical , biodistribution , perilymph , fluorescence , radical , biophysics , materials science , nanoparticle , in vitro , nanotechnology , medicine , biochemistry , radiology , quantum mechanics , physics , microbiology and biotechnology , organic chemistry , biology
The development of novel nanomaterials for the diagnosis and/or treatment of human diseases has become an important issue. In this work, a multifunctional theranostic agent was designed by covalently binding hydroxyl‐ and amino‐bearing C 60 derivatives (C 60 O ∼10 (OH) ∼16 (NH 2 ) ∼6 (NO 2 ) ∼6 ⋅ 24 H 2 O) with gadolinium diethylenetriaminepentaacetic acid (Gd‐DTPA) to yield C 60 O ∼10 (OH) ∼16 (NH 2 ) ∼6 (NO 2 ) ∼6 ⋅ 24 H 2 O/(Gd‐DTPA) 3 ( DF 1 Gd 3 ). The obtained DF 1 Gd 3 shows more than fourfold contrast improvement over commercial Gd‐DTPA along with multiwavelength fluorescent emission for dual‐modality diagnosis. An inner‐ear magnetic resonance imaging (MRI) study was designed as a model of biological barriers, including the blood/brain barrier (BBB) for DF 1 Gd 3 to investigate its in vivo behavior. This revealed that the fabricated contrast agent dramatically increases the local contrast but can not cross the middle ear/inner ear barrier and endolymph/perilymph barrier in the inner ear, and thus it is also BBB‐prohibited in normal individuals. In vivo biodistribution studies suggested that 1) DF 1 Gd 3 could circulate in vessels for a relatively long time and is mainly eliminated through liver and kidney, 2) DF 1 Gd 3 may potentially function as a liver‐specific MRI contrast agent. Interestingly, DF 1 Gd 3 also shows an excellent quenching effect on hydroxyl radicals, as revealed by the DMPO spin trap/ESR method. The combination of enhanced MRI/FL imaging and local treatment of lesions is unique to DF 1 Gd 3 and potentiates the medical paradigm of “detect and treat/prevent” in combating human diseases related to reactive oxygen.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom