Premium
Gd 3+ ‐Ion‐Doped Upconversion Nanoprobes: Relaxivity Mechanism Probing and Sensitivity Optimization
Author(s) -
Chen Feng,
Bu Wenbo,
Zhang Shengjian,
Liu Jianan,
Fan Wenpei,
Zhou Liangping,
Peng Weijun,
Shi Jianlin
Publication year - 2013
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.201201469
Subject(s) - nanoprobe , materials science , gadolinium , nanoparticle , doping , lanthanide , nuclear magnetic resonance , surface modification , paramagnetism , nanomaterials , nanotechnology , photon upconversion , analytical chemistry (journal) , ion , optoelectronics , chemistry , physics , organic chemistry , metallurgy , quantum mechanics , chromatography
Paramagnetic gadolinium (Gd‐III)‐ion‐doped upconversion nanoparticles (UCNPs) are attractive optical‐magnetic molecule imaging probes and are a highly promising nanoplatform for future theranostic nanomedicine design. However, the related relaxivity mechanism of this contrast agent is still not well understood and no significant breakthrough in relaxivity enhancement has been achieved. Here, the origin and optimization of both the longitudinal ( r 1 ) and transverse ( r 2 ) relaxivities are investigated using models of water soluble core@shell structured Gd 3+ ‐doped UCNPs. The longitudinal relaxivity enhancement of the nanoprobe is demonstrated to be co‐contributed by inner‐and outer‐sphere mechanisms for ligand‐free probes, and mainly by outer‐sphere mechanism for silica‐shielded probes. The origin of the transverse relaxivity is inferred to be mainly from an outer‐sphere mechanism regardless of surface‐coating, but with the r 2 values highly related to the surface‐state. Key factors that influence the observed relaxivities and r 2 / r 1 ratios are investigated in detail and found to be dependent on the thickness of the NaGdF 4 interlayer and the related surface modifications. A two orders of magnitude (105‐fold) enhancement in r 1 relaxivity and 18‐fold smaller r 2 / r 1 ratio compared to the first reported values are achieved, providing a new perspective for magnetic resonance (MR) sensitivity optimization and multimodality biological imaging using Gd 3+ ‐doped UCNPs.
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