Tuning the relaxation rates of dual-mode T?/T? nanoparticle contrast agents: a study into the ideal system

Magnetic resonance imaging (MRI) is an excellent imaging modality. However the low sensitivity of the technique poses a challenge to achieving an accurate image of function at the molecular level. To overcome this, contrast agents are used; typically gadolinium based agents for T? weighted imaging, or iron oxide based agents for T? imaging. Traditionally, only one imaging mode is used per diagnosis although several physiological situations are known to interfere with the signal induced by the contrast agents in each individual imaging mode acquisition. Recently, the combination of both T? and T? imaging capabilities into a single platform has emerged as a tool to reduce uncertainties in MR image analysis. To date, contradicting reports on the effect on the contrast of the coupling of a T? and T? agent have hampered the application of these specialised probes. Herein, we present a systematic experimental study on a range of gadolinium-labelled magnetite nanoparticles envisioned to bring some light into the mechanism of interaction between T? and T? components, and advance towards the design of efficient (dual) T? and T? MRI probes. Unexpected behaviours observed in some of the constructs will be discussed. In this study, we demonstrate that the relaxivity of such multimodal probes can be rationally tuned to obtain unmatched potentials in MR imaging, exemplified by preparation of the magnetite-based nanoparticle with the highest T? relaxivity described to date

A three orders of magnitude increase in nonlinear optical response by external electric field on Cryptand[2.2.2] (C222) based alkaline earthides

A new series of alkaline earthides based on Cryptand [2.2.2] (C222) containing nine complexes is designed by carefully placing alkali metals and alkaline earth metals inside and outside the C222 complexant, respectively i.e., M1(C222)M2 (M1 = Li, Na, K; M2 = Be, Mg, Ca). The designed complexes are reasonably stable both electronically and thermodynamically, as revealed through their vertical ionization potentials (VIPs) and interaction energies, respectively. Moreover, the true alkaline earthide nature of the complexes is confirmed through NBO and FMO analyses showing the negative charges and HOMOs over the alkaline earth metals, respectively. The further validity of true earthide characteristic is represented graphically by the spectra of partial density of states (PDOS). HOMO-LUMO gaps of the compounds are also very small (from 2.23 to 2.83 eV) when compared with pure cage's (C222) H-L gap i.e., 5.63 eV. All these features award these complexes with very small values of transition energies (ΔE) ranging from 0.68 to 2.06 eV ultimately resulting in remarkably high hyperpolarizability values up to 2.7 × 105 au (for Na+(C222)Mg−). Furthermore, applying external electric field (EEF) on the complexes enhances hyperpolarizability further. A remarkable increase of 1000 folds has been seen when hyperpolarizability of K+(C222)Ca− is calculated after EEF application i.e., from 8.79 × 104 au to 2.48 × 107 au; when subjected to 0.001 au external electric field