Rapid Catalyst Capture Enables Metal-Free Parahydrogen-Based Hyperpolarized Contrast Agents

Author(s):  
Danila Barskiy ◽  
Lucia Ke ◽  
Xingyang Li ◽  
Vincent Stevenson ◽  
Nevin Widarman ◽  
...  

<p>Hyperpolarization techniques based on the use of parahydrogen provide orders of magnitude signal enhancement for magnetic resonance spectroscopy and imaging. The main drawback limiting widespread applicability of parahydrogen-based techniques in biomedicine is the presence of organometallic compounds (the polarization transfer catalysts) in solution with hyperpolarized contrast agents. These catalysts are typically complexes of platinum-group metals and their administration in vivo should be avoided.</p> <p><br></p><p>Herein, we show how extraction of a hyperpolarized compound from an organic phase to an aqueous phase combined with a rapid (less than 10 seconds) Ir-based catalyst capture by metal scavenging agents can produce pure parahydrogen-based hyperpolarized contrast agents as demonstrated by high-resolution nuclear magnetic resonance (NMR) spectroscopy and inductively coupled plasma atomic emission spectroscopy (ICP-AES). The presented methodology enables fast and efficient means of producing pure hyperpolarized aqueous solutions for biomedical and other uses.</p>

2018 ◽  
Author(s):  
Danila Barskiy ◽  
Lucia Ke ◽  
Xingyang Li ◽  
Vincent Stevenson ◽  
Nevin Widarman ◽  
...  

<p>Hyperpolarization techniques based on the use of parahydrogen provide orders of magnitude signal enhancement for magnetic resonance spectroscopy and imaging. The main drawback limiting widespread applicability of parahydrogen-based techniques in biomedicine is the presence of organometallic compounds (the polarization transfer catalysts) in solution with hyperpolarized contrast agents. These catalysts are typically complexes of platinum-group metals and their administration in vivo should be avoided.</p> <p><br></p><p>Herein, we show how extraction of a hyperpolarized compound from an organic phase to an aqueous phase combined with a rapid (less than 10 seconds) Ir-based catalyst capture by metal scavenging agents can produce pure parahydrogen-based hyperpolarized contrast agents as demonstrated by high-resolution nuclear magnetic resonance (NMR) spectroscopy and inductively coupled plasma atomic emission spectroscopy (ICP-AES). The presented methodology enables fast and efficient means of producing pure hyperpolarized aqueous solutions for biomedical and other uses.</p>


2011 ◽  
Vol 412 ◽  
pp. 449-452 ◽  
Author(s):  
Chun Li Hao

Here we studied in vivo stability and biodistribution of quantum dots. Their distribution in vivo at various time points were determined by measuring the amount of cadmium ions and selenium ions in various organs by inductively coupled plasma-atomic emission spectrometry. The amount of cadmium ions was higher in liver than in other organs at all times. The amount of cadmium ions in kidney and spleen were increased gradually in time-dependent. There are also obviously increased cadmium ions in lung and heart at all times compared to the control. However the amount of selenium ions was high in all organs except for brain before the 3rd day.


2015 ◽  
Vol 1765 ◽  
pp. 71-76
Author(s):  
Ma.G. Joaquín-Morales ◽  
G. Vargas-Gutiérrez ◽  
J.L. Rodríguez-Galicia ◽  
G.I. Vazquez-Carbajal ◽  
J. López-Cuevas

ABSTRACTIn this work, we studied the dissolution of three different refractory compositions belonging to the ternary system SiO2-CaO-MgO into two Simulated Lung Fluids (SLF). The initial powder mixtures were uniaxially pressed and then sintered at 1300-1400 °C. The sintered samples were immersed for times from 1 to 21 days into a given SLF at 37 °C. The samples were characterized by X-Ray Diffraction (XRD) and Scanning Electron Microscopy (SEM). The dissolution of Ca2+, Mg2+ and Si4+ into the SLF was quantified by Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP-AES). The in vitro studies suggested that all the considered materials had a potential to show a diminished biopersistence in vivo, due to reasons that depended on their chemical and phase composition.


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