Evaluation of a custom single Peltier-cooled ablation cell for elemental imaging of biological samples in laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS)

2016 ◽  
Vol 31 (4) ◽  
pp. 1030-1033 ◽  
Author(s):  
J. S. Hamilton ◽  
E. L. Gorishek ◽  
P. M. Mach ◽  
D. Sturtevant ◽  
M. L. Ladage ◽  
...  

A new single Peltier element ablation cell is described and its applicability to biological sampling discussed to evaluate its performance.

2019 ◽  
Vol 11 (16) ◽  
pp. 2129-2137 ◽  
Author(s):  
Yuqiu Ke ◽  
Jianzong Zhou ◽  
Lei Qiao ◽  
Muhui Zhang ◽  
Wei Guo ◽  
...  

A methodology for high spatial resolution quantitative elemental imaging of foraminifer by LA-ICP-MS was developed.


2014 ◽  
Vol 29 (12) ◽  
pp. 2204-2228 ◽  
Author(s):  
Dirce Pozebon ◽  
Guilherme L. Scheffler ◽  
Valderi L. Dressler ◽  
Matheus A. G. Nunes

Laser ablation inductively coupled plasma mass spectrometry has been proven to be useful in life sciences as can be observed by the increasing number of publications in this field.


2021 ◽  
Vol 21 (11) ◽  
pp. 5436-5442
Author(s):  
Wenhe Luo ◽  
Tao Li ◽  
Meng Wang ◽  
Wanqin Dai ◽  
Chunlei Jiao ◽  
...  

Quantitatively studying the biodistribution and transformation of nanomaterials is of great importance for nanotoxicological evaluation. Recently, laser ablation inductively coupled plasma mass spectrometry has been employed to distinguish nanoparticles (NPs) with their dissolved ions in biological samples. The principle of the proposal is based on a hypothesis that the intact NPs sampled by laser ablation will generate discrete sharp pulses of signals in ICP-MS measurement, being totally different from the continuous, relatively lower signals generated by ions. However, it is still a controversy whether NPs could maintain their intactness during the laser ablation. This work found a way to exactly determine the number of NPs sampled for each LA-ICP-MS measurement. It made possible to reveal the signal profile of a single NP in LA-ICP-MS analysis. The results suggest that AuNR, AgNP and TIO2 NP were broken into much smaller secondary NPs during the laser ablation, therefore generating continuous signals in the analyzer. There was a certain probability that the fragmentation of large-sized NP or multiple NPs by laser ablation was not sufficient, leaving some NPs unbroken or some secondary NPs with relatively large sizes to generate discrete pulses of signals in the analyzer. When the intactness of NPs during laser ablation cannot be assured, it is impossible to determine the attribution of mass spectrum signals. These findings compromise the reliability of distinguishing NPs from their dissolved ions by LA-ICP-MS.


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