scholarly journals Analysis of Inorganic Antimicrobial Agents in Antimicrobial Products: Evaluation of a Screening Method by X-ray Fluorescence Spectrometry and the Measurement of Metals by Inductively Coupled Plasma Atomic Emission Spectroscopy

2007 ◽  
Vol 53 (4) ◽  
pp. 423-429 ◽  
Author(s):  
Harunobu Nakashima ◽  
Tomoko Ooshima
Keyword(s):  
Inductively Coupled Plasma ◽  
Emission Spectroscopy ◽  
Antimicrobial Agents ◽  
Screening Method ◽  
Atomic Emission ◽  
Atomic Emission Spectroscopy ◽  
Fluorescence Spectrometry ◽  
Plasma Atomic Emission ◽  
X Ray ◽  
Inductively Coupled

scholarly journals Arsenoplatin-Ferritin Nanocage: Structure and Cytotoxicity

2021 ◽  
Vol 22 (4) ◽  
pp. 1874
Author(s):  
Giarita Ferraro ◽  
Alessandro Pratesi ◽  
Damiano Cirri ◽  
Paola Imbimbo ◽  
Daria Maria Monti ◽  
...  
Keyword(s):  
Biological Activity ◽  
Diffraction Data ◽  
Inductively Coupled Plasma ◽  
Emission Spectroscopy ◽  
Atomic Emission ◽  
Side Chain ◽  
Plasma Atomic Emission ◽  
Average Amount ◽  
X Ray ◽  
Inductively Coupled

Arsenoplatin-1 (AP-1), the prototype of a novel class of metallodrugs containing a PtAs(OH)2 core, was encapsulated within the apoferritin (AFt) nanocage. UV-Vis absorption spectroscopy and inductively coupled plasma-atomic emission spectroscopy measurements confirmed metallodrug encapsulation and allowed us to determine the average amount of AP-1 trapped inside the cage. The X-ray structure of AP-1-encapsulated AFt was solved at 1.50 Å. Diffraction data revealed that an AP-1 fragment coordinates the side chain of a His residue. The biological activity of AP-1-loaded AFt was comparatively tested on a few representative cancer and non-cancer cell lines. Even though the presence of the cage reduces the overall cytotoxicity of AP-1, it improves its selectivity towards cancer cells.

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