A fast and accurate method for the determination of precious alloys caratage by Laser Induced Plasma Spectroscopy

2001 ◽  
Vol 13 (3) ◽  
pp. 373-377 ◽  
Author(s):  
M. Corsi ◽  
G. Cristoforetti ◽  
V. Palleschi ◽  
A. Salvetti ◽  
E. Tognoni
2018 ◽  
Vol 33 (11) ◽  
pp. 1917-1924 ◽  
Author(s):  
Violeta Lazic ◽  
Montserrat Filella ◽  
Andrew Turner

In this study, the feasibility of measuring the Sb content in different plastic materials by laser induced plasma spectroscopy (LIBS) is explored.


Author(s):  
Alessandro Ciucci ◽  
Vincenzo Palleschi ◽  
Simone Rastelli ◽  
Azenio Salvetti ◽  
Elisabetta Tognoni ◽  
...  

2000 ◽  
Vol 413 (1-2) ◽  
pp. 187-195 ◽  
Author(s):  
Q Sun ◽  
M Tran ◽  
B.W Smith ◽  
J.D Winefordner

2005 ◽  
Vol 54 (7) ◽  
pp. 637-641 ◽  
Author(s):  
Takahiro YASUDA ◽  
Mikio KUZUYA

2001 ◽  
Vol 16 (6) ◽  
pp. 628-632 ◽  
Author(s):  
Michael Tran ◽  
Qing Sun ◽  
Benjamin W. Smith ◽  
James D. Winefordner

2001 ◽  
Vol 55 (6) ◽  
pp. 739-744 ◽  
Author(s):  
Michael Tran ◽  
Qing Sun ◽  
Benjamin W. Smith ◽  
James D. Winefordner

2019 ◽  
Vol 15 (6) ◽  
pp. 568-573
Author(s):  
Soheil Sedaghat ◽  
Ommoleila Molavi ◽  
Akram Faridi ◽  
Ali Shayanfar ◽  
Mohammad Reza Rashidi

Background: Signal transducer and activator of transcription 3 (STAT3), an oncogenic protein found constitutively active in many types of human malignancies, is considered to be a promising target for cancer therapy. Objective: In this study for the first time, a simple and accurate method has been developed for the determination of a STAT3 dimerization inhibitor called stattic in aqueous and plasma samples. Methods: A reverse-phase high-performance liquid chromatography (RP-HPLC) composed of C18 column as stationary phase, and the mixture of acetonitrile (60%) and water (40%) as mobile phase with a UV detection at 215 nm were applied for quantification of stattic. The developed method was validated by Food and Drug Administration (FDA) guideline. Results: The method provided a linear range between 1-40 and 2.5-40 µg mL-1 for aqueous and plasma samples, respectively, with a correlation coefficient of 0.999. The accuracy (as recovery) of the developed method was found to be between 95-105% for aqueous medium and 85-115% for plasma samples. The precision (as relative standard deviation) for aqueous and plasma samples was less than 6% and 15%, respectively. The sensitivity of the developed method based on FDA guideline was 1 µg mL-1 for aqueous and 2.5 µg mL-1 for plasma samples. Conclusion: These results show that the established method is a fast and accurate quantification for stattic in aqueous and plasma samples.


Sign in / Sign up

Export Citation Format

Share Document