Highly sensitive and simple liquid chromatography assay with ion-pairing extraction and visible detection for quantification of gold from nanoparticles.

Talanta

Université de Lorraine, CITHEFOR EA 3452, "Cibles Thérapeutiques, Formulation et Expertise Préclinique du Médicament", Faculty of Pharmacy, Nancy, France. Electronic address:

Published: March 2018

AI Article Synopsis

  • A new HPLC method was developed to measure gold in nanoparticles (AuNP) using visible detection after oxidizing the nanoparticles.
  • The process involved forming an ion-pair with tetrachloroaurate and Rhodamine B dye, which was then extracted using an organic solvent for analysis.
  • The method was validated for accuracy and precision, with a detection range of 0.1 to 30.0µM, and was used to assess the quality of AuNP and check for gold leakage from polyelectrolyte films under stress.

Article Abstract

A simple isocratic HPLC method using visible detection was developed and validated for the quantification of gold in nanoparticles (AuNP). After a first step of oxidation of nanoparticles, an ion-pair between tetrachloroaurate anion and the cationic dye Rhodamine B was formed and extracted from the aqueous media with the help of an organic solvent. The corresponding Rhodamine B was finally quantified by reversed phase liquid chromatography using a Nucleosil C18 (150mm × 4.6mm, 3µm) column and with a mobile phase containing acetonitrile and 0.1% trifluoroacetic acid aqueous solution (25/75, V/V) at 1.0mLminand at a wavelength of 555nm. The method was validated using methodology described by the International Conference on Harmonization and was shown to be specific, precise (RSD < 11%), accurate and linear in the range of 0.1 - 30.0µM with a lower limit of quantification (LLOQ) of 0.1µM. This method was in a first time applied to AuNP quality control after their synthesis. In a second time, the absence of gold leakage (either as AuNP or gold salt form) from nanostructured multilayered polyelectrolyte films under shear stress was assessed.

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Source
http://dx.doi.org/10.1016/j.talanta.2017.11.016DOI Listing

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