Biochemistry & Pharmacology: Open Access
Open Access
ISSN: 2167-0501
ISSN: 2167-0501
James A O��?Hanlon and Melissa A Denecke
The University of Manchester, UK
Posters & Accepted Abstracts: Biochem Pharmacol (Los Angel)
Ethylene diamine tetra acetic acid (EDTA) is found in decontamination agents used throughout the nuclear industry,
therefore, is often found in repository consigned wastes. The Low-Level Waste Repository (LLWR) is the UK��?s Centre
for the disposal of low-level radioactive waste. LLWR maintain strict limits of acceptance on EDTA because, when present
in the waste, the ligand potentially solubilizes otherwise surface-bound radionuclides, making them more susceptible to
groundwater transportation into the wider geo/biosphere. A significant quantity of EDTA and radioactively-contaminated
ion-exchange resin sourced from decontamination operations during nuclear submarine maintenance is in radioactive decaystorage
in UK Naval dockyards. Before the material can be accepted for disposal at LLWR, it must be thermally conditioned to
remove EDTA; and then analyzed to confirm EDTA destruction. A simple method has been developed for the extraction and
quantification of EDTA from an incinerated ion-exchange resin matrix using reversed-phase ion-pair high-performance liquid
chromatography (HPLC) with ultraviolet detection. EDTA is extracted directly into an aqueous Fe (III) solution to undergo
complexation, separated on a monolithic silica column (Chromolith�?® HighResolution, Merck) and detected at 258 nm. The
linearity of the response is high (R2; 0.9999) and the limit of detection/quantification for the method has been determined
to be 0.23/0.62 mg/kg, respectively. From the standard addition method on four samples of incinerated resin containing 6%
EDTA prior to treatment, high recoveries were obtained (mean value; 78.3�?±3.34 %), with reasonably high intra- and inter-day
repeatability (RSD; 1.42��?12.4%). Absorption peaks at similar retention times were observed and, as they do not occur for the
resin incinerated without EDTA, are attributed to ferric complexes of EDTA thermal degradation products. Interfering peaks
were resolved by applying a least squares fit to the data.
Recent Publications
1. Wang G and Tomasella FP (2016) Ion-pairing HPLC methods to determine EDTA and DTPA in small molecule and
biological pharmaceutical formulations. Journal of Pharmaceutical Analysis 6(3):150-156.
2. Nowack B, Kari F G, Hilger S U and Sigg L (1996) Determination of dissolved and adsorbed EDTA species in water and
sediments by HPLC. Analytical Chemistry 68(3):561-6.
3. Kemmei T, Kodama S, Yamamoto A, Inoue Y and Hayakawa K (2013) Determination of ethylene diamine tetra acetic
acid in foods by reversed-phase high-performance liquid chromatography. Food Chemistry 138(2-3):866-869.
4. Kemmei T, Kodama S, Fujishima H, Yamamoto A, Inoue Y and Hayakawa K (2012) Determination of
ethylenediaminetetraacetic acid in sea water by solid-phase extraction and high-performance liquid chromatography.
Analytica Chimica Acta. 709:54-58.
5. Chiumiento F, D��?Aloise A, Marchegiani F and Melai V (2015) Determination of EDTA in feed and premix formulations
by HPLC-DAD. Food Chemistry 175:452-456.
James A O’Hanlon is pursuing his PhD at University of Manchester, School of Chemistry, in the group of Prof Melissa A Denecke. He has an Industrial Cooperative Awards in Science and Technology, studentship specially funded by the EPSRC (Engineering and Physical Sciences Research Council) to promote mutually beneficial research collaboration between academic and partner organizations.
E-mail: james.ohanlon@manchester.ac.uk