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High-performance liquid chromatographic determination of trace amounts of transition metals in parenteral solutions

Title
High-performance liquid chromatographic determination of trace amounts of transition metals in parenteral solutions
Type
Article in International Scientific Journal
Year
1998
Authors
Jun, X
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Journal
Title: The AnalystImported from Authenticus Search for Journal Publications
Vol. 123
Pages: 1283-1287
ISSN: 0003-2654
Scientific classification
FOS: Natural sciences > Chemical sciences
Other information
Authenticus ID: P-001-7QT
Abstract (EN): A high-performance liquid chromatographic (HPLC) method for the determination of trace levels of transition metals (Cu, Ph, Zn, Ni, Co, Cd and Mn) in parenteral solutions (large volume parenterals) was developed, The method involves a preconcentration step on a cation-chelating column (a Nova-Pak Cls guard column coated with Chrome Azurol S) and the separation of the different metals on a Nova-Pak C-18 column permanently coated with sodium hexadecanesulfonate, The eluent was a 100 mmol l(-1) tartrate solution of pH 3.1. Colorimetric detection (at 520 nm) after post-column reaction of the metals with 4-(2-pyridylazo)resorcinol was used. The conditions for the preconcentration and separation of the metals (composition, concentration and pH of the eluent) were studied, The repeatability of the results (n = 3) for a concentration level of about 50 mu g l(-1) was between 3.5 % (Cd) and 5.5% (Ni), The limits of quantification for a preconcentrated sample volume of 4 ml, expressed as mu g l(-1), were 0.40 (Cu), 2.1 (Pb), 0.50 (Zn), 0.33 (Ni), 0.23 (Co), 2.5 (Cd) and 2.6 (Mn), The results obtained with the developed HPLC method for ten commercial samples and seven spiked pooled samples were evaluated by comparison with those provided by electrothermal atomic absorption spectrometry (ETAAS), The developed procedure might be a rapid and inexpensive alternative to ETAAS for quality control in the pharmaceutical industry.
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 5
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