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Mass fraction assignment of amino acids in acidic aqueous solution (CCQM-K78.a)

Authors :
Marie-Pier Thibeault
Ralf D. Josephs
Vincent Delatour
André Henrion
Gökhan Bilsel
Maria Fernandes-Whaley
Kelly Wy Chan
Steven Westwood
Inchul Yang
Panagiota Giannikopoulou
Gustavo Martos
Jintana Nammoonnoy
Hongmei Li
Simay Gunduz
Hong Liu
Adeline Daireaux
Ting Huang
Ji-Seon Jeong
Ahmet C. Gören
O Sokolova
Taichi Yamazaki
Juris Meija
Sabine Biesenbruch
Rüdiger Ohlendorf
W H Lam
Wai-hong Fung
Elias Kakoulides
Wei Zhang
Charalampos Alexopoulos
Byung Joo Kim
Robert Wielgosz
M. Belyakov
Dewei Song
Tiphaine Choteau
Qinde Liu
Sharon Yong
Mark S. Lowenthal
Can Quan
Jeremy E. Melanson
Ha-Jeong Kwon
İlker Ün
S. Kharitonov
Déirée Prevoo-Franzsen
A. Krylov
E. Lopushanskaya
GÖREN, AHMET CEYHAN
Publication Year :
2019
Publisher :
IOP, 2019.

Abstract

The CCQM-K78.a comparison was coordinated by the BIPM on behalf of the CCQM Organic Analysis Working Group for NMIs and DIs which provide measurement services in organic analysis under the CIPM MRA. The key comparison forms part of the OAWG 10-year strategic plan of comparisons. CCQM-K78.a underpins the demonstration of capabilities for value assignment of high polarity calibration solutions. The model system selected was amino acids in aqueous solution. Participants were required to assign the mass fractions, expressed in μg/g, of phenylalanine (Phe), leucine (Leu), isoleucine (Ile) and proline (Pro) present in solution in 0.01 N hydrochloric acid. The content and analytical challenges of the selected analytes are representative of those for typical calibration solutions for polar organic analytes in aqueous solution. Participation in CCQM-K78, a benchmarked measurement capability for assigning the mass fraction content of polar organic compounds (pKow > -2) present at a mass fraction range between 50 μg/g and 500 μg/g in an aqueous solution. It also tested capabilities for the quantitative assignment of isomeric polar compounds of similar chromatographic retention time properties. A satisfactory level of agreement of the results was obtained between participants and with gravimetric values for amino acid content. In the cases where the agreement was not satisfactory, the participants were able to identify a technical cause for the inconsistency. The comparison demonstrated the trueness and precision of double IDMS-based methods as a primary measurement procedure for the quantification of polar analytes in aqueous solution when an isotopically labelled version of the analyte is available as the internal standard. It also demonstrated that amino acid quantification using pre- or post-column derivatization with UV or FLD detection can provide results with comparable levels of performance. In this case, where the purity of the primary calibrators had been assigned with a relative standard uncertainty below 0.2%, results consistent with the KCRV within a relative expanded uncertainty in the range 1% - 2% could be realized and levels of 2%-4% were routinely achieved. KEY WORDS FOR SEARCH Amino acid quantification, leucine, isoleucine, proline, phenylalanine, calibration solution, standard solution, IDMS, primary measurement procedure, polar solution, peptide quantification Main text To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by the CCQM, according to the provisions of the CIPM Mutual Recognition Arrangement (CIPM MRA).

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....debad9aab68690a381154a2d4bad1a13