scholarly journals Development of primary reference measurement procedure and reference materials for mass fraction of crude fat (oil content) in oilseeds and other products on their base

2021 ◽  
Vol 16 (3) ◽  
pp. 37-51
Author(s):  
A. S. Sergeeva ◽  
E. G. Parfenova ◽  
O. S. Golynets
2018 ◽  
Vol 64 (9) ◽  
pp. 1296-1307 ◽  
Author(s):  
Alexandra S Whale ◽  
Gerwyn M Jones ◽  
Jernej Pavšič ◽  
Tanja Dreo ◽  
Nicholas Redshaw ◽  
...  

Abstract BACKGROUND Genetic testing of tumor tissue and circulating cell-free DNA for somatic variants guides patient treatment of many cancers. Such measurements will be fundamental in the future support of precision medicine. However, there are currently no primary reference measurement procedures available for nucleic acid quantification that would support translation of tests for circulating tumor DNA into routine use. METHODS We assessed the accuracy of digital PCR (dPCR) for copy number quantification of a frequently occurring single-nucleotide variant in colorectal cancer (KRAS c.35G>A, p.Gly12Asp, from hereon termed G12D) by evaluating potential sources of uncertainty that influence dPCR measurement. RESULTS Concentration values for samples of KRAS G12D and wild-type plasmid templates varied by <1.2-fold when measured using 5 different assays with varying detection chemistry (hydrolysis, scorpion probes, and intercalating dyes) and <1.3-fold with 4 commercial dPCR platforms. Measurement trueness of a selected dPCR assay and platform was validated by comparison with an orthogonal method (inductively coupled plasma mass spectrometry). The candidate dPCR reference measurement procedure showed linear quantification over a wide range of copies per reaction and high repeatability and interlaboratory reproducibility (CV, 2%–8% and 5%–10%, respectively). CONCLUSIONS This work validates dPCR as an SI-traceable reference measurement procedure based on enumeration and demonstrates how it can be applied for assignment of copy number concentration and fractional abundance values to DNA reference materials in an aqueous solution. High-accuracy measurements using dPCR will support the implementation and traceable standardization of molecular diagnostic procedures needed for advancements in precision medicine.


Author(s):  
Sergej V. Medvedevskikh ◽  
Vasilisa B. Baranovskaya ◽  
Maria Yu. Medvedevskikh ◽  
Maria P. Krasheninina ◽  
Anna S. Sergeeva

2021 ◽  
Vol 17 (1) ◽  
pp. 21-33
Author(s):  
A. S. Sergeeva ◽  
N. L. Vostrikova ◽  
M. Yu. Medvedevskikh

The paper considers the contribution of experts from the Laboratory of Metrology of Moisture Measurement and Reference Materials to the improvement of the food industry metrological assurance system. The information on the results of the development of forty types of reference materials (RM) for the composition of various nutrition, food staples and nutritional supplement in the period 2008-2020 is generalized. The development of each new RM type included preparation of the material, research for its stability and homogeneity, and determination of certified value with the appliance of State primary (GET 173) and secondary (GVET 176-1) standards, as well as primary reference measurement procedures and conducting the interlaboratory experiment for checking the applicability of the RM. The creation in 2008 of GET 173 was accompanied by the development of RMs for the composition of grains and dry milk product. The approval in 2010 of GVET 176-1 allowed to add in the RM the certified value for the mass fraction of nitrogen (protein). As a result of successful participation in comparisons, UNIIM got 6 items of calibration and measurement capabilities on measurements of mass fraction of nitrogen in glycine, milk powder, grain, egg powder, cereal and feed-stuff in the BIPM database. 35 types of RM for the composition of dairy and meat products, egg powder, infant food, oil and starch products together with the development of primary reference measurement procedures for measurement of fat, crude fat, ash and carbohydrates mass fraction were created between 2016 and 2019. Moreover, the RM for the composition of nutritional supplement (glycine, melamine, cystine) and dairy products for metrological assurance of IR-analysers as well as RM for the composition of reconstituted milk were developed for the control of measurement results by the enzyme-linked immunosorbent assay (ELISA). Developed RM were systemized on fields of the appliance of Technical regulations of Customs Union and the sectors of the international food triangle model. These RMs allow providing the measurement uniformity of the identification indicators and the nutritional value of food products and food staples.


Author(s):  
Craig M. Jackson ◽  
M. Peter Esnouf ◽  
David L. Duewer

Thrombin, the proteolytic enzyme that catalyzes the transformation of soluble fibrinogen to the polymerized fibrin clot, participates in multiple reactions in blood coagulation in addition to the clotting reaction. Although reference materials have existed for many years, structural characterization and measurement of biological activity have never been sufficient to permit claims of clear metrological traceability for the thrombin preparations. Our current state-of-the-art methods for protein characterization and determination of the catalytic properties of thrombin now make it practical to develop and characterize a metrologically acceptable reference material and reference measurement procedure for thrombin. Specifically, α-thrombin, the biologically produced protease formed during prothrombin activation, is readily available and has been extensively characterized. Dependences of thrombin proteolytic and peptide hydrolytic activities on a variety of substrates, pH, specific ions, and temperature are established, although variability remains for the kinetic parameters that describe thrombin enzymatic action. The roles of specific areas on the surface of the thrombin molecule (exosites) in substrate recognition and catalytic efficiency are described and characterized. It is opportune to develop reference materials of high metrological order and technical feasibility. In this article, we review the properties of α-thrombin important for its preparation and suggest an approach suitable for producing a reference material and a reference measurement procedure that is sensitive to thrombin’s catalytic competency on a variety of substrates.


2019 ◽  
Vol 107 (2) ◽  
pp. 141-147 ◽  
Author(s):  
Iga Zuba ◽  
Halina Polkowska-Motrenko

Abstract Primary reference measurement procedure for Cr determination in biological samples by radiochemical neutron activation analysis (RNAA) has been elaborated. The procedure is based on quantitative and selective separation of chromium from neutron irradiated sample by column chromatography using MnO2-Resin and determination of 51Cr by γ-ray spectrometry. Quality components have been incorporated into the RNAA method which makes it possible to meet the requirements of the definition of ratio primary reference measurement procedure. The usefulness of the elaborated procedure to assign the certified values for Cr in new certified reference material (CRMs) based on animal tissues is demonstrated. The tentative certified values for Cr have been proposed for: MODAS M-4 Cormorant Tissue and M-5 Cod Tissue CRMs.


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