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  • 2024년 07월 03일(수) 13:30
 

  • P-ISSN1225-0163
  • E-ISSN2288-8985
  • SCOPUS, ESCI, KCI

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  • P-ISSN 1225-0163
  • E-ISSN 2288-8985

논문 상세

    Purity assignment of 17α-hydroxyprogesterone by mass balance method to establish traceability in measurement

    분석과학 / Analytical Science and Technology, (P)1225-0163; (E)2288-8985
    2019, v.32 no.6, pp.225-232
    https://doi.org/10.5806/AST.2019.32.6.225
    Hwa Shim Lee (Center for Bioanalysis, Division of Chemical and Medical Metrology, Korea Research Institute of Standards and Science)
    Su Jin Park (Cultural Heritage Conservation Science Center, National Research Institute of Cultural Heritage)
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    Abstract

    Traceability establishment in chemical measurements is a like a linkage established through an unbroken chain from the measured results to the international system (SI) of units. The primary process for traceability establishment is the purity assignment of a target material to be measured. In this study, we studied the purity assignment of 17α-hydroxyprogesterone (17-OHP). The presence of 17-OHP is indicative of congenital adrenal hyperplasia (CAH) and it builds up due to the deficiency of 21-hydroxylase and 11β-hydroxylase enzyme in the human blood. The purity assignment of 17-OHP was performed by the mass balance method, in which the impurities are categorized into four classes: total related structural impurities, water, residual organic solvents, and nonvolatiles/inorganics. The total related structural impurities were characterized by HPLC-UV; water content was determined by Karl-Fisher coulometer; and the total residual solvents and nonvolatiles/inorganics were determined by TGA. The purity of 17-OHP from a commercial manufacturer was calculated as 993.30 mg/g, and the expanded uncertainty was 0.58 mg/g. The proposed method was validated by uncertainty evaluation and comparing with the actual value of purity.

    keywords
    17-OHP, purity, traceability, mass balance method, CAH


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