Development of a new measurement method for serum calcium with chlorophosphonazo-III

Author:

Hokazono Eisaku12,Osawa Susumu1,Nakano Tomota3,Kawamoto Yukari3,Oguchi Yuji3,Hotta Taeko4,Kayamori Yuzo4,Kang Dongchon45,Cho Yuichiro2,Shiba Kiyoko6,Sato Kenji2

Affiliation:

1. Department of Health Sciences, Division of Biological Science and Technology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582

2. Anatomy and Physiological Science Department of Life Sciences and Bio-informatics, Division of Biomedical Laboratory Sciences, Graduate School of Health Sciences, Tokyo Medical and Dental University, Tokyo

3. Clinical Department of Isehara Research Laboratory, Technology & Department, Division, Kanto Chemical Co. Inc., Kanagawa

4. Department of Clinical Chemistry and Laboratory Medicine, Kyushu University Hospital, Fukuoka

5. Department of Basic Medicine, Faculty of Medical Sciences, Kyushu University, Fukuoka

6. Department of Clinical Laboratory Medicine, School of Health Science Technology, Bunkyo Gakuin University, Tokyo, Japan

Abstract

Background Although serum calcium has been measured using the o-cresolphthalein complexone (oCPC) method in the clinical laboratory, this method still has some problems regarding linearity and reagent stability. We developed a new measurement procedure using chlorophosphonazo-III (CPZ-III: 2,7-bis (4-chloro-2-phosphonophenylazo) -1,8- dihydroxy-3, 6-naphthalenedisulphonic acid, disodium salt) as a chelator with an acid medium for serum calcium measurement. The present method showed better linearity and reagent stability compared with the oCPC method. Methods Characteristics were studied in optimized conditions measuring wavelength by absorption spectra analysis, and interference of protein and metals with Mg2+, Fe2+, Cu2+ and Zn2+. The method was applied to an automated analyser (7170; Hitachi High Technologies Corp). The measurement performance was evaluated for accuracy, precision, recovery rate, linearity and reagent stability with a comparison study against atomic absorption spectrophotometry (AAS). Results The within-run and between-run variations (coefficient of variation [CV]) were 0.92–1.01% and 0.75–1.43%, respectively. The linearity was 0–7.0 mmol/L. The comparison study obtained y = 1.002 x (AAS) – 0.10, S y/x = 0.18 mmol/L, n = 50. Reagent stability was at least 20 d at 4°C without daily calibration. Conclusion The new calcium measurement method in serum was demonstrated to have reliable and acceptable performances as a routine test in clinical laboratory.

Publisher

SAGE Publications

Subject

Clinical Biochemistry,General Medicine

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