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Quantification of Urinary Hemoglobin by an Immunological Method
Nobuko WATANABE*1, Yoshiaki HASHIMOTO, MD*2, Azusa FUTAMURA*3,
Fumiko MASHIGE*4 and Kazuhiko NAKAHARA, MD*5
The quantification method of urinary hemoglobin has not been established.
We examined whether a reagent(Eiken, Tokyo) used to immunologically assay
fecal hemoglobin could be utilized to quantify urinary hemoglobin. The
coefficients of variation were 2.2`3.0% in the reproducibility of one-run
assays using urine and 4.3`5.7% in that of multiple-run assays using the
standard sample of hemoglobin. Urinary hemoglobin was unstable and decreased
in a time- and temperature-dependent manner. However, addition of the hemoglobin
stabilization buffer(50mM phosphate buffer, pH6.4)(Eiken) to urine made
urinary hemoglobin stable. Urinary hemoglobin levels did not change significantly
when stored at 4 for 7 days or at |80 for 30 days. The hemoglobin
concentration(mean}SD) of urine showing 1{, 2{ and 3{ with a test strip
was 385}165(n30), 1070}499(n40) and 4130}2770ng/ml(n20), respectively.
Urinary hemoglobin did not correlate with urinary albumin, transferrin,
immunoglobulin G, N-acetyl-ภ-D-glucosaminidase nor ฟ 1 microglobulin.
These results suggest that this immunological method using the hemoglobin
stabilization buffer can be utilized for quantification of urinary hemoglobin,
which may provide clinically important information.
[Rinsho Byori 51 : 403`408, 2003]
*1Department of Clinical Laboratory Medicine, The University of Tokyo Hospital, Bunkyo-ku, Tokyo 113-8655
yKey Wordszurinary hemoglobin(AwOr)Cimmunological assay(ฦuwIช่@)Cquantification of urinary hemoglobin(AwOr่ส)Cchronic glomerulonephritis(ซ
ฬt)
๓t2002N926๚E๓2003N319๚
*1`5ๅwใwฎa@ธ(ง113-8655 sถๆ{ฝ7-3-1)