A Liquid Chromatography of Urine 8nd lts Clinical Application

A clinical liquid chromatograph, which consists of a completely automated liquid chromatograph combined with a microcomputer for diagnosis, and it's application to rerlal function analyses are described.The analytical rate for urinary ultraviolet-absorbing constituents using anion-exchange chro...

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Published inJapanese Journal of Clinical Chemistry Vol. 12; no. 1; pp. 54 - 62
Main Authors YAMAGATA, YOH, MIYAGI, HIROYUKI, TAKATA, YOSHINORI, MIURA, JUNKICHI
Format Journal Article
LanguageJapanese
Published Japan Society of Clinical Chemistry 1983
一般社団法人 日本臨床化学会
Online AccessGet full text
ISSN0370-5633
2187-4077
DOI10.14921/jscc1971b.12.1_54

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Abstract A clinical liquid chromatograph, which consists of a completely automated liquid chromatograph combined with a microcomputer for diagnosis, and it's application to rerlal function analyses are described.The analytical rate for urinary ultraviolet-absorbing constituents using anion-exchange chromatography was twelve samples per day.The reproducibilities of retention time, peak area and absorbance ratio (A23nm/A250nm) were less than 1%, 5%, and 6%, respectively for continuous five days running. Approximately 90 morning fasting urhes were obtained from adult“healthy”subjects, inpatients and outpatients.The urine samples were stored at-20°C until used, and defrosted at room temperature in a water bath at 37°C. They were centrifuged and then the supernatant was filtered through a 0.1μm pore size membrane filter for the chromatography. Each chromatographic peak was numbered in accordance with peak identification parameters such as retention time and absorbance ratio.These peaks were rearranged in the order of peak number instead of retention time. The reconstructed chromatograms were used to discuss kidney functions in three ways. Those are (1) comparison of chromatograqhic profiles between normal and abnormal subjects,(2) correlation between creatinine clearance and a chromatographic peak,(3) correlation analysis of peak area between two specific peaks. These methods as mentioned above seem to be usefull for the estimation of pathological phases and metabolic change induced by drugs and diseases.
AbstractList A clinical liquid chromatograph, which consists of a completely automated liquid chromatograph combined with a microcomputer for diagnosis, and it's application to rerlal function analyses are described.The analytical rate for urinary ultraviolet-absorbing constituents using anion-exchange chromatography was twelve samples per day.The reproducibilities of retention time, peak area and absorbance ratio (A23nm/A250nm) were less than 1%, 5%, and 6%, respectively for continuous five days running.Approximately 90 morning fasting urhes were obtained from adult“healthy”subjects, inpatients and outpatients.The urine samples were stored at-20°C until used, and defrosted at room temperature in a water bath at 37°C. They were centrifuged and then the supernatant was filtered through a 0.1μm pore size membrane filter for the chromatography.Each chromatographic peak was numbered in accordance with peak identification parameters such as retention time and absorbance ratio.These peaks were rearranged in the order of peak number instead of retention time.The reconstructed chromatograms were used to discuss kidney functions in three ways. Those are (1) comparison of chromatograqhic profiles between normal and abnormal subjects,(2) correlation between creatinine clearance and a chromatographic peak,(3) correlation analysis of peak area between two specific peaks.These methods as mentioned above seem to be usefull for the estimation of pathological phases and metabolic change induced by drugs and diseases.
Author YAMAGATA, YOH
MIURA, JUNKICHI
TAKATA, YOSHINORI
MIYAGI, HIROYUKI
Author_FL 三浦 順吉
宮城 宏行
山形 陽
高田 芳矩
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DocumentTitleAlternate 尿の液体クロマトグラフィーと臨床応用への試み
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References 2) K. M. Riggin, R. L. Aicorn and P. T. Kissinger: Clin. Ckem., 22,782 (1976
3) L.Pauling: Sience, 160,(1968
8) W. N. Keiley and J. B. Wymgaarden: Clin. Ckem., 16,707 (1970
14) 山辺武郎, 高井信治: 生産研究, 22,485 (1970
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20) 岡野光夫, 片岡一則, 五ノ井いつみ, 赤池敏宏, 桜井靖久, 高井信治, 妹尾学, 中村亘志, 松崎充, 橋本勉, 中尾功: 第23回液体クロマトグラフ研究会講演要旨集 (1980
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18) H.Miyagi, J. Miura, Y. Takata and S. Ganno: Pittsburgh Conference on Amalytical Chemistry and Applied Spectroscopy. Atlantic City, N. J., 1980
1) 多田啓也: アミノ酸代謝異常, 東京医学社 (東京) P32 (-976
9) D. S. Young, J. A. Apley and P. Goldmam: Clin. Chem., 17,765 (1971
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References_xml – reference: 15) R. E. Majors: Anal.Chem., 44, 1722 (1972)
– reference: 5) C. D. Scott: Clin. Chem., 14,521 (1968)
– reference: 1) 多田啓也: アミノ酸代謝異常, 東京医学社 (東京) P32 (-976)
– reference: 2) K. M. Riggin, R. L. Aicorn and P. T. Kissinger: Clin. Ckem., 22,782 (1976)
– reference: 12) T. D. Beardmore and W. N. Kelley: Clin. Chem., 17,795 (1971)
– reference: 18) H.Miyagi, J. Miura, Y. Takata and S. Ganno: Pittsburgh Conference on Amalytical Chemistry and Applied Spectroscopy. Atlantic City, N. J., 1980
– reference: 13) E. W. Lis and K. F. Dehackbeil: Clin. Chem., 16,714 (1970)
– reference: 14) 山辺武郎, 高井信治: 生産研究, 22,485 (1970)
– reference: 17) H. Miyagi, J. Miura, Y. Takata and S. Ganno: Clin. Chem., 25, 1617 (1979)
– reference: 10) R. L. Stevenson and C. A. Burtis: Clin. Chem., 17,774 (1971)
– reference: 6) J. M. Vavich and R. R. Howell: Clin. Chem., 16,702 (1970)
– reference: 8) W. N. Keiley and J. B. Wymgaarden: Clin. Ckem., 16,707 (1970)
– reference: 9) D. S. Young, J. A. Apley and P. Goldmam: Clin. Chem., 17,765 (1971)
– reference: 4) C. D. Scott, J. E. Attril and N. G. Anderson: Proc. Soc. Exp. Biol. Med., 125,181 (1967)
– reference: 11) R. LJolley and C. D. Scott: Clin. Chem., 16,687 (1970)
– reference: 7) D. S. Young: Clin. Chem, 16,687 (1970)
– reference: 19) H. Miyagi, J. Miura, Y. Takata, S.kamitake, S.Ganno and Y. Yamagata: J. Chromatgr., 239,733 (1982)
– reference: 16) 高橋浩, 高井信治, 大坪修, 稲生綱政: 生産研究, 40,122 (1978)
– reference: 20) 岡野光夫, 片岡一則, 五ノ井いつみ, 赤池敏宏, 桜井靖久, 高井信治, 妹尾学, 中村亘志, 松崎充, 橋本勉, 中尾功: 第23回液体クロマトグラフ研究会講演要旨集 (1980)
– reference: 3) L.Pauling: Sience, 160,(1968)
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