URINARY ALBUMIN DETERMINATION BY GEL-FILTRATION HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY
スポンサーリンク
概要
- 論文の詳細を見る
To determine urinary albumin in a minute amount, a gel-filtration high-performance liquid chromatographic procedure was newly established. When urine of a normal rat was eluted isocratically at 0.6 ml/min by 100 mM Na sulfate in 20 mM Na, K-phosphate (pH 7.4), approximately 6 hrs for complete elution of urinary peak-forming substances was needed. Retention time of albumin was found to be 22.9 min. To shorten the analytic time, 100 mM Na sulfate in 20 mM Na, K-phosphate (pH 7.4) was first used during a 30 min period for separation of albumin. A mixture of acetonitrile/the above solvent=3/7 (v/v) was then flushed to wash away the peak-forming substances. By this elution mode, the analytic time could be reduced to 3 hrs. When the validity of this procedure was tested, the detection limit of albumin was 0.04 μg/injection, and a linearity was observed between 0.2 and 50 μg/injection. Rats then received single subcutaneous injections of puromycin aminonucleoside, which is a nephrotoxic agent. The plasma albumin concentrations fell at 5, 10 and 15 days after the administration, and the urinary excretions of albumin rose from the 1st day up to the 15th day. The results denoted that our procedure could be a good evaluative tool for nephrotoxicity studies where albuminuria was manifested.
- 日本トキシコロジー学会の論文
- 1992-08-25
著者
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Hayashi T
Department Of Clinical Pharmacology And Toxicology Faculty Of Pharmceutical Sciences Health Sciences
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Hayashi Taiji
Drug Safety Research Laboratory Taiho Pharmaceutical.co. Ltd.
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Hayashi Taiji
Department Of Urology Kaizuka City Hospital
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Hayashi Taiji
Department Of Toxicology And Clinical Pharmacology Faculty Of Pharmaceutical Sciences Higashi-nippon
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Hayashi Taiji
Dept. Of Toxicology And Clinical Pharmacology Fac. Of Pharmaceutical Sciences Higashi-nippon-gakuen
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Hayashi Taiji
Research Laboratory Taiho Pharmaceutical Co. Ltd.
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SUDO Jun-ichi
Department of Pharmacology, Faculty of Medicine, University of Tokyo
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Tateyama Midori
Department Of Biochemisty Faculty Of Pharmaceutical Science Higashi Nippon Gakuen Universiy
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Tateyama Midori
Department Of Toxicology And Clinical Pharmacology Faculty Of Pharmaceutical Sciences Higashi-nippon
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Tateyama Midori
Department Of Biochemistry Faculty Of Pharmaceutical Sciences Higashi Nippon Gakuen University
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Hayashi Taiji
Department Of Clinical Pharmacology And Toxicology Faculty Of Pharmceutical Sciences Health Sciences
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SUZUE Toshihiko
Department of Toxicology and Clinical Pharmacology, Faculty of Pharmaceutical Sciences, Higashi-Nipp
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TERUI Jun
Department of Toxicology and Clinical Pharmacology, Faculty of Pharmaceutical Sciences, Higashi-Nipp
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Terui J
Health Sci. Univ. Hokkaido Hokkaido Jpn
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Terui J
Department Of Clinical Pharmacology And Toxicology Faculty Of Pharmaceutical Sciences Health Science
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Terui Jun
Department Of Clinical Pharmacology And Toxicology Faculty Of Pharmaceutical Sciences Health Science
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Sudo J
Department Of Clinical Pharmacology And Toxicology Faculty Of Pharmceutical Sciences Health Sciences
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Sudo Jun-ichi
Department Of Clinical Pharmacology And Toxicology Faculty Of Pharmaceutical Sciences Health Science
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Soyama Momoko
Department of Clinical Pharmacology and Toxicology, Faculty of Pharmceutical Sciences, Health Scienc
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Soyama Momoko
Department Of Clinical Pharmacology And Toxicology Faculty Of Pharmceutical Sciences Health Sciences
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Suzue Toshihiko
Department Of Toxicology And Clinical Pharmacology Faculty Of Pharmaceutical Sciences Higashi-nippon
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Suzue Toshihiko
Department Of Physiology School Of Medicine Tokyo Medical And Dental University
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