Free Content Protein Binding of Glufosinate and Factors Affecting it Revealed by an Equilibrium Dialysis Technique

Authors: Hori Y.1; Koyama K.2; Fujisawa M.3; Nakajima M.3; Shimada K.4; Hirose Y.5; Kohda Y.2; Akuzawa H.6

Source: Journal of Analytical Toxicology, Volume 25, Number 6, September 2001 , pp. 439-442(4)

Publisher: Preston Publications

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Abstract:

We investigated the protein binding of glufosinate ammonium (GLF) and several factors affecting this binding using human serum albumin (HSA) and human volunteer serum under various conditions. The mean ratios of the free GLF (RFr-GLF) to 4% HSA were examined in the sera of patients described elsewhere at GLF levels from 1 mug/mL to 500 mug/mL; the range was found to be only from 0.80 to 0.88. Neither the incubation temperature nor buffers containing different chloride ion concentrations had any effect on the RFr-GLF to HSA. Moreover, the addition of heparin, glycoprotein-alpha1-acid (AAG), and sodium azide had no effect on the RFr-GLF. However, pH of the isotonic phosphate buffer and the addition of palmitic or oleic acid were seen to have an effect. In this study, the mean RFr-GLF to healthy human serum was 0.99. This high value was evidenced that GLF was rapidly excreted through the renal route.

Language: English

Document Type:

Affiliations: 1: Department of Analytical Chemistry, Niigata College of Pharmacy, Niigata, Japan; Emergency and Critical Care Medical Center, Niigata City General Hospital, Niigata, Japan, Correspondence Address: Emergency and Critical Care Medical Center, Niigat 2: Institute of Clinical Medicine, University of Tsukuba, Tsukuba, Japan 3: Department of Analytical Chemistry, Niigata College of Pharmacy, Niigata, Japan; Emergency and Critical Care Medical Center, Niigata City General Hospital, Niigata, Japan 4: Department of Analytical Chemistry, Niigata College of Pharmacy, Niigata, Japan 5: Emergency and Critical Care Medical Center, Niigata City General Hospital, Niigata, Japan 6: Forensic Science Laboratory of Gunma Police H.Q., Gunma, Japan

Publication date: 2001-09-01

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  • The Journal of Analytical Toxicology (JAT), established in 1977 and published 9 times a year, is the international source covering a broad range of clinical, forensic, and industrial laboratory topics regarding the isolation, identification, and quantitation of potentially toxic substances.

    With an emphasis on practical application, JAT articles provide improved and novel techniques for use in clinical, forensic, workplace, sports testing (doping), and other toxicology laboratories. Articles describe newly developed methods in immunoassay testing, gas chromatography, liquid chromatography, mass spectrometry, atomic absorption spectrometry, solid and liquid phase extraction techniques, and other analytical approaches. Worldwide readership includes toxicologists, pathologists, chemists, clinicians, researchers, and educators working in medical examiner and law enforcement laboratories, hospitals, university and independent analytical laboratories, as well as the drug manufacturing industry.

    Each year in October, we publish a special issue from the Society of Forensic Toxicologists.

    JAT, as determined by ISI Citation Index, is one of the two most referenced international journals in forensic science.

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