Search PubMed⌕ Search

Biomedical subjects

A Kono

Publications and source records attributed to A Kono.

At least 127 records · Page 7Linked to original sources

[Evaluation of the optimum method of administration of a new antineoplastic agent, HCFU, based on the serum 5-FU concentration following oral administration].

The serum concentration of HCFU and its metabolites was clinically studied to obtain the most useful information for optimal methods of oral administration of a new anticancer agent. In this paper, the serum level of the only 5-FU among metabolites of HCFU was discussed. High-performance liquid chromatography was used as monitoring the agent. The serum level of 5-FU usually reached a maximum one hour after oral administration of 200mg HCFU and remained more than 0.2 to 0.3 microgram/ml for at least two hours. When administered 200mg HCFU every 6 hours (800mg/day), the serum level of 5-FU could be maintained more than 0.1 micrograms/ml for 24 hours. When administered 200mg three times after each meal (600mg/day), its level could be maintained more than 0.1 microgram/ml only for daytime, but not at night. Consequently, we suggest that the most favorable therapeutic oral administration of HCFU might be 200 mg every 6 hours (800mg/day) to maintain the serum level of 5-FU over 0.1 microgram/ml for 24 hours.

Administration, Oral↗

A new series of Tc-99m-labeled hepatobiliary tracers: N'-acyl- and N'-sulfonyl ethylenediamine-N,N-diacetic acids.

Various Tc-99m-labeled N'-substituted derivatives of ethylenediamine-N,N-diacetic acid (EDDA) are evaluated as hepatobiliary imaging agents. N-substituted aromatic acyl and aromatic sulfonyl derivatives of EDDA, labeled with Tc-99m, were administered to rabbits and golden hamsters, and the distribution indicated clearance by the hepatobiliary system. N'-aromatic sulfonyl EDDAs were labeled with Tc-99m by the SnCl2 method with more than 99% yield. Clearance of Tc-99m-p-toluenesulfonyl EDDA from the blood and the liver was as rapid as that of TC-99m N-(2,6-diethylphenylcarbamoylmethyl)iminodiacetic acid (Tc-99m benzenesulfonyl EDDA lowered urinary excretion. It is concluded that the sulfonyl EDDAs provide a fruitful source for Tc-99m-labeled hepatobiliary radiopharmaceuticals.

Animals↗

Complex formed from 3-hydroxy-4-formylpyridine, glutamic acid, and technetium--a possible cholescintigraphic agent.

In order to obtain a technetium-99m-labeled cholescintigraphic agent suitable for kit preparation, reactions of a variety of aromatic aldehydes, amino acids, and [99mTc] pertechnetate were examined under mild conditions. Aqueous solutions of the three reactants were heated in a boiling-water bath and the products analyzed by means of thin-layer chromatography for the formation of organic technetium complexes. 3-Hydroxy-4-formylpyridine (HFP) and 1-methyl-3-hydroxy-4-formylpyridinium chloride (N-Me-HFP) formed the complex with excellent yields, whereas 3-hydroxy-2-formylpyridine, 4-nitrosalicylaldehyde, salicylaldehyde, and isonicotinaldehyde did not. The complex is concluded to be the Tc-99m chelate of the Schiff base formed from the aldehyde and amino acbbits administered with the complex of HFP, glutamic acid and Tc-99m. The results indicate that it is promising as a cholescintigraphic agent.

Animals↗