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Biomedical subjects

B Teichmann

Publications and source records attributed to B Teichmann.

At least 55 records · Page 3Linked to original sources
PubMed1976

[Substances with carcinogenic activity (second edition) (author's transl)].

A list of substances with carcinogenic activity is presented as a 2nd supplemented edition. The list includes synonyma and test routes of the substances and should be looked as information material for employers and managers in various fields of industry, agriculture etc., hygiene and occupational and health service. The list is available as a paper-back (265 pages).

Animals↗
PubMed1975

[Spectrophotometric investigations on aflatoxin B1 and aflatoxin G1 (author's transl)].

UV-spectrophotometric and fluorescence-spectrophotometric investigations have been performed on the aflatoxins B1 and G1 with the aim of their unequivocal identification and quantitative estimation in the routine examination. The lower limits of the quantitative and semiquantitative estimations have been found to be 0,4 ng (thin layer chromatography, semiquantitative), Imug/ml (UV-spectroscopy) and 10 ng/ml (fluorescence spectroscopy) for the aflatoxin B1 and 0,3 ng (TLC, semiquantitative), 1 mug/ml (UV-spectroscopy) and 1 ng/ml (fluorescence spectroscopy). Quinine sulfate in 0.1 n sulfuric acid was successfully utilized as a convenient standard substance for quantitative fluorescence spectroscopic estimations of the aflatoxins B1 and G1. In an extensive series of estimations the fluorescence intensity of aflatoxin B1 in chloroform in the range of 0,01-10 mug/ml has been compared with that of equally concentrated solutions of quinine sulfate in sulfuric acid. The ratio of the intensities was 0.5 : 1(0.509 : 1). Similar comparative estimations of aflatoxin G1 in chloroform in the range of 0.001 bis 1 mug/ml and quinine sulfate in sulfuric acid resulted in a ratio of 5 : 1 (4.99 : 1). These ratios have been found using a fluorescence spectrophotometer Beckman SF 1078.

Aflatoxins↗
PubMed1974

[Test of cellulose and cellulose derivatives for carcinogenic activity in rats, mice and rabbits].

Activated cellulose, p-aminobenzylcellulose, p-hydroxybenzylcellulose, cellulose-m-aminobenzoxymethylether and cellulose-m-hydroxybenzoxymethylether which are used as highmolecular inert components for the preparation of immunoadsorbents, have been tested for carcinogenic activity in Wistar-rats and CBA-mice by the subcutaneous and intramuscular route of administration. In the same manner the coupling products have been tested in rats, mice and rabbits of diazotized p-aminobenzylcellulose and cellulose-m-aminobenzoxymethylether with a) human gammaglobulin [(cellulose-p-benzylether)-azogammaglobulin and (cellulose-m-benzoxymethylether)-azogammaglobulin respectively] and b) 1-(m-hydroxyphenyl)-flavozole derivatives of saccharides of the isomaltodextrin- and maltodextrin series [saccharide-1-(3 ft.-hydroxy-4 ft.-(resp.-6 ft.-or-2 ft.-) [cellulose-p-benzylether]-azophenyl)-flavazoles and saccharide-1-(3 ft.-hydroxy-4 ft.-(resp. -6 ft;-or-2 ft.-) [cellulose-m-benzoxymethylether]-azophenyl)-flavazoles with isomaltotriose, isomaltotetraose, isomaltopentaose, isomaltohexaose, isomaltooctaose, maltotriose, maltotetraose, maltopentaose, maltohexaose and maltooctaose as saccharide moieties]. No tumours were found in rabbits. No statistical significant difference could be stated between the tumour incidence of experimental animals and controls in the rat and mouse groups.

Animals↗