PubMed Health⌕ Search

Biomedical subjects

K S Webb

Publications and source records attributed to K S Webb.

9 recordsLinked to original sources
PubMed1978

Diffusion of nitrosamines through protective gloves.

A simple experimental demonstration of the permeability of protective gloves to volatile nitrosamines has been carried out. Rubber and polyvinyl chloride (PVC) gloves were turned inside out and the fingers filled with dilute solutions of nitrosamines in hexane. The outer faces of the fingers were washed with water at various times and the nitrosamine content of these washings determined. From these measurements the proportions of the various nitrosamines passing through the gloves were calculated. For both types of gloves N-nitrosopyrrolidine (NPYR) permeated the fingers most rapidly and to the greatest extent. Only a relatively small amount of N-nitrosodibutylamine (NDBA) was transmitted. It was also established that the rubber gloves themselves did not contain any of the common volatile nitrosamines; N-nitrosomethylphenylamine and N-nitrosodiphenylamine were also absent.

Chromatography, Gas↗
PubMed1977

Simple chemiluminescent detector for the screening of foodstuffs for the presence of volatile nitrosamines.

The construction and subsequent evaluation of an apparatus for the detection of trace amounts of nitrosamines is described. The apparatus consists of a gas chromatograph, a catalytic chamber to generate nitric oxide from eluted nitrosamines, and a chemiluminescent detector to measure the infra-red emission resulting from interaction of this gas with ozone. Examples of the use of the system for determining the nitrosamine concentration in food extracts and other materials are given.

Chromatography, Gas↗
PubMed1977

Correlation of apparent molecular weight and antigenicity of viral proteins: an SDS-page separation followed by acrylamide-agarose electrophoresis and immunoprecipitation.

A simple method is described which combines a sodium dodecyl sulfate polyacrylamide gel electrophoresis (SOS-PAGE) in the first demension with a second electrophoresis, at right angles to the first, into an agarose matrix. The proteins, separated by SDS-PAGE, are exposed to appropriate antisera after the second stage electrophoresis and immunoprecipitates form in the agarose corresponding to the relative electrophoretic mobilities of proteins in the first stage SDS-PAGE separation. The method thus provides a simple, reproducible means for correlating antigenicity with apparent molecular weight of proteins. The technique is qualtitative, but requires smaller quantities of antisera than more conventional immunoelectrophoretic methods such as rocket electrophoresis.

Antigens, Viral↗