Results 251 to 260 of about 200,401 (305)
Some of the next articles are maybe not open access.

A Critical Review of the Toxicology of Glutaraldehyde

Critical Reviews in Toxicology, 1992
Glutaraldehyde, a low molecular weight aldehyde, has been investigated for toxicity in humans and animals. Examination of this dialdehyde was indicated from previous studies with other aldehydes in which carcinogenicity of formaldehyde and toxicity of acetaldehyde and malonaldehyde have been disclosed.
David O Clarke, Kevin T Morgan
exaly   +3 more sources

Glutaraldehyde

Medical Journal of Australia, 1992
This article discusses the potential toxicity of glutaraldehyde, a chemical commonly used in endoscopy units. The literature review cites adverse health effects experienced by workers exposed to glutaraldehyde. The sampling methodology for glutaraldehyde relative to the Occupational Safety and Health standard for glutaraldehyde is presented.
Leon A Le Leu, MB BS, E Michael Shanahan
openaire   +4 more sources

Glutaraldehyde as a fixative in bioprostheses and drug delivery matrices

open access: yesBiomaterials, 1996
The use of glutaraldehyde as a fixative in bioprostheses and drug delivery matrices is reviewed. The chemistry of glutaraldehyde cross-linking and its effect on the biological performance of a number of bioprostheses such as tissue heart valves, vascular
A Jayakrishnan
exaly   +3 more sources

Synthesis, Characterization, and Antibacterial Activity of Cross-Linked Chitosan-Glutaraldehyde

open access: yesMarine Drugs, 2013
This present study deals with synthesis, characterization and antibacterial activity of cross-linked chitosan-glutaraldehyde. Results from this study indicated that cross-linked chitosan-glutaraldehyde markedly inhibited the growth of antibiotic ...
Bin Li   +2 more
exaly   +2 more sources

Modification of a catalase by glutaraldehyde

Applied Biochemistry and Microbiology, 2006
Polycondensation of a catalase (EC 1.11.1.6) with glutaraldehyde in order to stabilize the quaternary structure of an enzyme, maintain its activity, and protect it from thermal denaturation was studied. Synthesis showed a superequivalent utilization of the aldehyde groups relative to the catalase amine groups, as a result of the formation of ...
R N, Mishaeva   +2 more
openaire   +2 more sources

Glutaraldehyde for electron microscopy: a practical investigation of commercial glutaraldehydes and glutaraldehyde-storage conditions

The Histochemical Journal, 1995
The paper takes issue with the use by glutaraldehyde suppliers of the term 'for electron microscopy', and the common practice of researchers giving insufficient or no data about the glutaraldehyde they use. Investigation of 11 commercial glutaraldehydes recommended for electron microscopy shows that only three or four of them are adequate for this ...
openaire   +2 more sources

Subcellular localization of glutaraldehyde

Dental Traumatology, 1990
Abstract Glutaraldehyde (GA) has been proposed as an alternative to formocresol for pulpotomies in primary teeth and as an irrigant in root canal therapy. These studies were undertaken to determine if GA can associate with the nucleus of living cells, thereby posing a mutagenic threat.
D M, Ranly, L, Amstutz, D, Horn
openaire   +2 more sources

Glutaraldehyde Nonbiologic Monitors

Infection Control & Hospital Epidemiology, 1990
Glutaraldehyde was first synthesized by Harries and Tank in 1908, and first marketed as a chemosterilizer in 1963. Since that time, glutaraldehyde has been used extensively as a disinfectant and chemical sterilizing solution. Even though it is generally agreed that moist heat is the preferred method of sterilization for medical, dental and hospital ...
D J, Kleier, R E, Averbach
openaire   +2 more sources

Reaction of proteins with glutaraldehyde

Archives of Biochemistry and Biophysics, 1968
Abstract Glutaraldehyde was found to react with the α-amino groups of amino acids, the N-terminal amino groups of some peptides and the sulfhydryl group of cysteine. The phenolic and the imidazole rings of tyrosine and histidine derivatives were partially reactive.
A J, Habeeb, R, Hiramoto
openaire   +2 more sources

Home - About - Disclaimer - Privacy