Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Sign In to gain access to subscriptions and/or personal tools.
Textile Research Journal
This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Morris, N. M.
Right arrow Articles by Catalano, E. A.
Right arrow Search for Related Content
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

A Chemical Method for Determining Endotoxins in Cotton Dust and Lint Without Extraction

Nancy M. Morris

USDA ARS, Southern Regional Research Center, New Orleans, Louisiana 70124, U.S.A.

Edwin A. Catalano

USDA ARS, Southern Regional Research Center, New Orleans, Louisiana 70124, U.S.A.

Endotoxins present on cotton and released during carding have been implicated as a cause of byssinosis, a lung dysfunction found in some textile mill workers. The endotoxin content of cotton lints and dusts is frequently determined by the Limulus amoebocyte lysate (LAL) test. Although this test is a very effective measure of endotoxin in drugs and parenteral solutions, it is subject to interferences and false positives from other components in a more complex matrix such as cotton dust. To obviate these problems, we are investigating the quantitation of endotoxins by determining the 3- hydroxymyristic acid content of the sample. This fatty acid is reported to be unique to the lipid A portion of lipopolysaccharides from gram-negative bacteria and has been reported as a marker for endotoxin by others. A major source of error in deter mining endotoxins in cotton lints and dusts appears to lie with the extraction procedures used to remove the endotoxin from the cellulosic matrix. This is true for both chemical and LAL assays. To eliminate this time-consuming and error-producing step, we are investigating the direct hydrolysis of the endotoxin while still on the cellulosic matrix. The amount of 3-hydroxymyristic acid is determined by HPLC of the phenacyl ester and related to endotoxin content using a calibration curve prepared from E. agglom erans, generally the predominant bacterial species on cotton fiber. Endotoxin values for direct hydrolysis are from 10 to 40 times greater than those obtained for aqueous or phenol-water extracts of the same lints or dusts, implying that endotoxin from both intact and lysed bacteria may be quantitated. Reproducibility is improved over that obtained for extracts of cotton lints and dusts.

Textile Research Journal, Vol. 60, No. 7, 421-426 (1990)
DOI: 10.1177/004051759006000708


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?