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Bacterial endotoxin test: difference between revisions

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Revision 1 — 22:34, 27 Aug 2024
SarcopeniaSefa (talk)
create article — method stub
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Revision 2 — 13:20, 1 Sep 2024
LedeLeander (talk)
clarify that area percent is not mass percent
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11Endotoxin is not a living organism and is not removed by sterilisation. A preparation can be sterile and pyrogenic at the same time: autoclaving kills bacteria but leaves their lipopolysaccharide intact and biologically active. Endotoxin is the commonest but not the only pyrogen, and a separate rabbit pyrogen test exists for the wider class.{{r|usp151}} This is why endotoxin and [[Sterility testing|sterility]] are separate determinations answering separate questions.{{r|usp85}}11Endotoxin is not a living organism and is not removed by sterilisation. A preparation can be sterile and pyrogenic at the same time: autoclaving kills bacteria but leaves their lipopolysaccharide intact and biologically active. Endotoxin is the commonest but not the only pyrogen, and a separate rabbit pyrogen test exists for the wider class.{{r|usp151}} This is why endotoxin and [[Sterility testing|sterility]] are separate determinations answering separate questions.{{r|usp85}}
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+13== Methods ==
+14Three variants are recognised. The gel-clot method observes whether a firm clot forms at a given dilution and gives a limit result rather than a number. The turbidimetric method follows the increase in turbidity as the cascade proceeds and is quantitative. The chromogenic method measures release of a coloured product from a synthetic substrate and is also quantitative.{{r|usp85}}
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+16Recombinant factor C assays, which use a recombinant version of the initiating enzyme rather than crab-derived lysate, have been introduced and are increasingly accepted. They avoid the animal-derived reagent and are more specific, since they respond only to endotoxin and not to β-glucans.
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13== References ==18== References ==
14{{reflist}}19{{reflist}}