Endotoxins!

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Skydweller007

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So, who are the CN vendors that test for - or at the very least, guarantee against - endotoxin levels being too high? Additionally, I don’t understand how mass and purity are so prevalent in testing, but not endotoxins. Starting to see a lot of bad endotoxin tests pop up, so I’m wondering who’s out there that is doing the right thing with this?
 
Don't be confused this isn't like best manufacturing practices. This is pure macro economics. The market has essentially dictated mass and purity. So the vendors have responded with tests or the appearance of tests that the market has demanded. They aren't going to do anything beyond that.
 
You are exposed to more germs touching a door handle. Herd immunity
 
Skydweller007 said:
So, who are the CN vendors that test for - or at the very least, guarantee against - endotoxin levels being too high? Additionally, I don’t understand how mass and purity are so prevalent in testing, but not endotoxins. Starting to see a lot of bad endotoxin tests pop up, so I’m wondering who’s out there that is doing the right thing with this?
Janoshik has said samples almost never fail endotoxins and any that do are already reconstituted peptides and completely failed sterility testing. If sterility is a concern it’s best to just filter your peptides for peace of mind.
 
Endotoxins won't get caught in a filter from my understanding (though any bacteria that could produce endotoxins will), but they're also just not a concern for peptides based on the testing done.
 
RuggerPanda said:
Janoshik has said samples almost never fail endotoxins and any that do are already reconstituted peptides and completely failed sterility testing. If sterility is a concern it’s best to just filter your peptides for peace of mind.
Can you say more about sterility testing? Newbie here. Do you mean they have bacteria present?
 
Read the FDA guidelines for acceptable levels of endotoxins. It's higher than you think it is. No vendor has failed endotoxin testing based on those guidelines.
 
Airborne Daddy said:
No one does and few pass sterility testing....

Eh?

While no vendors test for endotoxins, it’s palpably false to say few pass sterility. Spend time on FPPG and you’ll see those third party test results showing many pass sterility.
 
... I know that... Sometimes I have to work with them in my work

I said "reducing the risk"

I did not said " eliminating the risk"

I'm the case of lyophilized peptides I'm have more concern about not being sterile than having some endo (they have but normally not astronomical units)

👍
 
Lyophilized said:
... I know that... Sometimes I have to work with them in my work

I said "reducing the risk"

I did not said " eliminating the risk"

I'm the case of lyophilized peptides I'm have more concern about not being sterile than having some endo (they have but normally not astronomical units)

👍
I believe I read UV can break up endotoxins. Is that correct?
 
No.

The best way is high temperatures. Not applicable to these type of peptides

I think the only way for peptides would be by chromatography separation with anion exchange column... Expensive..

You probably will have more risk and problems with the lack of sterility than endotoxins..

For example

If the vial has for example 10 Eu of endotoxins total and you dilute in 10mL of BAC water and inject only 1mL of that you are injecting just 1EU every 5 or 7 days... Not a big problem and in the vial the quantity of endotoxins will be the same. They don't grow.. The concentration will always be the same

But when we are talking about bacteria, fungus, yeasts... And if you don't filter or use a low quality BAC water, they can grow.

On day one you can have 10 or 50 live cells and after a week the double or more

And also depend of the type... Some bacteria for example are not tottaly pathogenic and you don't have so much risks and there are bacteria highly pathogenic and can put you in the hospital..

That's why I mention

Filtering is reducing risk and for that you must buy good filters and good sterile vials
 
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