Do You Filter Your Peptides Before Use?

What olis BA? And how much do you add to a vial?
BA is benzyl alcohol. The amount needed is based off total liquid amount currently in your vial. Anything I personally brew I use 1% to 3% compared to .9%. I use 3% in stuff I know will last for 3 months roughly. If I have 3ml of liquid I'll add 1 unit of BA if it's been in the fridge a while. Likely not needed but it makes me feel better.
 
This was an entertaining read through. Never thought GLP1 would get close to meso level shit talking. but here we are.

Anywho. Filtering is great, but imo unnecessary in regards to subq injections. I have however read of mitigating risk of immunogenicity/immune response rxns.
 
That doesn't make sense to me....are you suggesting the original vial wasn't sterile to begin with? If that's the case, it's not going to matter regardless.. Or are you concerned with residual?
If there are no contaminates in the vial then you need not filter. If there are any contaminants in there and you filter it right back into it, you are defeating the purpose.
 
This was an entertaining read through. Never thought GLP1 would get close to meso level shit talking. but here we are.

Anywho. Filtering is great, but imo unnecessary in regards to subq injections. I have however read of mitigating risk of immunogenicity/immune response rxns.
Potentially we were cross contaminated and EWB had to filter out the contaminate?
I think it was a good use of filtering 🙂
 
If there are no contaminates in the vial then you need not filter. If there are any contaminants in there and you filter it right back into it, you are defeating the purpose.
This seems way over the top for a subq injection. The vial began sterile, peptide powder enters with possible contaminats, powder is diluted with BAC, and then withdrawn into a syringe large enough to withdraw 99+% of what's in the vial now mixed, the liquid passes through a filter (appropriate size) and then goes back into a vial with worse case scenario, a miniscule amount (if any) of contaminant remaining in the vial now diluted further in BAC. Then, it's injected subq, where infection rates are extremely low. Just saying....
If there are no contaminates in the vial then you need not filter. If there are any contaminants in there and you filter it right back into it, you are defeating the purpose.
 
This seems way over the top for a subq injection. The vial began sterile, peptide powder enters with possible contaminats, powder is diluted with BAC, and then withdrawn into a syringe large enough to withdraw 99+% of what's in the vial now mixed, the liquid passes through a filter (appropriate size) and then goes back into a vial with worse case scenario, a miniscule amount (if any) of contaminant remaining in the vial now diluted further in BAC. Then, it's injected subq, where infection rates are extremely low. Just saying....
If you don't want to filter, dont. But you're absolutely wrong about putting it back into the same vial. The vial often doesn't begin sterile and your description of "peptide powder" being put into the vial implies you don't understand how the manufacturing process works.
 
This seems way over the top for a subq injection. The vial began sterile, peptide powder enters with possible contaminats, powder is diluted with BAC, and then withdrawn into a syringe large enough to withdraw 99+% of what's in the vial now mixed, the liquid passes through a filter (appropriate size) and then goes back into a vial with worse case scenario, a miniscule amount (if any) of contaminant remaining in the vial now diluted further in BAC. Then, it's injected subq, where infection rates are extremely low. Just saying....
If the peptide was contaminated to start off with, then, the original vial that it was in, is contaminated also. It is possible the vial was not sterile and had some kind of contamination itself and not the peptide. Once the peptide enters the contaminated vial, the peptide becomes contaminated as well. I, myself, usually, don't filter, but it is something that I'm starting to think about.
 
This seems way over the top for a subq injection. The vial began sterile, peptide powder enters with possible contaminats, powder is diluted with BAC, and then withdrawn into a syringe large enough to withdraw 99+% of what's in the vial now mixed, the liquid passes through a filter (appropriate size) and then goes back into a vial with worse case scenario, a miniscule amount (if any) of contaminant remaining in the vial now diluted further in BAC. Then, it's injected subq, where infection rates are extremely low. Just saying....
I don’t filter. I also don’t discourage anyone from doing it. The OP stated they were filtering and then returning the filtered liquid back to the original vial. I’m simply saying that to do so is pointless. That’s like filtering puddle water and then putting it back into the puddle before you drink it.
 
Ive never filtered. I use only sterile water now too, no BAC. Its not a bad idea, though. I actually have syringe filters too.
 
If you don't want to filter, dont. But you're absolutely wrong about putting it back into the same vial. The vial often doesn't begin sterile and your description of "peptide powder" being put into the vial implies you don't understand how the manufacturing process works.
Not exactly, it was just descriptive. I don't claim to be a peptide manufacturer, but I've read enough to understand the process.
I haven't seen a single one of these providers posting their manufacturing process, so I think your assumptions or mine about sterility are just that.
 
If the peptide was contaminated to start off with, then, the original vial that it was in, is contaminated also. It is possible the vial was not sterile and had some kind of contamination itself and not the peptide. Once the peptide enters the contaminated vial, the peptide becomes contaminated as well. I, myself, usually, don't filter, but it is something that I'm starting to think about.
I think for the most part, you and I are saying the same thing, and we're both making assumptions whether or not the vial was sterile. My point was this seems an over the top concern to put it back into the vial for a sub q injection, especially if filtered and mixed with BAC. Im not condemning those who take all the steps.... I'm in intensive care Healthcare and some of this just doesn't jive with my sensibilities.
 
I think for the most part, you and I are saying the same thing, and we're both making assumptions whether or not the vial was sterile. My point was this seems an over the top concern to put it back into the vial for a sub q injection, especially if filtered and mixed with BAC. Im not condemning those who take all the steps.... I'm in intensive care Healthcare and some of this just doesn't jive with my sensibilities.
I do understand your point being that the med is only delivered sub q. That's why I never filtered before. If there were any issues I assume it would happen more locally at the injection site. Then again, I am not a doctor.🤷‍♀️
 
This was an entertaining read through. Never thought GLP1 would get close to meso level shit talking. but here we are.

Anywho. Filtering is great, but imo unnecessary in regards to subq injections. I have however read of mitigating risk of immunogenicity/immune response rxns.
wait till I enter the chat Ja! meso looks like a book club
 
Not exactly, it was just descriptive. I don't claim to be a peptide manufacturer, but I've read enough to understand the process.
I haven't seen a single one of these providers posting their manufacturing process, so I think your assumptions or mine about sterility are just that.
I'm not assuming anything about sterility, I've seen all the failed sterility tests. They failed so often we just stopped testing it last year.
 
Reconstituted my first vial today, decided to filter, I think it went pretty well. 15 but determined concentration based on test data of 17.2mg and did 1.7mL, figured that gives me 6 X 2.5mg draws and the extra 0.2mL can account for the filter holdback or whatever else lost volume.
 
Can someone please kindly help educate on filtering....I've never filtered.....should I be filtering ...if so what do I need I've googled I'm confused
 
Can someone please kindly help educate on filtering....I've never filtered.....should I be filtering ...if so what do I need I've googled I'm confused

Can someone please kindly help educate on filtering....I've never filtered.....should I be filtering ...if so what do I need I've googled I'm confused
@Skidude posted a great video on page 2 of this thread. Start from the beginning of this thread and go to page 2. You're doing very good. You just have to dig a little deeper.
 
And left handed screwdrivers! I THINK they filter on the way into the syringe from the ampule, then you just switch the hypodermic an inject a cleaner fluid.
There is a filter on the end before the media goes into the syringe. Buying filters is cheaper. And I only filter the vitamin c serum in an ampule. I’m not talented and always smash the top when popping open..
 
After being advised on here to filter, I ordered some of these: https://peptidetest.com/products/ti...4mm-sterile-individually-wrapped-exp-10-31-27

Seems a lot of folks don't have any trouble without filtering, but I figure I might as well. One filter per vial is not too expensive relative to other costs. After seeing posts about people finding visible stuff in their vials, I was pretty set on going the filter route. Maybe my room air isn't suitable for a biolab, but I rarely see shit floating in it.

As far as ampule filtering goes, I have these for ampules: https://www.amazon.com/dp/B07D95XVN6 and I would definitely recommend filtering any ampule draws to avoid injecting yourself with glass.
 

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