clearheaded
Member
I understand how filtering works but when you bash a bunch together to fit through the 0.2 do u think that causes less aggregation? lol ya know like pinching a hose, still big enough for water to fit through but causes alot more pressure... 
you are making many assumptions... and very much could be making FAR more aggregates and maybe so large doesn't filter out much of any aggregates anyway??
think, would squeezing ur peptide through a 30 gauge needle super hard and fast help or hinder aggregate formation? ya know, normal pharma tech is to no even have a weak stream against a peptide...
commercial producers use SPECIALIZED filters esp if for human use...a filter is not a filter(not the same and are highly specialized depending on use in science), if worked with them in actual science u would know this..
anyway, I think you should test this theory of yours before talking too much more about it as MAY be causing more harm. I def dont know, but I can reason pretty well not every peptide is going to like filtering the someway.
but ya getting coli DNA and bacteria out would be good, heck even extra charcoal filter would be great and might aswell add some resin filtering?
but ya, would need to run some tests before can come to any conclusions here my man.
EDIT:
not saying in theory not a good idea for variety of reasons but u simply have no idea if its doing anything other than filtering bacteria and minor insolubles.
and dude again ur making huge leaps from sterility to aggregates here... lol yes they make things sterile for lab rats... so what?

you are making many assumptions... and very much could be making FAR more aggregates and maybe so large doesn't filter out much of any aggregates anyway??
think, would squeezing ur peptide through a 30 gauge needle super hard and fast help or hinder aggregate formation? ya know, normal pharma tech is to no even have a weak stream against a peptide...
commercial producers use SPECIALIZED filters esp if for human use...a filter is not a filter(not the same and are highly specialized depending on use in science), if worked with them in actual science u would know this..
anyway, I think you should test this theory of yours before talking too much more about it as MAY be causing more harm. I def dont know, but I can reason pretty well not every peptide is going to like filtering the someway.
but ya getting coli DNA and bacteria out would be good, heck even extra charcoal filter would be great and might aswell add some resin filtering?
but ya, would need to run some tests before can come to any conclusions here my man.
EDIT:
not saying in theory not a good idea for variety of reasons but u simply have no idea if its doing anything other than filtering bacteria and minor insolubles.
and dude again ur making huge leaps from sterility to aggregates here... lol yes they make things sterile for lab rats... so what?